"geneId"	"geneSymbol"	"DSI"	"DPI"	"diseaseId"	"diseaseName"	"diseaseType"	"diseaseClass"	"diseaseSemanticType"	"score"	"EI"	"YearInitial"	"YearFinal"	"NofPmids"	"NofSnps"	"source"
"1"	"A1BG"	"0.857"	"0.172"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1"	"A1BG"	"0.857"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.848484848484849"	"1998"	"2016"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2004"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1987"	"2000"	"2"	"0"	"PSYGENET"
"2"	"A2M"	"0.564"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1987"	"2000"	"2"	"0"	"PSYGENET"
"2"	"A2M"	"0.564"	"0.724"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"0.5"	"1983"	"1989"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2005"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2004"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2004"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"3"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"1991"	"2004"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2"	"A2M"	"0.564"	"0.724"	"C3279661"	"alpha-2-Macroglobulin Deficiency"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1989"	"1989"	"0"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"9"	"NAT1"	"0.564"	"0.724"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9"	"1996"	"2018"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.904761904761905"	"1996"	"2018"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0028796"	"Dermatitis, Occupational"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0086457"	"Industrial Dermatosis"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9"	"NAT1"	"0.564"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"0.75"	"1999"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.964285714285714"	"1996"	"2017"	"5"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.972972972972973"	"1995"	"2017"	"5"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.914285714285714"	"1996"	"2017"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.31"	"1"	"2010"	"2013"	"3"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2016"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0028796"	"Dermatitis, Occupational"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2006"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0086457"	"Industrial Dermatosis"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"0.5"	"1995"	"2009"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"0.875"	"1998"	"2012"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.918918918918919"	"1996"	"2017"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2016"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2002"	"2016"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"		"2002"	"2010"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2016"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2016"	"4"	"0"	"CTD_human"
"10"	"NAT2"	"0.466"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2016"	"4"	"0"	"CTD_human"
"12"	"SERPINA3"	"0.572"	"0.69"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"12"	"SERPINA3"	"0.572"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"12"	"SERPINA3"	"0.572"	"0.69"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"12"	"SERPINA3"	"0.572"	"0.69"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"12"	"SERPINA3"	"0.572"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2008"	"1"	"0"	"CTD_human"
"13"	"AADAC"	"0.713"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"15"	"AANAT"	"0.696"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"15"	"AANAT"	"0.696"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"15"	"AANAT"	"0.696"	"0.414"	"C0393770"	"Delayed Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0494410"	"Nonorganic Sleep Wake Cycle Disorders"	"group"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0751758"	"Advanced Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0751759"	"Non-24 Hour Sleep-Wake Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0751760"	"Shift-Work Sleep Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"15"	"AANAT"	"0.696"	"0.414"	"C0877792"	"Sleep Disorders, Circadian Rhythm"	"group"	"C10;C24;F03"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"16"	"AARS"	"0.667"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"16"	"AARS"	"0.667"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.44"	"0.75"	"1993"	"2016"	"1"	"2"	"GENOMICS_ENGLAND"
"16"	"AARS"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2015"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"16"	"AARS"	"0.667"	"0.345"	"C2750090"	"Charcot-Marie-Tooth Disease, Axonal, Type 2n"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2010"	"2016"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"16"	"AARS"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"16"	"AARS"	"0.667"	"0.345"	"C4225361"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2018"	"2"	"3"	"CTD_human;UNIPROT"
"18"	"ABAT"	"0.639"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0017168"	"Gastroesophageal reflux disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0023380"	"Lethargy"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0034933"	"Reflex, Abnormal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0151572"	"Reflex, Corneal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0151888"	"Hyporeflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0151889"	"Hyperreflexia"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0234146"	"Absent reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0234784"	"Reflex, Gag, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0241772"	"Reflex, Deep Tendon, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"1989"	"2012"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0277839"	"Hoffman's Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0277850"	"Reflex, Pendular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0278211"	"Reflex, Corneal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0342708"	"Gamma aminobutyric acid transaminase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1984"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"18"	"ABAT"	"0.639"	"0.276"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0522345"	"Reflex, Acoustic, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"18"	"ABAT"	"0.639"	"0.276"	"C0558845"	"Reflex, Ankle, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0558846"	"Reflex, Triceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0558847"	"Reflex, Biceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0576612"	"Reflex, Anal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0743002"	"Abnormal Deep Tendon Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751468"	"Bulbocavernosus Reflex, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751469"	"Bulbocavernousus Reflex Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751470"	"Palmo-Mental Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751471"	"Reflex, Anal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751472"	"Reflex, Ankle, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751473"	"Reflex, Ankle, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751474"	"Reflex, Biceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751475"	"Reflex, Biceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751476"	"Reflex, Gag, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751477"	"Reflex, Knee, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751478"	"Reflex, Knee, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751479"	"Reflex, Moro, Asymmetric"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751480"	"Reflex, Triceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751481"	"Reflex, Triceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"18"	"ABAT"	"0.639"	"0.276"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"18"	"ABAT"	"0.639"	"0.276"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"18"	"ABAT"	"0.639"	"0.276"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"19"	"ABCA1"	"0.484"	"0.793"	"C0039292"	"Tangier Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.989473684210526"	"1999"	"2017"	"19"	"22"	"CTD_human;ORPHANET;UNIPROT"
"19"	"ABCA1"	"0.484"	"0.793"	"C0342898"	"Apolipoprotein A-I deficiency"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"ORPHANET"
"19"	"ABCA1"	"0.484"	"0.793"	"C0473527"	"Hypoalphalipoproteinemias"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.48"	"1"	"2003"	"2011"	"0"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C0751544"	"Tangier Disease Neuropathy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"3"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2003"	"2013"	"2"	"1"	"CTD_human;UNIPROT"
"19"	"ABCA1"	"0.484"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C1704429"	"Hypoalphalipoproteinemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.96551724137931"	"1995"	"2015"	"6"	"7"	"CTD_human;ORPHANET;UNIPROT"
"19"	"ABCA1"	"0.484"	"0.793"	"C2931838"	"Familial HDL deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1999"	"2017"	"7"	"5"	"CTD_human;UNIPROT"
"19"	"ABCA1"	"0.484"	"0.793"	"C3165209"	"High density lipoprotein deficiency"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2005"	"6"	"5"	"UNIPROT"
"19"	"ABCA1"	"0.484"	"0.793"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"19"	"ABCA1"	"0.484"	"0.793"	"C3711531"	"Hdl Deficiency, Type 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"21"	"ABCA3"	"0.614"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0020192"	"Hyaline Membrane Disease"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"21"	"ABCA3"	"0.614"	"0.448"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C0035220"	"Respiratory Distress Syndrome, Newborn"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.38"	"0.625"	"2006"	"2014"	"0"	"0"	"ORPHANET"
"21"	"ABCA3"	"0.614"	"0.448"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"21"	"ABCA3"	"0.614"	"0.448"	"C0852283"	"Respiratory Distress Syndrome"	"disease"		"Disease or Syndrome"	"0.34"	"0.75"	"2006"	"2012"	"0"	"0"	"ORPHANET"
"21"	"ABCA3"	"0.614"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"21"	"ABCA3"	"0.614"	"0.448"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2014"	"0"	"2"	"ORPHANET"
"21"	"ABCA3"	"0.614"	"0.448"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"21"	"ABCA3"	"0.614"	"0.448"	"C1970456"	"Surfactant Metabolism Dysfunction, Pulmonary, 3"	"disease"	"C08"	"Disease or Syndrome"	"0.70"		"2004"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"22"	"ABCB7"	"0.72"	"0.241"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22"	"ABCB7"	"0.72"	"0.241"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"2014"	"6"	"0"	"GENOMICS_ENGLAND"
"22"	"ABCB7"	"0.72"	"0.241"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2014"	"6"	"0"	"GENOMICS_ENGLAND"
"22"	"ABCB7"	"0.72"	"0.241"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22"	"ABCB7"	"0.72"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"22"	"ABCB7"	"0.72"	"0.241"	"C1845028"	"ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA"	"disease"	"C10;C15;C16"	"Disease or Syndrome"	"0.73"	"1"	"1985"	"2015"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"22"	"ABCB7"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1985"	"2002"	"2"	"0"	"GENOMICS_ENGLAND"
"23"	"ABCF1"	"0.743"	"0.31"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23"	"ABCF1"	"0.743"	"0.31"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2008"	"1"	"1"	"UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.41"	"1"	"2010"	"2017"	"1"	"13"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"0.956521739130435"	"1998"	"2018"	"1"	"6"	"CTD_human;ORPHANET"
"24"	"ABCA4"	"0.52"	"0.793"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.96875"	"1997"	"2018"	"1"	"0"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C0271093"	"Stargardt's disease"	"phenotype"	"C11"	"Disease or Syndrome"	"0.98"	"1"	"1997"	"2018"	"19"	"177"	"CTD_human;ORPHANET;UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C1855465"	"STARGARDT DISEASE 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"1.00"	"0.91304347826087"	"1997"	"2018"	"19"	"290"	"CTD_human;ORPHANET;UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2018"	"19"	"177"	"UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C1858806"	"CONE-ROD DYSTROPHY 3 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"1997"	"2017"	"3"	"35"	"CTD_human;UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C1866422"	"RETINITIS PIGMENTOSA 19"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2017"	"0"	"8"	"CTD_human"
"24"	"ABCA4"	"0.52"	"0.793"	"C3495438"	"Macular Degeneration, Age-Related, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1997"	"2014"	"2"	"11"	"CTD_human;UNIPROT"
"24"	"ABCA4"	"0.52"	"0.793"	"C4282180"	"Juvenile macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.70"		"1997"	"2018"	"19"	"175"	"CTD_human;UNIPROT"
"25"	"ABL1"	"0.475"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1990"	"2011"	"0"	"0"	"ORPHANET"
"25"	"ABL1"	"0.475"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25"	"ABL1"	"0.475"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0015544"	"Failure to Thrive"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.888888888888889"	"1993"	"2018"	"2"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2012"	"2"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.80"	"0.969945355191257"	"1983"	"2018"	"3"	"21"	"CGI;CTD_human;ORPHANET"
"25"	"ABL1"	"0.475"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25"	"ABL1"	"0.475"	"0.69"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25"	"ABL1"	"0.475"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25"	"ABL1"	"0.475"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2014"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"0.935483870967742"	"1991"	"2016"	"0"	"0"	"ORPHANET"
"25"	"ABL1"	"0.475"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.952380952380952"	"1998"	"2016"	"0"	"0"	"CGI;ORPHANET"
"25"	"ABL1"	"0.475"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.97752808988764"	"1988"	"2018"	"2"	"0"	"CGI;CTD_human"
"25"	"ABL1"	"0.475"	"0.69"	"C4539857"	"CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"26"	"AOC1"	"0.727"	"0.483"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"26"	"AOC1"	"0.727"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"26"	"AOC1"	"0.727"	"0.483"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1989"	"1991"	"2"	"0"	"PSYGENET"
"28"	"ABO"	"0.491"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1991"	"1991"	"1"	"0"	"PSYGENET"
"28"	"ABO"	"0.491"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2018"	"2"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1981"	"1995"	"4"	"0"	"PSYGENET"
"28"	"ABO"	"0.491"	"0.828"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"28"	"ABO"	"0.491"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"29"	"ABR"	"0.773"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"29"	"ABR"	"0.773"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C0268603"	"Acetyl-CoA: carboxylase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"31"	"ACACA"	"0.552"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"31"	"ACACA"	"0.552"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"32"	"ACACB"	"0.701"	"0.414"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"32"	"ACACB"	"0.701"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"32"	"ACACB"	"0.701"	"0.414"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"32"	"ACACB"	"0.701"	"0.414"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"33"	"ACADL"	"0.727"	"0.276"	"C0220711"	"Long chain acyl-CoA dehydrogenase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"33"	"ACADL"	"0.727"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"GENOMICS_ENGLAND"
"34"	"ACADM"	"0.696"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"34"	"ACADM"	"0.696"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"34"	"ACADM"	"0.696"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"34"	"ACADM"	"0.696"	"0.379"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"34"	"ACADM"	"0.696"	"0.379"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"34"	"ACADM"	"0.696"	"0.379"	"C0085605"	"Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"34"	"ACADM"	"0.696"	"0.379"	"C0220710"	"Medium-chain acyl-coenzyme A dehydrogenase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1984"	"2017"	"16"	"72"	"CTD_human;ORPHANET;UNIPROT"
"34"	"ACADM"	"0.696"	"0.379"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"34"	"ACADM"	"0.696"	"0.379"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"34"	"ACADM"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1984"	"2001"	"8"	"0"	"GENOMICS_ENGLAND"
"35"	"ACADS"	"0.762"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"35"	"ACADS"	"0.762"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"35"	"ACADS"	"0.762"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"35"	"ACADS"	"0.762"	"0.276"	"C0342783"	"Deficiency of butyryl-CoA dehydrogenase"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.97"	"1"	"1989"	"2017"	"3"	"32"	"CTD_human;ORPHANET;UNIPROT"
"35"	"ACADS"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"36"	"ACADSB"	"0.752"	"0.241"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"36"	"ACADSB"	"0.752"	"0.241"	"C1864912"	"2-Methylbutyryl-CoA Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2000"	"2007"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"36"	"ACADSB"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"37"	"ACADVL"	"0.735"	"0.345"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"37"	"ACADVL"	"0.735"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1996"	"2016"	"3"	"2"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"37"	"ACADVL"	"0.735"	"0.345"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"37"	"ACADVL"	"0.735"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"37"	"ACADVL"	"0.735"	"0.345"	"C3887523"	"Very long chain acyl-CoA dehydrogenase deficiency"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.98"	"0.875"	"1985"	"2017"	"4"	"72"	"CTD_human;ORPHANET;UNIPROT"
"38"	"ACAT1"	"0.577"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"38"	"ACAT1"	"0.577"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C1536500"	"Deficiency of acetyl-CoA acetyltransferase"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1973"	"2016"	"4"	"26"	"CTD_human;ORPHANET;UNIPROT"
"38"	"ACAT1"	"0.577"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"38"	"ACAT1"	"0.577"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"38"	"ACAT1"	"0.577"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"39"	"ACAT2"	"0.72"	"0.31"	"C0342735"	"Cytosolic acetoacetyl-CoA thiolase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"40"	"ASIC2"	"0.743"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"40"	"ASIC2"	"0.743"	"0.276"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"41"	"ASIC1"	"0.681"	"0.448"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.969230769230769"	"1991"	"2018"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"43"	"ACHE"	"0.494"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0353676"	"Organophosphorus Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"1987"	"2013"	"3"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0700359"	"Organophosphate poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"1987"	"2013"	"3"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C3494247"	"Organothiophosphonate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"1987"	"2013"	"3"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C3494248"	"Organothiophosphate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"1987"	"2013"	"3"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"43"	"ACHE"	"0.494"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"47"	"ACLY"	"0.652"	"0.414"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"48"	"ACO1"	"0.663"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"48"	"ACO1"	"0.663"	"0.483"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"48"	"ACO1"	"0.663"	"0.483"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50"	"ACO2"	"0.636"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"50"	"ACO2"	"0.636"	"0.483"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50"	"ACO2"	"0.636"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50"	"ACO2"	"0.636"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"50"	"ACO2"	"0.636"	"0.483"	"C3281192"	"INFANTILE CEREBELLAR-RETINAL DEGENERATION"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2012"	"2017"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"50"	"ACO2"	"0.636"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"50"	"ACO2"	"0.636"	"0.483"	"C4225384"	"OPTIC ATROPHY 9"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"51"	"ACOX1"	"0.639"	"0.448"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51"	"ACOX1"	"0.639"	"0.448"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51"	"ACOX1"	"0.639"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51"	"ACOX1"	"0.639"	"0.448"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51"	"ACOX1"	"0.639"	"0.448"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"51"	"ACOX1"	"0.639"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51"	"ACOX1"	"0.639"	"0.448"	"C1849678"	"Peroxisomal ACYL-COA oxidase deficiency"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.92"	"1"	"1994"	"2014"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"51"	"ACOX1"	"0.639"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2012"	"2"	"0"	"CTD_human"
"51"	"ACOX1"	"0.639"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"52"	"ACP1"	"0.582"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1990"	"2018"	"1"	"0"	"PSYGENET"
"52"	"ACP1"	"0.582"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"52"	"ACP1"	"0.582"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"53"	"ACP2"	"0.857"	"0.207"	"C0268410"	"Acid Phosphatase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54"	"ACP5"	"0.577"	"0.69"	"C0020503"	"Hyperparathyroidism, Secondary"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"54"	"ACP5"	"0.577"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54"	"ACP5"	"0.577"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"54"	"ACP5"	"0.577"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"1994"	"1994"	"0"	"0"	"GENOMICS_ENGLAND"
"54"	"ACP5"	"0.577"	"0.69"	"C0432222"	"Spondyloenchondrodysplasia"	"disease"	"C05;C16;C20"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"54"	"ACP5"	"0.577"	"0.69"	"C1842763"	"SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION"	"disease"	"C05;C16;C20"	"Disease or Syndrome"	"0.60"		"1958"	"2017"	"2"	"11"	"CTD_human;UNIPROT"
"54"	"ACP5"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55"	"ACPP"	"0.63"	"0.517"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55"	"ACPP"	"0.63"	"0.517"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55"	"ACPP"	"0.63"	"0.517"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"58"	"ACTA1"	"0.59"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2012"	"3"	"0"	"CLINGEN"
"58"	"ACTA1"	"0.59"	"0.586"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.967741935483871"	"1999"	"2018"	"0"	"0"	"ORPHANET"
"58"	"ACTA1"	"0.59"	"0.586"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.50"	"0.916666666666667"	"1999"	"2016"	"2"	"1"	"GENOMICS_ENGLAND"
"58"	"ACTA1"	"0.59"	"0.586"	"C0270969"	"Zebra body myopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"58"	"ACTA1"	"0.59"	"0.586"	"C0410180"	"Eichsfeld type congenital muscular dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"58"	"ACTA1"	"0.59"	"0.586"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"58"	"ACTA1"	"0.59"	"0.586"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.74"	"0.75"	"1993"	"2011"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"58"	"ACTA1"	"0.59"	"0.586"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"58"	"ACTA1"	"0.59"	"0.586"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"58"	"ACTA1"	"0.59"	"0.586"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2012"	"3"	"0"	"CLINGEN"
"58"	"ACTA1"	"0.59"	"0.586"	"C1834339"	"Myopathy, Actin, Congenital, with Excess of Thin Myofilaments"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"		"1997"	"2015"	"13"	"15"	"CTD_human;UNIPROT"
"58"	"ACTA1"	"0.59"	"0.586"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C2750536"	"Nemaline Myopathy 3, With Intranuclear Rods"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"		"1999"	"2015"	"13"	"15"	"CTD_human;UNIPROT"
"58"	"ACTA1"	"0.59"	"0.586"	"C2750537"	"Myopathy, Actin, Congenital, With Cores"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"		"1999"	"2015"	"13"	"15"	"CTD_human;UNIPROT"
"58"	"ACTA1"	"0.59"	"0.586"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58"	"ACTA1"	"0.59"	"0.586"	"C3711389"	"Actin-Accumulation Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.92"	"1"	"1997"	"2017"	"13"	"24"	"CTD_human;ORPHANET;UNIPROT"
"58"	"ACTA1"	"0.59"	"0.586"	"C4225181"	"MYOPATHY, SCAPULOHUMEROPERONEAL"	"disease"		"Disease or Syndrome"	"0.70"		"1966"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"59"	"ACTA2"	"0.54"	"0.69"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"59"	"ACTA2"	"0.54"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"59"	"ACTA2"	"0.54"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2016"	"7"	"0"	"CLINGEN"
"59"	"ACTA2"	"0.54"	"0.69"	"C0026654"	"Moyamoya Disease"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2009"	"2018"	"0"	"0"	"ORPHANET"
"59"	"ACTA2"	"0.54"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"59"	"ACTA2"	"0.54"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.32"	"1"	"2009"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"59"	"ACTA2"	"0.54"	"0.69"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C1619692"	"Nephrogenic Fibrosing Dermopathy"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"59"	"ACTA2"	"0.54"	"0.69"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59"	"ACTA2"	"0.54"	"0.69"	"C2673186"	"Aortic Aneurysm, Familial Thoracic 6"	"disease"	"C14;C17;C23"	"Disease or Syndrome"	"0.60"		"2007"	"2017"	"3"	"12"	"CTD_human;UNIPROT"
"59"	"ACTA2"	"0.54"	"0.69"	"C2931384"	"Moyamoya disease 1"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"59"	"ACTA2"	"0.54"	"0.69"	"C3151201"	"MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME"	"disease"		"Disease or Syndrome"	"0.64"	"1"	"1999"	"2017"	"1"	"1"	"ORPHANET;UNIPROT"
"59"	"ACTA2"	"0.54"	"0.69"	"C3279690"	"MOYAMOYA DISEASE 5"	"disease"		"Disease or Syndrome"	"0.60"		"1999"	"2012"	"1"	"3"	"CTD_human;UNIPROT"
"59"	"ACTA2"	"0.54"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"60"	"ACTB"	"0.453"	"0.862"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"60"	"ACTB"	"0.453"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.50"		"1989"	"2012"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"60"	"ACTB"	"0.453"	"0.862"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60"	"ACTB"	"0.453"	"0.862"	"C0013393"	"Dysostoses"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"60"	"ACTB"	"0.453"	"0.862"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2001"	"2014"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0263579"	"Pigmented hairy epidermal nevus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"60"	"ACTB"	"0.453"	"0.862"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C1846331"	"Juvenile-onset dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"1993"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"60"	"ACTB"	"0.453"	"0.862"	"C1855722"	"Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation"	"disease"	"C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.75"	"1"	"1992"	"2017"	"1"	"19"	"CTD_human;ORPHANET;UNIPROT"
"60"	"ACTB"	"0.453"	"0.862"	"C1858042"	"Becker Nevus Syndrome"	"disease"	"C04;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60"	"ACTB"	"0.453"	"0.862"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60"	"ACTB"	"0.453"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"1999"	"2013"	"2"	"0"	"CTD_human"
"60"	"ACTB"	"0.453"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"70"	"ACTC1"	"0.656"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.84"	"0.75"	"2002"	"2014"	"0"	"1"	"CTD_human;GENOMICS_ENGLAND"
"70"	"ACTC1"	"0.656"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.66"	"0.833333333333333"	"1999"	"2017"	"11"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"70"	"ACTC1"	"0.656"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"70"	"ACTC1"	"0.656"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C0034951"	"Refractive Errors"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"70"	"ACTC1"	"0.656"	"0.414"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"70"	"ACTC1"	"0.656"	"0.414"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"70"	"ACTC1"	"0.656"	"0.414"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1999"	"2017"	"11"	"2"	"CLINGEN"
"70"	"ACTC1"	"0.656"	"0.414"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2005"	"0"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C1527310"	"Ametropia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"70"	"ACTC1"	"0.656"	"0.414"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"70"	"ACTC1"	"0.656"	"0.414"	"C2677506"	"Cardiomyopathy, Familial Hypertrophic, 11"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1998"	"2017"	"4"	"8"	"CTD_human;UNIPROT"
"70"	"ACTC1"	"0.656"	"0.414"	"C2748552"	"Atrial Septal Defect 5"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"1998"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"70"	"ACTC1"	"0.656"	"0.414"	"C3150681"	"CARDIOMYOPATHY, DILATED, 1R"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2017"	"1"	"3"	"UNIPROT"
"70"	"ACTC1"	"0.656"	"0.414"	"C3150682"	"LEFT VENTRICULAR NONCOMPACTION 4"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2008"	"1"	"3"	"UNIPROT"
"70"	"ACTC1"	"0.656"	"0.414"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"71"	"ACTG1"	"0.567"	"0.759"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.51"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"71"	"ACTG1"	"0.567"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"71"	"ACTG1"	"0.567"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0266551"	"Congenital coloboma of iris"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"71"	"ACTG1"	"0.567"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"71"	"ACTG1"	"0.567"	"0.759"	"C1855722"	"Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation"	"disease"	"C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.36"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"71"	"ACTG1"	"0.567"	"0.759"	"C1858172"	"Deafness, Autosomal Dominant 20"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1968"	"2016"	"7"	"9"	"CTD_human;UNIPROT"
"71"	"ACTG1"	"0.567"	"0.759"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"71"	"ACTG1"	"0.567"	"0.759"	"C3281235"	"BARAITSER-WINTER SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.60"		"1988"	"2015"	"1"	"9"	"CTD_human;UNIPROT"
"71"	"ACTG1"	"0.567"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"72"	"ACTG2"	"0.639"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"72"	"ACTG2"	"0.639"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"72"	"ACTG2"	"0.639"	"0.379"	"C0042781"	"Visceral Myopathy"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"4"	"10"	"UNIPROT"
"72"	"ACTG2"	"0.639"	"0.379"	"C0266833"	"Visceral Myopathy, Familial"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"72"	"ACTG2"	"0.639"	"0.379"	"C1608393"	"Megacystis microcolon intestinal hypoperistalsis syndrome"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.65"	"1"	"2013"	"2016"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"72"	"ACTG2"	"0.639"	"0.379"	"C1835084"	"Megaduodenum and-or Megacystis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"4"	"14"	"ORPHANET;UNIPROT"
"72"	"ACTG2"	"0.639"	"0.379"	"C1864996"	"Visceral Neuropathy, Familial, Autosomal Dominant"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"4"	"10"	"UNIPROT"
"72"	"ACTG2"	"0.639"	"0.379"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"81"	"ACTN4"	"0.548"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"1"	"2003"	"2016"	"0"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"81"	"ACTN4"	"0.548"	"0.621"	"C0333497"	"Segmental glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2000"	"2016"	"7"	"6"	"UNIPROT"
"81"	"ACTN4"	"0.548"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"86"	"ACTL6A"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"87"	"ACTN1"	"0.743"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"87"	"ACTN1"	"0.743"	"0.379"	"C3554663"	"BLEEDING DISORDER, PLATELET-TYPE, 15"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2014"	"2"	"6"	"CTD_human;UNIPROT"
"87"	"ACTN1"	"0.743"	"0.379"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"88"	"ACTN2"	"0.743"	"0.207"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"88"	"ACTN2"	"0.743"	"0.207"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"88"	"ACTN2"	"0.743"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"88"	"ACTN2"	"0.743"	"0.207"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"88"	"ACTN2"	"0.743"	"0.207"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"88"	"ACTN2"	"0.743"	"0.207"	"C2677338"	"Cardiomyopathy, Dilated, 1AA"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2004"	"2015"	"4"	"6"	"CTD_human;UNIPROT"
"88"	"ACTN2"	"0.743"	"0.207"	"C4225403"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2015"	"4"	"6"	"UNIPROT"
"90"	"ACVR1"	"0.573"	"0.552"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90"	"ACVR1"	"0.573"	"0.552"	"C0016037"	"Fibrodysplasia Ossificans Progressiva"	"disease"	"C05"	"Disease or Syndrome"	"1.00"	"1"	"1972"	"2018"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"90"	"ACVR1"	"0.573"	"0.552"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2014"	"2014"	"3"	"0"	"CGI;CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"90"	"ACVR1"	"0.573"	"0.552"	"C0027122"	"Myositis Ossificans"	"disease"	"C05"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"0"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"3"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90"	"ACVR1"	"0.573"	"0.552"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"3"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90"	"ACVR1"	"0.573"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92"	"ACVR2A"	"0.681"	"0.345"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"92"	"ACVR2A"	"0.681"	"0.345"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"92"	"ACVR2A"	"0.681"	"0.345"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C0175707"	"Asplenia Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.50"		"1997"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C0265357"	"Polysplenia Syndrome"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.50"		"1997"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"93"	"ACVR2B"	"0.639"	"0.345"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"93"	"ACVR2B"	"0.639"	"0.345"	"C3151057"	"HETEROTAXY, VISCERAL, 4, AUTOSOMAL"	"disease"		"Disease or Syndrome"	"0.80"		"1997"	"1999"	"1"	"2"	"CTD_human;UNIPROT"
"93"	"ACVR2B"	"0.639"	"0.345"	"C3178805"	"Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C3178806"	"Right Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.50"		"1997"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C3178807"	"Left Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"93"	"ACVR2B"	"0.639"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"94"	"ACVRL1"	"0.57"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"94"	"ACVRL1"	"0.57"	"0.621"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.51"		"2004"	"2016"	"1"	"0"	"CTD_human"
"94"	"ACVRL1"	"0.57"	"0.621"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"1.00"	"1"	"1996"	"2017"	"4"	"2"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"94"	"ACVRL1"	"0.57"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"94"	"ACVRL1"	"0.57"	"0.621"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"94"	"ACVRL1"	"0.57"	"0.621"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"94"	"ACVRL1"	"0.57"	"0.621"	"C1832529"	"HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.40"		"1996"	"2016"	"13"	"39"	"UNIPROT"
"94"	"ACVRL1"	"0.57"	"0.621"	"C1838163"	"OSLER-RENDU-WEBER SYNDROME 2"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.66"	"0.833333333333333"	"1996"	"2017"	"13"	"45"	"CTD_human;UNIPROT"
"94"	"ACVRL1"	"0.57"	"0.621"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.40"		"1976"	"2016"	"24"	"0"	"GENOMICS_ENGLAND"
"94"	"ACVRL1"	"0.57"	"0.621"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.50"	"0.964285714285714"	"1976"	"2018"	"24"	"1"	"GENOMICS_ENGLAND"
"94"	"ACVRL1"	"0.57"	"0.621"	"C3850148"	"Vascular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94"	"ACVRL1"	"0.57"	"0.621"	"C3852953"	"Pulmonary Arterial Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"95"	"ACY1"	"0.667"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"95"	"ACY1"	"0.667"	"0.448"	"C1835922"	"Aminoacylase 1 deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2006"	"2015"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"95"	"ACY1"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"98"	"ACYP2"	"0.815"	"0.138"	"C2750088"	"HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"1989"	"2008"	"2"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0037928"	"Spinal Cord Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1989"	"1994"	"2"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1989"	"1994"	"2"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0268124"	"Adenosine deaminase deficiency"	"disease"		"Disease or Syndrome"	"0.60"	"1"	"1980"	"2017"	"0"	"0"	"ORPHANET"
"100"	"ADA"	"0.494"	"0.793"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1989"	"1994"	"2"	"0"	"CTD_human"
"100"	"ADA"	"0.494"	"0.793"	"C0392607"	"Severe combined immunodeficiency due to adenosine deaminase deficiency"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.70"	"0.972222222222222"	"1980"	"2018"	"11"	"28"	"CTD_human;ORPHANET;UNIPROT"
"100"	"ADA"	"0.494"	"0.793"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"1996"	"2008"	"2"	"1"	"UNIPROT"
"100"	"ADA"	"0.494"	"0.793"	"C1863236"	"SCID Due to ADA Deficiency, Early-Onset"	"disease"		"Disease or Syndrome"	"0.40"		"1975"	"2017"	"11"	"37"	"UNIPROT"
"100"	"ADA"	"0.494"	"0.793"	"C1863239"	"Partial adenosine deaminase deficiency"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.63"	"1"	"1984"	"2001"	"11"	"30"	"CTD_human;UNIPROT"
"100"	"ADA"	"0.494"	"0.793"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"101"	"ADAM8"	"0.636"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"101"	"ADAM8"	"0.636"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"101"	"ADAM8"	"0.636"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"101"	"ADAM8"	"0.636"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"101"	"ADAM8"	"0.636"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"101"	"ADAM8"	"0.636"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C0406811"	"Reticulate acropigmentation of Kitamura"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.71"	"1"	"2014"	"2014"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"102"	"ADAM10"	"0.552"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"102"	"ADAM10"	"0.552"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2007"	"2017"	"1"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C3714534"	"dowling-degos disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"102"	"ADAM10"	"0.552"	"0.724"	"C3810041"	"ALZHEIMER DISEASE 18"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2014"	"2"	"2"	"CTD_human;UNIPROT"
"103"	"ADAR"	"0.586"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2006"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"103"	"ADAR"	"0.586"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"103"	"ADAR"	"0.586"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"103"	"ADAR"	"0.586"	"0.655"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"103"	"ADAR"	"0.586"	"0.655"	"C0406775"	"Symmetrical dyschromatosis of extremities"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.80"	"1"	"2003"	"2016"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"103"	"ADAR"	"0.586"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"103"	"ADAR"	"0.586"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C0795996"	"STRIATONIGRAL DEGENERATION, INFANTILE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"103"	"ADAR"	"0.586"	"0.655"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.38"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"103"	"ADAR"	"0.586"	"0.655"	"C3539013"	"AICARDI-GOUTIERES SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"1"	"11"	"UNIPROT"
"103"	"ADAR"	"0.586"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"104"	"ADARB1"	"0.656"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.333333333333333"	"2004"	"2014"	"3"	"0"	"PSYGENET"
"104"	"ADARB1"	"0.656"	"0.586"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"104"	"ADARB1"	"0.656"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"104"	"ADARB1"	"0.656"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"104"	"ADARB1"	"0.656"	"0.586"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"105"	"ADARB2"	"0.762"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"105"	"ADARB2"	"0.762"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"107"	"ADCY1"	"0.762"	"0.31"	"C1857809"	"DEAFNESS, AUTOSOMAL RECESSIVE 44"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"1"	"1"	"CLINGEN;CTD_human"
"108"	"ADCY2"	"0.762"	"0.207"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"108"	"ADCY2"	"0.762"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2018"	"1"	"11"	"PSYGENET"
"109"	"ADCY3"	"0.701"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"109"	"ADCY3"	"0.701"	"0.31"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"109"	"ADCY3"	"0.701"	"0.31"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"109"	"ADCY3"	"0.701"	"0.31"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"109"	"ADCY3"	"0.701"	"0.31"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"109"	"ADCY3"	"0.701"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2010"	"2017"	"1"	"2"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.818181818181818"	"2010"	"2017"	"2"	"2"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0393584"	"Benign Hereditary Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"111"	"ADCY5"	"0.645"	"0.448"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"111"	"ADCY5"	"0.645"	"0.448"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"111"	"ADCY5"	"0.645"	"0.448"	"C1847627"	"Dyskinesia, Familial, with Facial Myokymia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.70"		"1993"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"111"	"ADCY5"	"0.645"	"0.448"	"C1859098"	"Chorea, Benign Familial"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"111"	"ADCY5"	"0.645"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"112"	"ADCY6"	"0.743"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"112"	"ADCY6"	"0.743"	"0.379"	"C4225385"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 8"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"113"	"ADCY7"	"0.685"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"2"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"113"	"ADCY7"	"0.685"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"113"	"ADCY7"	"0.685"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"114"	"ADCY8"	"0.735"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"114"	"ADCY8"	"0.735"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"114"	"ADCY8"	"0.735"	"0.345"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2010"	"2013"	"4"	"0"	"CTD_human;PSYGENET"
"114"	"ADCY8"	"0.735"	"0.345"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114"	"ADCY8"	"0.735"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2002"	"2010"	"4"	"0"	"PSYGENET"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"4"	"0"	"PSYGENET"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"4"	"0"	"PSYGENET"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0026205"	"Miosis disorder"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.75"	"2002"	"2017"	"4"	"0"	"PSYGENET"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0268849"	"Overactive Detrusor"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0392156"	"Akathisia"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C0878773"	"Overactive Bladder"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"116"	"ADCYAP1"	"0.598"	"0.586"	"C3887612"	"Psychomotor Agitation"	"phenotype"	"C10;C23;F01"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"117"	"ADCYAP1R1"	"0.633"	"0.483"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"117"	"ADCYAP1R1"	"0.633"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"117"	"ADCYAP1R1"	"0.633"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"117"	"ADCYAP1R1"	"0.633"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"PSYGENET"
"118"	"ADD1"	"0.607"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.870967741935484"	"1995"	"2016"	"2"	"0"	"CTD_human"
"118"	"ADD1"	"0.607"	"0.517"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.951219512195122"	"1995"	"2018"	"0"	"0"	"CTD_human"
"118"	"ADD1"	"0.607"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"118"	"ADD1"	"0.607"	"0.517"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"119"	"ADD2"	"0.72"	"0.448"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"120"	"ADD3"	"0.659"	"0.483"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"120"	"ADD3"	"0.659"	"0.483"	"C2751938"	"Cerebral Palsy, Spastic Quadriplegic, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"120"	"ADD3"	"0.659"	"0.483"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"120"	"ADD3"	"0.659"	"0.483"	"C4310767"	"CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"123"	"PLIN2"	"0.645"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123"	"PLIN2"	"0.645"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123"	"PLIN2"	"0.645"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123"	"PLIN2"	"0.645"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123"	"PLIN2"	"0.645"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123"	"PLIN2"	"0.645"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"124"	"ADH1A"	"0.676"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1999"	"2013"	"5"	"1"	"PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9"	"1994"	"2015"	"3"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"1994"	"2018"	"8"	"4"	"CTD_human;PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0007107"	"Malignant neoplasm of larynx"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2006"	"2015"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0023055"	"Laryngeal neoplasm"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0031347"	"Pharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"1994"	"2016"	"8"	"0"	"CTD_human;PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"		"2008"	"2016"	"1"	"1"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0153405"	"Malignant neoplasm of pharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.41"	"0"	"2001"	"2016"	"1"	"1"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0349464"	"Wernicke-Korsakoff Syndrome"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0393756"	"Hangover from alcohol"	"phenotype"		"Sign or Symptom"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"125"	"ADH1B"	"0.525"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"125"	"ADH1B"	"0.525"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2006"	"2015"	"1"	"0"	"CTD_human"
"126"	"ADH1C"	"0.567"	"0.655"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"126"	"ADH1C"	"0.567"	"0.655"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2015"	"5"	"0"	"PSYGENET"
"126"	"ADH1C"	"0.567"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"1991"	"2018"	"6"	"4"	"CTD_human;PSYGENET"
"126"	"ADH1C"	"0.567"	"0.655"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"126"	"ADH1C"	"0.567"	"0.655"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"1994"	"2012"	"5"	"0"	"CTD_human;PSYGENET"
"126"	"ADH1C"	"0.567"	"0.655"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"126"	"ADH1C"	"0.567"	"0.655"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"127"	"ADH4"	"0.672"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"127"	"ADH4"	"0.672"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2015"	"4"	"0"	"PSYGENET"
"127"	"ADH4"	"0.672"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"127"	"ADH4"	"0.672"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"128"	"ADH5"	"0.659"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2006"	"1"	"0"	"PSYGENET"
"130"	"ADH6"	"0.834"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"131"	"ADH7"	"0.656"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"131"	"ADH7"	"0.656"	"0.448"	"C0007107"	"Malignant neoplasm of larynx"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0023055"	"Laryngeal neoplasm"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0031347"	"Pharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0153405"	"Malignant neoplasm of pharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131"	"ADH7"	"0.656"	"0.448"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2015"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"132"	"ADK"	"0.639"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"132"	"ADK"	"0.639"	"0.483"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"132"	"ADK"	"0.639"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"132"	"ADK"	"0.639"	"0.483"	"C3280381"	"HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"132"	"ADK"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"133"	"ADM"	"0.471"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2014"	"3"	"0"	"PSYGENET"
"133"	"ADM"	"0.471"	"0.724"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"133"	"ADM"	"0.471"	"0.724"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2010"	"2"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2008"	"2"	"0"	"PSYGENET"
"133"	"ADM"	"0.471"	"0.724"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.38"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"133"	"ADM"	"0.471"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"134"	"ADORA1"	"0.616"	"0.552"	"C0038525"	"Subarachnoid Hemorrhage"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0270192"	"Perinatal Subarachnoid Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0472383"	"Subarachnoid Hemorrhage, Spontaneous"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751530"	"Subarachnoid Hemorrhage, Aneurysmal"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0795688"	"Subarachnoid Hemorrhage, Intracranial"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"134"	"ADORA1"	"0.616"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"134"	"ADORA1"	"0.616"	"0.552"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.888888888888889"	"2003"	"2013"	"4"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1992"	"2008"	"3"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0021603"	"Sleep Initiation and Maintenance Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0030319"	"Panic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.857142857142857"	"2003"	"2016"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0033139"	"Primary Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.75"	"1997"	"2014"	"4"	"0"	"PSYGENET"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2006"	"3"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2006"	"3"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0086769"	"Panic Attacks"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2006"	"3"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0270541"	"Rebound Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0349255"	"Nonorganic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2010"	"4"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0393759"	"Transient Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0541798"	"Early Awakening"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751249"	"Chronic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751250"	"Psychophysiological Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751251"	"Secondary Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751252"	"Sleep Initiation Dysfunction"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C0917801"	"Sleeplessness"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2010"	"4"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"135"	"ADORA2A"	"0.537"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"136"	"ADORA2B"	"0.656"	"0.483"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"140"	"ADORA3"	"0.701"	"0.31"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"140"	"ADORA3"	"0.701"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"140"	"ADORA3"	"0.701"	"0.31"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"2"	"0"	"CTD_human"
"140"	"ADORA3"	"0.701"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"142"	"PARP1"	"0.432"	"0.862"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.943396226415094"	"2005"	"2018"	"1"	"0"	"CTD_human;UNIPROT"
"142"	"PARP1"	"0.432"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0015697"	"Arterial Fatty Streak"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2004"	"2008"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0022821"	"Kyphosis deformity of spine"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2005"	"2017"	"1"	"1"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0042842"	"Vitamin A Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0264956"	"Atheroma"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.96"	"2003"	"2018"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"1999"	"2018"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C2936351"	"Fibroatheroma"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"142"	"PARP1"	"0.432"	"0.862"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"142"	"PARP1"	"0.432"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"143"	"PARP4"	"0.762"	"0.276"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"143"	"PARP4"	"0.762"	"0.276"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2002"	"2"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2002"	"2"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"147"	"ADRA1B"	"0.663"	"0.414"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2000"	"2018"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0600519"	"Ventricular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C0600520"	"Left Ventricle Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"148"	"ADRA1A"	"0.548"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"148"	"ADRA1A"	"0.548"	"0.69"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.53"	"0.75"	"2001"	"2011"	"4"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2001"	"2011"	"4"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"0.5"	"1999"	"2012"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0030319"	"Panic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2004"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2007"	"2015"	"4"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0086769"	"Panic Attacks"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2006"	"2"	"0"	"PSYGENET"
"150"	"ADRA2A"	"0.633"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"150"	"ADRA2A"	"0.633"	"0.414"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C0010520"	"Cyanosis"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C1832841"	"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"151"	"ADRA2B"	"0.545"	"0.69"	"C1842852"	"EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2002"	"2014"	"0"	"1"	"CTD_human"
"151"	"ADRA2B"	"0.545"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"1995"	"1"	"0"	"PSYGENET"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.5"	"2002"	"2013"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.5"	"2002"	"2013"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"152"	"ADRA2C"	"0.707"	"0.207"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"152"	"ADRA2C"	"0.707"	"0.207"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"153"	"ADRB1"	"0.586"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"153"	"ADRB1"	"0.586"	"0.586"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.933333333333333"	"1992"	"2017"	"5"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.935483870967742"	"1992"	"2016"	"5"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1993"	"2018"	"2"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"5"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.39"	"0.777777777777778"	"1997"	"2008"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"1998"	"2008"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"5"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2004"	"2006"	"2"	"0"	"PSYGENET"
"153"	"ADRB1"	"0.586"	"0.586"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"1998"	"2012"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"5"	"0"	"CTD_human"
"153"	"ADRB1"	"0.586"	"0.586"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1995"	"2011"	"5"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0001849"	"AIDS Dementia Complex"	"disease"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.950310559006211"	"1993"	"2017"	"0"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"154"	"ADRB2"	"0.479"	"0.793"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.31"		"1988"	"2008"	"3"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.879310344827586"	"1997"	"2018"	"1"	"1"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0206019"	"HIV Encephalopathy"	"disease"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0243010"	"Viral Encephalitis"	"group"	"C02;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C0936243"	"HIV-1-Associated Cognitive Motor Complex"	"phenotype"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1997"	"4"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"154"	"ADRB2"	"0.479"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"0"	"2001"	"2006"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.842696629213483"	"1995"	"2016"	"0"	"1"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"155"	"ADRB3"	"0.558"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"155"	"ADRB3"	"0.558"	"0.552"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"155"	"ADRB3"	"0.558"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"156"	"GRK2"	"0.58"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"156"	"GRK2"	"0.58"	"0.517"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.904761904761905"	"1994"	"2017"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.888888888888889"	"1994"	"2017"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"156"	"GRK2"	"0.58"	"0.517"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"156"	"GRK2"	"0.58"	"0.517"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"157"	"GRK3"	"0.672"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2004"	"2010"	"6"	"0"	"CTD_human;PSYGENET"
"157"	"GRK3"	"0.672"	"0.448"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"157"	"GRK3"	"0.672"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"157"	"GRK3"	"0.672"	"0.448"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"157"	"GRK3"	"0.672"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"157"	"GRK3"	"0.672"	"0.448"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"157"	"GRK3"	"0.672"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"158"	"ADSL"	"0.685"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"158"	"ADSL"	"0.685"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1989"	"2005"	"1"	"0"	"CTD_human"
"158"	"ADSL"	"0.685"	"0.379"	"C0268126"	"Adenylosuccinate lyase deficiency (disorder)"	"disease"	"C16;C18;F03"	"Disease or Syndrome"	"0.76"	"1"	"1984"	"2017"	"10"	"20"	"CTD_human;ORPHANET;UNIPROT"
"158"	"ADSL"	"0.685"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"158"	"ADSL"	"0.685"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1993"	"1993"	"0"	"0"	"GENOMICS_ENGLAND"
"159"	"ADSS"	"0.815"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"163"	"AP2B1"	"0.773"	"0.241"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"165"	"AEBP1"	"0.785"	"0.345"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"166"	"AES"	"0.752"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"173"	"AFM"	"0.72"	"0.379"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"0.818181818181818"	"1982"	"2016"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2001"	"2013"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C1863080"	"ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF"	"phenotype"		"Finding"	"0.40"		"1993"	"2004"	"0"	"1"	"ORPHANET"
"174"	"AFP"	"0.502"	"0.724"	"C1863081"	"alpha-Fetoprotein Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2005"	"2009"	"0"	"2"	"CTD_human;ORPHANET"
"174"	"AFP"	"0.502"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.958333333333333"	"1980"	"2018"	"3"	"0"	"CTD_human"
"174"	"AFP"	"0.502"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"175"	"AGA"	"0.627"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"175"	"AGA"	"0.627"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"175"	"AGA"	"0.627"	"0.724"	"C0268225"	"Aspartylglucosaminuria"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.945945945945946"	"1983"	"2018"	"6"	"42"	"CTD_human;ORPHANET;UNIPROT"
"175"	"AGA"	"0.627"	"0.724"	"C2931840"	"Aspartylglucosamidase (AGA) deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2001"	"6"	"13"	"ORPHANET;UNIPROT"
"175"	"AGA"	"0.627"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"176"	"ACAN"	"0.562"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.39"	"0.888888888888889"	"1998"	"2014"	"1"	"0"	"CTD_human"
"176"	"ACAN"	"0.562"	"0.724"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"176"	"ACAN"	"0.562"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"176"	"ACAN"	"0.562"	"0.724"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"176"	"ACAN"	"0.562"	"0.724"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"176"	"ACAN"	"0.562"	"0.724"	"C1842149"	"Spondyloepiphyseal Dysplasia, Kimberley Type"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.61"	"1"	"2006"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"176"	"ACAN"	"0.562"	"0.724"	"C2748544"	"Spondyloepimetaphyseal Dysplasia, Aggrecan Type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"176"	"ACAN"	"0.562"	"0.724"	"C3665488"	"Familial Osteochondritis Dissecans"	"disease"	"C05"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"176"	"ACAN"	"0.562"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"177"	"AGER"	"0.472"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.47"	"1"	"2003"	"2014"	"1"	"7"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.38"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2004"	"2012"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.36"	"0.75"	"2005"	"2014"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"3"	"PSYGENET"
"177"	"AGER"	"0.472"	"0.724"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0262593"	"Peripheral Nerve Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"177"	"AGER"	"0.472"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"178"	"AGL"	"0.681"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"178"	"AGL"	"0.681"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"178"	"AGL"	"0.681"	"0.448"	"C0017922"	"Glycogen Storage Disease Type III"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.973684210526316"	"1988"	"2017"	"4"	"74"	"CTD_human;ORPHANET;UNIPROT"
"178"	"AGL"	"0.681"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"178"	"AGL"	"0.681"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2010"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"178"	"AGL"	"0.681"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"178"	"AGL"	"0.681"	"0.448"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"178"	"AGL"	"0.681"	"0.448"	"C1968739"	"Glycogen Storage Disease IIIA"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1992"	"2017"	"1"	"12"	"UNIPROT"
"178"	"AGL"	"0.681"	"0.448"	"C1968740"	"Glycogen Storage Disease IIIB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1996"	"2014"	"1"	"7"	"UNIPROT"
"178"	"AGL"	"0.681"	"0.448"	"C1968741"	"Glycogen Storage Disease IIIC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2007"	"2010"	"1"	"2"	"UNIPROT"
"178"	"AGL"	"0.681"	"0.448"	"C1968742"	"Glycogen Storage Disease IIID"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"178"	"AGL"	"0.681"	"0.448"	"C2936915"	"Amylo-1,6-glucosidase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"178"	"AGL"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"181"	"AGRP"	"0.652"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.866666666666667"	"1997"	"2017"	"0"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C0010038"	"Corneal Opacity"	"phenotype"	"C11"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.31"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2002"	"3"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.33"	"0.666666666666667"	"1999"	"2014"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"182"	"JAG1"	"0.467"	"0.724"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.80"	"1"	"1999"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"182"	"JAG1"	"0.467"	"0.724"	"C0085280"	"Alagille Syndrome"	"disease"	"C06;C14;C16"	"Congenital Abnormality"	"0.80"	"0.925925925925926"	"1995"	"2018"	"15"	"13"	"CTD_human;UNIPROT"
"182"	"JAG1"	"0.467"	"0.724"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C1857761"	"Alagille Syndrome 2"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C1956125"	"Alagille Syndrome 1"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"2017"	"15"	"46"	"CTD_human;UNIPROT"
"182"	"JAG1"	"0.467"	"0.724"	"C2930797"	"Hepatic ductular hypoplasia"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2011"	"3"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"182"	"JAG1"	"0.467"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"182"	"JAG1"	"0.467"	"0.724"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0002063"	"Alkalosis"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0002949"	"Aneurysm, Dissecting"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0003460"	"Anuria"	"phenotype"	"C12;C13"	"Disease or Syndrome"	"0.40"		"1996"	"1996"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0003486"	"Aortic Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1991"	"1991"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.978723404255319"	"1998"	"2018"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2008"	"2"	"0"	"PSYGENET"
"183"	"AGT"	"0.406"	"0.862"	"C0007192"	"Cardiomyopathy, Alcoholic"	"disease"	"C14;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.953488372093023"	"1996"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0011071"	"Sudden death"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"183"	"AGT"	"0.406"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"183"	"AGT"	"0.406"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.865384615384615"	"1996"	"2016"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.54"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2016"	"4"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.55"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2017"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.54"	"0.75"	"1999"	"2012"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2010"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2016"	"18"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.96551724137931"	"1992"	"2018"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.961538461538462"	"1992"	"2018"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"		"2004"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.941952506596306"	"1980"	"2018"	"74"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020540"	"Malignant Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"1989"	"2017"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020544"	"Renal hypertension"	"disease"	"C12;C13;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2016"	"6"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.40"		"1990"	"1997"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2016"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.886363636363636"	"1995"	"2016"	"4"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1992"	"2011"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.54"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.930232558139535"	"1992"	"2017"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1991"	"2009"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1992"	"2003"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0029944"	"Drug Overdose"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0030922"	"Peptic Ulcer Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.35"		"1993"	"2008"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1979"	"2007"	"5"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0035344"	"Retinopathy of Prematurity"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.31"	"0"	"2013"	"2015"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.96"	"1988"	"2018"	"0"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2014"	"6"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2017"	"4"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1992"	"2011"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0266313"	"Allanson Pantzar McLeod syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.71"	"1"	"2001"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"183"	"AGT"	"0.406"	"0.862"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0340643"	"Dissection of aorta"	"disease"	"C14"	"Pathologic Function"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2016"	"4"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.35"	"0.8"	"1998"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"1997"	"2002"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2016"	"18"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.38"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2016"	"4"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1992"	"2011"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"2011"	"3"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C2678367"	"Renal Tubular Dysgenesis With Choanal Atresia And Athelia"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"183"	"AGT"	"0.406"	"0.862"	"C2936380"	"Neointima"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C2936381"	"Neointima Formation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"183"	"AGT"	"0.406"	"0.862"	"C3850148"	"Vascular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C3852953"	"Pulmonary Arterial Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4277533"	"Dissection, Blood Vessel"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"183"	"AGT"	"0.406"	"0.862"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2004"	"2009"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.35"	"0.8"	"2004"	"2010"	"2"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2014"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.898148148148148"	"1994"	"2017"	"4"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.60"	"0.923076923076923"	"1997"	"2015"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.980392156862745"	"1994"	"2018"	"0"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0266313"	"Allanson Pantzar McLeod syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.70"		"2005"	"2012"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"185"	"AGTR1"	"0.454"	"0.759"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"185"	"AGTR1"	"0.454"	"0.759"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"185"	"AGTR1"	"0.454"	"0.759"	"C2678367"	"Renal Tubular Dysgenesis With Choanal Atresia And Athelia"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"185"	"AGTR1"	"0.454"	"0.759"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"186"	"AGTR2"	"0.554"	"0.621"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2002"	"2013"	"5"	"0"	"CLINGEN;ORPHANET"
"186"	"AGTR2"	"0.554"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2002"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"189"	"AGXT"	"0.624"	"0.621"	"C0268164"	"Primary hyperoxaluria, type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2018"	"24"	"162"	"CTD_human;ORPHANET;UNIPROT"
"189"	"AGXT"	"0.624"	"0.621"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"189"	"AGXT"	"0.624"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"190"	"NR0B1"	"0.512"	"0.621"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"190"	"NR0B1"	"0.512"	"0.621"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"1995"	"2012"	"1"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"190"	"NR0B1"	"0.512"	"0.621"	"C0220766"	"Congenital hypoplasia of adrenal gland"	"disease"		"Congenital Abnormality"	"0.80"	"1"	"1995"	"2017"	"16"	"8"	"ORPHANET;UNIPROT"
"190"	"NR0B1"	"0.512"	"0.621"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"0.953125"	"1995"	"2017"	"1"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1999"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"190"	"NR0B1"	"0.512"	"0.621"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"1.00"	"0.985915492957746"	"1982"	"2018"	"23"	"26"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"190"	"NR0B1"	"0.512"	"0.621"	"C0432475"	"XX males"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"190"	"NR0B1"	"0.512"	"0.621"	"C0795887"	"Complex Glycerol Kinase Deficiency"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2007"	"2"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1995"	"1995"	"1"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C1848296"	"DOSAGE-SENSITIVE SEX REVERSAL"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"0"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C1868690"	"Hypoadrenocorticism, familial"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C2936419"	"46, XX Testicular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"190"	"NR0B1"	"0.512"	"0.621"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"190"	"NR0B1"	"0.512"	"0.621"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1995"	"1995"	"1"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C4505291"	"Xp21 Contiguous Gene Deletion Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"190"	"NR0B1"	"0.512"	"0.621"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"191"	"AHCY"	"0.627"	"0.621"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"191"	"AHCY"	"0.627"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0268621"	"Hepatic methionine adenosyltransferase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C1847720"	"Glycine N-Methyltransferase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"191"	"AHCY"	"0.627"	"0.621"	"C3151058"	"S-adenosylhomocysteine hydrolase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2004"	"2016"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"191"	"AHCY"	"0.627"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"191"	"AHCY"	"0.627"	"0.621"	"C4048705"	"Hypermethioninemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0005683"	"Urinary Bladder Calculi (disorder)"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"1993"	"2017"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0020578"	"Hyperventilation"	"phenotype"	"C08;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2016"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.92"	"1990"	"2018"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2002"	"2016"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0037997"	"Splenic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2002"	"2006"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0041955"	"Ureteral Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"1996"	"2011"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0153619"	"Malignant neoplasm of ureter"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0162834"	"Hyperpigmentation"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0236811"	"Chronobiology Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0242706"	"Hyperoxia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2002"	"2016"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0559470"	"Allergy to peanuts"	"phenotype"	"C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.966101694915254"	"1993"	"2017"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0700501"	"Congenital nystagmus"	"disease"	"C10;C11;C16"	"Congenital Abnormality"	"0.50"		"1997"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0813142"	"Circadian Rhythm Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0887800"	"Psychogenic Inversion of Circadian Rhythm"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"2"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C2931037"	"Pancreatic cancer, adult"	"disease"	"C04;C06;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"196"	"AHR"	"0.462"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.31"		"2002"	"2006"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C1859878"	"Alopecia-Mental Retardation Syndrome 1"	"disease"	"C10;C17;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"197"	"AHSG"	"0.577"	"0.69"	"C2931280"	"Perniola Krajewska Carnevale syndrome"	"disease"	"C10;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"199"	"AIF1"	"0.598"	"0.655"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"199"	"AIF1"	"0.598"	"0.655"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"203"	"AK1"	"0.735"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"203"	"AK1"	"0.735"	"0.379"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"203"	"AK1"	"0.735"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"203"	"AK1"	"0.735"	"0.379"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"203"	"AK1"	"0.735"	"0.379"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"203"	"AK1"	"0.735"	"0.379"	"C2675459"	"Adenylate Kinase Deficiency, Hemolytic Anemia Due To"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1989"	"2005"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"203"	"AK1"	"0.735"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"204"	"AK2"	"0.685"	"0.345"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.41"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"2"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0272167"	"Reticular dysgenesis"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.74"	"0.75"	"2009"	"2011"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"204"	"AK2"	"0.685"	"0.345"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C1282908"	"De Vaal's syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"204"	"AK2"	"0.685"	"0.345"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"204"	"AK2"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"204"	"AK2"	"0.685"	"0.345"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"205"	"AK4"	"0.773"	"0.276"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"205"	"AK4"	"0.773"	"0.276"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2003"	"2016"	"5"	"0"	"PSYGENET"
"207"	"AKT1"	"0.355"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.987012987012987"	"1999"	"2018"	"2"	"1"	"CGI;CTD_human;UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.42"	"1"	"2002"	"2016"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2018"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.893617021276596"	"2002"	"2018"	"0"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.45"	"1"	"2004"	"2016"	"0"	"1"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"5"	"0"	"PSYGENET"
"207"	"AKT1"	"0.355"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"5"	"0"	"PSYGENET"
"207"	"AKT1"	"0.355"	"0.862"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"0"	"0"	"ORPHANET"
"207"	"AKT1"	"0.355"	"0.862"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"3"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.983606557377049"	"2002"	"2018"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.67"	"1"	"2013"	"2018"	"1"	"0"	"CGI;CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.38"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.47"	"1"	"2005"	"2017"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.979166666666667"	"1997"	"2016"	"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.32"	"0.5"	"2007"	"2015"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2016"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.875"	"2000"	"2018"	"2"	"1"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.953488372093023"	"2004"	"2017"	"4"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0085261"	"Proteus Syndrome"	"disease"	"C04;C05;C16"	"Neoplastic Process"	"0.74"	"1"	"1993"	"2016"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.47"	"1"	"2002"	"2015"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2010"	"2016"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"2008"	"2017"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0206644"	"Histiocytoma, Benign Fibrous"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.948717948717949"	"2003"	"2017"	"3"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.985507246376812"	"2000"	"2018"	"2"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2006"	"2"	"0"	"PSYGENET"
"207"	"AKT1"	"0.355"	"0.862"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"207"	"AKT1"	"0.355"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.987012987012987"	"1999"	"2018"	"1"	"0"	"CGI;CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.41"	"1"	"2007"	"2012"	"0"	"1"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.64"	"1"	"2005"	"2016"	"2"	"1"	"CGI;CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"	"0.976744186046512"	"1997"	"2016"	"2"	"0"	"CGI;CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1153706"	"Endometrial adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2005"	"2016"	"1"	"1"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"207"	"AKT1"	"0.355"	"0.862"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"2002"	"2017"	"1"	"1"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.957446808510638"	"2002"	"2018"	"0"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C1866398"	"Proteus-Like Syndrome (disorder)"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C1867610"	"Macrocephaly mesodermal hamartoma spectrum"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"1"	"UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"207"	"AKT1"	"0.355"	"0.862"	"C3554519"	"COWDEN SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"207"	"AKT1"	"0.355"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"208"	"AKT2"	"0.512"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"208"	"AKT2"	"0.512"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2001"	"2015"	"1"	"0"	"CGI;CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.44"	"1"	"2008"	"2016"	"0"	"1"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.83"	"1"	"2001"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"208"	"AKT2"	"0.512"	"0.655"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2015"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.38"	"1"	"1996"	"2018"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.59"	"1"	"2001"	"2015"	"1"	"0"	"CGI;CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"1992"	"2009"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2016"	"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"208"	"AKT2"	"0.512"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2006"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2004"	"2009"	"2"	"1"	"UNIPROT"
"208"	"AKT2"	"0.512"	"0.655"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"208"	"AKT2"	"0.512"	"0.655"	"C3278384"	"HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"208"	"AKT2"	"0.512"	"0.655"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2004"	"2009"	"2"	"1"	"UNIPROT"
"210"	"ALAD"	"0.55"	"0.483"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2014"	"3"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0162533"	"Porphyrias, Hepatic"	"group"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1984"	"1991"	"2"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0268328"	"Porphobilinogen synthase deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.73"	"1"	"1988"	"2007"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"210"	"ALAD"	"0.55"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C0751859"	"Lead Poisoning, Nervous System"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C2748608"	"LEAD POISONING, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.50"		"1991"	"2007"	"5"	"4"	"ORPHANET;UNIPROT"
"210"	"ALAD"	"0.55"	"0.483"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"210"	"ALAD"	"0.55"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"211"	"ALAS1"	"0.785"	"0.276"	"C0032708"	"Disorders of Porphyrin Metabolism"	"group"	"C18"	"Disease or Syndrome"	"0.50"		"1995"	"1997"	"1"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"1"	"1992"	"2017"	"2"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"212"	"ALAS2"	"0.616"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"212"	"ALAS2"	"0.616"	"0.414"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"212"	"ALAS2"	"0.616"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"212"	"ALAS2"	"0.616"	"0.414"	"C0221018"	"Hereditary sideroblastic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.972222222222222"	"1992"	"2017"	"11"	"18"	"CTD_human;ORPHANET;UNIPROT"
"212"	"ALAS2"	"0.616"	"0.414"	"C2677889"	"Protoporphyria, Erythropoietic, X-Linked Dominant"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2013"	"0"	"4"	"CTD_human;ORPHANET"
"213"	"ALB"	"0.412"	"0.828"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0003460"	"Anuria"	"phenotype"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0004509"	"Azoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.923076923076923"	"1993"	"2015"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.878787878787879"	"1989"	"2016"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0013502"	"Echinococcosis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1980"	"2012"	"8"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0017662"	"Glomerulonephritis, Membranoproliferative"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.36"	"1"	"1994"	"2017"	"6"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1991"	"2012"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0019699"	"HIV Seropositivity"	"phenotype"	"C02;C20"	"Laboratory or Test Result"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0020522"	"Delayed Hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.857142857142857"	"1989"	"2016"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.40"		"1975"	"2001"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.878787878787879"	"1978"	"2016"	"8"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2017"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.75"	"1997"	"2016"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1988"	"2015"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0025290"	"Aseptic Meningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"3"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1980"	"2006"	"6"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2013"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"1991"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1991"	"2013"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1977"	"2008"	"9"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0035457"	"Rhinitis, Allergic, Perennial"	"disease"	"C08;C09;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0036830"	"Serum Sickness"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1978"	"1997"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2015"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2013"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1994"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1994"	"2007"	"6"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"0.6"	"1987"	"2018"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0239981"	"Hypoalbuminemia"	"disease"	"C15"	"Disease or Syndrome"	"0.45"	"0.8"	"1999"	"2017"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1994"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1994"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0342185"	"Hyperthyroxinemia, Familial Dysalbuminemic"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.70"	"0.896551724137931"	"1986"	"2017"	"5"	"2"	"CTD_human;UNIPROT"
"213"	"ALB"	"0.412"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1994"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0878666"	"Analbuminemia"	"phenotype"		"Finding"	"0.40"		"1988"	"2013"	"0"	"3"	"ORPHANET"
"213"	"ALB"	"0.412"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1991"	"2017"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.37"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1980"	"2010"	"8"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1994"	"2007"	"6"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1991"	"2017"	"4"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"213"	"ALB"	"0.412"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"214"	"ALCAM"	"0.562"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"215"	"ABCD1"	"0.604"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"215"	"ABCD1"	"0.604"	"0.69"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"1.00"	"0.933333333333333"	"1982"	"2018"	"28"	"57"	"CLINGEN;CTD_human;UNIPROT"
"215"	"ABCD1"	"0.604"	"0.69"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.34"	"0.75"	"1999"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"215"	"ABCD1"	"0.604"	"0.69"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"215"	"ABCD1"	"0.604"	"0.69"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.70"	"0.923076923076923"	"1985"	"2017"	"25"	"29"	"CTD_human;ORPHANET;UNIPROT"
"215"	"ABCD1"	"0.604"	"0.69"	"C1845408"	"Contiguous Abcd1-Dxs1375e Deletion Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"1"	"ORPHANET"
"215"	"ABCD1"	"0.604"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1988"	"1988"	"1"	"0"	"PSYGENET"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1983"	"2015"	"5"	"0"	"PSYGENET"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"PSYGENET"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"216"	"ALDH1A1"	"0.515"	"0.724"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1994"	"2018"	"2"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1983"	"2014"	"5"	"0"	"PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"1991"	"2018"	"7"	"1"	"CTD_human;PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2015"	"2"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2011"	"2016"	"2"	"0"	"PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0007172"	"Heart Rupture, Traumatic"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2000"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.977777777777778"	"1996"	"2017"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.902439024390244"	"1989"	"2018"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0018805"	"Heart Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0028796"	"Dermatitis, Occupational"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.59"	"1"	"1996"	"2016"	"7"	"0"	"CTD_human;PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0086457"	"Industrial Dermatosis"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0236664"	"Alcohol-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1993"	"2015"	"3"	"0"	"PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0236970"	"Alcohol-Induced Disorders"	"group"	"C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0349464"	"Wernicke-Korsakoff Syndrome"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0393756"	"Hangover from alcohol"	"phenotype"		"Sign or Symptom"	"0.34"	"1"	"2000"	"2018"	"4"	"0"	"PSYGENET"
"217"	"ALDH2"	"0.481"	"0.862"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2000"	"2016"	"1"	"0"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C2608086"	"HANGOVER, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"1983"	"2010"	"1"	"1"	"CTD_human"
"217"	"ALDH2"	"0.481"	"0.862"	"C2674838"	"ALCOHOL SENSITIVITY, ACUTE"	"phenotype"		"Finding"	"0.40"		"1983"	"2010"	"1"	"1"	"CTD_human"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C0339289"	"Injury of cornea"	"disease"	"C10;C11;C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C0349702"	"Corneal Scar"	"phenotype"	"C10;C11;C26"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"218"	"ALDH3A1"	"0.69"	"0.552"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"2"	"0"	"CTD_human"
"219"	"ALDH1B1"	"0.727"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C3554524"	"MICROPHTHALMIA, ISOLATED 8"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"7"	"5"	"CTD_human;UNIPROT"
"220"	"ALDH1A3"	"0.633"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"221"	"ALDH3B1"	"0.834"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2009"	"2"	"0"	"PSYGENET"
"221"	"ALDH3B1"	"0.834"	"0.31"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"222"	"ALDH3B2"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"224"	"ALDH3A2"	"0.636"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"224"	"ALDH3A2"	"0.636"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"224"	"ALDH3A2"	"0.636"	"0.655"	"C0037231"	"Sjogren-Larsson Syndrome"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.80"	"0.972972972972973"	"1981"	"2016"	"7"	"50"	"CTD_human;ORPHANET;UNIPROT"
"224"	"ALDH3A2"	"0.636"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"225"	"ABCD2"	"0.762"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"225"	"ABCD2"	"0.762"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"225"	"ABCD2"	"0.762"	"0.31"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"225"	"ABCD2"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1988"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"226"	"ALDOA"	"0.672"	"0.379"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"1988"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"226"	"ALDOA"	"0.672"	"0.379"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1988"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"226"	"ALDOA"	"0.672"	"0.379"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"226"	"ALDOA"	"0.672"	"0.379"	"C0272066"	"Glycogen Storage Disease XII"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1988"	"2004"	"5"	"3"	"CTD_human;ORPHANET;UNIPROT"
"226"	"ALDOA"	"0.672"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"226"	"ALDOA"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"229"	"ALDOB"	"0.648"	"0.483"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"229"	"ALDOB"	"0.648"	"0.483"	"C0016751"	"Hereditary fructose intolerance syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1983"	"2017"	"13"	"31"	"CTD_human;ORPHANET;UNIPROT"
"229"	"ALDOB"	"0.648"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"229"	"ALDOB"	"0.648"	"0.483"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"229"	"ALDOB"	"0.648"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"229"	"ALDOB"	"0.648"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"229"	"ALDOB"	"0.648"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.37"	"1"	"1993"	"2017"	"4"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.31"		"2007"	"2015"	"2"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"231"	"AKR1B1"	"0.536"	"0.621"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"238"	"ALK"	"0.448"	"0.724"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.61"	"1"	"2009"	"2013"	"1"	"3"	"CGI;CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.978632478632479"	"2007"	"2018"	"28"	"6"	"CGI;CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"238"	"ALK"	"0.448"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"238"	"ALK"	"0.448"	"0.724"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CGI"
"238"	"ALK"	"0.448"	"0.724"	"C0018199"	"Granuloma, Plasma Cell"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"CGI"
"238"	"ALK"	"0.448"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.80"	"0.935779816513761"	"1990"	"2018"	"12"	"14"	"CGI;CTD_human;ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.46"	"1"	"2012"	"2016"	"0"	"1"	"CGI"
"238"	"ALK"	"0.448"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"238"	"ALK"	"0.448"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0085269"	"Plasma Cell Granuloma, Pulmonary"	"disease"	"C08"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"238"	"ALK"	"0.448"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.978021978021978"	"2008"	"2018"	"8"	"6"	"CGI;CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.50"		"2013"	"2013"	"1"	"0"	"CGI;CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0206180"	"Ki-1+ Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"0.972696245733788"	"1995"	"2018"	"6"	"0"	"CGI;CTD_human;ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C0278601"	"Inflammatory Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.70"	"0.984848484848485"	"1999"	"2018"	"3"	"0"	"CGI;CTD_human;ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C1332079"	"Anaplastic Large Cell Lymphoma, ALK-Positive"	"disease"		"Neoplastic Process"	"0.40"	"0.916666666666667"	"1999"	"2018"	"0"	"0"	"ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C1333294"	"ALK positive large B-cell lymphoma"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2011"	"2017"	"0"	"0"	"ORPHANET"
"238"	"ALK"	"0.448"	"0.724"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"238"	"ALK"	"0.448"	"0.724"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"238"	"ALK"	"0.448"	"0.724"	"C2751681"	"NEUROBLASTOMA, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.40"		"1993"	"2012"	"4"	"13"	"UNIPROT"
"238"	"ALK"	"0.448"	"0.724"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"239"	"ALOX12"	"0.596"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"239"	"ALOX12"	"0.596"	"0.621"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"PSYGENET"
"239"	"ALOX12"	"0.596"	"0.621"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"239"	"ALOX12"	"0.596"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.88"	"1997"	"2016"	"0"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2008"	"2"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0009376"	"Colonic Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0016659"	"Fractures, Closed"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"1996"	"2004"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2010"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0524598"	"Fractures, Occult"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"240"	"ALOX5"	"0.482"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"2013"	"2016"	"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"241"	"ALOX5AP"	"0.633"	"0.552"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"242"	"ALOX12B"	"0.652"	"0.483"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.56"	"0.833333333333333"	"2005"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"242"	"ALOX12B"	"0.652"	"0.483"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2002"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"242"	"ALOX12B"	"0.652"	"0.483"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.65"	"0.8"	"2006"	"2015"	"1"	"1"	"CTD_human;ORPHANET"
"242"	"ALOX12B"	"0.652"	"0.483"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"242"	"ALOX12B"	"0.652"	"0.483"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2002"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"242"	"ALOX12B"	"0.652"	"0.483"	"C1855789"	"Self-Healing Collodion Baby"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"2002"	"2010"	"5"	"15"	"ORPHANET;UNIPROT"
"242"	"ALOX12B"	"0.652"	"0.483"	"C1855792"	"ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2002"	"2015"	"0"	"12"	"CTD_human"
"242"	"ALOX12B"	"0.652"	"0.483"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"242"	"ALOX12B"	"0.652"	"0.483"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"242"	"ALOX12B"	"0.652"	"0.483"	"C3888093"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2010"	"5"	"15"	"UNIPROT"
"246"	"ALOX15"	"0.543"	"0.69"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.882352941176471"	"2005"	"2013"	"1"	"0"	"CTD_human"
"246"	"ALOX15"	"0.543"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"246"	"ALOX15"	"0.543"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"246"	"ALOX15"	"0.543"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"246"	"ALOX15"	"0.543"	"0.69"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0002382"	"Alveolar Bone Loss"	"disease"	"C05;C07"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"249"	"ALPL"	"0.564"	"0.621"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0020503"	"Hyperparathyroidism, Secondary"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0020630"	"Hypophosphatasia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.973684210526316"	"1992"	"2018"	"1"	"9"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"0"	"2000"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"249"	"ALPL"	"0.564"	"0.621"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0220743"	"Childhood hypophosphatasia (disorder)"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.92"	"1"	"1992"	"2015"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"249"	"ALPL"	"0.564"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0268412"	"Infantile hypophosphatasia"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1988"	"2016"	"4"	"47"	"CTD_human;ORPHANET;UNIPROT"
"249"	"ALPL"	"0.564"	"0.621"	"C0268413"	"Adult hypophosphatasia (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.94"	"0.75"	"1988"	"2016"	"29"	"41"	"CTD_human;ORPHANET;UNIPROT"
"249"	"ALPL"	"0.564"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"249"	"ALPL"	"0.564"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C1840322"	"ODONTOHYPOPHOSPHATASIA (disorder)"	"disease"	"C07;C16;C18"	"Disease or Syndrome"	"0.81"	"1"	"1988"	"2016"	"29"	"40"	"ORPHANET;UNIPROT"
"249"	"ALPL"	"0.564"	"0.621"	"C2673477"	"Hypophosphatasia, Perinatal Lethal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"		"1995"	"2013"	"4"	"6"	"ORPHANET;UNIPROT"
"249"	"ALPL"	"0.564"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"249"	"ALPL"	"0.564"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"249"	"ALPL"	"0.564"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"2"	"0"	"CTD_human"
"251"	"ALPG"	"0.799"	"0.172"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"251"	"ALPG"	"0.799"	"0.172"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"257"	"ALX3"	"0.648"	"0.414"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"257"	"ALX3"	"0.648"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"257"	"ALX3"	"0.648"	"0.414"	"C1876203"	"Frontonasal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.75"	"1"	"1980"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"257"	"ALX3"	"0.648"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"258"	"AMBN"	"0.773"	"0.103"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.49"	"1"	"1997"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"258"	"AMBN"	"0.773"	"0.103"	"C0399367"	"Amelogenesis imperfecta local hypoplastic form"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"258"	"AMBN"	"0.773"	"0.103"	"C4225394"	"AMELOGENESIS IMPERFECTA, TYPE IF"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1996"	"2017"	"2"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1996"	"2017"	"2"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1996"	"2017"	"2"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"259"	"AMBP"	"0.621"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"265"	"AMELX"	"0.663"	"0.448"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.50"	"1"	"1991"	"2018"	"17"	"0"	"GENOMICS_ENGLAND"
"265"	"AMELX"	"0.663"	"0.448"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"265"	"AMELX"	"0.663"	"0.448"	"C1845052"	"AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.62"	"1"	"1967"	"2004"	"5"	"10"	"CTD_human;UNIPROT"
"265"	"AMELX"	"0.663"	"0.448"	"C1845053"	"Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2004"	"5"	"3"	"UNIPROT"
"266"	"AMELY"	"0.727"	"0.241"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"266"	"AMELY"	"0.727"	"0.241"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"267"	"AMFR"	"0.701"	"0.31"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"267"	"AMFR"	"0.701"	"0.31"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"268"	"AMH"	"0.562"	"0.517"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"268"	"AMH"	"0.562"	"0.517"	"C1849930"	"Persistent Mullerian duct syndrome"	"phenotype"	"C12;C13;C16;C19"	"Anatomical Abnormality"	"0.70"	"0.961538461538462"	"1989"	"2018"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"269"	"AMHR2"	"0.639"	"0.448"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"269"	"AMHR2"	"0.639"	"0.448"	"C1849930"	"Persistent Mullerian duct syndrome"	"phenotype"	"C12;C13;C16;C19"	"Anatomical Abnormality"	"0.85"	"1"	"1996"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"270"	"AMPD1"	"0.616"	"0.517"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"270"	"AMPD1"	"0.616"	"0.517"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2008"	"2"	"0"	"CTD_human"
"270"	"AMPD1"	"0.616"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2005"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"270"	"AMPD1"	"0.616"	"0.517"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2000"	"2000"	"1"	"0"	"CTD_human"
"270"	"AMPD1"	"0.616"	"0.517"	"C0268123"	"Muscle AMP deaminase deficiency"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"1993"	"2017"	"0"	"4"	"ORPHANET"
"270"	"AMPD1"	"0.616"	"0.517"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"270"	"AMPD1"	"0.616"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"270"	"AMPD1"	"0.616"	"0.517"	"C2931781"	"Adenosine monophosphate deaminase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1992"	"2001"	"3"	"0"	"CTD_human;ORPHANET"
"270"	"AMPD1"	"0.616"	"0.517"	"C3714933"	"MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.50"		"2001"	"2001"	"1"	"2"	"CTD_human;UNIPROT"
"271"	"AMPD2"	"0.672"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"271"	"AMPD2"	"0.672"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"271"	"AMPD2"	"0.672"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"271"	"AMPD2"	"0.672"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"271"	"AMPD2"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"271"	"AMPD2"	"0.672"	"0.379"	"C3810295"	"SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"271"	"AMPD2"	"0.672"	"0.379"	"C4014354"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 9"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"272"	"AMPD3"	"0.815"	"0.207"	"C0268123"	"Muscle AMP deaminase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"272"	"AMPD3"	"0.815"	"0.207"	"C2752073"	"Erythrocyte Amp Deaminase Deficiency"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"1994"	"2001"	"4"	"7"	"CTD_human;UNIPROT"
"272"	"AMPD3"	"0.815"	"0.207"	"C2931781"	"Adenosine monophosphate deaminase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"274"	"BIN1"	"0.573"	"0.621"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9375"	"2011"	"2018"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"274"	"BIN1"	"0.573"	"0.621"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2011"	"2014"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"274"	"BIN1"	"0.573"	"0.621"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2014"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0410204"	"Myopathy, Centronuclear, Autosomal Recessive"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.63"	"1"	"2007"	"2013"	"1"	"6"	"ORPHANET;UNIPROT"
"274"	"BIN1"	"0.573"	"0.621"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.923076923076923"	"2011"	"2018"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"274"	"BIN1"	"0.573"	"0.621"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"274"	"BIN1"	"0.573"	"0.621"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"274"	"BIN1"	"0.573"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"275"	"AMT"	"0.69"	"0.414"	"C0268560"	"Hyperglycinemia, Transient Neonatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"2018"	"8"	"11"	"UNIPROT"
"275"	"AMT"	"0.69"	"0.414"	"C0268561"	"Hyperglycinemia, Nonketotic, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"275"	"AMT"	"0.69"	"0.414"	"C0268562"	"Hyperglycinemia, Nonketotic, Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"275"	"AMT"	"0.69"	"0.414"	"C0751747"	"Hyperglycinemia, Nonketotic, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"275"	"AMT"	"0.69"	"0.414"	"C0751748"	"Nonketotic Hyperglycinemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.77"	"0.857142857142857"	"1974"	"2018"	"9"	"29"	"CTD_human;ORPHANET;UNIPROT"
"283"	"ANG"	"0.547"	"0.69"	"C0001349"	"Acute-Phase Reaction"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"283"	"ANG"	"0.547"	"0.69"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.96969696969697"	"2005"	"2017"	"0"	"0"	"ORPHANET"
"283"	"ANG"	"0.547"	"0.69"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"283"	"ANG"	"0.547"	"0.69"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"283"	"ANG"	"0.547"	"0.69"	"C2678468"	"Amyotrophic Lateral Sclerosis 9"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"8"	"10"	"CTD_human;UNIPROT"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2008"	"2"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"284"	"ANGPT1"	"0.495"	"0.69"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"285"	"ANGPT2"	"0.479"	"0.724"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"286"	"ANK1"	"0.586"	"0.828"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"286"	"ANK1"	"0.586"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"286"	"ANK1"	"0.586"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1991"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"286"	"ANK1"	"0.586"	"0.828"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"286"	"ANK1"	"0.586"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"286"	"ANK1"	"0.586"	"0.828"	"C0221409"	"Anemia, hereditary spherocytic hemolytic"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"286"	"ANK1"	"0.586"	"0.828"	"C2674218"	"SPHEROCYTOSIS, TYPE 1 (disorder)"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.81"	"1"	"1980"	"2015"	"2"	"7"	"CTD_human;UNIPROT"
"286"	"ANK1"	"0.586"	"0.828"	"C4304505"	"8p11.2 deletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"287"	"ANK2"	"0.663"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"287"	"ANK2"	"0.663"	"0.345"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.45"	"1"	"2004"	"2016"	"0"	"3"	"GENOMICS_ENGLAND"
"287"	"ANK2"	"0.663"	"0.345"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"287"	"ANK2"	"0.663"	"0.345"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"287"	"ANK2"	"0.663"	"0.345"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"287"	"ANK2"	"0.663"	"0.345"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"287"	"ANK2"	"0.663"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"287"	"ANK2"	"0.663"	"0.345"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"287"	"ANK2"	"0.663"	"0.345"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"287"	"ANK2"	"0.663"	"0.345"	"C1833154"	"Long Qt Syndrome 4"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2004"	"2"	"5"	"UNIPROT"
"287"	"ANK2"	"0.663"	"0.345"	"C1970119"	"CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.54"	"1"	"2003"	"2015"	"2"	"5"	"CTD_human;UNIPROT"
"288"	"ANK3"	"0.602"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"2009"	"2018"	"7"	"32"	"CTD_human;PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0033300"	"Progeria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"		"2007"	"2016"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2014"	"2015"	"2"	"0"	"PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2009"	"2016"	"3"	"3"	"PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2015"	"2"	"0"	"PSYGENET"
"288"	"ANK3"	"0.602"	"0.379"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"288"	"ANK3"	"0.602"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"288"	"ANK3"	"0.602"	"0.379"	"C3809672"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"290"	"ANPEP"	"0.534"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"290"	"ANPEP"	"0.534"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"290"	"ANPEP"	"0.534"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"290"	"ANPEP"	"0.534"	"0.621"	"C0149821"	"ACUTE ALCOHOL WITHDRAWAL"	"disease"		"Disease or Syndrome"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"290"	"ANPEP"	"0.534"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2013"	"2"	"0"	"PSYGENET"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.42"	"1"	"2000"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"291"	"SLC25A4"	"0.627"	"0.552"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"291"	"SLC25A4"	"0.627"	"0.552"	"C1834846"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"	"disease"	"C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"291"	"SLC25A4"	"0.627"	"0.552"	"C1836460"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.60"		"1996"	"2017"	"7"	"4"	"CTD_human;UNIPROT"
"291"	"SLC25A4"	"0.627"	"0.552"	"C1859317"	"Cataract and cardiomyopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"291"	"SLC25A4"	"0.627"	"0.552"	"C3809443"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"1989"	"2017"	"11"	"4"	"CLINGEN;CTD_human;UNIPROT"
"291"	"SLC25A4"	"0.627"	"0.552"	"C4310676"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"293"	"SLC25A6"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"301"	"ANXA1"	"0.498"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2006"	"2012"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2012"	"3"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2002"	"2016"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2007"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0038354"	"Stomach Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"301"	"ANXA1"	"0.498"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2012"	"3"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"302"	"ANXA2"	"0.485"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"306"	"ANXA3"	"0.696"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"306"	"ANXA3"	"0.696"	"0.448"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"307"	"ANXA4"	"0.636"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"308"	"ANXA5"	"0.49"	"0.69"	"C3280674"	"PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"309"	"ANXA6"	"0.569"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"309"	"ANXA6"	"0.569"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"309"	"ANXA6"	"0.569"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"310"	"ANXA7"	"0.659"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"310"	"ANXA7"	"0.659"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"311"	"ANXA11"	"0.752"	"0.379"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"311"	"ANXA11"	"0.752"	"0.379"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.47"	"0.857142857142857"	"2009"	"2016"	"1"	"4"	"CTD_human"
"313"	"AOAH"	"0.785"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"313"	"AOAH"	"0.785"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"313"	"AOAH"	"0.785"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"316"	"AOX1"	"0.834"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"316"	"AOX1"	"0.834"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2010"	"2"	"0"	"PSYGENET"
"317"	"APAF1"	"0.545"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"2"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"317"	"APAF1"	"0.545"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2010"	"2"	"0"	"PSYGENET"
"317"	"APAF1"	"0.545"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"318"	"NUDT2"	"0.834"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"318"	"NUDT2"	"0.834"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"318"	"NUDT2"	"0.834"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"318"	"NUDT2"	"0.834"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"321"	"APBA2"	"0.707"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"321"	"APBA2"	"0.707"	"0.379"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2016"	"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"323"	"APBB2"	"0.762"	"0.103"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.979591836734694"	"1993"	"2016"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.965034965034965"	"1990"	"2017"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0002886"	"Anemia, Macrocytic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"1994"	"2007"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0004991"	"Benign neoplasm of colon"	"disease"		"Neoplastic Process"	"0.30"		"1993"	"1996"	"6"	"0"	"CLINGEN"
"324"	"APC"	"0.397"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.947826086956522"	"1992"	"2016"	"7"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1994"	"2015"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.931034482758621"	"1990"	"2016"	"7"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.936708860759494"	"1990"	"2018"	"8"	"1"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.932432432432432"	"1990"	"2016"	"7"	"11"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0017097"	"Gardner Syndrome"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2016"	"10"	"15"	"ORPHANET;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0017181"	"Gastrointestinal Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.53"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"324"	"APC"	"0.397"	"0.828"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"1997"	"1997"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0018932"	"Hematochezia"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.36"	"0.666666666666667"	"1998"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.866666666666667"	"1994"	"2017"	"6"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0021846"	"Intestinal Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"	"0.8"	"1995"	"2015"	"3"	"1"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9"	"1992"	"2017"	"0"	"0"	"CGI;CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.928571428571429"	"1995"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"0.8"	"2002"	"2017"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.80"	"0.929054054054054"	"1989"	"2018"	"21"	"6"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.52"		"2007"	"2018"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2006"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"324"	"APC"	"0.397"	"0.828"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.63"	"0.666666666666667"	"1992"	"2008"	"0"	"2"	"CGI;CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0079218"	"Fibromatosis, Aggressive"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.977777777777778"	"1992"	"2016"	"1"	"0"	"CGI;CTD_human;ORPHANET"
"324"	"APC"	"0.397"	"0.828"	"C0085136"	"Central Nervous System Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"0"	"2007"	"2007"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2008"	"2015"	"0"	"1"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"324"	"APC"	"0.397"	"0.828"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2009"	"4"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"1995"	"2013"	"0"	"1"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0206646"	"Fibromatosis, Abdominal"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0206677"	"Adenomatous Polyps"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2008"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"1992"	"2017"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0265325"	"Turcot syndrome (disorder)"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.39"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2017"	"6"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.38"	"0.875"	"1992"	"2017"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0348374"	"Malignant Central Nervous System Neoplasm"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0685938"	"Malignant neoplasm of gastrointestinal tract"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"1995"	"2011"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"0.945652173913043"	"1991"	"2016"	"0"	"1"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.70"	"1"	"1992"	"2018"	"0"	"2"	"CGI;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"1995"	"2000"	"2"	"1"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1995"	"1995"	"0"	"0"	"CGI"
"324"	"APC"	"0.397"	"0.828"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"1992"	"2015"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1334970"	"Medulloblastoma with extensive nodularity"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.90"	"0.941558441558442"	"1990"	"2018"	"7"	"0"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1851124"	"Desmoid disease, hereditary"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.44"	"1"	"1992"	"2012"	"0"	"1"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C1859309"	"Syndactyly Cenani Lenz type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"324"	"APC"	"0.397"	"0.828"	"C1879526"	"Aberrant Crypt Foci"	"phenotype"	"C04"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.958333333333333"	"1992"	"2016"	"0"	"1"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C2673218"	"BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.40"		"1991"	"2016"	"10"	"8"	"UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C2674616"	"FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.40"	"0.95"	"1991"	"2016"	"10"	"6"	"UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C2675440"	"Desmoid Tumor Caused By Somatic Mutation"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.80"		"1990"	"2017"	"21"	"193"	"CTD_human;UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.50"		"1990"	"2017"	"11"	"0"	"CTD_human"
"324"	"APC"	"0.397"	"0.828"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"				"0"	"2"	"UNIPROT"
"324"	"APC"	"0.397"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1994"	"2001"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"0"	"0"	"UNIPROT"
"325"	"APCS"	"0.565"	"0.655"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2003"	"2015"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"325"	"APCS"	"0.565"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0006840"	"Candidiasis"	"disease"	"C01"	"Disease or Syndrome"	"0.40"	"0.833333333333333"	"2002"	"2011"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0085409"	"Polyendocrinopathies, Autoimmune"	"group"	"C19;C20"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0085859"	"Polyglandular Type I Autoimmune Syndrome"	"disease"	"C19;C20"	"Disease or Syndrome"	"1.00"	"0.94488188976378"	"1967"	"2018"	"21"	"51"	"CTD_human;ORPHANET;UNIPROT"
"326"	"AIRE"	"0.55"	"0.621"	"C0085860"	"Autoimmune Syndrome Type II, Polyglandular"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"326"	"AIRE"	"0.55"	"0.621"	"C1535942"	"Polyglandular Type III Autoimmune Syndrome"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C1855868"	"Polyglandular Deficiency Syndrome, Persian-Jewish Type"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.70"		"1997"	"2016"	"20"	"19"	"CTD_human;UNIPROT"
"326"	"AIRE"	"0.55"	"0.621"	"C1855869"	"Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.80"		"1997"	"2016"	"20"	"19"	"CTD_human;UNIPROT"
"326"	"AIRE"	"0.55"	"0.621"	"C2749602"	"AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.40"		"1967"	"2010"	"0"	"2"	"CTD_human"
"326"	"AIRE"	"0.55"	"0.621"	"C3494489"	"Autoimmune polyendocrinopathy syndrome, type 1"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.60"	"0.973684210526316"	"1999"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"326"	"AIRE"	"0.55"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"328"	"APEX1"	"0.495"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2005"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"328"	"APEX1"	"0.495"	"0.759"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2005"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"329"	"BIRC2"	"0.575"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2015"	"0"	"0"	"CGI"
"330"	"BIRC3"	"0.524"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"0"	"0"	"CGI"
"330"	"BIRC3"	"0.524"	"0.724"	"C0242647"	"Mucosa-Associated Lymphoid Tissue Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.95"	"1999"	"2017"	"0"	"0"	"CGI;ORPHANET"
"330"	"BIRC3"	"0.524"	"0.724"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"330"	"BIRC3"	"0.524"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"330"	"BIRC3"	"0.524"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C0549463"	"X-Linked Lymphoproliferative Disorder"	"disease"	"C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2006"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"331"	"XIAP"	"0.499"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"2000"	"2018"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C1845076"	"Lymphoproliferative Syndrome, X-Linked, 2"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.46"	"1"	"2006"	"2016"	"0"	"2"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"331"	"XIAP"	"0.499"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"332"	"BIRC5"	"0.479"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"		"2005"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2004"	"2009"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"		"2003"	"2009"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0023462"	"Acute Megakaryocytic Leukemias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2003"	"2011"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.39"		"2004"	"2009"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.59"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.57"		"2002"	"2008"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2013"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"		"2005"	"2009"	"4"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2016"	"4"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.952380952380952"	"2003"	"2015"	"2"	"0"	"CTD_human"
"332"	"BIRC5"	"0.479"	"0.655"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2007"	"2016"	"1"	"0"	"CTD_human"
"334"	"APLP2"	"0.727"	"0.31"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"334"	"APLP2"	"0.727"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2003"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.888888888888889"	"1986"	"2017"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"1998"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"335"	"APOA1"	"0.463"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.67"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"2"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"2"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0154251"	"Lipid Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0268389"	"Amyloidosis, familial visceral"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1969"	"2002"	"4"	"5"	"CTD_human;UNIPROT"
"335"	"APOA1"	"0.463"	"0.759"	"C0342898"	"Apolipoprotein A-I deficiency"	"phenotype"		"Pathologic Function"	"0.40"		"1989"	"1998"	"0"	"3"	"ORPHANET"
"335"	"APOA1"	"0.463"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0376297"	"Cardiac Death"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0473527"	"Hypoalphalipoproteinemias"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"1986"	"2012"	"0"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C1704429"	"Hypoalphalipoproteinemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.59"	"1"	"1986"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"335"	"APOA1"	"0.463"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C1848533"	"Ataxia with vitamin E deficiency"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.894736842105263"	"1986"	"2017"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2016"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C2362324"	"Pediatric Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"335"	"APOA1"	"0.463"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C4317171"	"Adolescent Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"335"	"APOA1"	"0.463"	"0.759"	"C4521075"	"Childhood Overweight"	"phenotype"	"C18;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"336"	"APOA2"	"0.619"	"0.552"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"336"	"APOA2"	"0.619"	"0.552"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"336"	"APOA2"	"0.619"	"0.552"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"336"	"APOA2"	"0.619"	"0.552"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"336"	"APOA2"	"0.619"	"0.552"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"337"	"APOA4"	"0.596"	"0.517"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"1994"	"2006"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"337"	"APOA4"	"0.596"	"0.517"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.986666666666667"	"1986"	"2017"	"1"	"1"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.943396226415094"	"1987"	"2016"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"0.964601769911504"	"1988"	"2018"	"3"	"14"	"CTD_human;GENOMICS_ENGLAND"
"338"	"APOB"	"0.477"	"0.724"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"1"	"1988"	"2014"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.39"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"338"	"APOB"	"0.477"	"0.724"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.963636363636364"	"1989"	"2018"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"338"	"APOB"	"0.477"	"0.724"	"C1704299"	"Hypobetalipoproteinemia, Familial, Apolipoprotein B"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"1995"	"3"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"0.90625"	"1989"	"2011"	"5"	"3"	"CTD_human;UNIPROT"
"338"	"APOB"	"0.477"	"0.724"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C1848533"	"Ataxia with vitamin E deficiency"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C1862596"	"Familial hypobetalipoproteinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.70"	"0.914285714285714"	"1979"	"2018"	"3"	"14"	"CTD_human;UNIPROT"
"338"	"APOB"	"0.477"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"338"	"APOB"	"0.477"	"0.724"	"C3888316"	"Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B"	"disease"		"Disease or Syndrome"	"0.30"		"1989"	"2011"	"4"	"2"	"UNIPROT"
"339"	"APOBEC1"	"0.681"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341"	"APOC1"	"0.604"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"343"	"AQP8"	"0.799"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"344"	"APOC2"	"0.619"	"0.483"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"1994"	"0"	"0"	"GENOMICS_ENGLAND"
"344"	"APOC2"	"0.619"	"0.483"	"C0023817"	"Hyperlipoproteinemia Type I"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.38"	"1"	"1981"	"2006"	"0"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C0268199"	"Familial apolipoprotein C-II deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"344"	"APOC2"	"0.619"	"0.483"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"344"	"APOC2"	"0.619"	"0.483"	"C1720779"	"Apolipoprotein C-II Deficiency (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"0.8"	"1986"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"344"	"APOC2"	"0.619"	"0.483"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"345"	"APOC3"	"0.552"	"0.586"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"1997"	"2016"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"345"	"APOC3"	"0.552"	"0.586"	"C0020476"	"Hyperlipoproteinemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0342883"	"Cholesteryl Ester Transfer Protein Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.42"	"1"	"1991"	"2014"	"0"	"0"	"ORPHANET"
"345"	"APOC3"	"0.552"	"0.586"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.958333333333333"	"1997"	"2016"	"1"	"0"	"CTD_human"
"345"	"APOC3"	"0.552"	"0.586"	"C3151467"	"Apolipoprotein C-III Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.61"	"1"	"1991"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"345"	"APOC3"	"0.552"	"0.586"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"346"	"APOC4"	"0.773"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"347"	"APOD"	"0.598"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"347"	"APOD"	"0.598"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.666666666666667"	"2002"	"2007"	"3"	"0"	"PSYGENET"
"347"	"APOD"	"0.598"	"0.483"	"C0086439"	"Hypokinesia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0233565"	"Bradykinesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0751701"	"Hypokinesia, Antiorthostatic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"347"	"APOD"	"0.598"	"0.483"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.75"	"2002"	"2008"	"4"	"0"	"PSYGENET"
"348"	"APOE"	"0.352"	"0.931"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.921821305841924"	"1991"	"2018"	"5"	"4"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.955182072829132"	"1993"	"2018"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0003850"	"Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.955555555555556"	"1983"	"2018"	"2"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.951923076923077"	"1983"	"2018"	"28"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"1997"	"2016"	"2"	"0"	"PSYGENET"
"348"	"APOE"	"0.352"	"0.931"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.905172413793103"	"1996"	"2016"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0007282"	"Carotid Stenosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.923076923076923"	"1997"	"2017"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.960526315789474"	"1983"	"2018"	"1"	"1"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"2007"	"2018"	"5"	"0"	"PSYGENET"
"348"	"APOE"	"0.352"	"0.931"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.892307692307692"	"1993"	"2018"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0015697"	"Arterial Fatty Streak"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2007"	"2015"	"7"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.955223880597015"	"1985"	"2018"	"4"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"0.65"	"1990"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"348"	"APOE"	"0.352"	"0.931"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.60"	"0.9375"	"1984"	"2016"	"4"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0020479"	"Hyperlipoproteinemia Type III"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.920634920634921"	"1981"	"2018"	"7"	"11"	"CTD_human;ORPHANET;UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.84"	"1994"	"2017"	"2"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2011"	"2"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0025427"	"Mercury Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.903225806451613"	"1995"	"2016"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"1986"	"2017"	"1"	"2"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.918918918918919"	"1989"	"2017"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.46"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.787878787878788"	"1996"	"2018"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0036489"	"Sea-Blue Histiocyte Syndrome"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"1"	"1"	"CTD_human;ORPHANET"
"348"	"APOE"	"0.352"	"0.931"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"0.916666666666667"	"1997"	"2016"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0085220"	"Cerebral Amyloid Angiopathy"	"disease"	"C10;C14;C18"	"Disease or Syndrome"	"0.50"	"0.950819672131147"	"1996"	"2018"	"1"	"1"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"348"	"APOE"	"0.352"	"0.931"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.50"	"0.938775510204082"	"1994"	"2016"	"1"	"1"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"2"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.94"	"1998"	"2017"	"1"	"1"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0264956"	"Atheroma"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2015"	"7"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.931034482758621"	"1993"	"2016"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0338582"	"Sporadic Cerebral Amyloid Angiopathy"	"disease"	"C10;C14;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0340569"	"Internal Carotid Artery Stenosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0393664"	"Multiple Sclerosis, Acute Relapsing"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.944915254237288"	"1993"	"2018"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"2014"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"1997"	"2017"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"0.736842105263158"	"1989"	"2016"	"4"	"3"	"CTD_human;UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"2014"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.85"	"1993"	"2017"	"5"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751633"	"Carotid Artery Plaque"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751634"	"Carotid Ulcer"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751635"	"Common Carotid Artery Stenosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751636"	"External Carotid Artery Stenosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0751967"	"Multiple Sclerosis, Relapsing-Remitting"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"0.5"	"2004"	"2010"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1997"	"2017"	"28"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.44"	"0.75"	"2006"	"2014"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1847200"	"ALZHEIMER DISEASE 4"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C1862556"	"Apolipoprotein E, Deficiency or Defect of"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862557"	"Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862558"	"Familial Hyperbeta- and Prebetalipoproteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862560"	"Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862561"	"Broad-Betalipoproteinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862562"	"Floating-Betalipoproteinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1862591"	"CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1989"	"2012"	"4"	"8"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1863051"	"ALZHEIMER DISEASE 2"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.928571428571429"	"1993"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C1864205"	"Macular Degeneration, Age-Related, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C2673196"	"LIPOPROTEIN GLOMERULOPATHY"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.80"	"1"	"1997"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C2676098"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5"	"phenotype"		"Finding"	"0.30"		"1989"	"2012"	"4"	"7"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C2936351"	"Fibroatheroma"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2007"	"2015"	"7"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"		"2013"	"2016"	"3"	"3"	"UNIPROT"
"348"	"APOE"	"0.352"	"0.931"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"348"	"APOE"	"0.352"	"0.931"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"350"	"APOH"	"0.611"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"350"	"APOH"	"0.611"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.90"	"0.967113276492083"	"1987"	"2018"	"57"	"13"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.97145993413831"	"1988"	"2018"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.909090909090909"	"2004"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"351"	"APP"	"0.43"	"0.862"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2018"	"5"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.982142857142857"	"1991"	"2018"	"33"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"351"	"APP"	"0.43"	"0.862"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"351"	"APP"	"0.43"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"351"	"APP"	"0.43"	"0.862"	"C0016667"	"Fragile X Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"7"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1996"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2002"	"2014"	"11"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0037928"	"Spinal Cord Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0085220"	"Cerebral Amyloid Angiopathy"	"disease"	"C10;C14;C18"	"Disease or Syndrome"	"0.50"	"0.939393939393939"	"1993"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0231341"	"Premature aging syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9375"	"1993"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0234985"	"Mental deterioration"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2014"	"2"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.972067039106145"	"1988"	"2018"	"33"	"0"	"CTD_human;ORPHANET"
"351"	"APP"	"0.43"	"0.862"	"C0333463"	"Senile Plaques"	"phenotype"	"C23"	"Acquired Abnormality"	"0.40"	"0.951754385964912"	"1988"	"2017"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0338582"	"Sporadic Cerebral Amyloid Angiopathy"	"disease"	"C10;C14;C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0338656"	"Impaired cognition"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.939024390243902"	"1993"	"2018"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1991"	"2018"	"33"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.970149253731343"	"1993"	"2018"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.91304347826087"	"1994"	"2016"	"2"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2018"	"33"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2018"	"33"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.96"	"1991"	"2018"	"33"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751156"	"FRAXA Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751157"	"FRAXE Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"7"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"7"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"7"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.49"	"1"	"2002"	"2018"	"15"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2014"	"2"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C1270972"	"Mild cognitive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2006"	"2017"	"7"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C1541844"	"PRESENILE AND SENILE DEMENTIA"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2005"	"26"	"11"	"UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C1863052"	"ALZHEIMER DISEASE, FAMILIAL, 1"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.41"	"1"	"1991"	"2008"	"26"	"12"	"UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C1863053"	"Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1991"	"2005"	"26"	"11"	"UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C2751494"	"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"		"1990"	"2010"	"6"	"3"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C2751536"	"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"		"1990"	"2010"	"6"	"5"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C2931672"	"Cerebral hemorrhage with amyloidosis, hereditary, Dutch type"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"		"1990"	"2010"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C2936349"	"Plaque, Amyloid"	"phenotype"	"C23"	"Acquired Abnormality"	"0.40"	"0.93010752688172"	"1988"	"2016"	"1"	"0"	"CTD_human"
"351"	"APP"	"0.43"	"0.862"	"C3549448"	"ALZHEIMER DISEASE, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2005"	"26"	"11"	"UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C3888307"	"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"		"1990"	"2010"	"6"	"3"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C3888308"	"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"		"1990"	"2010"	"6"	"3"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C3888309"	"CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"		"1990"	"2010"	"6"	"3"	"CTD_human;UNIPROT"
"351"	"APP"	"0.43"	"0.862"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"GENOMICS_ENGLAND"
"353"	"APRT"	"0.453"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1985"	"2014"	"5"	"0"	"PSYGENET"
"353"	"APRT"	"0.453"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1985"	"2014"	"5"	"0"	"PSYGENET"
"353"	"APRT"	"0.453"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"353"	"APRT"	"0.453"	"0.724"	"C0268120"	"Adenine phosphoribosyltransferase deficiency"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.99"	"1"	"1986"	"2013"	"8"	"11"	"CTD_human;ORPHANET;UNIPROT"
"353"	"APRT"	"0.453"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C0451641"	"Urolithiasis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1985"	"2012"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"353"	"APRT"	"0.453"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"353"	"APRT"	"0.453"	"0.724"	"C3665382"	"2,8-Dihydroxyadenine Urolithiasis"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1985"	"2012"	"8"	"5"	"CTD_human;ORPHANET;UNIPROT"
"354"	"KLK3"	"0.519"	"0.793"	"C0005001"	"Benign prostatic hypertrophy"	"phenotype"	"C12"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.964285714285714"	"1992"	"2016"	"11"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.95959595959596"	"1991"	"2018"	"11"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C0520477"	"Prostatic Adenoma"	"disease"	"C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C1334615"	"Malignant Phyllodes Tumor of Prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C1704272"	"Benign Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.40"	"0.868421052631579"	"1990"	"2018"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C1739363"	"Prostatic Hypertrophy"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"354"	"KLK3"	"0.519"	"0.793"	"C2937421"	"Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0002897"	"Anemia, Splenic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"0.958333333333333"	"1989"	"2016"	"3"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"355"	"FAS"	"0.393"	"0.862"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2000"	"2014"	"1"	"3"	"CGI;UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0020532"	"Hypersplenism"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"1995"	"2014"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.36"	"0"	"1998"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.54"	"1"	"1998"	"2010"	"1"	"2"	"CGI;UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C0024535"	"Malaria, Falciparum"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0032963"	"Pregnancy Complications, Cardiovascular"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"3"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"355"	"FAS"	"0.393"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"3"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0039338"	"Taste Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0042170"	"Uveomeningoencephalitic Syndrome"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"355"	"FAS"	"0.393"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234297"	"Taste Disorder, Primary"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234298"	"Taste Disorder, Primary, Sweet"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234299"	"Taste Disorder, Primary, Salt"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234300"	"Taste Disorder, Primary, Bitter"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234302"	"Taste Disorder, Anterior Tongue"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234303"	"Taste Disorder, Secondary"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234304"	"Taste Disorder, Secondary, Sweet"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234305"	"Taste Disorder, Secondary, Salt"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234306"	"Taste Disorder, Secondary, Bitter"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0234319"	"Taste Disorder, Posterior Tongue"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0240327"	"Taste, Metallic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"1999"	"2018"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"355"	"FAS"	"0.393"	"0.862"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"3"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"1.00"	"0.941176470588235"	"1978"	"2017"	"15"	"8"	"CTD_human;ORPHANET;UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C1846545"	"Autoimmune Lymphoproliferative Syndrome Type 2B"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C1866119"	"Autoimmune Lymphoproliferative Syndrome, Type IA"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.43"	"1"	"1967"	"2011"	"13"	"17"	"UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C1866120"	"Autoimmune Lymphoproliferative Syndrome, Type IB"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"13"	"8"	"UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C1866121"	"Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"13"	"8"	"UNIPROT"
"355"	"FAS"	"0.393"	"0.862"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2000"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C2717884"	"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"355"	"FAS"	"0.393"	"0.862"	"C3496549"	"Male Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"356"	"FASLG"	"0.462"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2004"	"2005"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0020474"	"Hyperlipidemia, Familial Combined"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"		"2004"	"2007"	"0"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.857142857142857"	"2001"	"2016"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0039584"	"Testicular Diseases"	"group"	"C12;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2008"	"0"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2006"	"2008"	"2"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.93"	"1"	"1984"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"356"	"FASLG"	"0.462"	"0.862"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C1846545"	"Autoimmune Lymphoproliferative Syndrome Type 2B"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"356"	"FASLG"	"0.462"	"0.862"	"C1866119"	"Autoimmune Lymphoproliferative Syndrome, Type IA"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2016"	"2"	"0"	"UNIPROT"
"356"	"FASLG"	"0.462"	"0.862"	"C1866120"	"Autoimmune Lymphoproliferative Syndrome, Type IB"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.40"		"1996"	"2016"	"2"	"1"	"UNIPROT"
"356"	"FASLG"	"0.462"	"0.862"	"C1866121"	"Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"1996"	"2016"	"2"	"0"	"UNIPROT"
"356"	"FASLG"	"0.462"	"0.862"	"C2717884"	"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"357"	"SHROOM2"	"0.834"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"357"	"SHROOM2"	"0.834"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"358"	"AQP1"	"0.518"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0008340"	"Choledochal Cyst"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0009439"	"Choledochal Cyst, Type I"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0013608"	"Edema, Cardiac"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2010"	"2012"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"358"	"AQP1"	"0.518"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C1257796"	"Choledochal Cyst, Type II"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C1257797"	"Choledochal Cyst, Type III"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C1257798"	"Choledochal Cyst, Type IV"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C1257799"	"Choledochal Cyst, Type V"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"358"	"AQP1"	"0.518"	"0.759"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"358"	"AQP1"	"0.518"	"0.759"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"358"	"AQP1"	"0.518"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"359"	"AQP2"	"0.648"	"0.448"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C0162283"	"Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.90"	"1"	"1988"	"2014"	"4"	"5"	"CTD_human;ORPHANET"
"359"	"AQP2"	"0.648"	"0.448"	"C0268443"	"Acquired Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"4"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C0677501"	"Congenital Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2011"	"4"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C1563705"	"Nephrogenic Diabetes Insipidus, Type I"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"0.970588235294118"	"1994"	"2016"	"4"	"1"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C1563706"	"Nephrogenic Diabetes Insipidus, Type II"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"1994"	"2014"	"20"	"22"	"CTD_human;UNIPROT"
"359"	"AQP2"	"0.648"	"0.448"	"C3542500"	"ADH-Resistant Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"4"	"0"	"CTD_human"
"359"	"AQP2"	"0.648"	"0.448"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"360"	"AQP3"	"0.577"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"360"	"AQP3"	"0.577"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"361"	"AQP4"	"0.525"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"361"	"AQP4"	"0.525"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"361"	"AQP4"	"0.525"	"0.793"	"C0027873"	"Neuromyelitis Optica"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.40"	"0.959459459459459"	"2005"	"2018"	"2"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"361"	"AQP4"	"0.525"	"0.793"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"361"	"AQP4"	"0.525"	"0.793"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"361"	"AQP4"	"0.525"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2017"	"8"	"0"	"GENOMICS_ENGLAND"
"362"	"AQP5"	"0.582"	"0.621"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"362"	"AQP5"	"0.582"	"0.621"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"362"	"AQP5"	"0.582"	"0.621"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"362"	"AQP5"	"0.582"	"0.621"	"C1833030"	"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"362"	"AQP5"	"0.582"	"0.621"	"C1838359"	"Diffuse palmoplantar keratoderma, Bothnian type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1995"	"2013"	"1"	"5"	"ORPHANET;UNIPROT"
"362"	"AQP5"	"0.582"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"363"	"AQP6"	"0.785"	"0.31"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"364"	"AQP7"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"364"	"AQP7"	"0.762"	"0.241"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.38"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"364"	"AQP7"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"366"	"AQP9"	"0.63"	"0.586"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"366"	"AQP9"	"0.63"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"2"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.39"	"0.888888888888889"	"2000"	"2014"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.940397350993378"	"1990"	"2018"	"2"	"2"	"CTD_human;UNIPROT"
"367"	"AR"	"0.38"	"0.793"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.60"	"0.9"	"2003"	"2016"	"0"	"0"	"CGI"
"367"	"AR"	"0.38"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"1994"	"2014"	"5"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"1994"	"2014"	"5"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0017412"	"Genital Diseases, Male"	"group"	"C12"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.40"	"0.947368421052632"	"1996"	"2016"	"3"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.97029702970297"	"1990"	"2018"	"21"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.666666666666667"	"1994"	"2006"	"1"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.34"	"1"	"2009"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"367"	"AR"	"0.38"	"0.793"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0039585"	"Androgen-Insensitivity Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"1.00"	"0.939597315436242"	"1970"	"2018"	"74"	"48"	"CTD_human;ORPHANET;UNIPROT"
"367"	"AR"	"0.38"	"0.793"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.50"	"0.857142857142857"	"2005"	"2015"	"1"	"11"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2009"	"2011"	"3"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0238033"	"Carcinoma of Male Breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2018"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0242788"	"Breast Neoplasms, Male"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1993"	"1994"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0268301"	"Reifenstein Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.80"	"0.967213114754098"	"1984"	"2018"	"41"	"26"	"CTD_human;ORPHANET;UNIPROT"
"367"	"AR"	"0.38"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.70"	"0.97997138769671"	"1985"	"2018"	"38"	"14"	"CTD_human;UNIPROT"
"367"	"AR"	"0.38"	"0.793"	"C0393547"	"Bulbospinal Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"1990"	"2011"	"0"	"0"	"ORPHANET"
"367"	"AR"	"0.38"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2018"	"1"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0556385"	"Craving for alcohol"	"phenotype"		"Finding"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"367"	"AR"	"0.38"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"1990"	"2018"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0752353"	"Atrophy, Muscular, Spinobulbar"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.979166666666667"	"1993"	"2015"	"0"	"0"	"ORPHANET"
"367"	"AR"	"0.38"	"0.793"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.32"	"1"	"2002"	"2011"	"3"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0860159"	"Partial androgen resistance"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"367"	"AR"	"0.38"	"0.793"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2003"	"2010"	"3"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C0936016"	"Testicular Feminization"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"0.957746478873239"	"1970"	"2018"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"1990"	"2016"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C1839259"	"Bulbo-Spinal Atrophy, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.982558139534884"	"1990"	"2018"	"0"	"4"	"ORPHANET"
"367"	"AR"	"0.38"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2017"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C2678098"	"Hypospadias 1, X-Linked"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.60"		"1993"	"1996"	"0"	"2"	"CTD_human;ORPHANET"
"367"	"AR"	"0.38"	"0.793"	"C2713546"	"Androgen Receptor Deficiency"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"0"	"1984"	"1994"	"2"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C2931395"	"Bulbospinal neuronopathy, X-linked recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.35"	"0.8"	"1992"	"1999"	"0"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C2931847"	"Type I familial incomplete male pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"1991"	"2004"	"41"	"20"	"UNIPROT"
"367"	"AR"	"0.38"	"0.793"	"C3658266"	"Prostatic Cancer, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2017"	"3"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C3658267"	"Prostatic Neoplasms, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2017"	"3"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"367"	"AR"	"0.38"	"0.793"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"2001"	"2015"	"1"	"0"	"CTD_human"
"367"	"AR"	"0.38"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"368"	"ABCC6"	"0.59"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"368"	"ABCC6"	"0.59"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"368"	"ABCC6"	"0.59"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"368"	"ABCC6"	"0.59"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"4"	"0"	"GENOMICS_ENGLAND"
"368"	"ABCC6"	"0.59"	"0.552"	"C0033847"	"Pseudoxanthoma Elasticum"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"1.00"	"0.905982905982906"	"2000"	"2018"	"22"	"268"	"CTD_human;ORPHANET;UNIPROT"
"368"	"ABCC6"	"0.59"	"0.552"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"368"	"ABCC6"	"0.59"	"0.552"	"C0264955"	"Idiopathic arterial calcification of infancy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"368"	"ABCC6"	"0.59"	"0.552"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"368"	"ABCC6"	"0.59"	"0.552"	"C0376359"	"Gronblad-Strandberg Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.50"		"2000"	"2015"	"22"	"76"	"CTD_human;UNIPROT"
"368"	"ABCC6"	"0.59"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"368"	"ABCC6"	"0.59"	"0.552"	"C1859727"	"Arterial calcification of infancy"	"disease"	"C18"	"Disease or Syndrome"	"0.55"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"368"	"ABCC6"	"0.59"	"0.552"	"C1867450"	"Pseudoxanthoma Elasticum, Incomplete"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"		"2001"	"2017"	"8"	"2"	"CTD_human"
"368"	"ABCC6"	"0.59"	"0.552"	"C3276161"	"ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2012"	"1"	"13"	"UNIPROT"
"368"	"ABCC6"	"0.59"	"0.552"	"C3279392"	"PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2015"	"15"	"76"	"UNIPROT"
"368"	"ABCC6"	"0.59"	"0.552"	"C3279393"	"PXE, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2015"	"15"	"76"	"UNIPROT"
"368"	"ABCC6"	"0.59"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"369"	"ARAF"	"0.701"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"369"	"ARAF"	"0.701"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.41"	"1"	"2014"	"2016"	"0"	"2"	"CGI"
"369"	"ARAF"	"0.701"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"369"	"ARAF"	"0.701"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"369"	"ARAF"	"0.701"	"0.414"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"369"	"ARAF"	"0.701"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"372"	"ARCN1"	"0.696"	"0.483"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"372"	"ARCN1"	"0.696"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"374"	"AREG"	"0.525"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2011"	"2"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1995"	"2018"	"3"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2006"	"3"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0162568"	"Erythropoietic Protoporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0349426"	"Ferrochelatase deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1992"	"2008"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2006"	"3"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374"	"AREG"	"0.525"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"375"	"ARF1"	"0.727"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"375"	"ARF1"	"0.727"	"0.379"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"375"	"ARF1"	"0.727"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"375"	"ARF1"	"0.727"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"375"	"ARF1"	"0.727"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2008"	"2016"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9"	"2003"	"2014"	"2"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"383"	"ARG1"	"0.551"	"0.724"	"C0018500"	"Hair Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0021053"	"Immune System Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.50"		"2004"	"2007"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.44"	"0.75"	"2013"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"383"	"ARG1"	"0.551"	"0.724"	"C0268548"	"Hyperargininemia"	"phenotype"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1979"	"2018"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"383"	"ARG1"	"0.551"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"383"	"ARG1"	"0.551"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"383"	"ARG1"	"0.551"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"383"	"ARG1"	"0.551"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.39"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2013"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"384"	"ARG2"	"0.627"	"0.586"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0000771"	"Abnormalities, Drug-Induced"	"phenotype"	"C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"387"	"RHOA"	"0.565"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0020981"	"Angioimmunoblastic Lymphadenopathy"	"disease"	"C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2014"	"2018"	"2"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2016"	"0"	"0"	"CGI"
"387"	"RHOA"	"0.565"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2018"	"3"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2005"	"2014"	"3"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"387"	"RHOA"	"0.565"	"0.586"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"387"	"RHOA"	"0.565"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2014"	"3"	"0"	"CTD_human"
"388"	"RHOB"	"0.672"	"0.31"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2012"	"2015"	"1"	"0"	"CTD_human"
"389"	"RHOC"	"0.656"	"0.31"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"389"	"RHOC"	"0.656"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"392"	"ARHGAP1"	"0.681"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"393"	"ARHGAP4"	"0.752"	"0.345"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"393"	"ARHGAP4"	"0.752"	"0.345"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"395"	"ARHGAP6"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C3808953"	"NEPHROTIC SYNDROME, TYPE 8"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"3"	"CTD_human"
"396"	"ARHGDIA"	"0.672"	"0.552"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"397"	"ARHGDIB"	"0.701"	"0.31"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"397"	"ARHGDIB"	"0.701"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"397"	"ARHGDIB"	"0.701"	"0.31"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"397"	"ARHGDIB"	"0.701"	"0.31"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"401"	"PHOX2A"	"0.735"	"0.276"	"C1302995"	"Congenital Fibrosis of the Extraocular Muscles"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.48"	"0.875"	"2001"	"2010"	"0"	"0"	"ORPHANET"
"401"	"PHOX2A"	"0.735"	"0.276"	"C1865915"	"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.63"	"0.666666666666667"	"2001"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"402"	"ARL2"	"0.799"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2006"	"2013"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"405"	"ARNT"	"0.602"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"406"	"ARNTL"	"0.569"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2017"	"3"	"0"	"PSYGENET"
"406"	"ARNTL"	"0.569"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2017"	"3"	"0"	"PSYGENET"
"406"	"ARNTL"	"0.569"	"0.621"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"406"	"ARNTL"	"0.569"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0268548"	"Hyperargininemia"	"phenotype"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406"	"ARNTL"	"0.569"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"406"	"ARNTL"	"0.569"	"0.621"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"408"	"ARRB1"	"0.616"	"0.552"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"408"	"ARRB1"	"0.616"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"408"	"ARRB1"	"0.616"	"0.552"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"408"	"ARRB1"	"0.616"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"408"	"ARRB1"	"0.616"	"0.552"	"C3178803"	"Social Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"409"	"ARRB2"	"0.604"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"409"	"ARRB2"	"0.604"	"0.621"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"409"	"ARRB2"	"0.604"	"0.621"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"409"	"ARRB2"	"0.604"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"409"	"ARRB2"	"0.604"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"410"	"ARSA"	"0.547"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1984"	"2002"	"4"	"0"	"PSYGENET"
"410"	"ARSA"	"0.547"	"0.724"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"410"	"ARSA"	"0.547"	"0.724"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"410"	"ARSA"	"0.547"	"0.724"	"C0023522"	"Leukodystrophy, Metachromatic"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.933774834437086"	"1980"	"2018"	"42"	"134"	"CTD_human;UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1997"	"1997"	"1"	"0"	"PSYGENET"
"410"	"ARSA"	"0.547"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"410"	"ARSA"	"0.547"	"0.724"	"C0751276"	"Metachromatic leukodystrophy, juvenile type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1983"	"2011"	"42"	"95"	"CTD_human;ORPHANET;UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C0751278"	"Metachromatic Leukodystrophy, Infant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1990"	"2011"	"42"	"93"	"CTD_human;ORPHANET;UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C0751279"	"Metachromatic Leukodystrophy, Adult-Type (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1983"	"2011"	"42"	"94"	"CTD_human;ORPHANET;UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1997"	"1997"	"1"	"0"	"PSYGENET"
"410"	"ARSA"	"0.547"	"0.724"	"C1855255"	"Pseudoarylsulfatase A Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"1984"	"2011"	"42"	"93"	"UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C2713319"	"Arylsulfatase A Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.55"	"1"	"1980"	"2018"	"42"	"93"	"CTD_human;UNIPROT"
"410"	"ARSA"	"0.547"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1990"	"2003"	"23"	"0"	"GENOMICS_ENGLAND"
"411"	"ARSB"	"0.667"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1993"	"2002"	"3"	"0"	"GENOMICS_ENGLAND"
"411"	"ARSB"	"0.667"	"0.586"	"C0026709"	"Mucopolysaccharidosis VI"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.90"	"1"	"1985"	"2017"	"11"	"20"	"CTD_human;UNIPROT"
"411"	"ARSB"	"0.667"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"411"	"ARSB"	"0.667"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2007"	"6"	"0"	"GENOMICS_ENGLAND"
"412"	"STS"	"0.487"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0019187"	"Hepatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0079588"	"Ichthyosis, X-Linked"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.80"	"0.923076923076923"	"1980"	"2017"	"6"	"5"	"CTD_human;ORPHANET;UNIPROT"
"412"	"STS"	"0.487"	"0.828"	"C0524610"	"Chronic Alcoholic Hepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C2677713"	"Ichthyosis, X-Linked, Complicated"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1992"	"2000"	"4"	"5"	"UNIPROT"
"412"	"STS"	"0.487"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"412"	"STS"	"0.487"	"0.828"	"C2717836"	"Steroid Sulfatase Deficiency Disease"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.70"	"0.928571428571429"	"1982"	"2006"	"6"	"5"	"CTD_human;ORPHANET;UNIPROT"
"412"	"STS"	"0.487"	"0.828"	"C2720163"	"Placental Steroid Sulfatase Deficiency"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.70"	"0.961538461538462"	"1980"	"2016"	"6"	"5"	"CTD_human;ORPHANET;UNIPROT"
"412"	"STS"	"0.487"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"1985"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"412"	"STS"	"0.487"	"0.828"	"C4274085"	"Syndromic recessive X-linked ichthyosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"415"	"ARSE"	"0.735"	"0.448"	"C0008445"	"Chondrodysplasia Punctata"	"disease"	"C05"	"Congenital Abnormality"	"0.35"	"0.8"	"1997"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"415"	"ARSE"	"0.735"	"0.448"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"415"	"ARSE"	"0.735"	"0.448"	"C1844853"	"Brachytelephalangic Chondrodysplasia Punctata"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"0.666666666666667"	"1989"	"2015"	"3"	"12"	"CTD_human;ORPHANET;UNIPROT"
"415"	"ARSE"	"0.735"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"416"	"ARSF"	"0.72"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"421"	"ARVCF"	"0.621"	"0.586"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"421"	"ARVCF"	"0.621"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2014"	"4"	"0"	"PSYGENET"
"421"	"ARVCF"	"0.621"	"0.586"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"421"	"ARVCF"	"0.621"	"0.586"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"421"	"ARVCF"	"0.621"	"0.586"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"421"	"ARVCF"	"0.621"	"0.586"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"421"	"ARVCF"	"0.621"	"0.586"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"421"	"ARVCF"	"0.621"	"0.586"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"427"	"ASAH1"	"0.57"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1997"	"2"	"0"	"GENOMICS_ENGLAND"
"427"	"ASAH1"	"0.57"	"0.69"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"427"	"ASAH1"	"0.57"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"427"	"ASAH1"	"0.57"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"427"	"ASAH1"	"0.57"	"0.69"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"427"	"ASAH1"	"0.57"	"0.69"	"C0268255"	"Farber Lipogranulomatosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1989"	"2015"	"8"	"6"	"CTD_human;ORPHANET;UNIPROT"
"427"	"ASAH1"	"0.57"	"0.69"	"C1834569"	"Jankovic Rivera syndrome"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"427"	"ASAH1"	"0.57"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1997"	"2008"	"4"	"0"	"GENOMICS_ENGLAND"
"429"	"ASCL1"	"0.569"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"0"	"1"	"CTD_human"
"429"	"ASCL1"	"0.569"	"0.552"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"429"	"ASCL1"	"0.569"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"430"	"ASCL2"	"0.713"	"0.103"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"430"	"ASCL2"	"0.713"	"0.103"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"434"	"ASIP"	"0.639"	"0.448"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"434"	"ASIP"	"0.639"	"0.448"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"434"	"ASIP"	"0.639"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"1995"	"2013"	"3"	"0"	"CTD_human"
"434"	"ASIP"	"0.639"	"0.448"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"434"	"ASIP"	"0.639"	"0.448"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"435"	"ASL"	"0.69"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"435"	"ASL"	"0.69"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.41"	"1"	"1991"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"435"	"ASL"	"0.69"	"0.345"	"C0268547"	"Argininosuccinic Aciduria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1987"	"2017"	"7"	"54"	"CTD_human;ORPHANET;UNIPROT"
"435"	"ASL"	"0.69"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1993"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"438"	"ASMT"	"0.72"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"438"	"ASMT"	"0.72"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"438"	"ASMT"	"0.72"	"0.276"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"438"	"ASMT"	"0.72"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"438"	"ASMT"	"0.72"	"0.276"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"438"	"ASMT"	"0.72"	"0.276"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"438"	"ASMT"	"0.72"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"440"	"ASNS"	"0.636"	"0.552"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"440"	"ASNS"	"0.636"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"440"	"ASNS"	"0.636"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"440"	"ASNS"	"0.636"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"440"	"ASNS"	"0.636"	"0.552"	"C3809971"	"ASPARAGINE SYNTHETASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2014"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"443"	"ASPA"	"0.611"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"1993"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"443"	"ASPA"	"0.611"	"0.586"	"C0206307"	"Canavan Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.933333333333333"	"1990"	"2018"	"15"	"40"	"CTD_human;UNIPROT"
"443"	"ASPA"	"0.611"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"443"	"ASPA"	"0.611"	"0.586"	"C0751663"	"Canavan Disease, Familial Form"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1994"	"2013"	"2"	"4"	"CTD_human"
"443"	"ASPA"	"0.611"	"0.586"	"C0751664"	"Canavan Disease, Neonatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2006"	"2007"	"2"	"0"	"CTD_human;ORPHANET"
"443"	"ASPA"	"0.611"	"0.586"	"C0751665"	"Canavan Disease, Sporadic Form"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"443"	"ASPA"	"0.611"	"0.586"	"C0751666"	"Canavan Disease, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2006"	"2007"	"2"	"0"	"CTD_human;ORPHANET"
"443"	"ASPA"	"0.611"	"0.586"	"C0751667"	"Canavan Disease, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2006"	"2007"	"2"	"0"	"CTD_human;ORPHANET"
"443"	"ASPA"	"0.611"	"0.586"	"C3542499"	"Aminoacylase 2 Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2007"	"2"	"0"	"CTD_human"
"443"	"ASPA"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"444"	"ASPH"	"0.648"	"0.448"	"C1832167"	"Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.71"	"1"	"2001"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"444"	"ASPH"	"0.648"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"445"	"ASS1"	"0.558"	"0.759"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"445"	"ASS1"	"0.558"	"0.759"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"445"	"ASS1"	"0.558"	"0.759"	"C0175683"	"Citrullinemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.972222222222222"	"1976"	"2017"	"16"	"67"	"CTD_human;UNIPROT"
"445"	"ASS1"	"0.558"	"0.759"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.45"	"1"	"1990"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"445"	"ASS1"	"0.558"	"0.759"	"C0751750"	"Argininosuccinic Acid Synthetase Deficiency Disease, Partial"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"445"	"ASS1"	"0.558"	"0.759"	"C0751751"	"Argininosuccinic Acid Synthetase Deficiency, Complete"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2015"	"0"	"0"	"CTD_human"
"445"	"ASS1"	"0.558"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"460"	"ASTN1"	"0.815"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"460"	"ASTN1"	"0.815"	"0.138"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"460"	"ASTN1"	"0.815"	"0.138"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"460"	"ASTN1"	"0.815"	"0.138"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"460"	"ASTN1"	"0.815"	"0.138"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"460"	"ASTN1"	"0.815"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1977"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"1984"	"2014"	"3"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0018674"	"Craniocerebral Trauma"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1995"	"2001"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.51"		"1983"	"2007"	"4"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.34"		"1976"	"2007"	"3"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0079102"	"Cerebral Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1980"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1983"	"2001"	"4"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"1976"	"2018"	"3"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0272375"	"Antithrombin III Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"1.00"	"0.941176470588235"	"1965"	"2018"	"37"	"35"	"CTD_human;ORPHANET;UNIPROT"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0347536"	"Head Injury, Superficial"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0451948"	"Head Injuries, Multiple"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0451981"	"Crushing Skull Injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0518454"	"Head Injury, Open"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0555305"	"Head Injury, Minor"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0751181"	"Frontal Region Trauma"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0751182"	"Occipital Region Trauma"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0751183"	"Parietal Region Trauma"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0751184"	"Temporal Region Trauma"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0752143"	"Intracranial Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0752144"	"Brain Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0936261"	"Brain Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0936263"	"Cerebral Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1979"	"2018"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"462"	"SERPINC1"	"0.554"	"0.621"	"C3658294"	"Hereditary Antithrombin Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"1984"	"2014"	"1"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"	"0.941176470588235"	"2009"	"2018"	"3"	"5"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2018"	"3"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.46"	"1"	"2012"	"2018"	"1"	"2"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"3"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2018"	"3"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2012"	"3"	"0"	"CTD_human"
"463"	"ZFHX3"	"0.656"	"0.517"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2012"	"3"	"0"	"CTD_human"
"466"	"ATF1"	"0.639"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"466"	"ATF1"	"0.639"	"0.345"	"C0206651"	"Clear Cell Sarcoma of Soft Tissue"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.967741935483871"	"1993"	"2016"	"0"	"0"	"ORPHANET"
"466"	"ATF1"	"0.639"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"467"	"ATF3"	"0.517"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"467"	"ATF3"	"0.517"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0848558"	"Hypospadias"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.36"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"467"	"ATF3"	"0.517"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2008"	"2"	"0"	"PSYGENET"
"468"	"ATF4"	"0.57"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"468"	"ATF4"	"0.57"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"468"	"ATF4"	"0.57"	"0.621"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"468"	"ATF4"	"0.57"	"0.621"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"468"	"ATF4"	"0.57"	"0.621"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0155003"	"Blindness, Transient"	"phenotype"	"C10;C11;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0221473"	"Blindness, Hysterical"	"disease"	"C10;C11;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0271215"	"Blindness, Legal"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0339730"	"Blindness, Acquired"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0376288"	"Amaurosis"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0456909"	"Blindness"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0750958"	"Blindness, Monocular"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C1837530"	"AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2004"	"2004"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"471"	"ATIC"	"0.607"	"0.621"	"C1879328"	"Blindness both eyes NOS (disorder)"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"471"	"ATIC"	"0.607"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"472"	"ATM"	"0.401"	"0.862"	"C0004135"	"Ataxia Telangiectasia"	"disease"	"C10;C14;C16;C18;C20"	"Disease or Syndrome"	"1.00"	"0.943548387096774"	"1978"	"2018"	"32"	"385"	"CTD_human;ORPHANET;UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.56"	"1"	"2008"	"2017"	"1"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.57"	"1"	"2008"	"2017"	"1"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.949275362318841"	"1996"	"2018"	"0"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.63"	"1"	"2011"	"2018"	"1"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.875"	"2004"	"2015"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2013"	"2017"	"6"	"0"	"CLINGEN"
"472"	"ATM"	"0.401"	"0.862"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"2001"	"2018"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1998"	"2017"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"0.95"	"1998"	"2017"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.904761904761905"	"1998"	"2017"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1998"	"2018"	"1"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2008"	"2017"	"1"	"1"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.38"	"1"	"2003"	"2018"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2018"	"4"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"472"	"ATM"	"0.401"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2001"	"2015"	"1"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"2"	"UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"1"	"2"	"UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"1999"	"2016"	"2"	"3"	"CGI;UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.923076923076923"	"1998"	"2016"	"5"	"11"	"CLINGEN"
"472"	"ATM"	"0.401"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"2001"	"2018"	"4"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0555202"	"Malignant lymphoma - lymphocytic, intermediate differentiation"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"472"	"ATM"	"0.401"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.946666666666667"	"1996"	"2018"	"0"	"0"	"CGI;CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.36"	"1"	"2008"	"2017"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.31"	"0"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"472"	"ATM"	"0.401"	"0.862"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2003"	"2003"	"0"	"0"	"CGI"
"472"	"ATM"	"0.401"	"0.862"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2017"	"6"	"0"	"CLINGEN"
"472"	"ATM"	"0.401"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.57"	"1"	"1998"	"2018"	"4"	"0"	"CGI;CLINGEN"
"472"	"ATM"	"0.401"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.50"		"2007"	"2007"	"1"	"5"	"CGI;UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"6"	"0"	"CLINGEN"
"472"	"ATM"	"0.401"	"0.862"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.818181818181818"	"1996"	"2015"	"0"	"2"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"472"	"ATM"	"0.401"	"0.862"	"C1876175"	"Ataxia-Telangiectasia Variant"	"disease"	"C10;C14;C16;C18;C20"	"Disease or Syndrome"	"0.60"		"1995"	"2016"	"27"	"28"	"ORPHANET;UNIPROT"
"472"	"ATM"	"0.401"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"472"	"ATM"	"0.401"	"0.862"	"C2363142"	"T-Cell Prolymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"1996"	"2014"	"2"	"7"	"CGI;UNIPROT"
"473"	"RERE"	"0.582"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"473"	"RERE"	"0.582"	"0.655"	"C1842870"	"Chromosome 1p36 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"473"	"RERE"	"0.582"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"473"	"RERE"	"0.582"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"473"	"RERE"	"0.582"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"473"	"RERE"	"0.582"	"0.655"	"C4310772"	"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2018"	"1"	"6"	"CTD_human;UNIPROT"
"474"	"ATOH1"	"0.659"	"0.276"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.875"	"2005"	"2014"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"474"	"ATOH1"	"0.659"	"0.276"	"C1879677"	"Alcohol Toxicity"	"disease"		"Injury or Poisoning"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"475"	"ATOX1"	"0.743"	"0.345"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"475"	"ATOX1"	"0.743"	"0.345"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1999"	"1999"	"1"	"0"	"PSYGENET"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0017162"	"Gastroenteritis, Transmissible, of Swine"	"disease"	"C02;C22"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.56"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"476"	"ATP1A1"	"0.667"	"0.552"	"C0206667"	"Adrenal Cortical Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"476"	"ATP1A1"	"0.667"	"0.552"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"477"	"ATP1A2"	"0.624"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"477"	"ATP1A2"	"0.624"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2001"	"2006"	"2"	"0"	"CTD_human"
"477"	"ATP1A2"	"0.624"	"0.31"	"C0270862"	"Hemiplegic migraine"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2004"	"2018"	"0"	"0"	"ORPHANET"
"477"	"ATP1A2"	"0.624"	"0.31"	"C0338488"	"Alternating hemiplegia of childhood"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.52"	"0.5"	"2004"	"2005"	"0"	"0"	"CTD_human;ORPHANET"
"477"	"ATP1A2"	"0.624"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"477"	"ATP1A2"	"0.624"	"0.31"	"C1865322"	"MIGRAINE, FAMILIAL HEMIPLEGIC, 2"	"disease"	"C10"	"Disease or Syndrome"	"0.69"	"1"	"1998"	"2016"	"5"	"11"	"CTD_human;UNIPROT"
"477"	"ATP1A2"	"0.624"	"0.31"	"C1865323"	"Migraine, Familial Basilar"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2003"	"2014"	"4"	"5"	"UNIPROT"
"477"	"ATP1A2"	"0.624"	"0.31"	"C3549447"	"ALTERNATING HEMIPLEGIA OF CHILDHOOD 1"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"477"	"ATP1A2"	"0.624"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2004"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"0.5"	"1998"	"2001"	"2"	"0"	"PSYGENET"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.47"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0338488"	"Alternating hemiplegia of childhood"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"	"0.964285714285714"	"2012"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C1832466"	"CAPOS syndrome"	"disease"	"C05;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.76"	"1"	"2014"	"2018"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"478"	"ATP1A3"	"0.58"	"0.379"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C1868681"	"DYSTONIA 12"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"0.90625"	"1993"	"2017"	"4"	"21"	"CTD_human;ORPHANET;UNIPROT"
"478"	"ATP1A3"	"0.58"	"0.379"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"478"	"ATP1A3"	"0.58"	"0.379"	"C3553788"	"ALTERNATING HEMIPLEGIA OF CHILDHOOD 2"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1993"	"2017"	"5"	"35"	"UNIPROT"
"478"	"ATP1A3"	"0.58"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"480"	"ATP1A4"	"0.928"	"0.138"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"481"	"ATP1B1"	"0.69"	"0.345"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"482"	"ATP1B2"	"0.752"	"0.207"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"482"	"ATP1B2"	"0.752"	"0.207"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"482"	"ATP1B2"	"0.752"	"0.207"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"1"	"1"	"CTD_human"
"482"	"ATP1B2"	"0.752"	"0.207"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"486"	"FXYD2"	"0.785"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"486"	"FXYD2"	"0.785"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"486"	"FXYD2"	"0.785"	"0.31"	"C0024473"	"Magnesium Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"486"	"FXYD2"	"0.785"	"0.31"	"C0268448"	"Primary hypomagnesemia (disorder)"	"disease"	"C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"486"	"FXYD2"	"0.785"	"0.31"	"C1835171"	"Hypomagnesemia 2, renal"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"		"1987"	"2002"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"487"	"ATP2A1"	"0.707"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"487"	"ATP2A1"	"0.707"	"0.276"	"C1832918"	"Brody myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.909090909090909"	"1996"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"487"	"ATP2A1"	"0.707"	"0.276"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"487"	"ATP2A1"	"0.707"	"0.276"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.14"	"1"	"2001"	"2017"	"1"	"0"	"PSYGENET"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2004"	"2"	"0"	"PSYGENET"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2004"	"2"	"0"	"PSYGENET"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.51"		"2005"	"2011"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.909090909090909"	"1996"	"2016"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.57"	"0.857142857142857"	"1996"	"2016"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0022595"	"Keratosis Follicularis"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"0.983333333333333"	"1999"	"2018"	"7"	"7"	"CTD_human;ORPHANET;UNIPROT"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2013"	"2017"	"1"	"1"	"PSYGENET"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0206145"	"Stunned Myocardium"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0206146"	"Myocardial Stunning"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0265971"	"Acrokeratosis Verruciformis of Hopf"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.73"	"1"	"2003"	"2013"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0376416"	"Hibernation, Myocardial"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0473575"	"Acantholytic Dyskeratotic Epidermal Nevus"	"disease"	"C16;C17"	"Neoplastic Process"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2002"	"2"	"0"	"PSYGENET"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2002"	"2015"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C1852296"	"Darier Disease, Acral Hemorrhagic Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2000"	"2018"	"5"	"6"	"UNIPROT"
"488"	"ATP2A2"	"0.572"	"0.552"	"C1852297"	"Darier Disease, Segmental"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2000"	"2018"	"5"	"7"	"UNIPROT"
"488"	"ATP2A2"	"0.572"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"488"	"ATP2A2"	"0.572"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"1"	"UNIPROT"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"489"	"ATP2A3"	"0.652"	"0.448"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.9375"	"1999"	"2017"	"1"	"3"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"490"	"ATP2B1"	"0.707"	"0.379"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2018"	"1"	"3"	"CTD_human"
"491"	"ATP2B2"	"0.743"	"0.345"	"C1832394"	"Deafness, Autosomal Recessive 12"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C0796205"	"SPINOCEREBELLAR ATAXIA, X-LINKED 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2000"	"2012"	"1"	"1"	"UNIPROT"
"492"	"ATP2B3"	"0.667"	"0.414"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"492"	"ATP2B3"	"0.667"	"0.414"	"C2678048"	"Spinocerebellar Ataxia, X-Linked 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"492"	"ATP2B3"	"0.667"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C3808899"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"498"	"ATP5F1A"	"0.639"	"0.448"	"C4015062"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C1291560"	"Deficiency of glutamate decarboxylase"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C1849508"	"EPILEPSY, PYRIDOXINE-DEPENDENT"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"1"	"2005"	"2017"	"3"	"19"	"CTD_human;ORPHANET;UNIPROT"
"501"	"ALDH7A1"	"0.594"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"506"	"ATP5F1B"	"0.773"	"0.276"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human"
"513"	"ATP5F1D"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"513"	"ATP5F1D"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"514"	"ATP5F1E"	"0.752"	"0.345"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"514"	"ATP5F1E"	"0.752"	"0.345"	"C3279708"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"522"	"ATP5PF"	"0.762"	"0.345"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"523"	"ATP6V1A"	"0.672"	"0.448"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"523"	"ATP6V1A"	"0.672"	"0.448"	"C0268355"	"Cutis Laxa, Autosomal Recessive, Type IIA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"523"	"ATP6V1A"	"0.672"	"0.448"	"C4479387"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"523"	"ATP6V1A"	"0.672"	"0.448"	"C4479409"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2017"	"0"	"2"	"CTD_human;ORPHANET;UNIPROT"
"525"	"ATP6V1B1"	"0.752"	"0.276"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.46"	"1"	"2001"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"525"	"ATP6V1B1"	"0.752"	"0.276"	"C0403554"	"Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness"	"disease"	"C09;C10;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.60"		"1999"	"2013"	"3"	"5"	"CTD_human;UNIPROT"
"525"	"ATP6V1B1"	"0.752"	"0.276"	"C1864498"	"RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2014"	"0"	"0"	"ORPHANET"
"525"	"ATP6V1B1"	"0.752"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C0796013"	"Zimmerman Laband syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C2675730"	"Deafness, Congenital, and Onychodystrophy, Autosomal Dominant"	"disease"	"C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.60"		"2014"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"526"	"ATP6V1B2"	"0.676"	"0.379"	"C4225321"	"ZIMMERMANN-LABAND SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2015"	"1"	"2"	"UNIPROT"
"529"	"ATP6V1E1"	"0.624"	"0.621"	"C0268355"	"Cutis Laxa, Autosomal Recessive, Type IIA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"529"	"ATP6V1E1"	"0.624"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"529"	"ATP6V1E1"	"0.624"	"0.621"	"C4479387"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"529"	"ATP6V1E1"	"0.624"	"0.621"	"C4479409"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"533"	"ATP6V0B"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"537"	"ATP6AP1"	"0.63"	"0.586"	"C4310819"	"IMMUNODEFICIENCY 47"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"538"	"ATP7A"	"0.518"	"0.655"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0003496"	"Aortic Rupture"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"1990"	"2016"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0022716"	"Menkes Kinky Hair Syndrome"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.958333333333333"	"1953"	"2018"	"40"	"83"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"538"	"ATP7A"	"0.518"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0027854"	"Neurologic Manifestations"	"group"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235031"	"Neurologic Symptoms"	"group"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0268353"	"Cutis laxa, x-linked"	"disease"	"C14;C15;C16;C17"	"Congenital Abnormality"	"0.80"	"0.956521739130435"	"1994"	"2016"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"538"	"ATP7A"	"0.518"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422837"	"Neurological observations"	"group"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0521654"	"Neurologic Deficits"	"group"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C0741160"	"Aortic Aneurysm, Ruptured"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"1990"	"2016"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0746857"	"Focal Neurologic Deficits"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751377"	"Neurologic Dysfunction"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751378"	"Neurologic Signs"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C1096660"	"Ehlers-Danlos syndrome type IX"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"538"	"ATP7A"	"0.518"	"0.655"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C1845359"	"Spinal Muscular Atrophy, Distal, X-Linked 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2004"	"2010"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"538"	"ATP7A"	"0.518"	"0.655"	"C2936380"	"Neointima"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C2936381"	"Neointima Formation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"538"	"ATP7A"	"0.518"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"538"	"ATP7A"	"0.518"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"540"	"ATP7B"	"0.547"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2007"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.976076555023923"	"1983"	"2018"	"124"	"207"	"CTD_human;ORPHANET;UNIPROT"
"540"	"ATP7B"	"0.547"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"540"	"ATP7B"	"0.547"	"0.621"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2000"	"2015"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"540"	"ATP7B"	"0.547"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2002"	"2009"	"3"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2002"	"2008"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"540"	"ATP7B"	"0.547"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"540"	"ATP7B"	"0.547"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2015"	"51"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"540"	"ATP7B"	"0.547"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"545"	"ATR"	"0.486"	"0.759"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2014"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2017"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.34"	"1"	"2006"	"2015"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"545"	"ATR"	"0.486"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"545"	"ATR"	"0.486"	"0.759"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.80"	"1"	"2005"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"545"	"ATR"	"0.486"	"0.759"	"C0280313"	"Squamous cell carcinoma of oropharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"545"	"ATR"	"0.486"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2000"	"2017"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"545"	"ATR"	"0.486"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2015"	"0"	"0"	"CGI"
"545"	"ATR"	"0.486"	"0.759"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"545"	"ATR"	"0.486"	"0.759"	"C3281203"	"CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL"	"disease"		"Neoplastic Process"	"0.70"		"2012"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"546"	"ATRX"	"0.489"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.958333333333333"	"2013"	"2018"	"2"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0030846"	"Penile Diseases"	"group"	"C12"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0039978"	"Thoracic Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"546"	"ATRX"	"0.489"	"0.69"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C0585216"	"Alpha-Thalassemia Myelodysplasia Syndrome"	"disease"	"C15;C16"	"Neoplastic Process"	"0.61"	"1"	"2003"	"2003"	"0"	"2"	"CTD_human;ORPHANET"
"546"	"ATRX"	"0.489"	"0.69"	"C0796003"	"Juberg-Marsidi syndrome"	"disease"	"C09;C10;C16;C19;C23"	"Disease or Syndrome"	"0.71"	"1"	"1996"	"2016"	"13"	"2"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"546"	"ATRX"	"0.489"	"0.69"	"C0796159"	"Mental retardation Smith Fineman Myers type"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"ORPHANET"
"546"	"ATRX"	"0.489"	"0.69"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C1328479"	"Pancreatic Endocrine Carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"546"	"ATRX"	"0.489"	"0.69"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"546"	"ATRX"	"0.489"	"0.69"	"C1845055"	"ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED"	"disease"	"C10;C15;C16"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"12"	"19"	"CTD_human;ORPHANET;UNIPROT"
"546"	"ATRX"	"0.489"	"0.69"	"C1845298"	"MENTAL RETARDATION, X-LINKED 52"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.46"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"546"	"ATRX"	"0.489"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1996"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"547"	"KIF1A"	"0.607"	"0.552"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1993"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"547"	"KIF1A"	"0.607"	"0.552"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"547"	"KIF1A"	"0.607"	"0.552"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"547"	"KIF1A"	"0.607"	"0.552"	"C0751540"	"Morvan's Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"547"	"KIF1A"	"0.607"	"0.552"	"C0796122"	"Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"547"	"KIF1A"	"0.607"	"0.552"	"C1835896"	"SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.91"	"1"	"2006"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"547"	"KIF1A"	"0.607"	"0.552"	"C1850055"	"PEHO syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2015"	"2017"	"0"	"3"	"ORPHANET"
"547"	"KIF1A"	"0.607"	"0.552"	"C2752089"	"Neuropathy, Hereditary Sensory And Autonomic, Type IIA"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2011"	"0"	"2"	"CTD_human"
"547"	"KIF1A"	"0.607"	"0.552"	"C3280168"	"NEUROPATHY, HEREDITARY SENSORY, TYPE IIC"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2017"	"0"	"4"	"CTD_human"
"547"	"KIF1A"	"0.607"	"0.552"	"C3280283"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 9"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2018"	"4"	"24"	"CTD_human;UNIPROT"
"547"	"KIF1A"	"0.607"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"549"	"AUH"	"0.727"	"0.207"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"549"	"AUH"	"0.727"	"0.207"	"C0342727"	"3-@METHYLGLUTACONIC ACIDURIA, TYPE I"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1982"	"2014"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"549"	"AUH"	"0.727"	"0.207"	"C0342728"	"3-Methylglutaconic aciduria type 1"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"549"	"AUH"	"0.727"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"551"	"AVP"	"0.486"	"0.759"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0002962"	"Angina Pectoris"	"phenotype"	"C14;C23"	"Sign or Symptom"	"0.30"		"2001"	"2002"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1996"	"2010"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0009178"	"Cocaine withdrawal"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0010398"	"Cruveilhier-Baumgarten Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0011175"	"Dehydration"	"phenotype"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0011848"	"Diabetes Insipidus"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.70"	"1"	"1981"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"551"	"AVP"	"0.486"	"0.759"	"C0013390"	"Dysmenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0017181"	"Gastrointestinal Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0018932"	"Hematochezia"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"1984"	"2016"	"5"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020541"	"Hypertension, Portal"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"1984"	"2009"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020625"	"Hyponatremia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"1982"	"2015"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.32"		"1987"	"2008"	"5"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0020683"	"Hypovolemic Shock"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0021141"	"Inappropriate ADH Syndrome"	"disease"	"C10;C18;C19"	"Disease or Syndrome"	"0.30"		"1979"	"1982"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1990"	"1999"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0029944"	"Drug Overdose"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0032617"	"Polyuria"	"phenotype"	"C12;C13;C23"	"Sign or Symptom"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1987"	"2015"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0036974"	"Shock"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0037019"	"Shy-Drager Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"1988"	"2004"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2012"	"2"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C0687720"	"Central Diabetes Insipidus"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"1.00"	"1"	"1982"	"2018"	"28"	"17"	"CTD_human;ORPHANET;UNIPROT"
"551"	"AVP"	"0.486"	"0.759"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"1991"	"2"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C1136135"	"Water Stress"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2009"	"1"	"0"	"PSYGENET"
"551"	"AVP"	"0.486"	"0.759"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"551"	"AVP"	"0.486"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"552"	"AVPR1A"	"0.681"	"0.414"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"552"	"AVPR1A"	"0.681"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"552"	"AVPR1A"	"0.681"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2007"	"2015"	"2"	"0"	"PSYGENET"
"552"	"AVPR1A"	"0.681"	"0.414"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"553"	"AVPR1B"	"0.735"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"553"	"AVPR1B"	"0.735"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"554"	"AVPR2"	"0.616"	"0.483"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"554"	"AVPR2"	"0.616"	"0.483"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0028961"	"Oliguria"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0162283"	"Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.90"	"1"	"1992"	"2017"	"5"	"15"	"CTD_human;ORPHANET"
"554"	"AVPR2"	"0.616"	"0.483"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0268443"	"Acquired Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"5"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0677501"	"Congenital Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.923076923076923"	"1994"	"2011"	"5"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C1138434"	"Genetic Diseases, X-Linked"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C1563705"	"Nephrogenic Diabetes Insipidus, Type I"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.70"	"0.947368421052632"	"1969"	"2016"	"28"	"23"	"CTD_human;UNIPROT"
"554"	"AVPR2"	"0.616"	"0.483"	"C1563706"	"Nephrogenic Diabetes Insipidus, Type II"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"5"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C1845202"	"Nephrogenic Syndrome of Inappropriate Antidiuresis"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.75"	"1"	"2005"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"554"	"AVPR2"	"0.616"	"0.483"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C3542500"	"ADH-Resistant Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"5"	"0"	"CTD_human"
"554"	"AVPR2"	"0.616"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"1992"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"554"	"AVPR2"	"0.616"	"0.483"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"558"	"AXL"	"0.529"	"0.517"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0206728"	"Plexiform Neurofibroma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"558"	"AXL"	"0.529"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0751374"	"Schwannomatosis, Plexiform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"558"	"AXL"	"0.529"	"0.517"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"		"2008"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"563"	"AZGP1"	"0.619"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0020455"	"Hypergammaglobulinemia"	"disease"	"C15;C20;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.42"	"1"	"1990"	"2014"	"3"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1990"	"2017"	"3"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"567"	"B2M"	"0.499"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0268389"	"Amyloidosis, familial visceral"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"567"	"B2M"	"0.499"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1990"	"2017"	"3"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C1855796"	"Hypoproteinemia, Hypercatabolic"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1969"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"567"	"B2M"	"0.499"	"0.759"	"C1858266"	"Bare Lymphocyte Syndrome, Type I"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"567"	"B2M"	"0.499"	"0.759"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1990"	"2017"	"3"	"0"	"CTD_human"
"567"	"B2M"	"0.499"	"0.759"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"567"	"B2M"	"0.499"	"0.759"	"C4302669"	"Autosomal dominant beta2-microglobulinic amyloidosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"570"	"BAAT"	"0.621"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"570"	"BAAT"	"0.621"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"570"	"BAAT"	"0.621"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"570"	"BAAT"	"0.621"	"0.483"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"570"	"BAAT"	"0.621"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"570"	"BAAT"	"0.621"	"0.483"	"C1843139"	"Hypercholanemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2003"	"2003"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"572"	"BAD"	"0.579"	"0.552"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"2"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"572"	"BAD"	"0.579"	"0.552"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"573"	"BAG1"	"0.573"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"573"	"BAG1"	"0.573"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"573"	"BAG1"	"0.573"	"0.621"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2002"	"2014"	"1"	"0"	"PSYGENET"
"573"	"BAG1"	"0.573"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"573"	"BAG1"	"0.573"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"578"	"BAK1"	"0.588"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"579"	"NKX3-2"	"0.886"	"0.103"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"579"	"NKX3-2"	"0.886"	"0.103"	"C2750066"	"Spondylo-Megaepiphyseal-Metaphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2010"	"0"	"3"	"CTD_human;ORPHANET"
"579"	"NKX3-2"	"0.886"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"580"	"BARD1"	"0.624"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.911764705882353"	"1997"	"2016"	"1"	"1"	"CGI;CTD_human;UNIPROT"
"580"	"BARD1"	"0.624"	"0.379"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2001"	"2016"	"4"	"0"	"CLINGEN"
"580"	"BARD1"	"0.624"	"0.379"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.47"	"1"	"2010"	"2017"	"2"	"13"	"CTD_human"
"580"	"BARD1"	"0.624"	"0.379"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.869565217391304"	"2001"	"2018"	"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2006"	"1"	"1"	"UNIPROT"
"580"	"BARD1"	"0.624"	"0.379"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.65"	"0.8"	"2001"	"2017"	"11"	"30"	"CLINGEN;GENOMICS_ENGLAND"
"580"	"BARD1"	"0.624"	"0.379"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.40"		"2010"	"2016"	"0"	"3"	"ORPHANET"
"580"	"BARD1"	"0.624"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.903225806451613"	"1997"	"2016"	"0"	"0"	"CGI;CTD_human"
"580"	"BARD1"	"0.624"	"0.379"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.44"	"1"	"1998"	"2006"	"0"	"0"	"CGI"
"580"	"BARD1"	"0.624"	"0.379"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2001"	"2016"	"4"	"0"	"CLINGEN"
"580"	"BARD1"	"0.624"	"0.379"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.857142857142857"	"1997"	"2018"	"3"	"0"	"CGI;CLINGEN"
"580"	"BARD1"	"0.624"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"580"	"BARD1"	"0.624"	"0.379"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2001"	"2016"	"4"	"0"	"CLINGEN"
"580"	"BARD1"	"0.624"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.55"	"1"	"2004"	"2009"	"0"	"0"	"CTD_human"
"580"	"BARD1"	"0.624"	"0.379"	"C1518693"	"Ovarian Clear Cell Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"581"	"BAX"	"0.45"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.818181818181818"	"1996"	"2014"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2003"	"0"	"0"	"UNIPROT"
"581"	"BAX"	"0.45"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2010"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2002"	"2007"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"1996"	"2014"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CGI"
"581"	"BAX"	"0.45"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"1998"	"2000"	"0"	"2"	"CGI"
"581"	"BAX"	"0.45"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"581"	"BAX"	"0.45"	"0.862"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"582"	"BBS1"	"0.639"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"582"	"BBS1"	"0.639"	"0.586"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.962962962962963"	"1993"	"2017"	"0"	"34"	"ORPHANET"
"582"	"BBS1"	"0.639"	"0.586"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"582"	"BBS1"	"0.639"	"0.586"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.84"	"1"	"2000"	"2015"	"8"	"13"	"CTD_human;UNIPROT"
"582"	"BBS1"	"0.639"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"582"	"BBS1"	"0.639"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"583"	"BBS2"	"0.602"	"0.552"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2002"	"2015"	"0"	"0"	"ORPHANET"
"583"	"BBS2"	"0.602"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"583"	"BBS2"	"0.602"	"0.552"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.958333333333333"	"1998"	"2017"	"0"	"10"	"ORPHANET"
"583"	"BBS2"	"0.602"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"583"	"BBS2"	"0.602"	"0.552"	"C2936863"	"Bardet-Biedl syndrome 2 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"1994"	"2016"	"7"	"17"	"CTD_human;UNIPROT"
"583"	"BBS2"	"0.602"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"583"	"BBS2"	"0.602"	"0.552"	"C4225281"	"RETINITIS PIGMENTOSA 74"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"583"	"BBS2"	"0.602"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"585"	"BBS4"	"0.639"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"1998"	"1998"	"0"	"0"	"GENOMICS_ENGLAND"
"585"	"BBS4"	"0.639"	"0.552"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9375"	"1993"	"2017"	"0"	"10"	"ORPHANET"
"585"	"BBS4"	"0.639"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"585"	"BBS4"	"0.639"	"0.552"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"585"	"BBS4"	"0.639"	"0.552"	"C2936864"	"Bardet-Biedl syndrome 4 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"1979"	"2016"	"6"	"9"	"CTD_human;UNIPROT"
"585"	"BBS4"	"0.639"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"585"	"BBS4"	"0.639"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"586"	"BCAT1"	"0.69"	"0.379"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"586"	"BCAT1"	"0.69"	"0.379"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0024776"	"Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0268568"	"Classic Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0268569"	"Intermittent Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C0751285"	"Maple Syrup Urine Disease, Thiamine Responsive"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"587"	"BCAT2"	"0.785"	"0.207"	"C1621920"	"Intermediate Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1986"	"1986"	"1"	"0"	"PSYGENET"
"590"	"BCHE"	"0.503"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.944444444444444"	"1995"	"2018"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0003578"	"Apnea"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.30"		"1967"	"2015"	"31"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1985"	"1985"	"1"	"0"	"PSYGENET"
"590"	"BCHE"	"0.503"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2016"	"8"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2010"	"2"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0015644"	"Muscular fasciculation"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1990"	"1990"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0018989"	"Hemiparesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0020529"	"Hypersomnia with Periodic Respiration"	"disease"	"C08;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1990"	"1990"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.39"	"1"	"2004"	"2017"	"4"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0030552"	"Paresis"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"4"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0032787"	"Postoperative Complications"	"group"	"C23"	"Pathologic Function"	"0.30"		"1967"	"1967"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0037315"	"Sleep Apnea Syndromes"	"group"	"C08;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0041105"	"Trismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1970"	"2011"	"10"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2016"	"8"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0239548"	"Fasciculation, Tongue"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0240302"	"Masseter Muscle Spasm"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0268379"	"Pseudocholinesterase deficiency"	"disease"	"C08;C16;C18;C23"	"Disease or Syndrome"	"0.50"		"1989"	"2015"	"23"	"27"	"CTD_human;UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C0270795"	"Monoparesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0338495"	"Sleep Apnea, Mixed Central and Obstructive"	"disease"	"C08;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0343495"	"Lockjaw"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0353676"	"Organophosphorus Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2016"	"7"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0376297"	"Cardiac Death"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2002"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"1999"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1970"	"2011"	"10"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0541957"	"Fasciculation, Skeletal Muscle"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"8"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0700359"	"Organophosphate poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2016"	"7"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751144"	"Fasciculation, Benign"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751409"	"Upper Extremity Paresis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751410"	"Lower Extremity Paresis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C0876994"	"Cardiotoxicity"	"disease"	"C23;C25;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1283400"	"Butyrylcholinesterase deficiency"	"disease"	"C08;C16;C18;C23"	"Disease or Syndrome"	"0.72"	"1"	"1957"	"2015"	"23"	"50"	"CTD_human;ORPHANET;UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1622434"	"Suxamethonium sensitivity"	"phenotype"	"C08;C16;C18;C23"	"Pathologic Function"	"0.50"		"1989"	"2015"	"23"	"27"	"CTD_human;UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1855794"	"Bamforth syndrome"	"disease"	"C05;C07;C16;C17;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C1867467"	"Acholinesterasemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1867468"	"Apnea, Postanesthetic"	"phenotype"	"C08;C16;C18;C23"	"Pathologic Function"	"0.60"		"1957"	"2015"	"23"	"27"	"CTD_human;UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1867469"	"Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1867470"	"Hypocholinesterasemia, Fluoride-Resistant, Japanese Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C1968699"	"Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate"	"disease"	"C05;C07;C16;C17;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C3494247"	"Organothiophosphonate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2016"	"7"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C3494248"	"Organothiophosphate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2016"	"7"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C3889586"	"BCHE, FLUORIDE 1 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889588"	"BCHE, FLUORIDE 2 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889589"	"BCHE, K VARIANT PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889591"	"BCHE, J VARIANT PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889592"	"BCHE, H VARIANT PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889596"	"BCHE NEWFOUNDLAND PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889604"	"BCHE, SILENT 1 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889605"	"BCHE CYNTHIANA PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C3889606"	"BCHE JOHANNESBURG PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4016356"	"APNEA, POSTANESTHETIC, DUE TO BCHE, ATYPICAL-1"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017543"	"BCHE, DIBUCAINE-RESISTANT I PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017544"	"CHE*70G PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017545"	"BCHE*70G PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017546"	"BCHE ANN ARBOR PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017547"	"CHE*FS117 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017548"	"BCHE*FS117 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017549"	"BCHE, FLUORIDE-RESISTANT I PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017550"	"CHE*243M PHENOTYPE"	"phenotype"		"Finding"	"0.40"		"1961"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017551"	"BCHE*243M PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017552"	"BCHE, FLUORIDE-RESISTANT II PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017553"	"CHE*390V PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017554"	"BCHE*390V PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017555"	"BCHE, QUANTITATIVE K POLYMORPHISM PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017556"	"CHE*539T PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017557"	"BCHE*539T PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017558"	"BCHE, QUANTITATIVE J VARIANT PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017559"	"BCHE, QUANTITATIVE H VARIANT PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4017560"	"BCHE*FS126 PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1989"	"2015"	"22"	"27"	"UNIPROT"
"590"	"BCHE"	"0.503"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"590"	"BCHE"	"0.503"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"2011"	"3"	"0"	"CTD_human"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0024776"	"Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1989"	"2016"	"9"	"38"	"CTD_human;UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0268568"	"Classic Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1989"	"2012"	"9"	"8"	"CTD_human;ORPHANET;UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0268569"	"Intermittent Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1989"	"2012"	"9"	"8"	"CTD_human;ORPHANET;UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"593"	"BCKDHA"	"0.69"	"0.276"	"C0751285"	"Maple Syrup Urine Disease, Thiamine Responsive"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1989"	"2012"	"9"	"8"	"CTD_human;ORPHANET;UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C1621920"	"Intermediate Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1989"	"2012"	"9"	"8"	"CTD_human;ORPHANET;UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C1855369"	"Maple Syrup Urine Disease, Type IA"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1989"	"2015"	"9"	"11"	"UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C1855371"	"MAPLE SYRUP URINE DISEASE, TYPE II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"9"	"8"	"UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C2930990"	"Maple syrup urine disease, type 1B"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1989"	"2012"	"9"	"8"	"UNIPROT"
"593"	"BCKDHA"	"0.69"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0024776"	"Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1991"	"2018"	"3"	"51"	"CTD_human;UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0268568"	"Classic Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0268569"	"Intermittent Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"594"	"BCKDHB"	"0.656"	"0.517"	"C0751285"	"Maple Syrup Urine Disease, Thiamine Responsive"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C1621920"	"Intermediate Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C1855369"	"Maple Syrup Urine Disease, Type IA"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"3"	"3"	"UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C1855371"	"MAPLE SYRUP URINE DISEASE, TYPE II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"3"	"3"	"UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C2930990"	"Maple syrup urine disease, type 1B"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"3"	"3"	"UNIPROT"
"594"	"BCKDHB"	"0.656"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"595"	"CCND1"	"0.365"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.981395348837209"	"1990"	"2018"	"6"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"595"	"CCND1"	"0.365"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.966666666666667"	"1997"	"2016"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.986842105263158"	"1989"	"2018"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.57"	"0.857142857142857"	"1997"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007528"	"Cecal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2014"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2014"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.5"	"2000"	"2007"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0019562"	"Von Hippel-Lindau Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2005"	"0"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0020502"	"Hyperparathyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2002"	"2011"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0021846"	"Intestinal Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"	"0"	"2003"	"2009"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.933333333333333"	"1992"	"2010"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.888888888888889"	"1988"	"2017"	"0"	"0"	"ORPHANET"
"595"	"CCND1"	"0.365"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.928571428571429"	"2001"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.38"	"0.666666666666667"	"1997"	"2008"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"1996"	"2015"	"0"	"0"	"CGI"
"595"	"CCND1"	"0.365"	"0.828"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.70"	"0.935064935064935"	"1991"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"595"	"CCND1"	"0.365"	"0.828"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1999"	"2009"	"1"	"0"	"PSYGENET"
"595"	"CCND1"	"0.365"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"595"	"CCND1"	"0.365"	"0.828"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2013"	"0"	"0"	"CGI"
"595"	"CCND1"	"0.365"	"0.828"	"C0153437"	"Malignant neoplasm of cecum"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.967741935483871"	"1990"	"2016"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.939393939393939"	"1996"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.963898916967509"	"1993"	"2018"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0555202"	"Malignant lymphoma - lymphocytic, intermediate differentiation"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"595"	"CCND1"	"0.365"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.977973568281938"	"1990"	"2018"	"6"	"1"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.39"	"1"	"1988"	"2003"	"0"	"0"	"ORPHANET"
"595"	"CCND1"	"0.365"	"0.828"	"C0919532"	"Genomic Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2014"	"6"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"595"	"CCND1"	"0.365"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2014"	"6"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"595"	"CCND1"	"0.365"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.986301369863014"	"1993"	"2018"	"5"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.933333333333333"	"1995"	"2017"	"1"	"0"	"CTD_human"
"595"	"CCND1"	"0.365"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"596"	"BCL2"	"0.312"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.891891891891892"	"1993"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.92"	"1994"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2011"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0004509"	"Azoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2013"	"3"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.966850828729282"	"1994"	"2017"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.967741935483871"	"1997"	"2018"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1988"	"2012"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2009"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.61"	"1"	"2007"	"2017"	"1"	"1"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.75"	"1996"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2013"	"2"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1998"	"2010"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.932584269662921"	"1987"	"2018"	"2"	"3"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9625"	"1990"	"2017"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.50"	"0.949458483754513"	"1987"	"2018"	"0"	"0"	"CGI"
"596"	"BCL2"	"0.312"	"0.862"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.954802259887006"	"1985"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"596"	"BCL2"	"0.312"	"0.862"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.957142857142857"	"1988"	"2017"	"2"	"0"	"CTD_human;UNIPROT"
"596"	"BCL2"	"0.312"	"0.862"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0025568"	"Metaplasia"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"0.95"	"1992"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2001"	"2008"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.54"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.32"		"2004"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.50"		"1996"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2015"	"2"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0037579"	"Soft Tissue Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.928571428571429"	"1997"	"2015"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.958677685950413"	"1991"	"2018"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"1988"	"2015"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2012"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1988"	"2004"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.35"	"0.8"	"1994"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0206637"	"Mesenchymal Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0206681"	"Adenocarcinoma, Clear Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.50"		"2002"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0276535"	"AIDS with Kaposi's sarcoma"	"disease"	"C01;C02;C03;C04;C20"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0334660"	"Angioendotheliomatosis"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"596"	"BCL2"	"0.312"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.981651376146789"	"1994"	"2018"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.333333333333333"	"1996"	"2016"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.963730569948187"	"1994"	"2017"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2014"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.952380952380952"	"1998"	"2016"	"3"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2004"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2014"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2012"	"2"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"596"	"BCL2"	"0.312"	"0.862"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"596"	"BCL2"	"0.312"	"0.862"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"597"	"BCL2A1"	"0.582"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2004"	"2008"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"1997"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2004"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.39"	"0.875"	"1998"	"2015"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2017"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.50"		"2002"	"2002"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2011"	"2"	"0"	"CTD_human"
"598"	"BCL2L1"	"0.471"	"0.828"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9"	"1996"	"2015"	"0"	"0"	"CGI"
"604"	"BCL6"	"0.488"	"0.655"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.927536231884058"	"1994"	"2018"	"0"	"0"	"ORPHANET"
"604"	"BCL6"	"0.488"	"0.655"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.953488372093023"	"1993"	"2015"	"1"	"0"	"CGI;CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"1994"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"604"	"BCL6"	"0.488"	"0.655"	"C0334660"	"Angioendotheliomatosis"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"ORPHANET"
"604"	"BCL6"	"0.488"	"0.655"	"C1292754"	"Mediastinal (Thymic) Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"604"	"BCL6"	"0.488"	"0.655"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"607"	"BCL9"	"0.656"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"607"	"BCL9"	"0.656"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"607"	"BCL9"	"0.656"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2016"	"2"	"1"	"PSYGENET"
"607"	"BCL9"	"0.656"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"607"	"BCL9"	"0.656"	"0.448"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"607"	"BCL9"	"0.656"	"0.448"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"607"	"BCL9"	"0.656"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"610"	"HCN2"	"0.713"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"611"	"OPN1SW"	"0.616"	"0.414"	"C0155017"	"Color Blindness, Blue"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.71"	"1"	"1986"	"1992"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"613"	"BCR"	"0.47"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2008"	"4"	"0"	"PSYGENET"
"613"	"BCR"	"0.47"	"0.759"	"C0005699"	"Blast Phase"	"disease"	"C04;C15;C23"	"Neoplastic Process"	"0.40"	"0.934065934065934"	"1981"	"2018"	"1"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"613"	"BCR"	"0.47"	"0.759"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9"	"1988"	"2018"	"0"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.70"	"0.95079086115993"	"1980"	"2018"	"3"	"0"	"CTD_human;ORPHANET"
"613"	"BCR"	"0.47"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.50"	"0.981481481481482"	"1989"	"2018"	"1"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"613"	"BCR"	"0.47"	"0.759"	"C0279680"	"Transitional cell carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"613"	"BCR"	"0.47"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"613"	"BCR"	"0.47"	"0.759"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.36"	"0.833333333333333"	"1991"	"2017"	"0"	"0"	"ORPHANET"
"613"	"BCR"	"0.47"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1989"	"2005"	"0"	"0"	"ORPHANET"
"613"	"BCR"	"0.47"	"0.759"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.888888888888889"	"1988"	"2018"	"0"	"0"	"CTD_human"
"613"	"BCR"	"0.47"	"0.759"	"C2678480"	"Chromosome 22q11.2 Deletion Syndrome, Distal"	"disease"	"C05;C14;C15;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"617"	"BCS1L"	"0.573"	"0.586"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"617"	"BCS1L"	"0.573"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"617"	"BCS1L"	"0.573"	"0.586"	"C0266006"	"Pili torti-deafness syndrome"	"disease"	"C09;C10;C17;C18;C23"	"Disease or Syndrome"	"0.74"	"1"	"1998"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"617"	"BCS1L"	"0.573"	"0.586"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2003"	"2018"	"0"	"0"	"ORPHANET"
"617"	"BCS1L"	"0.573"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"617"	"BCS1L"	"0.573"	"0.586"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"617"	"BCS1L"	"0.573"	"0.586"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"617"	"BCS1L"	"0.573"	"0.586"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"617"	"BCS1L"	"0.573"	"0.586"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"617"	"BCS1L"	"0.573"	"0.586"	"C1864002"	"GRACILE SYNDROME (disorder)"	"disease"	"C06;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.76"	"1"	"2001"	"2016"	"2"	"16"	"CTD_human;ORPHANET;UNIPROT"
"617"	"BCS1L"	"0.573"	"0.586"	"C3541471"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2014"	"6"	"9"	"CTD_human;UNIPROT"
"617"	"BCS1L"	"0.573"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1998"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"622"	"BDH1"	"0.735"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"622"	"BDH1"	"0.735"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"623"	"BDKRB1"	"0.642"	"0.517"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.56"	"0.833333333333333"	"2000"	"2017"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1993"	"2005"	"2"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"624"	"BDKRB2"	"0.619"	"0.621"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"624"	"BDKRB2"	"0.619"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.975806451612903"	"1992"	"2018"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2002"	"2017"	"7"	"0"	"CTD_human;PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2009"	"2012"	"2"	"1"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2010"	"7"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.888888888888889"	"2007"	"2016"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2003"	"2018"	"5"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2003"	"2018"	"7"	"0"	"CTD_human;PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.888888888888889"	"1993"	"2018"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.33"		"2003"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1997"	"2009"	"5"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.37"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.857142857142857"	"2006"	"2015"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2016"	"0"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.952380952380952"	"1996"	"2018"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.827586206896552"	"2005"	"2017"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.941935483870968"	"1999"	"2018"	"4"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"1"	"1997"	"2018"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.53"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2005"	"2018"	"7"	"0"	"CTD_human;PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.666666666666667"	"2003"	"2015"	"3"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0206115"	"WAGR Syndrome"	"disease"	"C04;C10;C11;C12;C13;C16;C19"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2014"	"0"	"0"	"ORPHANET"
"627"	"BDNF"	"0.382"	"0.828"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2010"	"7"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2013"	"3"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2005"	"2016"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2018"	"5"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2018"	"7"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2018"	"5"	"0"	"PSYGENET"
"627"	"BDNF"	"0.382"	"0.828"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.62"	"1"	"2002"	"2004"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"627"	"BDNF"	"0.382"	"0.828"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"2002"	"2002"	"1"	"1"	"CTD_human;UNIPROT"
"627"	"BDNF"	"0.382"	"0.828"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C2267227"	"Bulimia Nervosa"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2015"	"0"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C2931803"	"Deletion 11p13"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"627"	"BDNF"	"0.382"	"0.828"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2018"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"627"	"BDNF"	"0.382"	"0.828"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2011"	"3"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"		"2008"	"2016"	"1"	"1"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.952380952380952"	"2006"	"2016"	"1"	"4"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C2752038"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.60"		"1981"	"2010"	"2"	"6"	"ORPHANET;UNIPROT"
"629"	"CFB"	"0.588"	"0.724"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.55"	"1"	"2007"	"2018"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"629"	"CFB"	"0.588"	"0.724"	"C3809653"	"MACULAR DEGENERATION, AGE-RELATED, 14"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C3809654"	"MACULAR DEGENERATION, AGE-RELATED, REDUCED RISK OF"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"629"	"CFB"	"0.588"	"0.724"	"C3809950"	"COMPLEMENT FACTOR B DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"2"	"CTD_human"
"631"	"BFSP1"	"0.799"	"0.034"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"631"	"BFSP1"	"0.799"	"0.034"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"631"	"BFSP1"	"0.799"	"0.034"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"631"	"BFSP1"	"0.799"	"0.034"	"C1969644"	"Cataract, Cortical, Juvenile-Onset"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"631"	"BFSP1"	"0.799"	"0.034"	"C3808107"	"CATARACT 33, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.40"		"2007"	"2017"	"3"	"2"	"UNIPROT"
"632"	"BGLAP"	"0.528"	"0.621"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"632"	"BGLAP"	"0.528"	"0.621"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"633"	"BGN"	"0.523"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"633"	"BGN"	"0.523"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"633"	"BGN"	"0.523"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"633"	"BGN"	"0.523"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"633"	"BGN"	"0.523"	"0.655"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2007"	"2018"	"2"	"0"	"CLINGEN"
"633"	"BGN"	"0.523"	"0.655"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"633"	"BGN"	"0.523"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"633"	"BGN"	"0.523"	"0.655"	"C1848097"	"Spondyloepimetaphyseal Dysplasia, X-Linked"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1994"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"633"	"BGN"	"0.523"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"633"	"BGN"	"0.523"	"0.655"	"C4310811"	"MEESTER-LOEYS SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2018"	"2018"	"1"	"3"	"CTD_human;UNIPROT"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"634"	"CEACAM1"	"0.59"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2011"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0000832"	"Abruptio Placentae"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"635"	"BHMT"	"0.616"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.32"	"0.5"	"2004"	"2014"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"635"	"BHMT"	"0.616"	"0.483"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"637"	"BID"	"0.642"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"637"	"BID"	"0.642"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"637"	"BID"	"0.642"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"637"	"BID"	"0.642"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"637"	"BID"	"0.642"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"637"	"BID"	"0.642"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"638"	"BIK"	"0.685"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"639"	"PRDM1"	"0.6"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"0.333333333333333"	"2010"	"2015"	"3"	"0"	"CTD_human"
"639"	"PRDM1"	"0.6"	"0.621"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"2"	"CTD_human"
"639"	"PRDM1"	"0.6"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.55"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"639"	"PRDM1"	"0.6"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"2006"	"2017"	"0"	"0"	"CGI"
"639"	"PRDM1"	"0.6"	"0.621"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"639"	"PRDM1"	"0.6"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"639"	"PRDM1"	"0.6"	"0.621"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"640"	"BLK"	"0.648"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.36"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"640"	"BLK"	"0.648"	"0.586"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.875"	"2008"	"2017"	"1"	"3"	"CTD_human"
"640"	"BLK"	"0.648"	"0.586"	"C0026691"	"Mucocutaneous Lymph Node Syndrome"	"disease"	"C14;C15;C17"	"Disease or Syndrome"	"0.44"	"1"	"2012"	"2015"	"1"	"38"	"CTD_human"
"640"	"BLK"	"0.648"	"0.586"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"640"	"BLK"	"0.648"	"0.586"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"640"	"BLK"	"0.648"	"0.586"	"C3150618"	"Maturity-onset diabetes of the young, type 11"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"1"	"CTD_human"
"641"	"BLM"	"0.562"	"0.69"	"C0005859"	"Bloom Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.947916666666667"	"1981"	"2018"	"4"	"81"	"CTD_human;ORPHANET;UNIPROT"
"641"	"BLM"	"0.562"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"641"	"BLM"	"0.562"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"641"	"BLM"	"0.562"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2002"	"2005"	"0"	"0"	"CGI"
"641"	"BLM"	"0.562"	"0.69"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2002"	"2002"	"0"	"0"	"CGI"
"641"	"BLM"	"0.562"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"641"	"BLM"	"0.562"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"641"	"BLM"	"0.562"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"1998"	"2"	"0"	"GENOMICS_ENGLAND"
"641"	"BLM"	"0.562"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"642"	"BLMH"	"0.696"	"0.379"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.39"	"1"	"1998"	"2011"	"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"642"	"BLMH"	"0.696"	"0.379"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"643"	"CXCR5"	"0.577"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"0"	"0"	"UNIPROT"
"643"	"CXCR5"	"0.577"	"0.724"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"643"	"CXCR5"	"0.577"	"0.724"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"643"	"CXCR5"	"0.577"	"0.724"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"644"	"BLVRA"	"0.735"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"644"	"BLVRA"	"0.735"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"644"	"BLVRA"	"0.735"	"0.345"	"C3279964"	"HYPERBILIVERDINEMIA"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2011"	"0"	"2"	"CTD_human;ORPHANET"
"645"	"BLVRB"	"0.735"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"645"	"BLVRB"	"0.735"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"645"	"BLVRB"	"0.735"	"0.379"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"645"	"BLVRB"	"0.735"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0023472"	"Leukemia, Myeloid, Accelerated Phase"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"648"	"BMI1"	"0.477"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"649"	"BMP1"	"0.624"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"0"	"0"	"UNIPROT"
"649"	"BMP1"	"0.624"	"0.655"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"649"	"BMP1"	"0.624"	"0.655"	"C3553887"	"OSTEOGENESIS IMPERFECTA, TYPE XIII"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2015"	"3"	"6"	"CTD_human;UNIPROT"
"650"	"BMP2"	"0.491"	"0.759"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1704436"	"Peripheral Arterial Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1832702"	"BRACHYDACTYLY, TYPE A2"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.65"	"1"	"2005"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"650"	"BMP2"	"0.491"	"0.759"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"650"	"BMP2"	"0.491"	"0.759"	"C4304539"	"20p12.3 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"652"	"BMP4"	"0.477"	"0.724"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"652"	"BMP4"	"0.477"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"2008"	"2015"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.53"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0042842"	"Vitamin A Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"652"	"BMP4"	"0.477"	"0.724"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.41"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"652"	"BMP4"	"0.477"	"0.724"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"652"	"BMP4"	"0.477"	"0.724"	"C0344452"	"Microprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0344453"	"Macroprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C1306214"	"ACTH-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"2008"	"2015"	"1"	"0"	"CTD_human"
"652"	"BMP4"	"0.477"	"0.724"	"C1833563"	"Cleft Lip, Congenital Healed"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"4"	"UNIPROT"
"652"	"BMP4"	"0.477"	"0.724"	"C1864689"	"MICROPHTHALMIA, SYNDROMIC 6 (disorder)"	"disease"	"C05;C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.70"		"2008"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"652"	"BMP4"	"0.477"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"652"	"BMP4"	"0.477"	"0.724"	"C2677434"	"OROFACIAL CLEFT 11"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.61"	"1"	"2007"	"2011"	"1"	"5"	"CTD_human;UNIPROT"
"652"	"BMP4"	"0.477"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"654"	"BMP6"	"0.557"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.33"	"0.333333333333333"	"2009"	"2016"	"2"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2010"	"2"	"0"	"CTD_human"
"654"	"BMP6"	"0.557"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"655"	"BMP7"	"0.535"	"0.655"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"655"	"BMP7"	"0.535"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0015802"	"Femoral Fractures"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2010"	"2"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"655"	"BMP7"	"0.535"	"0.655"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2012"	"2"	"0"	"CTD_human"
"655"	"BMP7"	"0.535"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"655"	"BMP7"	"0.535"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0345893"	"Juvenile polyposis syndrome"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"1.00"	"1"	"2000"	"2017"	"7"	"20"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"657"	"BMPR1A"	"0.58"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1832587"	"POLYPOSIS SYNDROME, HEREDITARY MIXED, 1"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1832940"	"JUVENILE POLYPOSIS OF STOMACH"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.80"		"2001"	"2007"	"7"	"5"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1864730"	"Polyposis Syndrome, Hereditary Mixed, 2"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C1868081"	"Juvenile Polyposis Coli"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.80"		"2001"	"2007"	"7"	"5"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"657"	"BMPR1A"	"0.58"	"0.517"	"C2677290"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"657"	"BMPR1A"	"0.58"	"0.517"	"C2677291"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 15"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"657"	"BMPR1A"	"0.58"	"0.517"	"C3714239"	"Bmpr1a-Related Juvenile Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C3714240"	"Smad4-Related Juvenile Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"657"	"BMPR1A"	"0.58"	"0.517"	"C3896578"	"Familial Colorectal Cancer Type X"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0265260"	"Chondrodysplasia, Grebe type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1300268"	"Brachydactyly syndrome type C"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1832702"	"BRACHYDACTYLY, TYPE A2"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.76"	"0.833333333333333"	"2003"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1836182"	"Chondrodysplasia, acromesomelic, with genital anomalies"	"disease"	"C05;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1856738"	"Fibular hypoplasia and complex brachydactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1862103"	"Brachydactyly type C"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C1862151"	"BRACHYDACTYLY, TYPE A1 (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"658"	"BMPR1B"	"0.604"	"0.483"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"658"	"BMPR1B"	"0.604"	"0.483"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"658"	"BMPR1B"	"0.604"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"658"	"BMPR1B"	"0.604"	"0.483"	"C4225183"	"BRACHYDACTYLY, TYPE A1, D"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"658"	"BMPR1B"	"0.604"	"0.483"	"C4225404"	"ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2016"	"3"	"4"	"UNIPROT"
"659"	"BMPR2"	"0.573"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.37"		"2002"	"2014"	"9"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C0034091"	"Pulmonary Veno-Occlusive Disease (disorder)"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.62"	"1"	"2006"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"659"	"BMPR2"	"0.573"	"0.552"	"C0206081"	"Hyperandrogenism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"659"	"BMPR2"	"0.573"	"0.552"	"C0340544"	"Pulmonary arterial hypertension induced by drug"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"659"	"BMPR2"	"0.573"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"659"	"BMPR2"	"0.573"	"0.552"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"659"	"BMPR2"	"0.573"	"0.552"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"2000"	"2017"	"10"	"13"	"CTD_human;UNIPROT"
"659"	"BMPR2"	"0.573"	"0.552"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2000"	"2017"	"10"	"10"	"CTD_human;UNIPROT"
"659"	"BMPR2"	"0.573"	"0.552"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"1993"	"2017"	"15"	"0"	"GENOMICS_ENGLAND"
"659"	"BMPR2"	"0.573"	"0.552"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.80"	"0.954887218045113"	"1993"	"2018"	"21"	"10"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"659"	"BMPR2"	"0.573"	"0.552"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2000"	"2017"	"10"	"10"	"CTD_human;UNIPROT"
"660"	"BMX"	"0.727"	"0.276"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"664"	"BNIP3"	"0.569"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"664"	"BNIP3"	"0.569"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"667"	"DST"	"0.611"	"0.724"	"C1832926"	"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human"
"667"	"DST"	"0.611"	"0.724"	"C3539003"	"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"667"	"DST"	"0.611"	"0.724"	"C3809470"	"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2017"	"0"	"2"	"ORPHANET"
"668"	"FOXL2"	"0.561"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"668"	"FOXL2"	"0.561"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"668"	"FOXL2"	"0.561"	"0.448"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"668"	"FOXL2"	"0.561"	"0.448"	"C0220663"	"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder)"	"disease"	"C11;C12;C13;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2016"	"12"	"55"	"CTD_human;ORPHANET;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C0334401"	"Malignant Granulosa Cell Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"668"	"FOXL2"	"0.561"	"0.448"	"C1332218"	"Adult Type Ovarian Granulosa Cell Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"668"	"FOXL2"	"0.561"	"0.448"	"C1370419"	"Ovarian Granulosa Cell Tumor"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"668"	"FOXL2"	"0.561"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"668"	"FOXL2"	"0.561"	"0.448"	"C1567257"	"Granulosa Cell Cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"668"	"FOXL2"	"0.561"	"0.448"	"C1837008"	"PREMATURE OVARIAN FAILURE 3 (disorder)"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.60"		"2002"	"2009"	"2"	"2"	"CTD_human;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1862260"	"BPES, TYPE I"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"12"	"9"	"UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1862261"	"BPES, TYPE II"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2001"	"2011"	"12"	"9"	"UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1862262"	"Bpes With Ovarian Failure"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2010"	"13"	"9"	"CTD_human;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1862263"	"Bpes Without Ovarian Failure"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2010"	"13"	"9"	"CTD_human;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1862264"	"Bpes With Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2010"	"13"	"9"	"CTD_human;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C1970106"	"Bpes, Type I, Autosomal Recessive"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2010"	"13"	"9"	"CTD_human;UNIPROT"
"668"	"FOXL2"	"0.561"	"0.448"	"C2931135"	"Blepharophimosis syndrome type 1"	"disease"	"C11;C13;C16;C17"	"Disease or Syndrome"	"0.40"		"2001"	"2012"	"3"	"10"	"CTD_human"
"668"	"FOXL2"	"0.561"	"0.448"	"C3714208"	"Blepharophimosis, Ptosis, and Epicanthus Inversus Type II"	"disease"	"C11;C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"669"	"BPGM"	"0.815"	"0.138"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1969"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"669"	"BPGM"	"0.815"	"0.138"	"C1291620"	"Deficiency of bisphosphoglycerate mutase"	"disease"		"Disease or Syndrome"	"0.70"		"1978"	"2004"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.941829484902309"	"1987"	"2018"	"35"	"85"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2004"	"2018"	"1"	"0"	"CGI;CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"672"	"BRCA1"	"0.41"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1998"	"2013"	"5"	"0"	"PSYGENET"
"672"	"BRCA1"	"0.41"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1998"	"2013"	"5"	"0"	"PSYGENET"
"672"	"BRCA1"	"0.41"	"0.862"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"672"	"BRCA1"	"0.41"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2012"	"2"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.945836701697656"	"1992"	"2018"	"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.52"		"2005"	"2015"	"1"	"0"	"CGI;CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"672"	"BRCA1"	"0.41"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"672"	"BRCA1"	"0.41"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2018"	"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.936567164179104"	"1993"	"2018"	"22"	"141"	"ORPHANET;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.60"	"1"	"2002"	"2018"	"1"	"0"	"CGI;CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.876712328767123"	"1995"	"2018"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"672"	"BRCA1"	"0.41"	"0.862"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.70"	"0.953917050691244"	"1990"	"2018"	"2"	"687"	"CTD_human;ORPHANET"
"672"	"BRCA1"	"0.41"	"0.862"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.95"	"1994"	"2018"	"4"	"10"	"UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.941643323996265"	"1987"	"2018"	"12"	"2"	"CGI;CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CGI"
"672"	"BRCA1"	"0.41"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.98780487804878"	"1994"	"2016"	"5"	"2"	"CGI;CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.80"	"0.946944257891202"	"1992"	"2018"	"9"	"13"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"2017"	"12"	"0"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C1336076"	"Sporadic Breast Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.938053097345133"	"1994"	"2018"	"2"	"3"	"UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.936507936507937"	"1987"	"2017"	"12"	"45"	"CTD_human"
"672"	"BRCA1"	"0.41"	"0.862"	"C1514428"	"Primary peritoneal carcinoma"	"disease"		"Neoplastic Process"	"0.45"	"1"	"2003"	"2018"	"0"	"0"	"ORPHANET"
"672"	"BRCA1"	"0.41"	"0.862"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"1994"	"2018"	"22"	"85"	"UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C2676676"	"BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.70"		"1976"	"2018"	"14"	"1978"	"CLINGEN;CTD_human;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C2676677"	"BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.60"		"1994"	"2018"	"14"	"5"	"CLINGEN;CTD_human;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C2676678"	"OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.60"		"1994"	"2018"	"14"	"5"	"CLINGEN;CTD_human;UNIPROT"
"672"	"BRCA1"	"0.41"	"0.862"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"672"	"BRCA1"	"0.41"	"0.862"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.55"	"1"	"1999"	"2018"	"12"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0002448"	"Ameloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2014"	"2018"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.50"	"1"	"2011"	"2016"	"0"	"3"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.973333333333333"	"2003"	"2018"	"0"	"2"	"UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.42"	"0.5"	"2006"	"2016"	"0"	"6"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0007115"	"Malignant neoplasm of thyroid"	"disease"		"Neoplastic Process"	"0.40"	"0.982142857142857"	"2003"	"2017"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2003"	"2003"	"1"	"2"	"UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.976744186046512"	"2002"	"2018"	"1"	"16"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.970198675496689"	"2002"	"2018"	"4"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.967741935483871"	"2002"	"2017"	"4"	"9"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0010276"	"Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2018"	"1"	"0"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0019621"	"Histiocytosis, Langerhans-Cell"	"disease"	"C08;C15"	"Neoplastic Process"	"0.40"	"0.866666666666667"	"2010"	"2018"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.43"	"1"	"2008"	"2016"	"0"	"6"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0023443"	"Hairy Cell Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.92"	"2011"	"2018"	"0"	"0"	"CGI;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.42"	"1"	"2012"	"2016"	"0"	"1"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.54"	"1"	"2005"	"2016"	"0"	"0"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.61"	"1"	"2004"	"2004"	"1"	"3"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2003"	"2013"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0024694"	"Mandibular Neoplasms"	"group"	"C04;C05;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"1.00"	"0.972222222222222"	"1986"	"2018"	"22"	"30"	"CGI;CTD_human;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.49"	"0.666666666666667"	"2004"	"2018"	"0"	"11"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.64"	"1"	"2007"	"2014"	"1"	"3"	"CTD_human;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.944444444444444"	"2003"	"2017"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"0.5"	"2007"	"2018"	"2"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"0"	"2003"	"2007"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.70"	"0.925"	"2003"	"2016"	"4"	"3"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2015"	"1"	"5"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.35"	"0.6"	"2003"	"2016"	"4"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.915254237288136"	"2003"	"2018"	"0"	"12"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.80"	"1"	"2003"	"2016"	"3"	"14"	"CGI;CTD_human;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2015"	"0"	"2"	"ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.42"	"1"	"2009"	"2016"	"1"	"2"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2015"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"2002"	"2017"	"0"	"1"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.90"	"0.933649289099526"	"2003"	"2018"	"2"	"1"	"CTD_human;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"1"	"2003"	"2018"	"0"	"0"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0278600"	"Childhood Brain Stem Glioma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0278875"	"Adult Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2013"	"2015"	"1"	"0"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2008"	"2017"	"1"	"0"	"CGI;CTD_human;ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"0.75"	"2007"	"2018"	"2"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0431128"	"Papillary craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0431129"	"Adamantinous Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"673"	"BRAF"	"0.352"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.965317919075145"	"2003"	"2018"	"4"	"0"	"CGI;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.54"	"1"	"2007"	"2016"	"1"	"0"	"CLINGEN;CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.872881355932203"	"2003"	"2018"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.70"	"1"	"2002"	"2018"	"1"	"10"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.70"	"0.968253968253968"	"2002"	"2017"	"4"	"5"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.36"	"0.666666666666667"	"2003"	"2013"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0751061"	"Craniopharyngioma, Child"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0878675"	"Erdheim-Chester Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"2013"	"2016"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2002"	"2015"	"0"	"0"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"	"0.923076923076923"	"2002"	"2017"	"1"	"1"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C1266158"	"Nongerminomatous Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.40"		"2004"	"2004"	"0"	"1"	"CGI"
"673"	"BRAF"	"0.352"	"0.793"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"1.00"	"0.956521739130435"	"1993"	"2017"	"9"	"34"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C1275336"	"Hashimoto-Pritzker syndrome"	"disease"	"C08;C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"673"	"BRAF"	"0.352"	"0.793"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.56"	"0.833333333333333"	"2002"	"2016"	"2"	"3"	"CGI;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.96816976127321"	"2002"	"2018"	"8"	"5"	"CTD_human;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C1968782"	"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"673"	"BRAF"	"0.352"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2003"	"2016"	"1"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C3150970"	"NOONAN SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C3150971"	"LEOPARD SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"673"	"BRAF"	"0.352"	"0.793"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"0"	"2005"	"2017"	"2"	"0"	"CTD_human"
"673"	"BRAF"	"0.352"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"675"	"BRCA2"	"0.426"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.952156862745098"	"1989"	"2018"	"24"	"14"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.40"	"0.950617283950617"	"1998"	"2018"	"0"	"0"	"ORPHANET"
"675"	"BRCA2"	"0.426"	"0.793"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.50"		"2014"	"2014"	"1"	"0"	"CGI;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2003"	"2015"	"0"	"8"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.785714285714286"	"1996"	"2016"	"0"	"0"	"UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.62"	"1"	"2010"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"675"	"BRCA2"	"0.426"	"0.793"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"0.941529235382309"	"1994"	"2018"	"0"	"2"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.54"	"1"	"2003"	"2017"	"2"	"0"	"CGI;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"675"	"BRCA2"	"0.426"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0206720"	"Squamous Cell Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.924528301886792"	"1995"	"2017"	"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.65"	"0.8"	"2014"	"2016"	"1"	"0"	"CGI;CTD_human;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.80"	"0.946524064171123"	"1993"	"2018"	"21"	"107"	"GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.928571428571429"	"1996"	"2018"	"2"	"0"	"CGI;CTD_human;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.70"	"0.9125"	"1996"	"2018"	"1"	"7"	"CTD_human;GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"		"2006"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.70"	"0.966386554621849"	"1990"	"2018"	"1"	"840"	"CTD_human;ORPHANET"
"675"	"BRCA2"	"0.426"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.955268389662028"	"1989"	"2018"	"3"	"2"	"CGI;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.45"	"0.8"	"2000"	"2017"	"0"	"2"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0751688"	"Malignant Squamous Cell Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"675"	"BRCA2"	"0.426"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"1"	"1996"	"2015"	"1"	"1"	"CGI;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.80"	"0.945397815912636"	"1994"	"2018"	"1"	"4"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"3"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.94047619047619"	"1995"	"2017"	"3"	"37"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C1838457"	"FANCONI ANEMIA, COMPLEMENTATION GROUP D1"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"1999"	"2016"	"4"	"22"	"CTD_human;ORPHANET;UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"5"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2014"	"21"	"14"	"UNIPROT"
"675"	"BRCA2"	"0.426"	"0.793"	"C2675520"	"BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.60"		"1988"	"2018"	"10"	"2343"	"CLINGEN;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C2675521"	"BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.50"		"1996"	"2017"	"10"	"0"	"CLINGEN;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C2675522"	"OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.50"		"1996"	"2017"	"10"	"0"	"CLINGEN;CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"675"	"BRCA2"	"0.426"	"0.793"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"2002"	"2018"	"0"	"0"	"ORPHANET"
"675"	"BRCA2"	"0.426"	"0.793"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2016"	"0"	"0"	"ORPHANET"
"675"	"BRCA2"	"0.426"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"675"	"BRCA2"	"0.426"	"0.793"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2001"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"676"	"BRDT"	"0.834"	"0.138"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"676"	"BRDT"	"0.834"	"0.138"	"C4539991"	"SPERMATOGENIC FAILURE 21"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"678"	"ZFP36L2"	"0.72"	"0.31"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2010"	"2017"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C0015697"	"Arterial Fatty Streak"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"682"	"BSG"	"0.5"	"0.759"	"C0264956"	"Atheroma"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"682"	"BSG"	"0.5"	"0.759"	"C2936351"	"Fibroatheroma"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"683"	"BST1"	"0.785"	"0.345"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"683"	"BST1"	"0.785"	"0.345"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.8125"	"2010"	"2017"	"1"	"7"	"CTD_human"
"685"	"BTC"	"0.713"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"685"	"BTC"	"0.713"	"0.31"	"C0162568"	"Erythropoietic Protoporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"685"	"BTC"	"0.713"	"0.31"	"C0349426"	"Ferrochelatase deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C0220754"	"Biotinidase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2017"	"3"	"148"	"CTD_human;ORPHANET;UNIPROT"
"686"	"BTD"	"0.633"	"0.483"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"686"	"BTD"	"0.633"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"686"	"BTD"	"0.633"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"686"	"BTD"	"0.633"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C1854698"	"Multiple Carboxylase Deficiency, Juvenile-Onset"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1997"	"1999"	"3"	"9"	"ORPHANET;UNIPROT"
"686"	"BTD"	"0.633"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"686"	"BTD"	"0.633"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"686"	"BTD"	"0.633"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"687"	"KLF9"	"0.681"	"0.276"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"687"	"KLF9"	"0.681"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"687"	"KLF9"	"0.681"	"0.276"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"687"	"KLF9"	"0.681"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"688"	"KLF5"	"0.596"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2014"	"0"	"0"	"UNIPROT"
"688"	"KLF5"	"0.596"	"0.483"	"C2936380"	"Neointima"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"688"	"KLF5"	"0.596"	"0.483"	"C2936381"	"Neointima Formation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"694"	"BTG1"	"0.639"	"0.517"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"694"	"BTG1"	"0.639"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"694"	"BTG1"	"0.639"	"0.517"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"694"	"BTG1"	"0.639"	"0.517"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"694"	"BTG1"	"0.639"	"0.517"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"695"	"BTK"	"0.524"	"0.69"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.50"	"1"	"1994"	"2016"	"1"	"1"	"CTD_human"
"695"	"BTK"	"0.524"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"695"	"BTK"	"0.524"	"0.69"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.50"	"0.964285714285714"	"2011"	"2018"	"0"	"1"	"CGI"
"695"	"BTK"	"0.524"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"695"	"BTK"	"0.524"	"0.69"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.33"	"1"	"1993"	"2004"	"1"	"0"	"CTD_human"
"695"	"BTK"	"0.524"	"0.69"	"C0221026"	"X-linked agammaglobulinemia"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"1.00"	"0.936781609195402"	"1975"	"2018"	"26"	"47"	"CTD_human;ORPHANET;UNIPROT"
"695"	"BTK"	"0.524"	"0.69"	"C0241932"	"X-linked hypogammaglobulinemia"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"0"	"1994"	"2006"	"26"	"23"	"UNIPROT"
"695"	"BTK"	"0.524"	"0.69"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"695"	"BTK"	"0.524"	"0.69"	"C0472813"	"X-linked agammaglobulinemia with growth hormone deficiency"	"disease"	"C05;C10;C15;C16;C19;C20"	"Disease or Syndrome"	"0.60"		"1994"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"695"	"BTK"	"0.524"	"0.69"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"695"	"BTK"	"0.524"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"695"	"BTK"	"0.524"	"0.69"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"695"	"BTK"	"0.524"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"699"	"BUB1"	"0.586"	"0.655"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"UNIPROT"
"699"	"BUB1"	"0.586"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2013"	"2"	"3"	"UNIPROT"
"699"	"BUB1"	"0.586"	"0.655"	"C1850343"	"MOSAIC VARIEGATED ANEUPLOIDY SYNDROME"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"699"	"BUB1"	"0.586"	"0.655"	"C2931286"	"Warburton Anyane Yeboa syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"701"	"BUB1B"	"0.532"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2010"	"0"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"701"	"BUB1B"	"0.532"	"0.724"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"701"	"BUB1B"	"0.532"	"0.724"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2013"	"0"	"0"	"CGI"
"701"	"BUB1B"	"0.532"	"0.724"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"701"	"BUB1B"	"0.532"	"0.724"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0206656"	"Embryonal Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"1999"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"701"	"BUB1B"	"0.532"	"0.724"	"C1850343"	"MOSAIC VARIEGATED ANEUPLOIDY SYNDROME"	"disease"	"C16"	"Disease or Syndrome"	"0.96"	"1"	"2004"	"2017"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"701"	"BUB1B"	"0.532"	"0.724"	"C1864389"	"PREMATURE CHROMATID SEPARATION TRAIT"	"disease"		"Disease or Syndrome"	"0.64"	"1"	"1999"	"2014"	"1"	"4"	"CTD_human;UNIPROT"
"701"	"BUB1B"	"0.532"	"0.724"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C2931286"	"Warburton Anyane Yeboa syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"701"	"BUB1B"	"0.532"	"0.724"	"C2931383"	"Chromosomal mosaicism due to mitotic instability"	"disease"	"C16"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"701"	"BUB1B"	"0.532"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"701"	"BUB1B"	"0.532"	"0.724"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"706"	"TSPO"	"0.525"	"0.655"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0745744"	"End Stage Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"706"	"TSPO"	"0.525"	"0.655"	"C2936476"	"Chronic Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"708"	"C1QBP"	"0.636"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"708"	"C1QBP"	"0.636"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"708"	"C1QBP"	"0.636"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"708"	"C1QBP"	"0.636"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"708"	"C1QBP"	"0.636"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"708"	"C1QBP"	"0.636"	"0.483"	"C4540209"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"710"	"SERPING1"	"0.607"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0019243"	"Angioedemas, Hereditary"	"group"	"C14;C16;C17;C20"	"Disease or Syndrome"	"0.60"	"0.985294117647059"	"1981"	"2018"	"22"	"17"	"CTD_human;UNIPROT"
"710"	"SERPING1"	"0.607"	"0.655"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0024143"	"Lupus Nephritis"	"disease"	"C12;C13;C17;C20"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C0398775"	"Hereditary C1 esterase inhibitor deficiency - deficient factor"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"710"	"SERPING1"	"0.607"	"0.655"	"C0398776"	"Hereditary C1 esterase inhibitor deficiency - dysfunctional factor"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"710"	"SERPING1"	"0.607"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C1852700"	"Complement Component 4, Partial Deficiency Of"	"disease"	"C20"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"710"	"SERPING1"	"0.607"	"0.655"	"C1862892"	"Hereditary Angioedema Type II"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.70"		"1988"	"2014"	"19"	"18"	"CTD_human;ORPHANET;UNIPROT"
"710"	"SERPING1"	"0.607"	"0.655"	"C2717905"	"Hereditary Angioedema Types I and II"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.30"		"1992"	"2009"	"3"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C2717906"	"Hereditary Angioedema Type I"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.73"	"0.666666666666667"	"1988"	"2018"	"19"	"21"	"CTD_human;ORPHANET;UNIPROT"
"710"	"SERPING1"	"0.607"	"0.655"	"C2931758"	"Acquired angioedema"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1989"	"2017"	"2"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"710"	"SERPING1"	"0.607"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0015230"	"Exanthema"	"phenotype"	"C17"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1996"	"2015"	"2"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0017662"	"Glomerulonephritis, Membranoproliferative"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0020951"	"Immune Complex Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.56"	"0.833333333333333"	"1996"	"2013"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"712"	"C1QA"	"0.667"	"0.483"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C3150902"	"C1q DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"1995"	"2012"	"0"	"2"	"CTD_human"
"712"	"C1QA"	"0.667"	"0.483"	"C3280742"	"SYSTEMIC LUPUS ERYTHEMATOSUS 16"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"713"	"C1QB"	"0.72"	"0.379"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"713"	"C1QB"	"0.72"	"0.379"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"713"	"C1QB"	"0.72"	"0.379"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"713"	"C1QB"	"0.72"	"0.379"	"C3150902"	"C1q DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"1988"	"2015"	"7"	"1"	"CLINGEN;CTD_human;UNIPROT"
"714"	"C1QC"	"0.815"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"714"	"C1QC"	"0.815"	"0.241"	"C3150902"	"C1q DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"1982"	"2014"	"1"	"4"	"CTD_human;UNIPROT"
"715"	"C1R"	"0.69"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"715"	"C1R"	"0.69"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"715"	"C1R"	"0.69"	"0.483"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"715"	"C1R"	"0.69"	"0.483"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"715"	"C1R"	"0.69"	"0.483"	"C0268347"	"Ehlers-Danlos Syndrome, Type VIII"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.70"		"1977"	"2016"	"1"	"14"	"CTD_human;ORPHANET;UNIPROT"
"715"	"C1R"	"0.69"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"715"	"C1R"	"0.69"	"0.483"	"C3150274"	"COMPLEMENT COMPONENT C1r/C1s DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"716"	"C1S"	"0.707"	"0.31"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C0268347"	"Ehlers-Danlos Syndrome, Type VIII"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"ORPHANET"
"716"	"C1S"	"0.707"	"0.31"	"C0677607"	"Hashimoto Disease"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C1862892"	"Hereditary Angioedema Type II"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C2717905"	"Hereditary Angioedema Types I and II"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C2717906"	"Hereditary Angioedema Type I"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C3151078"	"Complement Component C1s Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.40"		"2001"	"2001"	"0"	"1"	"CTD_human"
"716"	"C1S"	"0.707"	"0.31"	"C4310681"	"EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"717"	"C2"	"0.645"	"0.552"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.47"	"1"	"2006"	"2014"	"1"	"8"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C3150275"	"COMPLEMENT COMPONENT 2 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.64"	"0.75"	"1985"	"2013"	"2"	"4"	"CTD_human;UNIPROT"
"717"	"C2"	"0.645"	"0.552"	"C3809653"	"MACULAR DEGENERATION, AGE-RELATED, 14"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"717"	"C2"	"0.645"	"0.552"	"C3809654"	"MACULAR DEGENERATION, AGE-RELATED, REDUCED RISK OF"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2012"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.50"		"2000"	"2016"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0030807"	"Pemphigus"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0030809"	"Pemphigus Vulgaris"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0034152"	"Henoch-Schoenlein Purpura"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0042386"	"Vasculitis, Hemorrhagic"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0086922"	"Rheumatoid Purpura"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2018"	"4"	"3"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0242461"	"Purpura, Nonthrombocytopenic"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0263313"	"Pemphigus Foliaceus"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0376362"	"Purpura Hemorrhagica"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2012"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C1969651"	"Macular Degeneration, Age-Related, 9"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2007"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"718"	"C3"	"0.484"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C2752037"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5"	"phenotype"		"Finding"	"0.60"		"1993"	"2010"	"2"	"8"	"ORPHANET;UNIPROT"
"718"	"C3"	"0.484"	"0.828"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.57"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"718"	"C3"	"0.484"	"0.828"	"C3151071"	"COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE"	"disease"	"C20"	"Disease or Syndrome"	"0.60"		"1994"	"1994"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"718"	"C3"	"0.484"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"718"	"C3"	"0.484"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"720"	"C4A"	"0.604"	"0.69"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"720"	"C4A"	"0.604"	"0.69"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"720"	"C4A"	"0.604"	"0.69"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"720"	"C4A"	"0.604"	"0.69"	"C3280642"	"Complement Component 4a Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"1990"	"0"	"0"	"CTD_human"
"720"	"C4A"	"0.604"	"0.69"	"C3280742"	"SYSTEMIC LUPUS ERYTHEMATOSUS 16"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"721"	"C4B"	"0.627"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"1996"	"2010"	"2"	"0"	"CTD_human"
"721"	"C4B"	"0.627"	"0.724"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.35"	"1"	"1984"	"2012"	"1"	"0"	"CTD_human"
"721"	"C4B"	"0.627"	"0.724"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"721"	"C4B"	"0.627"	"0.724"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"721"	"C4B"	"0.627"	"0.724"	"C3280641"	"Decreased serum complement C4b"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"1999"	"2017"	"0"	"0"	"CTD_human"
"722"	"C4BPA"	"0.648"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"725"	"C4BPB"	"0.762"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"726"	"CAPN5"	"0.735"	"0.448"	"C0242852"	"Proliferative vitreoretinopathy"	"disease"	"C11"	"Disease or Syndrome"	"0.70"		"1990"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"727"	"C5"	"0.611"	"0.655"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"727"	"C5"	"0.611"	"0.655"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"727"	"C5"	"0.611"	"0.655"	"C0031154"	"Peritonitis"	"disease"	"C01;C06"	"Pathologic Function"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"727"	"C5"	"0.611"	"0.655"	"C0343047"	"Complement component 5 deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.40"		"1995"	"2005"	"0"	"4"	"CTD_human"
"727"	"C5"	"0.611"	"0.655"	"C1449646"	"Primary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"727"	"C5"	"0.611"	"0.655"	"C1449647"	"Secondary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"728"	"C5AR1"	"0.59"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"728"	"C5AR1"	"0.59"	"0.655"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"728"	"C5AR1"	"0.59"	"0.655"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"728"	"C5AR1"	"0.59"	"0.655"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"729"	"C6"	"0.752"	"0.379"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729"	"C6"	"0.752"	"0.379"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729"	"C6"	"0.752"	"0.379"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729"	"C6"	"0.752"	"0.379"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729"	"C6"	"0.752"	"0.379"	"C2676232"	"Complement Component 6 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.42"	"1"	"1988"	"2013"	"0"	"2"	"CTD_human"
"730"	"C7"	"0.799"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"730"	"C7"	"0.799"	"0.276"	"C1864694"	"Complement Component 7 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.62"	"1"	"1989"	"2015"	"3"	"8"	"CTD_human;UNIPROT"
"731"	"C8A"	"0.815"	"0.138"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"731"	"C8A"	"0.815"	"0.138"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"731"	"C8A"	"0.815"	"0.138"	"C0025289"	"Meningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1998"	"1998"	"1"	"0"	"CTD_human"
"731"	"C8A"	"0.815"	"0.138"	"C0030167"	"Pachymeningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"731"	"C8A"	"0.815"	"0.138"	"C0085396"	"Neisseriaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"731"	"C8A"	"0.815"	"0.138"	"C3151081"	"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0025289"	"Meningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0030167"	"Pachymeningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0085396"	"Neisseriaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C3151080"	"COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II"	"disease"		"Disease or Syndrome"	"0.42"	"0.5"	"1991"	"2013"	"0"	"7"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"732"	"C8B"	"0.785"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"733"	"C8G"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"2"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0015456"	"Facial Dermatoses"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0015704"	"Favre-Racouchot Syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"2"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0025294"	"Meningococcal meningitis"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0041834"	"Erythema"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2014"	"2016"	"1"	"1"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0343097"	"Nodular Elastoidosis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C1135745"	"Meningitis, Meningococcal, Serogroup A"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C1135746"	"Meningitis, Meningococcal, Serogroup B"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C1135747"	"Meningitis, Meningococcal, Serogroup C"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C1136209"	"Meningitis, Meningococcal, Serogroup Y"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C1136210"	"Meningitis, Meningococcal, Serogroup W-135"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"735"	"C9"	"0.652"	"0.517"	"C3151189"	"C9 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.65"	"1"	"1990"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"735"	"C9"	"0.652"	"0.517"	"C3810042"	"MACULAR DEGENERATION, AGE-RELATED, 15"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"740"	"MRPL49"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"741"	"ZNHIT2"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"750"	"GAS8-AS1"	"1"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"752"	"FMNL1"	"0.785"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"755"	"C21orf2"	"0.663"	"0.414"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"755"	"C21orf2"	"0.663"	"0.414"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"755"	"C21orf2"	"0.663"	"0.414"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"755"	"C21orf2"	"0.663"	"0.414"	"C1865695"	"Spondylometaphyseal dysplasia, axial"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"4"	"8"	"UNIPROT"
"755"	"C21orf2"	"0.663"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"755"	"C21orf2"	"0.663"	"0.414"	"C4479651"	"RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2017"	"2"	"3"	"UNIPROT"
"759"	"CA1"	"0.672"	"0.379"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"759"	"CA1"	"0.672"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"1993"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"760"	"CA2"	"0.557"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C0345407"	"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.88"	"1"	"1972"	"2016"	"5"	"3"	"CTD_human;UNIPROT"
"760"	"CA2"	"0.557"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C1849435"	"Renal tubular acidosis, distal, type 3"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"760"	"CA2"	"0.557"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"760"	"CA2"	"0.557"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"761"	"CA3"	"0.69"	"0.379"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"761"	"CA3"	"0.69"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.50"		"2007"	"2015"	"1"	"0"	"CTD_human"
"761"	"CA3"	"0.69"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"761"	"CA3"	"0.69"	"0.379"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"762"	"CA4"	"0.685"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.47"	"1"	"1997"	"2010"	"0"	"0"	"ORPHANET"
"762"	"CA4"	"0.685"	"0.483"	"C1833245"	"Retinitis Pigmentosa 17"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.64"	"1"	"1995"	"2011"	"3"	"3"	"CTD_human;UNIPROT"
"763"	"CA5A"	"0.773"	"0.241"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"763"	"CA5A"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"763"	"CA5A"	"0.773"	"0.241"	"C3810404"	"CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"767"	"CA8"	"0.636"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"767"	"CA8"	"0.636"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"767"	"CA8"	"0.636"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"767"	"CA8"	"0.636"	"0.552"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"767"	"CA8"	"0.636"	"0.552"	"C0394006"	"Dysequilibrium syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"767"	"CA8"	"0.636"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"767"	"CA8"	"0.636"	"0.552"	"C2750509"	"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.80"		"2009"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"767"	"CA8"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"768"	"CA9"	"0.537"	"0.586"	"C0002793"	"Anaplasia"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"2001"	"2008"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0007124"	"Noninfiltrating Intraductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C1176475"	"Ductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"768"	"CA9"	"0.537"	"0.586"	"C1332347"	"Atypical Ductal Breast Hyperplasia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"771"	"CA12"	"0.672"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"771"	"CA12"	"0.672"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"771"	"CA12"	"0.672"	"0.586"	"C1840437"	"Isolated hyperchlorhidrosis"	"phenotype"		"Finding"	"0.60"		"2011"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0270862"	"Hemiplegic migraine"	"disease"		"Disease or Syndrome"	"0.40"	"0.888888888888889"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0338488"	"Alternating hemiplegia of childhood"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2007"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.979166666666667"	"1997"	"2016"	"7"	"6"	"CTD_human;ORPHANET;UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"2"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C1720416"	"Episodic ataxia type 2 (disorder)"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"1.00"	"0.962264150943396"	"1996"	"2017"	"14"	"35"	"CTD_human;ORPHANET;UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C1832884"	"Hemiplegic migraine, familial type 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.70"	"0.9"	"1995"	"2017"	"11"	"16"	"CTD_human;UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C1832903"	"MIGRAINE, SPORADIC HEMIPLEGIC"	"disease"	"C10"	"Disease or Syndrome"	"0.46"	"0.833333333333333"	"1996"	"2017"	"9"	"15"	"UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"773"	"CACNA1A"	"0.534"	"0.552"	"C3494934"	"Benign paroxysmal torticollis of infancy"	"disease"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"773"	"CACNA1A"	"0.534"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"		"2008"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"773"	"CACNA1A"	"0.534"	"0.552"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"773"	"CACNA1A"	"0.534"	"0.552"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"773"	"CACNA1A"	"0.534"	"0.552"	"C4310716"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2017"	"2"	"4"	"CTD_human;UNIPROT"
"773"	"CACNA1A"	"0.534"	"0.552"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2017"	"2"	"1"	"PSYGENET"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"				"0"	"0"	"CTD_human"
"774"	"CACNA1B"	"0.834"	"0.069"	"C3538999"	"DYSTONIA 23"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2015"	"1"	"1"	"UNIPROT"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"0.8"	"2009"	"2018"	"8"	"20"	"CTD_human;PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.45"	"1"	"2004"	"2017"	"1"	"3"	"GENOMICS_ENGLAND"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2011"	"2016"	"3"	"1"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2009"	"2018"	"4"	"8"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"2010"	"2015"	"5"	"3"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"2"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2011"	"2015"	"5"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.66"	"1"	"2007"	"2015"	"0"	"1"	"GENOMICS_ENGLAND;ORPHANET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2010"	"2015"	"5"	"0"	"PSYGENET"
"775"	"CACNA1C"	"0.575"	"0.517"	"C1832916"	"Timothy syndrome"	"disease"	"C05;C14;C16;C23;F03"	"Disease or Syndrome"	"1.00"	"0.944444444444444"	"1993"	"2016"	"6"	"4"	"CTD_human;ORPHANET;UNIPROT"
"775"	"CACNA1C"	"0.575"	"0.517"	"C2678478"	"Brugada Syndrome 3"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"775"	"CACNA1C"	"0.575"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2013"	"2016"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0004331"	"Auriculo-Ventricular Dissociation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0018794"	"Heart Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0039240"	"Supraventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0428908"	"Sinus Node Dysfunction (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C3554018"	"SINOATRIAL NODE DYSFUNCTION AND DEAFNESS"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"2"	"ORPHANET"
"776"	"CACNA1D"	"0.594"	"0.483"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"776"	"CACNA1D"	"0.594"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"776"	"CACNA1D"	"0.594"	"0.483"	"C3809609"	"PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"ORPHANET;UNIPROT"
"776"	"CACNA1D"	"0.594"	"0.483"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"778"	"CACNA1F"	"0.611"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"778"	"CACNA1F"	"0.611"	"0.414"	"C0268505"	"Ocular albinism, type II"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.66"	"1"	"1989"	"2014"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"778"	"CACNA1F"	"0.611"	"0.414"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"	"1"	"1994"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"778"	"CACNA1F"	"0.611"	"0.414"	"C1845407"	"CONE-ROD DYSTROPHY, X-LINKED, 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2001"	"2014"	"0"	"4"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.90"	"1"	"1993"	"2016"	"7"	"10"	"CTD_human;UNIPROT"
"778"	"CACNA1F"	"0.611"	"0.414"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2003"	"0"	"0"	"CTD_human"
"778"	"CACNA1F"	"0.611"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"778"	"CACNA1F"	"0.611"	"0.414"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0024591"	"Malignant hyperpyrexia due to anesthesia"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2018"	"0"	"0"	"ORPHANET"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0238357"	"Hyperkalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0238358"	"Hypokalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.967741935483871"	"1994"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0268446"	"Thyrotoxic periodic paralysis"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2003"	"2007"	"0"	"3"	"ORPHANET"
"779"	"CACNA1S"	"0.685"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"779"	"CACNA1S"	"0.685"	"0.517"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C1866077"	"MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5"	"phenotype"		"Finding"	"0.30"		"1997"	"1997"	"1"	"1"	"UNIPROT"
"779"	"CACNA1S"	"0.685"	"0.517"	"C2749982"	"THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C2930984"	"Malignant hyperthermia susceptibility type 5"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"1995"	"2017"	"0"	"3"	"CTD_human"
"779"	"CACNA1S"	"0.685"	"0.517"	"C3714580"	"Hypokalemic periodic paralysis type 1"	"disease"		"Disease or Syndrome"	"0.70"	"0.9375"	"1987"	"2017"	"5"	"7"	"CTD_human;UNIPROT"
"780"	"DDR1"	"0.533"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2015"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2007"	"2018"	"1"	"1"	"PSYGENET"
"780"	"DDR1"	"0.533"	"0.69"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"780"	"DDR1"	"0.533"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"780"	"DDR1"	"0.533"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.52"	"1"	"2007"	"2011"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C1865020"	"Short QT Syndrome 1"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"781"	"CACNA2D1"	"0.696"	"0.379"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2013"	"3"	"0"	"CTD_human"
"782"	"CACNB1"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"783"	"CACNB2"	"0.696"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2014"	"1"	"1"	"PSYGENET"
"783"	"CACNB2"	"0.696"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"783"	"CACNB2"	"0.696"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2018"	"1"	"4"	"PSYGENET"
"783"	"CACNB2"	"0.696"	"0.414"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"783"	"CACNB2"	"0.696"	"0.414"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"		"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"783"	"CACNB2"	"0.696"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"783"	"CACNB2"	"0.696"	"0.414"	"C2678477"	"Brugada Syndrome 4"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"784"	"CACNB3"	"0.857"	"0.207"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"784"	"CACNB3"	"0.857"	"0.207"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"GENOMICS_ENGLAND"
"785"	"CACNB4"	"0.676"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"785"	"CACNB4"	"0.676"	"0.207"	"C0014548"	"Epilepsy, Generalized"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0017332"	"Generalized Nonconvulsive Seizure Disorder"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0086236"	"Epilepsy, Atonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0086241"	"Epilepsy, Tonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0270850"	"Idiopathic generalized epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"785"	"CACNB4"	"0.676"	"0.207"	"C0270854"	"Symptomatic Generalized Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0311334"	"Generalized convulsive epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0347869"	"Epilepsy, Akinetic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0393676"	"Panayiotopoulos Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"785"	"CACNB4"	"0.676"	"0.207"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"785"	"CACNB4"	"0.676"	"0.207"	"C1866039"	"EPISODIC ATAXIA, TYPE 5"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"788"	"SLC25A20"	"0.619"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"788"	"SLC25A20"	"0.619"	"0.586"	"C0342791"	"Carnitine-Acylcarnitine Translocase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1992"	"2017"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"788"	"SLC25A20"	"0.619"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2003"	"5"	"0"	"GENOMICS_ENGLAND"
"790"	"CAD"	"0.557"	"0.655"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0023440"	"Acute Erythroblastic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"790"	"CAD"	"0.557"	"0.655"	"C0949116"	"Congenital hypoplastic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"790"	"CAD"	"0.557"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2016"	"1"	"1"	"UNIPROT"
"790"	"CAD"	"0.557"	"0.655"	"C4225320"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"793"	"CALB1"	"0.676"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"793"	"CALB1"	"0.676"	"0.448"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"793"	"CALB1"	"0.676"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"794"	"CALB2"	"0.642"	"0.379"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"794"	"CALB2"	"0.642"	"0.379"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"794"	"CALB2"	"0.642"	"0.379"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"794"	"CALB2"	"0.642"	"0.379"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"794"	"CALB2"	"0.642"	"0.379"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"794"	"CALB2"	"0.642"	"0.379"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"796"	"CALCA"	"0.456"	"0.828"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"1998"	"2001"	"1"	"0"	"PSYGENET"
"796"	"CALCA"	"0.456"	"0.828"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1983"	"1984"	"3"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"1975"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"1991"	"2011"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1975"	"2003"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.91304347826087"	"2003"	"2017"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0149940"	"Sciatic Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0154748"	"Lesion of Sciatic Nerve"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1983"	"1984"	"3"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0242013"	"Sciatic Neuritis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"0.5"	"2001"	"2017"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"796"	"CALCA"	"0.456"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1983"	"1998"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1983"	"1984"	"2"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751924"	"Neuralgia-Neuritis, Sciatic Nerve"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0751925"	"Sciatic Nerve Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"4"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"796"	"CALCA"	"0.456"	"0.828"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.38"	"0.875"	"2000"	"2015"	"0"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"799"	"CALCR"	"0.588"	"0.586"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"800"	"CALD1"	"0.607"	"0.552"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"800"	"CALD1"	"0.607"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"800"	"CALD1"	"0.607"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"800"	"CALD1"	"0.607"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9"	"1992"	"2016"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"801"	"CALM1"	"0.469"	"0.793"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"801"	"CALM1"	"0.469"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.10"	"0.888888888888889"	"1997"	"2013"	"1"	"0"	"PSYGENET"
"801"	"CALM1"	"0.469"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0340485"	"Familial ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.63"	"0.666666666666667"	"2013"	"2016"	"0"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"801"	"CALM1"	"0.469"	"0.793"	"C2677794"	"Stress-induced polymorphic ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"801"	"CALM1"	"0.469"	"0.793"	"C3554047"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"4"	"2"	"UNIPROT"
"801"	"CALM1"	"0.469"	"0.793"	"C4015671"	"LONG QT SYNDROME 14"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"5"	"4"	"CTD_human;UNIPROT"
"805"	"CALM2"	"0.472"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2014"	"2"	"0"	"PSYGENET"
"805"	"CALM2"	"0.472"	"0.793"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2005"	"2014"	"5"	"0"	"PSYGENET"
"805"	"CALM2"	"0.472"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2005"	"2014"	"5"	"0"	"PSYGENET"
"805"	"CALM2"	"0.472"	"0.793"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"805"	"CALM2"	"0.472"	"0.793"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.40"				"0"	"4"	"ORPHANET"
"805"	"CALM2"	"0.472"	"0.793"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"805"	"CALM2"	"0.472"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"805"	"CALM2"	"0.472"	"0.793"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"0"	"0"	"ORPHANET"
"805"	"CALM2"	"0.472"	"0.793"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.54"	"0.75"	"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"805"	"CALM2"	"0.472"	"0.793"	"C4015695"	"LONG QT SYNDROME 15"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"6"	"5"	"CTD_human;UNIPROT"
"808"	"CALM3"	"0.479"	"0.793"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"808"	"CALM3"	"0.479"	"0.793"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.53"	"0.666666666666667"	"2013"	"2016"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"810"	"CALML3"	"0.773"	"0.276"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"810"	"CALML3"	"0.773"	"0.276"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"0.60"	"0.952380952380952"	"2013"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"811"	"CALR"	"0.492"	"0.793"	"C0004565"	"Melanoma, B16"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0009075"	"Melanoma, Cloudman S91"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"811"	"CALR"	"0.492"	"0.793"	"C0018598"	"Melanoma, Harding-Passey"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0025205"	"Melanoma, Experimental"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0026987"	"Myelofibrosis"	"disease"		"Neoplastic Process"	"0.50"	"0.916666666666667"	"2014"	"2018"	"0"	"0"	"ORPHANET"
"811"	"CALR"	"0.492"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"2"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0036939"	"Shared Paranoid Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.60"	"0.907692307692308"	"2013"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"811"	"CALR"	"0.492"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"811"	"CALR"	"0.492"	"0.793"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"811"	"CALR"	"0.492"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"811"	"CALR"	"0.492"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"811"	"CALR"	"0.492"	"0.793"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"811"	"CALR"	"0.492"	"0.793"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"813"	"CALU"	"0.762"	"0.172"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"814"	"CAMK4"	"0.659"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2008"	"2018"	"1"	"0"	"PSYGENET"
"814"	"CAMK4"	"0.659"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"814"	"CAMK4"	"0.659"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"814"	"CAMK4"	"0.659"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"814"	"CAMK4"	"0.659"	"0.621"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"814"	"CAMK4"	"0.659"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human;PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"815"	"CAMK2A"	"0.672"	"0.31"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"815"	"CAMK2A"	"0.672"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"		"2001"	"2010"	"2"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"816"	"CAMK2B"	"0.69"	"0.345"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"816"	"CAMK2B"	"0.69"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"817"	"CAMK2D"	"0.773"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"817"	"CAMK2D"	"0.773"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"817"	"CAMK2D"	"0.773"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"817"	"CAMK2D"	"0.773"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"818"	"CAMK2G"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"821"	"CANX"	"0.633"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"822"	"CAPG"	"0.616"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0029134"	"Optic Neuritis"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0085582"	"Retrobulbar Neuritis"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C0524679"	"Neuropapillitis"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"823"	"CAPN1"	"0.627"	"0.621"	"C4310800"	"SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"824"	"CAPN2"	"0.636"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"824"	"CAPN2"	"0.636"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"824"	"CAPN2"	"0.636"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"825"	"CAPN3"	"0.609"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"825"	"CAPN3"	"0.609"	"0.483"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"0.948717948717949"	"1993"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"825"	"CAPN3"	"0.609"	"0.483"	"C1299884"	"Eosinophilic myositis (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.83"	"1"	"1995"	"2017"	"10"	"33"	"CTD_human;UNIPROT"
"825"	"CAPN3"	"0.609"	"0.483"	"C1869123"	"Limb-girdle muscular dystrophy type 2A"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"0.96551724137931"	"1993"	"2018"	"10"	"112"	"CTD_human;ORPHANET;UNIPROT"
"826"	"CAPNS1"	"0.743"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"826"	"CAPNS1"	"0.743"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"827"	"CAPN6"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"829"	"CAPZA1"	"0.857"	"0.103"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"831"	"CAST"	"0.565"	"0.724"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"831"	"CAST"	"0.565"	"0.724"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"831"	"CAST"	"0.565"	"0.724"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"831"	"CAST"	"0.565"	"0.724"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"831"	"CAST"	"0.565"	"0.724"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"831"	"CAST"	"0.565"	"0.724"	"C4225381"	"PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1986"	"2015"	"0"	"3"	"CTD_human;ORPHANET"
"832"	"CAPZB"	"0.773"	"0.241"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"832"	"CAPZB"	"0.773"	"0.241"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"833"	"CARS"	"0.773"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"833"	"CARS"	"0.773"	"0.345"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"834"	"CASP1"	"0.468"	"0.828"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"0.5"	"2003"	"2014"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"834"	"CASP1"	"0.468"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"835"	"CASP2"	"0.611"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"836"	"CASP3"	"0.391"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"		"2002"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.50"		"2003"	"2009"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.50"		"2008"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0014476"	"Eperythrozoonosis"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0026936"	"Mycoplasma Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"836"	"CASP3"	"0.391"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2010"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0038525"	"Subarachnoid Hemorrhage"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0270192"	"Perinatal Subarachnoid Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0472383"	"Subarachnoid Hemorrhage, Spontaneous"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0751530"	"Subarachnoid Hemorrhage, Aneurysmal"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0795688"	"Subarachnoid Hemorrhage, Intracranial"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2009"	"2"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"836"	"CASP3"	"0.391"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"837"	"CASP4"	"0.701"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"837"	"CASP4"	"0.701"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"2"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"840"	"CASP7"	"0.611"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"841"	"CASP8"	"0.443"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2004"	"2016"	"3"	"0"	"CGI;CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.833333333333333"	"2003"	"2014"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2000"	"2015"	"2"	"1"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"841"	"CASP8"	"0.443"	"0.793"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0343641"	"Human papilloma virus infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"841"	"CASP8"	"0.443"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0585362"	"Squamous cell carcinoma of mouth"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"841"	"CASP8"	"0.443"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"1"	"2004"	"2018"	"3"	"1"	"CGI;CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"841"	"CASP8"	"0.443"	"0.793"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2012"	"3"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.818181818181818"	"2003"	"2014"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C1846545"	"Autoimmune Lymphoproliferative Syndrome Type 2B"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.92"	"1"	"2002"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"841"	"CASP8"	"0.443"	"0.793"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"1"	"1999"	"2017"	"0"	"1"	"CGI;CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C2717884"	"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"841"	"CASP8"	"0.443"	"0.793"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2001"	"2012"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"842"	"CASP9"	"0.516"	"0.724"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.73"	"1"	"2002"	"2010"	"1"	"3"	"CGI;CTD_human;UNIPROT"
"843"	"CASP10"	"0.561"	"0.517"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2002"	"2004"	"0"	"0"	"CGI;CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"		"2002"	"2002"	"0"	"2"	"CGI;CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"843"	"CASP10"	"0.561"	"0.517"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"843"	"CASP10"	"0.561"	"0.517"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"843"	"CASP10"	"0.561"	"0.517"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.63"	"1"	"2002"	"2010"	"1"	"1"	"CGI;UNIPROT"
"843"	"CASP10"	"0.561"	"0.517"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"843"	"CASP10"	"0.561"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"843"	"CASP10"	"0.561"	"0.517"	"C1858968"	"Autoimmune Lymphoproliferative Syndrome, Type IIA"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.63"	"0.666666666666667"	"1993"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"843"	"CASP10"	"0.561"	"0.517"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"843"	"CASP10"	"0.561"	"0.517"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"844"	"CASQ1"	"0.773"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"844"	"CASQ1"	"0.773"	"0.276"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.51"	"1"	"2018"	"2018"	"1"	"2"	"ORPHANET;UNIPROT"
"844"	"CASQ1"	"0.773"	"0.276"	"C4011726"	"MYOPATHY, TUBULAR AGGREGATE, 1"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"2"	"UNIPROT"
"844"	"CASQ1"	"0.773"	"0.276"	"C4015624"	"MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES"	"disease"		"Disease or Syndrome"	"0.70"		"2006"	"2018"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"845"	"CASQ2"	"0.667"	"0.345"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"845"	"CASQ2"	"0.667"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"845"	"CASQ2"	"0.667"	"0.345"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.68"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"845"	"CASQ2"	"0.667"	"0.345"	"C0340485"	"Familial ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"845"	"CASQ2"	"0.667"	"0.345"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"845"	"CASQ2"	"0.667"	"0.345"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.80"	"0.947368421052632"	"2002"	"2018"	"1"	"5"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"845"	"CASQ2"	"0.667"	"0.345"	"C2677794"	"Stress-induced polymorphic ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.82"	"1"	"1993"	"2016"	"6"	"8"	"CTD_human;UNIPROT"
"845"	"CASQ2"	"0.667"	"0.345"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"846"	"CASR"	"0.47"	"0.655"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.918918918918919"	"1997"	"2017"	"1"	"1"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0020502"	"Hyperparathyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.70"	"0.9375"	"1997"	"2015"	"2"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0020598"	"Hypocalcemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.50"	"1"	"1995"	"2018"	"2"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0020626"	"Hypoparathyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.85"	"1996"	"2015"	"1"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"846"	"CASR"	"0.47"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.46"	"0.666666666666667"	"1997"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"846"	"CASR"	"0.47"	"0.655"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"846"	"CASR"	"0.47"	"0.655"	"C0270850"	"Idiopathic generalized epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0342342"	"Idiopathic Hypoparathyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.38"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C0342637"	"Hypocalciuric hypercalcemia, familial, type 1"	"disease"	"C18"	"Disease or Syndrome"	"1.00"	"0.974358974358974"	"1994"	"2017"	"26"	"43"	"CTD_human;ORPHANET;UNIPROT"
"846"	"CASR"	"0.47"	"0.655"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"846"	"CASR"	"0.47"	"0.655"	"C1809471"	"Familial benign hypercalcemia"	"disease"		"Disease or Syndrome"	"0.50"	"0.975609756097561"	"1948"	"2017"	"0"	"21"	"ORPHANET"
"846"	"CASR"	"0.47"	"0.655"	"C1832612"	"Hypocalcemia, Autosomal Dominant, with Bartter Syndrome"	"disease"	"C12;C13;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C1832615"	"HYPERPARATHYROIDISM, NEONATAL SEVERE"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.80"	"0.974358974358974"	"1982"	"2017"	"7"	"9"	"CTD_human;ORPHANET;UNIPROT"
"846"	"CASR"	"0.47"	"0.655"	"C1832648"	"Hypoparathyroidism familial isolated"	"disease"	"C19"	"Disease or Syndrome"	"0.42"	"0.5"	"1997"	"2017"	"1"	"1"	"CTD_human"
"846"	"CASR"	"0.47"	"0.655"	"C1840348"	"Hypocalciuric Hypercalcemia, Acquired"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"1994"	"2017"	"26"	"25"	"UNIPROT"
"846"	"CASR"	"0.47"	"0.655"	"C2752062"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8"	"phenotype"		"Finding"	"0.40"		"2008"	"2010"	"1"	"3"	"UNIPROT"
"846"	"CASR"	"0.47"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"846"	"CASR"	"0.47"	"0.655"	"C3715128"	"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1"	"disease"		"Disease or Syndrome"	"0.82"	"1"	"1995"	"2016"	"21"	"22"	"ORPHANET;UNIPROT"
"846"	"CASR"	"0.47"	"0.655"	"C4048195"	"Autosomal dominant hypocalcemia"	"disease"		"Disease or Syndrome"	"0.80"	"1"	"1995"	"2018"	"21"	"21"	"ORPHANET;UNIPROT"
"847"	"CAT"	"0.397"	"0.828"	"C0000771"	"Abnormalities, Drug-Induced"	"phenotype"	"C16"	"Congenital Abnormality"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1996"	"2015"	"2"	"0"	"PSYGENET"
"847"	"CAT"	"0.397"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2010"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"1996"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2003"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"6"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2007"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0008909"	"Claustrophobia"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2010"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2017"	"2"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"0"	"1995"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.59"	"0.875"	"2001"	"2016"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2010"	"2013"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0022593"	"Keratosis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0022594"	"Keratosis Blennorrhagica"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2006"	"2010"	"2"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"1996"	"2016"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0033626"	"Protein Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1993"	"2013"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2001"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"1991"	"2007"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2010"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0041408"	"Turner Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"847"	"CAT"	"0.397"	"0.828"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0086501"	"Keratoma"	"phenotype"	"C17"	"Acquired Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0242526"	"Gonadal Dysgenesis, 45,X"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0268419"	"Acatalasia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"0.916666666666667"	"1988"	"2015"	"5"	"0"	"CTD_human;ORPHANET"
"847"	"CAT"	"0.397"	"0.828"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0349231"	"Phobic anxiety disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2016"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0752048"	"Hypocatalasemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2015"	"5"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0814154"	"Alcohol Related Neurodevelopmental Disorder"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"0.5"	"2000"	"2014"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human;PSYGENET"
"847"	"CAT"	"0.397"	"0.828"	"C1456865"	"Ureteral Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.857142857142857"	"1991"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1527168"	"Bonnevie-Ullrich Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"0.5"	"1995"	"2013"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C2931868"	"Catalase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1990"	"2015"	"5"	"0"	"CTD_human;ORPHANET"
"847"	"CAT"	"0.397"	"0.828"	"C2936847"	"Acatalasemia Japanese type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2015"	"5"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C2936848"	"Acatalasemia Swiss type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1990"	"2015"	"5"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3146244"	"Alcohol Related Birth Defect"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3661483"	"Partial Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"847"	"CAT"	"0.397"	"0.828"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.49"	"0.888888888888889"	"2010"	"2017"	"2"	"4"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.80"	"0.985507246376812"	"1998"	"2017"	"4"	"0"	"CTD_human;UNIPROT"
"857"	"CAV1"	"0.416"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0011859"	"Lipoatrophic Diabetes Mellitus"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.56"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.920634920634921"	"1999"	"2018"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"857"	"CAV1"	"0.416"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C0221032"	"Familial generalized lipodystrophy"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2009"	"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.52"	"1"	"2017"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.964912280701754"	"1998"	"2016"	"4"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2011"	"4"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1258104"	"Diffuse Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1999"	"2013"	"4"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"857"	"CAV1"	"0.416"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C2675861"	"Lipodystrophy, Congenital Generalized, Type 3"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2016"	"0"	"3"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1993"	"2018"	"9"	"0"	"GENOMICS_ENGLAND"
"857"	"CAV1"	"0.416"	"0.828"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.70"	"0.909090909090909"	"1993"	"2018"	"9"	"0"	"CTD_human;GENOMICS_ENGLAND"
"857"	"CAV1"	"0.416"	"0.828"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C3807567"	"PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"857"	"CAV1"	"0.416"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"858"	"CAV2"	"0.627"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"858"	"CAV2"	"0.627"	"0.621"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.48"	"1"	"2000"	"2017"	"0"	"3"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"859"	"CAV3"	"0.592"	"0.414"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2014"	"1"	"3"	"UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C0205700"	"Asymmetric Septal Hypertrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C0241005"	"Creatine phosphokinase serum increased"	"phenotype"		"Finding"	"0.60"		"1975"	"2009"	"4"	"4"	"CTD_human;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2006"	"1"	"1"	"UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"859"	"CAV3"	"0.592"	"0.414"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C1832560"	"RIPPLING MUSCLE DISEASE 2 (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"1975"	"2012"	"7"	"9"	"CTD_human;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C1832567"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.92"	"1"	"1975"	"2016"	"7"	"11"	"CTD_human;ORPHANET;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C1838254"	"RIPPLING MUSCLE DISEASE 1"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C1853698"	"Rippling muscle disease"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"	"1"	"2001"	"2017"	"7"	"8"	"CTD_human;ORPHANET;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C2678485"	"LONG QT SYNDROME 9 (disorder)"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"2006"	"2014"	"2"	"6"	"CTD_human;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C2931337"	"Chromosome 3, monosomy 3p25"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"859"	"CAV3"	"0.592"	"0.414"	"C3280443"	"MYOPATHY, DISTAL, TATEYAMA TYPE"	"disease"		"Disease or Syndrome"	"0.70"		"1999"	"2009"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"859"	"CAV3"	"0.592"	"0.414"	"C3495498"	"Cardiomyopathy, Familial Hypertrophic, 1 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"860"	"RUNX2"	"0.49"	"0.621"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0008928"	"Cleidocranial Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"0.975"	"1993"	"2018"	"21"	"15"	"CTD_human;ORPHANET;UNIPROT"
"860"	"RUNX2"	"0.49"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"860"	"RUNX2"	"0.49"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"860"	"RUNX2"	"0.49"	"0.621"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"2000"	"2018"	"2"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0243057"	"Stomatognathic System Abnormalities"	"group"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C0949690"	"Spondylarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C1834969"	"Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"860"	"RUNX2"	"0.49"	"0.621"	"C1838416"	"CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.40"		"1997"	"2018"	"18"	"8"	"UNIPROT"
"860"	"RUNX2"	"0.49"	"0.621"	"C1861516"	"Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1997"	"2018"	"18"	"9"	"UNIPROT"
"860"	"RUNX2"	"0.49"	"0.621"	"C3549874"	"METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"860"	"RUNX2"	"0.49"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"861"	"RUNX1"	"0.467"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.38"	"0.875"	"2004"	"2013"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"861"	"RUNX1"	"0.467"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"861"	"RUNX1"	"0.467"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.97979797979798"	"1996"	"2018"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.982905982905983"	"1990"	"2018"	"2"	"4"	"CGI;CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2014"	"0"	"0"	"ORPHANET"
"861"	"RUNX1"	"0.467"	"0.69"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0032197"	"Platelet Storage Pool Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2018"	"0"	"0"	"ORPHANET"
"861"	"RUNX1"	"0.467"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"861"	"RUNX1"	"0.467"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"861"	"RUNX1"	"0.467"	"0.69"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"0.95"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"861"	"RUNX1"	"0.467"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C1832388"	"Platelet Disorder, Familial, with Associated Myeloid Malignancy"	"disease"	"C04;C15;C16"	"Disease or Syndrome"	"0.72"	"1"	"1999"	"2017"	"7"	"11"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"861"	"RUNX1"	"0.467"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2016"	"2"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"861"	"RUNX1"	"0.467"	"0.69"	"C2931875"	"Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"861"	"RUNX1"	"0.467"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.50"	"0.985915492957746"	"1993"	"2017"	"1"	"0"	"CTD_human"
"862"	"RUNX1T1"	"0.567"	"0.759"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.983606557377049"	"1993"	"2018"	"2"	"0"	"CTD_human"
"862"	"RUNX1T1"	"0.567"	"0.759"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"862"	"RUNX1T1"	"0.567"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"862"	"RUNX1T1"	"0.567"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"862"	"RUNX1T1"	"0.567"	"0.759"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1994"	"2016"	"2"	"0"	"CTD_human"
"863"	"CBFA2T3"	"0.672"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"864"	"RUNX3"	"0.494"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.38"	"0.875"	"2004"	"2016"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.962264150943396"	"2002"	"2017"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"1"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"864"	"RUNX3"	"0.494"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"UNIPROT"
"865"	"CBFB"	"0.627"	"0.414"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.976744186046512"	"1993"	"2017"	"2"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0023479"	"Acute myelomonocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"0.75"	"2000"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"865"	"CBFB"	"0.627"	"0.414"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C0029396"	"Heterotopic Ossification"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"865"	"CBFB"	"0.627"	"0.414"	"C2861596"	"AML M4 Eo with inv(16) or t(16;16)"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C1852529"	"Corticosteroid-Binding Globulin Deficiency"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.94"	"1"	"1992"	"2010"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"866"	"SERPINA6"	"0.627"	"0.655"	"C1969107"	"Corticosteroid-Binding Globulin, Elevated"	"disease"	"C15"	"Disease or Syndrome"	"0.50"		"1992"	"2010"	"3"	"2"	"UNIPROT"
"866"	"SERPINA6"	"0.627"	"0.655"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"866"	"SERPINA6"	"0.627"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"867"	"CBL"	"0.55"	"0.586"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"867"	"CBL"	"0.55"	"0.586"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"0"	"0"	"CGI"
"867"	"CBL"	"0.55"	"0.586"	"C0027019"	"Myelomonocytic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"867"	"CBL"	"0.55"	"0.586"	"C0042384"	"Vasculitis"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"867"	"CBL"	"0.55"	"0.586"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.70"	"1"	"2009"	"2016"	"3"	"2"	"CTD_human;ORPHANET"
"867"	"CBL"	"0.55"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.61"	"1"	"2012"	"2017"	"1"	"2"	"CGI;GENOMICS_ENGLAND"
"867"	"CBL"	"0.55"	"0.586"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"867"	"CBL"	"0.55"	"0.586"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"867"	"CBL"	"0.55"	"0.586"	"C3150803"	"NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2009"	"2016"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"867"	"CBL"	"0.55"	"0.586"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.39"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"867"	"CBL"	"0.55"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"868"	"CBLB"	"0.743"	"0.241"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"868"	"CBLB"	"0.743"	"0.241"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"868"	"CBLB"	"0.743"	"0.241"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CGI"
"868"	"CBLB"	"0.743"	"0.241"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.44"	"0.75"	"2010"	"2017"	"1"	"1"	"CTD_human"
"868"	"CBLB"	"0.743"	"0.241"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"868"	"CBLB"	"0.743"	"0.241"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.56"	"1"	"1998"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0729264"	"Preterm premature rupture of membranes (disorder)"	"phenotype"	"C13"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"871"	"SERPINH1"	"0.57"	"0.69"	"C3151211"	"OSTEOGENESIS IMPERFECTA, TYPE X"	"disease"		"Disease or Syndrome"	"0.80"		"2010"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"873"	"CBR1"	"0.609"	"0.517"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2015"	"2016"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2000"	"2012"	"1"	"0"	"CTD_human"
"873"	"CBR1"	"0.609"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"875"	"CBS"	"0.503"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"0.875"	"1996"	"2016"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"875"	"CBS"	"0.503"	"0.793"	"C0019880"	"Homocystinuria"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.70"	"0.960526315789474"	"1988"	"2018"	"0"	"8"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"875"	"CBS"	"0.503"	"0.793"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"875"	"CBS"	"0.503"	"0.793"	"C0162429"	"Malnutrition"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"875"	"CBS"	"0.503"	"0.793"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"875"	"CBS"	"0.503"	"0.793"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"875"	"CBS"	"0.503"	"0.793"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"875"	"CBS"	"0.503"	"0.793"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"0.911764705882353"	"1995"	"2018"	"3"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C0751202"	"Cystathionine beta-Synthase Deficiency Disease"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2018"	"40"	"54"	"CTD_human;ORPHANET;UNIPROT"
"875"	"CBS"	"0.503"	"0.793"	"C3150344"	"HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED"	"disease"		"Disease or Syndrome"	"0.40"		"1984"	"2017"	"40"	"75"	"UNIPROT"
"875"	"CBS"	"0.503"	"0.793"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"875"	"CBS"	"0.503"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"883"	"KYAT1"	"0.785"	"0.138"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"883"	"KYAT1"	"0.785"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"1998"	"2005"	"2"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2014"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1985"	"1985"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2014"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2011"	"2"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1981"	"1994"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1999"	"2004"	"6"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0041657"	"Unconscious State"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1985"	"1985"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.02"	"1"	"1999"	"2000"	"1"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1986"	"2002"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2005"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0564408"	"Manic mood"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"885"	"CCK"	"0.513"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1986"	"1987"	"2"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"885"	"CCK"	"0.513"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"886"	"CCKAR"	"0.642"	"0.31"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"886"	"CCKAR"	"0.642"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"0.8"	"1999"	"2005"	"6"	"0"	"CTD_human;PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"886"	"CCKAR"	"0.642"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2000"	"2013"	"5"	"0"	"PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"886"	"CCKAR"	"0.642"	"0.31"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"886"	"CCKAR"	"0.642"	"0.31"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"886"	"CCKAR"	"0.642"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"887"	"CCKBR"	"0.579"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0030319"	"Panic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9"	"1996"	"2013"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2002"	"2"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1998"	"2002"	"2"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0086769"	"Panic Attacks"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1998"	"2002"	"2"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"887"	"CCKBR"	"0.579"	"0.448"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"889"	"KRIT1"	"0.551"	"0.724"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"889"	"KRIT1"	"0.551"	"0.724"	"C0752160"	"Hemangioma, Cavernous, Central Nervous System"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C0752161"	"Cavernous Hemangioma, Extracerebral"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C0752164"	"Cavernous Hemangioma, Intracerebral"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C1140710"	"Cerebral Cavernous Hemangioma"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C1366911"	"Cerebral Cavernous Malformations 1"	"disease"		"Disease or Syndrome"	"0.44"	"0.75"	"1988"	"2013"	"1"	"4"	"UNIPROT"
"889"	"KRIT1"	"0.551"	"0.724"	"C1861785"	"Cavernous Malformations of CNS and Retina"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"UNIPROT"
"889"	"KRIT1"	"0.551"	"0.724"	"C1861786"	"Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations"	"disease"	"C10;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"UNIPROT"
"889"	"KRIT1"	"0.551"	"0.724"	"C1956260"	"Cavernous Angioma, Central Nervous System"	"disease"	"C04;C10;C14;C15;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"889"	"KRIT1"	"0.551"	"0.724"	"C2919945"	"Cavernous Hemangioma of Brain"	"phenotype"	"C04;C10;C14;C15;C16"	"Anatomical Abnormality"	"0.70"	"0.975609756097561"	"1993"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"889"	"KRIT1"	"0.551"	"0.724"	"C2931263"	"Familial cerebral cavernous malformation"	"disease"	"C04;C10;C14;C15;C16"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2017"	"0"	"0"	"ORPHANET"
"889"	"KRIT1"	"0.551"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"890"	"CCNA2"	"0.546"	"0.724"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"890"	"CCNA2"	"0.546"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"890"	"CCNA2"	"0.546"	"0.724"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"890"	"CCNA2"	"0.546"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"890"	"CCNA2"	"0.546"	"0.724"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"890"	"CCNA2"	"0.546"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"891"	"CCNB1"	"0.54"	"0.655"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"891"	"CCNB1"	"0.54"	"0.655"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"894"	"CCND2"	"0.519"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2018"	"1"	"1"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"894"	"CCND2"	"0.519"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CGI"
"894"	"CCND2"	"0.519"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"894"	"CCND2"	"0.519"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"894"	"CCND2"	"0.519"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CGI"
"894"	"CCND2"	"0.519"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"894"	"CCND2"	"0.519"	"0.655"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"894"	"CCND2"	"0.519"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C1863924"	"Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"894"	"CCND2"	"0.519"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"894"	"CCND2"	"0.519"	"0.655"	"C1879677"	"Alcohol Toxicity"	"disease"		"Injury or Poisoning"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"894"	"CCND2"	"0.519"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"894"	"CCND2"	"0.519"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"894"	"CCND2"	"0.519"	"0.655"	"C4014742"	"MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2014"	"1"	"6"	"UNIPROT"
"896"	"CCND3"	"0.58"	"0.517"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"896"	"CCND3"	"0.58"	"0.517"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2017"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.875"	"2003"	"2016"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"898"	"CCNE1"	"0.59"	"0.517"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"0"	"0"	"CGI"
"898"	"CCNE1"	"0.59"	"0.517"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"898"	"CCNE1"	"0.59"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.857142857142857"	"2003"	"2016"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.50"		"2011"	"2011"	"1"	"0"	"CGI;CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"	"1"	"2008"	"2018"	"1"	"0"	"CGI;CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"898"	"CCNE1"	"0.59"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"899"	"CCNF"	"0.727"	"0.414"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.42"	"1"	"2016"	"2018"	"0"	"0"	"ORPHANET"
"900"	"CCNG1"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"900"	"CCNG1"	"0.681"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"900"	"CCNG1"	"0.681"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"902"	"CCNH"	"0.648"	"0.517"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"914"	"CD2"	"0.672"	"0.414"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"914"	"CD2"	"0.672"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"914"	"CD2"	"0.672"	"0.414"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"914"	"CD2"	"0.672"	"0.414"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"914"	"CD2"	"0.672"	"0.414"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"915"	"CD3D"	"0.663"	"0.483"	"C3810147"	"IMMUNODEFICIENCY 19"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2000"	"2017"	"0"	"3"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2011"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C3810127"	"IMMUNODEFICIENCY 18"	"disease"		"Disease or Syndrome"	"0.60"		"1991"	"2015"	"6"	"2"	"CLINGEN;CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C3810128"	"IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT"	"disease"		"Disease or Syndrome"	"0.60"		"1991"	"2015"	"6"	"1"	"CLINGEN;CTD_human"
"916"	"CD3E"	"0.648"	"0.448"	"C3810129"	"IMMUNODEFICIENCY 18, SCID VARIANT"	"disease"		"Disease or Syndrome"	"0.50"		"1991"	"2015"	"6"	"0"	"CLINGEN;CTD_human"
"917"	"CD3G"	"0.735"	"0.276"	"C3810107"	"IMMUNODEFICIENCY 17"	"disease"		"Disease or Syndrome"	"0.60"		"1991"	"2007"	"0"	"3"	"CTD_human;ORPHANET"
"919"	"CD247"	"0.577"	"0.621"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.43"	"1"	"1998"	"2012"	"1"	"1"	"CTD_human"
"919"	"CD247"	"0.577"	"0.621"	"C1857798"	"Immunodeficiency due to Defect in CD3-Zeta"	"disease"	"C20"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"0"	"5"	"CTD_human"
"919"	"CD247"	"0.577"	"0.621"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"920"	"CD4"	"0.648"	"0.621"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"920"	"CD4"	"0.648"	"0.621"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"920"	"CD4"	"0.648"	"0.621"	"C0162526"	"AIDS-Related Opportunistic Infections"	"group"	"C01;C02;C03;C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"920"	"CD4"	"0.648"	"0.621"	"C0917713"	"Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"920"	"CD4"	"0.648"	"0.621"	"C3542021"	"Duchenne and Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"921"	"CD5"	"0.713"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"921"	"CD5"	"0.713"	"0.241"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2008"	"1"	"0"	"CTD_human"
"922"	"CD5L"	"0.727"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"923"	"CD6"	"0.54"	"0.586"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.43"	"1"	"2009"	"2016"	"2"	"1"	"CTD_human"
"923"	"CD6"	"0.54"	"0.586"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"2"	"0"	"CTD_human"
"924"	"CD7"	"0.752"	"0.345"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"924"	"CD7"	"0.752"	"0.345"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"924"	"CD7"	"0.752"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"924"	"CD7"	"0.752"	"0.345"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"924"	"CD7"	"0.752"	"0.345"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"925"	"CD8A"	"0.648"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"925"	"CD8A"	"0.648"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"925"	"CD8A"	"0.648"	"0.414"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"925"	"CD8A"	"0.648"	"0.414"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"925"	"CD8A"	"0.648"	"0.414"	"C1837065"	"CD8 Deficiency, Familial"	"disease"	"C20"	"Disease or Syndrome"	"0.70"		"2001"	"2001"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"926"	"CD8B"	"0.735"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"926"	"CD8B"	"0.735"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"926"	"CD8B"	"0.735"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2007"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"928"	"CD9"	"0.54"	"0.759"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.885245901639344"	"2001"	"2017"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0013595"	"Eczema"	"disease"	"C17"	"Disease or Syndrome"	"0.38"	"0.875"	"2002"	"2016"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"929"	"CD14"	"0.429"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"929"	"CD14"	"0.429"	"0.828"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"930"	"CD19"	"0.483"	"0.724"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"930"	"CD19"	"0.483"	"0.724"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"930"	"CD19"	"0.483"	"0.724"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"930"	"CD19"	"0.483"	"0.724"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.43"	"1"	"1991"	"2006"	"1"	"0"	"CTD_human"
"930"	"CD19"	"0.483"	"0.724"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"930"	"CD19"	"0.483"	"0.724"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"931"	"MS4A1"	"0.472"	"0.759"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"931"	"MS4A1"	"0.472"	"0.759"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"939"	"CD27"	"0.555"	"0.69"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"939"	"CD27"	"0.555"	"0.69"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"939"	"CD27"	"0.555"	"0.69"	"C3554540"	"LYMPHOPROLIFERATIVE SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2012"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"940"	"CD28"	"0.488"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2016"	"3"	"1"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0026948"	"Mycosis Fungoides"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1994"	"1994"	"0"	"0"	"ORPHANET"
"940"	"CD28"	"0.488"	"0.793"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"940"	"CD28"	"0.488"	"0.793"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.42"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"940"	"CD28"	"0.488"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"941"	"CD80"	"0.509"	"0.724"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"942"	"CD86"	"0.524"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"942"	"CD86"	"0.524"	"0.724"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.974683544303797"	"1987"	"2017"	"2"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"943"	"TNFRSF8"	"0.516"	"0.724"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.95"	"2011"	"2018"	"2"	"1"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.983606557377049"	"1991"	"2017"	"1"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2011"	"2018"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"945"	"CD33"	"0.567"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2006"	"1"	"0"	"CTD_human"
"946"	"SIGLEC6"	"0.886"	"0.103"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"946"	"SIGLEC6"	"0.886"	"0.103"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"947"	"CD34"	"0.414"	"0.793"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"947"	"CD34"	"0.414"	"0.793"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"947"	"CD34"	"0.414"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"947"	"CD34"	"0.414"	"0.793"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"947"	"CD34"	"0.414"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"948"	"CD36"	"0.505"	"0.828"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2001"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2012"	"0"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"948"	"CD36"	"0.505"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"0.962962962962963"	"1992"	"2016"	"0"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0038160"	"Staphylococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"948"	"CD36"	"0.505"	"0.828"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C1318973"	"Staphylococcus aureus infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2001"	"1"	"0"	"CTD_human"
"948"	"CD36"	"0.505"	"0.828"	"C1842090"	"Platelet Glycoprotein IV Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.90"	"0.933333333333333"	"1993"	"2016"	"2"	"8"	"CTD_human;UNIPROT"
"949"	"SCARB1"	"0.584"	"0.621"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0016427"	"Follicular cyst"	"phenotype"	"C04"	"Acquired Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"949"	"SCARB1"	"0.584"	"0.621"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C1853096"	"HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6"	"phenotype"		"Finding"	"0.40"		"2011"	"2016"	"0"	"4"	"CTD_human"
"949"	"SCARB1"	"0.584"	"0.621"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"950"	"SCARB2"	"0.633"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"950"	"SCARB2"	"0.633"	"0.483"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.79"	"1"	"1993"	"2015"	"4"	"19"	"CTD_human;ORPHANET;UNIPROT"
"950"	"SCARB2"	"0.633"	"0.483"	"C0751785"	"Unverricht-Lundborg Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"950"	"SCARB2"	"0.633"	"0.483"	"C1961835"	"Gaucher Disease, Type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"950"	"SCARB2"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"952"	"CD38"	"0.481"	"0.828"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"952"	"CD38"	"0.481"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"952"	"CD38"	"0.481"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"953"	"ENTPD1"	"0.569"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"953"	"ENTPD1"	"0.569"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"953"	"ENTPD1"	"0.569"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"953"	"ENTPD1"	"0.569"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"953"	"ENTPD1"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"953"	"ENTPD1"	"0.569"	"0.655"	"C3810289"	"SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"954"	"ENTPD2"	"0.785"	"0.103"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"954"	"ENTPD2"	"0.785"	"0.103"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"954"	"ENTPD2"	"0.785"	"0.103"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"955"	"ENTPD6"	"0.886"	"0.138"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"955"	"ENTPD6"	"0.886"	"0.138"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.909090909090909"	"2002"	"2016"	"3"	"2"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0026691"	"Mucocutaneous Lymph Node Syndrome"	"disease"	"C14;C15;C17"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"0.923076923076923"	"2000"	"2016"	"1"	"1"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0272236"	"Hyperimmunoglobulin M syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2014"	"0"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2006"	"1"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C1720956"	"Hyper-IgM Immunodeficiency Syndrome, Type 2"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C1720957"	"Hyper-IgM Immunodeficiency Syndrome, Type 3"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.70"		"2001"	"2016"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"958"	"CD40"	"0.433"	"0.862"	"C1720958"	"Hyper-IgM Immunodeficiency Syndrome, Type 5"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"958"	"CD40"	"0.433"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"959"	"CD40LG"	"0.447"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2005"	"2015"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0398689"	"Hyper-IgM Immunodeficiency Syndrome, Type 1"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.80"	"0.967032967032967"	"1992"	"2017"	"8"	"12"	"CTD_human;ORPHANET;UNIPROT"
"959"	"CD40LG"	"0.447"	"0.828"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"959"	"CD40LG"	"0.447"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2015"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"2"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.972972972972973"	"1993"	"2018"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.948412698412698"	"1990"	"2018"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"960"	"CD44"	"0.389"	"0.862"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"962"	"CD48"	"0.667"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"962"	"CD48"	"0.667"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"963"	"CD53"	"0.607"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"965"	"CD58"	"0.639"	"0.552"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2014"	"2"	"4"	"CTD_human"
"965"	"CD58"	"0.639"	"0.552"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"965"	"CD58"	"0.639"	"0.552"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"2"	"0"	"CTD_human"
"966"	"CD59"	"0.496"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1992"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"966"	"CD59"	"0.496"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1992"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"966"	"CD59"	"0.496"	"0.724"	"C2676767"	"CD59 Deficiency"	"disease"	"C12;C13;C15;C23"	"Disease or Syndrome"	"0.75"	"1"	"1992"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"967"	"CD63"	"0.614"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"967"	"CD63"	"0.614"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"967"	"CD63"	"0.614"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"967"	"CD63"	"0.614"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"967"	"CD63"	"0.614"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"968"	"CD68"	"0.48"	"0.793"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0003864"	"Arthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"2"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0162323"	"Polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"969"	"CD69"	"0.562"	"0.759"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"972"	"CD74"	"0.569"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"973"	"CD79A"	"0.596"	"0.621"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.41"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human"
"973"	"CD79A"	"0.596"	"0.621"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"0"	"0"	"CGI"
"973"	"CD79A"	"0.596"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.54"	"1"	"2003"	"2014"	"1"	"0"	"CGI;CTD_human"
"973"	"CD79A"	"0.596"	"0.621"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"973"	"CD79A"	"0.596"	"0.621"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"974"	"CD79B"	"0.614"	"0.517"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"974"	"CD79B"	"0.614"	"0.517"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"974"	"CD79B"	"0.614"	"0.517"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2013"	"0"	"0"	"CGI"
"974"	"CD79B"	"0.614"	"0.517"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.56"	"1"	"2010"	"2017"	"1"	"0"	"CGI;CTD_human"
"974"	"CD79B"	"0.614"	"0.517"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"974"	"CD79B"	"0.614"	"0.517"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"974"	"CD79B"	"0.614"	"0.517"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"974"	"CD79B"	"0.614"	"0.517"	"C3150207"	"AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"975"	"CD81"	"0.607"	"0.621"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"975"	"CD81"	"0.607"	"0.621"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.945945945945946"	"1998"	"2017"	"1"	"0"	"CTD_human"
"975"	"CD81"	"0.607"	"0.621"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"975"	"CD81"	"0.607"	"0.621"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"976"	"ADGRE5"	"0.667"	"0.448"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"977"	"CD151"	"0.621"	"0.552"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"977"	"CD151"	"0.621"	"0.552"	"C1836823"	"Nephropathy with Pretibial Epidermolysis Bullosa and Deafness"	"disease"	"C09;C10;C12;C13;C16;C17;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"978"	"CDA"	"0.611"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"978"	"CDA"	"0.611"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"978"	"CDA"	"0.611"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2000"	"2015"	"2"	"0"	"CTD_human"
"978"	"CDA"	"0.611"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2000"	"2015"	"2"	"0"	"CTD_human"
"983"	"CDK1"	"0.538"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"983"	"CDK1"	"0.538"	"0.69"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"983"	"CDK1"	"0.538"	"0.69"	"C1306067"	"Drug-induced paranoid state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"987"	"LRBA"	"0.648"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"987"	"LRBA"	"0.648"	"0.517"	"C3553512"	"IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"989"	"SEPT7"	"0.815"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"990"	"CDC6"	"0.604"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"990"	"CDC6"	"0.604"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"990"	"CDC6"	"0.604"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"990"	"CDC6"	"0.604"	"0.621"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.53"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"990"	"CDC6"	"0.604"	"0.621"	"C3151126"	"MEIER-GORLIN SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2011"	"1"	"1"	"UNIPROT"
"990"	"CDC6"	"0.604"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"994"	"CDC25B"	"0.633"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"994"	"CDC25B"	"0.633"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"994"	"CDC25B"	"0.633"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"994"	"CDC25B"	"0.633"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"994"	"CDC25B"	"0.633"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"994"	"CDC25B"	"0.633"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"995"	"CDC25C"	"0.621"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2016"	"1"	"1"	"PSYGENET"
"996"	"CDC27"	"0.773"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"996"	"CDC27"	"0.773"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"996"	"CDC27"	"0.773"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2018"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"998"	"CDC42"	"0.511"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2016"	"4"	"0"	"PSYGENET"
"998"	"CDC42"	"0.511"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"998"	"CDC42"	"0.511"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"998"	"CDC42"	"0.511"	"0.828"	"C4225222"	"TAKENOUCHI-KOSAKI SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"998"	"CDC42"	"0.511"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.58"	"0.875"	"2001"	"2016"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.962264150943396"	"1997"	"2017"	"5"	"2"	"CTD_human;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"999"	"CDH1"	"0.432"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2001"	"2017"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9"	"1997"	"2016"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.964285714285714"	"1999"	"2018"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2010"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1998"	"2016"	"6"	"0"	"CLINGEN"
"999"	"CDH1"	"0.432"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0014476"	"Eperythrozoonosis"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"999"	"CDH1"	"0.432"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1996"	"2007"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.947368421052632"	"1997"	"2018"	"6"	"1"	"CGI;CTD_human;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0026936"	"Mycoplasma Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.96875"	"1993"	"2016"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0027645"	"Neoplasm Seeding"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.37"	"1"	"1994"	"2016"	"1"	"1"	"UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"		"2002"	"2008"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0"	"1997"	"2018"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1998"	"2017"	"6"	"0"	"CGI;CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"999"	"CDH1"	"0.432"	"0.759"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"999"	"CDH1"	"0.432"	"0.759"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"999"	"CDH1"	"0.432"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"1"	"1996"	"2013"	"2"	"0"	"CGI;CTD_human;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"999"	"CDH1"	"0.432"	"0.759"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"999"	"CDH1"	"0.432"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2001"	"2012"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.866666666666667"	"1997"	"2018"	"3"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.50"	"0.909090909090909"	"1994"	"2016"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"999"	"CDH1"	"0.432"	"0.759"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2007"	"2"	"1"	"UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"1"	"1994"	"2013"	"1"	"1"	"UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.96875"	"1992"	"2017"	"4"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.70"	"0.940828402366864"	"1994"	"2018"	"0"	"0"	"CGI;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"1994"	"2008"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"1998"	"2016"	"6"	"0"	"CLINGEN"
"999"	"CDH1"	"0.432"	"0.759"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.55"	"1"	"1994"	"2016"	"1"	"0"	"CLINGEN;CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2013"	"4"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2016"	"6"	"0"	"CLINGEN"
"999"	"CDH1"	"0.432"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8"	"2002"	"2016"	"4"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.931034482758621"	"1997"	"2018"	"2"	"1"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.80"	"0.925925925925926"	"1964"	"2018"	"20"	"45"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C1861536"	"Blepharo-cheilo-dontic syndrome"	"disease"	"C05;C07;C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"2018"	"2018"	"1"	"1"	"ORPHANET;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2006"	"2"	"0"	"CTD_human"
"999"	"CDH1"	"0.432"	"0.759"	"C3149287"	"GASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFT PALATE"	"disease"		"Neoplastic Process"	"0.50"		"1991"	"2016"	"14"	"1"	"CLINGEN;UNIPROT"
"999"	"CDH1"	"0.432"	"0.759"	"C3549742"	"Breast cancer, lobular"	"disease"		"Neoplastic Process"	"0.60"	"1"	"1991"	"2016"	"14"	"1"	"CLINGEN;UNIPROT"
"1000"	"CDH2"	"0.59"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"1000"	"CDH2"	"0.59"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1001"	"CDH3"	"0.604"	"0.517"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1001"	"CDH3"	"0.604"	"0.517"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1001"	"CDH3"	"0.604"	"0.517"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1001"	"CDH3"	"0.604"	"0.517"	"C1832162"	"HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY"	"disease"	"C11;C17"	"Disease or Syndrome"	"0.70"		"2001"	"2003"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1001"	"CDH3"	"0.604"	"0.517"	"C1857041"	"Ectodermal dysplasia, ectrodactyly, and macular dystrophy"	"disease"	"C05;C11;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.73"	"1"	"1956"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1001"	"CDH3"	"0.604"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1003"	"CDH5"	"0.656"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1003"	"CDH5"	"0.656"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0232347"	"No-Reflow Phenomenon"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1003"	"CDH5"	"0.656"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"1004"	"CDH6"	"0.762"	"0.172"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1005"	"CDH7"	"0.815"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1005"	"CDH7"	"0.815"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1005"	"CDH7"	"0.815"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1005"	"CDH7"	"0.815"	"0.103"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1005"	"CDH7"	"0.815"	"0.103"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1005"	"CDH7"	"0.815"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1006"	"CDH8"	"0.815"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1007"	"CDH9"	"0.834"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1007"	"CDH9"	"0.834"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1008"	"CDH10"	"0.799"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1008"	"CDH10"	"0.799"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1008"	"CDH10"	"0.799"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1008"	"CDH10"	"0.799"	"0.207"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1009"	"CDH11"	"0.561"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"1009"	"CDH11"	"0.561"	"0.724"	"C0809936"	"Branchio-skeleto-genital syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1009"	"CDH11"	"0.561"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"1010"	"CDH12"	"0.815"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"1010"	"CDH12"	"0.815"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1010"	"CDH12"	"0.815"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"1012"	"CDH13"	"0.529"	"0.793"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2002"	"2012"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1012"	"CDH13"	"0.529"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1012"	"CDH13"	"0.529"	"0.793"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"2"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2010"	"2016"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"1012"	"CDH13"	"0.529"	"0.793"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1013"	"CDH15"	"0.696"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1013"	"CDH15"	"0.696"	"0.517"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1013"	"CDH15"	"0.696"	"0.517"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1013"	"CDH15"	"0.696"	"0.517"	"C2675488"	"Mental Retardation, Autosomal Dominant 3"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"4"	"CTD_human;UNIPROT"
"1013"	"CDH15"	"0.696"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"1015"	"CDH17"	"0.609"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2008"	"2"	"0"	"PSYGENET"
"1015"	"CDH17"	"0.609"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1015"	"CDH17"	"0.609"	"0.552"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1015"	"CDH17"	"0.609"	"0.552"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1015"	"CDH17"	"0.609"	"0.552"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1016"	"CDH18"	"0.928"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1017"	"CDK2"	"0.478"	"0.69"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1995"	"1997"	"0"	"0"	"CGI"
"1017"	"CDK2"	"0.478"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.868421052631579"	"1994"	"2016"	"1"	"0"	"CTD_human"
"1017"	"CDK2"	"0.478"	"0.69"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2008"	"0"	"0"	"CGI"
"1017"	"CDK2"	"0.478"	"0.69"	"C1332201"	"Adult Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1017"	"CDK2"	"0.478"	"0.69"	"C1332967"	"Childhood Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1017"	"CDK2"	"0.478"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2017"	"0"	"0"	"UNIPROT"
"1018"	"CDK3"	"0.799"	"0.138"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1019"	"CDK4"	"0.449"	"0.724"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"1019"	"CDK4"	"0.449"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2017"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2016"	"2"	"0"	"CGI;CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2017"	"0"	"0"	"CGI"
"1019"	"CDK4"	"0.449"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2014"	"3"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.956521739130435"	"1994"	"2018"	"0"	"1"	"CGI;GENOMICS_ENGLAND"
"1019"	"CDK4"	"0.449"	"0.724"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"2000"	"2017"	"0"	"2"	"CGI"
"1019"	"CDK4"	"0.449"	"0.724"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2003"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"1019"	"CDK4"	"0.449"	"0.724"	"C0205825"	"Liposarcoma, Pleomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0677866"	"Brain Stem Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0751886"	"Brain Stem Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0751887"	"Medullary Neoplasms"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0751888"	"Mesencephalic Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C0751889"	"Pontine Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2003"	"2"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C1370889"	"Liposarcoma, well differentiated"	"disease"		"Neoplastic Process"	"0.38"	"0.875"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"1019"	"CDK4"	"0.449"	"0.724"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C1836892"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.60"		"1969"	"2013"	"4"	"3"	"CTD_human;UNIPROT"
"1019"	"CDK4"	"0.449"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"1019"	"CDK4"	"0.449"	"0.724"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1020"	"CDK5"	"0.542"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1020"	"CDK5"	"0.542"	"0.69"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"1020"	"CDK5"	"0.542"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"1020"	"CDK5"	"0.542"	"0.69"	"C0949664"	"Tauopathies"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"1020"	"CDK5"	"0.542"	"0.69"	"C4225359"	"LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.35"	"0.6"	"2000"	"2015"	"1"	"1"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1021"	"CDK6"	"0.508"	"0.69"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1021"	"CDK6"	"0.508"	"0.69"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2014"	"0"	"0"	"CGI"
"1021"	"CDK6"	"0.508"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1021"	"CDK6"	"0.508"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1021"	"CDK6"	"0.508"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2014"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"1021"	"CDK6"	"0.508"	"0.69"	"C0677866"	"Brain Stem Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751886"	"Brain Stem Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751887"	"Medullary Neoplasms"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751888"	"Mesencephalic Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751889"	"Pontine Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1021"	"CDK6"	"0.508"	"0.69"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"1021"	"CDK6"	"0.508"	"0.69"	"C4015156"	"MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"1024"	"CDK8"	"0.663"	"0.414"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1024"	"CDK8"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.961538461538462"	"1997"	"2013"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2008"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2003"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.59"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0025267"	"Multiple Endocrine Neoplasia Type 1"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2003"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"1998"	"2008"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.53"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9"	"1998"	"2015"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.967741935483871"	"1995"	"2014"	"2"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1026"	"CDKN1A"	"0.415"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2017"	"1"	"0"	"CGI;CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1998"	"2015"	"8"	"0"	"CLINGEN"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2010"	"3"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0025267"	"Multiple Endocrine Neoplasia Type 1"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.40"	"0.882352941176471"	"2007"	"2018"	"0"	"0"	"ORPHANET"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.70"	"1"	"1997"	"2016"	"1"	"0"	"CGI;CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"3"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2002"	"2004"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2009"	"2016"	"1"	"3"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0262587"	"Parathyroid Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.43"	"1"	"2011"	"2014"	"0"	"0"	"CGI"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.851851851851852"	"1996"	"2018"	"3"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1996"	"2017"	"1"	"0"	"CGI;CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2006"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"1998"	"2015"	"8"	"0"	"CLINGEN"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1998"	"2015"	"8"	"0"	"CLINGEN"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1336005"	"Small Intestinal Neuroendocrine Neoplasm"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C1970712"	"Multiple Endocrine Neoplasia, Type IV"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.68"	"1"	"2007"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"1027"	"CDKN1B"	"0.424"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2016"	"2"	"17"	"CTD_human;UNIPROT"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0014173"	"Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2007"	"2013"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"	"0.916666666666667"	"1996"	"2016"	"5"	"1"	"GENOMICS_ENGLAND;ORPHANET"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2011"	"2"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0349578"	"Complex Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0349579"	"Atypical Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0456483"	"Simple Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C1846009"	"Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies"	"disease"	"C05;C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.78"	"1"	"1993"	"2017"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C1851719"	"BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION"	"phenotype"		"Finding"	"0.30"		"2016"	"2016"	"1"	"4"	"UNIPROT"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C1859977"	"Adrenal Hypoplasia, Cytomegalic Type"	"disease"	"C05;C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1028"	"CDKN1C"	"0.479"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.94949494949495"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"2"	"UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.973684210526316"	"1995"	"2018"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2018"	"2"	"0"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.928571428571429"	"1995"	"2017"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.957746478873239"	"1995"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2015"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.53"	"1"	"2001"	"2018"	"2"	"0"	"CGI;CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.952830188679245"	"1994"	"2016"	"3"	"3"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.955665024630542"	"1994"	"2018"	"2"	"2"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0008628"	"Chromosome Deletion"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2016"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2014"	"3"	"0"	"PSYGENET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2014"	"3"	"0"	"PSYGENET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0013403"	"Dysplastic Nevus Syndrome"	"disease"	"C04;C16"	"Neoplastic Process"	"0.35"	"0.25"	"1997"	"2006"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1994"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.935185185185185"	"1994"	"2016"	"2"	"0"	"CGI;CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0022783"	"Vulvar Lichen Sclerosus"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"1994"	"2016"	"0"	"1"	"UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"2000"	"2016"	"3"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2016"	"4"	"0"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.911111111111111"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.967741935483871"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.94047619047619"	"1994"	"2018"	"1"	"4"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.925"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.50"	"0.941176470588235"	"1997"	"2016"	"1"	"1"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2014"	"0"	"1"	"UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2018"	"2"	"7"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.952380952380952"	"1995"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"1"	"1996"	"2015"	"2"	"1"	"CGI;CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.935483870967742"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2002"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.875"	"1997"	"2013"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0040100"	"Thymoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0040715"	"Chromosomal translocation"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0041107"	"Trisomy"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0042065"	"Genitourinary Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.96"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0085390"	"Li-Fraumeni Syndrome"	"disease"	"C04;C16;C18"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2011"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2009"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.909090909090909"	"1995"	"2016"	"1"	"7"	"CGI;CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2007"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205747"	"Familial Atypical Multiple Mole-Melanoma"	"disease"	"C04;C16"	"Neoplastic Process"	"0.38"	"1"	"1995"	"2010"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0206727"	"Nerve Sheath Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.37"	"0.833333333333333"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.60"	"0.987341772151899"	"1995"	"2018"	"1"	"1"	"CGI;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.931818181818182"	"1994"	"2017"	"4"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.947368421052632"	"1994"	"2016"	"1"	"1"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1996"	"2016"	"3"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"3"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2018"	"2"	"0"	"CGI;CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.894736842105263"	"1995"	"2012"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.899350649350649"	"1994"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0677866"	"Brain Stem Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.918918918918919"	"1994"	"2018"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751569"	"Genitourinary Cancer"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751689"	"Peripheral Nerve Sheath Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751691"	"Perineurioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751886"	"Brain Stem Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751887"	"Medullary Neoplasms"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751888"	"Mesencephalic Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0751889"	"Pontine Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.973684210526316"	"1994"	"2018"	"2"	"7"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.48"	"1"	"1995"	"2014"	"0"	"1"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1297882"	"Partial Trisomy"	"disease"	"C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.818181818181818"	"1995"	"2015"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1512419"	"Hereditary Melanoma"	"disease"		"Neoplastic Process"	"0.50"	"0.952941176470588"	"1994"	"2017"	"0"	"29"	"UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2008"	"2"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1835042"	"Melanoma astrocytoma syndrome"	"disease"	"C04;C10"	"Neoplastic Process"	"0.51"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human;ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1835044"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.60"		"1994"	"2013"	"12"	"22"	"CTD_human;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1838547"	"MELANOMA-PANCREATIC CANCER SYNDROME"	"disease"	"C04;C06;C16;C19"	"Disease or Syndrome"	"0.70"		"1995"	"2017"	"0"	"8"	"CTD_human;ORPHANET;UNIPROT"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.833333333333333"	"1996"	"2014"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.948979591836735"	"1996"	"2017"	"1"	"3"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.37"	"1"	"1995"	"2009"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C2930745"	"Partial Monosomy"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.39"	"1"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"1029"	"CDKN2A"	"0.321"	"0.828"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.34"	"0.75"	"2011"	"2017"	"1"	"4"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.952380952380952"	"1995"	"2013"	"2"	"0"	"CGI;CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0025267"	"Multiple Endocrine Neoplasia Type 1"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2009"	"2"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2018"	"1"	"2"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1030"	"CDKN2B"	"0.438"	"0.759"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"1995"	"2013"	"1"	"0"	"CTD_human"
"1031"	"CDKN2C"	"0.573"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"1031"	"CDKN2C"	"0.573"	"0.483"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1031"	"CDKN2C"	"0.573"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2013"	"0"	"0"	"CGI"
"1031"	"CDKN2C"	"0.573"	"0.483"	"C0025267"	"Multiple Endocrine Neoplasia Type 1"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2011"	"0"	"0"	"ORPHANET"
"1031"	"CDKN2C"	"0.573"	"0.483"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2012"	"0"	"0"	"CGI"
"1032"	"CDKN2D"	"0.584"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1032"	"CDKN2D"	"0.584"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1032"	"CDKN2D"	"0.584"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1032"	"CDKN2D"	"0.584"	"0.655"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1033"	"CDKN3"	"0.518"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1033"	"CDKN3"	"0.518"	"0.724"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"1033"	"CDKN3"	"0.518"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2010"	"1"	"2"	"UNIPROT"
"1033"	"CDKN3"	"0.518"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"1997"	"2017"	"1"	"2"	"UNIPROT"
"1033"	"CDKN3"	"0.518"	"0.724"	"C2676033"	"Hepatoblastoma Caused By Somatic Mutation"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"1036"	"CDO1"	"0.701"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1036"	"CDO1"	"0.701"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1036"	"CDO1"	"0.701"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2015"	"0"	"0"	"UNIPROT"
"1040"	"CDS1"	"0.701"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1040"	"CDS1"	"0.701"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1040"	"CDS1"	"0.701"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1041"	"CDSN"	"0.611"	"0.621"	"C1840299"	"Hypotrichosis Simplex of Scalp"	"disease"	"C17"	"Disease or Syndrome"	"0.60"		"1987"	"2003"	"0"	"2"	"CTD_human;ORPHANET"
"1041"	"CDSN"	"0.611"	"0.621"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"1987"	"2014"	"4"	"4"	"CTD_human;GENOMICS_ENGLAND"
"1048"	"CEACAM5"	"0.502"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1048"	"CEACAM5"	"0.502"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2012"	"6"	"0"	"GENOMICS_ENGLAND"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"1.00"	"0.986666666666667"	"1993"	"2018"	"5"	"11"	"CGI;CTD_human;UNIPROT"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2010"	"2"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0027666"	"Neoplasms, Radiation-Induced"	"group"	"C04;C26"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2012"	"6"	"0"	"GENOMICS_ENGLAND"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0751366"	"Radiation-Induced Cancer"	"disease"	"C04;C26"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2018"	"2"	"0"	"CTD_human"
"1050"	"CEBPA"	"0.533"	"0.586"	"C3275959"	"LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2001"	"2004"	"3"	"1"	"UNIPROT"
"1050"	"CEBPA"	"0.533"	"0.586"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.38"	"0.857142857142857"	"2002"	"2015"	"0"	"0"	"CGI"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"1051"	"CEBPB"	"0.538"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0344452"	"Microprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C0344453"	"Macroprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1052"	"CEBPD"	"0.6"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1053"	"CEBPE"	"0.713"	"0.241"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"1053"	"CEBPE"	"0.713"	"0.241"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1053"	"CEBPE"	"0.713"	"0.241"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"1053"	"CEBPE"	"0.713"	"0.241"	"C0398593"	"Specific granule deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"1053"	"CEBPE"	"0.713"	"0.241"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"2"	"CTD_human"
"1053"	"CEBPE"	"0.713"	"0.241"	"C4479548"	"SPECIFIC GRANULE DEFICIENCY 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1055"	"CECR"	"0.773"	"0.345"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1055"	"CECR"	"0.773"	"0.345"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1055"	"CECR"	"0.773"	"0.345"	"C0265493"	"Cat eye syndrome"	"disease"	"C11;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"1055"	"CECR"	"0.773"	"0.345"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1056"	"CEL"	"0.579"	"0.621"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"0.5"	"2013"	"2015"	"1"	"0"	"CTD_human"
"1056"	"CEL"	"0.579"	"0.621"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.45"	"1"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"1056"	"CEL"	"0.579"	"0.621"	"C1853297"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.44"	"1"	"2006"	"2014"	"0"	"2"	"CTD_human"
"1057"	"CELP"	"0.834"	"0.241"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"1061"	"CENPCP1"	"0.928"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1061"	"CENPCP1"	"0.928"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1061"	"CENPCP1"	"0.928"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1062"	"CENPE"	"0.633"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1062"	"CENPE"	"0.633"	"0.517"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"1062"	"CENPE"	"0.633"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1062"	"CENPE"	"0.633"	"0.517"	"C4015080"	"MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"1063"	"CENPF"	"0.672"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"1063"	"CENPF"	"0.672"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1063"	"CENPF"	"0.672"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1063"	"CENPF"	"0.672"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1063"	"CENPF"	"0.672"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"1063"	"CENPF"	"0.672"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1063"	"CENPF"	"0.672"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"1063"	"CENPF"	"0.672"	"0.448"	"C1855705"	"Jejunal Atresia with Microcephaly and Ocular Anomalies"	"disease"	"C05;C06;C10;C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"1063"	"CENPF"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1063"	"CENPF"	"0.672"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1066"	"CES1"	"0.63"	"0.655"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1066"	"CES1"	"0.63"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1068"	"CETN1"	"0.596"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"2"	"0"	"PSYGENET"
"1071"	"CETP"	"0.555"	"0.655"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.938461538461538"	"1995"	"2018"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.964285714285714"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.59"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1071"	"CETP"	"0.555"	"0.655"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.44"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0020476"	"Hyperlipoproteinemias"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2002"	"2"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.38"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"0.923076923076923"	"1996"	"2017"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0342883"	"Cholesteryl Ester Transfer Protein Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.891891891891892"	"1990"	"2015"	"0"	"0"	"ORPHANET"
"1071"	"CETP"	"0.555"	"0.655"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C2362324"	"Pediatric Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C3149462"	"HYPERALPHALIPOPROTEINEMIA 1"	"disease"		"Disease or Syndrome"	"0.60"	"0.846153846153846"	"1990"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"1071"	"CETP"	"0.555"	"0.655"	"C3149463"	"HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 10"	"phenotype"		"Finding"	"0.50"		"1990"	"2002"	"3"	"2"	"CTD_human;UNIPROT"
"1071"	"CETP"	"0.555"	"0.655"	"C4317171"	"Adolescent Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1071"	"CETP"	"0.555"	"0.655"	"C4521075"	"Childhood Overweight"	"phenotype"	"C18;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1072"	"CFL1"	"0.639"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1073"	"CFL2"	"0.735"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1073"	"CFL2"	"0.735"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"1073"	"CFL2"	"0.735"	"0.31"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"1073"	"CFL2"	"0.735"	"0.31"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.32"	"1"	"2007"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"1073"	"CFL2"	"0.735"	"0.31"	"C1853154"	"Nemaline Myopathy 7"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"1075"	"CTSC"	"0.6"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0030360"	"Papillon-Lefevre Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"0.976744186046512"	"1999"	"2016"	"15"	"20"	"CTD_human;ORPHANET;UNIPROT"
"1075"	"CTSC"	"0.6"	"0.586"	"C0031090"	"Periodontal Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2001"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0031106"	"Periodontitis, Juvenile"	"disease"	"C07"	"Disease or Syndrome"	"0.69"	"0.888888888888889"	"1999"	"2016"	"2"	"3"	"CTD_human;UNIPROT"
"1075"	"CTSC"	"0.6"	"0.586"	"C0034219"	"Alveolar pyorrhea"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C0600298"	"Periodontosis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1075"	"CTSC"	"0.6"	"0.586"	"C1855627"	"HAIM-MUNK SYNDROME"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.75"	"1"	"2000"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1075"	"CTSC"	"0.6"	"0.586"	"C2713394"	"Haim-Monk Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2005"	"2"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"1080"	"CFTR"	"0.453"	"0.793"	"C0004509"	"Azoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.50"	"0.916666666666667"	"1996"	"2017"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0008340"	"Choledochal Cyst"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"1080"	"CFTR"	"0.453"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0009439"	"Choledochal Cyst, Type I"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"1.00"	"0.947806354009077"	"1989"	"2018"	"85"	"427"	"CTD_human;ORPHANET;UNIPROT"
"1080"	"CFTR"	"0.453"	"0.793"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.50"	"1"	"1995"	"2018"	"2"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"0.918918918918919"	"1998"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1080"	"CFTR"	"0.453"	"0.793"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2018"	"1"	"1"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2015"	"0"	"49"	"CTD_human;ORPHANET"
"1080"	"CFTR"	"0.453"	"0.793"	"C0339985"	"Idiopathic bronchiectasis"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2006"	"2008"	"0"	"0"	"ORPHANET"
"1080"	"CFTR"	"0.453"	"0.793"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.36"	"1"	"1991"	"2016"	"15"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0403814"	"Congenital bilateral aplasia of vas deferens"	"disease"	"C12"	"Congenital Abnormality"	"0.80"	"0.945054945054945"	"1990"	"2017"	"8"	"37"	"CTD_human;ORPHANET;UNIPROT"
"1080"	"CFTR"	"0.453"	"0.793"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"1080"	"CFTR"	"0.453"	"0.793"	"C1257796"	"Choledochal Cyst, Type II"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1257797"	"Choledochal Cyst, Type III"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1257798"	"Choledochal Cyst, Type IV"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1257799"	"Choledochal Cyst, Type V"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2012"	"15"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C2749757"	"BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1"	"disease"	"C08"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C4080064"	"Autosomal Dominant Hereditary Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1080"	"CFTR"	"0.453"	"0.793"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0001621"	"Adrenal Gland Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0018991"	"Hemiplegia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0029928"	"Ovarian Diseases"	"group"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0042131"	"Uterine Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0085622"	"Monoplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0154693"	"Hemiplegia, Flaccid"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0154694"	"Hemiplegia, Spastic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0278110"	"Hemiplegia, Crossed"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0392550"	"Hemiplegia, Infantile"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0521662"	"Hemiplegia, Transient"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C0751195"	"Hemiplegia, Post-Ictal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C1720816"	"Endometrial Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1081"	"CGA"	"0.586"	"0.586"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1082"	"CGB3"	"0.63"	"0.483"	"C0015951"	"Fetal Resorption"	"disease"	"C13;C23"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"1082"	"CGB3"	"0.63"	"0.483"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"1997"	"2"	"0"	"CTD_human"
"1082"	"CGB3"	"0.63"	"0.483"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"1997"	"2"	"0"	"CTD_human"
"1082"	"CGB3"	"0.63"	"0.483"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"1997"	"2"	"0"	"CTD_human"
"1082"	"CGB3"	"0.63"	"0.483"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"1997"	"2"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1986"	"1986"	"1"	"0"	"PSYGENET"
"1103"	"CHAT"	"0.559"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"1103"	"CHAT"	"0.559"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"1103"	"CHAT"	"0.559"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"1103"	"CHAT"	"0.559"	"0.655"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2000"	"2007"	"2"	"0"	"PSYGENET"
"1103"	"CHAT"	"0.559"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0393929"	"Familial infantile myasthenia"	"disease"	"C08;C10;C20;C23"	"Disease or Syndrome"	"0.81"	"1"	"2001"	"2017"	"2"	"14"	"CTD_human;UNIPROT"
"1103"	"CHAT"	"0.559"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.48"	"1"	"1993"	"2018"	"2"	"1"	"GENOMICS_ENGLAND"
"1103"	"CHAT"	"0.559"	"0.655"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1103"	"CHAT"	"0.559"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1103"	"CHAT"	"0.559"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1105"	"CHD1"	"0.815"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1105"	"CHD1"	"0.815"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"1105"	"CHD1"	"0.815"	"0.138"	"C4540131"	"PILAROWSKI-BJORNSSON SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"UNIPROT"
"1106"	"CHD2"	"0.624"	"0.31"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0238111"	"Lennox-Gastaut syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"1106"	"CHD2"	"0.624"	"0.31"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"1106"	"CHD2"	"0.624"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2013"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"1106"	"CHD2"	"0.624"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1106"	"CHD2"	"0.624"	"0.31"	"C3809278"	"EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"2"	"26"	"UNIPROT"
"1107"	"CHD3"	"0.815"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1107"	"CHD3"	"0.815"	"0.31"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1107"	"CHD3"	"0.815"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1108"	"CHD4"	"0.642"	"0.483"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1108"	"CHD4"	"0.642"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1108"	"CHD4"	"0.642"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1108"	"CHD4"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1108"	"CHD4"	"0.642"	"0.483"	"C4310688"	"SIFRIM-HITZ-WEISS SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"2"	"7"	"UNIPROT"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2011"	"2013"	"2"	"0"	"CTD_human;PSYGENET"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"1109"	"AKR1C4"	"0.659"	"0.586"	"C1839840"	"MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"1972"	"2011"	"0"	"1"	"CTD_human;ORPHANET"
"1111"	"CHEK1"	"0.53"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1111"	"CHEK1"	"0.53"	"0.724"	"C0032578"	"Polyploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1111"	"CHEK1"	"0.53"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1111"	"CHEK1"	"0.53"	"0.724"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CLINGEN"
"1111"	"CHEK1"	"0.53"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1111"	"CHEK1"	"0.53"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2016"	"0"	"0"	"CLINGEN"
"1111"	"CHEK1"	"0.53"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1111"	"CHEK1"	"0.53"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1113"	"CHGA"	"0.54"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"1113"	"CHGA"	"0.54"	"0.621"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1986"	"2014"	"1"	"0"	"CTD_human"
"1113"	"CHGA"	"0.54"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"PSYGENET"
"1113"	"CHGA"	"0.54"	"0.621"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1113"	"CHGA"	"0.54"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1114"	"CHGB"	"0.69"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2017"	"3"	"0"	"PSYGENET"
"1114"	"CHGB"	"0.69"	"0.31"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9375"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"2002"	"2017"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.31"		"2005"	"2011"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.34"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.875"	"2003"	"2012"	"0"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"0.8"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1116"	"CHI3L1"	"0.502"	"0.793"	"C2677770"	"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"1118"	"CHIT1"	"0.58"	"0.621"	"C0017205"	"Gaucher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"1118"	"CHIT1"	"0.58"	"0.621"	"C0268250"	"Gaucher Disease, Type 2 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1118"	"CHIT1"	"0.58"	"0.621"	"C0268251"	"Gaucher Disease, Type 3 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1118"	"CHIT1"	"0.58"	"0.621"	"C1961835"	"Gaucher Disease, Type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1119"	"CHKA"	"0.624"	"0.517"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1119"	"CHKA"	"0.624"	"0.517"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1119"	"CHKA"	"0.624"	"0.517"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1120"	"CHKB"	"0.648"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1120"	"CHKB"	"0.648"	"0.483"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2014"	"1"	"1"	"CTD_human"
"1120"	"CHKB"	"0.648"	"0.483"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1120"	"CHKB"	"0.648"	"0.483"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"1"	"CTD_human"
"1120"	"CHKB"	"0.648"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1120"	"CHKB"	"0.648"	"0.483"	"C1865233"	"Muscular Dystrophy, Congenital, Megaconial Type"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.82"	"1"	"1998"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"1120"	"CHKB"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1121"	"CHM"	"0.663"	"0.379"	"C0008525"	"Choroideremia"	"disease"	"C11;C16"	"Disease or Syndrome"	"1.00"	"0.962962962962963"	"1988"	"2018"	"3"	"13"	"CTD_human;ORPHANET;UNIPROT"
"1121"	"CHM"	"0.663"	"0.379"	"C0344297"	"Choroidal sclerosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1994"	"2012"	"3"	"1"	"UNIPROT"
"1123"	"CHN1"	"0.696"	"0.31"	"C0013261"	"Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.68"	"0.875"	"2007"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"1123"	"CHN1"	"0.696"	"0.31"	"C0751083"	"Duane Retraction Syndrome, Type 2"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"2000"	"2011"	"1"	"9"	"CTD_human;UNIPROT"
"1123"	"CHN1"	"0.696"	"0.31"	"C0751084"	"Duane Retraction Syndrome, Type 3"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1123"	"CHN1"	"0.696"	"0.31"	"C0994516"	"Type 1 Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1123"	"CHN1"	"0.696"	"0.31"	"C1623209"	"Okihiro Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1124"	"CHN2"	"0.785"	"0.379"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1124"	"CHN2"	"0.785"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1124"	"CHN2"	"0.785"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1124"	"CHN2"	"0.785"	"0.379"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.5"	"2003"	"2016"	"4"	"0"	"PSYGENET"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1128"	"CHRM1"	"0.639"	"0.448"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2003"	"5"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2005"	"2014"	"5"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0005697"	"Neurogenic Urinary Bladder"	"disease"	"C10;C12;C13;C23"	"Disease or Syndrome"	"0.31"		"2004"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2002"	"2011"	"4"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2011"	"4"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0149622"	"Neurogenic Urinary Bladder, Atonic"	"disease"	"C10;C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0392115"	"Neurogenic Urinary Bladder, Uninhibited"	"disease"	"C10;C12;C13;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0750953"	"Urinary Bladder Neurogenesis"	"disease"	"C10;C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0750955"	"Neurogenic Urinary Bladder, Spastic"	"disease"	"C10;C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2010"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1129"	"CHRM2"	"0.596"	"0.586"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1130"	"LYST"	"0.633"	"0.586"	"C0007965"	"Chediak-Higashi Syndrome"	"disease"	"C15;C20"	"Disease or Syndrome"	"1.00"	"0.952380952380952"	"1963"	"2017"	"2"	"41"	"CTD_human;ORPHANET;UNIPROT"
"1130"	"LYST"	"0.633"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"1130"	"LYST"	"0.633"	"0.586"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.41"	"1"	"1993"	"1999"	"4"	"0"	"GENOMICS_ENGLAND"
"1130"	"LYST"	"0.633"	"0.586"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"1993"	"1999"	"4"	"0"	"GENOMICS_ENGLAND"
"1130"	"LYST"	"0.633"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1130"	"LYST"	"0.633"	"0.586"	"C4304022"	"Attenuated Chédiak-Higashi syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0003962"	"Ascites"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0005686"	"Urinary Bladder Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0033770"	"Prune Belly Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.62"	"1"	"2005"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0265363"	"Urethral obstruction sequence"	"disease"	"C12;C13;C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1131"	"CHRM3"	"0.546"	"0.724"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1131"	"CHRM3"	"0.546"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1131"	"CHRM3"	"0.546"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0007398"	"Catatonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2013"	"2"	"0"	"PSYGENET"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0338650"	"Catatonia, Organic"	"disease"	"C10;C23;F01"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0750992"	"Catatonia, Malignant"	"disease"	"C10;C23;F01"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0750993"	"Schizophreniform Catatonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1132"	"CHRM4"	"0.799"	"0.172"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1133"	"CHRM5"	"0.815"	"0.138"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.36"	"1"	"1995"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C1837122"	"Myasthenic Syndrome, Congenital, Fast-Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1981"	"2004"	"0"	"4"	"CTD_human"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.70"		"1982"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C2931107"	"Myasthenic syndrome, congenital, postsynaptic slow-channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C4084823"	"MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2006"	"5"	"7"	"UNIPROT"
"1134"	"CHRNA1"	"0.624"	"0.552"	"C4225405"	"MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2004"	"2"	"4"	"UNIPROT"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2009"	"2"	"0"	"PSYGENET"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C1835905"	"Epilepsy, Nocturnal Frontal Lobe, Type 4"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"1"	"1"	"CTD_human;UNIPROT"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"1135"	"CHRNA2"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2009"	"2014"	"4"	"0"	"CTD_human;PSYGENET"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2008"	"2015"	"1"	"1"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2010"	"2018"	"1"	"3"	"PSYGENET"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2014"	"2"	"0"	"PSYGENET"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1136"	"CHRNA3"	"0.584"	"0.448"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"4"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"3"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"3"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2001"	"2016"	"4"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.35"	"0.8"	"2001"	"2016"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0085541"	"Epilepsy, Frontal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2015"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2008"	"2012"	"3"	"0"	"PSYGENET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393671"	"Frontal Epilepsy, Benign, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393683"	"Epilepsy, Supplementary Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393684"	"Epilepsy, Cingulate"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0393688"	"Epilepsy, Opercular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751642"	"Epilepsy, Anterior Fronto-Polar"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0751643"	"Epilepsy, Orbito-Frontal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"3"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C1838049"	"Epilepsy, Nocturnal Frontal Lobe, Type 1"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"2"	"4"	"CTD_human;UNIPROT"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.967741935483871"	"1995"	"2016"	"0"	"0"	"ORPHANET"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1137"	"CHRNA4"	"0.521"	"0.586"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"2009"	"2013"	"5"	"0"	"CTD_human;PSYGENET"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2018"	"2"	"1"	"PSYGENET"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.95"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"4"	"0"	"PSYGENET"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1138"	"CHRNA5"	"0.598"	"0.414"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0004310"	"Auditory Perceptual Disorders"	"group"	"C09;C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0014548"	"Epilepsy, Generalized"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0017332"	"Generalized Nonconvulsive Seizure Disorder"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2014"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.75"	"1998"	"2016"	"4"	"0"	"PSYGENET"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.34"	"1"	"1998"	"2015"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0037917"	"Spina Bifida Cystica"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0086236"	"Epilepsy, Atonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0086241"	"Epilepsy, Tonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0270854"	"Symptomatic Generalized Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0311334"	"Generalized convulsive epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0347869"	"Epilepsy, Akinetic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0750942"	"Auditory Inattention"	"disease"	"C09;C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0795690"	"Congenital omphalocele"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C0917813"	"Spina Bifida, Open"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C1306503"	"Congenital exomphalos"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C2677613"	"Chromosome 15q13.3 Microdeletion Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1139"	"CHRNA7"	"0.55"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"5"	"0"	"CTD_human"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"1996"	"2012"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C1837092"	"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1140"	"CHRNB1"	"0.72"	"0.379"	"C4225374"	"MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL"	"disease"		"Disease or Syndrome"	"0.40"		"1996"	"2017"	"3"	"3"	"UNIPROT"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"		"2003"	"2008"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0034933"	"Reflex, Abnormal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2008"	"2"	"0"	"PSYGENET"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2003"	"2012"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0085541"	"Epilepsy, Frontal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0151572"	"Reflex, Corneal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0151888"	"Hyporeflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0151889"	"Hyperreflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0234146"	"Absent reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0234784"	"Reflex, Gag, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0241772"	"Reflex, Deep Tendon, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0277839"	"Hoffman's Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0277850"	"Reflex, Pendular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0278211"	"Reflex, Corneal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0393671"	"Frontal Epilepsy, Benign, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0393683"	"Epilepsy, Supplementary Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0393684"	"Epilepsy, Cingulate"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0393688"	"Epilepsy, Opercular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0522345"	"Reflex, Acoustic, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0558845"	"Reflex, Ankle, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0558846"	"Reflex, Triceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0558847"	"Reflex, Biceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0576612"	"Reflex, Anal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0743002"	"Abnormal Deep Tendon Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751468"	"Bulbocavernosus Reflex, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751469"	"Bulbocavernousus Reflex Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751470"	"Palmo-Mental Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751471"	"Reflex, Anal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751472"	"Reflex, Ankle, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751473"	"Reflex, Ankle, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751474"	"Reflex, Biceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751475"	"Reflex, Biceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751476"	"Reflex, Gag, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751477"	"Reflex, Knee, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751478"	"Reflex, Knee, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751479"	"Reflex, Moro, Asymmetric"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751480"	"Reflex, Triceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751481"	"Reflex, Triceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751642"	"Epilepsy, Anterior Fronto-Polar"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0751643"	"Epilepsy, Orbito-Frontal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C1854335"	"Epilepsy, Nocturnal Frontal Lobe, Type 3"	"disease"	"C10"	"Disease or Syndrome"	"0.80"		"1993"	"2012"	"1"	"5"	"CTD_human;UNIPROT"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2001"	"2013"	"0"	"0"	"ORPHANET"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"1141"	"CHRNB2"	"0.619"	"0.207"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1142"	"CHRNB3"	"0.727"	"0.207"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2012"	"3"	"0"	"PSYGENET"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2014"	"2"	"0"	"PSYGENET"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1143"	"CHRNB4"	"0.642"	"0.345"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"1144"	"CHRND"	"0.663"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1144"	"CHRND"	"0.663"	"0.448"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2018"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1144"	"CHRND"	"0.663"	"0.448"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1144"	"CHRND"	"0.663"	"0.448"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C1837092"	"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C1837122"	"Myasthenic Syndrome, Congenital, Fast-Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1144"	"CHRND"	"0.663"	"0.448"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.70"		"2008"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1144"	"CHRND"	"0.663"	"0.448"	"C4225370"	"MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2008"	"2"	"1"	"UNIPROT"
"1144"	"CHRND"	"0.663"	"0.448"	"C4225371"	"MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2008"	"2"	"5"	"UNIPROT"
"1144"	"CHRND"	"0.663"	"0.448"	"C4225372"	"MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"2002"	"2"	"2"	"UNIPROT"
"1145"	"CHRNE"	"0.663"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"1145"	"CHRNE"	"0.663"	"0.414"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"1993"	"2018"	"5"	"3"	"GENOMICS_ENGLAND"
"1145"	"CHRNE"	"0.663"	"0.414"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1145"	"CHRNE"	"0.663"	"0.414"	"C1837091"	"MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"		"1996"	"2013"	"1"	"15"	"CTD_human;UNIPROT"
"1145"	"CHRNE"	"0.663"	"0.414"	"C1837122"	"Myasthenic Syndrome, Congenital, Fast-Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"1145"	"CHRNE"	"0.663"	"0.414"	"C1853949"	"MYASTHENIA, FAMILIAL INFANTILE, 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1987"	"2017"	"0"	"11"	"CTD_human"
"1145"	"CHRNE"	"0.663"	"0.414"	"C4225369"	"MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2012"	"2"	"6"	"UNIPROT"
"1145"	"CHRNE"	"0.663"	"0.414"	"C4225413"	"MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL"	"disease"		"Disease or Syndrome"	"0.50"		"1995"	"2016"	"5"	"4"	"UNIPROT"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0265261"	"Multiple pterygium syndrome"	"disease"	"C16;C17;C23"	"Congenital Abnormality"	"0.74"	"1"	"2005"	"2015"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"1994"	"2017"	"6"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1146"	"CHRNG"	"0.609"	"0.552"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1146"	"CHRNG"	"0.609"	"0.552"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1146"	"CHRNG"	"0.609"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1147"	"CHUK"	"0.586"	"0.586"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0013949"	"Embryopathies"	"disease"	"C13;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0015929"	"Fetal Diseases"	"group"	"C13;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"3"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1147"	"CHUK"	"0.586"	"0.586"	"C3150891"	"COCOON SYNDROME"	"disease"		"Disease or Syndrome"	"0.82"	"1"	"1999"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"1147"	"CHUK"	"0.586"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1149"	"CIDEA"	"0.752"	"0.207"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1982"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2012"	"1"	"0"	"PSYGENET"
"1152"	"CKB"	"0.636"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"0"	"1987"	"1988"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C0857501"	"Acute schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1152"	"CKB"	"0.636"	"0.483"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1152"	"CKB"	"0.636"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1153"	"CIRBP"	"0.663"	"0.448"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1153"	"CIRBP"	"0.663"	"0.448"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1153"	"CIRBP"	"0.663"	"0.448"	"C0751865"	"Alcohol-Induced Disorders, Nervous System"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1153"	"CIRBP"	"0.663"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C0004610"	"Bacteremia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1154"	"CISH"	"0.541"	"0.724"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1155"	"TBCB"	"0.928"	"0.103"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1988"	"2002"	"2"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1158"	"CKM"	"0.815"	"0.241"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0009207"	"Cockayne Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.964285714285714"	"1996"	"2016"	"2"	"0"	"CTD_human"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0020241"	"Hydroa Vacciniforme"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0751037"	"Cockayne Syndrome, Type III"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"2"	"0"	"CTD_human;ORPHANET"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0751038"	"Cockayne Syndrome, Type II"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.53"	"0.666666666666667"	"2004"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"1161"	"ERCC8"	"0.6"	"0.655"	"C0751039"	"Cockayne Syndrome, Type I"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.78"	"1"	"1995"	"2018"	"5"	"11"	"CTD_human;ORPHANET;UNIPROT"
"1161"	"ERCC8"	"0.6"	"0.655"	"C1833561"	"UV-Sensitive Syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"1161"	"ERCC8"	"0.6"	"0.655"	"C3553298"	"UV-SENSITIVE SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"1161"	"ERCC8"	"0.6"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1164"	"CKS2"	"0.696"	"0.31"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1164"	"CKS2"	"0.696"	"0.31"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1174"	"AP1S1"	"0.735"	"0.345"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1174"	"AP1S1"	"0.735"	"0.345"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1174"	"AP1S1"	"0.735"	"0.345"	"C1836330"	"ERYTHROKERATODERMIA VARIABILIS 3 (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"1174"	"AP1S1"	"0.735"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1175"	"AP2S1"	"0.69"	"0.31"	"C1833372"	"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1992"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1176"	"AP3S1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1180"	"CLCN1"	"0.672"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"1180"	"CLCN1"	"0.672"	"0.31"	"C0027127"	"Myotonia Congenita"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.90"	"0.979591836734694"	"1982"	"2016"	"1"	"24"	"CTD_human;ORPHANET"
"1180"	"CLCN1"	"0.672"	"0.31"	"C0270959"	"Myotonia Levior"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1994"	"2017"	"13"	"13"	"CTD_human;UNIPROT"
"1180"	"CLCN1"	"0.672"	"0.31"	"C0751360"	"Becker Generalized Myotonia"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2017"	"21"	"36"	"CTD_human;UNIPROT"
"1180"	"CLCN1"	"0.672"	"0.31"	"C2936781"	"Generalized Myotonia of Thomsen"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.982142857142857"	"1992"	"2017"	"13"	"24"	"CTD_human;ORPHANET;UNIPROT"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.53"	"1"	"2014"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0270850"	"Idiopathic generalized epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2014"	"0"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2009"	"0"	"0"	"ORPHANET"
"1181"	"CLCN2"	"0.663"	"0.379"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C1854107"	"Hyperaldosteronism, Familial, Type II"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"1"	"2"	"CTD_human"
"1181"	"CLCN2"	"0.663"	"0.379"	"C2750893"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11"	"disease"		"Finding"	"0.30"		"2009"	"2009"	"2"	"3"	"UNIPROT"
"1181"	"CLCN2"	"0.663"	"0.379"	"C2750894"	"EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8"	"phenotype"		"Finding"	"0.30"		"2009"	"2009"	"2"	"3"	"UNIPROT"
"1181"	"CLCN2"	"0.663"	"0.379"	"C2750895"	"EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.30"		"2009"	"2009"	"2"	"3"	"UNIPROT"
"1181"	"CLCN2"	"0.663"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"1181"	"CLCN2"	"0.663"	"0.379"	"C3810242"	"LEUKOENCEPHALOPATHY WITH ATAXIA"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2015"	"1"	"18"	"CTD_human;ORPHANET;UNIPROT"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1182"	"CLCN3"	"0.667"	"0.483"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1183"	"CLCN4"	"0.713"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1183"	"CLCN4"	"0.713"	"0.414"	"C0796221"	"MENTAL RETARDATION, X-LINKED 15"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"1183"	"CLCN4"	"0.713"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2018"	"3"	"0"	"CLINGEN;ORPHANET"
"1183"	"CLCN4"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1999"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1183"	"CLCN4"	"0.713"	"0.414"	"C3887959"	"MENTAL RETARDATION, X-LINKED 49"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0018021"	"Goiter"	"phenotype"	"C19"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0403720"	"X-linked recessive nephrolithiasis with renal failure"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.62"	"0.5"	"1996"	"2001"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0733682"	"Hypophosphatemic Rickets, X-Linked Dominant"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C0878681"	"Dent's disease"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"	"0.870967741935484"	"1995"	"2017"	"3"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C1839874"	"Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"1996"	"2009"	"3"	"3"	"CTD_human;UNIPROT"
"1184"	"CLCN5"	"0.63"	"0.483"	"C1845168"	"Hypophosphatemic Rickets, X-Linked Recessive"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2011"	"2"	"1"	"CTD_human;UNIPROT"
"1184"	"CLCN5"	"0.63"	"0.483"	"C1848336"	"Dent disease 1"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.94"	"1"	"1993"	"2016"	"14"	"23"	"CTD_human;ORPHANET;UNIPROT"
"1184"	"CLCN5"	"0.63"	"0.483"	"C3536983"	"Familial Hypophosphatemic Rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2018"	"0"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C3536984"	"Vitamin D-Resistant Rickets, X-Linked"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C3540852"	"Rickets, X-Linked Hypophosphatemic"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1184"	"CLCN5"	"0.63"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1978"	"1978"	"1"	"0"	"GENOMICS_ENGLAND"
"1186"	"CLCN7"	"0.642"	"0.517"	"C0029454"	"Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.972222222222222"	"2001"	"2016"	"0"	"0"	"CTD_human"
"1186"	"CLCN7"	"0.642"	"0.517"	"C0432261"	"Osteopetrosis - intermediate type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1186"	"CLCN7"	"0.642"	"0.517"	"C1318518"	"Infantile malignant osteopetrosis"	"disease"		"Congenital Abnormality"	"0.35"	"1"	"2001"	"2016"	"0"	"0"	"ORPHANET"
"1186"	"CLCN7"	"0.642"	"0.517"	"C1850126"	"Osteopetrosis, mild autosomal recessive form"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"UNIPROT"
"1186"	"CLCN7"	"0.642"	"0.517"	"C1969093"	"Osteopetrosis, Autosomal Recessive 6"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1186"	"CLCN7"	"0.642"	"0.517"	"C1969106"	"Osteopetrosis, Autosomal Recessive 4"	"disease"	"C05"	"Disease or Syndrome"	"0.80"		"1993"	"2016"	"6"	"14"	"CTD_human;UNIPROT"
"1186"	"CLCN7"	"0.642"	"0.517"	"C3179239"	"Osteopetrosis Autosomal Dominant Type 2"	"disease"	"C05"	"Disease or Syndrome"	"0.90"		"2002"	"2016"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1186"	"CLCN7"	"0.642"	"0.517"	"C3645711"	"Congenital Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1186"	"CLCN7"	"0.642"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1187"	"CLCNKA"	"0.713"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"1187"	"CLCNKA"	"0.713"	"0.379"	"C2751312"	"BARTTER SYNDROME, TYPE 4B"	"disease"	"C09;C10;C12;C13;C19;C23"	"Disease or Syndrome"	"0.40"		"2004"	"2008"	"0"	"2"	"CTD_human"
"1187"	"CLCNKA"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1187"	"CLCNKA"	"0.713"	"0.379"	"C4310805"	"BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"1"	"UNIPROT"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C0004775"	"Bartter Disease"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.961538461538462"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C0268450"	"Gitelman Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.36"	"1"	"1999"	"2015"	"0"	"0"	"ORPHANET"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C1846343"	"Bartter syndrome, type 3"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.80"	"1"	"1997"	"2018"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C1846344"	"Bartter Syndrome, Type 3, with Hypocalciuria"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"		"1997"	"2004"	"1"	"6"	"UNIPROT"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C2751312"	"BARTTER SYNDROME, TYPE 4B"	"disease"	"C09;C10;C12;C13;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1188"	"CLCNKB"	"0.672"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2004"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"1191"	"CLU"	"0.456"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.963414634146341"	"1991"	"2018"	"3"	"5"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"1999"	"2018"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2010"	"2017"	"6"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.35"	"0.8"	"2004"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"2"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"1191"	"CLU"	"0.456"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2015"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"6"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2017"	"6"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1191"	"CLU"	"0.456"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1192"	"CLIC1"	"0.681"	"0.31"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1193"	"CLIC2"	"0.735"	"0.207"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1193"	"CLIC2"	"0.735"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1193"	"CLIC2"	"0.735"	"0.207"	"C3550913"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC 32"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1193"	"CLIC2"	"0.735"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1200"	"TPP1"	"0.611"	"0.586"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1200"	"TPP1"	"0.611"	"0.586"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0022340"	"Late-Infantile Neuronal Ceroid Lipfuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"16"	"25"	"CTD_human;UNIPROT"
"1200"	"TPP1"	"0.611"	"0.586"	"C0022797"	"Adult Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1999"	"2008"	"2"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0027877"	"Neuronal Ceroid-Lipofuscinoses"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.9375"	"1991"	"2017"	"2"	"12"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1200"	"TPP1"	"0.611"	"0.586"	"C0268281"	"Infantile neuronal ceroid lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1200"	"TPP1"	"0.611"	"0.586"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C0751383"	"Juvenile Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"1999"	"2014"	"2"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C1834207"	"Ceroid Lipofuscinosis, Neuronal, Parry Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"1200"	"TPP1"	"0.611"	"0.586"	"C1836474"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"2015"	"1"	"3"	"ORPHANET;UNIPROT"
"1200"	"TPP1"	"0.611"	"0.586"	"C1876161"	"CEROID LIPOFUSCINOSIS, NEURONAL, 2"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.98"	"1"	"1993"	"2016"	"14"	"45"	"CTD_human;ORPHANET;UNIPROT"
"1200"	"TPP1"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1201"	"CLN3"	"0.614"	"0.586"	"C0022340"	"Late-Infantile Neuronal Ceroid Lipfuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2016"	"0"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0022797"	"Adult Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1999"	"2016"	"0"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0027877"	"Neuronal Ceroid-Lipofuscinoses"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.951219512195122"	"1993"	"2017"	"0"	"3"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1201"	"CLN3"	"0.614"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0268281"	"Infantile neuronal ceroid lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1201"	"CLN3"	"0.614"	"0.586"	"C0751383"	"Juvenile Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.990909090909091"	"1991"	"2016"	"4"	"62"	"CTD_human;ORPHANET;UNIPROT"
"1201"	"CLN3"	"0.614"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C1834207"	"Ceroid Lipofuscinosis, Neuronal, Parry Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1201"	"CLN3"	"0.614"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1203"	"CLN5"	"0.72"	"0.241"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1203"	"CLN5"	"0.72"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1203"	"CLN5"	"0.72"	"0.241"	"C1850442"	"CEROID LIPOFUSCINOSIS, NEURONAL, 5"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.91"	"1"	"1993"	"2016"	"10"	"42"	"CTD_human;ORPHANET;UNIPROT"
"1203"	"CLN5"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1207"	"CLNS1A"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1209"	"CLPTM1"	"0.773"	"0.207"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1209"	"CLPTM1"	"0.773"	"0.207"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1212"	"CLTB"	"0.928"	"0.103"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1212"	"CLTB"	"0.928"	"0.103"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1213"	"CLTC"	"0.659"	"0.483"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1213"	"CLTC"	"0.659"	"0.483"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2008"	"0"	"0"	"ORPHANET"
"1213"	"CLTC"	"0.659"	"0.483"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1215"	"CMA1"	"0.575"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1215"	"CMA1"	"0.575"	"0.517"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"1215"	"CMA1"	"0.575"	"0.517"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1215"	"CMA1"	"0.575"	"0.517"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"1230"	"CCR1"	"0.558"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"1230"	"CCR1"	"0.558"	"0.724"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1232"	"CCR3"	"0.57"	"0.759"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1233"	"CCR4"	"0.573"	"0.655"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.9375"	"2002"	"2013"	"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"PSYGENET"
"1234"	"CCR5"	"0.431"	"0.897"	"C0043124"	"West Nile Fever"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.34"	"0.75"	"2006"	"2016"	"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0751583"	"Encephalitis, West Nile Fever"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0751584"	"West Nile Fever Meningitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0751585"	"West Nile Fever Meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C0751586"	"West Nile Fever Myelitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C2675864"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 22 (disorder)"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1234"	"CCR5"	"0.431"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1235"	"CCR6"	"0.522"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2016"	"3"	"8"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1235"	"CCR6"	"0.522"	"0.724"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1235"	"CCR6"	"0.522"	"0.724"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1235"	"CCR6"	"0.522"	"0.724"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C1258104"	"Diffuse Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1235"	"CCR6"	"0.522"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1235"	"CCR6"	"0.522"	"0.724"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1236"	"CCR7"	"0.477"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1236"	"CCR7"	"0.477"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1237"	"CCR8"	"0.659"	"0.414"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1240"	"CMKLR1"	"0.696"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1240"	"CMKLR1"	"0.696"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1241"	"LTB4R"	"0.624"	"0.552"	"C0002792"	"anaphylaxis"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1241"	"LTB4R"	"0.624"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2000"	"2005"	"1"	"0"	"CTD_human"
"1241"	"LTB4R"	"0.624"	"0.552"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1241"	"LTB4R"	"0.624"	"0.552"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.78"	"0.875"	"2000"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2009"	"2012"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2014"	"3"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0020433"	"Hyperbilirubinemia"	"disease"	"C23"	"Disease or Syndrome"	"0.57"	"0.857142857142857"	"1996"	"2018"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0022350"	"Jaundice, Chronic Idiopathic"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1996"	"2016"	"9"	"19"	"CTD_human;ORPHANET;UNIPROT"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2014"	"3"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"1244"	"ABCC2"	"0.495"	"0.69"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1244"	"ABCC2"	"0.495"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1258"	"CNGB1"	"0.663"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.63"	"0.666666666666667"	"2001"	"2017"	"1"	"8"	"CTD_human;ORPHANET"
"1258"	"CNGB1"	"0.663"	"0.517"	"C3151066"	"RETINITIS PIGMENTOSA 45"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"4"	"CTD_human;UNIPROT"
"1259"	"CNGA1"	"0.701"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.64"	"1"	"1995"	"2017"	"1"	"6"	"CTD_human;ORPHANET"
"1259"	"CNGA1"	"0.701"	"0.31"	"C3151059"	"RETINITIS PIGMENTOSA 49"	"disease"		"Disease or Syndrome"	"0.60"		"1995"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"1260"	"CNGA2"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"1260"	"CNGA2"	"0.928"	"0.138"	"C0393778"	"Congenital anosmia"	"disease"	"C10;C23"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"1261"	"CNGA3"	"0.676"	"0.138"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"1261"	"CNGA3"	"0.676"	"0.138"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.50"	"0.967741935483871"	"2000"	"2017"	"0"	"9"	"ORPHANET"
"1261"	"CNGA3"	"0.676"	"0.138"	"C1857618"	"Achromatopsia 2"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.82"	"1"	"1998"	"2017"	"8"	"35"	"CTD_human;UNIPROT"
"1265"	"CNN2"	"0.727"	"0.207"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1265"	"CNN2"	"0.727"	"0.207"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1265"	"CNN2"	"0.727"	"0.207"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1265"	"CNN2"	"0.727"	"0.207"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1265"	"CNN2"	"0.727"	"0.207"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1265"	"CNN2"	"0.727"	"0.207"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1266"	"CNN3"	"0.799"	"0.207"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1267"	"CNP"	"0.652"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1267"	"CNP"	"0.652"	"0.483"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1267"	"CNP"	"0.652"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"1267"	"CNP"	"0.652"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1267"	"CNP"	"0.652"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1999"	"2013"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2001"	"2012"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.35"	"0.8"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0026838"	"Muscle Spasticity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2001"	"2014"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.972972972972973"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.35"	"0.8"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.966666666666667"	"2001"	"2018"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2013"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2016"	"4"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2012"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0277820"	"Clasp-Knife Spasticity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0443306"	"Spastic"	"disease"	"C05;C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0596170"	"Binge eating disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2006"	"2013"	"4"	"0"	"CTD_human;PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1999"	"2013"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2016"	"4"	"0"	"PSYGENET"
"1268"	"CNR1"	"0.47"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1997"	"2012"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"1999"	"2011"	"3"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1268"	"CNR1"	"0.47"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2014"	"5"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2007"	"2014"	"5"	"0"	"CTD_human;PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0021053"	"Immune System Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"		"2003"	"2004"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2010"	"2015"	"4"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1269"	"CNR2"	"0.554"	"0.621"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2010"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"1269"	"CNR2"	"0.554"	"0.621"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1270"	"CNTF"	"0.621"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2012"	"4"	"0"	"PSYGENET"
"1270"	"CNTF"	"0.621"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2012"	"4"	"0"	"PSYGENET"
"1270"	"CNTF"	"0.621"	"0.414"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1270"	"CNTF"	"0.621"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.25"	"1997"	"2008"	"4"	"0"	"PSYGENET"
"1270"	"CNTF"	"0.621"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1270"	"CNTF"	"0.621"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"0"	"2002"	"2002"	"1"	"0"	"CTD_human"
"1270"	"CNTF"	"0.621"	"0.414"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1272"	"CNTN1"	"0.667"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1272"	"CNTN1"	"0.667"	"0.31"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"1272"	"CNTN1"	"0.667"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1272"	"CNTN1"	"0.667"	"0.31"	"C2675527"	"Myopathy, Congenital, Compton-North"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"		"2009"	"2011"	"0"	"1"	"CTD_human;ORPHANET"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0002949"	"Aneurysm, Dissecting"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.59"	"1"	"1989"	"2017"	"10"	"0"	"GENOMICS_ENGLAND"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0020497"	"Cortical Congenital Hyperostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.31"	"1"	"1993"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"4"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2016"	"3"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0023931"	"Lobstein Disease"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"1.00"	"0.962962962962963"	"1989"	"2018"	"13"	"102"	"CTD_human;ORPHANET;UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.90"	"0.975206611570248"	"1975"	"2018"	"1"	"26"	"CTD_human;GENOMICS_ENGLAND"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2014"	"0"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"4"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268335"	"Ehlers-Danlos syndrome type 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"0"	"2"	"CTD_human;ORPHANET"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268336"	"Ehlers-Danlos syndrome type 2"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268345"	"EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"1984"	"1991"	"0"	"2"	"CTD_human;ORPHANET"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268358"	"Osteogenesis imperfecta, dominant perinatal lethal"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.88"	"1"	"1986"	"2016"	"37"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.96"	"1"	"1989"	"2016"	"15"	"16"	"CTD_human;ORPHANET;UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.96"	"1"	"1989"	"2016"	"11"	"15"	"CTD_human;ORPHANET;UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0340643"	"Dissection of aorta"	"disease"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2004"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0392784"	"Dermatofibrosarcoma Protuberans"	"disease"		"Neoplastic Process"	"0.40"	"0.959183673469388"	"1997"	"2018"	"0"	"0"	"ORPHANET"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C1619692"	"Nephrogenic Fibrosing Dermopathy"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C4225429"	"Ehlers-Danlos syndrome classic type"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2007"	"2"	"0"	"UNIPROT"
"1277"	"COL1A1"	"0.472"	"0.724"	"C4277533"	"Dissection, Blood Vessel"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1277"	"COL1A1"	"0.472"	"0.724"	"C4303786"	"Ehlers-Danlos syndrome vascular-like type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"1987"	"2017"	"12"	"0"	"GENOMICS_ENGLAND"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2005"	"2016"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0023931"	"Lobstein Disease"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.89"	"1"	"1982"	"2018"	"5"	"35"	"ORPHANET;UNIPROT"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2007"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.70"	"0.973451327433628"	"1981"	"2018"	"0"	"9"	"GENOMICS_ENGLAND"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.35"	"1"	"1986"	"2016"	"0"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.888888888888889"	"1987"	"2014"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1987"	"2016"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0268345"	"EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.39"	"1"	"1988"	"2000"	"0"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0268358"	"Osteogenesis imperfecta, dominant perinatal lethal"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.68"	"0.875"	"1985"	"2009"	"15"	"27"	"CTD_human;ORPHANET;UNIPROT"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.95"	"1"	"1984"	"2016"	"15"	"33"	"CTD_human;ORPHANET;UNIPROT"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.80"	"1"	"1986"	"2016"	"10"	"28"	"CTD_human;ORPHANET;UNIPROT"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1278"	"COL1A2"	"0.526"	"0.724"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1278"	"COL1A2"	"0.526"	"0.724"	"C1851801"	"EDS VIIB"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"		"1980"	"1994"	"0"	"3"	"ORPHANET"
"1278"	"COL1A2"	"0.526"	"0.724"	"C1857034"	"Ehlers-Danlos syndrome, cardiac valvular form"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.60"		"1988"	"2006"	"1"	"4"	"CTD_human;ORPHANET"
"1278"	"COL1A2"	"0.526"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0003864"	"Arthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2016"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"7"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"		"2005"	"2017"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0008479"	"Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.34"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"2015"	"2017"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"1985"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0015814"	"Femur Head Necrosis"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.42"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0023234"	"Legg-Calve-Perthes Disease"	"disease"	"C05"	"Disease or Syndrome"	"0.75"	"1"	"2005"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"		"1993"	"2015"	"2"	"1"	"CTD_human;GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2015"	"1"	"1"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.894736842105263"	"1993"	"2016"	"2"	"1"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.43"	"1"	"1993"	"2018"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.45"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"	"1"	"1989"	"2016"	"1"	"11"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0039103"	"Synovitis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"		"2005"	"2015"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0041834"	"Erythema"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.61"	"1"	"1993"	"1993"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0162323"	"Polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0220685"	"Achondrogenesis type 2"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.96"	"1"	"1989"	"2014"	"9"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0265279"	"Kniest dysplasia"	"disease"	"C05;C07;C08;C16;C17;C19"	"Congenital Abnormality"	"0.80"	"1"	"1952"	"2016"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2004"	"2"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0410480"	"Avascular Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Disease or Syndrome"	"0.70"		"2005"	"2011"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0410574"	"Synovial Hypertrophy"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0432214"	"Namaqualand hip dysplasia"	"disease"		"Congenital Abnormality"	"0.50"		"1990"	"1995"	"4"	"1"	"ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0432221"	"Spondylometaphyseal dysplasia, 'corner fracture' type"	"disease"	"C05;C16;C23;C26"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0524595"	"Aseptic Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0542428"	"Hypochondrogenesis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.87"	"1"	"1989"	"2008"	"8"	"6"	"ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0700635"	"Strudwick syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"1993"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0796173"	"Spondyloperipheral dysplasia short ulna"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.65"	"1"	"1996"	"2013"	"0"	"5"	"CTD_human;ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"7"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"7"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1835437"	"Platyspondylic Lethal Skeletal Dysplasia, Torrance Type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"2000"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1836080"	"Stickler Syndrome, Type I, Nonsyndromic Ocular"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1978"	"2008"	"5"	"7"	"CTD_human;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1836081"	"RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2008"	"5"	"5"	"ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1836683"	"Czech dysplasia, metatarsal type"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.73"	"1"	"1994"	"2016"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.32"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1840452"	"Hyaloideoretinal degeneration of Wagner"	"disease"	"C11"	"Disease or Syndrome"	"0.36"	"1"	"1993"	"2003"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1848488"	"Pierre Robin syndrome with fetal chondrodysplasia"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1851536"	"Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness"	"disease"	"C05;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.70"		"1999"	"1999"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1855310"	"Megaepiphyseal dwarfism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1858079"	"Osteoarthritis with Mild Chondrodysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1990"	"1998"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C1866688"	"Spondylometaphyseal dysplasia, Algerian type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.80"	"0.942307692307692"	"1988"	"2017"	"4"	"37"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C2745959"	"Spondyloepiphyseal dysplasia, congenita"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.90"	"0.972972972972973"	"1989"	"2016"	"8"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1993"	"1994"	"1"	"0"	"CTD_human"
"1280"	"COL2A1"	"0.474"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1280"	"COL2A1"	"0.474"	"0.724"	"C4225273"	"SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"1991"	"2016"	"5"	"2"	"CLINGEN;ORPHANET;UNIPROT"
"1280"	"COL2A1"	"0.474"	"0.724"	"C4302548"	"Dysspondyloenchondromatosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C4479260"	"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1280"	"COL2A1"	"0.474"	"0.724"	"C4520892"	"Otospondylomegaepiphyseal dysplasia"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1986"	"2018"	"9"	"1"	"CTD_human;GENOMICS_ENGLAND"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1989"	"2009"	"5"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2002"	"2015"	"2"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"1987"	"2016"	"10"	"0"	"CLINGEN"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0238590"	"Acrogeria"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"1996"	"2004"	"0"	"0"	"ORPHANET"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1989"	"2006"	"5"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0268337"	"Ehlers-Danlos syndrome, type 3 (disorder)"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.60"		"1995"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0268338"	"Ehlers-Danlos Syndrome, Type IV"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1957"	"2017"	"27"	"354"	"CTD_human;ORPHANET;UNIPROT"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0406584"	"Acrogeria, gottron type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"2"	"UNIPROT"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1853365"	"AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C1862932"	"ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1281"	"COL3A1"	"0.51"	"0.759"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1281"	"COL3A1"	"0.51"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0266484"	"Schizencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.42"	"1"	"2013"	"2016"	"1"	"1"	"UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0302892"	"Congenital porencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.60"	"1"	"2005"	"2016"	"0"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2008"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1843512"	"BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.92"	"1"	"1981"	"2017"	"8"	"12"	"CTD_human;ORPHANET;UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1862876"	"STROKE, HEMORRHAGIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1867327"	"RETINAL ARTERIES, TORTUOSITY OF"	"phenotype"		"Finding"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C1867983"	"PORENCEPHALY, FAMILIAL"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.84"	"1"	"2005"	"2014"	"3"	"0"	"CTD_human;ORPHANET;UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C2673195"	"Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps"	"disease"	"C05;C10;C14;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2015"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C2675650"	"Brain Small Vessel Disease With Axenfeld-Rieger Anomaly"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.70"		"2005"	"2015"	"8"	"0"	"CTD_human;UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C2930808"	"Familial vascular leukoencephalopathy"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1282"	"COL4A1"	"0.512"	"0.69"	"C2931870"	"Familial schizencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1282"	"COL4A1"	"0.512"	"0.69"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C3281105"	"HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C3698507"	"Post-traumatic Porencephaly"	"phenotype"	"C05;C10;C16"	"Acquired Abnormality"	"0.50"		"2005"	"2006"	"0"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C4013035"	"BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES"	"disease"		"Disease or Syndrome"	"0.50"		"2005"	"2015"	"8"	"0"	"UNIPROT"
"1282"	"COL4A1"	"0.512"	"0.69"	"C4082173"	"Porencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"0"	"0"	"CTD_human"
"1282"	"COL4A1"	"0.512"	"0.69"	"C4082301"	"Developmental Porencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0302892"	"Congenital porencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.35"	"1"	"2012"	"2016"	"0"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1284"	"COL4A2"	"0.642"	"0.448"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1284"	"COL4A2"	"0.642"	"0.448"	"C1867983"	"PORENCEPHALY, FAMILIAL"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"1284"	"COL4A2"	"0.642"	"0.448"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C3280970"	"PORENCEPHALY 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"1284"	"COL4A2"	"0.642"	"0.448"	"C3698507"	"Post-traumatic Porencephaly"	"phenotype"	"C05;C10;C16"	"Acquired Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1284"	"COL4A2"	"0.642"	"0.448"	"C4082173"	"Porencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2012"	"2016"	"0"	"0"	"CTD_human"
"1284"	"COL4A2"	"0.642"	"0.448"	"C4082301"	"Developmental Porencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"1285"	"COL4A3"	"0.572"	"0.586"	"C0027706"	"Hereditary nephritis"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.38"	"1"	"1989"	"2008"	"1"	"0"	"CTD_human"
"1285"	"COL4A3"	"0.572"	"0.586"	"C0241908"	"Hematuria, Benign Familial"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.69"	"0.888888888888889"	"1996"	"2018"	"1"	"5"	"CTD_human;UNIPROT"
"1285"	"COL4A3"	"0.572"	"0.586"	"C0403440"	"Thin basement membrane disease"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.60"	"1"	"2001"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"1285"	"COL4A3"	"0.572"	"0.586"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"1285"	"COL4A3"	"0.572"	"0.586"	"C1567741"	"Alport Syndrome"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.50"	"0.96969696969697"	"1986"	"2018"	"1"	"1"	"CTD_human"
"1285"	"COL4A3"	"0.572"	"0.586"	"C1567742"	"Alport Syndrome, X-Linked"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.39"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"1285"	"COL4A3"	"0.572"	"0.586"	"C1567743"	"Alport Syndrome, Autosomal Dominant"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.72"	"1"	"1997"	"2015"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1285"	"COL4A3"	"0.572"	"0.586"	"C1567744"	"Alport Syndrome, Autosomal Recessive"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2015"	"3"	"17"	"CTD_human;ORPHANET;UNIPROT"
"1285"	"COL4A3"	"0.572"	"0.586"	"C2931253"	"Alport syndrome, dominant type"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1285"	"COL4A3"	"0.572"	"0.586"	"C2931254"	"Alport syndrome, recessive type"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1285"	"COL4A3"	"0.572"	"0.586"	"C2931861"	"Hemorrhagic hereditary nephritis"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1285"	"COL4A3"	"0.572"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1286"	"COL4A4"	"0.667"	"0.379"	"C0241908"	"Hematuria, Benign Familial"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2018"	"3"	"5"	"UNIPROT"
"1286"	"COL4A4"	"0.667"	"0.379"	"C0403440"	"Thin basement membrane disease"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2017"	"3"	"3"	"UNIPROT"
"1286"	"COL4A4"	"0.667"	"0.379"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2002"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"1286"	"COL4A4"	"0.667"	"0.379"	"C1567743"	"Alport Syndrome, Autosomal Dominant"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2018"	"0"	"0"	"ORPHANET"
"1286"	"COL4A4"	"0.667"	"0.379"	"C1567744"	"Alport Syndrome, Autosomal Recessive"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.90"	"0.928571428571429"	"1995"	"2018"	"2"	"8"	"ORPHANET;UNIPROT"
"1286"	"COL4A4"	"0.667"	"0.379"	"C2931253"	"Alport syndrome, dominant type"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1286"	"COL4A4"	"0.667"	"0.379"	"C2931254"	"Alport syndrome, recessive type"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1286"	"COL4A4"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1287"	"COL4A5"	"0.584"	"0.621"	"C0086533"	"Leiomyoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1287"	"COL4A5"	"0.584"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1287"	"COL4A5"	"0.584"	"0.621"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"1"	"GENOMICS_ENGLAND"
"1287"	"COL4A5"	"0.584"	"0.621"	"C1567742"	"Alport Syndrome, X-Linked"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"1.00"	"0.953125"	"1991"	"2018"	"22"	"505"	"CTD_human;ORPHANET;UNIPROT"
"1287"	"COL4A5"	"0.584"	"0.621"	"C1839884"	"Leiomyomatosis, esophageal and vulval, with nephropathy"	"disease"	"C04;C12;C13;C16;C17"	"Disease or Syndrome"	"0.32"	"0.5"	"1993"	"2014"	"0"	"0"	"ORPHANET"
"1288"	"COL4A6"	"0.69"	"0.345"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1288"	"COL4A6"	"0.69"	"0.345"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1288"	"COL4A6"	"0.69"	"0.345"	"C0086533"	"Leiomyoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1288"	"COL4A6"	"0.69"	"0.345"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1288"	"COL4A6"	"0.69"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1288"	"COL4A6"	"0.69"	"0.345"	"C1839884"	"Leiomyomatosis, esophageal and vulval, with nephropathy"	"disease"	"C04;C12;C13;C16;C17"	"Disease or Syndrome"	"0.31"	"0"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"1288"	"COL4A6"	"0.69"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1288"	"COL4A6"	"0.69"	"0.345"	"C3806737"	"DEAFNESS, X-LINKED 6"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0268335"	"Ehlers-Danlos syndrome type 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2017"	"3"	"26"	"CTD_human;ORPHANET"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0268336"	"Ehlers-Danlos syndrome type 2"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"1995"	"1998"	"2"	"0"	"CTD_human;ORPHANET"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0268338"	"Ehlers-Danlos Syndrome, Type IV"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2000"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1289"	"COL5A1"	"0.586"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1289"	"COL5A1"	"0.586"	"0.621"	"C4225429"	"Ehlers-Danlos syndrome classic type"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2009"	"5"	"2"	"UNIPROT"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0268335"	"Ehlers-Danlos syndrome type 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.80"		"1998"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0268336"	"Ehlers-Danlos syndrome type 2"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"ORPHANET"
"1290"	"COL5A2"	"0.633"	"0.483"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1290"	"COL5A2"	"0.633"	"0.483"	"C4225429"	"Ehlers-Danlos syndrome classic type"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2016"	"3"	"0"	"UNIPROT"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2005"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0410179"	"Scleroatonic muscular dystrophy"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.70"	"0.944444444444444"	"2003"	"2017"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"1291"	"COL6A1"	"0.645"	"0.621"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1291"	"COL6A1"	"0.645"	"0.621"	"C1834674"	"Bethlem myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1996"	"2014"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1291"	"COL6A1"	"0.645"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2017"	"9"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0410179"	"Scleroatonic muscular dystrophy"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.70"	"1"	"2001"	"2010"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"1292"	"COL6A2"	"0.645"	"0.552"	"C1611706"	"Myosclerosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1292"	"COL6A2"	"0.645"	"0.552"	"C1834674"	"Bethlem myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"1996"	"2014"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1292"	"COL6A2"	"0.645"	"0.552"	"C1850671"	"Myosclerosis, Autosomal Recessive"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2014"	"0"	"2"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1998"	"2017"	"8"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0410179"	"Scleroatonic muscular dystrophy"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.90"	"1"	"2002"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C1834674"	"Bethlem myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1997"	"2014"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"1293"	"COL6A3"	"0.611"	"0.69"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1293"	"COL6A3"	"0.611"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1293"	"COL6A3"	"0.611"	"0.69"	"C4225336"	"DYSTONIA 27"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"6"	"ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2006"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"	"0.916666666666667"	"1992"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0079136"	"Cockayne-Touraine Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"0.916666666666667"	"1989"	"2015"	"16"	"13"	"CTD_human;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0079294"	"Epidermolysis Bullosa Dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2017"	"0"	"3"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0079474"	"Hallopeau-Siemens Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"0.960526315789474"	"1993"	"2018"	"14"	"35"	"CTD_human;ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0268371"	"Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"		"1966"	"1996"	"0"	"2"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0432321"	"Epidermolysis bullosa, pretibial"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.74"	"1"	"1995"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0432322"	"Dominant dystrophic epidermolysis bullosa, albopapular type (disorder)"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.77"	"1"	"1989"	"2015"	"16"	"15"	"CTD_human;ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1275114"	"Epidermolysis Bullosa Pruriginosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"0.9"	"1999"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1843477"	"Epidermolysis Bullosa Simplex Superficialis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1843761"	"TOENAIL DYSTROPHY, ISOLATED"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.60"		"1995"	"2007"	"1"	"4"	"CTD_human;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C1851573"	"Transient bullous dermolysis of the newborn"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2007"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C2673611"	"Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"1993"	"2010"	"14"	"17"	"ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C2673612"	"Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"1993"	"2010"	"14"	"19"	"ORPHANET;UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C2675683"	"Epidermolysis Bullosa Dystrophica With Subcorneal Cleavage"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1989"	"2010"	"16"	"13"	"UNIPROT"
"1294"	"COL7A1"	"0.552"	"0.586"	"C4302547"	"Dystrophic epidermolysis bullosa nails only"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1294"	"COL7A1"	"0.552"	"0.586"	"C4511056"	"Centripetalis recessive dystrophic epidermolysis bullosa"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1294"	"COL7A1"	"0.552"	"0.586"	"C4518087"	"Acral dystrophic epidermolysis bullosa"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1295"	"COL8A1"	"0.727"	"0.448"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1296"	"COL8A2"	"0.69"	"0.414"	"C0016781"	"Fuchs Endothelial Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"1296"	"COL8A2"	"0.69"	"0.414"	"C0339284"	"Polymorphous corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"1296"	"COL8A2"	"0.69"	"0.414"	"C1850959"	"Corneal dystrophy, Fuchs' endothelial, 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"1979"	"2013"	"1"	"8"	"CTD_human;UNIPROT"
"1296"	"COL8A2"	"0.69"	"0.414"	"C1852795"	"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1979"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"1296"	"COL8A2"	"0.69"	"0.414"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2002"	"2012"	"5"	"0"	"GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.70"	"0.909090909090909"	"2000"	"2012"	"8"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.31"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0265253"	"Stickler syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2005"	"2014"	"4"	"0"	"CLINGEN"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1297"	"COL9A1"	"0.596"	"0.517"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2014"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"1297"	"COL9A1"	"0.596"	"0.517"	"C2675767"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 6"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C3279941"	"STICKLER SYNDROME, TYPE IV"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2011"	"0"	"2"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1297"	"COL9A1"	"0.596"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2011"	"5"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"	"0.9"	"1999"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.53"	"1"	"1999"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"1298"	"COL9A2"	"0.607"	"0.517"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1298"	"COL9A2"	"0.607"	"0.517"	"C1838429"	"Epiphyseal dysplasia, multiple, 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1298"	"COL9A2"	"0.607"	"0.517"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2014"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"1298"	"COL9A2"	"0.607"	"0.517"	"C2675551"	"LUMBAR DISC DEGENERATION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"1298"	"COL9A2"	"0.607"	"0.517"	"C2676840"	"LUMBAR DISC HERNIATION, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"1298"	"COL9A2"	"0.607"	"0.517"	"C3280342"	"STICKLER SYNDROME, TYPE V"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2011"	"0"	"1"	"CTD_human"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"	"0.8"	"1993"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2015"	"0"	"0"	"CTD_human"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2000"	"2000"	"2"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1299"	"COL9A3"	"0.616"	"0.586"	"C1832998"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"1299"	"COL9A3"	"0.616"	"0.586"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"1299"	"COL9A3"	"0.616"	"0.586"	"C3152083"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 3, WITH MYOPATHY"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2015"	"1"	"1"	"UNIPROT"
"1300"	"COL10A1"	"0.676"	"0.379"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1300"	"COL10A1"	"0.676"	"0.379"	"C0265289"	"Metaphyseal chondrodysplasia Schmid type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.94"	"0.75"	"1994"	"2015"	"9"	"14"	"CTD_human;ORPHANET;UNIPROT"
"1300"	"COL10A1"	"0.676"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2014"	"5"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2016"	"2"	"1"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0021818"	"Intervertebral Disk Displacement"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0265235"	"Marshall syndrome"	"disease"	"C05;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"1958"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0265282"	"Fibrochondrogenesis"	"disease"	"C05;C16;C19;C23"	"Congenital Abnormality"	"0.63"	"1"	"2011"	"2014"	"0"	"3"	"CTD_human;ORPHANET"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C1858084"	"STICKLER SYNDROME, TYPE II (disorder)"	"disease"	"C11;C17"	"Disease or Syndrome"	"0.95"	"1"	"1971"	"2015"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1301"	"COL11A1"	"0.524"	"0.586"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.56"	"1"	"1971"	"2014"	"0"	"0"	"ORPHANET"
"1301"	"COL11A1"	"0.524"	"0.586"	"C3278138"	"FIBROCHONDROGENESIS 1"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"UNIPROT"
"1301"	"COL11A1"	"0.524"	"0.586"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1301"	"COL11A1"	"0.524"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2015"	"10"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2015"	"1"	"1"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1995"	"2005"	"3"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0265253"	"Stickler syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"1995"	"2015"	"14"	"0"	"CLINGEN"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0265282"	"Fibrochondrogenesis"	"disease"	"C05;C16;C19;C23"	"Congenital Abnormality"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.50"		"1999"	"2001"	"1"	"0"	"CLINGEN"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2015"	"3"	"0"	"CLINGEN"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1848488"	"Pierre Robin syndrome with fetal chondrodysplasia"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.82"	"1"	"1995"	"2005"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CLINGEN"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1855310"	"Megaepiphyseal dwarfism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1861481"	"Stickler syndrome, type 3"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"		"1964"	"2005"	"0"	"5"	"ORPHANET"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1864746"	"Deafness, Autosomal Recessive 53"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.61"	"1"	"2006"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"1302"	"COL11A2"	"0.478"	"0.69"	"C1866095"	"Deafness, Autosomal Dominant 13"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.81"	"1"	"1999"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"1302"	"COL11A2"	"0.478"	"0.69"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.55"	"1"	"1995"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1302"	"COL11A2"	"0.478"	"0.69"	"C4520892"	"Otospondylomegaepiphyseal dysplasia"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.80"		"1995"	"2006"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0410179"	"Scleroatonic muscular dystrophy"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1303"	"COL12A1"	"0.676"	"0.517"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"1303"	"COL12A1"	"0.676"	"0.517"	"C1834674"	"Bethlem myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1303"	"COL12A1"	"0.676"	"0.517"	"C4225313"	"BETHLEM MYOPATHY 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"2"	"3"	"UNIPROT"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1305"	"COL13A1"	"0.685"	"0.414"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1306"	"COL15A1"	"0.72"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1306"	"COL15A1"	"0.72"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1308"	"COL17A1"	"0.59"	"0.552"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"1996"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"1308"	"COL17A1"	"0.59"	"0.552"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"	"0.75"	"1995"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"1308"	"COL17A1"	"0.59"	"0.552"	"C0079297"	"Epidermolysis Bullosa Progressiva"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2002"	"5"	"2"	"UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C0079301"	"Junctional Epidermolysis Bullosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"	"0.939393939393939"	"1995"	"2016"	"5"	"3"	"UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C0268374"	"Adult junctional epidermolysis bullosa (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1996"	"2014"	"6"	"9"	"CTD_human;UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C1852551"	"Epithelial Recurrent Erosion Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.72"	"1"	"1989"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C2608084"	"EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1996"	"2014"	"6"	"3"	"CTD_human;UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C2673609"	"Epidermolysis bullosa inversa dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2002"	"5"	"2"	"UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C2673610"	"JEB-I"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2002"	"5"	"2"	"UNIPROT"
"1308"	"COL17A1"	"0.59"	"0.552"	"C4304724"	"Late-onset junctional epidermolysis bullosa"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1310"	"COL19A1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"1311"	"COMP"	"0.577"	"0.586"	"C0022410"	"Joint Instability"	"phenotype"	"C05"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1311"	"COMP"	"0.577"	"0.586"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"	"0.939393939393939"	"1995"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1311"	"COMP"	"0.577"	"0.586"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.944444444444444"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1311"	"COMP"	"0.577"	"0.586"	"C0029410"	"Osteoarthritis of hip"	"disease"	"C05"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1311"	"COMP"	"0.577"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1311"	"COMP"	"0.577"	"0.586"	"C0086437"	"Joint laxity"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1311"	"COMP"	"0.577"	"0.586"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1311"	"COMP"	"0.577"	"0.586"	"C0410538"	"Pseudoachondroplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"1"	"1993"	"2018"	"13"	"14"	"CTD_human;ORPHANET;UNIPROT"
"1311"	"COMP"	"0.577"	"0.586"	"C1838280"	"Epiphyseal dysplasia, multiple, 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2012"	"10"	"13"	"CTD_human;ORPHANET;UNIPROT"
"1311"	"COMP"	"0.577"	"0.586"	"C1851537"	"Fairbank disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"9"	"7"	"UNIPROT"
"1311"	"COMP"	"0.577"	"0.586"	"C1851538"	"Epiphyseal Dysplasia, Ribbing Type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"9"	"7"	"UNIPROT"
"1311"	"COMP"	"0.577"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1312"	"COMT"	"0.426"	"0.897"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2007"	"2011"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.956521739130435"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1997"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"0.5"	"2002"	"2006"	"3"	"0"	"CTD_human;PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.983050847457627"	"1998"	"2017"	"3"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1983"	"2018"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1983"	"2018"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.60"	"0.866666666666667"	"1997"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2016"	"3"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0026858"	"Musculoskeletal Pain"	"phenotype"	"C05;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.927710843373494"	"2003"	"2017"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0030319"	"Panic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"0"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.923076923076923"	"1984"	"2018"	"4"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0039494"	"Temporomandibular Joint Disorders"	"group"	"C05;C07"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2016"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1983"	"1983"	"1"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0086769"	"Panic Attacks"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.60"	"0.85"	"1997"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"2"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1982"	"2015"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0525046"	"Schizophrenia Spectrum and Other Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2009"	"2011"	"3"	"0"	"CTD_human;PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.983050847457627"	"1998"	"2017"	"3"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"1997"	"1997"	"1"	"0"	"CTD_human;ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"2005"	"3"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.918367346938776"	"1996"	"2018"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2018"	"5"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C1306067"	"Drug-induced paranoid state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"		"1998"	"2008"	"3"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1991"	"2004"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C2750088"	"HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2011"	"0"	"0"	"ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1312"	"COMT"	"0.426"	"0.897"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2018"	"2"	"0"	"PSYGENET"
"1312"	"COMT"	"0.426"	"0.897"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1312"	"COMT"	"0.426"	"0.897"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C0003864"	"Arthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C0162323"	"Polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C0206061"	"Pneumonia, Interstitial"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C0206062"	"Lung Diseases, Interstitial"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1314"	"COPA"	"0.785"	"0.241"	"C4225334"	"AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2015"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1316"	"KLF6"	"0.534"	"0.69"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2010"	"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1316"	"KLF6"	"0.534"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.54"	"1"	"2005"	"2012"	"0"	"0"	"CGI;CTD_human"
"1316"	"KLF6"	"0.534"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2013"	"0"	"0"	"CTD_human"
"1316"	"KLF6"	"0.534"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.61"		"2005"	"2005"	"0"	"1"	"CGI;CTD_human"
"1316"	"KLF6"	"0.534"	"0.69"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.9"	"2002"	"2013"	"0"	"0"	"CTD_human"
"1316"	"KLF6"	"0.534"	"0.69"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.46"	"0.833333333333333"	"2005"	"2012"	"0"	"0"	"CGI"
"1316"	"KLF6"	"0.534"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1317"	"SLC31A1"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1326"	"MAP3K8"	"0.555"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1326"	"MAP3K8"	"0.555"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2013"	"0"	"0"	"CTD_human"
"1326"	"MAP3K8"	"0.555"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1326"	"MAP3K8"	"0.555"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"0"	"0"	"CTD_human"
"1327"	"COX4I1"	"0.735"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1329"	"COX5B"	"0.886"	"0.172"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1329"	"COX5B"	"0.886"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1337"	"COX6A1"	"0.762"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1337"	"COX6A1"	"0.762"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1337"	"COX6A1"	"0.762"	"0.138"	"C4015029"	"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D"	"disease"		"Disease or Syndrome"	"0.80"		"2014"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"1340"	"COX6B1"	"0.713"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.70"		"2008"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1340"	"COX6B1"	"0.713"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1340"	"COX6B1"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1345"	"COX6C"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1346"	"COX7A1"	"0.886"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1347"	"COX7A2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1349"	"COX7B"	"0.707"	"0.345"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1349"	"COX7B"	"0.707"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1349"	"COX7B"	"0.707"	"0.345"	"C0796070"	"MICROPHTHALMIA, SYNDROMIC 7"	"disease"	"C11;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"1349"	"COX7B"	"0.707"	"0.345"	"C3550921"	"LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2013"	"0"	"3"	"CTD_human"
"1349"	"COX7B"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1350"	"COX7C"	"1"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1350"	"COX7C"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1351"	"COX8A"	"0.461"	"0.793"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"1351"	"COX8A"	"0.461"	"0.793"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.44"	"1"	"1998"	"2016"	"0"	"1"	"ORPHANET"
"1351"	"COX8A"	"0.461"	"0.793"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1352"	"COX10"	"0.624"	"0.552"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"1352"	"COX10"	"0.624"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2000"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"1352"	"COX10"	"0.624"	"0.552"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.94"	"1"	"2000"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1352"	"COX10"	"0.624"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1352"	"COX10"	"0.624"	"0.552"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1352"	"COX10"	"0.624"	"0.552"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1352"	"COX10"	"0.624"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1352"	"COX10"	"0.624"	"0.552"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1352"	"COX10"	"0.624"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1998"	"2012"	"15"	"0"	"GENOMICS_ENGLAND"
"1355"	"COX15"	"0.63"	"0.448"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1991"	"2017"	"9"	"3"	"CLINGEN;CTD_human;UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1355"	"COX15"	"0.63"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1355"	"COX15"	"0.63"	"0.448"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2017"	"9"	"0"	"CLINGEN;CTD_human"
"1355"	"COX15"	"0.63"	"0.448"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1355"	"COX15"	"0.63"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1355"	"COX15"	"0.63"	"0.448"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1991"	"2011"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C1858424"	"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1355"	"COX15"	"0.63"	"0.448"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"2"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C3554534"	"CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2"	"disease"		"Disease or Syndrome"	"0.40"		"1991"	"2011"	"1"	"1"	"UNIPROT"
"1355"	"COX15"	"0.63"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1356"	"CP"	"0.5"	"0.586"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0011156"	"Deficiency Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.45"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2010"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0012715"	"Iron Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.53"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.40"	"0.827586206896552"	"1987"	"2013"	"3"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0022716"	"Menkes Kinky Hair Syndrome"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0085397"	"Pasteurellaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0282193"	"Iron Overload"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2001"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1980"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0878682"	"Ceruloplasmin deficiency"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.90"	"1"	"1966"	"2017"	"3"	"44"	"CTD_human;ORPHANET"
"1356"	"CP"	"0.5"	"0.586"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2013"	"3"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"2000"	"2009"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C2931082"	"Familial apoceruloplasmin deficiency"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1356"	"CP"	"0.5"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1357"	"CPA1"	"0.752"	"0.241"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"1357"	"CPA1"	"0.752"	"0.241"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"1357"	"CPA1"	"0.752"	"0.241"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1358"	"CPA2"	"0.928"	"0.138"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1358"	"CPA2"	"0.928"	"0.138"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1358"	"CPA2"	"0.928"	"0.138"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1358"	"CPA2"	"0.928"	"0.138"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1361"	"CPB2"	"0.594"	"0.586"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1361"	"CPB2"	"0.594"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1361"	"CPB2"	"0.594"	"0.586"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1362"	"CPD"	"0.72"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1363"	"CPE"	"0.633"	"0.448"	"C0014130"	"Endocrine System Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.54"	"1"	"1990"	"2016"	"2"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1363"	"CPE"	"0.633"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"1"	"UNIPROT"
"1364"	"CLDN4"	"0.573"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1364"	"CLDN4"	"0.573"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"1365"	"CLDN3"	"0.607"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2006"	"2012"	"1"	"0"	"CTD_human"
"1365"	"CLDN3"	"0.607"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1365"	"CLDN3"	"0.607"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"1365"	"CLDN3"	"0.607"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"1365"	"CLDN3"	"0.607"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1366"	"CLDN7"	"0.555"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"1366"	"CLDN7"	"0.555"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1366"	"CLDN7"	"0.555"	"0.655"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1368"	"CPM"	"0.72"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1368"	"CPM"	"0.72"	"0.276"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1368"	"CPM"	"0.72"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1369"	"CPN1"	"0.799"	"0.276"	"C0398782"	"Carboxypeptidase N Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"1371"	"CPOX"	"0.554"	"0.724"	"C0162531"	"Hereditary Coproporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.875"	"1983"	"2017"	"11"	"9"	"CTD_human;ORPHANET;UNIPROT"
"1371"	"CPOX"	"0.554"	"0.724"	"C0162566"	"Porphyria Cutanea Tarda"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1371"	"CPOX"	"0.554"	"0.724"	"C0342859"	"Harderoporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.46"	"0.833333333333333"	"1983"	"2011"	"10"	"10"	"UNIPROT"
"1373"	"CPS1"	"0.645"	"0.379"	"C0009421"	"Comatose"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0031190"	"Persistent Fetal Circulation Syndrome"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.70"	"0.923076923076923"	"1993"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1373"	"CPS1"	"0.645"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C0751753"	"Carbamoyl-Phosphate Synthase I Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"1993"	"2017"	"16"	"48"	"CTD_human;ORPHANET;UNIPROT"
"1373"	"CPS1"	"0.645"	"0.379"	"C0860634"	"Psychogenic coma"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1373"	"CPS1"	"0.645"	"0.379"	"C3714958"	"PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1373"	"CPS1"	"0.645"	"0.379"	"C4082171"	"Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1993"	"2016"	"16"	"43"	"CTD_human;UNIPROT"
"1373"	"CPS1"	"0.645"	"0.379"	"C4085580"	"Carbamoyl Phosphate Synthase 1 Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2007"	"2"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.52"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1374"	"CPT1A"	"0.621"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1374"	"CPT1A"	"0.621"	"0.448"	"C1829703"	"Carnitine palmitoyl transferase 1A deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"		"1998"	"2017"	"7"	"16"	"CTD_human;ORPHANET;UNIPROT"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.35"	"0.8"	"2008"	"2014"	"1"	"1"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"1"	"CTD_human"
"1375"	"CPT1B"	"0.701"	"0.31"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1376"	"CPT2"	"0.596"	"0.483"	"C0006112"	"Brain Diseases, Metabolic"	"group"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.43"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.42"		"2000"	"2018"	"3"	"1"	"GENOMICS_ENGLAND"
"1376"	"CPT2"	"0.596"	"0.483"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1376"	"CPT2"	"0.596"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"1376"	"CPT2"	"0.596"	"0.483"	"C0750968"	"Central Nervous System Metabolic Disorders"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C0751743"	"Metabolic Disorder, Central Nervous System, Acquired"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C0751744"	"Brain Diseases, Metabolic, Acquired"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C1135773"	"Acquired Metabolic Diseases, Nervous System"	"phenotype"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1376"	"CPT2"	"0.596"	"0.483"	"C1833508"	"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.70"		"1978"	"2015"	"12"	"36"	"CTD_human;ORPHANET;UNIPROT"
"1376"	"CPT2"	"0.596"	"0.483"	"C1833511"	"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1991"	"2015"	"2"	"28"	"CTD_human;ORPHANET;UNIPROT"
"1376"	"CPT2"	"0.596"	"0.483"	"C1833518"	"CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1998"	"2015"	"0"	"19"	"CTD_human;ORPHANET"
"1376"	"CPT2"	"0.596"	"0.483"	"C3280160"	"ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.46"	"1"	"2009"	"2018"	"2"	"8"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2001"	"2015"	"0"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0024535"	"Malaria, Falciparum"	"disease"	"C03"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2009"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1378"	"CR1"	"0.607"	"0.621"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1380"	"CR2"	"0.569"	"0.621"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.59"	"1"	"2009"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"1380"	"CR2"	"0.569"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.37"	"1"	"2004"	"2017"	"0"	"0"	"CTD_human"
"1380"	"CR2"	"0.569"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1380"	"CR2"	"0.569"	"0.621"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"1380"	"CR2"	"0.569"	"0.621"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1381"	"CRABP1"	"0.648"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1382"	"CRABP2"	"0.645"	"0.448"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1382"	"CRABP2"	"0.645"	"0.448"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"3"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.666666666666667"	"2008"	"2016"	"3"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"3"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2014"	"5"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.666666666666667"	"2000"	"2016"	"3"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2001"	"2015"	"5"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0206651"	"Clear Cell Sarcoma of Soft Tissue"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2017"	"0"	"0"	"ORPHANET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"3"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2002"	"2009"	"4"	"0"	"CTD_human;PSYGENET"
"1385"	"CREB1"	"0.494"	"0.793"	"C1266127"	"Histiocytoma, Angiomatoid Fibrous"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"0"	"0"	"CTD_human"
"1385"	"CREB1"	"0.494"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2001"	"2016"	"5"	"0"	"PSYGENET"
"1386"	"ATF2"	"0.594"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"2002"	"2017"	"0"	"0"	"UNIPROT"
"1386"	"ATF2"	"0.594"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1386"	"ATF2"	"0.594"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1386"	"ATF2"	"0.594"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1386"	"ATF2"	"0.594"	"0.724"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"1"	"2"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1996"	"2018"	"0"	"0"	"CGI"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0035934"	"Rubinstein-Taybi Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1995"	"2018"	"11"	"80"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2011"	"2018"	"0"	"0"	"CGI"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2017"	"2"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1864648"	"CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1387"	"CREBBP"	"0.451"	"0.862"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"1387"	"CREBBP"	"0.451"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1387"	"CREBBP"	"0.451"	"0.862"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1387"	"CREBBP"	"0.451"	"0.862"	"C4511003"	"Acute myeloid leukemia with t(8;16)(p11;p13) translocation"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1390"	"CREM"	"0.594"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1390"	"CREM"	"0.594"	"0.586"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1390"	"CREM"	"0.594"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1390"	"CREM"	"0.594"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1390"	"CREM"	"0.594"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1390"	"CREM"	"0.594"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2013"	"5"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2015"	"11"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"1998"	"2014"	"3"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0005899"	"Body Rocking"	"phenotype"	"F03"	"Individual Behavior"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0008031"	"Chest Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2009"	"5"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0010481"	"Cushing Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.54"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1992"	"2018"	"5"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1992"	"2018"	"7"	"0"	"CTD_human;PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0018672"	"Head Banging"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1984"	"1992"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0032001"	"Pituitary Apoplexy"	"disease"	"C10;C14;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0035333"	"Retinitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1991"	"2014"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0038273"	"Stereotypic Movement Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1992"	"2016"	"7"	"0"	"CTD_human;PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2004"	"2010"	"1"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0154874"	"Neuroretinitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2009"	"5"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2012"	"11"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1992"	"2010"	"5"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1392"	"CRH"	"0.456"	"0.759"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2009"	"5"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1992"	"2016"	"5"	"0"	"PSYGENET"
"1392"	"CRH"	"0.456"	"0.759"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2012"	"11"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C3203733"	"Precordial Catch Syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2013"	"0"	"2"	"ORPHANET"
"1392"	"CRH"	"0.456"	"0.759"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1392"	"CRH"	"0.456"	"0.759"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"6"	"0"	"CTD_human"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2012"	"3"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"1997"	"2010"	"2"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2010"	"3"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2008"	"2"	"0"	"PSYGENET"
"1393"	"CRHBP"	"0.701"	"0.345"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1393"	"CRHBP"	"0.701"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2016"	"5"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2012"	"2014"	"4"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0030201"	"Pain, Postoperative"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2012"	"2"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2016"	"5"	"0"	"CTD_human;PSYGENET"
"1394"	"CRHR1"	"0.545"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2012"	"2"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1394"	"CRHR1"	"0.545"	"0.69"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2003"	"2012"	"4"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2009"	"4"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2006"	"3"	"0"	"PSYGENET"
"1395"	"CRHR2"	"0.596"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1395"	"CRHR2"	"0.596"	"0.655"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1398"	"CRK"	"0.486"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"1399"	"CRKL"	"0.604"	"0.586"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2006"	"1"	"0"	"CTD_human"
"1399"	"CRKL"	"0.604"	"0.586"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2001"	"2006"	"1"	"0"	"CTD_human"
"1399"	"CRKL"	"0.604"	"0.586"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1399"	"CRKL"	"0.604"	"0.586"	"C2678480"	"Chromosome 22q11.2 Deletion Syndrome, Distal"	"disease"	"C05;C14;C15;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1400"	"CRMP1"	"0.624"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1400"	"CRMP1"	"0.624"	"0.621"	"C3178803"	"Social Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1401"	"CRP"	"0.399"	"0.862"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.60"	"0.939393939393939"	"1989"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.929411764705882"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.936"	"2000"	"2018"	"2"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.893617021276596"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2002"	"2014"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0020503"	"Hyperparathyroidism, Secondary"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.9375"	"2003"	"2016"	"4"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.34"	"0.75"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"2001"	"2011"	"3"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.958333333333333"	"1987"	"2018"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0025289"	"Meningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.96078431372549"	"2001"	"2017"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0030167"	"Pachymeningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0031051"	"Pericementitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0031099"	"Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.38"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.666666666666667"	"2007"	"2017"	"3"	"0"	"PSYGENET"
"1401"	"CRP"	"0.399"	"0.862"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"1401"	"CRP"	"0.399"	"0.862"	"C0085397"	"Pasteurellaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"1401"	"CRP"	"0.399"	"0.862"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.941176470588235"	"2002"	"2017"	"2"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2012"	"2017"	"2"	"0"	"PSYGENET"
"1401"	"CRP"	"0.399"	"0.862"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.885057471264368"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"1990"	"2016"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.35"		"1988"	"2008"	"1"	"0"	"CTD_human"
"1401"	"CRP"	"0.399"	"0.862"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1404"	"HAPLN1"	"0.727"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"1406"	"CRX"	"0.59"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"1406"	"CRX"	"0.59"	"0.517"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1406"	"CRX"	"0.59"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"0.964285714285714"	"1997"	"2015"	"5"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1406"	"CRX"	"0.59"	"0.517"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"0.933333333333333"	"1998"	"2017"	"2"	"1"	"CTD_human;ORPHANET"
"1406"	"CRX"	"0.59"	"0.517"	"C3151192"	"LEBER CONGENITAL AMAUROSIS 7"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2014"	"5"	"4"	"CTD_human;UNIPROT"
"1406"	"CRX"	"0.59"	"0.517"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1998"	"1999"	"2"	"0"	"CTD_human"
"1406"	"CRX"	"0.59"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"1407"	"CRY1"	"0.619"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"2005"	"2013"	"3"	"0"	"PSYGENET"
"1407"	"CRY1"	"0.619"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1407"	"CRY1"	"0.619"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"2"	"0"	"PSYGENET"
"1407"	"CRY1"	"0.619"	"0.586"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1407"	"CRY1"	"0.619"	"0.586"	"C0393770"	"Delayed Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0494410"	"Nonorganic Sleep Wake Cycle Disorders"	"group"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0751758"	"Advanced Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0751759"	"Non-24 Hour Sleep-Wake Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0751760"	"Shift-Work Sleep Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"1407"	"CRY1"	"0.619"	"0.586"	"C0877792"	"Sleep Disorders, Circadian Rhythm"	"group"	"C10;C24;F03"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"1408"	"CRY2"	"0.648"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2013"	"4"	"0"	"PSYGENET"
"1408"	"CRY2"	"0.648"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"3"	"0"	"PSYGENET"
"1408"	"CRY2"	"0.648"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2014"	"4"	"0"	"PSYGENET"
"1408"	"CRY2"	"0.648"	"0.552"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1408"	"CRY2"	"0.648"	"0.552"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1409"	"CRYAA"	"0.663"	"0.345"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1409"	"CRYAA"	"0.663"	"0.345"	"C1855179"	"CATARACT, ANTERIOR POLAR"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C1858679"	"CATARACT, AUTOSOMAL DOMINANT"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"1996"	"2017"	"7"	"7"	"CTD_human;UNIPROT"
"1409"	"CRYAA"	"0.663"	"0.345"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"1409"	"CRYAA"	"0.663"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1409"	"CRYAA"	"0.663"	"0.345"	"C3888098"	"Cataract, Autosomal Recessive Congenital 1"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"1996"	"2013"	"7"	"4"	"UNIPROT"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2006"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0266537"	"Congenital lamellar cataract"	"disease"		"Congenital Abnormality"	"0.50"		"2013"	"2013"	"0"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"ORPHANET"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"ORPHANET"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C1837317"	"Alpha-B Crystallinopathy"	"disease"	"C05;C10;C11;C14"	"Disease or Syndrome"	"0.90"		"1978"	"2015"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1410"	"CRYAB"	"0.546"	"0.621"	"C3151065"	"Cataract, Posterior Polar, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2006"	"2013"	"0"	"3"	"CTD_human"
"1410"	"CRYAB"	"0.546"	"0.621"	"C3151236"	"MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"1410"	"CRYAB"	"0.546"	"0.621"	"C3554649"	"CARDIOMYOPATHY, DILATED, 1II"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2018"	"2"	"3"	"CTD_human;UNIPROT"
"1410"	"CRYAB"	"0.546"	"0.621"	"C3808377"	"CATARACT 16, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2013"	"0"	"0"	"CTD_human"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C1833229"	"Cataract, Congenital Zonular, with Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1998"	"2015"	"0"	"1"	"CTD_human"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1411"	"CRYBA1"	"0.727"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1412"	"CRYBA2"	"0.815"	"0.172"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1412"	"CRYBA2"	"0.815"	"0.172"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1412"	"CRYBA2"	"0.815"	"0.172"	"C1855179"	"CATARACT, ANTERIOR POLAR"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1412"	"CRYBA2"	"0.815"	"0.172"	"C4011454"	"CATARACT 42"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;UNIPROT"
"1413"	"CRYBA4"	"0.762"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.44"	"0.5"	"2003"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"1413"	"CRYBA4"	"0.762"	"0.172"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1413"	"CRYBA4"	"0.762"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1413"	"CRYBA4"	"0.762"	"0.172"	"C3808012"	"CATARACT 23, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2010"	"2"	"3"	"CTD_human;UNIPROT"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.64"	"0.5"	"2003"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"0.5"	"2012"	"2013"	"0"	"0"	"ORPHANET"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C1969062"	"Cataract, Congenital Nuclear, Autosomal Recessive 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2003"	"2013"	"3"	"4"	"CTD_human;UNIPROT"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1414"	"CRYBB1"	"0.701"	"0.172"	"C3888124"	"CATARACT 17, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2013"	"3"	"0"	"UNIPROT"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.50"	"1"	"2000"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0344523"	"Cataract, congenital, cerulean type 1"	"disease"	"C11"	"Congenital Abnormality"	"0.62"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1832175"	"Cataract, Congenital, Cerulean Type, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1980"	"2017"	"0"	"2"	"CTD_human"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1415"	"CRYBB2"	"0.681"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2005"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C1855179"	"CATARACT, ANTERIOR POLAR"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C1857853"	"Cataract, Congenital Nuclear, Autosomal Recessive 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2013"	"2"	"2"	"CTD_human;UNIPROT"
"1417"	"CRYBB3"	"0.785"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1418"	"CRYGA"	"0.834"	"0.207"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"1419"	"CRYGB"	"0.785"	"0.207"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1419"	"CRYGB"	"0.785"	"0.207"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1419"	"CRYGB"	"0.785"	"0.207"	"C1855179"	"CATARACT, ANTERIOR POLAR"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1419"	"CRYGB"	"0.785"	"0.207"	"C3808800"	"CATARACT 39, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.60"		"1984"	"2013"	"0"	"2"	"CTD_human"
"1420"	"CRYGC"	"0.672"	"0.345"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.68"	"1"	"1999"	"2012"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1420"	"CRYGC"	"0.672"	"0.345"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1420"	"CRYGC"	"0.672"	"0.345"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2000"	"2002"	"2"	"0"	"CTD_human"
"1420"	"CRYGC"	"0.672"	"0.345"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1420"	"CRYGC"	"0.672"	"0.345"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2000"	"2002"	"2"	"0"	"CTD_human"
"1420"	"CRYGC"	"0.672"	"0.345"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"1420"	"CRYGC"	"0.672"	"0.345"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.90"		"1999"	"2015"	"7"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1420"	"CRYGC"	"0.672"	"0.345"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1420"	"CRYGC"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1421"	"CRYGD"	"0.575"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1421"	"CRYGD"	"0.575"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1421"	"CRYGD"	"0.575"	"0.69"	"C0344523"	"Cataract, congenital, cerulean type 1"	"disease"	"C11"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1392104"	"Coralliform cataract"	"disease"		"Congenital Abnormality"	"0.33"	"1"	"2004"	"2014"	"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1837023"	"CATARACT, CONGENITAL, CERULEAN TYPE, 3"	"disease"	"C11"	"Disease or Syndrome"	"0.70"		"1999"	"2011"	"11"	"4"	"CTD_human;UNIPROT"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1421"	"CRYGD"	"0.575"	"0.69"	"C1861832"	"CATARACT, CRYSTALLINE ACULEIFORM"	"phenotype"	"C11"	"Finding"	"0.80"		"1999"	"2017"	"11"	"6"	"CTD_human;UNIPROT"
"1421"	"CRYGD"	"0.575"	"0.69"	"C3540850"	"CATARACT 4, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.70"		"1999"	"2011"	"11"	"4"	"CTD_human;UNIPROT"
"1421"	"CRYGD"	"0.575"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1421"	"CRYGD"	"0.575"	"0.69"	"C3888390"	"Cataract, Punctate, Progressive Juvenile-Onset"	"disease"	"C11"	"Disease or Syndrome"	"0.70"		"1999"	"2011"	"11"	"4"	"CTD_human;UNIPROT"
"1421"	"CRYGD"	"0.575"	"0.69"	"C3888391"	"Nonnuclear polymorphic congenital cataract"	"disease"		"Congenital Abnormality"	"0.70"		"1999"	"2011"	"11"	"4"	"CTD_human;UNIPROT"
"1423"	"CRYGFP"	"1"	"0.034"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1427"	"CRYGS"	"0.799"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.56"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1427"	"CRYGS"	"0.799"	"0.172"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"1"	"CTD_human"
"1427"	"CRYGS"	"0.799"	"0.172"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1427"	"CRYGS"	"0.799"	"0.172"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1427"	"CRYGS"	"0.799"	"0.172"	"C3805410"	"CATARACT 20, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.70"		"1983"	"2006"	"1"	"1"	"CTD_human;UNIPROT"
"1428"	"CRYM"	"0.785"	"0.276"	"C4084708"	"DEAFNESS, AUTOSOMAL DOMINANT 40"	"disease"		"Disease or Syndrome"	"0.70"		"2003"	"2017"	"6"	"2"	"CLINGEN;CTD_human;UNIPROT"
"1429"	"CRYZ"	"0.554"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.666666666666667"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"1429"	"CRYZ"	"0.554"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1431"	"CS"	"0.659"	"0.517"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1431"	"CS"	"0.659"	"0.517"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"PSYGENET"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1432"	"MAPK14"	"0.449"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2000"	"2007"	"1"	"0"	"CTD_human"
"1434"	"CSE1L"	"0.621"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"0"	"0"	"UNIPROT"
"1435"	"CSF1"	"0.51"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"1435"	"CSF1"	"0.51"	"0.655"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"1435"	"CSF1"	"0.51"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1989"	"2015"	"1"	"0"	"CTD_human"
"1435"	"CSF1"	"0.51"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2015"	"1"	"0"	"CTD_human"
"1435"	"CSF1"	"0.51"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1991"	"2006"	"1"	"0"	"CTD_human"
"1435"	"CSF1"	"0.51"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.51"	"1"	"1992"	"2018"	"1"	"0"	"CGI;CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.975"	"1988"	"2016"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2013"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.42"	"1"	"1992"	"2018"	"1"	"4"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.46"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"1990"	"2009"	"0"	"5"	"CGI"
"1436"	"CSF1R"	"0.508"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2014"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1436"	"CSF1R"	"0.508"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.39"	"1"	"1990"	"1998"	"0"	"0"	"CGI"
"1436"	"CSF1R"	"0.508"	"0.655"	"C3711381"	"Hereditary Diffuse Leukoencephalopathy with Spheroids"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"1"	"1989"	"2018"	"2"	"43"	"CTD_human;ORPHANET;UNIPROT"
"1436"	"CSF1R"	"0.508"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1437"	"CSF2"	"0.356"	"0.966"	"C0001824"	"Agranulocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2001"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"1993"	"2009"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"1992"	"2010"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.96551724137931"	"1989"	"2017"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0015423"	"Eyelid Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0017181"	"Gastrointestinal Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2003"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0018932"	"Hematochezia"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2013"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.949367088607595"	"1986"	"2016"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2018"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1981"	"2007"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.38"	"0.75"	"1993"	"2014"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"1980"	"2009"	"1"	"0"	"PSYGENET"
"1437"	"CSF2"	"0.356"	"0.966"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0085090"	"Lymphoma, AIDS-Related"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"1998"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"2002"	"2"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0242594"	"Residual Cancer"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0242596"	"Neoplasm, Residual"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0543478"	"Residual Tumor"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1990"	"2014"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"0.75"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C2931245"	"Bone Marrow failure syndromes"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1993"	"2001"	"3"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2001"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C3808553"	"Bone marrow failure syndrome 1"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C3810350"	"Bone marrow failure syndrome 2"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"1437"	"CSF2"	"0.356"	"0.966"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1438"	"CSF2RA"	"0.72"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"1438"	"CSF2RA"	"0.72"	"0.483"	"C2677877"	"Surfactant Metabolism Dysfunction, Pulmonary, 4"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"2"	"1"	"UNIPROT"
"1438"	"CSF2RA"	"0.72"	"0.483"	"C2931035"	"Pulmonary alveolar proteinosis, congenital"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1438"	"CSF2RA"	"0.72"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2011"	"3"	"0"	"PSYGENET"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C2931035"	"Pulmonary alveolar proteinosis, congenital"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1439"	"CSF2RB"	"0.752"	"0.31"	"C3280574"	"SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"0"	"1"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0001824"	"Agranulocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2010"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.37"	"1"	"1992"	"2006"	"6"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0003862"	"Arthralgia"	"phenotype"	"C05;C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2007"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2007"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2014"	"8"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2003"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1995"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0011644"	"Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1993"	"2016"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018681"	"Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0019156"	"Hepatic Veno-Occlusive Disease"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0020433"	"Hyperbilirubinemia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0021308"	"Infarction"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023269"	"leiomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"1987"	"2016"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.837837837837838"	"1995"	"2017"	"4"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1996"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1987"	"2015"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1994"	"2016"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.833333333333333"	"1993"	"2017"	"13"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0028838"	"Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"0.5"	"1995"	"2016"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2007"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0036420"	"Localized scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0037579"	"Soft Tissue Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0038160"	"Staphylococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0038362"	"Stomatitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2002"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1993"	"2016"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2004"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0085090"	"Lymphoma, AIDS-Related"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0162296"	"Polyarthralgia"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1992"	"2006"	"6"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205815"	"Leiomyosarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0205816"	"Leiomyosarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"0.888888888888889"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0263409"	"Linear Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0282609"	"Bone Marrow Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"1995"	"2006"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0423618"	"Throbbing Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0423623"	"Bilateral Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0474366"	"Generalized Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2014"	"8"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751186"	"Orthostatic Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751187"	"Periorbital Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751189"	"Retro-Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751190"	"Sharp Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751192"	"Vertex Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"2000"	"3"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752255"	"Impairment, Light Touch Sensation"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752256"	"Pain Sensation Diminished"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752257"	"Pinprick Sensation Diminished"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752258"	"Position Sense Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752260"	"Proprioceptive Disorders"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752261"	"Thermal Sensation Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0752262"	"Somatosensory Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0877781"	"Hemicrania"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1993"	"2006"	"8"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1318973"	"Staphylococcus aureus infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2015"	"8"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1527383"	"Morphea"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1568868"	"Oral Mucositis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1440"	"CSF3"	"0.421"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1997"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.933333333333333"	"1998"	"2017"	"0"	"0"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.945945945945946"	"1995"	"2016"	"0"	"1"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.43"	"1"	"1997"	"2014"	"0"	"2"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0023481"	"Chronic Neutrophilic Leukemia"	"disease"	"C15"	"Neoplastic Process"	"0.60"	"0.904761904761905"	"1998"	"2017"	"0"	"0"	"CGI;ORPHANET"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C0543669"	"Neutrophilia, Hereditary"	"disease"	"C15"	"Disease or Syndrome"	"0.93"	"1"	"1998"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1441"	"CSF3R"	"0.596"	"0.448"	"C1292772"	"Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative"	"disease"	"C04;C15"	"Neoplastic Process"	"0.59"	"0.888888888888889"	"2013"	"2017"	"0"	"0"	"CGI;ORPHANET"
"1441"	"CSF3R"	"0.596"	"0.448"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.49"	"1"	"1998"	"2014"	"0"	"0"	"CGI"
"1441"	"CSF3R"	"0.596"	"0.448"	"C4310764"	"NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1442"	"CSH1"	"0.656"	"0.483"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2004"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1445"	"CSK"	"0.633"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1447"	"CSN2"	"0.727"	"0.345"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1448"	"CSN3"	"0.752"	"0.241"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1452"	"CSNK1A1"	"0.743"	"0.207"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1452"	"CSNK1A1"	"0.743"	"0.207"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"0"	"0"	"UNIPROT"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C1858496"	"Advanced Sleep-Phase Syndrome, Familial"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human;ORPHANET"
"1453"	"CSNK1D"	"0.696"	"0.276"	"C3808874"	"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2014"	"2"	"2"	"UNIPROT"
"1454"	"CSNK1E"	"0.707"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2003"	"2016"	"5"	"0"	"PSYGENET"
"1454"	"CSNK1E"	"0.707"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1454"	"CSNK1E"	"0.707"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2013"	"2"	"0"	"PSYGENET"
"1454"	"CSNK1E"	"0.707"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1454"	"CSNK1E"	"0.707"	"0.414"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1457"	"CSNK2A1"	"0.619"	"0.655"	"C4310739"	"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"1459"	"CSNK2A2"	"0.69"	"0.379"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1459"	"CSNK2A2"	"0.69"	"0.379"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1459"	"CSNK2A2"	"0.69"	"0.379"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1460"	"CSNK2B"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"1462"	"VCAN"	"0.523"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1462"	"VCAN"	"0.523"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1462"	"VCAN"	"0.523"	"0.759"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1462"	"VCAN"	"0.523"	"0.759"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1462"	"VCAN"	"0.523"	"0.759"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1462"	"VCAN"	"0.523"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1462"	"VCAN"	"0.523"	"0.759"	"C1840452"	"Hyaloideoretinal degeneration of Wagner"	"disease"	"C11"	"Disease or Syndrome"	"0.60"	"1"	"1999"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"1463"	"NCAN"	"0.727"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2011"	"2016"	"5"	"1"	"PSYGENET"
"1463"	"NCAN"	"0.727"	"0.345"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1463"	"NCAN"	"0.727"	"0.345"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1463"	"NCAN"	"0.727"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0014173"	"Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0349578"	"Complex Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0349579"	"Atypical Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0456483"	"Simple Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1465"	"CSRP1"	"0.696"	"0.379"	"C0746402"	"manic symptom"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1468"	"SLC25A10"	"0.799"	"0.276"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C0018621"	"Hay fever"	"disease"	"C08;C09;C20"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1469"	"CST1"	"0.707"	"0.345"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.944444444444444"	"1989"	"2015"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1996"	"2010"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2014"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0268393"	"Familial Cerebral Amyloid Angiopathy"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.833333333333333"	"2000"	"2009"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1510489"	"Cerebral Amyloid Angiopathy, Hereditary"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1983"	"2009"	"3"	"1"	"CTD_human;UNIPROT"
"1471"	"CST3"	"0.5"	"0.724"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1527338"	"Hereditary Cerebral Amyloid Angiopathy, Icelandic Type"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1988"	"2013"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1471"	"CST3"	"0.5"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C1956349"	"Cerebral Amyloid Angiopathy, Genetic"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C2677774"	"Age-Related Macular Degeneration type 11"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1989"	"2015"	"3"	"1"	"CTD_human;UNIPROT"
"1471"	"CST3"	"0.5"	"0.724"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1471"	"CST3"	"0.5"	"0.724"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"GENOMICS_ENGLAND"
"1472"	"CST4"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1474"	"CST6"	"0.6"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1474"	"CST6"	"0.6"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.833333333333333"	"2004"	"2017"	"1"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C1838440"	"ICHTHYOSIS EXFOLIATIVA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1475"	"CSTA"	"0.633"	"0.483"	"C1842797"	"Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2003"	"2016"	"0"	"4"	"CTD_human"
"1475"	"CSTA"	"0.633"	"0.483"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"1475"	"CSTA"	"0.633"	"0.483"	"C1853354"	"Peeling skin syndrome, acral type"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1475"	"CSTA"	"0.633"	"0.483"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1476"	"CSTB"	"0.559"	"0.483"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1476"	"CSTB"	"0.559"	"0.483"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C0751785"	"Unverricht-Lundborg Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.931818181818182"	"1993"	"2017"	"3"	"13"	"CTD_human;ORPHANET;UNIPROT"
"1476"	"CSTB"	"0.559"	"0.483"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1476"	"CSTB"	"0.559"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"2004"	"4"	"0"	"GENOMICS_ENGLAND"
"1478"	"CSTF2"	"0.857"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.45"	"1"	"2007"	"2017"	"1"	"1"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.61"	"1"	"2003"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.48"	"1"	"2005"	"2016"	"0"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0027126"	"Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.96"	"0.833333333333333"	"2000"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.50"		"2003"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0149630"	"Bicuspid aortic valve"	"disease"	"C14"	"Congenital Abnormality"	"0.42"	"0.5"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0152101"	"Hypoplastic Left Heart Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.82"	"1"	"2003"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.50"		"2003"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0266283"	"Ectopic thyroid tissue (disorder)"	"phenotype"	"C16;C19"	"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.42"	"1"	"2003"	"2009"	"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0410226"	"Congenital Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0685889"	"Splenic Hypoplasia"	"disease"	"C20"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.60"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2003"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1260873"	"Aortic valve disorder"	"group"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2003"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C1879286"	"Hereditary bundle branch system defect"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C2673630"	"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5 (disorder)"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"3"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C2931574"	"Chromosome 5, monosomy 5q35"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C2931689"	"Dystrophia myotonica 2"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3276096"	"ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS"	"disease"		"Disease or Syndrome"	"0.80"		"1976"	"2017"	"5"	"26"	"CTD_human;UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3280785"	"VENTRICULAR SEPTAL DEFECT 3"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2011"	"2011"	"2"	"3"	"UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3280795"	"HYPOPLASTIC LEFT HEART SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2005"	"2"	"1"	"UNIPROT"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3502353"	"Atrial Septal Defect with Atrioventricular Conduction Defects"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1482"	"NKX2-5"	"0.543"	"0.621"	"C3887892"	"Aortic Valve Disease 1"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1487"	"CTBP1"	"0.598"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1487"	"CTBP1"	"0.598"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1487"	"CTBP1"	"0.598"	"0.655"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1487"	"CTBP1"	"0.598"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1487"	"CTBP1"	"0.598"	"0.655"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1488"	"CTBP2"	"0.696"	"0.31"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1488"	"CTBP2"	"0.696"	"0.31"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1488"	"CTBP2"	"0.696"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1488"	"CTBP2"	"0.696"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"1489"	"CTF1"	"0.667"	"0.345"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1489"	"CTF1"	"0.667"	"0.345"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1489"	"CTF1"	"0.667"	"0.345"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2005"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2006"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"0.8"	"1999"	"2016"	"3"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.70"	"0.833333333333333"	"1998"	"2018"	"4"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.925"	"1995"	"2018"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2016"	"4"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1490"	"CTGF"	"0.443"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"3"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1490"	"CTGF"	"0.443"	"0.759"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C1258104"	"Diffuse Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"1490"	"CTGF"	"0.443"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1490"	"CTGF"	"0.443"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1491"	"CTH"	"0.743"	"0.379"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1491"	"CTH"	"0.743"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"1491"	"CTH"	"0.743"	"0.379"	"C0035320"	"Retinal Neovascularization"	"phenotype"	"C11;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1491"	"CTH"	"0.743"	"0.379"	"C0220993"	"Cystathioninuria"	"phenotype"		"Disease or Syndrome"	"0.83"	"0.666666666666667"	"2003"	"2015"	"2"	"3"	"ORPHANET;UNIPROT"
"1491"	"CTH"	"0.743"	"0.379"	"C0268616"	"Gamma-cystathionase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"0.666666666666667"	"2003"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"1491"	"CTH"	"0.743"	"0.379"	"C3495552"	"Cystathionase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2008"	"2"	"2"	"UNIPROT"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2010"	"2016"	"1"	"1"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"1998"	"2017"	"2"	"1"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2011"	"2"	"0"	"PSYGENET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.903225806451613"	"1981"	"2016"	"0"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.40"	"0.932432432432432"	"1995"	"2016"	"3"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"1998"	"2008"	"0"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"2008"	"2018"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0026948"	"Mycosis Fungoides"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2016"	"3"	"0"	"PSYGENET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2001"	"2011"	"2"	"0"	"PSYGENET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C0677607"	"Hashimoto Disease"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.9375"	"1998"	"2015"	"0"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2001"	"2011"	"2"	"0"	"PSYGENET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C1832392"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 12"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C3495801"	"Granulomatosis with polyangiitis"	"disease"	"C08;C14;C20"	"Disease or Syndrome"	"0.36"	"1"	"2000"	"2005"	"0"	"0"	"ORPHANET"
"1493"	"CTLA4"	"0.434"	"0.862"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1493"	"CTLA4"	"0.434"	"0.862"	"C4015214"	"CTLA4 Haploinsufficiency"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2015"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1493"	"CTLA4"	"0.434"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"				"0"	"0"	"CLINGEN"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"2007"	"2014"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"CLINGEN"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"				"0"	"0"	"CLINGEN"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1837029"	"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"1970"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1868569"	"Patterned dystrophy of retinal pigment epithelium"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1495"	"CTNNA1"	"0.636"	"0.483"	"C4511237"	"Butterfly-shaped pigmentary macular dystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1496"	"CTNNA2"	"0.785"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1496"	"CTNNA2"	"0.785"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1496"	"CTNNA2"	"0.785"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1496"	"CTNNA2"	"0.785"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1496"	"CTNNA2"	"0.785"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1497"	"CTNS"	"0.627"	"0.448"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"1497"	"CTNS"	"0.627"	"0.448"	"C0268626"	"Juvenile nephropathic cystinosis (disorder)"	"disease"	"C12;C13;C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.71"	"1"	"1998"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1497"	"CTNS"	"0.627"	"0.448"	"C2749685"	"CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2012"	"9"	"12"	"UNIPROT"
"1497"	"CTNS"	"0.627"	"0.448"	"C2931013"	"Cystinosis, benign, nonnephropathic"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1497"	"CTNS"	"0.627"	"0.448"	"C2931187"	"Nephropathic cystinosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.918918918918919"	"1998"	"2018"	"10"	"12"	"CTD_human;UNIPROT"
"1497"	"CTNS"	"0.627"	"0.448"	"C3537440"	"Cystinosis, Infantile Nephropathic"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1998"	"2012"	"9"	"12"	"ORPHANET;UNIPROT"
"1497"	"CTNS"	"0.627"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1497"	"CTNS"	"0.627"	"0.448"	"C4316899"	"Cystinosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1998"	"2012"	"10"	"12"	"CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.857142857142857"	"2000"	"2011"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.904761904761905"	"1999"	"2016"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"0"	"2"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8"	"2001"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2014"	"9"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2009"	"2018"	"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0007528"	"Cecal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"9"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"4"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"1999"	"2016"	"4"	"5"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0010276"	"Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.66"	"0.833333333333333"	"2004"	"2016"	"1"	"2"	"CTD_human;ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2014"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.8125"	"1998"	"2016"	"2"	"8"	"CGI;CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.888888888888889"	"1996"	"2015"	"0"	"10"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.875"	"2001"	"2017"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.40"	"0.846153846153846"	"2003"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.36"	"1"	"1998"	"2014"	"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.58"	"1"	"2002"	"2018"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2016"	"2"	"0"	"PSYGENET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0079218"	"Fibromatosis, Aggressive"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1997"	"2017"	"0"	"0"	"CGI;ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.43"	"1"	"2001"	"2016"	"0"	"9"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.41"	"1"	"2001"	"2016"	"0"	"9"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0153437"	"Malignant neoplasm of cecum"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2004"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.95"	"1999"	"2016"	"1"	"1"	"CGI;CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0206667"	"Adrenal Cortical Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2012"	"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.43"	"1"	"2005"	"2016"	"1"	"5"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0206711"	"Pilomatrixoma"	"disease"	"C04"	"Neoplastic Process"	"0.75"	"1"	"1997"	"2015"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0232347"	"No-Reflow Phenomenon"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0262587"	"Parathyroid Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2013"	"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"8"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0278875"	"Adult Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0279606"	"Childhood Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.41"	"1"	"2007"	"2015"	"0"	"1"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0342649"	"Vascular calcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"0.928571428571429"	"2000"	"2018"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0431128"	"Papillary craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0431129"	"Adamantinous Craniopharyngioma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.818181818181818"	"1998"	"2018"	"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2013"	"1"	"2"	"UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.866666666666667"	"1996"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"1"	"1997"	"2014"	"1"	"2"	"UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0751061"	"Craniopharyngioma, Child"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2000"	"2002"	"2"	"2"	"CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.84"	"1"	"1999"	"2016"	"1"	"1"	"CGI;CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.81"	"1"	"1999"	"2014"	"2"	"2"	"CGI;CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2015"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1334970"	"Medulloblastoma with extensive nodularity"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2002"	"2"	"2"	"UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.957446808510638"	"1997"	"2017"	"5"	"1"	"CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"ORPHANET"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C1879526"	"Aberrant Crypt Foci"	"phenotype"	"C04"	"Finding"	"0.30"		"2000"	"2003"	"3"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.80"	"0.955882352941177"	"1998"	"2017"	"5"	"12"	"CGI;CTD_human;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C3554449"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 19"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2015"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1499"	"CTNNB1"	"0.417"	"0.759"	"C4539767"	"EXUDATIVE VITREORETINOPATHY 7"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"1500"	"CTNND1"	"0.572"	"0.586"	"C1861536"	"Blepharo-cheilo-dontic syndrome"	"disease"	"C05;C07;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0010314"	"Cri-du-Chat Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2015"	"0"	"0"	"ORPHANET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"PSYGENET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1501"	"CTNND2"	"0.596"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"1501"	"CTNND2"	"0.596"	"0.483"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1501"	"CTNND2"	"0.596"	"0.483"	"C1832841"	"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C2931860"	"Monosomy 5p"	"disease"	"C10;C16"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"1501"	"CTNND2"	"0.596"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1503"	"CTPS1"	"0.799"	"0.172"	"C4014617"	"IMMUNODEFICIENCY 24"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"1504"	"CTRB1"	"0.834"	"0.241"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1504"	"CTRB1"	"0.834"	"0.241"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1504"	"CTRB1"	"0.834"	"0.241"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1504"	"CTRB1"	"0.834"	"0.241"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1504"	"CTRB1"	"0.834"	"0.241"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1506"	"CTRL"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1508"	"CTSB"	"0.49"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1995"	"2012"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2002"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1508"	"CTSB"	"0.49"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C0406756"	"Keratolytic winter erythema"	"disease"	"C16;C17;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"1508"	"CTSB"	"0.49"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1508"	"CTSB"	"0.49"	"0.828"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1509"	"CTSD"	"0.505"	"0.759"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C1864669"	"NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"		"1995"	"2015"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1509"	"CTSD"	"0.505"	"0.759"	"C1864670"	"Neuronal Ceroid Lipofuscinosis, Congenital"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1995"	"2012"	"3"	"2"	"CTD_human;UNIPROT"
"1509"	"CTSD"	"0.505"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"1509"	"CTSD"	"0.505"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1510"	"CTSE"	"0.659"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1510"	"CTSE"	"0.659"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.43"	"1"	"2008"	"2016"	"1"	"2"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"1512"	"CTSH"	"0.663"	"0.517"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"1"	"ORPHANET"
"1512"	"CTSH"	"0.663"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1512"	"CTSH"	"0.663"	"0.517"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1512"	"CTSH"	"0.663"	"0.517"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1513"	"CTSK"	"0.534"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"1513"	"CTSK"	"0.534"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1513"	"CTSK"	"0.534"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1513"	"CTSK"	"0.534"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"1513"	"CTSK"	"0.534"	"0.724"	"C0238402"	"Pycnodysostosis"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2017"	"7"	"24"	"CTD_human;ORPHANET;UNIPROT"
"1513"	"CTSK"	"0.534"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1513"	"CTSK"	"0.534"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1513"	"CTSK"	"0.534"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1514"	"CTSL"	"0.518"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1514"	"CTSL"	"0.518"	"0.655"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1520"	"CTSS"	"0.642"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1520"	"CTSS"	"0.642"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1520"	"CTSS"	"0.642"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1520"	"CTSS"	"0.642"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"1520"	"CTSS"	"0.642"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1522"	"CTSZ"	"0.676"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1522"	"CTSZ"	"0.676"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1522"	"CTSZ"	"0.676"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1522"	"CTSZ"	"0.676"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1523"	"CUX1"	"0.52"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2017"	"0"	"0"	"UNIPROT"
"1523"	"CUX1"	"0.52"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1523"	"CUX1"	"0.52"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2013"	"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1994"	"2012"	"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"2008"	"2014"	"3"	"0"	"PSYGENET"
"1523"	"CUX1"	"0.52"	"0.655"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1523"	"CUX1"	"0.52"	"0.655"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"1523"	"CUX1"	"0.52"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.666666666666667"	"2008"	"2016"	"3"	"0"	"PSYGENET"
"1523"	"CUX1"	"0.52"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1523"	"CUX1"	"0.52"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2010"	"0"	"0"	"UNIPROT"
"1523"	"CUX1"	"0.52"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2001"	"2013"	"0"	"0"	"CTD_human"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"2000"	"2015"	"0"	"0"	"CTD_human"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C3151079"	"MACULAR DEGENERATION, AGE-RELATED, 12"	"disease"		"Disease or Syndrome"	"0.50"		"2007"	"2007"	"0"	"0"	"CTD_human"
"1524"	"CX3CR1"	"0.496"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1525"	"CXADR"	"0.57"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"1994"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0268285"	"Adrenal hyperplasia, congenital, type 5"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1528"	"CYB5A"	"0.633"	"0.448"	"C0272087"	"Congenital Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"1992"	"0"	"0"	"ORPHANET"
"1528"	"CYB5A"	"0.633"	"0.448"	"C2673427"	"METHEMOGLOBINEMIA TYPE IV"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"1986"	"1994"	"0"	"1"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"2000"	"2012"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"1535"	"CYBA"	"0.55"	"0.655"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.8125"	"2002"	"2016"	"3"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C1844376"	"Granulomatous Disease, Chronic, X-Linked"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"1535"	"CYBA"	"0.55"	"0.655"	"C1856255"	"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.60"		"1990"	"2014"	"9"	"12"	"CTD_human;UNIPROT"
"1535"	"CYBA"	"0.55"	"0.655"	"C3661525"	"Autosomal Recessive Chronic Granulomatous Disease"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.33"	"1"	"1990"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.90"	"0.956896551724138"	"1987"	"2017"	"2"	"2"	"CTD_human;ORPHANET"
"1536"	"CYBB"	"0.503"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"0.666666666666667"	"2003"	"2016"	"3"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2004"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0393953"	"Anterior Cerebral Circulation Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0751952"	"Anterior Circulation Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0751953"	"Brain Infarction, Posterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0751954"	"Venous Infarction, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C0751955"	"Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C1844376"	"Granulomatous Disease, Chronic, X-Linked"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.70"	"0.983870967741935"	"1988"	"2017"	"24"	"61"	"CTD_human;UNIPROT"
"1536"	"CYBB"	"0.503"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1536"	"CYBB"	"0.503"	"0.793"	"C1970859"	"Atypical Mycobacteriosis, Familial, X-Linked 2"	"disease"	"C01;C16"	"Disease or Syndrome"	"0.70"		"2007"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1536"	"CYBB"	"0.503"	"0.793"	"C3661525"	"Autosomal Recessive Chronic Granulomatous Disease"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"2"	"0"	"CTD_human"
"1537"	"CYC1"	"0.707"	"0.276"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1537"	"CYC1"	"0.707"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1537"	"CYC1"	"0.707"	"0.276"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1537"	"CYC1"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1537"	"CYC1"	"0.707"	"0.276"	"C3809553"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"1540"	"CYLD"	"0.561"	"0.586"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1540"	"CYLD"	"0.561"	"0.586"	"C0023860"	"Listeriosis"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C0040100"	"Thymoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1540"	"CYLD"	"0.561"	"0.586"	"C1275122"	"Familial multiple trichoepitheliomata"	"disease"	"C04;C16;C17"	"Neoplastic Process"	"0.80"	"1"	"2003"	"2016"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1540"	"CYLD"	"0.561"	"0.586"	"C1305968"	"Eccrine dermal cylindroma"	"disease"	"C04;C16;C17"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C1851526"	"Ancell-Spiegler cylindromas"	"phenotype"		"Pathologic Function"	"0.40"		"2000"	"2006"	"0"	"19"	"ORPHANET"
"1540"	"CYLD"	"0.561"	"0.586"	"C1857941"	"Brooke-Spiegler syndrome"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.70"	"0.944444444444444"	"2002"	"2016"	"5"	"7"	"CTD_human;UNIPROT"
"1540"	"CYLD"	"0.561"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"1540"	"CYLD"	"0.561"	"0.586"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0003860"	"Arteritis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.901408450704225"	"1989"	"2018"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0018552"	"Hamartoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2008"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0039239"	"Sinus Tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0085096"	"Peripheral Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0242706"	"Hyperoxia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"2001"	"2013"	"2"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.907894736842105"	"1989"	"2018"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2010"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.878787878787879"	"1983"	"2017"	"1"	"0"	"CTD_human"
"1543"	"CYP1A1"	"0.458"	"0.828"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2007"	"2012"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2007"	"2011"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0025637"	"Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2000"	"2014"	"1"	"0"	"PSYGENET"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0037997"	"Splenic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0162566"	"Porphyria Cutanea Tarda"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.36"	"0.666666666666667"	"2001"	"2012"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1544"	"CYP1A2"	"0.509"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.927272727272727"	"1995"	"2016"	"2"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2011"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0020302"	"Hydrophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"	"1"	"1996"	"2018"	"19"	"29"	"ORPHANET;UNIPROT"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0344559"	"Irido-corneo-trabecular dysgenesis (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.65"	"1"	"1997"	"2015"	"0"	"3"	"CTD_human;ORPHANET"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"2003"	"2018"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.927272727272727"	"1995"	"2016"	"2"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"2005"	"2007"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"2001"	"2014"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2010"	"2"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1832977"	"GLAUCOMA 3, PRIMARY INFANTILE, B"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1842028"	"GLAUCOMA 1, OPEN ANGLE, A"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1856439"	"GLAUCOMA 3, PRIMARY CONGENITAL, A"	"disease"	"C11"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"1997"	"2017"	"19"	"34"	"CTD_human;UNIPROT"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1862839"	"Anterior segment mesenchymal dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C2981140"	"Glaucoma of childhood"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"2002"	"2013"	"0"	"0"	"ORPHANET"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C3278152"	"GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2008"	"19"	"29"	"UNIPROT"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C3278153"	"GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2008"	"19"	"29"	"UNIPROT"
"1545"	"CYP1B1"	"0.489"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.34"	"0.666666666666667"	"2002"	"2009"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2016"	"6"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.923076923076923"	"1999"	"2016"	"4"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0029106"	"Opisthorchiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2003"	"2017"	"4"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2016"	"4"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0206704"	"Carcinoma, Large Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"1999"	"2017"	"6"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0277004"	"Opisthorchis felineus Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0277005"	"Opisthorchis viverrini Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2016"	"4"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0750384"	"Coumarin Resistance"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2001"	"2010"	"2"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1548"	"CYP2A6"	"0.546"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"1553"	"CYP2A13"	"0.681"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1553"	"CYP2A13"	"0.681"	"0.379"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1553"	"CYP2A13"	"0.681"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2006"	"2"	"0"	"PSYGENET"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"PSYGENET"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2001"	"2"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"PSYGENET"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C3281153"	"EFAVIRENZ, POOR METABOLISM OF"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C3281154"	"EFAVIRENZ CENTRAL NERVOUS SYSTEM TOXICITY, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1555"	"CYP2B6"	"0.437"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2012"	"4"	"0"	"PSYGENET"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2012"	"4"	"0"	"PSYGENET"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2003"	"2012"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1996"	"2017"	"5"	"0"	"PSYGENET"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1996"	"2017"	"5"	"0"	"PSYGENET"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C1836023"	"Drug Metabolism, Poor, CYP2C19-Related"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1557"	"CYP2C19"	"0.501"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"2"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2014"	"2017"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.50"		"2005"	"2011"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1558"	"CYP2C8"	"0.639"	"0.517"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2002"	"2013"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2016"	"5"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0030922"	"Peptic Ulcer Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2004"	"2014"	"4"	"1"	"PSYGENET"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2002"	"2013"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0750384"	"Coumarin Resistance"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2018"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C2608079"	"WARFARIN SENSITIVITY (disorder)"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"1559"	"CYP2C9"	"0.542"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"1562"	"CYP2C18"	"0.69"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1562"	"CYP2C18"	"0.69"	"0.517"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1562"	"CYP2C18"	"0.69"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.964285714285714"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.936708860759494"	"1996"	"2018"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0009421"	"Comatose"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1996"	"2014"	"5"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1996"	"2014"	"5"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0026837"	"Muscle Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.892857142857143"	"1992"	"2014"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"1995"	"2015"	"5"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"1996"	"2015"	"5"	"2"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0151564"	"Cogwheel Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0231519"	"Gegenhalten"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0233608"	"Catatonic Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0239325"	"Extensor Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0277821"	"Extrapyramidal Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.936708860759494"	"1996"	"2018"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C0860634"	"Psychogenic coma"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"1996"	"2014"	"5"	"0"	"PSYGENET"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1320474"	"Nuchal Rigidity"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"		"2007"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C1837154"	"Drug Metabolism, Poor, CYP2D6-Related"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1565"	"CYP2D6"	"0.461"	"0.724"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1995"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0015696"	"Fatty Liver, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2009"	"2016"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2018"	"4"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.38"	"0.857142857142857"	"2002"	"2013"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1991"	"2009"	"2"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.58"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.37"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2012"	"1"	"0"	"PSYGENET"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"1992"	"2014"	"6"	"0"	"CTD_human;PSYGENET"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0236664"	"Alcohol-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0"	"1999"	"2001"	"2"	"0"	"PSYGENET"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"0.75"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2018"	"4"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2018"	"4"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"2003"	"2015"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C2718067"	"Alcoholic Steatohepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"4"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"4"	"0"	"CTD_human"
"1571"	"CYP2E1"	"0.473"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2018"	"4"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.888888888888889"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2004"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2015"	"1"	"0"	"PSYGENET"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0040479"	"Torsades de Pointes"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.777777777777778"	"1998"	"2015"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.882352941176471"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1576"	"CYP3A4"	"0.492"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"2"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2005"	"2008"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2011"	"3"	"0"	"PSYGENET"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"0.777777777777778"	"2003"	"2015"	"1"	"0"	"CTD_human"
"1577"	"CYP3A5"	"0.541"	"0.724"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1580"	"CYP4B1"	"0.762"	"0.276"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1580"	"CYP4B1"	"0.762"	"0.276"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"1581"	"CYP7A1"	"0.63"	"0.379"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"1998"	"2012"	"2"	"0"	"CTD_human"
"1581"	"CYP7A1"	"0.63"	"0.379"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"1581"	"CYP7A1"	"0.63"	"0.379"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1582"	"CYP8B1"	"0.752"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0001623"	"Adrenal gland hypofunction"	"phenotype"	"C19"	"Disease or Syndrome"	"0.47"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2003"	"2013"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2008"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0238395"	"Male Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0342474"	"Lipoid congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C2751824"	"46, XY Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C3151055"	"ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2001"	"2015"	"5"	"7"	"ORPHANET;UNIPROT"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C3489793"	"46,XY Sex Reversal 3"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C3502132"	"Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1583"	"CYP11A1"	"0.555"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.43"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C0268292"	"Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.80"	"1"	"1982"	"2017"	"12"	"33"	"CTD_human;ORPHANET;UNIPROT"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C1260386"	"Glucocorticoid-remediable aldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.60"	"0.923076923076923"	"1992"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.39"	"0.777777777777778"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1584"	"CYP11B1"	"0.588"	"0.552"	"C3669121"	"11-Beta-hydroxylase deficiency"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2016"	"0"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0020428"	"Hyperaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.933333333333333"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0020595"	"Hypoaldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"0.9"	"1999"	"2013"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0268293"	"Corticosterone Methyl Oxidase Type I Deficiency"	"disease"	"C19"	"Disease or Syndrome"	"0.61"	"0"	"1997"	"2001"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0376185"	"Hypoaldosteronism, Hyporeninemic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C1260386"	"Glucocorticoid-remediable aldosteronism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.9"	"1992"	"2016"	"0"	"0"	"ORPHANET"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C1384514"	"Conn Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1585"	"CYP11B2"	"0.572"	"0.483"	"C3463917"	"Corticosterone Methyl Oxidase Type II Deficiency"	"disease"		"Disease or Syndrome"	"0.41"	"0"	"1991"	"2004"	"5"	"6"	"UNIPROT"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.50"	"1"	"1988"	"2016"	"1"	"1"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.897959183673469"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0020461"	"Hyperkalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0020540"	"Malignant Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0020635"	"Hypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0028949"	"Oligomenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2008"	"5"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0242342"	"Sheehan Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0268285"	"Adrenal hyperplasia, congenital, type 5"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.80"	"0.944444444444444"	"1989"	"2016"	"18"	"19"	"CTD_human;ORPHANET;UNIPROT"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.914893617021277"	"1999"	"2018"	"5"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.897959183673469"	"1997"	"2017"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.5"	"2001"	"2009"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C3277849"	"17,20-Lyase Deficiency, Isolated"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.46"	"1"	"1989"	"2015"	"18"	"18"	"UNIPROT"
"1586"	"CYP17A1"	"0.486"	"0.655"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1587"	"ADAM3A"	"0.928"	"0.103"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.939130434782609"	"1994"	"2018"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.60"	"0.964285714285714"	"2002"	"2017"	"2"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0020635"	"Hypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.48"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0029928"	"Ovarian Diseases"	"group"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.60"	"0.9375"	"1994"	"2018"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"		"2006"	"2009"	"2"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0242341"	"Sexual Infantilism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0242342"	"Sheehan Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2009"	"2014"	"2"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2014"	"2"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.946428571428571"	"1994"	"2018"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0853662"	"Oestrogen deficiency"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2007"	"2011"	"0"	"0"	"ORPHANET"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"1994"	"2012"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2017"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"4"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1563718"	"Genital Infantilism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1960539"	"Aromatase deficiency"	"disease"	"C12;C13;C16;C17;C18;C19"	"Disease or Syndrome"	"0.79"	"1"	"1991"	"2016"	"6"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C1970109"	"AROMATASE EXCESS SYNDROME"	"disease"	"C12;C13;C16;C17;C18;C19"	"Disease or Syndrome"	"0.58"	"1"	"1998"	"2015"	"0"	"0"	"ORPHANET"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1588"	"CYP19A1"	"0.482"	"0.69"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.40"	"0.979591836734694"	"1983"	"2018"	"2"	"0"	"CTD_human"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C0342467"	"Late onset congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C1859995"	"Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"1985"	"2016"	"53"	"35"	"UNIPROT"
"1589"	"CYP21A2"	"0.607"	"0.586"	"C2936858"	"Congenital adrenal hyperplasia due to 21 hydroxylase deficiency"	"disease"	"C12;C13;C16;C18;C19"	"Congenital Abnormality"	"0.60"	"0.943548387096774"	"1981"	"2017"	"53"	"35"	"CTD_human;UNIPROT"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.833333333333333"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.95"	"2011"	"2018"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0020438"	"Hypercalciuria"	"phenotype"	"C23"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2006"	"2018"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0268080"	"Hypercalcemia, Idiopathic, of Infancy"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1986"	"2014"	"1"	"8"	"ORPHANET;UNIPROT"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0392525"	"Nephrolithiasis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.36"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0475732"	"Hypercalcemia, Infantile"	"phenotype"	"C18"	"Finding"	"0.40"		"2011"	"2017"	"0"	"1"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.785714285714286"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C4310232"	"Hypercalcemia, Infantile, 1"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1591"	"CYP24A1"	"0.532"	"0.69"	"C4310473"	"Hypercalcemia, infantile, 2"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1592"	"CYP26A1"	"0.636"	"0.414"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"1"	"2001"	"2014"	"2"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2010"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0238052"	"Xanthomatosis, Cerebrotendinous"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.970149253731343"	"1983"	"2018"	"8"	"53"	"CTD_human;ORPHANET;UNIPROT"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2018"	"8"	"0"	"GENOMICS_ENGLAND"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2010"	"2"	"0"	"CTD_human"
"1593"	"CYP27A1"	"0.582"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0035579"	"Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.69"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0085655"	"Polymyositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0263984"	"Polymyositis Ossificans"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0268689"	"Vitamin D-dependent rickets, type 1"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2016"	"4"	"18"	"CTD_human;ORPHANET;UNIPROT"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1594"	"CYP27B1"	"0.542"	"0.69"	"C0554591"	"Polymyositis, Idiopathic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1595"	"CYP51A1"	"0.773"	"0.31"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1600"	"DAB1"	"0.672"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1600"	"DAB1"	"0.672"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"1600"	"DAB1"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1600"	"DAB1"	"0.672"	"0.483"	"C3889636"	"SPINOCEREBELLAR ATAXIA 37"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1604"	"CD55"	"0.57"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0020800"	"Idiopathic Hypercatabolic Hypoproteinemia"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0033680"	"Protein-Losing Enteropathies"	"group"	"C06"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"5"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1604"	"CD55"	"0.57"	"0.759"	"C4538570"	"COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"UNIPROT"
"1605"	"DAG1"	"0.522"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C0023092"	"Lassa Fever"	"disease"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"	"0.958333333333333"	"1998"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"1605"	"DAG1"	"0.522"	"0.655"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.39"	"1"	"2001"	"2015"	"0"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2014"	"0"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"0.95"	"1996"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.60"	"1"	"1997"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2017"	"0"	"0"	"CTD_human"
"1605"	"DAG1"	"0.522"	"0.655"	"C3151184"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9"	"disease"		"Disease or Syndrome"	"0.90"		"2011"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1605"	"DAG1"	"0.522"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2004"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1605"	"DAG1"	"0.522"	"0.655"	"C4225291"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"2"	"2"	"UNIPROT"
"1607"	"DGKB"	"0.785"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1607"	"DGKB"	"0.785"	"0.207"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1607"	"DGKB"	"0.785"	"0.207"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"1608"	"DGKG"	"0.834"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1609"	"DGKQ"	"0.886"	"0.207"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1609"	"DGKQ"	"0.886"	"0.207"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1609"	"DGKQ"	"0.886"	"0.207"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1610"	"DAO"	"0.667"	"0.414"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.42"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"1610"	"DAO"	"0.667"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1610"	"DAO"	"0.667"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2004"	"2012"	"5"	"0"	"PSYGENET"
"1610"	"DAO"	"0.667"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1610"	"DAO"	"0.667"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.947368421052632"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1610"	"DAO"	"0.667"	"0.414"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1610"	"DAO"	"0.667"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"1610"	"DAO"	"0.667"	"0.414"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1610"	"DAO"	"0.667"	"0.414"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2008"	"1"	"0"	"PSYGENET"
"1611"	"DAP"	"0.542"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2017"	"1"	"3"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0009759"	"Conjunctival Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.5"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.35"	"0.8"	"2010"	"2016"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1612"	"DAPK1"	"0.513"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1613"	"DAPK3"	"0.645"	"0.448"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1613"	"DAPK3"	"0.645"	"0.448"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1615"	"DARS"	"0.834"	"0.207"	"C3809008"	"HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2013"	"2015"	"1"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1616"	"DAXX"	"0.602"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"1616"	"DAXX"	"0.602"	"0.552"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"1616"	"DAXX"	"0.602"	"0.552"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1616"	"DAXX"	"0.602"	"0.552"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"1616"	"DAXX"	"0.602"	"0.552"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"1616"	"DAXX"	"0.602"	"0.552"	"C1328479"	"Pancreatic Endocrine Carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1617"	"DAZ1"	"0.727"	"0.345"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"1617"	"DAZ1"	"0.727"	"0.345"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1617"	"DAZ1"	"0.727"	"0.345"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1618"	"DAZL"	"0.785"	"0.172"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1620"	"BRINP1"	"0.667"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1621"	"DBH"	"0.557"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"1983"	"2015"	"5"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1995"	"2013"	"5"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"1994"	"2014"	"5"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1994"	"2014"	"5"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"1989"	"2015"	"1"	"0"	"CTD_human"
"1621"	"DBH"	"0.557"	"0.621"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"1621"	"DBH"	"0.557"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2015"	"3"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0342687"	"dopamine beta hydroxylase deficiency"	"disease"	"C10"	"Disease or Syndrome"	"0.91"	"1"	"1993"	"2013"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"1621"	"DBH"	"0.557"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1982"	"2009"	"4"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1621"	"DBH"	"0.557"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2015"	"3"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C1306067"	"Drug-induced paranoid state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2015"	"3"	"0"	"PSYGENET"
"1621"	"DBH"	"0.557"	"0.621"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2000"	"2015"	"3"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1622"	"DBI"	"0.727"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2005"	"2012"	"1"	"0"	"PSYGENET"
"1622"	"DBI"	"0.727"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1622"	"DBI"	"0.727"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1627"	"DBN1"	"0.69"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1627"	"DBN1"	"0.69"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1627"	"DBN1"	"0.69"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2013"	"3"	"0"	"PSYGENET"
"1628"	"DBP"	"0.672"	"0.552"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1629"	"DBT"	"0.659"	"0.345"	"C0024776"	"Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1991"	"2017"	"2"	"21"	"CTD_human;UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1629"	"DBT"	"0.659"	"0.345"	"C0268568"	"Classic Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1991"	"1998"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C0268569"	"Intermittent Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1991"	"1998"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1629"	"DBT"	"0.659"	"0.345"	"C0751285"	"Maple Syrup Urine Disease, Thiamine Responsive"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1991"	"1998"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C1621920"	"Intermediate Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1991"	"1998"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C1855369"	"Maple Syrup Urine Disease, Type IA"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"1998"	"2"	"1"	"UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C1855371"	"MAPLE SYRUP URINE DISEASE, TYPE II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1991"	"2015"	"2"	"4"	"UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C2930990"	"Maple syrup urine disease, type 1B"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"1998"	"2"	"1"	"UNIPROT"
"1629"	"DBT"	"0.659"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1630"	"DCC"	"0.504"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.90625"	"1990"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"1630"	"DCC"	"0.504"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1992"	"2008"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1630"	"DCC"	"0.504"	"0.655"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.51"	"1"	"1992"	"1992"	"0"	"0"	"CGI;CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1630"	"DCC"	"0.504"	"0.655"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.50"		"1994"	"1994"	"1"	"1"	"CGI;UNIPROT"
"1630"	"DCC"	"0.504"	"0.655"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1630"	"DCC"	"0.504"	"0.655"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1630"	"DCC"	"0.504"	"0.655"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1630"	"DCC"	"0.504"	"0.655"	"C0175754"	"Agenesis of corpus callosum"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.41"	"1"	"2017"	"2017"	"1"	"8"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1630"	"DCC"	"0.504"	"0.655"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1630"	"DCC"	"0.504"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1630"	"DCC"	"0.504"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.923076923076923"	"1990"	"2015"	"1"	"0"	"CTD_human;UNIPROT"
"1630"	"DCC"	"0.504"	"0.655"	"C1834870"	"MIRROR MOVEMENTS 1"	"phenotype"		"Finding"	"0.60"		"1993"	"2017"	"2"	"16"	"CTD_human;UNIPROT"
"1630"	"DCC"	"0.504"	"0.655"	"C1846496"	"Gaze Palsy, Familial Horizontal, with Progressive Scoliosis"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C3179058"	"Corpus Callosum Malformation"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1630"	"DCC"	"0.504"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1630"	"DCC"	"0.504"	"0.655"	"C4479640"	"GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"1634"	"DCN"	"0.505"	"0.69"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1634"	"DCN"	"0.505"	"0.69"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1634"	"DCN"	"0.505"	"0.69"	"C1864738"	"Corneal Dystrophy, Congenital Stromal"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.85"	"1"	"1968"	"2015"	"0"	"4"	"CTD_human;ORPHANET"
"1636"	"ACE"	"0.367"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.31"		"2006"	"2013"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"3"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.859375"	"1998"	"2018"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"	"0.954545454545455"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.55"	"0.5"	"2000"	"2011"	"4"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.902597402597403"	"1994"	"2018"	"3"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.785714285714286"	"1995"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"1636"	"ACE"	"0.367"	"0.897"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.895833333333333"	"1992"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.862068965517241"	"1992"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0010200"	"Coughing"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.40"	"0.954545454545455"	"1997"	"2016"	"2"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0011071"	"Sudden death"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9"	"1998"	"2015"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.892307692307692"	"1994"	"2016"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0017205"	"Gaucher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"	"0.951219512195122"	"1995"	"2016"	"2"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.33"	"1"	"1994"	"2017"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0017924"	"Glycogen Storage Disease Type V"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.96969696969697"	"1992"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.953846153846154"	"1992"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"1998"	"0"	"0"	"GENOMICS_ENGLAND"
"1636"	"ACE"	"0.367"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.851963746223565"	"1986"	"2018"	"2"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.32"		"2003"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.40"		"1987"	"1987"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0021295"	"Infant, Premature, Diseases"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2002"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.872"	"1994"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"	"0.857142857142857"	"1995"	"2017"	"2"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.54"	"0.75"	"1998"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0025303"	"Meningococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.908571428571429"	"1992"	"2016"	"2"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0032310"	"Pneumonia, Viral"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.34"		"2003"	"2008"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.733333333333333"	"1996"	"2014"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2018"	"4"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0038160"	"Staphylococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2005"	"2010"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.811320754716981"	"1994"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2017"	"2"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.32"	"1"	"1995"	"2015"	"1"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"	"0.842857142857143"	"1993"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2014"	"1"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0266313"	"Allanson Pantzar McLeod syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.64"	"1"	"2005"	"2016"	"2"	"7"	"CTD_human;ORPHANET"
"1636"	"ACE"	"0.367"	"0.897"	"C0268250"	"Gaucher Disease, Type 2 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0268251"	"Gaucher Disease, Type 3 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2013"	"2014"	"3"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2014"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0455503"	"H/O: depression"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1999"	"2015"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C0948480"	"Coronary Restenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1175175"	"Severe Acute Respiratory Syndrome"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.32"	"0.5"	"2004"	"2007"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2017"	"2"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C1318973"	"Staphylococcus aureus infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.39"	"0.555555555555556"	"1997"	"2007"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1636"	"ACE"	"0.367"	"0.897"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.883870967741936"	"1992"	"2017"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C1961835"	"Gaucher Disease, Type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C2675470"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C2678367"	"Renal Tubular Dysgenesis With Choanal Atresia And Athelia"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"1636"	"ACE"	"0.367"	"0.897"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1636"	"ACE"	"0.367"	"0.897"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1637"	"DCR"	"0.785"	"0.31"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"1994"	"2010"	"0"	"0"	"CTD_human"
"1637"	"DCR"	"0.785"	"0.31"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1637"	"DCR"	"0.785"	"0.31"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1637"	"DCR"	"0.785"	"0.31"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.45"	"0.8"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"1993"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C1843315"	"Neuronopathy, Distal Hereditary Motor, Type Viib"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"5"	"1"	"CTD_human;UNIPROT"
"1639"	"DCTN1"	"0.604"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.60"		"2003"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"1639"	"DCTN1"	"0.604"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2017"	"2"	"4"	"CTD_human;UNIPROT"
"1639"	"DCTN1"	"0.604"	"0.414"	"C1868594"	"Perry Syndrome"	"disease"	"C08;C10;C23;F01"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"6"	"8"	"CTD_human;ORPHANET;UNIPROT"
"1639"	"DCTN1"	"0.604"	"0.414"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C3203358"	"Hypoventilation"	"phenotype"	"C08;C23"	"Pathologic Function"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1639"	"DCTN1"	"0.604"	"0.414"	"C3542025"	"AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"4"	"UNIPROT"
"1639"	"DCTN1"	"0.604"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1641"	"DCX"	"0.569"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1641"	"DCX"	"0.569"	"0.517"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1641"	"DCX"	"0.569"	"0.517"	"C0265219"	"Miller Dieker syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human"
"1641"	"DCX"	"0.569"	"0.517"	"C0431375"	"Classical Lissencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2013"	"0"	"0"	"CTD_human"
"1641"	"DCX"	"0.569"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1641"	"DCX"	"0.569"	"0.517"	"C1848070"	"Lissencephaly and agenesis of corpus callosum"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"1998"	"2016"	"15"	"21"	"UNIPROT"
"1641"	"DCX"	"0.569"	"0.517"	"C1848199"	"X-Linked Lissencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2016"	"15"	"24"	"CTD_human;ORPHANET;UNIPROT"
"1641"	"DCX"	"0.569"	"0.517"	"C1848200"	"SUBCORTICAL BAND HETEROTOPIA, X-LINKED"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"15"	"21"	"UNIPROT"
"1641"	"DCX"	"0.569"	"0.517"	"C1848201"	"Subcortical Band Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.972972972972973"	"1998"	"2017"	"15"	"21"	"CTD_human;ORPHANET;UNIPROT"
"1641"	"DCX"	"0.569"	"0.517"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1641"	"DCX"	"0.569"	"0.517"	"C1955870"	"Classical Lissencephalies and Subcortical Band Heterotopias"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"1641"	"DCX"	"0.569"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1999"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"1642"	"DDB1"	"0.735"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1642"	"DDB1"	"0.735"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1642"	"DDB1"	"0.735"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1642"	"DDB1"	"0.735"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1643"	"DDB2"	"0.607"	"0.552"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"1643"	"DDB2"	"0.607"	"0.552"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1643"	"DDB2"	"0.607"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"CGI"
"1643"	"DDB2"	"0.607"	"0.552"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.59"	"1"	"1999"	"2011"	"0"	"0"	"ORPHANET"
"1643"	"DDB2"	"0.607"	"0.552"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"1643"	"DDB2"	"0.607"	"0.552"	"C1848411"	"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.90"	"0.833333333333333"	"1996"	"2014"	"2"	"4"	"CTD_human;UNIPROT"
"1643"	"DDB2"	"0.607"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1644"	"DDC"	"0.554"	"0.621"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.666666666666667"	"1996"	"2003"	"3"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"1"	"1988"	"2014"	"2"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2012"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.05"	"1"	"1998"	"2015"	"4"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0085633"	"Mood swings"	"disease"		"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0342686"	"Aromatic amino acid decarboxylase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"2004"	"2018"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"1644"	"DDC"	"0.554"	"0.621"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C1291564"	"Deficiency of aromatic-L-amino-acid decarboxylase"	"disease"		"Disease or Syndrome"	"0.80"		"1992"	"2015"	"2"	"9"	"ORPHANET;UNIPROT"
"1644"	"DDC"	"0.554"	"0.621"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1996"	"2003"	"2"	"0"	"PSYGENET"
"1644"	"DDC"	"0.554"	"0.621"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1644"	"DDC"	"0.554"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"1644"	"DDC"	"0.554"	"0.621"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0019269"	"Hermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0027661"	"Neoplasms, Hormone-Dependent"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0033804"	"Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0266362"	"Ambiguous Genitalia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C2930618"	"Intersex Conditions"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1645"	"AKR1C1"	"0.609"	"0.483"	"C2930619"	"Sex Differentiation Disorders"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0019269"	"Hermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0027661"	"Neoplasms, Hormone-Dependent"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0033804"	"Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0266362"	"Ambiguous Genitalia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C1839840"	"MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"		"1972"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C2930618"	"Intersex Conditions"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C2930619"	"Sex Differentiation Disorders"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1646"	"AKR1C2"	"0.624"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"		"2002"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"2004"	"2007"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1647"	"GADD45A"	"0.546"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"0"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0028840"	"Ocular Hypertension"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0041582"	"Ulcer"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0206634"	"Liposarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.944444444444444"	"1993"	"2018"	"3"	"0"	"CTD_human;ORPHANET"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"1649"	"DDIT3"	"0.489"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1649"	"DDIT3"	"0.489"	"0.724"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1650"	"DDOST"	"0.713"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1650"	"DDOST"	"0.713"	"0.552"	"C3281084"	"Congenital disorder of glycosylation type 1r"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.70"		"2012"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1650"	"DDOST"	"0.713"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1653"	"DDX1"	"0.672"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0014173"	"Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0349578"	"Complex Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0349579"	"Atypical Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0456483"	"Simple Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1653"	"DDX1"	"0.672"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2017"	"0"	"0"	"UNIPROT"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1654"	"DDX3X"	"0.607"	"0.655"	"C0796184"	"Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence"	"disease"	"C05;C07;C10;C12;C13;C14;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"1654"	"DDX3X"	"0.607"	"0.655"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1654"	"DDX3X"	"0.607"	"0.655"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1654"	"DDX3X"	"0.607"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1654"	"DDX3X"	"0.607"	"0.655"	"C4085582"	"MENTAL RETARDATION, X-LINKED 102"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"1"	"19"	"CTD_human;UNIPROT"
"1655"	"DDX5"	"0.676"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1655"	"DDX5"	"0.676"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1656"	"DDX6"	"0.72"	"0.345"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1657"	"DMXL1"	"0.799"	"0.138"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1657"	"DMXL1"	"0.799"	"0.138"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1657"	"DMXL1"	"0.799"	"0.138"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1662"	"DDX10"	"0.834"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"1663"	"DDX11"	"0.663"	"0.552"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1663"	"DDX11"	"0.663"	"0.552"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1663"	"DDX11"	"0.663"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"1663"	"DDX11"	"0.663"	"0.552"	"C3150658"	"WARSAW BREAKAGE SYNDROME"	"disease"		"Disease or Syndrome"	"0.78"	"1"	"2010"	"2018"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1663"	"DDX11"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"1665"	"DHX15"	"0.773"	"0.241"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1665"	"DHX15"	"0.773"	"0.241"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1665"	"DHX15"	"0.773"	"0.241"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1666"	"DECR1"	"0.472"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1666"	"DECR1"	"0.472"	"0.759"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"1666"	"DECR1"	"0.472"	"0.759"	"C1857252"	"2,4-Dienoyl-CoA Reductase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1666"	"DECR1"	"0.472"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"1668"	"DEFA3"	"0.72"	"0.448"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1669"	"DEFA4"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0031269"	"Peutz-Jeghers Syndrome"	"disease"	"C04;C06;C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1670"	"DEFA5"	"0.743"	"0.345"	"C0206677"	"Adenomatous Polyps"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1671"	"DEFA6"	"0.857"	"0.069"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1672"	"DEFB1"	"0.555"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1672"	"DEFB1"	"0.555"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1672"	"DEFB1"	"0.555"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1672"	"DEFB1"	"0.555"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"1672"	"DEFB1"	"0.555"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1673"	"DEFB4A"	"0.551"	"0.724"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1996"	"2013"	"0"	"2"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.33"	"1"	"1995"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2007"	"0"	"0"	"ORPHANET"
"1674"	"DES"	"0.503"	"0.759"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.45"	"1"	"2010"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"0.5"	"1994"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1674"	"DES"	"0.503"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C1832370"	"MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED"	"disease"	"C05;C10;C14;C16"	"Disease or Syndrome"	"1.00"	"1"	"1989"	"2017"	"32"	"41"	"CLINGEN;ORPHANET;UNIPROT"
"1674"	"DES"	"0.503"	"0.759"	"C1858154"	"CARDIOMYOPATHY, DILATED, 1I"	"disease"	"C14"	"Disease or Syndrome"	"0.80"		"1996"	"2016"	"3"	"3"	"CTD_human;UNIPROT"
"1674"	"DES"	"0.503"	"0.759"	"C1867005"	"Scapuloperoneal Syndrome, Neurogenic, Kaeser Type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1964"	"2015"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1674"	"DES"	"0.503"	"0.759"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C2678065"	"Myofibrillar Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"	"0.962962962962963"	"2000"	"2016"	"0"	"5"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C3148763"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1674"	"DES"	"0.503"	"0.759"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1674"	"DES"	"0.503"	"0.759"	"C3809137"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R"	"disease"		"Disease or Syndrome"	"0.60"		"2000"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"1675"	"CFD"	"0.672"	"0.448"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0025303"	"Meningococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0085396"	"Neisseriaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C0398764"	"Complement Factor D Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.70"		"2001"	"2006"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1675"	"CFD"	"0.672"	"0.448"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1675"	"CFD"	"0.672"	"0.448"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1678"	"TIMM8A"	"0.558"	"0.724"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1678"	"TIMM8A"	"0.558"	"0.724"	"C0796074"	"MOHR-TRANEBJAERG SYNDROME"	"disease"	"C09;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.80"	"0.944444444444444"	"1992"	"2014"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"1678"	"TIMM8A"	"0.558"	"0.724"	"C1839564"	"Jensen syndrome"	"disease"	"C09;C10;C11;C23;F03"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2002"	"4"	"1"	"CTD_human;UNIPROT"
"1678"	"TIMM8A"	"0.558"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1687"	"GSDME"	"0.743"	"0.276"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1687"	"GSDME"	"0.743"	"0.276"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"		"2008"	"2012"	"1"	"0"	"CTD_human"
"1687"	"GSDME"	"0.743"	"0.276"	"C1832932"	"DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"CTD_human"
"1690"	"COCH"	"0.735"	"0.172"	"C1832425"	"Deafness, Autosomal Dominant 9"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.86"	"1"	"1997"	"2016"	"13"	"10"	"CTD_human;UNIPROT"
"1690"	"COCH"	"0.735"	"0.172"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"1714"	"DGCR"	"0.707"	"0.483"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2015"	"0"	"0"	"CTD_human"
"1714"	"DGCR"	"0.707"	"0.483"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2011"	"0"	"0"	"CTD_human"
"1714"	"DGCR"	"0.707"	"0.483"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1716"	"DGUOK"	"0.616"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1716"	"DGUOK"	"0.616"	"0.448"	"C0010398"	"Cruveilhier-Baumgarten Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1716"	"DGUOK"	"0.616"	"0.448"	"C0020541"	"Hypertension, Portal"	"disease"	"C06"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"1716"	"DGUOK"	"0.616"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1716"	"DGUOK"	"0.616"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"1716"	"DGUOK"	"0.616"	"0.448"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"1716"	"DGUOK"	"0.616"	"0.448"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2002"	"2002"	"2"	"0"	"GENOMICS_ENGLAND"
"1716"	"DGUOK"	"0.616"	"0.448"	"C3151513"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2014"	"2"	"12"	"CTD_human;ORPHANET;UNIPROT"
"1716"	"DGUOK"	"0.616"	"0.448"	"C3711385"	"Deoxyguanosine Kinase Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1716"	"DGUOK"	"0.616"	"0.448"	"C4310733"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1716"	"DGUOK"	"0.616"	"0.448"	"C4310735"	"PORTAL HYPERTENSION, NONCIRRHOTIC"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2017"	"2"	"1"	"ORPHANET;UNIPROT"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0175694"	"Smith-Lemli-Opitz Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.976744186046512"	"1993"	"2018"	"17"	"63"	"CTD_human;ORPHANET;UNIPROT"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0282643"	"Smith-Lemli-Opitz Syndrome, Type I"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2017"	"10"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0282644"	"Smith-Lemli-Opitz Syndrome, Type II"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2017"	"10"	"0"	"CTD_human"
"1717"	"DHCR7"	"0.527"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1717"	"DHCR7"	"0.527"	"0.759"	"C2713347"	"7-Dehydrocholesterol Reductase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2017"	"10"	"0"	"CTD_human;ORPHANET"
"1717"	"DHCR7"	"0.527"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2000"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.95"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2001"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0034362"	"Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0519066"	"Acute Q fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C1443892"	"Chronic Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C1865596"	"Desmosterolosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"2001"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1718"	"DHCR24"	"0.572"	"0.655"	"C2973787"	"Coxiella burnetii Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1718"	"DHCR24"	"0.572"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1719"	"DHFR"	"0.54"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0002888"	"Anemia, Megaloblastic"	"disease"	"C15"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"1987"	"2014"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1983"	"2017"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"1719"	"DHFR"	"0.54"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0016412"	"Folic Acid Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"1719"	"DHFR"	"0.54"	"0.759"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1983"	"2017"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2017"	"2"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C2751584"	"Neurodegeneration Due To Cerebral Folate Transport Deficiency"	"phenotype"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"1719"	"DHFR"	"0.54"	"0.759"	"C3151205"	"Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.71"	"1"	"1975"	"2011"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1719"	"DHFR"	"0.54"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1719"	"DHFR"	"0.54"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1719"	"DHFR"	"0.54"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0023440"	"Acute Erythroblastic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C0265257"	"Genee-Wiedemann syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.74"	"1"	"2010"	"2013"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"1723"	"DHODH"	"0.621"	"0.621"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"1723"	"DHODH"	"0.621"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C0010520"	"Cyanosis"	"phenotype"	"C23"	"Sign or Symptom"	"0.43"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C0025637"	"Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"1"	"1983"	"2011"	"1"	"0"	"CTD_human"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C0268193"	"NADH cytochrome B5 reductase deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.50"		"1991"	"2010"	"11"	"9"	"CTD_human;UNIPROT"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C0272087"	"Congenital Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"1"	"1980"	"2013"	"0"	"1"	"ORPHANET"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C2749559"	"Methemoglobinemia, Type I"	"disease"	"C15"	"Disease or Syndrome"	"0.66"	"1"	"1948"	"2011"	"11"	"11"	"CTD_human;UNIPROT"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C2749560"	"Methemoglobinemia, Type Ii"	"disease"	"C15"	"Disease or Syndrome"	"0.63"	"1"	"1990"	"2011"	"11"	"17"	"CTD_human;UNIPROT"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C2749561"	"Nadh-Cytochrome B5 Reductase Deficiency, Type I"	"disease"	"C15"	"Disease or Syndrome"	"0.50"		"1991"	"2010"	"11"	"9"	"CTD_human;UNIPROT"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C2749562"	"Nadh-Cytochrome B5 Reductase Deficiency, Type Ii"	"disease"	"C15"	"Disease or Syndrome"	"0.50"		"1991"	"2010"	"11"	"9"	"CTD_human;UNIPROT"
"1727"	"CYB5R3"	"0.672"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1987"	"1987"	"0"	"0"	"GENOMICS_ENGLAND"
"1728"	"NQO1"	"0.467"	"0.724"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.38"	"0.875"	"2003"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.58"	"0.875"	"1996"	"2015"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.923076923076923"	"1996"	"2015"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.88"	"2000"	"2017"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"2"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2012"	"2017"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2002"	"2010"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2012"	"2"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"2011"	"2"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"1997"	"2007"	"4"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.05"	"0.6"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"1728"	"NQO1"	"0.467"	"0.724"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.01"	"0"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1728"	"NQO1"	"0.467"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1728"	"NQO1"	"0.467"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.884615384615385"	"2000"	"2017"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C2608079"	"WARFARIN SENSITIVITY (disorder)"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1728"	"NQO1"	"0.467"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.70"		"1997"	"2018"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C4225261"	"SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"1729"	"DIAPH1"	"0.659"	"0.517"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1730"	"DIAPH2"	"0.773"	"0.207"	"C1845293"	"Premature Ovarian Failure 2a"	"disease"	"C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1730"	"DIAPH2"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1733"	"DIO1"	"0.696"	"0.448"	"C0020551"	"Hyperthyroxinemia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"1733"	"DIO1"	"0.696"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"1733"	"DIO1"	"0.696"	"0.448"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1733"	"DIO1"	"0.696"	"0.448"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1734"	"DIO2"	"0.642"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1734"	"DIO2"	"0.642"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1734"	"DIO2"	"0.642"	"0.448"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1734"	"DIO2"	"0.642"	"0.448"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1734"	"DIO2"	"0.642"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1734"	"DIO2"	"0.642"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1735"	"DIO3"	"0.663"	"0.517"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1735"	"DIO3"	"0.663"	"0.517"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1736"	"DKC1"	"0.575"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1998"	"2000"	"4"	"0"	"GENOMICS_ENGLAND"
"1736"	"DKC1"	"0.575"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2000"	"4"	"0"	"GENOMICS_ENGLAND"
"1736"	"DKC1"	"0.575"	"0.69"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.90"	"1"	"1998"	"2018"	"2"	"2"	"CTD_human;ORPHANET"
"1736"	"DKC1"	"0.575"	"0.69"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"1998"	"2000"	"2"	"0"	"GENOMICS_ENGLAND"
"1736"	"DKC1"	"0.575"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"1736"	"DKC1"	"0.575"	"0.69"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"0.916666666666667"	"1986"	"2018"	"13"	"38"	"CTD_human;UNIPROT"
"1736"	"DKC1"	"0.575"	"0.69"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2017"	"11"	"22"	"ORPHANET;UNIPROT"
"1736"	"DKC1"	"0.575"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1736"	"DKC1"	"0.575"	"0.69"	"C3806774"	"GROWTH RETARDATION, PRENATAL, WITH PROGRESSIVE PANCYTOPENIA AND CEREBELLAR HYPOPLASIA"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2015"	"11"	"22"	"UNIPROT"
"1737"	"DLAT"	"0.602"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1737"	"DLAT"	"0.602"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1737"	"DLAT"	"0.602"	"0.655"	"C1855565"	"Pyruvate Dehydrogenase E2 Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"1737"	"DLAT"	"0.602"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1738"	"DLD"	"0.572"	"0.621"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1738"	"DLD"	"0.572"	"0.621"	"C0268193"	"NADH cytochrome B5 reductase deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.59"	"1"	"1981"	"2014"	"12"	"10"	"ORPHANET;UNIPROT"
"1738"	"DLD"	"0.572"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1738"	"DLD"	"0.572"	"0.621"	"C3492932"	"Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"1738"	"DLD"	"0.572"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"1739"	"DLG1"	"0.696"	"0.552"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1739"	"DLG1"	"0.696"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2002"	"2018"	"3"	"0"	"CTD_human"
"1739"	"DLG1"	"0.696"	"0.552"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1739"	"DLG1"	"0.696"	"0.552"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1739"	"DLG1"	"0.696"	"0.552"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1739"	"DLG1"	"0.696"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"1740"	"DLG2"	"0.743"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2007"	"2"	"0"	"PSYGENET"
"1740"	"DLG2"	"0.743"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1740"	"DLG2"	"0.743"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"0.75"	"2003"	"2016"	"4"	"1"	"PSYGENET"
"1740"	"DLG2"	"0.743"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1740"	"DLG2"	"0.743"	"0.31"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"1740"	"DLG2"	"0.743"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1740"	"DLG2"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1741"	"DLG3"	"0.575"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2008"	"4"	"0"	"PSYGENET"
"1741"	"DLG3"	"0.575"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.4"	"2003"	"2008"	"5"	"0"	"PSYGENET"
"1741"	"DLG3"	"0.575"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2008"	"3"	"0"	"PSYGENET"
"1741"	"DLG3"	"0.575"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2006"	"2"	"0"	"PSYGENET"
"1741"	"DLG3"	"0.575"	"0.414"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1984"	"2011"	"1"	"0"	"CTD_human"
"1741"	"DLG3"	"0.575"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2008"	"3"	"0"	"PSYGENET"
"1741"	"DLG3"	"0.575"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1741"	"DLG3"	"0.575"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1741"	"DLG3"	"0.575"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2017"	"0"	"0"	"ORPHANET"
"1741"	"DLG3"	"0.575"	"0.414"	"C3275443"	"MENTAL RETARDATION, X-LINKED 90 (disorder)"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2017"	"0"	"5"	"CTD_human"
"1741"	"DLG3"	"0.575"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.833333333333333"	"1999"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1742"	"DLG4"	"0.648"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2017"	"4"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1742"	"DLG4"	"0.648"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.333333333333333"	"2001"	"2017"	"3"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2018"	"4"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1742"	"DLG4"	"0.648"	"0.448"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2012"	"3"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1742"	"DLG4"	"0.648"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2018"	"4"	"0"	"PSYGENET"
"1742"	"DLG4"	"0.648"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1742"	"DLG4"	"0.648"	"0.448"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1742"	"DLG4"	"0.648"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"1743"	"DLST"	"0.815"	"0.345"	"C0349464"	"Wernicke-Korsakoff Syndrome"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"1743"	"DLST"	"0.815"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1745"	"DLX1"	"0.752"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1745"	"DLX1"	"0.752"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"1745"	"DLX1"	"0.752"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"PSYGENET"
"1745"	"DLX1"	"0.752"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"1745"	"DLX1"	"0.752"	"0.31"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"PSYGENET"
"1745"	"DLX1"	"0.752"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1745"	"DLX1"	"0.752"	"0.31"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1746"	"DLX2"	"0.735"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1746"	"DLX2"	"0.735"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"1747"	"DLX3"	"0.707"	"0.31"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.45"	"1"	"1998"	"2017"	"6"	"1"	"GENOMICS_ENGLAND"
"1747"	"DLX3"	"0.707"	"0.31"	"C0265333"	"Tricho-dento-osseous syndrome (disorder)"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.70"	"0.923076923076923"	"1998"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"1747"	"DLX3"	"0.707"	"0.31"	"C0399373"	"Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1747"	"DLX3"	"0.707"	"0.31"	"C1863012"	"Amelogenesis Imperfecta, Type IV"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.61"	"1"	"2005"	"2008"	"0"	"1"	"CTD_human;ORPHANET"
"1748"	"DLX4"	"0.656"	"0.448"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1748"	"DLX4"	"0.656"	"0.448"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1748"	"DLX4"	"0.656"	"0.448"	"C4225209"	"OROFACIAL CLEFT 15"	"disease"		"Congenital Abnormality"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"1749"	"DLX5"	"0.636"	"0.552"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1749"	"DLX5"	"0.636"	"0.552"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.52"	"1"	"2002"	"2015"	"0"	"0"	"ORPHANET"
"1749"	"DLX5"	"0.636"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1999"	"2016"	"3"	"0"	"CTD_human"
"1749"	"DLX5"	"0.636"	"0.552"	"C1857344"	"Split-Hand-Foot Malformation With Sensorineural Hearing Loss"	"disease"	"C05;C09;C10;C16;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1750"	"DLX6"	"0.713"	"0.517"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"		"2002"	"2008"	"0"	"0"	"ORPHANET"
"1750"	"DLX6"	"0.713"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1755"	"DMBT1"	"0.573"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"1755"	"DMBT1"	"0.573"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1755"	"DMBT1"	"0.573"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2002"	"0"	"1"	"UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.90"	"0.9375"	"1993"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"0.968794326241135"	"1982"	"2018"	"16"	"350"	"CTD_human;ORPHANET;UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0023269"	"leiomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"	"0.962655601659751"	"1985"	"2018"	"4"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0026851"	"Muscular Dystrophy, Animal"	"disease"	"C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"3"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.50"	"0.869565217391304"	"1987"	"2018"	"1"	"1"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0205815"	"Leiomyosarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0205816"	"Leiomyosarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0206656"	"Embryonal Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2010"	"0"	"0"	"ORPHANET"
"1756"	"DMD"	"0.477"	"0.724"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"0.947368421052632"	"1989"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"1996"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1756"	"DMD"	"0.477"	"0.724"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.90625"	"1993"	"2016"	"3"	"1"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C0917713"	"Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.970037453183521"	"1984"	"2018"	"11"	"191"	"CTD_human;ORPHANET;UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.941176470588235"	"1994"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1756"	"DMD"	"0.477"	"0.724"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C3542021"	"Duchenne and Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"0.970588235294118"	"1987"	"2018"	"10"	"0"	"CTD_human"
"1756"	"DMD"	"0.477"	"0.724"	"C3668940"	"Dmd-Associated Dilated Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2018"	"3"	"120"	"CTD_human;UNIPROT"
"1756"	"DMD"	"0.477"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.923076923076923"	"1991"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1757"	"SARDH"	"0.611"	"0.552"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1757"	"SARDH"	"0.611"	"0.552"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1757"	"SARDH"	"0.611"	"0.552"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1757"	"SARDH"	"0.611"	"0.552"	"C0268563"	"Sarcosinemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2013"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1757"	"SARDH"	"0.611"	"0.552"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1758"	"DMP1"	"0.609"	"0.517"	"C0342643"	"Autosomal recessive hypophosphatemic vitamin D refractory rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.84"	"1"	"2007"	"2011"	"0"	"4"	"CTD_human;ORPHANET"
"1758"	"DMP1"	"0.609"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1759"	"DNM1"	"0.667"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"PSYGENET"
"1759"	"DNM1"	"0.667"	"0.345"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2016"	"10"	"0"	"CLINGEN"
"1759"	"DNM1"	"0.667"	"0.345"	"C0238111"	"Lennox-Gastaut syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1759"	"DNM1"	"0.667"	"0.345"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2016"	"10"	"0"	"CLINGEN"
"1759"	"DNM1"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2014"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"1759"	"DNM1"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1759"	"DNM1"	"0.667"	"0.345"	"C4225357"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"3"	"6"	"CTD_human;UNIPROT"
"1760"	"DMPK"	"0.627"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1993"	"2"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0027125"	"Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C0027126"	"Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"0.973451327433628"	"1992"	"2018"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1760"	"DMPK"	"0.627"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0410226"	"Congenital Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1760"	"DMPK"	"0.627"	"0.69"	"C0751358"	"Myotonic Phenomenon"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C0751359"	"Percussion Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C2931689"	"Dystrophia myotonica 2"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1760"	"DMPK"	"0.627"	"0.69"	"C3250443"	"MYOTONIC DYSTROPHY 1"	"disease"		"Disease or Syndrome"	"0.50"	"0.974358974358974"	"1995"	"2017"	"0"	"1"	"ORPHANET"
"1760"	"DMPK"	"0.627"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1761"	"DMRT1"	"0.592"	"0.414"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1763"	"DNA2"	"0.663"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1763"	"DNA2"	"0.663"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1763"	"DNA2"	"0.663"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1763"	"DNA2"	"0.663"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1763"	"DNA2"	"0.663"	"0.552"	"C3554599"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 6"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1763"	"DNA2"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"1767"	"DNAH5"	"0.659"	"0.448"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1767"	"DNAH5"	"0.659"	"0.448"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2016"	"0"	"2"	"ORPHANET"
"1767"	"DNAH5"	"0.659"	"0.448"	"C1837618"	"CILIARY DYSKINESIA, PRIMARY, 3"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2017"	"4"	"17"	"CTD_human;UNIPROT"
"1767"	"DNAH5"	"0.659"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1767"	"DNAH5"	"0.659"	"0.448"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2014"	"4"	"0"	"PSYGENET"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1769"	"DNAH8"	"0.51"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"UNIPROT"
"1769"	"DNAH8"	"0.51"	"0.759"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1770"	"DNAH9"	"0.857"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"1773"	"DNASE1"	"0.588"	"0.552"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2016"	"0"	"0"	"CTD_human"
"1773"	"DNASE1"	"0.588"	"0.552"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1773"	"DNASE1"	"0.588"	"0.552"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1773"	"DNASE1"	"0.588"	"0.552"	"C3280742"	"SYSTEMIC LUPUS ERYTHEMATOSUS 16"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1775"	"DNASE1L2"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1775"	"DNASE1L2"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2011"	"2"	"2"	"UNIPROT"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.44"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C0343206"	"Hypocomplementemic urticarial vasculitis"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1776"	"DNASE1L3"	"0.645"	"0.483"	"C3280742"	"SYSTEMIC LUPUS ERYTHEMATOSUS 16"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.47"	"1"	"1993"	"2016"	"2"	"2"	"GENOMICS_ENGLAND"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0043116"	"HMN (Hereditary Motor Neuropathy) Proximal Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0152109"	"Juvenile Spinal Muscular Atrophy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0393538"	"Muscular Atrophy, Spinal, Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0700595"	"Spinal Muscular Atrophies of Childhood"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C1834690"	"Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2003"	"2018"	"6"	"8"	"ORPHANET;UNIPROT"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.53"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C2931358"	"Muscular atrophy, spinal, infantile chronic form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3280220"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3281202"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 13"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2010"	"2018"	"4"	"14"	"CTD_human;UNIPROT"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.66"	"1"	"2010"	"2018"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1778"	"DYNC1H1"	"0.596"	"0.552"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1780"	"DYNC1I1"	"0.886"	"0.069"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1783"	"DYNC1LI2"			"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.95"	"2005"	"2017"	"0"	"1"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.43"	"1"	"2007"	"2014"	"1"	"1"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"	"0.928571428571429"	"2006"	"2017"	"10"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1785"	"DNM2"	"0.54"	"0.655"	"C1847902"	"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2005"	"2017"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"1785"	"DNM2"	"0.54"	"0.655"	"C1847903"	"Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2009"	"4"	"4"	"UNIPROT"
"1785"	"DNM2"	"0.54"	"0.655"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1785"	"DNM2"	"0.54"	"0.655"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1785"	"DNM2"	"0.54"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1785"	"DNM2"	"0.54"	"0.655"	"C3809272"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2016"	"2"	"0"	"PSYGENET"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0020074"	"HSAN Type IV"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.75"	"2001"	"2018"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0027889"	"Hereditary Sensory and Autonomic Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2016"	"4"	"0"	"PSYGENET"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2011"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0086405"	"Hereditary Sensory Radicular Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0699739"	"Sensory Neuropathy, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2018"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2005"	"2018"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C1858804"	"Cerebellar Ataxia, Deafness, and Narcolepsy"	"disease"	"C09;C10;C23;F03"	"Disease or Syndrome"	"0.62"	"1"	"1996"	"2017"	"9"	"3"	"CLINGEN;CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C2931852"	"Clear-cell metastatic renal cell carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1786"	"DNMT1"	"0.438"	"0.759"	"C3279885"	"Hereditary Sensory and Autonomic Neuropathy Type Ie"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"1995"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1786"	"DNMT1"	"0.438"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1786"	"DNMT1"	"0.438"	"0.759"	"C3807295"	"CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.65"	"1"	"2011"	"2017"	"9"	"3"	"CLINGEN;ORPHANET;UNIPROT"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2010"	"2017"	"1"	"2"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0020981"	"Angioimmunoblastic Lymphadenopathy"	"disease"	"C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0023465"	"Acute monocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.982758620689655"	"2009"	"2018"	"0"	"2"	"CGI;CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"3"	"UNIPROT"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C2931852"	"Clear-cell metastatic renal cell carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1788"	"DNMT3A"	"0.507"	"0.69"	"C4014545"	"TATTON-BROWN-RAHMAN SYNDROME"	"disease"		"Disease or Syndrome"	"0.73"	"1"	"2014"	"2018"	"3"	"16"	"CTD_human;ORPHANET;UNIPROT"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"0.875"	"2004"	"2015"	"2"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.44"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0398788"	"Immunodeficiency syndrome, variable"	"disease"	"C20"	"Disease or Syndrome"	"0.82"	"1"	"1988"	"2016"	"11"	"13"	"CTD_human;UNIPROT"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"2004"	"2015"	"2"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.5"	"2004"	"2012"	"2"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1656427"	"Early onset schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C1834671"	"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"1789"	"DNMT3B"	"0.495"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2008"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1793"	"DOCK1"	"0.69"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1794"	"DOCK2"	"0.799"	"0.138"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1794"	"DOCK2"	"0.799"	"0.138"	"C4225328"	"IMMUNODEFICIENCY 40"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1795"	"DOCK3"	"0.707"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"1796"	"DOK1"	"0.707"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1796"	"DOK1"	"0.707"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1796"	"DOK1"	"0.707"	"0.345"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1796"	"DOK1"	"0.707"	"0.345"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.56"	"1"	"2012"	"2017"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C2931004"	"Congenital disorder of glycosylation type 1J"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"2004"	"2016"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C3553645"	"MYASTHENIC SYNDROME, CONGENITAL, 13"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"7"	"UNIPROT"
"1798"	"DPAGT1"	"0.63"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"1800"	"DPEP1"	"0.667"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"1"	"UNIPROT"
"1801"	"DPH1"	"0.663"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2011"	"0"	"2"	"UNIPROT"
"1801"	"DPH1"	"0.663"	"0.517"	"C4310801"	"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1803"	"DPP4"	"0.5"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"1803"	"DPP4"	"0.5"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"1803"	"DPP4"	"0.5"	"0.69"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"1804"	"DPP6"	"0.652"	"0.552"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.47"	"0.857142857142857"	"2008"	"2014"	"1"	"1"	"CTD_human"
"1804"	"DPP6"	"0.652"	"0.552"	"C0220693"	"Microcephaly autosomal dominant"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"1804"	"DPP6"	"0.652"	"0.552"	"C0340493"	"Paroxysmal familial ventricular fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.53"	"1"	"2009"	"2016"	"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1804"	"DPP6"	"0.652"	"0.552"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1804"	"DPP6"	"0.652"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1804"	"DPP6"	"0.652"	"0.552"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1804"	"DPP6"	"0.652"	"0.552"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human"
"1804"	"DPP6"	"0.652"	"0.552"	"C2751898"	"Ventricular Fibrillation, Paroxysmal Familial, 1"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1804"	"DPP6"	"0.652"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1804"	"DPP6"	"0.652"	"0.552"	"C4017668"	"VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"1804"	"DPP6"	"0.652"	"0.552"	"C4225375"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 33"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"1805"	"DPT"	"0.696"	"0.517"	"C0042345"	"Varicosity"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1805"	"DPT"	"0.696"	"0.517"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"1806"	"DPYD"	"0.52"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1806"	"DPYD"	"0.52"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.966666666666667"	"1998"	"2018"	"5"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.833333333333333"	"1999"	"2009"	"5"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2016"	"3"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0034139"	"Purine-Pyrimidine Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1988"	"2005"	"2"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2016"	"2"	"2"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2016"	"3"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0274576"	"Poisoning by fluorouracil"	"disease"		"Injury or Poisoning"	"0.50"		"1997"	"2006"	"4"	"3"	"ORPHANET;UNIPROT"
"1806"	"DPYD"	"0.52"	"0.69"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2011"	"2"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1806"	"DPYD"	"0.52"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"		"2002"	"2009"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"1998"	"2018"	"5"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C1959620"	"Dihydropyrimidine Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.870967741935484"	"1988"	"2017"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1806"	"DPYD"	"0.52"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C3495551"	"Dihydropyrimidinuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"1806"	"DPYD"	"0.52"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"1806"	"DPYD"	"0.52"	"0.69"	"C4304578"	"1p21.3 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1807"	"DPYS"	"0.681"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1807"	"DPYS"	"0.681"	"0.414"	"C0342803"	"Dihydropyrimidinase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1997"	"2007"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1807"	"DPYS"	"0.681"	"0.414"	"C3495551"	"Dihydropyrimidinuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1998"	"2010"	"1"	"3"	"ORPHANET;UNIPROT"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.75"	"2003"	"2009"	"4"	"0"	"PSYGENET"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0011251"	"Delusional disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1808"	"DPYSL2"	"0.63"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1811"	"SLC26A3"	"0.624"	"0.621"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"0"	"2002"	"2010"	"1"	"0"	"CTD_human"
"1811"	"SLC26A3"	"0.624"	"0.621"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1811"	"SLC26A3"	"0.624"	"0.621"	"C0267662"	"Congenital chloride diarrhea"	"disease"	"C16;C18;C23"	"Disease or Syndrome"	"0.99"	"0.888888888888889"	"1996"	"2018"	"10"	"54"	"CTD_human;ORPHANET;UNIPROT"
"1812"	"DRD1"	"0.555"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"1812"	"DRD1"	"0.555"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1992"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"1812"	"DRD1"	"0.555"	"0.517"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1995"	"3"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2010"	"4"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2007"	"2014"	"3"	"0"	"PSYGENET"
"1812"	"DRD1"	"0.555"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2014"	"3"	"0"	"PSYGENET"
"1812"	"DRD1"	"0.555"	"0.517"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1992"	"2003"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.52"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.96"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1991"	"2008"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1992"	"1992"	"1"	"0"	"PSYGENET"
"1812"	"DRD1"	"0.555"	"0.517"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1988"	"1995"	"3"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2010"	"4"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2014"	"4"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1812"	"DRD1"	"0.555"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1990"	"2017"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2010"	"5"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1991"	"2016"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1998"	"4"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2000"	"2014"	"14"	"0"	"CTD_human;PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"2"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1993"	"2014"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.38"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2010"	"5"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.37"	"0.857142857142857"	"2002"	"2018"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2004"	"2016"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1992"	"2003"	"4"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0021122"	"Disruptive, Impulse Control, and Conduct Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2007"	"2012"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0021776"	"Intermittent Explosive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0022734"	"Kleptomania"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0023015"	"Language Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.5"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"1983"	"2012"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.935483870967742"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.916666666666667"	"1991"	"2018"	"4"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1993"	"2010"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"1998"	"2016"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"1994"	"2016"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1992"	"1992"	"1"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1988"	"1998"	"4"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2010"	"10"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1990"	"2015"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1992"	"2000"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0454560"	"Acquired Language Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1996"	"2015"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1994"	"2014"	"15"	"0"	"CTD_human;PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1993"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2010"	"5"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2014"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2004"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.954545454545455"	"2000"	"2016"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"1998"	"2016"	"5"	"0"	"PSYGENET"
"1813"	"DRD2"	"0.454"	"0.724"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C1834570"	"Myoclonic dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.57"	"1"	"1999"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"1813"	"DRD2"	"0.454"	"0.724"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"1997"	"2013"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1813"	"DRD2"	"0.454"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1813"	"DRD2"	"0.454"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2002"	"3"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1996"	"2015"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1993"	"2014"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1999"	"2010"	"6"	"0"	"CTD_human;PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1996"	"2010"	"2"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2013"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2013"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0016995"	"Gambling"	"phenotype"	"F01;F03"	"Individual Behavior"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0021122"	"Disruptive, Impulse Control, and Conduct Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0021776"	"Intermittent Explosive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0022734"	"Kleptomania"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0030662"	"Gambling, Pathological"	"disease"	"F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.908163265306122"	"1993"	"2016"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0040517"	"Gilles de la Tourette syndrome"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.34"	"0.75"	"1995"	"2015"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1993"	"2015"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1993"	"1993"	"1"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2010"	"5"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2002"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1994"	"2000"	"4"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"0.666666666666667"	"1999"	"2010"	"7"	"0"	"CTD_human;PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1993"	"2015"	"5"	"0"	"PSYGENET"
"1814"	"DRD3"	"0.527"	"0.552"	"C1860861"	"TREMOR, HEREDITARY ESSENTIAL, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1814"	"DRD3"	"0.527"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.666666666666667"	"2005"	"2007"	"3"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2016"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0003477"	"Separation Anxiety Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"1994"	"2015"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0008074"	"Child Development Disorders, Pervasive"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0008701"	"Chronic Motor or Vocal Tic Disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2018"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2018"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0012734"	"Disruptive Behavior Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2012"	"2014"	"4"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0029121"	"Oppositional Defiant Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.729166666666667"	"1994"	"2015"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0040188"	"Tic disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0040702"	"Transient Tic Disorder"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2010"	"4"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2016"	"2"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0236964"	"Attention Deficit and Disruptive Behavior Disorders"	"phenotype"	"F03"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0338468"	"Tic Disorders, Vocal"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0524528"	"Pervasive Development Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1994"	"2007"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C0683303"	"RISK-TAKING BEHAVIOR"	"phenotype"		"Individual Behavior"	"0.30"				"0"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0751553"	"Childhood Tic Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0751554"	"Motor Tic Disorders"	"group"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C0751555"	"Post-Traumatic Tic Disorder"	"disease"	"C10;F03"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.948051948051948"	"1997"	"2018"	"3"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"1815"	"DRD4"	"0.536"	"0.414"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C1866430"	"NOVELTY SEEKING PERSONALITY TRAIT"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1815"	"DRD4"	"0.536"	"0.414"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1816"	"DRD5"	"0.636"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"1998"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"1816"	"DRD5"	"0.636"	"0.241"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0005747"	"Blepharospasm"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0040485"	"Torticollis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0152116"	"Spasmodic torticollis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0349785"	"Torticollis, Psychogenic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0426785"	"Torticollis, Intermittent"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C0949445"	"Cervical Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2001"	"2003"	"1"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.944444444444444"	"2000"	"2013"	"2"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"1816"	"DRD5"	"0.636"	"0.241"	"C2930898"	"Benign essential blepharospasm"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human"
"1821"	"DRP2"	"0.815"	"0.103"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1822"	"ATN1"	"0.442"	"0.828"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.947368421052632"	"1995"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"1822"	"ATN1"	"0.442"	"0.828"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1822"	"ATN1"	"0.442"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"1823"	"DSC1"	"0.799"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.50"	"0.9"	"2006"	"2017"	"0"	"6"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"1824"	"DSC2"	"0.624"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C1864850"	"Arrhythmogenic Right Ventricular Dysplasia, Familial, 11"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2017"	"4"	"9"	"CTD_human;UNIPROT"
"1824"	"DSC2"	"0.624"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1824"	"DSC2"	"0.624"	"0.345"	"C4310824"	"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2017"	"4"	"3"	"UNIPROT"
"1825"	"DSC3"	"0.685"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1825"	"DSC3"	"0.685"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1825"	"DSC3"	"0.685"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1825"	"DSC3"	"0.685"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1825"	"DSC3"	"0.685"	"0.31"	"C2751292"	"Hypotrichosis And Recurrent Skin Vesicles"	"disease"	"C17;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"1"	"ORPHANET"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1826"	"DSCAM"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"GENOMICS_ENGLAND"
"1826"	"DSCAM"	"0.707"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.975"	"1996"	"2016"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1827"	"RCAN1"	"0.63"	"0.586"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"	"0.9"	"2001"	"2018"	"1"	"2"	"GENOMICS_ENGLAND"
"1828"	"DSG1"	"0.639"	"0.414"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"1828"	"DSG1"	"0.639"	"0.414"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C2931122"	"Keratosis palmoplantaris striata 1"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1995"	"2009"	"0"	"6"	"CTD_human"
"1828"	"DSG1"	"0.639"	"0.414"	"C3809719"	"ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE"	"disease"		"Disease or Syndrome"	"0.63"	"0.666666666666667"	"2013"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"1829"	"DSG2"	"0.645"	"0.448"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1829"	"DSG2"	"0.645"	"0.448"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.50"	"1"	"2006"	"2017"	"0"	"9"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1829"	"DSG2"	"0.645"	"0.448"	"C1857777"	"Arrhythmogenic Right Ventricular Dysplasia, Familial, 10"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2017"	"4"	"15"	"CTD_human;UNIPROT"
"1829"	"DSG2"	"0.645"	"0.448"	"C2752072"	"Cardiomyopathy, Dilated, 1BB"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"5"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C0039584"	"Testicular Diseases"	"group"	"C12;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1831"	"TSC22D3"	"0.667"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2000"	"2015"	"0"	"17"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CLINGEN"
"1832"	"DSP"	"0.532"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.31"		"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"	"1"	"1999"	"2017"	"11"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.40"		"2010"	"2015"	"1"	"1"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"1832"	"DSP"	"0.532"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.50"	"0.956521739130435"	"2003"	"2018"	"0"	"23"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2000"	"2017"	"11"	"0"	"GENOMICS_ENGLAND"
"1832"	"DSP"	"0.532"	"0.69"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"1832"	"DSP"	"0.532"	"0.69"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C1720824"	"Sudden Cardiac Arrest"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"2013"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"1832"	"DSP"	"0.532"	"0.69"	"C1843292"	"Skin Fragility-Woolly Hair Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.72"	"1"	"2002"	"2011"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1832"	"DSP"	"0.532"	"0.69"	"C1843896"	"Arrhythmogenic Right Ventricular Dysplasia, Familial, 8"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.80"		"2000"	"2017"	"3"	"24"	"CTD_human;UNIPROT"
"1832"	"DSP"	"0.532"	"0.69"	"C1852127"	"KERATOSIS PALMOPLANTARIS STRIATA II"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1999"	"2011"	"0"	"3"	"CTD_human"
"1832"	"DSP"	"0.532"	"0.69"	"C1854063"	"Cardiomyopathy dilated with Woolly hair and keratoderma"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.86"	"0.833333333333333"	"1996"	"2017"	"1"	"11"	"CTD_human;ORPHANET"
"1832"	"DSP"	"0.532"	"0.69"	"C1864826"	"Epidermolysis bullosa, lethal acantholytic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.63"	"1"	"2005"	"2011"	"0"	"4"	"CTD_human;ORPHANET"
"1832"	"DSP"	"0.532"	"0.69"	"C3809719"	"ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1832"	"DSP"	"0.532"	"0.69"	"C4014393"	"CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2013"	"3"	"4"	"CTD_human;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1834"	"DSPP"	"0.633"	"0.483"	"C0011436"	"Dentinogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.50"	"0.935483870967742"	"1992"	"2017"	"0"	"0"	"CTD_human"
"1834"	"DSPP"	"0.633"	"0.483"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1834"	"DSPP"	"0.633"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1834"	"DSPP"	"0.633"	"0.483"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"1834"	"DSPP"	"0.633"	"0.483"	"C0205730"	"Hereditary Opalescent Dentin (disorder)"	"disease"	"C07;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2001"	"2012"	"0"	"3"	"CTD_human"
"1834"	"DSPP"	"0.633"	"0.483"	"C0399378"	"Dentinogenesis imperfecta - Shield's type III (disorder)"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.71"	"1"	"2001"	"2013"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C0399379"	"Dentin dysplasia, type 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"1834"	"DSPP"	"0.633"	"0.483"	"C0399380"	"Dentin dyspalsia, Shields type 2"	"disease"	"C07"	"Congenital Abnormality"	"0.67"	"1"	"1998"	"2015"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C1527284"	"Dental Pulp Stone"	"disease"	"C07"	"Disease or Syndrome"	"0.60"		"2003"	"2009"	"2"	"1"	"CTD_human;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C1854146"	"Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1"	"disease"	"C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.50"		"2001"	"2012"	"2"	"2"	"CTD_human;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C2973527"	"Dentinogenesis imperfecta without osteogenesis imperfecta"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.66"	"1"	"1998"	"2012"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1834"	"DSPP"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1834"	"DSPP"	"0.633"	"0.483"	"C4049050"	"Opalescent dentin"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2001"	"0"	"0"	"CTD_human"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0013447"	"Ear Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0022821"	"Kyphosis deformity of spine"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.49"	"0.888888888888889"	"2001"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0220726"	"Diastrophic dysplasia"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.90"	"1"	"1972"	"2017"	"0"	"48"	"CTD_human;ORPHANET"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0265274"	"Achondrogenesis, type IB (disorder)"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.79"	"1"	"1994"	"2017"	"1"	"30"	"CTD_human;ORPHANET;UNIPROT"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C1847593"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 4"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"1994"	"2017"	"2"	"32"	"CTD_human;ORPHANET;UNIPROT"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C1850554"	"Atelosteogenesis type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.77"	"1"	"1994"	"2017"	"1"	"30"	"CTD_human;ORPHANET;UNIPROT"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C1850555"	"De La Chapelle Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1972"	"2009"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1836"	"SLC26A2"	"0.6"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1837"	"DTNA"	"0.696"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1837"	"DTNA"	"0.696"	"0.241"	"C1858725"	"NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"1"	"CTD_human;UNIPROT"
"1837"	"DTNA"	"0.696"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"1837"	"DTNA"	"0.696"	"0.241"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2001"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1837"	"DTNA"	"0.696"	"0.241"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1995"	"2001"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"1995"	"2001"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2002"	"2005"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1839"	"HBEGF"	"0.545"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1840"	"DTX1"	"0.696"	"0.414"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1842"	"ECM2"	"1"	"0.034"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1842"	"ECM2"	"1"	"0.034"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"2005"	"2015"	"4"	"0"	"PSYGENET"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1843"	"DUSP1"	"0.528"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1844"	"DUSP2"	"0.624"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1844"	"DUSP2"	"0.624"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1844"	"DUSP2"	"0.624"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1845"	"DUSP3"	"0.799"	"0.172"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"1846"	"DUSP4"	"0.659"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"1846"	"DUSP4"	"0.659"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"1846"	"DUSP4"	"0.659"	"0.448"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1846"	"DUSP4"	"0.659"	"0.448"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1846"	"DUSP4"	"0.659"	"0.448"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1847"	"DUSP5"	"0.72"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2001"	"2012"	"3"	"0"	"PSYGENET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1848"	"DUSP6"	"0.548"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"1848"	"DUSP6"	"0.548"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1848"	"DUSP6"	"0.548"	"0.724"	"C3808981"	"HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"1850"	"DUSP8"	"0.857"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"1855"	"DVL1"	"0.582"	"0.655"	"C0265205"	"Robinow Syndrome"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.53"	"1"	"2015"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"1855"	"DVL1"	"0.582"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1857"	"DVL3"	"0.609"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1857"	"DVL3"	"0.609"	"0.552"	"C0265205"	"Robinow Syndrome"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.61"	"1"	"2016"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"1857"	"DVL3"	"0.609"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.36"	"1"	"2008"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2008"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C3279839"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 7"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2018"	"0"	"23"	"CTD_human"
"1859"	"DYRK1A"	"0.607"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.942528735632184"	"1991"	"2018"	"3"	"1"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0013423"	"Dystonia Musculorum Deformans"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.963636363636364"	"1990"	"2015"	"0"	"0"	"ORPHANET"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.941520467836257"	"1991"	"2018"	"1"	"1"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2005"	"2015"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"0.8"	"1999"	"2014"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"1997"	"2015"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"0.5"	"1997"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"1861"	"TOR1A"	"0.586"	"0.586"	"C1834570"	"Myoclonic dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2009"	"0"	"0"	"ORPHANET"
"1861"	"TOR1A"	"0.586"	"0.586"	"C1851945"	"DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.88"	"1"	"1993"	"2017"	"12"	"3"	"ORPHANET;UNIPROT"
"1861"	"TOR1A"	"0.586"	"0.586"	"C3888090"	"Early onset torsion dystonia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1994"	"2017"	"12"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1861"	"TOR1A"	"0.586"	"0.586"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.947368421052632"	"2000"	"2017"	"2"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"1869"	"E2F1"	"0.491"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"2"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1879"	"EBF1"	"0.656"	"0.345"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1880"	"GPR183"	"0.815"	"0.276"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1880"	"GPR183"	"0.815"	"0.276"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1880"	"GPR183"	"0.815"	"0.276"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"1998"	"1999"	"2"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"1889"	"ECE1"	"0.58"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.63"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0393912"	"Segmental Autonomic Dysfunction"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0750944"	"Peripheral Autonomic Nervous System Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0750945"	"Nervous System Diseases, Parasympathetic"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C0750946"	"Nervous System Diseases, Sympathetic"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C1145628"	"Autonomic nervous system disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1889"	"ECE1"	"0.58"	"0.483"	"C3151237"	"Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction"	"disease"	"C06;C10;C14;C16"	"Disease or Syndrome"	"0.60"		"1995"	"1999"	"1"	"1"	"CTD_human;UNIPROT"
"1889"	"ECE1"	"0.58"	"0.483"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"1890"	"TYMP"	"0.513"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2010"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2010"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2003"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1890"	"TYMP"	"0.513"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2007"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1890"	"TYMP"	"0.513"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"1996"	"2015"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1890"	"TYMP"	"0.513"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"1998"	"2008"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2003"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2003"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2003"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2003"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2002"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"1890"	"TYMP"	"0.513"	"0.655"	"C0872218"	"MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"4"	"64"	"CTD_human;ORPHANET;UNIPROT"
"1890"	"TYMP"	"0.513"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C2749862"	"Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C3501849"	"Mngie Without Leukoencephalopathy"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"1890"	"TYMP"	"0.513"	"0.655"	"C3711125"	"Mitochondrial DNA Depletion Syndrome 8A"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.43"	"1"	"2015"	"2015"	"2"	"2"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1892"	"ECHS1"	"0.69"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1892"	"ECHS1"	"0.69"	"0.379"	"C4225391"	"MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"6"	"19"	"CTD_human;UNIPROT"
"1893"	"ECM1"	"0.639"	"0.483"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1893"	"ECM1"	"0.639"	"0.483"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1893"	"ECM1"	"0.639"	"0.483"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2008"	"2016"	"1"	"0"	"CTD_human"
"1893"	"ECM1"	"0.639"	"0.483"	"C0023795"	"Lipoid Proteinosis of Urbach and Wiethe"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"1894"	"ECT2"	"0.676"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1894"	"ECT2"	"0.676"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1896"	"EDA"	"0.582"	"0.621"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.50"	"0.882352941176471"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"1896"	"EDA"	"0.582"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1896"	"EDA"	"0.582"	"0.621"	"C0162359"	"Christ-Siemens-Touraine syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"0.952380952380952"	"1992"	"2017"	"25"	"31"	"CTD_human;ORPHANET;UNIPROT"
"1896"	"EDA"	"0.582"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1896"	"EDA"	"0.582"	"0.621"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1896"	"EDA"	"0.582"	"0.621"	"C1970757"	"Tooth Agenesis, Selective, X-Linked, 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2016"	"7"	"8"	"CTD_human;UNIPROT"
"1896"	"EDA"	"0.582"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1896"	"EDA"	"0.582"	"0.621"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.49"	"0.888888888888889"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1901"	"S1PR1"	"0.639"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0003126"	"Anosmia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0015927"	"Fetal Death"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2009"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0553757"	"Olfaction Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C1510410"	"Sense of smell altered"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1902"	"LPAR1"	"0.586"	"0.552"	"C3888024"	"Cacosmia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2002"	"2008"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.38"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.59"	"0.888888888888889"	"1999"	"2016"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1994"	"2014"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1994"	"2010"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0019212"	"Hepatorenal Syndrome"	"disease"	"C06;C12;C13"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.943396226415094"	"1993"	"2017"	"14"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.53"		"1995"	"2011"	"5"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.31"		"1992"	"2008"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.37"	"1"	"1996"	"2011"	"3"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2003"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"2006"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0024799"	"Marginal ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1995"	"1997"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.35"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0030920"	"Peptic Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.32"		"2007"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.58"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"1992"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2004"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0038525"	"Subarachnoid Hemorrhage"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0080274"	"Urinary Retention"	"phenotype"	"C12;C13"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2007"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0149745"	"Oral Ulcer"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2008"	"3"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"2006"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0241832"	"Cerebrovascular Insufficiency"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.51"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0268849"	"Overactive Detrusor"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0270192"	"Perinatal Subarachnoid Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1994"	"2011"	"4"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1992"	"1993"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0472383"	"Subarachnoid Hemorrhage, Spontaneous"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1906"	"EDN1"	"0.417"	"0.828"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0596298"	"Cerebrovascular Occlusion"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751530"	"Subarachnoid Hemorrhage, Aneurysmal"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0795688"	"Subarachnoid Hemorrhage, Intracranial"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C0878773"	"Overactive Bladder"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2004"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1865295"	"Auriculo-condylar syndrome"	"disease"	"C09"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"1906"	"EDN1"	"0.417"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"2006"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"2006"	"7"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C2748545"	"QUESTION MARK EARS, ISOLATED"	"phenotype"		"Anatomical Abnormality"	"0.41"	"1"	"2013"	"2014"	"1"	"2"	"UNIPROT"
"1906"	"EDN1"	"0.417"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1906"	"EDN1"	"0.417"	"0.828"	"C3810332"	"AURICULOCONDYLAR SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2014"	"1"	"2"	"UNIPROT"
"1907"	"EDN2"	"0.762"	"0.276"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1907"	"EDN2"	"0.762"	"0.276"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"	"1"	"1964"	"2011"	"4"	"0"	"CTD_human;ORPHANET"
"1908"	"EDN3"	"0.652"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1992"	"1995"	"2"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.32"	"1"	"1996"	"2010"	"4"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1996"	"1998"	"4"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.50"		"1996"	"1996"	"1"	"0"	"CTD_human;ORPHANET"
"1908"	"EDN3"	"0.652"	"0.379"	"C1848519"	"WAARDENBURG SYNDROME, TYPE 4A"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.55"	"1"	"1996"	"2011"	"3"	"0"	"CTD_human;ORPHANET"
"1908"	"EDN3"	"0.652"	"0.379"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1908"	"EDN3"	"0.652"	"0.379"	"C2750457"	"Waardenburg Syndrome, Type 4b"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"		"1994"	"2017"	"10"	"5"	"CLINGEN;CTD_human;UNIPROT"
"1908"	"EDN3"	"0.652"	"0.379"	"C3150975"	"HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"1908"	"EDN3"	"0.652"	"0.379"	"C3266898"	"Waardenburg Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"ORPHANET"
"1908"	"EDN3"	"0.652"	"0.379"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.50"		"1996"	"1998"	"4"	"0"	"CTD_human;ORPHANET"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2012"	"0"	"0"	"UNIPROT"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"1998"	"1999"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2011"	"0"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.50"		"2007"	"2009"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2007"	"2"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0520679"	"Sleep Apnea, Obstructive"	"disease"	"C08;C10"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0751761"	"Upper Airway Resistance Sleep Apnea Syndrome"	"disease"	"C08;C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1909"	"EDNRA"	"0.469"	"0.828"	"C3887485"	"MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"1909"	"EDNRA"	"0.469"	"0.828"	"C4225349"	"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA"	"disease"		"Disease or Syndrome"	"0.91"	"1"	"2006"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"	"1"	"1966"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2004"	"2008"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0038525"	"Subarachnoid Hemorrhage"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.33"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0270192"	"Perinatal Subarachnoid Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0472383"	"Subarachnoid Hemorrhage, Spontaneous"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0751530"	"Subarachnoid Hemorrhage, Aneurysmal"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C0795688"	"Subarachnoid Hemorrhage, Intracranial"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2004"	"2006"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1838099"	"ABCD syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.41"	"1"	"1995"	"2002"	"0"	"1"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1838564"	"HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.40"		"1995"	"2017"	"5"	"4"	"UNIPROT"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1848519"	"WAARDENBURG SYNDROME, TYPE 4A"	"disease"	"C06;C16"	"Disease or Syndrome"	"1.00"	"1"	"1994"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1910"	"EDNRB"	"0.492"	"0.793"	"C2700265"	"Waardenburg Syndrome Type 2"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"1910"	"EDNRB"	"0.492"	"0.793"	"C3266898"	"Waardenburg Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.40"		"2010"	"2015"	"0"	"1"	"ORPHANET"
"1910"	"EDNRB"	"0.492"	"0.793"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.51"	"1"	"1996"	"1998"	"1"	"0"	"CTD_human;ORPHANET"
"1910"	"EDNRB"	"0.492"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"GENOMICS_ENGLAND"
"1911"	"PHC1"	"0.676"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1911"	"PHC1"	"0.676"	"0.552"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.41"	"1"	"2013"	"2015"	"2"	"1"	"GENOMICS_ENGLAND"
"1911"	"PHC1"	"0.676"	"0.552"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1911"	"PHC1"	"0.676"	"0.552"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1911"	"PHC1"	"0.676"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1911"	"PHC1"	"0.676"	"0.552"	"C3809431"	"MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1915"	"EEF1A1"	"0.63"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C4225337"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33"	"disease"		"Disease or Syndrome"	"0.60"		"1988"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"1917"	"EEF1A2"	"0.51"	"0.69"	"C4225343"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 38"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1933"	"EEF1B2"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1938"	"EEF2"	"0.627"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2011"	"1"	"0"	"CTD_human"
"1938"	"EEF2"	"0.627"	"0.586"	"C1836395"	"SPINOCEREBELLAR ATAXIA 26"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2005"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1942"	"EFNA1"	"0.627"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2005"	"2012"	"1"	"0"	"CTD_human"
"1942"	"EFNA1"	"0.627"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2005"	"2012"	"1"	"0"	"CTD_human"
"1942"	"EFNA1"	"0.627"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1942"	"EFNA1"	"0.627"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1945"	"EFNA4"	"0.886"	"0.172"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"1946"	"EFNA5"	"0.701"	"0.414"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.64"	"1"	"2004"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0020534"	"Orbital separation excessive"	"phenotype"	"C05;C16"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0220767"	"Craniofrontonasal dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"0.95"	"1993"	"2017"	"3"	"13"	"CTD_human;ORPHANET;UNIPROT"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C1876203"	"Frontonasal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1947"	"EFNB1"	"0.579"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"PSYGENET"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1948"	"EFNB2"	"0.621"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.884615384615385"	"1987"	"2017"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"1950"	"EGF"	"0.386"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.973958333333333"	"1987"	"2018"	"3"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2003"	"2009"	"3"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.970149253731343"	"1988"	"2017"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0025568"	"Metaplasia"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2016"	"4"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9625"	"1989"	"2018"	"2"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2014"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.08"	"1"	"2004"	"2014"	"1"	"0"	"PSYGENET"
"1950"	"EGF"	"0.386"	"0.897"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2006"	"2"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1950"	"EGF"	"0.386"	"0.897"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"1950"	"EGF"	"0.386"	"0.897"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.953846153846154"	"1994"	"2016"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.974358974358974"	"1987"	"2018"	"3"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2013"	"3"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1950"	"EGF"	"0.386"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2016"	"3"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2018"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C2673648"	"Hypomagnesemia 4, Renal"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"1950"	"EGF"	"0.386"	"0.897"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1950"	"EGF"	"0.386"	"0.897"	"C4510731"	"Familial primary hypomagnesemia with normocalciuria and normocalcemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1952"	"CELSR2"	"0.701"	"0.414"	"C0014173"	"Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1952"	"CELSR2"	"0.701"	"0.414"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"1952"	"CELSR2"	"0.701"	"0.414"	"C0349578"	"Complex Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1952"	"CELSR2"	"0.701"	"0.414"	"C0349579"	"Atypical Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1952"	"CELSR2"	"0.701"	"0.414"	"C0456483"	"Simple Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1954"	"MEGF8"	"0.604"	"0.517"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"1954"	"MEGF8"	"0.604"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1954"	"MEGF8"	"0.604"	"0.517"	"C1275078"	"Acrocephalopolysyndactyly type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"1954"	"MEGF8"	"0.604"	"0.517"	"C3554247"	"CARPENTER SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"3"	"UNIPROT"
"1954"	"MEGF8"	"0.604"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"1956"	"EGFR"	"0.325"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.955315870570108"	"1989"	"2018"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0005396"	"Bile Duct Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.50"	"0.972222222222222"	"1988"	"2016"	"0"	"7"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.986631016042781"	"1987"	"2018"	"6"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.957746478873239"	"1990"	"2016"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.38"	"0.875"	"2007"	"2016"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.973528069374715"	"1989"	"2018"	"16"	"27"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.965217391304348"	"1984"	"2018"	"3"	"2"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"		"2004"	"2011"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.95583596214511"	"1992"	"2018"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.923076923076923"	"2002"	"2017"	"2"	"1"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"1994"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.958333333333333"	"1988"	"2018"	"3"	"0"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.972027972027972"	"1988"	"2018"	"3"	"7"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.973451327433628"	"1987"	"2018"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.62"	"1"	"2004"	"2016"	"3"	"3"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2001"	"2004"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.943661971830986"	"1994"	"2017"	"7"	"0"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1996"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.8"	"1994"	"2014"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1987"	"2013"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.944250871080139"	"1989"	"2018"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.952380952380952"	"1997"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"1996"	"2015"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.50"	"1"	"1994"	"2015"	"3"	"1"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1995"	"2016"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2010"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.50"	"0.941176470588235"	"2007"	"2018"	"0"	"3"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2018"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.974658869395711"	"1990"	"2018"	"2"	"4"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"1"	"1988"	"2018"	"0"	"1"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2011"	"2017"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2018"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"2016"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"2016"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"2016"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"2016"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1989"	"2016"	"5"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2004"	"2008"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.97622027534418"	"1988"	"2018"	"7"	"0"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.981818181818182"	"1989"	"2018"	"3"	"0"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.971428571428571"	"1994"	"2017"	"1"	"1"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2009"	"2016"	"3"	"0"	"CTD_human;ORPHANET"
"1956"	"EGFR"	"0.325"	"0.862"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"0.714285714285714"	"2005"	"2016"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.976470588235294"	"1986"	"2018"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0349566"	"Squamous cell carcinoma of tongue"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2007"	"2009"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.976470588235294"	"1994"	"2018"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.933333333333333"	"1991"	"2016"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.91304347826087"	"1988"	"2018"	"3"	"0"	"CGI;CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.984210526315789"	"1987"	"2018"	"6"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.50"	"0.976811594202899"	"1988"	"2018"	"0"	"1"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C0740277"	"Bile duct carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0745730"	"Multiple lipomata"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1956"	"EGFR"	"0.325"	"0.862"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.985507246376812"	"1991"	"2017"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1153706"	"Endometrial adenocarcinoma"	"disease"		"Neoplastic Process"	"0.33"	"1"	"1991"	"2011"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.965277777777778"	"1992"	"2018"	"0"	"4"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2013"	"6"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2018"	"1"	"0"	"PSYGENET"
"1956"	"EGFR"	"0.325"	"0.862"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.38"	"0.875"	"1993"	"2015"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.955555555555556"	"1990"	"2016"	"6"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.955128205128205"	"1993"	"2018"	"2"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.957627118644068"	"1988"	"2018"	"3"	"2"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"3"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.986111111111111"	"1992"	"2018"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"1956"	"EGFR"	"0.325"	"0.862"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.37"	"1"	"1989"	"2018"	"0"	"0"	"CGI"
"1956"	"EGFR"	"0.325"	"0.862"	"C4015130"	"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"1956"	"EGFR"	"0.325"	"0.862"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2018"	"3"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0020295"	"Hydronephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"1958"	"EGR1"	"0.459"	"0.793"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1958"	"EGR1"	"0.459"	"0.793"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1958"	"EGR1"	"0.459"	"0.793"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1959"	"EGR2"	"0.579"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"1959"	"EGR2"	"0.579"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"1998"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1959"	"EGR2"	"0.579"	"0.621"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.93"	"1"	"1993"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"1959"	"EGR2"	"0.579"	"0.621"	"C0019816"	"Hereditary, Type VII, Motor and Sensory Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0027888"	"Hereditary Motor and Sensory Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2009"	"0"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0035372"	"Rett Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.333333333333333"	"2011"	"2016"	"3"	"0"	"PSYGENET"
"1959"	"EGR2"	"0.579"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C0393818"	"Congenital hypomyelinating neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.99"	"1"	"1993"	"2012"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"1959"	"EGR2"	"0.579"	"0.621"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2012"	"2016"	"1"	"1"	"CTD_human"
"1959"	"EGR2"	"0.579"	"0.621"	"C1843247"	"Charcot-Marie-Tooth disease, Type 1D (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2012"	"7"	"6"	"CTD_human;ORPHANET;UNIPROT"
"1959"	"EGR2"	"0.579"	"0.621"	"C3551756"	"NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.50"		"1998"	"2012"	"2"	"1"	"UNIPROT"
"1959"	"EGR2"	"0.579"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1960"	"EGR3"	"0.645"	"0.586"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2011"	"3"	"0"	"PSYGENET"
"1960"	"EGR3"	"0.645"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1960"	"EGR3"	"0.645"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"1960"	"EGR3"	"0.645"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.5"	"2007"	"2017"	"2"	"0"	"PSYGENET"
"1960"	"EGR3"	"0.645"	"0.586"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1960"	"EGR3"	"0.645"	"0.586"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"1961"	"EGR4"	"0.762"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2013"	"2"	"0"	"PSYGENET"
"1961"	"EGR4"	"0.762"	"0.414"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0015624"	"Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0341703"	"Adult Fanconi syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0342870"	"Bifunctional peroxisomal enzyme deficiency"	"phenotype"	"C09;C10;C12;C13;C16;C19;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"ORPHANET"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1962"	"EHHADH"	"0.685"	"0.414"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C1857395"	"De Toni-Debre-Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C3495427"	"Fanconi-Bickel Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1962"	"EHHADH"	"0.685"	"0.414"	"C3810100"	"FANCONI RENOTUBULAR SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"1992"	"2014"	"1"	"1"	"UNIPROT"
"1962"	"EHHADH"	"0.685"	"0.414"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1964"	"EIF1AX"	"0.773"	"0.31"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"1964"	"EIF1AX"	"0.773"	"0.31"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.35"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"1964"	"EIF1AX"	"0.773"	"0.31"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"ORPHANET"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1965"	"EIF2S1"	"0.598"	"0.517"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.39"	"0.888888888888889"	"2004"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.64"	"1"	"2002"	"2008"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"1967"	"EIF2B1"	"0.701"	"0.414"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"0.947368421052632"	"2001"	"2016"	"2"	"7"	"ORPHANET;UNIPROT"
"1968"	"EIF2S3"	"0.627"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1968"	"EIF2S3"	"0.627"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"1968"	"EIF2S3"	"0.627"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"1968"	"EIF2S3"	"0.627"	"0.655"	"C1846278"	"MENTAL RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND HYPOGENITALISM, MICROCEPHALY, AND OBESITY (disorder)"	"disease"	"C05;C10;C16;C18;C19;C23"	"Disease or Syndrome"	"0.70"		"2013"	"2018"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"1968"	"EIF2S3"	"0.627"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.35"	"1"	"2009"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"		"2010"	"2010"	"0"	"1"	"CGI"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1969"	"EPHA2"	"0.526"	"0.69"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1969"	"EPHA2"	"0.526"	"0.69"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"1969"	"EPHA2"	"0.526"	"0.69"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"1969"	"EPHA2"	"0.526"	"0.69"	"C1861825"	"CATARACT, POSTERIOR POLAR, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"2006"	"2017"	"4"	"4"	"CTD_human;UNIPROT"
"1973"	"EIF4A1"	"0.735"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1973"	"EIF4A1"	"0.735"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1974"	"EIF4A2"	"0.659"	"0.517"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1974"	"EIF4A2"	"0.659"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"UNIPROT"
"1974"	"EIF4A2"	"0.659"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1974"	"EIF4A2"	"0.659"	"0.517"	"C0394996"	"Acute alcoholic intoxication"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"1975"	"EIF4B"	"0.773"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1975"	"EIF4B"	"0.773"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"1977"	"EIF4E"	"0.489"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"1977"	"EIF4E"	"0.489"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"1977"	"EIF4E"	"0.489"	"0.724"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"1977"	"EIF4E"	"0.489"	"0.724"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1978"	"EIF4EBP1"	"0.529"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"1981"	"EIF4G1"	"0.63"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.823529411764706"	"2011"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"1981"	"EIF4G1"	"0.63"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"1981"	"EIF4G1"	"0.63"	"0.586"	"C3280271"	"PARKINSON DISEASE 18"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"1981"	"EIF4G1"	"0.63"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"1981"	"EIF4G1"	"0.63"	"0.586"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"1983"	"EIF5"	"0.785"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1983"	"EIF5"	"0.785"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1984"	"EIF5A"	"0.633"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"1990"	"CELA1"	"0.743"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1990"	"CELA1"	"0.743"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"1991"	"ELANE"	"0.506"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"1991"	"ELANE"	"0.506"	"0.759"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.882352941176471"	"2001"	"2015"	"1"	"0"	"CTD_human"
"1991"	"ELANE"	"0.506"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"1991"	"ELANE"	"0.506"	"0.759"	"C0221023"	"Cyclic neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2018"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"1991"	"ELANE"	"0.506"	"0.759"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"1991"	"ELANE"	"0.506"	"0.759"	"C1859966"	"Neutropenia, Severe Congenital, Autosomal Dominant 1"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"13"	"18"	"CTD_human;ORPHANET;UNIPROT"
"1991"	"ELANE"	"0.506"	"0.759"	"C3671688"	"Cyclic Hematopoesis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"1991"	"ELANE"	"0.506"	"0.759"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"1993"	"ELAVL2"	"0.6"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2013"	"1"	"0"	"PSYGENET"
"1993"	"ELAVL2"	"0.6"	"0.621"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"1994"	"ELAVL1"	"0.607"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1994"	"ELAVL1"	"0.607"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1995"	"ELAVL3"	"0.735"	"0.31"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1995"	"ELAVL3"	"0.735"	"0.31"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1998"	"ELF2"	"0.815"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1998"	"ELF2"	"0.815"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1998"	"ELF2"	"0.815"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"1999"	"ELF3"	"0.611"	"0.586"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1999"	"ELF3"	"0.611"	"0.586"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"1999"	"ELF3"	"0.611"	"0.586"	"C0750952"	"Biliary Tract Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"1999"	"ELF3"	"0.611"	"0.586"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2000"	"ELF4"	"0.707"	"0.448"	"C0472813"	"X-linked agammaglobulinemia with growth hormone deficiency"	"disease"	"C05;C10;C15;C16;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2002"	"ELK1"	"0.582"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"2004"	"ELK3"	"0.592"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2004"	"ELK3"	"0.592"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2004"	"ELK3"	"0.592"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2004"	"ELK3"	"0.592"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0003499"	"Supravalvular aortic stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1988"	"2017"	"2"	"26"	"CTD_human;ORPHANET"
"2006"	"ELN"	"0.455"	"0.828"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"2006"	"ELN"	"0.455"	"0.828"	"C0010495"	"Cutis Laxa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"	"1"	"1981"	"2012"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"2006"	"ELN"	"0.455"	"0.828"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"1987"	"2018"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.48"	"1"	"1990"	"2014"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2016"	"2"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2006"	"ELN"	"0.455"	"0.828"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.60"	"0.986666666666667"	"1988"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"2006"	"ELN"	"0.455"	"0.828"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C0268350"	"Cutis Laxa, Autosomal Dominant"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.56"	"1"	"1998"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"2006"	"ELN"	"0.455"	"0.828"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"2006"	"ELN"	"0.455"	"0.828"	"C1305147"	"Congenital supravalvular aortic stenosis"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"ORPHANET"
"2006"	"ELN"	"0.455"	"0.828"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2006"	"ELN"	"0.455"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1997"	"1998"	"0"	"0"	"GENOMICS_ENGLAND"
"2009"	"EML1"	"0.72"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2009"	"EML1"	"0.72"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2009"	"EML1"	"0.72"	"0.379"	"C1838239"	"Band Heterotopia of Brain"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"3"	"CTD_human"
"2009"	"EML1"	"0.72"	"0.379"	"C1848201"	"Subcortical Band Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2009"	"EML1"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2009"	"EML1"	"0.72"	"0.379"	"C4284594"	"BAND HETEROTOPIA"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"2010"	"EMD"	"0.614"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0410189"	"Muscular Dystrophy, Emery-Dreifuss"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"0.935483870967742"	"1991"	"2016"	"0"	"0"	"CTD_human"
"2010"	"EMD"	"0.614"	"0.552"	"C0410190"	"Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human"
"2010"	"EMD"	"0.614"	"0.552"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2010"	"EMD"	"0.614"	"0.552"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.96"	"1997"	"2017"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"2010"	"EMD"	"0.614"	"0.552"	"C1450051"	"Autosomal Recessive Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2010"	"EMD"	"0.614"	"0.552"	"C2930996"	"Muscular dystrophy, tardive Emery-Dreifuss type, with contractures"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2006"	"4"	"2"	"UNIPROT"
"2011"	"MARK2"	"0.554"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2011"	"MARK2"	"0.554"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2011"	"MARK2"	"0.554"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2012"	"2"	"0"	"PSYGENET"
"2011"	"MARK2"	"0.554"	"0.655"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2012"	"EMP1"	"0.633"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"2012"	"EMP1"	"0.633"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2013"	"EMP2"	"0.681"	"0.414"	"C4014507"	"NEPHROTIC SYNDROME, TYPE 10"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"2014"	"EMP3"	"0.681"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2014"	"EMP3"	"0.681"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2015"	"ADGRE1"	"0.799"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"1993"	"2017"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C0023531"	"Leukoplakia"	"disease"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C1704317"	"Leukokeratosis"	"phenotype"	"C04;C23"	"Anatomical Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2017"	"CTTN"	"0.6"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2018"	"EMX2"	"0.672"	"0.31"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2018"	"EMX2"	"0.672"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2018"	"EMX2"	"0.672"	"0.31"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2018"	"EMX2"	"0.672"	"0.31"	"C0266484"	"Schizencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.46"	"1"	"1997"	"2008"	"0"	"0"	"ORPHANET"
"2018"	"EMX2"	"0.672"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2018"	"EMX2"	"0.672"	"0.31"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2018"	"EMX2"	"0.672"	"0.31"	"C2931870"	"Familial schizencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2005"	"0"	"0"	"CTD_human"
"2018"	"EMX2"	"0.672"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"2019"	"EN1"	"0.799"	"0.276"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2019"	"EN1"	"0.799"	"0.276"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2019"	"EN1"	"0.799"	"0.276"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2019"	"EN1"	"0.799"	"0.276"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2019"	"EN1"	"0.799"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2019"	"EN1"	"0.799"	"0.276"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2020"	"EN2"	"0.735"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2004"	"2015"	"4"	"0"	"CTD_human"
"2020"	"EN2"	"0.735"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2004"	"2014"	"2"	"0"	"PSYGENET"
"2020"	"EN2"	"0.735"	"0.276"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"2020"	"EN2"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2022"	"ENG"	"0.477"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"2022"	"ENG"	"0.477"	"0.655"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2022"	"ENG"	"0.477"	"0.655"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"1.00"	"0.984615384615385"	"1989"	"2017"	"16"	"36"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"2022"	"ENG"	"0.477"	"0.655"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2022"	"ENG"	"0.477"	"0.655"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C0345893"	"Juvenile polyposis syndrome"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.55"	"0.8"	"2005"	"2016"	"3"	"0"	"CLINGEN;ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C1832940"	"JUVENILE POLYPOSIS OF STOMACH"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2016"	"3"	"0"	"CLINGEN;ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C1862932"	"ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C1868081"	"Juvenile Polyposis Coli"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2016"	"3"	"0"	"CLINGEN;ORPHANET"
"2022"	"ENG"	"0.477"	"0.655"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2016"	"12"	"0"	"GENOMICS_ENGLAND"
"2022"	"ENG"	"0.477"	"0.655"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"1"	"1995"	"2016"	"12"	"0"	"GENOMICS_ENGLAND"
"2023"	"ENO1"	"0.516"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"		"2003"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2023"	"ENO1"	"0.516"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2016"	"2"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2023"	"ENO1"	"0.516"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2026"	"ENO2"	"0.559"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2026"	"ENO2"	"0.559"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2027"	"ENO3"	"0.857"	"0.138"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2027"	"ENO3"	"0.857"	"0.138"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2001"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2027"	"ENO3"	"0.857"	"0.138"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2027"	"ENO3"	"0.857"	"0.138"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2027"	"ENO3"	"0.857"	"0.138"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2027"	"ENO3"	"0.857"	"0.138"	"C2752027"	"Glycogen Storage Disease XIII"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2001"	"2001"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2028"	"ENPEP"	"0.648"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"UNIPROT"
"2028"	"ENPEP"	"0.648"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2028"	"ENPEP"	"0.648"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2028"	"ENPEP"	"0.648"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2029"	"ENSA"	"0.886"	"0.172"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"2"	"0"	"PSYGENET"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0586323"	"Alcohol Withdrawal Seizures"	"disease"	"C10;C23;C25"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0751868"	"Alcohol Withdrawal-Induced Major Motor Seizure"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C0751869"	"Status Epilepticus, Alcohol Withdrawal-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2030"	"SLC29A1"	"0.604"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2033"	"EP300"	"0.489"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1993"	"1993"	"1"	"0"	"PSYGENET"
"2033"	"EP300"	"0.489"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.62"	"1"	"2004"	"2018"	"1"	"0"	"CGI;CTD_human;UNIPROT"
"2033"	"EP300"	"0.489"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2004"	"0"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2005"	"2013"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2013"	"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2033"	"EP300"	"0.489"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0035934"	"Rubinstein-Taybi Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2018"	"0"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2018"	"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"2"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;UNIPROT"
"2033"	"EP300"	"0.489"	"0.828"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.52"	"1"	"2004"	"2018"	"1"	"0"	"CGI;CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2015"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2000"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"2033"	"EP300"	"0.489"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"2033"	"EP300"	"0.489"	"0.828"	"C3150941"	"RUBINSTEIN-TAYBI SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2018"	"0"	"16"	"ORPHANET"
"2033"	"EP300"	"0.489"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2033"	"EP300"	"0.489"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"1"	"2001"	"2018"	"1"	"18"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2016"	"3"	"0"	"CLINGEN"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2016"	"3"	"0"	"CLINGEN"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.846153846153846"	"2011"	"2018"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2016"	"3"	"0"	"CLINGEN"
"2034"	"EPAS1"	"0.509"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2016"	"3"	"0"	"CLINGEN"
"2034"	"EPAS1"	"0.509"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2034"	"EPAS1"	"0.509"	"0.586"	"C1318533"	"Secondary polycythemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2034"	"EPAS1"	"0.509"	"0.586"	"C2673187"	"Erythrocytosis, Familial, 4"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2008"	"2012"	"4"	"2"	"CTD_human;UNIPROT"
"2035"	"EPB41"	"0.752"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1986"	"1992"	"3"	"0"	"GENOMICS_ENGLAND"
"2035"	"EPB41"	"0.752"	"0.276"	"C0013902"	"Elliptocytosis, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.62"	"1"	"1999"	"2016"	"0"	"1"	"ORPHANET"
"2035"	"EPB41"	"0.752"	"0.276"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2035"	"EPB41"	"0.752"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1986"	"1992"	"3"	"0"	"GENOMICS_ENGLAND"
"2035"	"EPB41"	"0.752"	"0.276"	"C2678497"	"Elliptocytosis 1"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1992"	"1995"	"0"	"1"	"CTD_human"
"2036"	"EPB41L1"	"0.928"	"0.034"	"C3280285"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 11"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"2036"	"EPB41L1"	"0.928"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"2037"	"EPB41L2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2038"	"EPB42"	"0.762"	"0.103"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1990"	"2004"	"5"	"0"	"GENOMICS_ENGLAND"
"2038"	"EPB42"	"0.762"	"0.103"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"2038"	"EPB42"	"0.762"	"0.103"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1990"	"2004"	"5"	"0"	"GENOMICS_ENGLAND"
"2038"	"EPB42"	"0.762"	"0.103"	"C0221409"	"Anemia, hereditary spherocytic hemolytic"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2038"	"EPB42"	"0.762"	"0.103"	"C2675192"	"Spherocytosis, Type 5"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1990"	"2002"	"5"	"9"	"CTD_human;UNIPROT"
"2040"	"STOM"	"0.707"	"0.414"	"C1861455"	"STOMATOCYTOSIS I"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2003"	"0"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9"	"2010"	"2018"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2015"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2041"	"EPHA1"	"0.596"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2042"	"EPHA3"	"0.552"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2042"	"EPHA3"	"0.552"	"0.586"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2042"	"EPHA3"	"0.552"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2042"	"EPHA3"	"0.552"	"0.586"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2042"	"EPHA3"	"0.552"	"0.586"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"2042"	"EPHA3"	"0.552"	"0.586"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"2042"	"EPHA3"	"0.552"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"2043"	"EPHA4"	"0.609"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.44"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"2043"	"EPHA4"	"0.609"	"0.586"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1997"	"2007"	"1"	"1"	"UNIPROT"
"2043"	"EPHA4"	"0.609"	"0.586"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2044"	"EPHA5"	"0.743"	"0.241"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2044"	"EPHA5"	"0.743"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2005"	"2007"	"1"	"2"	"UNIPROT"
"2044"	"EPHA5"	"0.743"	"0.241"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2045"	"EPHA7"	"0.659"	"0.379"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2045"	"EPHA7"	"0.659"	"0.379"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2045"	"EPHA7"	"0.659"	"0.379"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2045"	"EPHA7"	"0.659"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"1"	"UNIPROT"
"2046"	"EPHA8"	"0.656"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"2046"	"EPHA8"	"0.656"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2046"	"EPHA8"	"0.656"	"0.414"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2046"	"EPHA8"	"0.656"	"0.414"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2046"	"EPHA8"	"0.656"	"0.414"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2047"	"EPHB1"	"0.6"	"0.724"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2047"	"EPHB1"	"0.6"	"0.724"	"C0346167"	"Undifferentiated carcinoma of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2017"	"2"	"4"	"UNIPROT"
"2048"	"EPHB2"	"0.425"	"0.759"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C1863600"	"PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding)"	"phenotype"		"Finding"	"0.40"		"2004"	"2006"	"0"	"4"	"CTD_human"
"2048"	"EPHB2"	"0.425"	"0.759"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"2049"	"EPHB3"	"0.762"	"0.207"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2050"	"EPHB4"	"0.569"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2050"	"EPHB4"	"0.569"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2050"	"EPHB4"	"0.569"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"2050"	"EPHB4"	"0.569"	"0.586"	"C4310629"	"HYDROPS FETALIS, NONIMMUNE, AND/OR ATRIAL SEPTAL DEFECT, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"2051"	"EPHB6"	"0.656"	"0.345"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2051"	"EPHB6"	"0.656"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2051"	"EPHB6"	"0.656"	"0.345"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0000771"	"Abnormalities, Drug-Induced"	"phenotype"	"C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1994"	"2015"	"3"	"0"	"CLINGEN"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.954545454545455"	"1997"	"2016"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"		"2003"	"2009"	"2"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.32"		"2001"	"2007"	"2"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.38"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.96"	"1998"	"2014"	"2"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"3"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"1994"	"2015"	"3"	"0"	"CLINGEN"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1994"	"2015"	"3"	"0"	"CLINGEN"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1843139"	"Hypercholanemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2052"	"EPHX1"	"0.51"	"0.759"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.818181818181818"	"1995"	"2014"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2052"	"EPHX1"	"0.51"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2000"	"2005"	"0"	"1"	"GENOMICS_ENGLAND"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2053"	"EPHX2"	"0.633"	"0.448"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2054"	"STX2"	"0.676"	"0.31"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2054"	"STX2"	"0.676"	"0.31"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2054"	"STX2"	"0.676"	"0.31"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2055"	"CLN8"	"0.667"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2055"	"CLN8"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2055"	"CLN8"	"0.667"	"0.345"	"C1838570"	"CEROID LIPOFUSCINOSIS, NEURONAL, 8"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.93"	"1"	"1986"	"2016"	"7"	"30"	"CTD_human;ORPHANET;UNIPROT"
"2055"	"CLN8"	"0.667"	"0.345"	"C1864923"	"Northern epilepsy syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2055"	"CLN8"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"2056"	"EPO"	"0.425"	"0.759"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.959677419354839"	"1985"	"2018"	"64"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2012"	"3"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2010"	"3"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2010"	"3"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0007682"	"CNS disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0015672"	"Fatigue"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"1992"	"2016"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.36"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2012"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1991"	"2018"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0030472"	"Paraneoplastic Syndromes"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"4"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0036214"	"Sarcoma, Engelbreth-Holm-Swarm"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0036216"	"Sarcoma, Experimental"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0036219"	"Sarcoma, Jensen"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"4"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0036980"	"Shock, Cardiogenic"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0086525"	"Lassitude"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0152025"	"Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2010"	"3"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0271683"	"Polyneuropathy, Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0393851"	"Polyneuropathy, Critical Illness"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751448"	"Polyneuropathy, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751449"	"Acquired Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"4"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"1987"	"2017"	"0"	"0"	"UNIPROT"
"2056"	"EPO"	"0.425"	"0.759"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C2675471"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2003"	"2005"	"2"	"0"	"CTD_human"
"2056"	"EPO"	"0.425"	"0.759"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.40"	"0.863636363636364"	"1990"	"2016"	"2"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0023440"	"Acute Erythroblastic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.35"	"1"	"1994"	"2009"	"0"	"1"	"UNIPROT"
"2057"	"EPOR"	"0.555"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"		"2004"	"2006"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.70"	"0.846153846153846"	"1993"	"2015"	"6"	"1"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"2057"	"EPOR"	"0.555"	"0.552"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"2057"	"EPOR"	"0.555"	"0.552"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2059"	"EPS8"	"0.685"	"0.276"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2059"	"EPS8"	"0.685"	"0.276"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"6"	"0"	"CLINGEN"
"2059"	"EPS8"	"0.685"	"0.276"	"C3892050"	"DEAFNESS, AUTOSOMAL RECESSIVE 102"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2002"	"2010"	"1"	"3"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2063"	"NR2F6"	"0.762"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.976635514018692"	"1986"	"2018"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"	"1"	"1994"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.80"	"0.970725630644659"	"1987"	"2018"	"40"	"0"	"CGI;CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2004"	"2010"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.97752808988764"	"1989"	"2018"	"1"	"9"	"CGI;UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.785714285714286"	"1989"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9375"	"1997"	"2015"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"0"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.97737556561086"	"1986"	"2018"	"3"	"0"	"CGI;CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"2014"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.931880108991826"	"1989"	"2018"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.973404255319149"	"1989"	"2018"	"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"1997"	"2013"	"3"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.875"	"1989"	"2015"	"3"	"1"	"CGI;CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"1"	"1991"	"2017"	"1"	"7"	"CGI;UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1988"	"2012"	"2"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0206725"	"Subependymal Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2000"	"2012"	"3"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.986842105263158"	"1989"	"2018"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2004"	"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.932432432432432"	"1992"	"2018"	"3"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.85"	"1997"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.952879581151832"	"1989"	"2018"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.983333333333333"	"1989"	"2018"	"2"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.975866095757104"	"1987"	"2018"	"40"	"0"	"CGI;CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"	"0.969230769230769"	"1989"	"2018"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0685938"	"Malignant neoplasm of gastrointestinal tract"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.70"	"0.972881355932203"	"1986"	"2018"	"2"	"1"	"CGI;UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.936170212765957"	"1990"	"2017"	"2"	"1"	"CGI;CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.962962962962963"	"1990"	"2017"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.973154362416107"	"1989"	"2018"	"4"	"1"	"CGI;CTD_human;UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2000"	"2015"	"40"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2000"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CGI"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.958241758241758"	"1987"	"2018"	"40"	"14"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.45"	"0.8"	"1995"	"2016"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"3"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C1842010"	"Glioma of Brain, Familial"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C2750850"	"GLIOMA SUSCEPTIBILITY 1"	"phenotype"		"Finding"	"0.40"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"1"	"UNIPROT"
"2064"	"ERBB2"	"0.352"	"0.862"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"2064"	"ERBB2"	"0.352"	"0.862"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2003"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.987012987012987"	"1996"	"2018"	"2"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"		"2006"	"2008"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.333333333333333"	"2004"	"2010"	"3"	"0"	"PSYGENET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.42"		"2008"	"2013"	"0"	"1"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.42"	"1"	"2016"	"2016"	"0"	"3"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2018"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.975"	"1991"	"2017"	"2"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.38"	"1"	"1998"	"2016"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.38"	"1"	"2003"	"2018"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"2065"	"ERBB3"	"0.473"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2065"	"ERBB3"	"0.473"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"1990"	"2017"	"2"	"3"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C1843478"	"Lethal Congenital Contracture Syndrome 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2065"	"ERBB3"	"0.473"	"0.69"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2065"	"ERBB3"	"0.473"	"0.69"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"0"	"0"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.978260869565217"	"1995"	"2018"	"0"	"0"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.916666666666667"	"2009"	"2016"	"1"	"6"	"CGI;CTD_human"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2017"	"4"	"0"	"PSYGENET"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.978723404255319"	"1995"	"2015"	"0"	"1"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2066"	"ERBB4"	"0.494"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2066"	"ERBB4"	"0.494"	"0.69"	"C3715155"	"AMYOTROPHIC LATERAL SCLEROSIS 19"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.976744186046512"	"2003"	"2018"	"2"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.38"		"2003"	"2009"	"0"	"0"	"CGI"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0220722"	"Cerebrooculofacioskeletal Syndrome 1"	"disease"	"C05;C10;C16;C18"	"Congenital Abnormality"	"0.32"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9"	"2005"	"2016"	"0"	"0"	"CGI"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"	"0.9"	"2005"	"2016"	"0"	"0"	"CGI"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0751038"	"Cockayne Syndrome, Type II"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C1853100"	"CEREBROOCULOFACIOSKELETAL SYNDROME 4"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2007"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"2067"	"ERCC1"	"0.463"	"0.724"	"C1859312"	"CAMFAK syndrome"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2067"	"ERCC1"	"0.463"	"0.724"	"C2931277"	"Pena Shokeir syndrome Type 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2067"	"ERCC1"	"0.463"	"0.724"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.37"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"2067"	"ERCC1"	"0.463"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"2067"	"ERCC1"	"0.463"	"0.724"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.916666666666667"	"2001"	"2016"	"2"	"0"	"CGI;CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.947368421052632"	"2001"	"2016"	"2"	"0"	"CGI;CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"1995"	"2010"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"		"2006"	"2006"	"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2002"	"2017"	"1"	"0"	"CGI;CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"2004"	"2015"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2002"	"2008"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2016"	"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0038814"	"Sunburn"	"disease"	"C17;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.70"	"0.895522388059702"	"1989"	"2016"	"0"	"1"	"ORPHANET"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0079153"	"Hyperkeratosis, Epidermolytic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"2004"	"2013"	"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0220722"	"Cerebrooculofacioskeletal Syndrome 1"	"disease"	"C05;C10;C16;C18"	"Congenital Abnormality"	"0.43"	"1"	"2001"	"2016"	"0"	"1"	"ORPHANET"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0268138"	"Xeroderma Pigmentosum, Complementation Group D"	"disease"	"C04;C16;C17;C18"	"Disease or Syndrome"	"0.90"	"0.921052631578947"	"1986"	"2015"	"7"	"17"	"CTD_human;UNIPROT"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.40"	"0.916666666666667"	"2001"	"2014"	"0"	"0"	"CGI"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"2004"	"2015"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1853102"	"Cerebrooculofacioskeletal Syndrome 2"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"3"	"CTD_human;UNIPROT"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1859312"	"CAMFAK syndrome"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1866504"	"Photosensitive Trichothiodystrophy"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1994"	"2015"	"6"	"12"	"CTD_human;UNIPROT"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1866505"	"Ichthyosis, Congenital, with Trichothiodystrophy"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"1994"	"2001"	"6"	"10"	"CTD_human;UNIPROT"
"2068"	"ERCC2"	"0.447"	"0.828"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"0.951612903225806"	"1992"	"2016"	"0"	"0"	"ORPHANET"
"2068"	"ERCC2"	"0.447"	"0.828"	"C2931277"	"Pena Shokeir syndrome Type 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2068"	"ERCC2"	"0.447"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1995"	"1995"	"0"	"0"	"GENOMICS_ENGLAND"
"2069"	"EREG"	"0.602"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"2069"	"EREG"	"0.602"	"0.621"	"C0162568"	"Erythropoietic Protoporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2069"	"EREG"	"0.602"	"0.621"	"C0349426"	"Ferrochelatase deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2069"	"EREG"	"0.602"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2069"	"EREG"	"0.602"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"2070"	"EYA4"	"0.645"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.44"	"1"	"2005"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2070"	"EYA4"	"0.645"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2070"	"EYA4"	"0.645"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2070"	"EYA4"	"0.645"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2070"	"EYA4"	"0.645"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.53"	"1"	"2006"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"2070"	"EYA4"	"0.645"	"0.414"	"C1832476"	"Deafness, Autosomal Dominant 10"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.62"	"1"	"2001"	"2016"	"4"	"2"	"CTD_human;UNIPROT"
"2070"	"EYA4"	"0.645"	"0.414"	"C1854368"	"Cardiomyopathy, Dilated, 1J"	"disease"	"C09;C10;C14;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.60"	"0.939393939393939"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0268136"	"Xeroderma pigmentosum, group B"	"disease"	"C04;C16;C17;C18"	"Disease or Syndrome"	"0.77"	"1"	"1991"	"2012"	"3"	"1"	"CTD_human;UNIPROT"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2071"	"ERCC3"	"0.541"	"0.793"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"	"0.952380952380952"	"1995"	"2016"	"0"	"0"	"ORPHANET"
"2071"	"ERCC3"	"0.541"	"0.793"	"C1970808"	"Xeroderma Pigmentosum B-Cockayne Syndrome"	"disease"	"C04;C05;C10;C16;C17;C18"	"Disease or Syndrome"	"0.60"		"1974"	"2009"	"3"	"3"	"UNIPROT"
"2071"	"ERCC3"	"0.541"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2071"	"ERCC3"	"0.541"	"0.793"	"C4225344"	"TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"1997"	"1"	"1"	"CTD_human;UNIPROT"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2012"	"2015"	"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.45"	"1"	"2007"	"2017"	"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2016"	"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.31"		"2004"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.60"	"1"	"1998"	"2016"	"0"	"0"	"ORPHANET"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.42"	"1"	"2013"	"2017"	"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0268140"	"Xeroderma pigmentosum, group F"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.90"	"1"	"1988"	"2015"	"4"	"7"	"CTD_human;UNIPROT"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0751039"	"Cockayne Syndrome, Type I"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2016"	"0"	"0"	"CGI"
"2072"	"ERCC4"	"0.503"	"0.724"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2072"	"ERCC4"	"0.503"	"0.724"	"C1970416"	"XFE Progeroid Syndrome"	"disease"	"C04;C05;C10;C16;C17;C18"	"Disease or Syndrome"	"0.62"	"1"	"2007"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"2072"	"ERCC4"	"0.503"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2072"	"ERCC4"	"0.503"	"0.724"	"C3806565"	"XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2015"	"4"	"6"	"UNIPROT"
"2072"	"ERCC4"	"0.503"	"0.724"	"C3808988"	"FANCONI ANEMIA, COMPLEMENTATION GROUP Q"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2014"	"2"	"4"	"CTD_human;UNIPROT"
"2072"	"ERCC4"	"0.503"	"0.724"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2009"	"0"	"0"	"CGI"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2007"	"2015"	"0"	"0"	"CGI"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.70"	"1"	"1994"	"2016"	"0"	"1"	"ORPHANET"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.42"	"1"	"2007"	"2011"	"0"	"0"	"CGI"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0220722"	"Cerebrooculofacioskeletal Syndrome 1"	"disease"	"C05;C10;C16;C18"	"Congenital Abnormality"	"0.32"	"1"	"2001"	"2015"	"0"	"0"	"ORPHANET"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0268141"	"Xeroderma pigmentosum, group G"	"disease"	"C04;C16;C17;C18"	"Disease or Syndrome"	"0.90"	"1"	"1978"	"2015"	"6"	"13"	"CTD_human;UNIPROT"
"2073"	"ERCC5"	"0.518"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1997"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"2073"	"ERCC5"	"0.518"	"0.69"	"C1851443"	"Cerebrooculofacioskeletal Syndrome 3"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"2073"	"ERCC5"	"0.518"	"0.69"	"C1859312"	"CAMFAK syndrome"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2073"	"ERCC5"	"0.518"	"0.69"	"C1968561"	"Xeroderma Pigmentosum, Type G-Cockayne Syndrome"	"disease"	"C04;C05;C10;C16;C17;C18"	"Disease or Syndrome"	"0.60"		"1994"	"2013"	"6"	"8"	"UNIPROT"
"2073"	"ERCC5"	"0.518"	"0.69"	"C2931277"	"Pena Shokeir syndrome Type 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2073"	"ERCC5"	"0.518"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2018"	"0"	"0"	"UNIPROT"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0009207"	"Cockayne Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.984615384615385"	"1993"	"2017"	"7"	"1"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0020241"	"Hydroa Vacciniforme"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"		"2008"	"2009"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CGI"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.60"		"2008"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0220722"	"Cerebrooculofacioskeletal Syndrome 1"	"disease"	"C05;C10;C16;C18"	"Congenital Abnormality"	"0.74"	"1"	"1982"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0231341"	"Premature aging syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0265201"	"De Sanctis-Cacchione syndrome"	"disease"	"C04;C05;C10;C16;C17;C18;C19;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"1998"	"2000"	"1"	"1"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0751037"	"Cockayne Syndrome, Type III"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1998"	"2016"	"7"	"0"	"CTD_human;ORPHANET"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0751038"	"Cockayne Syndrome, Type II"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"9"	"30"	"CTD_human;ORPHANET;UNIPROT"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0751039"	"Cockayne Syndrome, Type I"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"7"	"0"	"CTD_human;ORPHANET"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"0"	"0"	"UNIPROT"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1833561"	"UV-Sensitive Syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.64"	"1"	"1981"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1859312"	"CAMFAK syndrome"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2074"	"ERCC6"	"0.507"	"0.69"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"2"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C2931277"	"Pena Shokeir syndrome Type 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2074"	"ERCC6"	"0.507"	"0.69"	"C3151063"	"MACULAR DEGENERATION, AGE-RELATED, 5"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"1"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2074"	"ERCC6"	"0.507"	"0.69"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2000"	"2008"	"2"	"0"	"CTD_human"
"2074"	"ERCC6"	"0.507"	"0.69"	"C4310783"	"PREMATURE OVARIAN FAILURE 11"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0003803"	"Arnold Chiari Malformation"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2077"	"ERF"	"0.596"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"2077"	"ERF"	"0.596"	"0.448"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"2077"	"ERF"	"0.596"	"0.448"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0555206"	"Chiari malformation type II"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0750929"	"Arnold-Chiari Malformation, Type I"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0750931"	"Arnold-Chiari Malformation, Type III"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0750932"	"Arnold-Chiari Malformation, Type IV"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2013"	"2016"	"1"	"7"	"CTD_human;ORPHANET"
"2077"	"ERF"	"0.596"	"0.448"	"C1860050"	"Cloverleaf skull"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"2077"	"ERF"	"0.596"	"0.448"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2077"	"ERF"	"0.596"	"0.448"	"C2931196"	"Craniofacial dysostosis type 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2077"	"ERF"	"0.596"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2077"	"ERF"	"0.596"	"0.448"	"C3806917"	"CRANIOSYNOSTOSIS 4"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"2077"	"ERF"	"0.596"	"0.448"	"C4310679"	"CHITAYAT SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"2078"	"ERG"	"0.511"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2018"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2018"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.96875"	"2006"	"2017"	"7"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0279980"	"Extraosseous Ewings sarcoma-primitive neuroepithelial tumor"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"ORPHANET"
"2078"	"ERG"	"0.511"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.969491525423729"	"2005"	"2018"	"7"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"1994"	"2016"	"0"	"0"	"ORPHANET"
"2078"	"ERG"	"0.511"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2078"	"ERG"	"0.511"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"2081"	"ERN1"	"0.588"	"0.69"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2081"	"ERN1"	"0.588"	"0.69"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2081"	"ERN1"	"0.588"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"1"	"UNIPROT"
"2081"	"ERN1"	"0.588"	"0.69"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2081"	"ERN1"	"0.588"	"0.69"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2081"	"ERN1"	"0.588"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2081"	"ERN1"	"0.588"	"0.69"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2081"	"ERN1"	"0.588"	"0.69"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2081"	"ERN1"	"0.588"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"2091"	"FBL"	"0.681"	"0.276"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"1991"	"2009"	"3"	"0"	"CTD_human"
"2091"	"FBL"	"0.681"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2091"	"FBL"	"0.681"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2091"	"FBL"	"0.681"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2091"	"FBL"	"0.681"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2091"	"FBL"	"0.681"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2098"	"ESD"	"0.735"	"0.414"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.884615384615385"	"1991"	"2017"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2000"	"2012"	"5"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.97044494965898"	"1983"	"2018"	"15"	"1"	"CGI;CTD_human;UNIPROT"
"2099"	"ESR1"	"0.355"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.96"	"1998"	"2018"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.857142857142857"	"2000"	"2014"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"2011"	"2018"	"5"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"2011"	"2018"	"5"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0015799"	"Feminization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"2099"	"ESR1"	"0.355"	"0.897"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2006"	"2015"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.939393939393939"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0026858"	"Musculoskeletal Pain"	"phenotype"	"C05;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.916666666666667"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.952755905511811"	"1992"	"2018"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2099"	"ESR1"	"0.355"	"0.897"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.50"	"0.941176470588235"	"1997"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.926470588235294"	"1990"	"2018"	"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2009"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2002"	"2013"	"5"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0036939"	"Shared Paranoid Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.931034482758621"	"1995"	"2014"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.8"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.923076923076923"	"1999"	"2017"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.47"	"0.857142857142857"	"1995"	"2013"	"0"	"1"	"GENOMICS_ENGLAND"
"2099"	"ESR1"	"0.355"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.970588235294118"	"1996"	"2017"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.60"	"0.954022988505747"	"1991"	"2018"	"1"	"0"	"CGI;CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"4"	"0"	"PSYGENET"
"2099"	"ESR1"	"0.355"	"0.897"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.972105464272067"	"1981"	"2018"	"14"	"4"	"CGI;CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.34"	"0.75"	"2003"	"2015"	"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2014"	"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.929824561403509"	"1994"	"2018"	"0"	"0"	"CGI"
"2099"	"ESR1"	"0.355"	"0.897"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"14"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.964769647696477"	"1988"	"2018"	"14"	"5"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.925925925925926"	"1998"	"2014"	"2"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C3809250"	"ESTROGEN RESISTANCE"	"disease"		"Disease or Syndrome"	"0.70"	"1"	"1994"	"2017"	"2"	"3"	"ORPHANET;UNIPROT"
"2099"	"ESR1"	"0.355"	"0.897"	"C3887485"	"MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2099"	"ESR1"	"0.355"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2100"	"ESR2"	"0.445"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.857142857142857"	"2002"	"2013"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.956896551724138"	"1998"	"2018"	"3"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.33"		"2003"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.40"	"0.947368421052632"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0023869"	"Lithiasis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"6"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2002"	"2012"	"3"	"0"	"PSYGENET"
"2100"	"ESR2"	"0.445"	"0.828"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.934782608695652"	"2001"	"2016"	"6"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2100"	"ESR2"	"0.445"	"0.828"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.956140350877193"	"1998"	"2018"	"3"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"2100"	"ESR2"	"0.445"	"0.828"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"1999"	"2017"	"3"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C1833921"	"Familial medullary thyroid carcinoma"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2100"	"ESR2"	"0.445"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2100"	"ESR2"	"0.445"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"2002"	"2017"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"2002"	"2017"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2101"	"ESRRA"	"0.619"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"2103"	"ESRRB"	"0.667"	"0.483"	"C1837857"	"DEAFNESS, AUTOSOMAL RECESSIVE 35"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2008"	"1"	"5"	"CTD_human;UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2108"	"ETFA"	"0.611"	"0.655"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2108"	"ETFA"	"0.611"	"0.655"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2108"	"ETFA"	"0.611"	"0.655"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2108"	"ETFA"	"0.611"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2108"	"ETFA"	"0.611"	"0.655"	"C0268596"	"Multiple Acyl Coenzyme A Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.64"	"0.75"	"1991"	"2016"	"4"	"4"	"CTD_human;UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C1856401"	"Glutaric Aciduria IIA"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2003"	"4"	"3"	"CTD_human;UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C1856403"	"Glutaric Aciduria IIB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2003"	"4"	"3"	"CTD_human;UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C1856405"	"Glutaric Aciduria IIC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2003"	"4"	"3"	"CTD_human;UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2108"	"ETFA"	"0.611"	"0.655"	"C3278154"	"GLUTARIC ACIDEMIA IIA"	"disease"		"Disease or Syndrome"	"0.40"		"1991"	"2003"	"4"	"3"	"UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C3278155"	"GLUTARIC ACIDEMIA IIB"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2003"	"4"	"3"	"UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C3278156"	"GLUTARIC ACIDEMIA IIC"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2003"	"4"	"3"	"UNIPROT"
"2108"	"ETFA"	"0.611"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2009"	"6"	"0"	"GENOMICS_ENGLAND"
"2109"	"ETFB"	"0.701"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2109"	"ETFB"	"0.701"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2109"	"ETFB"	"0.701"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2109"	"ETFB"	"0.701"	"0.448"	"C0268596"	"Multiple Acyl Coenzyme A Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"1994"	"2013"	"2"	"2"	"CTD_human;UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C1856401"	"Glutaric Aciduria IIA"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1994"	"2003"	"2"	"2"	"CTD_human;UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C1856403"	"Glutaric Aciduria IIB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1994"	"2003"	"2"	"2"	"CTD_human;UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C1856405"	"Glutaric Aciduria IIC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1994"	"2003"	"2"	"2"	"CTD_human;UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C3278154"	"GLUTARIC ACIDEMIA IIA"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"2003"	"2"	"2"	"UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C3278155"	"GLUTARIC ACIDEMIA IIB"	"disease"		"Disease or Syndrome"	"0.40"		"1994"	"2003"	"2"	"2"	"UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C3278156"	"GLUTARIC ACIDEMIA IIC"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"2003"	"2"	"2"	"UNIPROT"
"2109"	"ETFB"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0268596"	"Multiple Acyl Coenzyme A Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"2003"	"2018"	"6"	"17"	"CTD_human;UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2110"	"ETFDH"	"0.667"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C1856401"	"Glutaric Aciduria IIA"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"6"	"12"	"CTD_human;UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C1856403"	"Glutaric Aciduria IIB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"6"	"12"	"CTD_human;UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C1856405"	"Glutaric Aciduria IIC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2011"	"6"	"12"	"CTD_human;UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C3278154"	"GLUTARIC ACIDEMIA IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2011"	"6"	"12"	"UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C3278155"	"GLUTARIC ACIDEMIA IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2011"	"6"	"12"	"UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C3278156"	"GLUTARIC ACIDEMIA IIC"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2011"	"6"	"13"	"UNIPROT"
"2110"	"ETFDH"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2113"	"ETS1"	"0.481"	"0.69"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"		"2010"	"2012"	"1"	"2"	"CTD_human"
"2113"	"ETS1"	"0.481"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.9375"	"2000"	"2017"	"1"	"1"	"CTD_human"
"2113"	"ETS1"	"0.481"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2113"	"ETS1"	"0.481"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2114"	"ETS2"	"0.557"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1987"	"2014"	"1"	"0"	"CTD_human"
"2115"	"ETV1"	"0.707"	"0.31"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2115"	"ETV1"	"0.707"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2016"	"3"	"0"	"CTD_human"
"2115"	"ETV1"	"0.707"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.942857142857143"	"2005"	"2018"	"3"	"0"	"CTD_human"
"2115"	"ETV1"	"0.707"	"0.31"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2004"	"0"	"0"	"ORPHANET"
"2117"	"ETV3"	"0.799"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2117"	"ETV3"	"0.799"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2012"	"0"	"0"	"ORPHANET"
"2118"	"ETV4"	"0.59"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2118"	"ETV4"	"0.59"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"2119"	"ETV5"	"0.607"	"0.552"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2119"	"ETV5"	"0.607"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"2119"	"ETV5"	"0.607"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0016057"	"Fibrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.989473684210526"	"1995"	"2018"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.974358974358974"	"1996"	"2017"	"0"	"2"	"CGI"
"2120"	"ETV6"	"0.509"	"0.655"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2007"	"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.44"	"1"	"2015"	"2017"	"2"	"2"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C0376544"	"Hematopoietic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.70"	"1"	"1995"	"2017"	"3"	"3"	"CTD_human;GENOMICS_ENGLAND"
"2120"	"ETV6"	"0.509"	"0.655"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"0.933333333333333"	"1995"	"2016"	"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C1332965"	"Congenital Mesoblastic Nephroma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"1"	"1998"	"2006"	"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C1832388"	"Platelet Disorder, Familial, with Associated Myeloid Malignancy"	"disease"	"C04;C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2120"	"ETV6"	"0.509"	"0.655"	"C1838656"	"Macrocytosis, Familial"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2120"	"ETV6"	"0.509"	"0.655"	"C4015537"	"THROMBOCYTOPENIA 5"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"2120"	"ETV6"	"0.509"	"0.655"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2121"	"EVC"	"0.611"	"0.517"	"C0013903"	"Ellis-Van Creveld Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.96"	"1"	"1964"	"2017"	"6"	"11"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2121"	"EVC"	"0.611"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2121"	"EVC"	"0.611"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2121"	"EVC"	"0.611"	"0.517"	"C0457013"	"Weyers acrofacial dysostosis"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.72"	"1"	"1995"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2121"	"EVC"	"0.611"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2121"	"EVC"	"0.611"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2122"	"MECOM"	"0.551"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0026985"	"Myelodysplasia"	"disease"		"Congenital Abnormality"	"0.36"	"1"	"1995"	"2015"	"0"	"0"	"ORPHANET"
"2122"	"MECOM"	"0.551"	"0.552"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.40"		"2010"	"2016"	"1"	"1"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2122"	"MECOM"	"0.551"	"0.552"	"C1854273"	"Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia"	"disease"	"C05;C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"2122"	"MECOM"	"0.551"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.40"	"0.962962962962963"	"1995"	"2016"	"0"	"0"	"ORPHANET"
"2122"	"MECOM"	"0.551"	"0.552"	"C4225221"	"RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2016"	"1"	"3"	"UNIPROT"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0206651"	"Clear Cell Sarcoma of Soft Tissue"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"1993"	"2017"	"0"	"0"	"ORPHANET"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"1993"	"2013"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0279980"	"Extraosseous Ewings sarcoma-primitive neuroepithelial tumor"	"disease"		"Neoplastic Process"	"0.34"	"1"	"1996"	"2016"	"0"	"0"	"ORPHANET"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0281508"	"Desmoplastic Small Round Cell Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.967261904761905"	"1993"	"2018"	"3"	"0"	"CTD_human;ORPHANET"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2130"	"EWSR1"	"0.534"	"0.586"	"C1275278"	"Extraskeletal Myxoid Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"0"	"0"	"ORPHANET"
"2131"	"EXT1"	"0.577"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"2131"	"EXT1"	"0.577"	"0.655"	"C0008479"	"Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.875"	"1995"	"2015"	"0"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2131"	"EXT1"	"0.577"	"0.655"	"C0015306"	"Hereditary Multiple Exostoses"	"disease"	"C04;C05;C16"	"Congenital Abnormality"	"1.00"	"0.96875"	"1995"	"2018"	"13"	"6"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2131"	"EXT1"	"0.577"	"0.655"	"C0023003"	"Langer-Giedion Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2015"	"0"	"0"	"ORPHANET"
"2131"	"EXT1"	"0.577"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2131"	"EXT1"	"0.577"	"0.655"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"2131"	"EXT1"	"0.577"	"0.655"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"GENOMICS_ENGLAND"
"2131"	"EXT1"	"0.577"	"0.655"	"C0206641"	"Osteochondromatosis"	"disease"	"C04;C05"	"Neoplastic Process"	"0.40"	"0.958333333333333"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"2131"	"EXT1"	"0.577"	"0.655"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"2131"	"EXT1"	"0.577"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2002"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2132"	"EXT2"	"0.627"	"0.483"	"C0015306"	"Hereditary Multiple Exostoses"	"disease"	"C04;C05;C16"	"Congenital Abnormality"	"0.90"	"0.986111111111111"	"1994"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"2132"	"EXT2"	"0.627"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2132"	"EXT2"	"0.627"	"0.483"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2132"	"EXT2"	"0.627"	"0.483"	"C0206641"	"Osteochondromatosis"	"disease"	"C04;C05"	"Neoplastic Process"	"0.40"	"0.9375"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"2132"	"EXT2"	"0.627"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"2132"	"EXT2"	"0.627"	"0.483"	"C1832588"	"Chromosome 11p11.2 Deletion Syndrome"	"disease"	"C04;C05;C16;C23"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"2132"	"EXT2"	"0.627"	"0.483"	"C1851413"	"EXOSTOSES, MULTIPLE, TYPE II"	"disease"	"C04;C05;C16;C23"	"Disease or Syndrome"	"0.60"		"1996"	"2017"	"8"	"13"	"CTD_human;UNIPROT"
"2132"	"EXT2"	"0.627"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2132"	"EXT2"	"0.627"	"0.483"	"C4225248"	"SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"2"	"ORPHANET;UNIPROT"
"2134"	"EXTL1"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2137"	"EXTL3"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2137"	"EXTL3"	"0.672"	"0.483"	"C4479452"	"IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"2138"	"EYA1"	"0.559"	"0.655"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C0018777"	"Conductive hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2138"	"EYA1"	"0.559"	"0.655"	"C0265234"	"Branchio-Oto-Renal Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"1.00"	"0.975609756097561"	"1969"	"2018"	"7"	"21"	"CTD_human;ORPHANET;UNIPROT"
"2138"	"EYA1"	"0.559"	"0.655"	"C0376524"	"Branchio-Oculo-Facial Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C1833691"	"Otofaciocervical Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2006"	"0"	"0"	"CTD_human;ORPHANET"
"2138"	"EYA1"	"0.559"	"0.655"	"C1865143"	"BRANCHIOOTIC SYNDROME 1"	"disease"	"C16"	"Disease or Syndrome"	"0.72"	"1"	"1998"	"2016"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2138"	"EYA1"	"0.559"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2138"	"EYA1"	"0.559"	"0.655"	"C1970479"	"Branchiootorenal Syndrome 2"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2138"	"EYA1"	"0.559"	"0.655"	"C2931416"	"Fara Chlupackova syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2138"	"EYA1"	"0.559"	"0.655"	"C3551443"	"ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT"	"disease"		"Disease or Syndrome"	"0.50"		"1998"	"2006"	"4"	"3"	"ORPHANET;UNIPROT"
"2138"	"EYA1"	"0.559"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2146"	"EZH2"	"0.421"	"0.759"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.977777777777778"	"2003"	"2018"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2146"	"EZH2"	"0.421"	"0.759"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2018"	"0"	"3"	"CGI"
"2146"	"EZH2"	"0.421"	"0.759"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2010"	"2018"	"1"	"0"	"CGI;CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2013"	"3"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"0"	"0"	"CGI"
"2146"	"EZH2"	"0.421"	"0.759"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"2010"	"2017"	"1"	"0"	"CGI;CTD_human;UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2146"	"EZH2"	"0.421"	"0.759"	"C0220765"	"Weaver-Like Syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2018"	"5"	"6"	"UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0265210"	"Weaver syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.78"	"1"	"1993"	"2018"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.37"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"2146"	"EZH2"	"0.421"	"0.759"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.985294117647059"	"2002"	"2018"	"3"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.977272727272727"	"2003"	"2018"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C0749794"	"Upper Extremity Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1301355"	"Myelodysplastic-Myeloproliferative Diseases"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1332201"	"Adult Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C1332967"	"Childhood Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"2146"	"EZH2"	"0.421"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"2146"	"EZH2"	"0.421"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2147"	"F2"	"0.466"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"1980"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2010"	"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"		"2003"	"2007"	"2"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.52"	"1"	"1991"	"2013"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0020640"	"Inherited Factor II deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.916666666666667"	"1983"	"2013"	"13"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2147"	"F2"	"0.466"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.78125"	"1997"	"2017"	"3"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.54"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2018"	"1"	"1"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0037198"	"Sinus Thrombosis, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.923076923076923"	"1995"	"2016"	"1"	"1"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.42"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.58"		"1992"	"2013"	"4"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.37"		"1999"	"2013"	"3"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0085605"	"Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2012"	"2"	"0"	"PSYGENET"
"2147"	"F2"	"0.466"	"0.793"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"2007"	"4"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.949152542372881"	"1998"	"2016"	"3"	"1"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0162819"	"Skin Diseases, Vascular"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0267412"	"Mesenteric Venous Thrombosis"	"phenotype"	"C06;C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0272317"	"Hereditary factor II deficiency disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.76"	"1"	"1955"	"2009"	"12"	"12"	"CTD_human;ORPHANET;UNIPROT"
"2147"	"F2"	"0.466"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.60"	"0.963963963963964"	"1992"	"2017"	"1"	"1"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751500"	"Petrous Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751501"	"Intracranial Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751502"	"Petrous Sinus Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2009"	"2"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C1412000"	"Mesenteric vascular insufficiency"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.50"	"0.8"	"2002"	"2018"	"1"	"2"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2018"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3203356"	"Factor II deficiency"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1983"	"2009"	"0"	"0"	"ORPHANET"
"2147"	"F2"	"0.466"	"0.793"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3280672"	"PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3852984"	"Acute Mesenteric Arterial Embolus"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3852985"	"Occlusive Mesenteric Arterial Ischemia"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3852986"	"Nonocclusive Mesenteric Ischemia"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2147"	"F2"	"0.466"	"0.793"	"C3852987"	"Acute Mesenteric Arterial Thrombosis"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2009"	"2011"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2149"	"F2R"	"0.478"	"0.759"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"2150"	"F2RL1"	"0.514"	"0.724"	"C0017160"	"Gastroenteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2150"	"F2RL1"	"0.514"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.34"		"2003"	"2015"	"2"	"0"	"CTD_human"
"2150"	"F2RL1"	"0.514"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2150"	"F2RL1"	"0.514"	"0.724"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2150"	"F2RL1"	"0.514"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.60"	"0.928571428571429"	"1994"	"2016"	"3"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0034155"	"Purpura, Thrombotic Thrombocytopenic"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.34"		"2002"	"2015"	"2"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2015"	"2"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C1268935"	"Congenital Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.666666666666667"	"2005"	"2016"	"1"	"0"	"CTD_human"
"2152"	"F3"	"0.458"	"0.724"	"C1956258"	"Familial Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"1996"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.36"	"0.8"	"1995"	"2016"	"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0015499"	"Hereditary Factor V Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.77"	"1"	"1996"	"2012"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2153"	"F5"	"0.468"	"0.69"	"C0019154"	"Hepatic Vein Thrombosis"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.56"	"1"	"2000"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2153"	"F5"	"0.468"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.869565217391304"	"1995"	"2013"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0035328"	"Retinal Vein Occlusion"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.38"	"0.857142857142857"	"1998"	"2017"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.50"	"0.866666666666667"	"1995"	"2018"	"1"	"1"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"2004"	"2010"	"2"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.38"		"1998"	"2007"	"2"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.50"		"2002"	"2012"	"5"	"11"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1998"	"2001"	"2"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.96969696969697"	"1996"	"2018"	"5"	"11"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0267412"	"Mesenteric Venous Thrombosis"	"phenotype"	"C06;C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0338575"	"Sagittal Sinus Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0600433"	"Activated Protein C Resistance"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"	"0.9375"	"1994"	"2017"	"9"	"3"	"UNIPROT"
"2153"	"F5"	"0.468"	"0.69"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751823"	"Septic Phlebitis, Sagittal Sinus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751824"	"Sagittal Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0856761"	"Budd-Chiari Syndrome"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2153"	"F5"	"0.468"	"0.69"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2003"	"2009"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C1412000"	"Mesenteric vascular insufficiency"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"2153"	"F5"	"0.468"	"0.69"	"C1527411"	"Thrombosis of retinal vein"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C1853831"	"Bleeding Disorder, East Texas Type"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2153"	"F5"	"0.468"	"0.69"	"C1861171"	"THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.62"	"1"	"1994"	"2006"	"9"	"4"	"CTD_human;UNIPROT"
"2153"	"F5"	"0.468"	"0.69"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.50"	"0.75"	"1996"	"2018"	"2"	"11"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C2584620"	"Thrombophilia, hereditary"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C3280670"	"PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2153"	"F5"	"0.468"	"0.69"	"C3852984"	"Acute Mesenteric Arterial Embolus"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C3852985"	"Occlusive Mesenteric Arterial Ischemia"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C3852986"	"Nonocclusive Mesenteric Ischemia"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2153"	"F5"	"0.468"	"0.69"	"C3852987"	"Acute Mesenteric Arterial Thrombosis"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0015503"	"Factor VII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1983"	"2017"	"27"	"57"	"CTD_human;ORPHANET;UNIPROT"
"2155"	"F7"	"0.547"	"0.69"	"C0018965"	"Hematuria"	"phenotype"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2003"	"2007"	"3"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0019087"	"Hemorrhagic Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.866666666666667"	"1995"	"2007"	"0"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0032787"	"Postoperative Complications"	"group"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2008"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0151699"	"Intracranial Hemorrhages"	"group"	"C10;C14;C23"	"Disease or Syndrome"	"0.45"	"1"	"1999"	"2010"	"5"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0273058"	"Traumatic intracranial hemorrhage"	"disease"	"C10;C14;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0553692"	"Brain hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2010"	"5"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0749098"	"Hematoma, Subdural, Acute"	"phenotype"	"C10;C14;C23;C26"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0751797"	"Intracranial Hematoma, Traumatic"	"phenotype"	"C10;C14;C26"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C0751893"	"Posterior Fossa Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2010"	"5"	"0"	"CTD_human"
"2155"	"F7"	"0.547"	"0.69"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.31"		"2006"	"2011"	"2"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C0019069"	"Hemophilia A"	"disease"	"C15;C16"	"Disease or Syndrome"	"1.00"	"0.958823529411765"	"1980"	"2018"	"82"	"209"	"CTD_human;ORPHANET;UNIPROT"
"2157"	"F8"	"0.586"	"0.655"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.33"		"2002"	"2008"	"1"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C0272322"	"Severe hereditary factor VIII deficiency disease"	"disease"		"Disease or Syndrome"	"0.40"	"0.948717948717949"	"1988"	"2017"	"0"	"0"	"ORPHANET"
"2157"	"F8"	"0.586"	"0.655"	"C0272324"	"Mild hereditary factor VIII deficiency disease"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1986"	"2016"	"0"	"0"	"ORPHANET"
"2157"	"F8"	"0.586"	"0.655"	"C0272325"	"Factor 8 deficiency, acquired"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C3494186"	"Autosomal Hemophilia A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2005"	"2"	"0"	"CTD_human"
"2157"	"F8"	"0.586"	"0.655"	"C3494187"	"Factor VIII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.41"	"1"	"1997"	"2005"	"2"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"1987"	"1997"	"4"	"0"	"PSYGENET"
"2158"	"F9"	"0.511"	"0.759"	"C0008533"	"Hemophilia B"	"disease"	"C15;C16"	"Disease or Syndrome"	"1.00"	"0.976027397260274"	"1952"	"2018"	"40"	"73"	"CTD_human;ORPHANET;UNIPROT"
"2158"	"F9"	"0.511"	"0.759"	"C0019069"	"Hemophilia A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"0.931034482758621"	"1982"	"2018"	"1"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C0750384"	"Coumarin Resistance"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C2749016"	"Thrombophilia, X-Linked, Due To Factor Ix Defect"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2158"	"F9"	"0.511"	"0.759"	"C3275410"	"DEEP VENOUS THROMBOSIS, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"2158"	"F9"	"0.511"	"0.759"	"C3494186"	"Autosomal Hemophilia A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2158"	"F9"	"0.511"	"0.759"	"C3494187"	"Factor VIII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2159"	"F10"	"0.636"	"0.448"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"1977"	"2018"	"1"	"0"	"CTD_human"
"2159"	"F10"	"0.636"	"0.448"	"C0015519"	"Factor X Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.75"	"1"	"1989"	"2016"	"21"	"22"	"CTD_human;ORPHANET;UNIPROT"
"2159"	"F10"	"0.636"	"0.448"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"2159"	"F10"	"0.636"	"0.448"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"2160"	"F11"	"0.656"	"0.414"	"C0015523"	"Hereditary Factor XI Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"1.00"	"1"	"1981"	"2017"	"21"	"90"	"CTD_human;ORPHANET;UNIPROT"
"2160"	"F11"	"0.656"	"0.414"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0015526"	"Factor XII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.96"	"1"	"1981"	"2011"	"9"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2161"	"F12"	"0.727"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0019243"	"Angioedemas, Hereditary"	"group"	"C14;C16;C17;C20"	"Disease or Syndrome"	"0.50"	"0.923076923076923"	"1984"	"2015"	"1"	"1"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2161"	"F12"	"0.727"	"0.379"	"C1857728"	"Hereditary Angioedema Type III"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.74"	"1"	"2000"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2161"	"F12"	"0.727"	"0.379"	"C1960459"	"Hereditary angioedema with normal C1 esterase inhibitor activity"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2162"	"F13A1"	"0.602"	"0.586"	"C0015530"	"Hereditary Factor XIII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.76"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"2162"	"F13A1"	"0.602"	"0.586"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2162"	"F13A1"	"0.602"	"0.586"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"2162"	"F13A1"	"0.602"	"0.586"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"1999"	"2008"	"1"	"0"	"CTD_human"
"2162"	"F13A1"	"0.602"	"0.586"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2162"	"F13A1"	"0.602"	"0.586"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2162"	"F13A1"	"0.602"	"0.586"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2162"	"F13A1"	"0.602"	"0.586"	"C2750514"	"Factor Xiii, A Subunit, Deficiency Of"	"phenotype"	"C15;C16"	"Finding"	"0.60"		"1981"	"2016"	"6"	"15"	"CTD_human;UNIPROT"
"2165"	"F13B"	"0.707"	"0.414"	"C0015530"	"Hereditary Factor XIII Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"1990"	"1990"	"1"	"0"	"CTD_human;ORPHANET"
"2165"	"F13B"	"0.707"	"0.414"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2165"	"F13B"	"0.707"	"0.414"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2165"	"F13B"	"0.707"	"0.414"	"C2750481"	"Factor XIII, B Subunit, Deficiency Of"	"phenotype"	"C15;C16"	"Finding"	"0.60"		"1993"	"2015"	"4"	"6"	"CTD_human;UNIPROT"
"2166"	"FAAH"	"0.555"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"2166"	"FAAH"	"0.555"	"0.517"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2007"	"2016"	"3"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.91304347826087"	"2005"	"2017"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0032962"	"Pregnancy Complications"	"group"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2010"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2166"	"FAAH"	"0.555"	"0.517"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2002"	"2014"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2166"	"FAAH"	"0.555"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2006"	"0"	"0"	"UNIPROT"
"2167"	"FABP4"	"0.59"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2167"	"FABP4"	"0.59"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2168"	"FABP1"	"0.676"	"0.448"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2168"	"FABP1"	"0.676"	"0.448"	"C0022672"	"Acute Kidney Tubular Necrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2168"	"FABP1"	"0.676"	"0.448"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"2169"	"FABP2"	"0.645"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"2169"	"FABP2"	"0.645"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2170"	"FABP3"	"0.659"	"0.483"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2170"	"FABP3"	"0.659"	"0.483"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2170"	"FABP3"	"0.659"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2015"	"2016"	"1"	"0"	"PSYGENET"
"2171"	"FABP5"	"0.633"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"2171"	"FABP5"	"0.633"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2171"	"FABP5"	"0.633"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"2173"	"FABP7"	"0.642"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"2"	"0"	"PSYGENET"
"2173"	"FABP7"	"0.642"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"2173"	"FABP7"	"0.642"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"2173"	"FABP7"	"0.642"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"PSYGENET"
"2173"	"FABP7"	"0.642"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"2173"	"FABP7"	"0.642"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2173"	"FABP7"	"0.642"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2175"	"FANCA"	"0.567"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.954545454545455"	"1995"	"2018"	"1"	"29"	"CTD_human;ORPHANET"
"2175"	"FANCA"	"0.567"	"0.621"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2175"	"FANCA"	"0.567"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2004"	"0"	"0"	"CGI"
"2175"	"FANCA"	"0.567"	"0.621"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"1996"	"1998"	"2"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C1856796"	"Estren-Dameshek Variant of Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.50"		"1998"	"2008"	"8"	"17"	"UNIPROT"
"2175"	"FANCA"	"0.567"	"0.621"	"C1856797"	"Estren-Dameshek Variant of Fanconi Pancytopenia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.50"		"1998"	"2008"	"8"	"17"	"UNIPROT"
"2175"	"FANCA"	"0.567"	"0.621"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2175"	"FANCA"	"0.567"	"0.621"	"C3469521"	"FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)"	"disease"		"Disease or Syndrome"	"0.70"	"0.951219512195122"	"1993"	"2018"	"8"	"39"	"UNIPROT"
"2175"	"FANCA"	"0.567"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2175"	"FANCA"	"0.567"	"0.621"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2017"	"2017"	"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.955223880597015"	"1993"	"2017"	"1"	"21"	"CTD_human;ORPHANET"
"2176"	"FANCC"	"0.569"	"0.655"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"2176"	"FANCC"	"0.569"	"0.655"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.41"		"2008"	"2008"	"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2176"	"FANCC"	"0.569"	"0.655"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2176"	"FANCC"	"0.569"	"0.655"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2176"	"FANCC"	"0.569"	"0.655"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2176"	"FANCC"	"0.569"	"0.655"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"2176"	"FANCC"	"0.569"	"0.655"	"C3468041"	"FANCONI ANEMIA, COMPLEMENTATION GROUP C"	"disease"		"Disease or Syndrome"	"0.83"	"1"	"1992"	"2017"	"7"	"44"	"CTD_human;UNIPROT"
"2176"	"FANCC"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2176"	"FANCC"	"0.569"	"0.655"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1992"	"1992"	"1"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.952"	"1998"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2015"	"0"	"0"	"CGI"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"0"	"0"	"CGI"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2177"	"FANCD2"	"0.534"	"0.724"	"C3160738"	"FANCONI ANEMIA, COMPLEMENTATION GROUP D2"	"disease"		"Disease or Syndrome"	"0.88"	"1"	"2001"	"2018"	"1"	"5"	"CTD_human;UNIPROT"
"2177"	"FANCD2"	"0.534"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2177"	"FANCD2"	"0.534"	"0.724"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1995"	"1999"	"4"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2014"	"0"	"0"	"ORPHANET"
"2178"	"FANCE"	"0.636"	"0.586"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2178"	"FANCE"	"0.636"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2178"	"FANCE"	"0.636"	"0.586"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"1999"	"4"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2178"	"FANCE"	"0.636"	"0.586"	"C3160739"	"FANCONI ANEMIA, COMPLEMENTATION GROUP E"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1995"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"2178"	"FANCE"	"0.636"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2178"	"FANCE"	"0.636"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1995"	"1999"	"4"	"0"	"GENOMICS_ENGLAND"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.53"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2180"	"ACSL1"	"0.685"	"0.31"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0041834"	"Erythema"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2182"	"ACSL4"	"0.609"	"0.552"	"C1845672"	"Mental Retardation, X-Linked 63"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2003"	"1"	"3"	"CTD_human;UNIPROT"
"2182"	"ACSL4"	"0.609"	"0.552"	"C1846242"	"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis"	"disease"	"C05;C10;C12;C13;C15;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2182"	"ACSL4"	"0.609"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"2182"	"ACSL4"	"0.609"	"0.552"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2017"	"7"	"0"	"CLINGEN;ORPHANET"
"2182"	"ACSL4"	"0.609"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"1998"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"2184"	"FAH"	"0.624"	"0.483"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2184"	"FAH"	"0.624"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2184"	"FAH"	"0.624"	"0.483"	"C0268483"	"Tyrosinemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1985"	"2017"	"2"	"0"	"CTD_human"
"2184"	"FAH"	"0.624"	"0.483"	"C0268487"	"Tyrosine Transaminase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"2184"	"FAH"	"0.624"	"0.483"	"C0268490"	"Tyrosinemia, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.975"	"1990"	"2017"	"16"	"39"	"CTD_human;ORPHANET;UNIPROT"
"2184"	"FAH"	"0.624"	"0.483"	"C0268623"	"Tyrosinemia, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"2184"	"FAH"	"0.624"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"2184"	"FAH"	"0.624"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2185"	"PTK2B"	"0.502"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2186"	"BPTF"	"0.743"	"0.31"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2186"	"BPTF"	"0.743"	"0.31"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2186"	"BPTF"	"0.743"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2186"	"BPTF"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.45"	"1"	"2002"	"2017"	"0"	"1"	"ORPHANET"
"2187"	"FANCB"	"0.52"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C1845292"	"FANCONI ANEMIA, COMPLEMENTATION GROUP B"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2187"	"FANCB"	"0.52"	"0.586"	"C1848599"	"VACTERL Association With Hydrocephalus"	"disease"	"C05;C06;C10;C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human;ORPHANET"
"2187"	"FANCB"	"0.52"	"0.586"	"C1848600"	"Vater Association With Hydrocephalus"	"disease"	"C05;C06;C08;C10;C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2187"	"FANCB"	"0.52"	"0.586"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2187"	"FANCB"	"0.52"	"0.586"	"C2749240"	"Vater Association With Macrocephaly And Ventriculomegaly"	"disease"	"C05;C06;C08;C10;C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2187"	"FANCB"	"0.52"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"2187"	"FANCB"	"0.52"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.50"	"0.888888888888889"	"2000"	"2017"	"0"	"3"	"ORPHANET"
"2188"	"FANCF"	"0.627"	"0.552"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2188"	"FANCF"	"0.627"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CGI"
"2188"	"FANCF"	"0.627"	"0.552"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2188"	"FANCF"	"0.627"	"0.552"	"C3469526"	"FANCONI ANEMIA, COMPLEMENTATION GROUP F"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1997"	"2017"	"0"	"6"	"CTD_human"
"2188"	"FANCF"	"0.627"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2188"	"FANCF"	"0.627"	"0.552"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.925925925925926"	"1993"	"2017"	"2"	"5"	"CTD_human;ORPHANET"
"2189"	"FANCG"	"0.648"	"0.483"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2189"	"FANCG"	"0.648"	"0.483"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2189"	"FANCG"	"0.648"	"0.483"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2189"	"FANCG"	"0.648"	"0.483"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2189"	"FANCG"	"0.648"	"0.483"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2189"	"FANCG"	"0.648"	"0.483"	"C3469527"	"fanconi anemia complementation group g"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2009"	"2"	"8"	"CTD_human;UNIPROT"
"2189"	"FANCG"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2189"	"FANCG"	"0.648"	"0.483"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2192"	"FBLN1"	"0.619"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2192"	"FBLN1"	"0.619"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2192"	"FBLN1"	"0.619"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2192"	"FBLN1"	"0.619"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"2192"	"FBLN1"	"0.619"	"0.552"	"C1842422"	"Synpolydactyly 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2194"	"FASN"	"0.516"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"2"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"3"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2194"	"FASN"	"0.516"	"0.793"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0205825"	"Liposarcoma, Pleomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"2"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2011"	"2"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"3"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2009"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2194"	"FASN"	"0.516"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2194"	"FASN"	"0.516"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"2195"	"FAT1"	"0.573"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2196"	"FAT2"	"0.886"	"0.138"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2199"	"FBLN2"	"0.735"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2199"	"FBLN2"	"0.735"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2199"	"FBLN2"	"0.735"	"0.448"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2199"	"FBLN2"	"0.735"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0003496"	"Aortic Rupture"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0003706"	"Arachnodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.46"	"1"	"1995"	"2017"	"1"	"2"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"1996"	"1996"	"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0013581"	"Ectopia Lentis"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"	"1"	"1994"	"2016"	"1"	"3"	"CTD_human;ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2004"	"2016"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"1.00"	"0.957236842105263"	"1973"	"2018"	"54"	"369"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2200"	"FBN1"	"0.469"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1997"	"2017"	"1"	"36"	"CTD_human;GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0265287"	"Acromicric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.75"	"1"	"1991"	"2016"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"2200"	"FBN1"	"0.469"	"0.69"	"C0265313"	"Weill-Marchesani syndrome"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.90"	"1"	"1997"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.32"	"1"	"2001"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C0741160"	"Aortic Aneurysm, Ruptured"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1321551"	"Shprintzen-Goldberg syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"1996"	"2007"	"0"	"0"	"ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C1851286"	"Ectopia lentis isolated"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.45"	"1"	"1994"	"2015"	"0"	"8"	"ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1858556"	"OVERLAP CONNECTIVE TISSUE DISEASE"	"disease"	"C11;C14;C17"	"Disease or Syndrome"	"0.44"	"1"	"1989"	"2016"	"0"	"7"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1861456"	"Stiff Skin Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.73"	"1"	"1991"	"2016"	"1"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2200"	"FBN1"	"0.469"	"0.69"	"C1869114"	"Weill-Marchesani Syndrome, Autosomal Recessive"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"0"	"0"	"CTD_human"
"2200"	"FBN1"	"0.469"	"0.69"	"C1869115"	"Weill-Marchesani Syndrome, Autosomal Dominant"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.81"	"1"	"2003"	"2015"	"0"	"7"	"CTD_human;ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C2746069"	"Familial ectopia lentis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C2931588"	"GEMSS syndrome"	"disease"	"C05;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C3280054"	"GELEOPHYSIC DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1991"	"2016"	"1"	"10"	"UNIPROT"
"2200"	"FBN1"	"0.469"	"0.69"	"C3489726"	"Geleophysic dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.57"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2200"	"FBN1"	"0.469"	"0.69"	"C3541518"	"ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.50"		"1994"	"2007"	"5"	"3"	"CTD_human;UNIPROT"
"2200"	"FBN1"	"0.469"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"2200"	"FBN1"	"0.469"	"0.69"	"C4310796"	"MARFAN LIPODYSTROPHY SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2017"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2201"	"FBN2"	"0.541"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2201"	"FBN2"	"0.541"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"2201"	"FBN2"	"0.541"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2201"	"FBN2"	"0.541"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1998"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"2201"	"FBN2"	"0.541"	"0.69"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.48"	"1"	"1994"	"2016"	"6"	"1"	"CLINGEN"
"2201"	"FBN2"	"0.541"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"2201"	"FBN2"	"0.541"	"0.69"	"C0220668"	"Congenital contractural arachnodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"1"	"1994"	"2017"	"9"	"19"	"CTD_human;ORPHANET;UNIPROT"
"2201"	"FBN2"	"0.541"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2201"	"FBN2"	"0.541"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"2201"	"FBN2"	"0.541"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2201"	"FBN2"	"0.541"	"0.69"	"C4015286"	"MACULAR DEGENERATION, EARLY-ONSET"	"disease"		"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1832174"	"DOYNE HONEYCOMB RETINAL DYSTROPHY"	"disease"	"C10;C11"	"Disease or Syndrome"	"1.00"	"0.833333333333333"	"1999"	"2015"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1852020"	"Malattia Leventinese"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.99"	"0.777777777777778"	"1999"	"2015"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2202"	"EFEMP1"	"0.572"	"0.552"	"C1852021"	"Drusen, Radial, Autosomal Dominant"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2008"	"4"	"1"	"ORPHANET;UNIPROT"
"2203"	"FBP1"	"0.667"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0016756"	"Fructose-1,6-Diphosphatase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1995"	"2016"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2203"	"FBP1"	"0.667"	"0.379"	"C0019489"	"Deficiency, Hexosediphosphatase"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2203"	"FBP1"	"0.667"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2203"	"FBP1"	"0.667"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"2203"	"FBP1"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2205"	"FCER1A"	"0.727"	"0.276"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2205"	"FCER1A"	"0.727"	"0.276"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"2205"	"FCER1A"	"0.727"	"0.276"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"2205"	"FCER1A"	"0.727"	"0.276"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2206"	"MS4A2"	"0.752"	"0.31"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2007"	"2010"	"3"	"0"	"CTD_human"
"2206"	"MS4A2"	"0.752"	"0.31"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2206"	"MS4A2"	"0.752"	"0.31"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2206"	"MS4A2"	"0.752"	"0.31"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2207"	"FCER1G"	"0.735"	"0.448"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"2207"	"FCER1G"	"0.735"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2208"	"FCER2"	"0.598"	"0.621"	"C0014038"	"Encephalitis"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"2208"	"FCER2"	"0.598"	"0.621"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2001"	"1"	"0"	"CTD_human"
"2208"	"FCER2"	"0.598"	"0.621"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2208"	"FCER2"	"0.598"	"0.621"	"C0393484"	"Rasmussen Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2208"	"FCER2"	"0.598"	"0.621"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2209"	"FCGR1A"	"0.611"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.764705882352941"	"2003"	"2016"	"2"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.45"	"1"	"2010"	"2017"	"2"	"3"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.892857142857143"	"1996"	"2017"	"1"	"2"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.39"	"0.714285714285714"	"2004"	"2014"	"0"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0026691"	"Mucocutaneous Lymph Node Syndrome"	"disease"	"C14;C15;C17"	"Disease or Syndrome"	"0.49"	"1"	"2012"	"2017"	"2"	"1"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2001"	"2002"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2212"	"FCGR2A"	"0.511"	"0.724"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2213"	"FCGR2B"	"0.582"	"0.655"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2213"	"FCGR2B"	"0.582"	"0.655"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.60"	"0.96551724137931"	"1996"	"2016"	"0"	"0"	"CTD_human"
"2213"	"FCGR2B"	"0.582"	"0.655"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.55"	"1"	"2004"	"2016"	"0"	"0"	"CTD_human"
"2213"	"FCGR2B"	"0.582"	"0.655"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2213"	"FCGR2B"	"0.582"	"0.655"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2214"	"FCGR3A"	"0.466"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2214"	"FCGR3A"	"0.466"	"0.793"	"C0752332"	"Lupus Vasculitis, Central Nervous System"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2214"	"FCGR3A"	"0.466"	"0.793"	"C0752334"	"Lupus Meningoencephalitis"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2214"	"FCGR3A"	"0.466"	"0.793"	"C0752335"	"Neuropsychiatric Systemic Lupus Erythematosus"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2214"	"FCGR3A"	"0.466"	"0.793"	"C3810342"	"IMMUNODEFICIENCY 20"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2013"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0024143"	"Lupus Nephritis"	"disease"	"C12;C13;C17;C20"	"Disease or Syndrome"	"0.36"	"0.666666666666667"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0752332"	"Lupus Vasculitis, Central Nervous System"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0752334"	"Lupus Meningoencephalitis"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C0752335"	"Neuropsychiatric Systemic Lupus Erythematosus"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2215"	"FCGR3B"	"0.49"	"0.759"	"C3495801"	"Granulomatosis with polyangiitis"	"disease"	"C08;C14;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2218"	"FKTN"	"0.522"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2218"	"FKTN"	"0.522"	"0.586"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1998"	"2008"	"4"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"2218"	"FKTN"	"0.522"	"0.586"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.66"	"1"	"2007"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"2218"	"FKTN"	"0.522"	"0.586"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"1998"	"1999"	"2"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2218"	"FKTN"	"0.522"	"0.586"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2018"	"4"	"14"	"CTD_human;ORPHANET;UNIPROT"
"2218"	"FKTN"	"0.522"	"0.586"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"2218"	"FKTN"	"0.522"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2004"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2218"	"FKTN"	"0.522"	"0.586"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2218"	"FKTN"	"0.522"	"0.586"	"C1969024"	"CARDIOMYOPATHY, DILATED, 1X"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"2218"	"FKTN"	"0.522"	"0.586"	"C1969040"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2015"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2218"	"FKTN"	"0.522"	"0.586"	"C2751052"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4"	"disease"		"Disease or Syndrome"	"0.80"		"2001"	"2015"	"4"	"2"	"CTD_human;UNIPROT"
"2218"	"FKTN"	"0.522"	"0.586"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"2218"	"FKTN"	"0.522"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"0.714285714285714"	"2001"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"2219"	"FCN1"	"0.743"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2219"	"FCN1"	"0.743"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2220"	"FCN2"	"0.584"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2220"	"FCN2"	"0.584"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2222"	"FDFT1"	"0.642"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2224"	"FDPS"	"0.72"	"0.448"	"C0265970"	"Porokeratosis, Disseminated Superficial Actinic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2224"	"FDPS"	"0.72"	"0.448"	"C4225262"	"POROKERATOSIS 9, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"2232"	"FDXR"	"0.815"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2232"	"FDXR"	"0.815"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2232"	"FDXR"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2232"	"FDXR"	"0.815"	"0.241"	"C4521678"	"AUDITORY NEUROPATHY AND OPTIC ATROPHY"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"2235"	"FECH"	"0.636"	"0.414"	"C0005395"	"Bile Duct Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2235"	"FECH"	"0.636"	"0.414"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2235"	"FECH"	"0.636"	"0.414"	"C0162568"	"Erythropoietic Protoporphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.956043956043956"	"1982"	"2018"	"17"	"18"	"CTD_human;ORPHANET;UNIPROT"
"2235"	"FECH"	"0.636"	"0.414"	"C0349426"	"Ferrochelatase deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1992"	"2007"	"17"	"8"	"CTD_human;UNIPROT"
"2235"	"FECH"	"0.636"	"0.414"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2237"	"FEN1"	"0.607"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2237"	"FEN1"	"0.607"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2237"	"FEN1"	"0.607"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2239"	"GPC4"	"0.596"	"0.621"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.41"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human"
"2239"	"GPC4"	"0.596"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2239"	"GPC4"	"0.596"	"0.621"	"C0796154"	"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1"	"disease"	"C05;C10;C14;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.54"	"0.75"	"1998"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"2239"	"GPC4"	"0.596"	"0.621"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2241"	"FER"	"0.696"	"0.379"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2241"	"FER"	"0.696"	"0.379"	"C0346163"	"Endometrioid carcinoma ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2243"	"FGA"	"0.594"	"0.586"	"C0001733"	"Afibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"1992"	"2010"	"4"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"		"1993"	"1996"	"2"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.50"		"2000"	"2012"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0268389"	"Amyloidosis, familial visceral"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2008"	"1"	"4"	"CTD_human;UNIPROT"
"2243"	"FGA"	"0.594"	"0.586"	"C0272350"	"Dysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2243"	"FGA"	"0.594"	"0.586"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0740340"	"Amyloidosis, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"1996"	"2"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C1859970"	"Hypodysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2006"	"2"	"3"	"UNIPROT"
"2243"	"FGA"	"0.594"	"0.586"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.41"		"2007"	"2012"	"1"	"1"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C2584774"	"Congenital hypofibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.79"	"1"	"1992"	"2016"	"5"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2243"	"FGA"	"0.594"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"2243"	"FGA"	"0.594"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2243"	"FGA"	"0.594"	"0.586"	"C4316812"	"Fibrinogen Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1992"	"2002"	"4"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0001733"	"Afibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.36"	"1"	"2000"	"2015"	"0"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C0272350"	"Dysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.61"	"1"	"1992"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2244"	"FGB"	"0.604"	"0.552"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2244"	"FGB"	"0.604"	"0.552"	"C1859970"	"Hypodysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"1"	"UNIPROT"
"2244"	"FGB"	"0.604"	"0.552"	"C2584774"	"Congenital hypofibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.76"	"1"	"2000"	"2018"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2244"	"FGB"	"0.604"	"0.552"	"C4316812"	"Fibrinogen Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2245"	"FGD1"	"0.621"	"0.621"	"C0016508"	"Congenital Foot Deformity"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"1994"	"2002"	"4"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2245"	"FGD1"	"0.621"	"0.621"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0042063"	"Urogenital Abnormalities"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.30"		"1994"	"2000"	"3"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0175701"	"Aarskog syndrome"	"disease"	"C05;C14;C16;C19"	"Disease or Syndrome"	"0.80"	"0.961538461538462"	"1994"	"2018"	"9"	"14"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2245"	"FGD1"	"0.621"	"0.621"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C1844569"	"Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.50"		"1994"	"2011"	"7"	"2"	"CLINGEN;UNIPROT"
"2245"	"FGD1"	"0.621"	"0.621"	"C1856871"	"Autosomal recessive facio-digito-genital syndrome"	"disease"	"C05;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"1994"	"2007"	"6"	"0"	"CTD_human"
"2245"	"FGD1"	"0.621"	"0.621"	"C3275558"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC 16"	"disease"		"Disease or Syndrome"	"0.50"		"1994"	"2011"	"7"	"2"	"CLINGEN;UNIPROT"
"2245"	"FGD1"	"0.621"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2246"	"FGF1"	"0.572"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1991"	"2007"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2006"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2246"	"FGF1"	"0.572"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.942857142857143"	"1990"	"2017"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.666666666666667"	"2004"	"2015"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0031030"	"Periapical Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"0.666666666666667"	"1997"	"2015"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"2247"	"FGF2"	"0.404"	"0.897"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0085109"	"Corneal Neovascularization"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2008"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"1997"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2004"	"2"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.875"	"1989"	"2014"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0393953"	"Anterior Cerebral Circulation Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0524686"	"Periodontitis, Acute Nonsuppurative"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"2247"	"FGF2"	"0.404"	"0.897"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751952"	"Anterior Circulation Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751953"	"Brain Infarction, Posterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751954"	"Venous Infarction, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C0751955"	"Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2247"	"FGF2"	"0.404"	"0.897"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.954545454545455"	"1987"	"2016"	"1"	"0"	"CGI;CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0038368"	"Stomatognathic Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2248"	"FGF3"	"0.554"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.962962962962963"	"1989"	"2016"	"1"	"0"	"CGI;CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2248"	"FGF3"	"0.554"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2012"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C1704330"	"Dental Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C1833693"	"Otodental Dysplasia"	"disease"	"C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2017"	"0"	"0"	"ORPHANET"
"2248"	"FGF3"	"0.554"	"0.69"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C1853144"	"Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia"	"disease"	"C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.73"	"1"	"1993"	"2011"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"2248"	"FGF3"	"0.554"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"2248"	"FGF3"	"0.554"	"0.69"	"C2750325"	"Oculootodental Syndrome"	"disease"	"C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2248"	"FGF3"	"0.554"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2249"	"FGF4"	"0.616"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.56"	"1"	"1989"	"2012"	"1"	"0"	"CGI;CTD_human"
"2249"	"FGF4"	"0.616"	"0.483"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2249"	"FGF4"	"0.616"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1989"	"2012"	"1"	"0"	"CGI;CTD_human"
"2249"	"FGF4"	"0.616"	"0.483"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2249"	"FGF4"	"0.616"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2249"	"FGF4"	"0.616"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"2249"	"FGF4"	"0.616"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1990"	"2015"	"1"	"0"	"CTD_human"
"2250"	"FGF5"	"0.762"	"0.345"	"C0854699"	"Trichomegaly"	"phenotype"		"Finding"	"0.40"		"2014"	"2014"	"1"	"3"	"UNIPROT"
"2251"	"FGF6"	"0.799"	"0.138"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2251"	"FGF6"	"0.799"	"0.138"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0005001"	"Benign prostatic hypertrophy"	"phenotype"	"C12"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0017566"	"Gingival Hyperplasia"	"phenotype"	"C07"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C0520477"	"Prostatic Adenoma"	"disease"	"C12"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C1704272"	"Benign Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C1739363"	"Prostatic Hypertrophy"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2252"	"FGF7"	"0.533"	"0.621"	"C2937421"	"Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.42"	"1"	"2011"	"2018"	"1"	"3"	"GENOMICS_ENGLAND"
"2253"	"FGF8"	"0.543"	"0.655"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.55"	"0.8"	"2010"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2253"	"FGF8"	"0.543"	"0.655"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"2253"	"FGF8"	"0.543"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2253"	"FGF8"	"0.543"	"0.655"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2253"	"FGF8"	"0.543"	"0.655"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"2"	"ORPHANET"
"2253"	"FGF8"	"0.543"	"0.655"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"2253"	"FGF8"	"0.543"	"0.655"	"C3552574"	"HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2013"	"2"	"6"	"UNIPROT"
"2254"	"FGF9"	"0.577"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2254"	"FGF9"	"0.577"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0175700"	"Multiple synostosis syndrome"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2009"	"2017"	"0"	"0"	"ORPHANET"
"2254"	"FGF9"	"0.577"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C0342282"	"Multiple synostoses syndrome 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2254"	"FGF9"	"0.577"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2254"	"FGF9"	"0.577"	"0.621"	"C2751826"	"Multiple Synostoses Syndrome 3"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2255"	"FGF10"	"0.569"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2255"	"FGF10"	"0.569"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2255"	"FGF10"	"0.569"	"0.621"	"C0158667"	"Aplasia of Lacrimal and Salivary Glands"	"disease"	"C07;C11"	"Congenital Abnormality"	"0.63"	"1"	"2005"	"2009"	"0"	"4"	"CTD_human;ORPHANET"
"2255"	"FGF10"	"0.569"	"0.621"	"C0265269"	"Lacrimoauriculodentodigital syndrome"	"disease"	"C05;C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.93"	"1"	"2005"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2255"	"FGF10"	"0.569"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2012"	"1"	"1"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2255"	"FGF10"	"0.569"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2255"	"FGF10"	"0.569"	"0.621"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2257"	"FGF12"	"0.735"	"0.241"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2257"	"FGF12"	"0.735"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2257"	"FGF12"	"0.735"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"2257"	"FGF12"	"0.735"	"0.241"	"C4310685"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"2258"	"FGF13"	"0.532"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"0.8"	"1996"	"2012"	"1"	"0"	"CTD_human"
"2258"	"FGF13"	"0.532"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2258"	"FGF13"	"0.532"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2259"	"FGF14"	"0.727"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2259"	"FGF14"	"0.727"	"0.379"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2259"	"FGF14"	"0.727"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2259"	"FGF14"	"0.727"	"0.379"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"2259"	"FGF14"	"0.727"	"0.379"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2259"	"FGF14"	"0.727"	"0.379"	"C1836383"	"SPINOCEREBELLAR ATAXIA 27"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.91"	"1"	"2002"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2259"	"FGF14"	"0.727"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"1994"	"2016"	"1"	"5"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.95"	"1999"	"2018"	"2"	"0"	"CGI;CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.894736842105263"	"1999"	"2018"	"2"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"2008"	"2018"	"2"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.43"	"1"	"2007"	"2016"	"1"	"1"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.34"	"0.666666666666667"	"2004"	"2008"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"	"0.8"	"1995"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.8"	"2004"	"2013"	"5"	"0"	"PSYGENET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2004"	"2013"	"5"	"0"	"CTD_human;PSYGENET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.40"	"0.971428571428571"	"1998"	"2017"	"2"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2018"	"1"	"1"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.666666666666667"	"2006"	"2013"	"4"	"0"	"CTD_human;PSYGENET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"		"2009"	"2017"	"2"	"2"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2011"	"2018"	"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"0.974358974358974"	"2003"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0220658"	"Pfeiffer Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"	"1"	"1994"	"2018"	"1"	"1"	"UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.63"	"0.666666666666667"	"2001"	"2007"	"0"	"0"	"CTD_human;ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2014"	"0"	"0"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"1"	"2003"	"2016"	"2"	"8"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0406612"	"Encephalocraniocutaneous lipomatosis"	"disease"	"C10;C11;C16;C17;C18"	"Congenital Abnormality"	"0.71"	"1"	"2000"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"1"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0432122"	"Interfrontal craniofaciosynostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2001"	"2006"	"1"	"1"	"UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0432283"	"Osteoglophonic dwarfism"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.71"	"1"	"1980"	"2006"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.958333333333333"	"1994"	"2018"	"2"	"0"	"CGI;CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"1"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0795998"	"JACKSON-WEISS SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1995"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"2008"	"2013"	"3"	"0"	"PSYGENET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2013"	"2"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.62"	"0.5"	"1983"	"2017"	"15"	"38"	"CTD_human;UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.33"	"0.666666666666667"	"2004"	"2008"	"1"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1845146"	"Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2017"	"2"	"10"	"ORPHANET;UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C2931888"	"Pfeiffer type acrocephalosyndactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2260"	"FGFR1"	"0.388"	"0.759"	"C3150773"	"CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME"	"disease"		"Disease or Syndrome"	"0.39"	"0.888888888888889"	"1999"	"2017"	"0"	"0"	"ORPHANET"
"2260"	"FGFR1"	"0.388"	"0.759"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"2260"	"FGFR1"	"0.388"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2260"	"FGFR1"	"0.388"	"0.759"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2260"	"FGFR1"	"0.388"	"0.759"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0001080"	"Achondroplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"0.965811965811966"	"1994"	"2018"	"10"	"6"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.80"	"0.92"	"1996"	"2018"	"6"	"4"	"CGI;CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.953488372093023"	"2001"	"2018"	"4"	"0"	"CGI;CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0007847"	"Malignant tumor of cervix"	"disease"		"Neoplastic Process"	"0.33"	"0.666666666666667"	"2000"	"2013"	"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.52"	"1"	"2005"	"2006"	"0"	"0"	"CGI;CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"		"2001"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2016"	"0"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"	"0.944444444444444"	"1995"	"2017"	"2"	"8"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0014145"	"Yolk Sac Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1994"	"1994"	"1"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0022603"	"Seborrheic keratosis"	"disease"	"C17"	"Neoplastic Process"	"0.50"	"1"	"1995"	"2016"	"1"	"7"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.70"	"0.958333333333333"	"1995"	"2018"	"1"	"2"	"CGI;CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0039743"	"Thanatophoric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"	"0.962962962962963"	"1995"	"2018"	"1"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.64"	"1"	"2013"	"2017"	"0"	"1"	"CGI;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0175699"	"Saethre-Chotzen Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"1996"	"2016"	"0"	"1"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0238451"	"Teratoma of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0265269"	"Lacrimoauriculodentodigital syndrome"	"disease"	"C05;C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0265529"	"Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"1998"	"2002"	"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0302592"	"Cervix carcinoma"	"disease"		"Neoplastic Process"	"0.46"	"0.833333333333333"	"1996"	"2013"	"0"	"1"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0334082"	"NEVUS, EPIDERMAL (disorder)"	"disease"	"C04"	"Disease or Syndrome"	"0.68"	"1"	"1994"	"2011"	"1"	"3"	"CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0334517"	"Spermatocytic seminoma"	"disease"		"Neoplastic Process"	"0.40"		"1995"	"2009"	"1"	"1"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0343114"	"Woolly hair nevus"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0410529"	"Hypochondroplasia (disorder)"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.80"	"0.927272727272727"	"1973"	"2018"	"6"	"17"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.50"	"0.926470588235294"	"2001"	"2018"	"0"	"6"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1266158"	"Nongerminomatous Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1300257"	"Thanatophoric dysplasia, type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.79"	"0.888888888888889"	"1993"	"2014"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.50"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.54"	"1"	"2000"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1834928"	"Cloverleaf skull micromelia thoracic dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1864436"	"Muenke Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"1"	"1996"	"2015"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1864852"	"CATSHL syndrome"	"disease"	"C05;C09;C10;C16;C23"	"Disease or Syndrome"	"0.70"		"2006"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C1868678"	"THANATOPHORIC DYSPLASIA, TYPE I (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"0.967741935483871"	"1993"	"2018"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C2674173"	"Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.70"	"1"	"1999"	"2018"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C2677099"	"CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.77"	"1"	"1996"	"2017"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C2931282"	"Skeletal dysplasia, San Diego type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2261"	"FGFR3"	"0.417"	"0.759"	"C3463918"	"EMBRYONAL CELL CARCINOMA"	"disease"		"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1987"	"2015"	"11"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C3854181"	"Nevus sebaceous"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"3"	"UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C4011754"	"Nevus, Keratinocytic, Nonepidermolytic"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2006"	"2006"	"1"	"3"	"CTD_human;UNIPROT"
"2261"	"FGFR3"	"0.417"	"0.759"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2261"	"FGFR3"	"0.417"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.53"	"0.666666666666667"	"1999"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"2262"	"GPC5"	"0.701"	"0.414"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2262"	"GPC5"	"0.701"	"0.414"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0001193"	"Apert syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.80"	"1"	"1995"	"2016"	"11"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0003090"	"Ankylosis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.948453608247423"	"1991"	"2018"	"3"	"0"	"CTD_human;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2015"	"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0010273"	"Craniofacial Dysostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2016"	"1"	"24"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"	"0.895522388059702"	"1995"	"2018"	"8"	"4"	"CTD_human;GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.40"		"2007"	"2015"	"1"	"10"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"		"2014"	"2014"	"0"	"1"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"1995"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2018"	"2"	"0"	"CGI;CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.62"		"1999"	"2012"	"2"	"1"	"CGI;CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.63"	"0.666666666666667"	"2014"	"2017"	"0"	"3"	"CGI;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.42"	"1"	"2008"	"2017"	"0"	"5"	"UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"		"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0175699"	"Saethre-Chotzen Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.64"	"0.75"	"1997"	"2016"	"4"	"1"	"CTD_human;ORPHANET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0220658"	"Pfeiffer Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2018"	"16"	"11"	"CTD_human;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0265269"	"Lacrimoauriculodentodigital syndrome"	"disease"	"C05;C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2008"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0265326"	"Bannayan-Riley-Ruvalcaba Syndrome"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1997"	"2011"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"1997"	"2008"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0391826"	"Lhermitte-Duclos disease"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.70"	"1"	"1995"	"2018"	"1"	"2"	"CGI;CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.953271028037383"	"1996"	"2018"	"3"	"17"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"1"	"1993"	"2017"	"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0795998"	"JACKSON-WEISS SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.75"	"1"	"1995"	"2016"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1153706"	"Endometrial adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2008"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"		"2017"	"2017"	"0"	"1"	"UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1450010"	"Plagiocephaly, Nonsynostotic"	"phenotype"	"C05;C16"	"Anatomical Abnormality"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.888888888888889"	"1991"	"2016"	"3"	"4"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1510455"	"Acrocephalosyndactylia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.88"		"1997"	"2010"	"4"	"1"	"CTD_human;ORPHANET"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1852406"	"Cutis Gyrata Syndrome of Beare And Stevenson"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.97"	"1"	"1996"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1860042"	"Antley-Bixler Syndrome with Disordered Steroidogenesis"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1863389"	"Apert-Crouzon Disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"1995"	"2009"	"11"	"3"	"CTD_human;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1863391"	"Vogt Cephalodactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2004"	"8"	"3"	"UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1865070"	"SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2005"	"2007"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C1959582"	"PTEN Hamartoma Tumor Syndrome"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C2350233"	"Antley-Bixler Syndrome Phenotype"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1997"	"2006"	"3"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C2931196"	"Craniofacial dysostosis type 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2015"	"16"	"22"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C2931888"	"Pfeiffer type acrocephalosyndactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C2936791"	"Antley-Bixler Syndrome, Autosomal Dominant"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C3281247"	"BENT BONE DYSPLASIA SYNDROME"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2012"	"2018"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2263"	"FGFR2"	"0.398"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2006"	"2013"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2263"	"FGFR2"	"0.398"	"0.759"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2263"	"FGFR2"	"0.398"	"0.759"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2263"	"FGFR2"	"0.398"	"0.759"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2005"	"2008"	"1"	"0"	"CTD_human"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2005"	"2014"	"0"	"2"	"CGI"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2014"	"0"	"0"	"UNIPROT"
"2264"	"FGFR4"	"0.507"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2015"	"5"	"1"	"CTD_human;UNIPROT"
"2266"	"FGG"	"0.681"	"0.379"	"C0001733"	"Afibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.53"	"1"	"2000"	"2004"	"0"	"0"	"CTD_human"
"2266"	"FGG"	"0.681"	"0.379"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2266"	"FGG"	"0.681"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2266"	"FGG"	"0.681"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2266"	"FGG"	"0.681"	"0.379"	"C0272350"	"Dysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.61"	"1"	"1986"	"2016"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2266"	"FGG"	"0.681"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2266"	"FGG"	"0.681"	"0.379"	"C1859970"	"Hypodysfibrinogenemia, Congenital"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1986"	"2005"	"4"	"4"	"UNIPROT"
"2266"	"FGG"	"0.681"	"0.379"	"C2584774"	"Congenital hypofibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.74"	"1"	"1992"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2266"	"FGG"	"0.681"	"0.379"	"C4316812"	"Fibrinogen Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"2268"	"FGR"	"0.701"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2271"	"FH"	"0.533"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"2271"	"FH"	"0.533"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1992"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2017"	"0"	"0"	"CGI"
"2271"	"FH"	"0.533"	"0.69"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2016"	"6"	"0"	"CLINGEN"
"2271"	"FH"	"0.533"	"0.69"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2016"	"6"	"0"	"CLINGEN"
"2271"	"FH"	"0.533"	"0.69"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C0342770"	"Fumarase deficiency"	"disease"	"C10;C16;C18;C23;F01"	"Disease or Syndrome"	"0.73"	"1"	"1994"	"2017"	"1"	"38"	"CTD_human;ORPHANET;UNIPROT"
"2271"	"FH"	"0.533"	"0.69"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2016"	"6"	"0"	"CLINGEN"
"2271"	"FH"	"0.533"	"0.69"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2016"	"6"	"0"	"CLINGEN"
"2271"	"FH"	"0.533"	"0.69"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2017"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2271"	"FH"	"0.533"	"0.69"	"C1378703"	"Renal carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"0"	"0"	"CGI"
"2271"	"FH"	"0.533"	"0.69"	"C1708350"	"Hereditary Leiomyomatosis and Renal Cell Cancer"	"disease"	"C04;C13;C16;C17"	"Neoplastic Process"	"0.80"	"0.951612903225806"	"1993"	"2018"	"3"	"51"	"CTD_human;ORPHANET;UNIPROT"
"2271"	"FH"	"0.533"	"0.69"	"C2936826"	"Fumaric aciduria"	"disease"	"C10;C16;C18;C23;F01"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2271"	"FH"	"0.533"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2272"	"FHIT"	"0.45"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.928571428571429"	"1997"	"2017"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2014"	"2"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2004"	"2008"	"2"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"0"	"1998"	"2009"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.10"		"2013"	"2018"	"1"	"1"	"PSYGENET"
"2272"	"FHIT"	"0.45"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2006"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2002"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2272"	"FHIT"	"0.45"	"0.828"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2272"	"FHIT"	"0.45"	"0.828"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2273"	"FHL1"	"0.582"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.48"	"1"	"2009"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2273"	"FHL1"	"0.582"	"0.586"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0270970"	"Reducing-body myopathy"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"2273"	"FHL1"	"0.582"	"0.586"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"0"	"0"	"ORPHANET"
"2273"	"FHL1"	"0.582"	"0.586"	"C2678015"	"Myopathy, Reducing Body, X-Linked, Childhood-Onset"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2009"	"0"	"3"	"CTD_human"
"2273"	"FHL1"	"0.582"	"0.586"	"C2678027"	"Myopathy, Reducing Body, X-Linked, Early-Onset, Severe"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"1995"	"2009"	"0"	"5"	"CTD_human"
"2273"	"FHL1"	"0.582"	"0.586"	"C2678055"	"MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2008"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2273"	"FHL1"	"0.582"	"0.586"	"C2678061"	"SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.92"	"1"	"2008"	"2016"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2273"	"FHL1"	"0.582"	"0.586"	"C2749106"	"Emery-Dreifuss Muscular Dystrophy 6, X-Linked"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2010"	"3"	"4"	"UNIPROT"
"2273"	"FHL1"	"0.582"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2273"	"FHL1"	"0.582"	"0.586"	"C4225159"	"REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2013"	"4"	"3"	"UNIPROT"
"2273"	"FHL1"	"0.582"	"0.586"	"C4225423"	"REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2009"	"3"	"5"	"UNIPROT"
"2274"	"FHL2"	"0.588"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2008"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"2274"	"FHL2"	"0.588"	"0.517"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2274"	"FHL2"	"0.588"	"0.517"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2274"	"FHL2"	"0.588"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2008"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"2274"	"FHL2"	"0.588"	"0.517"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2277"	"VEGFD"	"0.573"	"0.552"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2277"	"VEGFD"	"0.573"	"0.552"	"C0751674"	"Lymphangioleiomyomatosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.666666666666667"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2280"	"FKBP1A"	"0.707"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"2280"	"FKBP1A"	"0.707"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2280"	"FKBP1A"	"0.707"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2286"	"FKBP2"	"0.834"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2286"	"FKBP2"	"0.834"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2286"	"FKBP2"	"0.834"	"0.172"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2286"	"FKBP2"	"0.834"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2288"	"FKBP4"	"0.59"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"2288"	"FKBP4"	"0.59"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.666666666666667"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2009"	"2016"	"5"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"2008"	"2018"	"5"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"2008"	"2018"	"5"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0021290"	"Neonatal disorder"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2013"	"2018"	"1"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2018"	"1"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2010"	"2015"	"5"	"0"	"PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"2009"	"2018"	"5"	"0"	"CTD_human;PSYGENET"
"2289"	"FKBP5"	"0.572"	"0.655"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"2289"	"FKBP5"	"0.572"	"0.655"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.59"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.43"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0796147"	"Acrocallosal Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2013"	"0"	"0"	"ORPHANET"
"2290"	"FOXG1"	"0.561"	"0.517"	"C3150705"	"FOXG1 syndrome"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2008"	"2017"	"3"	"35"	"CTD_human;UNIPROT"
"2290"	"FOXG1"	"0.561"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2290"	"FOXG1"	"0.561"	"0.517"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4305240"	"14q12 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2290"	"FOXG1"	"0.561"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0024899"	"Mastocytosis"	"disease"	"C04;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0031190"	"Persistent Fetal Circulation Syndrome"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2017"	"3"	"3"	"UNIPROT"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C0600260"	"Lung Diseases, Obstructive"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C2677362"	"Alveolar capillary dysplasia"	"disease"	"C08;C16"	"Congenital Abnormality"	"0.56"	"1"	"2009"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"2294"	"FOXF1"	"0.579"	"0.517"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2294"	"FOXF1"	"0.579"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"2295"	"FOXF2"	"0.696"	"0.379"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2295"	"FOXF2"	"0.696"	"0.379"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0003076"	"Aniridia"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2008"	"2009"	"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0010964"	"Dandy-Walker Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0265341"	"Rieger syndrome"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.44"	"1"	"2002"	"2004"	"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0266548"	"Axenfeld anomaly (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.48"	"1"	"1998"	"2013"	"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"0.5"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0344559"	"Irido-corneo-trabecular dysgenesis (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2003"	"2008"	"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C1839928"	"IRIS HYPOPLASIA WITH GLAUCOMA"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2011"	"6"	"5"	"UNIPROT"
"2296"	"FOXC1"	"0.517"	"0.724"	"C1866560"	"IRIDOGONIODYSGENESIS, TYPE 1 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1998"	"2011"	"6"	"6"	"CTD_human;UNIPROT"
"2296"	"FOXC1"	"0.517"	"0.724"	"C1866561"	"Glaucoma Iridogoniodysplasia, Familial"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1998"	"2011"	"6"	"5"	"UNIPROT"
"2296"	"FOXC1"	"0.517"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2296"	"FOXC1"	"0.517"	"0.724"	"C2678503"	"AXENFELD-RIEGER SYNDROME, TYPE 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2017"	"20"	"23"	"CTD_human;UNIPROT"
"2296"	"FOXC1"	"0.517"	"0.724"	"C3495488"	"Axenfeld-Rieger syndrome"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C3495489"	"Rieger eye malformation sequence"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2296"	"FOXC1"	"0.517"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"2296"	"FOXC1"	"0.517"	"0.724"	"C3714873"	"Axenfeld-Rieger Syndrome, Type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2296"	"FOXC1"	"0.517"	"0.724"	"C3887633"	"Dandy-Walker Syndrome, Familial"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2299"	"FOXI1"	"0.752"	"0.31"	"C0271829"	"Pendred's syndrome"	"disease"	"C09;C10;C19;C23"	"Disease or Syndrome"	"0.83"	"0.666666666666667"	"2003"	"2011"	"0"	"1"	"CTD_human;ORPHANET"
"2299"	"FOXI1"	"0.752"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2299"	"FOXI1"	"0.752"	"0.31"	"C3538946"	"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2001"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0344559"	"Irido-corneo-trabecular dysgenesis (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"2301"	"FOXE3"	"0.63"	"0.448"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2301"	"FOXE3"	"0.63"	"0.448"	"C1853230"	"Aphakia, congenital primary"	"disease"	"C11"	"Congenital Abnormality"	"0.74"	"1"	"1987"	"2015"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2301"	"FOXE3"	"0.63"	"0.448"	"C1862839"	"Anterior segment mesenchymal dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2001"	"0"	"0"	"CTD_human;ORPHANET"
"2301"	"FOXE3"	"0.63"	"0.448"	"C2751822"	"Cataract, Autosomal Recessive Congenital 3"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2007"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"2301"	"FOXE3"	"0.63"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2301"	"FOXE3"	"0.63"	"0.448"	"C4479235"	"AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0265345"	"Lymphedema distichiasis syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2014"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1998"	"2"	"0"	"CTD_human"
"2303"	"FOXC2"	"0.554"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2303"	"FOXC2"	"0.554"	"0.655"	"C2675066"	"Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus"	"disease"	"C12;C13;C15;C18;C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"3"	"1"	"UNIPROT"
"2303"	"FOXC2"	"0.554"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2304"	"FOXE1"	"0.602"	"0.517"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.44"	"1"	"1998"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"2304"	"FOXE1"	"0.602"	"0.517"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.70"	"1"	"1998"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"2304"	"FOXE1"	"0.602"	"0.517"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"2304"	"FOXE1"	"0.602"	"0.517"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.64"	"1"	"1998"	"2018"	"4"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"2304"	"FOXE1"	"0.602"	"0.517"	"C1855794"	"Bamforth syndrome"	"disease"	"C05;C07;C16;C17;C19"	"Disease or Syndrome"	"0.93"	"1"	"1989"	"2015"	"5"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2304"	"FOXE1"	"0.602"	"0.517"	"C1968699"	"Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate"	"disease"	"C05;C07;C16;C17;C19"	"Disease or Syndrome"	"0.40"		"2006"	"2011"	"1"	"1"	"CTD_human"
"2304"	"FOXE1"	"0.602"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2304"	"FOXE1"	"0.602"	"0.517"	"C4225293"	"THYROID CANCER, NONMEDULLARY, 4"	"disease"		"Neoplastic Process"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"2"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"2305"	"FOXM1"	"0.484"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"2"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0022578"	"Keratoconus"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"		"2003"	"2018"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2016"	"0"	"0"	"CGI"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0206655"	"Alveolar rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.974358974358974"	"1994"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"2308"	"FOXO1"	"0.49"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"2308"	"FOXO1"	"0.49"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2014"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"2309"	"FOXO3"	"0.489"	"0.759"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.946236559139785"	"2005"	"2018"	"4"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0013595"	"Eczema"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.930348258706468"	"2005"	"2018"	"1"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0079584"	"Ichthyosis Vulgaris"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.50"	"1"	"1985"	"2018"	"2"	"8"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"4"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2312"	"FLG"	"0.55"	"0.655"	"C0678306"	"alcohol sensitivity"	"phenotype"		"Finding"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2312"	"FLG"	"0.55"	"0.655"	"C1853965"	"Dermatitis, Atopic, 2"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0032197"	"Platelet Storage Pool Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0279980"	"Extraosseous Ewings sarcoma-primitive neuroepithelial tumor"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.970588235294118"	"1993"	"2016"	"3"	"0"	"CTD_human;ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C0684337"	"Ewings sarcoma-primitive neuroectodermal tumor (PNET)"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"1993"	"2012"	"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C0795841"	"Jacobsen Distal 11q Deletion Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.39"	"0.888888888888889"	"2000"	"2016"	"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2313"	"FLI1"	"0.53"	"0.621"	"C1861178"	"Thrombocytopenia Paris-Trousseau type"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C1956093"	"Paris-Trousseau Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C2931875"	"Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2313"	"FLI1"	"0.53"	"0.621"	"C4479515"	"BLEEDING DISORDER, PLATELET-TYPE, 21"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2018"	"3"	"6"	"CTD_human;UNIPROT"
"2314"	"FLII"	"0.567"	"0.655"	"C0795864"	"Smith-Magenis syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2315"	"MLANA"	"0.648"	"0.517"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2315"	"MLANA"	"0.648"	"0.517"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.959677419354839"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2315"	"MLANA"	"0.648"	"0.517"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2315"	"MLANA"	"0.648"	"0.517"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2315"	"MLANA"	"0.648"	"0.517"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2315"	"MLANA"	"0.648"	"0.517"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2316"	"FLNA"	"0.456"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0010701"	"Phyllodes Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"2316"	"FLNA"	"0.456"	"0.793"	"C0021847"	"Intestinal Pseudo-Obstruction"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2013"	"0"	"0"	"ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"7"	"0"	"CLINGEN"
"2316"	"FLNA"	"0.456"	"0.793"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"1983"	"2011"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0220769"	"FG syndrome"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0262436"	"Cardiac valvular dysplasia, X-linked"	"disease"	"C04;C14;C16"	"Congenital Abnormality"	"0.61"	"1"	"1993"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C0265251"	"Oto-Palato-digital syndrome type 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"2003"	"2017"	"4"	"16"	"CTD_human;ORPHANET;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C0265293"	"Frontometaphyseal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.70"	"0.909090909090909"	"1997"	"2017"	"2"	"4"	"CTD_human;ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2316"	"FLNA"	"0.456"	"0.793"	"C0600066"	"Malignant Cystosarcoma Phyllodes"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C1844696"	"OTOPALATODIGITAL SYNDROME, TYPE II"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.80"	"0.9"	"2003"	"2017"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C1845235"	"Heterotopia, Periventricular, Ehlers-Danlos Variant"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.60"		"2002"	"2006"	"6"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C1845546"	"FG SYNDROME 4 (disorder)"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C1845567"	"FG SYNDROME 3"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C1845902"	"FG SYNDROME 2"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C1846129"	"Terminal Osseous Dysplasia and Pigmentary Defects"	"disease"	"C05;C16;C17;C23"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2010"	"0"	"1"	"CTD_human;ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C1848213"	"Periventricular Heterotopia, X-Linked"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.90"	"1"	"1987"	"2017"	"7"	"54"	"CTD_human;UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C1848214"	"Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"6"	"4"	"UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C1855733"	"Neuronal intestinal pseudoobstruction"	"disease"	"C06;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C1857034"	"Ehlers-Danlos syndrome, cardiac valvular form"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C1868720"	"Periventricular Nodular Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2316"	"FLNA"	"0.456"	"0.793"	"C2746068"	"Congenital idiopathic intestinal pseudoobstruction"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2018"	"0"	"4"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C2748918"	"Otopalatodigital Spectrum Disorder"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2003"	"2017"	"3"	"6"	"UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C2748919"	"Frontootopalatodigital Osteodysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2017"	"3"	"4"	"UNIPROT"
"2316"	"FLNA"	"0.456"	"0.793"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2316"	"FLNA"	"0.456"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"2316"	"FLNA"	"0.456"	"0.793"	"C4273726"	"Congenital dysplasia of cardiac valve"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2316"	"FLNA"	"0.456"	"0.793"	"C4281559"	"FRONTOMETAPHYSEAL DYSPLASIA 1"	"disease"		"Congenital Abnormality"	"0.30"		"2003"	"2017"	"3"	"3"	"UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2317"	"FLNB"	"0.501"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2317"	"FLNB"	"0.501"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2317"	"FLNB"	"0.501"	"0.862"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2317"	"FLNB"	"0.501"	"0.862"	"C0175778"	"Larsen syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.69"	"1"	"2004"	"2018"	"2"	"12"	"ORPHANET;UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C0265283"	"Atelosteogenesis, type 1"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.75"	"1"	"1993"	"2015"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C0432201"	"Boomerang dysplasia"	"disease"	"C05;C16;C19;C23"	"Disease or Syndrome"	"0.73"	"1"	"2003"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C1848934"	"SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2017"	"1"	"8"	"CTD_human;ORPHANET"
"2317"	"FLNB"	"0.501"	"0.862"	"C2931648"	"Larsen syndrome, dominant type"	"disease"	"C05;C07;C16;C26"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"2317"	"FLNB"	"0.501"	"0.862"	"C3668942"	"Atelosteogenesis Type 3"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.71"	"1"	"1993"	"2006"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2317"	"FLNB"	"0.501"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0007196"	"Restrictive cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"2318"	"FLNC"	"0.624"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2318"	"FLNC"	"0.624"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2318"	"FLNC"	"0.624"	"0.448"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0348616"	"Other restrictive cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2318"	"FLNC"	"0.624"	"0.448"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"2318"	"FLNC"	"0.624"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2318"	"FLNC"	"0.624"	"0.448"	"C1836050"	"Filaminopathy, autosomal dominant"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.90"		"1998"	"2017"	"12"	"5"	"CLINGEN;CTD_human;ORPHANET"
"2318"	"FLNC"	"0.624"	"0.448"	"C3279722"	"MYOPATHY, DISTAL, 4"	"disease"		"Disease or Syndrome"	"0.70"		"2005"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2318"	"FLNC"	"0.624"	"0.448"	"C4310748"	"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5"	"disease"		"Disease or Syndrome"	"0.50"		"2015"	"2016"	"2"	"3"	"CTD_human;UNIPROT"
"2318"	"FLNC"	"0.624"	"0.448"	"C4310749"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2017"	"2"	"8"	"CTD_human;UNIPROT"
"2321"	"FLT1"	"0.453"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.60"		"2005"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"2321"	"FLT1"	"0.453"	"0.793"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"2321"	"FLT1"	"0.453"	"0.793"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0279680"	"Transitional cell carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2321"	"FLT1"	"0.453"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2321"	"FLT1"	"0.453"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2006"	"0"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023464"	"Acute biphenotypic leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"1.00"	"0.979020979020979"	"1992"	"2018"	"13"	"28"	"CGI;CTD_human;UNIPROT"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023479"	"Acute myelomonocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2011"	"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.954545454545455"	"1997"	"2016"	"3"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.31"		"2004"	"2017"	"2"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2002"	"2017"	"13"	"0"	"CTD_human;ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"2322"	"FLT3"	"0.503"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"2322"	"FLT3"	"0.503"	"0.517"	"C0522631"	"Acute myeloid leukemia, minimal differentiation"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.34"	"0.75"	"1994"	"2012"	"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2006"	"2017"	"13"	"0"	"CTD_human;ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"0.833333333333333"	"2004"	"2016"	"0"	"0"	"ORPHANET"
"2322"	"FLT3"	"0.503"	"0.517"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"2004"	"2018"	"1"	"4"	"CGI;CTD_human;UNIPROT"
"2322"	"FLT3"	"0.503"	"0.517"	"C2861596"	"AML M4 Eo with inv(16) or t(16;16)"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2324"	"FLT4"	"0.51"	"0.724"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2324"	"FLT4"	"0.51"	"0.724"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"2324"	"FLT4"	"0.51"	"0.724"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"2324"	"FLT4"	"0.51"	"0.724"	"C0024236"	"Lymphedema"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.954545454545455"	"2000"	"2016"	"0"	"0"	"CTD_human"
"2324"	"FLT4"	"0.51"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2324"	"FLT4"	"0.51"	"0.724"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2324"	"FLT4"	"0.51"	"0.724"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"2324"	"FLT4"	"0.51"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2324"	"FLT4"	"0.51"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2324"	"FLT4"	"0.51"	"0.724"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2324"	"FLT4"	"0.51"	"0.724"	"C1704423"	"Milroy Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2016"	"10"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2324"	"FLT4"	"0.51"	"0.724"	"C1865871"	"HEMANGIOMA, CAPILLARY INFANTILE"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.50"		"2002"	"2002"	"1"	"1"	"CTD_human;UNIPROT"
"2324"	"FLT4"	"0.51"	"0.724"	"C2931852"	"Clear-cell metastatic renal cell carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"2324"	"FLT4"	"0.51"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2326"	"FMO1"	"0.815"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"2326"	"FMO1"	"0.815"	"0.241"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2326"	"FMO1"	"0.815"	"0.241"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2327"	"FMO2"	"0.857"	"0.103"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2327"	"FMO2"	"0.857"	"0.103"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C0342739"	"Trimethylaminuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1976"	"2016"	"7"	"11"	"CTD_human;UNIPROT"
"2328"	"FMO3"	"0.645"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2328"	"FMO3"	"0.645"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.888888888888889"	"2002"	"2018"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2332"	"FMR1"	"0.492"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"1993"	"2017"	"5"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.909090909090909"	"2000"	"2018"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0016667"	"Fragile X Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.978805394990366"	"1991"	"2018"	"27"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2332"	"FMR1"	"0.492"	"0.69"	"C0018051"	"Gonadal Dysgenesis"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2332"	"FMR1"	"0.492"	"0.69"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2010"	"2"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2010"	"2"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1996"	"2018"	"2"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.40"	"0.923076923076923"	"1994"	"2018"	"0"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0338908"	"Mixed anxiety and depressive disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0751156"	"FRAXA Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2000"	"2017"	"8"	"0"	"CTD_human;ORPHANET"
"2332"	"FMR1"	"0.492"	"0.69"	"C0751157"	"FRAXE Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2017"	"8"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2010"	"2"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C0949331"	"Gonadal Agenesis"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C1839780"	"FRAGILE X TREMOR/ATAXIA SYNDROME"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.80"	"0.978102189781022"	"2004"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"2332"	"FMR1"	"0.492"	"0.69"	"C2678248"	"Mood instability"	"phenotype"		"Finding"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2332"	"FMR1"	"0.492"	"0.69"	"C3275521"	"CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2332"	"FMR1"	"0.492"	"0.69"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2332"	"FMR1"	"0.492"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.978102189781022"	"1992"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2334"	"AFF2"	"0.707"	"0.345"	"C0016667"	"Fragile X Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2012"	"0"	"0"	"CTD_human"
"2334"	"AFF2"	"0.707"	"0.345"	"C0751156"	"FRAXA Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2334"	"AFF2"	"0.707"	"0.345"	"C0751157"	"FRAXE Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2004"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"2334"	"AFF2"	"0.707"	"0.345"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2014"	"10"	"0"	"CLINGEN"
"2334"	"AFF2"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.944444444444444"	"1996"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"2335"	"FN1"	"0.399"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2018"	"2"	"1"	"CTD_human;UNIPROT"
"2335"	"FN1"	"0.399"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"1994"	"2007"	"2"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"2335"	"FN1"	"0.399"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2335"	"FN1"	"0.399"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0432221"	"Spondylometaphyseal dysplasia, 'corner fracture' type"	"disease"	"C05;C16;C23;C26"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2335"	"FN1"	"0.399"	"0.828"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2016"	"0"	"0"	"UNIPROT"
"2335"	"FN1"	"0.399"	"0.828"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2335"	"FN1"	"0.399"	"0.828"	"C1866075"	"GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.70"		"1992"	"2008"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2335"	"FN1"	"0.399"	"0.828"	"C3888104"	"Glomerulopathy with fibronectin deposits"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.63"	"1"	"1999"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2346"	"FOLH1"	"0.584"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2346"	"FOLH1"	"0.584"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2346"	"FOLH1"	"0.584"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"2"	"0"	"CTD_human"
"2346"	"FOLH1"	"0.584"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"2346"	"FOLH1"	"0.584"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.97979797979798"	"1996"	"2018"	"2"	"0"	"CTD_human"
"2346"	"FOLH1"	"0.584"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2004"	"0"	"0"	"UNIPROT"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.34"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"1"	"GENOMICS_ENGLAND"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0752107"	"Brain Diseases, Metabolic, Inherited"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0752109"	"Brain Diseases, Metabolic, Inborn"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0752110"	"Central Nervous System Inborn Metabolic Diseases"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.909090909090909"	"1991"	"2017"	"1"	"0"	"CTD_human"
"2348"	"FOLR1"	"0.557"	"0.724"	"C2751584"	"Neurodegeneration Due To Cerebral Folate Transport Deficiency"	"phenotype"	"C10"	"Disease or Syndrome"	"0.76"	"1"	"1999"	"2017"	"13"	"2"	"CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET"
"2348"	"FOLR1"	"0.557"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2009"	"2012"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2350"	"FOLR2"	"0.663"	"0.379"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2012"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0011859"	"Lipoatrophic Diabetes Mellitus"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2353"	"FOS"	"0.436"	"0.862"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"0"	"2008"	"2013"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0016063"	"Osteitis Fibrosa Disseminata"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2353"	"FOS"	"0.436"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0221032"	"Familial generalized lipodystrophy"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"2353"	"FOS"	"0.436"	"0.862"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2012"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"2353"	"FOS"	"0.436"	"0.862"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.933333333333333"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2353"	"FOS"	"0.436"	"0.862"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2353"	"FOS"	"0.436"	"0.862"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"4"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"4"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0021122"	"Disruptive, Impulse Control, and Conduct Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0021776"	"Intermittent Explosive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0022734"	"Kleptomania"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"4"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2354"	"FOSB"	"0.504"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"4"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2354"	"FOSB"	"0.504"	"0.759"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2355"	"FOSL2"	"0.656"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2005"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"2356"	"FPGS"	"0.639"	"0.276"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2358"	"FPR2"	"0.607"	"0.655"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"2358"	"FPR2"	"0.607"	"0.655"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2358"	"FPR2"	"0.607"	"0.655"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2358"	"FPR2"	"0.607"	"0.655"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2358"	"FPR2"	"0.607"	"0.655"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2395"	"FXN"	"0.527"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1981"	"1981"	"0"	"0"	"GENOMICS_ENGLAND"
"2395"	"FXN"	"0.527"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.46"	"0.833333333333333"	"1996"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2395"	"FXN"	"0.527"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2395"	"FXN"	"0.527"	"0.586"	"C0016719"	"Friedreich Ataxia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.996124031007752"	"1990"	"2018"	"15"	"7"	"CLINGEN;CTD_human;ORPHANET"
"2395"	"FXN"	"0.527"	"0.586"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2395"	"FXN"	"0.527"	"0.586"	"C1847416"	"FRIEDREICH ATAXIA WITH RETAINED REFLEXES"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2011"	"13"	"8"	"CLINGEN;UNIPROT"
"2395"	"FXN"	"0.527"	"0.586"	"C1856689"	"FRIEDREICH ATAXIA 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.966442953020134"	"1996"	"2018"	"13"	"9"	"CLINGEN;CTD_human;UNIPROT"
"2395"	"FXN"	"0.527"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"2414"	"FRA7G"	"0.707"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"2444"	"FRK"	"0.735"	"0.276"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2464"	"FRA16E"	"0.857"	"0.172"	"C1850985"	"Fragile Site 16p12"	"disease"	"C05;C14;C16;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2464"	"FRA16E"	"0.857"	"0.172"	"C3149276"	"CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2018"	"1"	"7"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2009"	"2012"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"2475"	"MTOR"	"0.399"	"0.793"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"2009"	"2018"	"1"	"0"	"CGI;CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.46"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2475"	"MTOR"	"0.399"	"0.793"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.37"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0588006"	"Mild depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2475"	"MTOR"	"0.399"	"0.793"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"2475"	"MTOR"	"0.399"	"0.793"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"2004"	"2010"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"2475"	"MTOR"	"0.399"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2015"	"0"	"0"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C1846385"	"FOCAL CORTICAL DYSPLASIA OF TAYLOR"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"2015"	"2017"	"4"	"7"	"CTD_human;UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C1846386"	"Focal Cortical Dysplasia of Taylor, Type IIa"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C1846388"	"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"4"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C1846389"	"Focal Cortical Dysplasia of Taylor, Type IIb"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2016"	"4"	"4"	"CTD_human;UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2016"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2475"	"MTOR"	"0.399"	"0.793"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.964285714285714"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"2475"	"MTOR"	"0.399"	"0.793"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"2475"	"MTOR"	"0.399"	"0.793"	"C4225259"	"SMITH-KINGSMORE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"3"	"6"	"ORPHANET;UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C4478700"	"FOCAL CORTICAL DYSPLASIA, TYPE IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"4"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C4478701"	"FOCAL CORTICAL DYSPLASIA, TYPE IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"4"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C4479708"	"FCD IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"4"	"UNIPROT"
"2475"	"MTOR"	"0.399"	"0.793"	"C4479709"	"FCD IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"4"	"UNIPROT"
"2483"	"FRG1"	"0.72"	"0.414"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"0.91304347826087"	"1997"	"2018"	"0"	"0"	"ORPHANET"
"2483"	"FRG1"	"0.72"	"0.414"	"C1834673"	"Facioscapulohumeral muscular dystrophy 1a"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2487"	"FRZB"	"0.598"	"0.448"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.95"	"1998"	"2016"	"0"	"2"	"CTD_human"
"2487"	"FRZB"	"0.598"	"0.448"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2487"	"FRZB"	"0.598"	"0.448"	"C3887876"	"OSTEOARTHRITIS SUSCEPTIBILITY 1"	"disease"		"Finding"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"2488"	"FSHB"	"0.648"	"0.483"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"2014"	"3"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.32"	"1"	"1980"	"2016"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.41"	"1"	"1974"	"2013"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0043019"	"Lateral Medullary Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.41"	"1"	"1994"	"2016"	"3"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"2488"	"FSHB"	"0.648"	"0.483"	"C0342386"	"Follicle stimulating hormone deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2488"	"FSHB"	"0.648"	"0.483"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1994"	"2014"	"3"	"0"	"CTD_human"
"2488"	"FSHB"	"0.648"	"0.483"	"C1856716"	"Follicle-stimulating hormone deficiency, isolated"	"disease"	"C12"	"Disease or Syndrome"	"0.71"	"1"	"1972"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2488"	"FSHB"	"0.648"	"0.483"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1994"	"2014"	"3"	"0"	"CTD_human"
"2492"	"FSHR"	"0.551"	"0.517"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2018"	"1"	"3"	"CTD_human"
"2492"	"FSHR"	"0.551"	"0.517"	"C0085083"	"Ovarian Hyperstimulation Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.80"	"0.952380952380952"	"1996"	"2017"	"7"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2492"	"FSHR"	"0.551"	"0.517"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"ORPHANET"
"2492"	"FSHR"	"0.551"	"0.517"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.75"	"1"	"1995"	"2016"	"7"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2492"	"FSHR"	"0.551"	"0.517"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2492"	"FSHR"	"0.551"	"0.517"	"C3494162"	"Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.50"		"2003"	"2015"	"7"	"2"	"CTD_human;UNIPROT"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0003128"	"Anovulation"	"phenotype"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.38"	"0.875"	"2010"	"2017"	"2"	"0"	"CTD_human"
"2494"	"NR5A2"	"0.609"	"0.483"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0282193"	"Iron Overload"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2495"	"FTH1"	"0.627"	"0.517"	"C1851316"	"Iron Overload, Autosomal Dominant"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2512"	"FTL"	"0.582"	"0.586"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0012715"	"Iron Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2008"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"2512"	"FTL"	"0.582"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2512"	"FTL"	"0.582"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.44"	"1"	"1997"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2512"	"FTL"	"0.582"	"0.586"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2512"	"FTL"	"0.582"	"0.586"	"C0751870"	"Heredodegenerative Disorders, Nervous System"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2512"	"FTL"	"0.582"	"0.586"	"C1833213"	"Hyperferritinemia, hereditary, with congenital cataracts"	"disease"	"C11;C18"	"Disease or Syndrome"	"0.80"	"1"	"1996"	"2018"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"2512"	"FTL"	"0.582"	"0.586"	"C1853578"	"Neuroferritinopathy"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.80"	"0.947368421052632"	"2001"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2512"	"FTL"	"0.582"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2512"	"FTL"	"0.582"	"0.586"	"C3810090"	"L-FERRITIN DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2004"	"0"	"1"	"CTD_human;ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0001623"	"Adrenal gland hypofunction"	"phenotype"	"C19"	"Disease or Syndrome"	"0.40"	"0.952380952380952"	"1999"	"2017"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.38"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2015"	"3"	"0"	"CTD_human;ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.37"	"1"	"2011"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.40"	"0.933333333333333"	"2009"	"2016"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0238395"	"Male Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0266361"	"True Hermaphroditism (disorder)"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0432475"	"XX males"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2015"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.51"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C2748895"	"Ovotesticular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C2751824"	"46, XY Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.50"	"1"	"1999"	"2017"	"0"	"15"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C2751825"	"PREMATURE OVARIAN FAILURE 7 (disorder)"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.60"		"2001"	"2016"	"3"	"9"	"CTD_human;UNIPROT"
"2516"	"NR5A1"	"0.512"	"0.586"	"C2936419"	"46, XX Testicular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.50"		"1999"	"2004"	"3"	"0"	"CTD_human;ORPHANET"
"2516"	"NR5A1"	"0.512"	"0.586"	"C3151406"	"SPERMATOGENIC FAILURE 8"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"5"	"CTD_human;UNIPROT"
"2516"	"NR5A1"	"0.512"	"0.586"	"C3489793"	"46,XY Sex Reversal 3"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.50"		"1999"	"2018"	"8"	"8"	"CTD_human;UNIPROT"
"2516"	"NR5A1"	"0.512"	"0.586"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2516"	"NR5A1"	"0.512"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2516"	"NR5A1"	"0.512"	"0.586"	"C4479552"	"46,XX SEX REVERSAL 4"	"disease"		"Congenital Abnormality"	"0.40"		"2017"	"2018"	"4"	"2"	"UNIPROT"
"2516"	"NR5A1"	"0.512"	"0.586"	"C4479664"	"ADRENAL INSUFFICIENCY, NR5A1-RELATED"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2016"	"3"	"5"	"UNIPROT"
"2516"	"NR5A1"	"0.512"	"0.586"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2517"	"FUCA1"	"0.636"	"0.621"	"C0016788"	"Fucosidase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.78"	"1"	"1975"	"2017"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2517"	"FUCA1"	"0.636"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2517"	"FUCA1"	"0.636"	"0.621"	"C0268221"	"Fucosidosis Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2517"	"FUCA1"	"0.636"	"0.621"	"C0268222"	"Fucosidosis Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2517"	"FUCA1"	"0.636"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2517"	"FUCA1"	"0.636"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2520"	"GAST"	"0.512"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2016"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.941176470588235"	"1986"	"2016"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1986"	"2007"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2001"	"2004"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.96551724137931"	"1988"	"2018"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0024799"	"Marginal ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0030920"	"Peptic Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"1987"	"2016"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2520"	"GAST"	"0.512"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2521"	"FUS"	"0.533"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.979057591623037"	"2009"	"2018"	"0"	"0"	"ORPHANET"
"2521"	"FUS"	"0.533"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2018"	"0"	"0"	"UNIPROT"
"2521"	"FUS"	"0.533"	"0.586"	"C0206634"	"Liposarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.975609756097561"	"1993"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"2521"	"FUS"	"0.533"	"0.586"	"C1842675"	"AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2003"	"2016"	"5"	"13"	"UNIPROT"
"2521"	"FUS"	"0.533"	"0.586"	"C2750729"	"Amyotrophic Lateral Sclerosis 6, Autosomal Recessive"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"1"	"CTD_human"
"2521"	"FUS"	"0.533"	"0.586"	"C3468114"	"Juvenile amyotrophic lateral sclerosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2521"	"FUS"	"0.533"	"0.586"	"C3539195"	"TREMOR, HEREDITARY ESSENTIAL, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2012"	"1"	"3"	"CTD_human;UNIPROT"
"2521"	"FUS"	"0.533"	"0.586"	"C3714524"	"Fibromyxosarcoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2001"	"2011"	"0"	"0"	"ORPHANET"
"2521"	"FUS"	"0.533"	"0.586"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2524"	"FUT2"	"0.579"	"0.586"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.48"	"1"	"2010"	"2017"	"1"	"4"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0162677"	"Caliciviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0206044"	"Infections, Calicivirus"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C2674252"	"VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.40"		"1996"	"2015"	"0"	"1"	"CTD_human"
"2524"	"FUT2"	"0.579"	"0.586"	"C3534585"	"Infection caused by Norovirus"	"group"	"C02"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2526"	"FUT4"	"0.537"	"0.552"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2526"	"FUT4"	"0.537"	"0.552"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2529"	"FUT7"	"0.743"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2529"	"FUT7"	"0.743"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2530"	"FUT8"	"0.676"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2015"	"2"	"0"	"PSYGENET"
"2530"	"FUT8"	"0.676"	"0.345"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2531"	"KDSR"	"0.707"	"0.31"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2531"	"KDSR"	"0.707"	"0.31"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2531"	"KDSR"	"0.707"	"0.31"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2531"	"KDSR"	"0.707"	"0.31"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2531"	"KDSR"	"0.707"	"0.31"	"C4479620"	"ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"4"	"UNIPROT"
"2532"	"ACKR1"	"0.636"	"0.655"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"0.928571428571429"	"1998"	"2017"	"0"	"0"	"CTD_human"
"2533"	"FYB1"	"0.773"	"0.379"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2533"	"FYB1"	"0.773"	"0.379"	"C2678311"	"Thrombocytopenia 3"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2015"	"2016"	"0"	"2"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2534"	"FYN"	"0.594"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2009"	"1"	"0"	"PSYGENET"
"2534"	"FYN"	"0.594"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2009"	"2"	"0"	"PSYGENET"
"2534"	"FYN"	"0.594"	"0.621"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"0.5"	"2000"	"2017"	"2"	"1"	"PSYGENET"
"2534"	"FYN"	"0.594"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2534"	"FYN"	"0.594"	"0.621"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2534"	"FYN"	"0.594"	"0.621"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2534"	"FYN"	"0.594"	"0.621"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2534"	"FYN"	"0.594"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2535"	"FZD2"	"0.639"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2535"	"FZD2"	"0.639"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2535"	"FZD2"	"0.639"	"0.483"	"C0265205"	"Robinow Syndrome"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2535"	"FZD2"	"0.639"	"0.483"	"C2750355"	"Omodysplasia 2"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2537"	"IFI6"	"0.773"	"0.31"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2537"	"IFI6"	"0.773"	"0.31"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2537"	"IFI6"	"0.773"	"0.31"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2538"	"G6PC"	"0.584"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2538"	"G6PC"	"0.584"	"0.517"	"C0017920"	"Glycogen Storage Disease Type I"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.953488372093023"	"1983"	"2017"	"24"	"23"	"CTD_human;ORPHANET;UNIPROT"
"2538"	"G6PC"	"0.584"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2538"	"G6PC"	"0.584"	"0.517"	"C2919796"	"Glycogen storage disease type Ia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2018"	"0"	"32"	"CTD_human;ORPHANET"
"2539"	"G6PD"	"0.476"	"0.724"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"1974"	"2016"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1974"	"1996"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0002882"	"Anemia, Hemolytic, Congenital Nonspherocytic"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"1973"	"2001"	"2"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1974"	"1996"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1981"	"2007"	"5"	"0"	"PSYGENET"
"2539"	"G6PD"	"0.476"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"2539"	"G6PD"	"0.476"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1991"	"1991"	"1"	"0"	"GENOMICS_ENGLAND"
"2539"	"G6PD"	"0.476"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0015702"	"Favism"	"disease"	"C15;C16;C25"	"Disease or Syndrome"	"0.60"	"1"	"1981"	"2015"	"2"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"1973"	"1994"	"1"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1970"	"1979"	"2"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1974"	"1979"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"0.963636363636364"	"1980"	"2018"	"0"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0031306"	"Phagocyte Bactericidal Dysfunction"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"GENOMICS_ENGLAND"
"2539"	"G6PD"	"0.476"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1974"	"1996"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1970"	"1979"	"2"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1970"	"1979"	"2"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1974"	"1979"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C1844376"	"Granulomatous Disease, Chronic, X-Linked"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"1973"	"1994"	"1"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1974"	"1979"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C2720289"	"ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.60"		"1982"	"2017"	"18"	"53"	"CTD_human;UNIPROT"
"2539"	"G6PD"	"0.476"	"0.724"	"C2939465"	"Deficiency of glucose-6-phosphate dehydrogenase"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.40"	"0.933823529411765"	"1973"	"2017"	"3"	"0"	"CTD_human"
"2539"	"G6PD"	"0.476"	"0.724"	"C3661525"	"Autosomal Recessive Chronic Granulomatous Disease"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0268146"	"Glucose-6-phosphate transport defect"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"19"	"40"	"CTD_human;ORPHANET;UNIPROT"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0342749"	"GLYCOGEN STORAGE DISEASE Ic"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2000"	"1"	"4"	"CTD_human;UNIPROT"
"2542"	"SLC37A4"	"0.624"	"0.517"	"C0342750"	"Glycogen storage disease type Id"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"2"	"UNIPROT"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2543"	"GAGE1"	"0.743"	"0.172"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2547"	"XRCC6"	"0.586"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"0.5"	"2001"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0017921"	"Glycogen storage disease type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.955882352941177"	"1965"	"2018"	"55"	"136"	"CLINGEN;CTD_human;UNIPROT"
"2548"	"GAA"	"0.607"	"0.655"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0342751"	"Generalized glycogen storage disease of infants"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"0.955882352941177"	"1992"	"2018"	"5"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C0751172"	"Adult Glycogen Storage Disease Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2012"	"5"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C0751173"	"Glycogen Storage Disease Type II, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1991"	"2012"	"5"	"5"	"CTD_human;ORPHANET"
"2548"	"GAA"	"0.607"	"0.655"	"C0751174"	"Glycogen Storage Disease Type II, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2012"	"5"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2548"	"GAA"	"0.607"	"0.655"	"C2931347"	"Cardiac form of generalized glycogenosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1965"	"2015"	"50"	"64"	"CLINGEN;UNIPROT"
"2548"	"GAA"	"0.607"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2548"	"GAA"	"0.607"	"0.655"	"C3888924"	"Glycogen storage disease due to acid maltase deficiency, infantile onset"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2548"	"GAA"	"0.607"	"0.655"	"C3888925"	"Pompe's disease adult onset"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2549"	"GAB1"	"0.627"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2015"	"0"	"0"	"UNIPROT"
"2549"	"GAB1"	"0.627"	"0.517"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"2549"	"GAB1"	"0.627"	"0.517"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.54"	"0.5"	"1999"	"2016"	"5"	"0"	"CTD_human;PSYGENET"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"2"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2003"	"2016"	"2"	"0"	"PSYGENET"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2550"	"GABBR1"	"0.633"	"0.552"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2551"	"GABPA"	"0.454"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2551"	"GABPA"	"0.454"	"0.828"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"PSYGENET"
"2551"	"GABPA"	"0.454"	"0.828"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2553"	"GABPB1"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2003"	"2010"	"3"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2005"	"2012"	"4"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0270736"	"Essential Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.56"	"1"	"2002"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0393615"	"Familial Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0393676"	"Panayiotopoulos Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"1999"	"2004"	"4"	"0"	"PSYGENET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"0"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2554"	"GABRA1"	"0.596"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2554"	"GABRA1"	"0.596"	"0.414"	"C1970160"	"Epilepsy, Childhood Absence, Susceptibility To, 4"	"phenotype"	"C10"	"Finding"	"0.30"		"2002"	"2012"	"2"	"2"	"UNIPROT"
"2554"	"GABRA1"	"0.596"	"0.414"	"C2749942"	"EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5 (disorder)"	"phenotype"		"Finding"	"0.40"		"2002"	"2017"	"2"	"4"	"UNIPROT"
"2554"	"GABRA1"	"0.596"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"2554"	"GABRA1"	"0.596"	"0.414"	"C3810400"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"2"	"9"	"CTD_human;UNIPROT"
"2554"	"GABRA1"	"0.596"	"0.414"	"C4013473"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13"	"disease"		"Finding"	"0.30"		"2002"	"2012"	"2"	"2"	"UNIPROT"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.714285714285714"	"2009"	"2015"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"2004"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2010"	"2013"	"3"	"0"	"CTD_human;PSYGENET"
"2555"	"GABRA2"	"0.663"	"0.207"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2555"	"GABRA2"	"0.663"	"0.207"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2555"	"GABRA2"	"0.663"	"0.207"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2556"	"GABRA3"	"0.663"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2556"	"GABRA3"	"0.663"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1990"	"2004"	"5"	"0"	"PSYGENET"
"2556"	"GABRA3"	"0.663"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2556"	"GABRA3"	"0.663"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2556"	"GABRA3"	"0.663"	"0.483"	"C0268446"	"Thyrotoxic periodic paralysis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0270496"	"Schizoaffective disorder, bipolar type"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2557"	"GABRA4"	"0.773"	"0.207"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1998"	"2011"	"5"	"0"	"PSYGENET"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0150080"	"Social Communication Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C3711376"	"Isodicentric Chromosome 15 Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2558"	"GABRA5"	"0.652"	"0.276"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2558"	"GABRA5"	"0.652"	"0.276"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"1999"	"2005"	"3"	"0"	"PSYGENET"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2559"	"GABRA6"	"0.672"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2006"	"5"	"0"	"PSYGENET"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2013"	"2"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0270496"	"Schizoaffective disorder, bipolar type"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2560"	"GABRB1"	"0.696"	"0.345"	"C4310691"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"3"	"3"	"CTD_human;UNIPROT"
"2561"	"GABRB2"	"0.743"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.666666666666667"	"2005"	"2010"	"3"	"0"	"PSYGENET"
"2561"	"GABRB2"	"0.743"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2561"	"GABRB2"	"0.743"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"2561"	"GABRB2"	"0.743"	"0.276"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2561"	"GABRB2"	"0.743"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2013"	"4"	"0"	"PSYGENET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.833333333333333"	"1998"	"2014"	"2"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2011"	"2"	"0"	"PSYGENET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2013"	"5"	"0"	"PSYGENET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2013"	"5"	"0"	"PSYGENET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.44"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"1999"	"2015"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0021603"	"Sleep Initiation and Maintenance Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0033139"	"Primary Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2006"	"2015"	"2"	"0"	"PSYGENET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0162635"	"Angelman Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2007"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0238111"	"Lennox-Gastaut syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0270541"	"Rebound Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0349255"	"Nonorganic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0393759"	"Transient Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0541798"	"Early Awakening"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2013"	"2018"	"0"	"2"	"GENOMICS_ENGLAND"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751249"	"Chronic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751250"	"Psychophysiological Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751251"	"Secondary Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0751252"	"Sleep Initiation Dysfunction"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C0917801"	"Sleeplessness"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.63"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2562"	"GABRB3"	"0.572"	"0.517"	"C2677087"	"EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5"	"phenotype"		"Finding"	"0.40"		"2008"	"2017"	"2"	"2"	"UNIPROT"
"2562"	"GABRB3"	"0.572"	"0.517"	"C3711376"	"Isodicentric Chromosome 15 Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"2562"	"GABRB3"	"0.572"	"0.517"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2562"	"GABRB3"	"0.572"	"0.517"	"C4310712"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"6"	"6"	"CTD_human;UNIPROT"
"2562"	"GABRB3"	"0.572"	"0.517"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2563"	"GABRD"	"0.648"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2563"	"GABRD"	"0.648"	"0.379"	"C0270850"	"Idiopathic generalized epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2563"	"GABRD"	"0.648"	"0.379"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"2563"	"GABRD"	"0.648"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2563"	"GABRD"	"0.648"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2563"	"GABRD"	"0.648"	"0.379"	"C1842870"	"Chromosome 1p36 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2563"	"GABRD"	"0.648"	"0.379"	"C2751603"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10"	"disease"		"Finding"	"0.30"		"2005"	"2005"	"1"	"2"	"UNIPROT"
"2563"	"GABRD"	"0.648"	"0.379"	"C2751604"	"EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7"	"phenotype"		"Finding"	"0.30"		"2005"	"2005"	"1"	"2"	"UNIPROT"
"2563"	"GABRD"	"0.648"	"0.379"	"C3150399"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2005"	"2005"	"1"	"2"	"UNIPROT"
"2563"	"GABRD"	"0.648"	"0.379"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2010"	"0"	"0"	"ORPHANET"
"2565"	"GABRG1"	"0.785"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"4"	"0"	"PSYGENET"
"2565"	"GABRG1"	"0.785"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2005"	"2015"	"3"	"0"	"CTD_human;PSYGENET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"	"0.75"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2012"	"0"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2005"	"2015"	"4"	"0"	"PSYGENET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0376532"	"Epilepsy, Rolandic"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2018"	"0"	"1"	"ORPHANET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2014"	"0"	"0"	"ORPHANET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C1843244"	"EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2017"	"1"	"4"	"UNIPROT"
"2566"	"GABRG2"	"0.6"	"0.31"	"C1858674"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"		"1999"	"2013"	"2"	"5"	"CTD_human;UNIPROT"
"2566"	"GABRG2"	"0.6"	"0.31"	"C1969810"	"FEBRILE CONVULSIONS, FAMILIAL, 8"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2017"	"2"	"7"	"UNIPROT"
"2566"	"GABRG2"	"0.6"	"0.31"	"C2363129"	"Benign Rolandic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"1"	"ORPHANET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2014"	"0"	"0"	"ORPHANET"
"2566"	"GABRG2"	"0.6"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2566"	"GABRG2"	"0.6"	"0.31"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2566"	"GABRG2"	"0.6"	"0.31"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"PSYGENET"
"2567"	"GABRG3"	"0.752"	"0.345"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C3711376"	"Isodicentric Chromosome 15 Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2567"	"GABRG3"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2568"	"GABRP"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"0"	"0"	"UNIPROT"
"2569"	"GABRR1"	"0.834"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2569"	"GABRR1"	"0.834"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"2"	"0"	"PSYGENET"
"2569"	"GABRR1"	"0.834"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2570"	"GABRR2"	"0.815"	"0.103"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1988"	"2014"	"5"	"0"	"PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2001"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.962962962962963"	"2000"	"2016"	"4"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2571"	"GAD1"	"0.542"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2005"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"2571"	"GAD1"	"0.542"	"0.724"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2571"	"GAD1"	"0.542"	"0.724"	"C2751938"	"Cerebral Palsy, Spastic Quadriplegic, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"1997"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2571"	"GAD1"	"0.542"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2572"	"GAD2"	"0.557"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.666666666666667"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"2572"	"GAD2"	"0.557"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1997"	"2013"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"2572"	"GAD2"	"0.557"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2572"	"GAD2"	"0.557"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"2580"	"GAK"	"0.886"	"0.103"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2017"	"1"	"3"	"CTD_human"
"2581"	"GALC"	"0.648"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2001"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"2581"	"GALC"	"0.648"	"0.448"	"C0023521"	"Globoid cell leukodystrophy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1982"	"2017"	"8"	"69"	"CTD_human;UNIPROT"
"2581"	"GALC"	"0.648"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2581"	"GALC"	"0.648"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2581"	"GALC"	"0.648"	"0.448"	"C0268252"	"Late-Onset Globoid Cell Leukodystrophy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.55"	"1"	"1982"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"2581"	"GALC"	"0.648"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2581"	"GALC"	"0.648"	"0.448"	"C0751273"	"Infantile Globoid Cell Leukodystrophy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.56"	"0.833333333333333"	"1995"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"2581"	"GALC"	"0.648"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"2582"	"GALE"	"0.752"	"0.276"	"C0016952"	"Galactosemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"2582"	"GALE"	"0.752"	"0.276"	"C0268151"	"Classical galactosemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"2582"	"GALE"	"0.752"	"0.276"	"C0268155"	"Deficiency of galactokinase"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2582"	"GALE"	"0.752"	"0.276"	"C0751161"	"UDPglucose 4-epimerase deficiency disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1993"	"2015"	"9"	"17"	"CTD_human;UNIPROT"
"2582"	"GALE"	"0.752"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2583"	"B4GALNT1"	"0.773"	"0.207"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2583"	"B4GALNT1"	"0.773"	"0.207"	"C1836632"	"SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"6"	"ORPHANET;UNIPROT"
"2583"	"B4GALNT1"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2584"	"GALK1"	"0.735"	"0.276"	"C0016952"	"Galactosemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"	"0.875"	"1988"	"2018"	"1"	"0"	"CTD_human"
"2584"	"GALK1"	"0.735"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"0.909090909090909"	"1986"	"2004"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2584"	"GALK1"	"0.735"	"0.276"	"C0268151"	"Classical galactosemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"0.75"	"1988"	"2018"	"1"	"0"	"CTD_human"
"2584"	"GALK1"	"0.735"	"0.276"	"C0268155"	"Deficiency of galactokinase"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1986"	"2005"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2584"	"GALK1"	"0.735"	"0.276"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2584"	"GALK1"	"0.735"	"0.276"	"C0751161"	"UDPglucose 4-epimerase deficiency disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2001"	"1"	"0"	"CTD_human"
"2584"	"GALK1"	"0.735"	"0.276"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2584"	"GALK1"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2587"	"GALR1"	"0.713"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2587"	"GALR1"	"0.713"	"0.207"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2587"	"GALR1"	"0.713"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2587"	"GALR1"	"0.713"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2587"	"GALR1"	"0.713"	"0.207"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2587"	"GALR1"	"0.713"	"0.207"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2588"	"GALNS"	"0.616"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1987"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"2588"	"GALNS"	"0.616"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2588"	"GALNS"	"0.616"	"0.655"	"C0026707"	"Mucopolysaccharidosis IV"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.70"	"1"	"1980"	"2015"	"0"	"3"	"CTD_human"
"2588"	"GALNS"	"0.616"	"0.655"	"C0086651"	"Mucopolysaccharidosis, MPS-IV-A"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"1988"	"2017"	"12"	"69"	"CTD_human;ORPHANET;UNIPROT"
"2588"	"GALNS"	"0.616"	"0.655"	"C0086652"	"Mucopolysaccharidosis type IVB"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2588"	"GALNS"	"0.616"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2588"	"GALNS"	"0.616"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2588"	"GALNS"	"0.616"	"0.655"	"C3179194"	"GALNS Deficiency"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2006"	"0"	"0"	"CTD_human;ORPHANET"
"2588"	"GALNS"	"0.616"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.33"		"2004"	"2008"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0085681"	"Hyperphosphatemia (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2591"	"GALNT3"	"0.627"	"0.586"	"C1876187"	"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1961"	"2015"	"0"	"14"	"ORPHANET"
"2592"	"GALT"	"0.63"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2592"	"GALT"	"0.63"	"0.517"	"C0016952"	"Galactosemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"	"0.948717948717949"	"1982"	"2018"	"1"	"1"	"CTD_human"
"2592"	"GALT"	"0.63"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.43"	"1"	"1993"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"2592"	"GALT"	"0.63"	"0.517"	"C0268151"	"Classical galactosemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.945454545454545"	"1982"	"2018"	"28"	"224"	"CTD_human;ORPHANET;UNIPROT"
"2592"	"GALT"	"0.63"	"0.517"	"C0268155"	"Deficiency of galactokinase"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2592"	"GALT"	"0.63"	"0.517"	"C0751161"	"UDPglucose 4-epimerase deficiency disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"2592"	"GALT"	"0.63"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2592"	"GALT"	"0.63"	"0.517"	"C3278146"	"GALACTOSEMIA, DUARTE VARIANT"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2017"	"27"	"113"	"UNIPROT"
"2592"	"GALT"	"0.63"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2593"	"GAMT"	"0.667"	"0.241"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2593"	"GAMT"	"0.667"	"0.241"	"C0574080"	"Guanidinoacetate methyltransferase deficiency"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.94"	"1"	"1993"	"2016"	"11"	"13"	"CTD_human;ORPHANET;UNIPROT"
"2593"	"GAMT"	"0.667"	"0.241"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2005"	"2005"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2593"	"GAMT"	"0.667"	"0.241"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2593"	"GAMT"	"0.667"	"0.241"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1999"	"2012"	"4"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2596"	"GAP43"	"0.624"	"0.517"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2596"	"GAP43"	"0.624"	"0.517"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2597"	"GAPDH"	"0.484"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2016"	"2"	"0"	"CTD_human"
"2617"	"GARS"	"0.656"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2617"	"GARS"	"0.656"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2617"	"GARS"	"0.656"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2617"	"GARS"	"0.656"	"0.276"	"C1832274"	"Charcot-Marie-Tooth disease, Type 2D"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.97"	"0.857142857142857"	"1997"	"2018"	"9"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2617"	"GARS"	"0.656"	"0.276"	"C1833308"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"1"	"1996"	"2016"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2618"	"GART"	"0.735"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2618"	"GART"	"0.735"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2619"	"GAS1"	"0.645"	"0.483"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2619"	"GAS1"	"0.645"	"0.483"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"2619"	"GAS1"	"0.645"	"0.483"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"2619"	"GAS1"	"0.645"	"0.483"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"2619"	"GAS1"	"0.645"	"0.483"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"2620"	"GAS2"	"0.834"	"0.172"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2620"	"GAS2"	"0.834"	"0.172"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2620"	"GAS2"	"0.834"	"0.172"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2001"	"2006"	"4"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2006"	"4"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2621"	"GAS6"	"0.554"	"0.621"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2622"	"GAS8"	"0.752"	"0.241"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"2622"	"GAS8"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2622"	"GAS8"	"0.752"	"0.241"	"C4225230"	"CILIARY DYSKINESIA, PRIMARY, 33"	"disease"		"Disease or Syndrome"	"0.80"		"2016"	"2017"	"3"	"3"	"CTD_human;UNIPROT"
"2622"	"GAS8"	"0.752"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2622"	"GAS8"	"0.752"	"0.241"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2000"	"2014"	"5"	"0"	"GENOMICS_ENGLAND"
"2623"	"GATA1"	"0.51"	"0.69"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.989130434782609"	"2002"	"2017"	"0"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C0023437"	"Acute Basophilic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C0023462"	"Acute Megakaryocytic Leukemias"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.955555555555556"	"2002"	"2016"	"0"	"1"	"CGI"
"2623"	"GATA1"	"0.51"	"0.69"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.70"	"0.9"	"1995"	"2012"	"1"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2014"	"5"	"0"	"GENOMICS_ENGLAND"
"2623"	"GATA1"	"0.51"	"0.69"	"C0162530"	"Porphyria, Erythropoietic"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2016"	"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2623"	"GATA1"	"0.51"	"0.69"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.37"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C1834582"	"MYELOPROLIFERATIVE SYNDROME, TRANSIENT"	"disease"	"C10;C15;C16"	"Neoplastic Process"	"0.40"	"0.928571428571429"	"2003"	"2017"	"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C1839161"	"Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.70"		"1977"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2623"	"GATA1"	"0.51"	"0.69"	"C1845837"	"Dyserythropoietic Anemia with Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2014"	"0"	"10"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C1860788"	"Transient Myeloproliferative Disorder of Down Syndrome"	"disease"	"C10;C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"2623"	"GATA1"	"0.51"	"0.69"	"C2718078"	"Deficiency of Uroporphyrinogen III Synthase"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2623"	"GATA1"	"0.51"	"0.69"	"C3550789"	"THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA"	"disease"		"Disease or Syndrome"	"0.50"		"2000"	"2002"	"4"	"4"	"CTD_human;UNIPROT"
"2623"	"GATA1"	"0.51"	"0.69"	"C3550856"	"ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2624"	"GATA2"	"0.536"	"0.621"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1994"	"2016"	"2"	"2"	"CGI;CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"2624"	"GATA2"	"0.536"	"0.621"	"C0024236"	"Lymphedema"	"disease"	"C15"	"Disease or Syndrome"	"0.44"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0026985"	"Myelodysplasia"	"disease"		"Congenital Abnormality"	"0.35"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"2624"	"GATA2"	"0.536"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"2"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.33"	"0.666666666666667"	"2009"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2624"	"GATA2"	"0.536"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C1704423"	"Milroy Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2011"	"2017"	"3"	"0"	"CTD_human"
"2624"	"GATA2"	"0.536"	"0.621"	"C3279664"	"Emberger syndrome"	"disease"		"Disease or Syndrome"	"0.75"	"1"	"2010"	"2017"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2624"	"GATA2"	"0.536"	"0.621"	"C3280030"	"GATA2 Deficiency"	"disease"		"Disease or Syndrome"	"0.76"	"1"	"1989"	"2014"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2624"	"GATA2"	"0.536"	"0.621"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.80"	"1"	"2002"	"2017"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2625"	"GATA3"	"0.477"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.42"	"1"	"2005"	"2014"	"1"	"2"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.951219512195122"	"1999"	"2018"	"0"	"0"	"CGI;UNIPROT"
"2625"	"GATA3"	"0.477"	"0.793"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2625"	"GATA3"	"0.477"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.45"	"1"	"2005"	"2017"	"1"	"4"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0025568"	"Metaplasia"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2625"	"GATA3"	"0.477"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.944444444444444"	"1999"	"2018"	"0"	"0"	"CGI"
"2625"	"GATA3"	"0.477"	"0.793"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2625"	"GATA3"	"0.477"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"		"2014"	"2014"	"0"	"1"	"ORPHANET"
"2625"	"GATA3"	"0.477"	"0.793"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2625"	"GATA3"	"0.477"	"0.793"	"C1840333"	"Barakat syndrome"	"disease"	"C09;C10;C12;C13;C19;C23"	"Disease or Syndrome"	"1.00"	"0.96969696969697"	"2000"	"2017"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2625"	"GATA3"	"0.477"	"0.793"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2626"	"GATA4"	"0.482"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2009"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.50"	"0.941176470588235"	"2007"	"2018"	"0"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"2007"	"2008"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"2626"	"GATA4"	"0.482"	"0.724"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.80"	"0.866666666666667"	"2006"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2626"	"GATA4"	"0.482"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.36"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"2626"	"GATA4"	"0.482"	"0.724"	"C0344735"	"Partial atrioventricular canal"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"2626"	"GATA4"	"0.482"	"0.724"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C1389016"	"ATRIOVENTRICULAR CANAL DEFECT"	"phenotype"	"C14;C16"	"Anatomical Abnormality"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C1389018"	"Atrioventricular Septal Defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"2626"	"GATA4"	"0.482"	"0.724"	"C1842778"	"Atrial septal defect 2"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.80"		"2003"	"2016"	"7"	"7"	"CTD_human;UNIPROT"
"2626"	"GATA4"	"0.482"	"0.724"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2626"	"GATA4"	"0.482"	"0.724"	"C2931638"	"Chromosome 8, monosomy 8p23 1"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2626"	"GATA4"	"0.482"	"0.724"	"C3280777"	"VENTRICULAR SEPTAL DEFECT 1"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2008"	"2012"	"4"	"7"	"UNIPROT"
"2626"	"GATA4"	"0.482"	"0.724"	"C3280781"	"ATRIOVENTRICULAR SEPTAL DEFECT 4"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2008"	"2011"	"1"	"2"	"UNIPROT"
"2626"	"GATA4"	"0.482"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2626"	"GATA4"	"0.482"	"0.724"	"C3809858"	"TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"2626"	"GATA4"	"0.482"	"0.724"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2627"	"GATA6"	"0.51"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2627"	"GATA6"	"0.51"	"0.621"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.73"	"1"	"2011"	"2013"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.62"	"1"	"2009"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"3"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"2627"	"GATA6"	"0.51"	"0.621"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C0344735"	"Partial atrioventricular canal"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C1389016"	"ATRIOVENTRICULAR CANAL DEFECT"	"phenotype"	"C14;C16"	"Anatomical Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"2627"	"GATA6"	"0.51"	"0.621"	"C1389018"	"Atrioventricular Septal Defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"2627"	"GATA6"	"0.51"	"0.621"	"C1838780"	"Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease"	"disease"	"C14;C16;C18;C19"	"Disease or Syndrome"	"0.60"		"1994"	"2015"	"1"	"10"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C2931296"	"Yorifuji Okuno syndrome"	"disease"	"C10;C12;C13;C14;C18;C19;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2627"	"GATA6"	"0.51"	"0.621"	"C3280939"	"ATRIOVENTRICULAR SEPTAL DEFECT 5"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C3280943"	"ATRIAL SEPTAL DEFECT 9"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2627"	"GATA6"	"0.51"	"0.621"	"C3888085"	"PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"5"	"CTD_human;UNIPROT"
"2627"	"GATA6"	"0.51"	"0.621"	"C4012454"	"HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"5"	"CTD_human;UNIPROT"
"2628"	"GATM"	"0.672"	"0.517"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2628"	"GATM"	"0.672"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2628"	"GATM"	"0.672"	"0.517"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2628"	"GATM"	"0.672"	"0.517"	"C2675179"	"Arginine:Glycine Amidinotransferase Deficiency"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2016"	"6"	"16"	"CTD_human;ORPHANET;UNIPROT"
"2628"	"GATM"	"0.672"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"0"	"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0017205"	"Gaucher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"	"0.96969696969697"	"1982"	"2018"	"6"	"25"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.40"		"1984"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2018"	"2"	"1"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.49"	"1"	"2005"	"2016"	"1"	"1"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0268250"	"Gaucher Disease, Type 2 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.93"	"1"	"1987"	"2016"	"8"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C0268251"	"Gaucher Disease, Type 3 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.93"	"1"	"1987"	"2016"	"7"	"12"	"CTD_human;ORPHANET;UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2018"	"1"	"1"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C1842704"	"GAUCHER DISEASE, PERINATAL LETHAL"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1988"	"2015"	"0"	"12"	"CTD_human;ORPHANET"
"2629"	"GBA"	"0.521"	"0.724"	"C1856476"	"Gaucher Disease, Type Iiic"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1989"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"2629"	"GBA"	"0.521"	"0.724"	"C1856491"	"Gaucher Disease, Type IIIa"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2011"	"1"	"1"	"UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C1856492"	"Gaucher Disease, Type IIIb"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2011"	"1"	"1"	"UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C1856493"	"Gaucher Disease, Norrbottnian Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2011"	"1"	"1"	"UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C1961835"	"Gaucher Disease, Type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.909090909090909"	"1983"	"2016"	"46"	"114"	"CTD_human;ORPHANET;UNIPROT"
"2629"	"GBA"	"0.521"	"0.724"	"C2931585"	"Gaucher-like disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2629"	"GBA"	"0.521"	"0.724"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"1987"	"2016"	"0"	"4"	"CTD_human"
"2629"	"GBA"	"0.521"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2629"	"GBA"	"0.521"	"0.724"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2632"	"GBE1"	"0.621"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0017922"	"Glycogen Storage Disease Type III"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"2632"	"GBE1"	"0.621"	"0.517"	"C0017923"	"Glycogen Storage Disease Type IV"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1993"	"2017"	"2"	"15"	"CTD_human;UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.40"		"1999"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2005"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2632"	"GBE1"	"0.621"	"0.517"	"C1849722"	"Polyglucosan Body Disease, Adult Form"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856301"	"GSD IV, Classic Hepatic"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1996"	"2017"	"2"	"8"	"UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856302"	"GSD IV, Nonprogressive Hepatic"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"2005"	"2"	"7"	"UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856303"	"GSD IV, Neuromuscular Form, Fatal Perinatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2005"	"2"	"7"	"ORPHANET;UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856304"	"GSD IV, Neuromuscular Form, Congenital"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1994"	"2009"	"2"	"13"	"ORPHANET;UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856305"	"GSD IV, Neuromuscular Form, Childhood"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1996"	"2005"	"2"	"8"	"ORPHANET;UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C1856306"	"GSD IV, Neuromuscular Form, Adult, with Isolated Myopathy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"2005"	"2"	"7"	"UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C2936914"	"Cirrhosis, familial, with deposition of abnormal glycogen"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"2005"	"2"	"7"	"UNIPROT"
"2632"	"GBE1"	"0.621"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2633"	"GBP1"	"0.676"	"0.448"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2634"	"GBP2"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2634"	"GBP2"	"0.815"	"0.172"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2637"	"GBX2"	"0.799"	"0.345"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2637"	"GBX2"	"0.799"	"0.345"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"1985"	"2012"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"1989"	"2015"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1983"	"2015"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.32"		"1996"	"2008"	"2"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"0"	"2008"	"2018"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2638"	"GC"	"0.525"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2639"	"GCDH"	"0.727"	"0.276"	"C0268595"	"Glutaric aciduria, type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1989"	"2017"	"8"	"78"	"CTD_human;ORPHANET;UNIPROT"
"2639"	"GCDH"	"0.727"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2001"	"5"	"0"	"GENOMICS_ENGLAND"
"2641"	"GCG"	"0.529"	"0.655"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"2008"	"2012"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0009421"	"Comatose"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0009806"	"Constipation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.979381443298969"	"1986"	"2018"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.966666666666667"	"1981"	"2018"	"2"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.38"	"0.875"	"1986"	"2018"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1988"	"1993"	"2"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.964285714285714"	"1996"	"2016"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0037763"	"Spasm"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0038354"	"Stomach Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0039239"	"Sinus Tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0151911"	"Generalized Spasms"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0235229"	"Ciliary Body Spasm"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0237326"	"Dyschezia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1985"	"1998"	"5"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C0860634"	"Psychogenic coma"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1257861"	"Colonic Inertia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"1986"	"2009"	"2"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1879526"	"Aberrant Crypt Foci"	"phenotype"	"C04"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2641"	"GCG"	"0.529"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2642"	"GCGR"	"0.727"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.894736842105263"	"1995"	"2017"	"0"	"1"	"CTD_human"
"2642"	"GCGR"	"0.727"	"0.207"	"C1857451"	"Acth-Independent Macronodular Adrenal Hyperplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2005"	"2013"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.955555555555556"	"1991"	"2017"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0026837"	"Muscle Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0026858"	"Musculoskeletal Pain"	"phenotype"	"C05;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.88"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"2643"	"GCH1"	"0.534"	"0.724"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0086439"	"Hypokinesia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0151564"	"Cogwheel Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0231519"	"Gegenhalten"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0233565"	"Bradykinesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0233608"	"Catatonic Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0239325"	"Extensor Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0268467"	"Hyperphenylalaninemia, BH4-Deficient, B"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1995"	"2008"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2643"	"GCH1"	"0.534"	"0.724"	"C0277821"	"Extrapyramidal Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2643"	"GCH1"	"0.534"	"0.724"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.42"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C0751701"	"Hypokinesia, Antiorthostatic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2643"	"GCH1"	"0.534"	"0.724"	"C1320474"	"Nuchal Rigidity"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2643"	"GCH1"	"0.534"	"0.724"	"C1851920"	"Dopa-Responsive Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"0.900900900900901"	"1990"	"2018"	"15"	"13"	"CTD_human;ORPHANET;UNIPROT"
"2643"	"GCH1"	"0.534"	"0.724"	"C2673535"	"DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"1996"	"2006"	"2"	"6"	"UNIPROT"
"2643"	"GCH1"	"0.534"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2644"	"GCHFR"	"0.681"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.921985815602837"	"1992"	"2018"	"4"	"3"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9875"	"1992"	"2017"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.37"	"1"	"2004"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"2645"	"GCK"	"0.547"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.938931297709924"	"1992"	"2018"	"0"	"0"	"ORPHANET"
"2645"	"GCK"	"0.547"	"0.586"	"C0342277"	"Diabetes mellitus autosomal dominant type II (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.80"	"0.954545454545455"	"1992"	"2015"	"20"	"26"	"CTD_human;UNIPROT"
"2645"	"GCK"	"0.547"	"0.586"	"C1833102"	"DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES"	"disease"	"C10;C18;C19;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"2"	"7"	"UNIPROT"
"2645"	"GCK"	"0.547"	"0.586"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2015"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2645"	"GCK"	"0.547"	"0.586"	"C1853564"	"Developmental Delay, Epilepsy, and Neonatal Diabetes"	"disease"	"C10;C16;C18;C19;C23;F01"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"2"	"7"	"UNIPROT"
"2645"	"GCK"	"0.547"	"0.586"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C1865290"	"Hyperinsulinemic hypoglycemia, familial, 3"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1998"	"2018"	"8"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2645"	"GCK"	"0.547"	"0.586"	"C2931832"	"Hyperinsulinemic hypoglycemia, familial, 1"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C2931833"	"Hyperinsulinemic hypoglycemia, familial, 2"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2645"	"GCK"	"0.547"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2645"	"GCK"	"0.547"	"0.586"	"C3888018"	"Congenital Hyperinsulinism"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.40"	"0.846153846153846"	"1997"	"2015"	"1"	"0"	"CTD_human"
"2646"	"GCKR"	"0.636"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.933333333333333"	"2005"	"2018"	"1"	"1"	"CTD_human"
"2646"	"GCKR"	"0.636"	"0.414"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.45"	"0.8"	"2010"	"2017"	"1"	"2"	"CTD_human"
"2647"	"BLOC1S1"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2650"	"GCNT1"	"0.713"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2650"	"GCNT1"	"0.713"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2650"	"GCNT1"	"0.713"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"2651"	"GCNT2"	"0.701"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2004"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2651"	"GCNT2"	"0.701"	"0.414"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2651"	"GCNT2"	"0.701"	"0.414"	"C3805373"	"CATARACT 13 WITH ADULT i PHENOTYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2002"	"1"	"2"	"CTD_human;UNIPROT"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C0155016"	"Color Blindness, Red-Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2002"	"2"	"4"	"CTD_human;UNIPROT"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C0339537"	"Cone monochromatism"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.72"	"1"	"1989"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C2931753"	"Achromatopsia incomplete, X-linked"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C3887937"	"CONE DYSTROPHY 5, X-LINKED"	"disease"		"Disease or Syndrome"	"0.40"		"1996"	"2010"	"2"	"2"	"UNIPROT"
"2652"	"OPN1MW"	"0.667"	"0.448"	"C3887938"	"COLORBLINDNESS, PARTIAL, DEUTAN SERIES"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"1990"	"2002"	"2"	"3"	"CTD_human;UNIPROT"
"2653"	"GCSH"	"0.743"	"0.276"	"C0268561"	"Hyperglycinemia, Nonketotic, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2653"	"GCSH"	"0.743"	"0.276"	"C0268562"	"Hyperglycinemia, Nonketotic, Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2653"	"GCSH"	"0.743"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2653"	"GCSH"	"0.743"	"0.276"	"C0751747"	"Hyperglycinemia, Nonketotic, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2653"	"GCSH"	"0.743"	"0.276"	"C0751748"	"Nonketotic Hyperglycinemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.68"	"1"	"1990"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"2653"	"GCSH"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2657"	"GDF1"	"0.565"	"0.483"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.61"	"1"	"2006"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.71"	"1"	"2007"	"2007"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C0040761"	"Transposition of Great Vessels"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.51"	"1"	"2007"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C0175707"	"Asplenia Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.60"		"2010"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"2657"	"GDF1"	"0.565"	"0.483"	"C0265357"	"Polysplenia Syndrome"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C1956410"	"Double Outlet Right Ventricle, Noncommitted VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C1956411"	"Double Outlet Right Ventricle, Subaortic VSD"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C1956412"	"Double Outlet Right Ventricle, Subpulmonary VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C1956413"	"Taussig-Bing Anomaly"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C3151221"	"TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 3"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"2"	"CTD_human;UNIPROT"
"2657"	"GDF1"	"0.565"	"0.483"	"C3178805"	"Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C3178806"	"Right Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C3178807"	"Left Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2657"	"GDF1"	"0.565"	"0.483"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2658"	"GDF2"	"0.656"	"0.448"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2658"	"GDF2"	"0.656"	"0.448"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2658"	"GDF2"	"0.656"	"0.448"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2658"	"GDF2"	"0.656"	"0.448"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.62"	"1"	"2013"	"2016"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"2658"	"GDF2"	"0.656"	"0.448"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2658"	"GDF2"	"0.656"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"2014"	"2014"	"1"	"0"	"CTD_human"
"2658"	"GDF2"	"0.656"	"0.448"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"2658"	"GDF2"	"0.656"	"0.448"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"2658"	"GDF2"	"0.656"	"0.448"	"C3809710"	"TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"2660"	"MSTN"	"0.602"	"0.586"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C0236033"	"Muscle hypertrophy"	"phenotype"		"Organ or Tissue Function"	"0.40"		"1993"	"2004"	"0"	"1"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2660"	"MSTN"	"0.602"	"0.586"	"C2931112"	"Myostatin-related muscle hypertrophy"	"disease"	"C05;C10;C23"	"Congenital Abnormality"	"0.70"		"1997"	"2009"	"2"	"0"	"CTD_human;ORPHANET"
"2661"	"GDF9"	"0.735"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"2661"	"GDF9"	"0.735"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2662"	"GDF10"	"0.69"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2662"	"GDF10"	"0.69"	"0.276"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"2662"	"GDF10"	"0.69"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2662"	"GDF10"	"0.69"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2662"	"GDF10"	"0.69"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2664"	"GDI1"	"0.59"	"0.448"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2002"	"2"	"0"	"CTD_human"
"2664"	"GDI1"	"0.59"	"0.448"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2664"	"GDI1"	"0.59"	"0.448"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2664"	"GDI1"	"0.59"	"0.448"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1996"	"2017"	"13"	"0"	"CLINGEN;ORPHANET"
"2664"	"GDI1"	"0.59"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1998"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2664"	"GDI1"	"0.59"	"0.448"	"C3887939"	"MENTAL RETARDATION, X-LINKED 41"	"disease"		"Disease or Syndrome"	"0.80"		"1996"	"2012"	"2"	"4"	"CTD_human;UNIPROT"
"2665"	"GDI2"	"0.928"	"0.138"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"2668"	"GDNF"	"0.463"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2005"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"	"0.931034482758621"	"1996"	"2014"	"2"	"0"	"CTD_human;ORPHANET"
"2668"	"GDNF"	"0.463"	"0.759"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0027854"	"Neurologic Manifestations"	"group"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.985915492957746"	"1993"	"2017"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"1"	"1997"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"2668"	"GDNF"	"0.463"	"0.759"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.5"	"2002"	"2015"	"4"	"0"	"PSYGENET"
"2668"	"GDNF"	"0.463"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"2668"	"GDNF"	"0.463"	"0.759"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1996"	"1997"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CLINGEN"
"2668"	"GDNF"	"0.463"	"0.759"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CLINGEN"
"2668"	"GDNF"	"0.463"	"0.759"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0235031"	"Neurologic Symptoms"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2005"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2014"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CLINGEN"
"2668"	"GDNF"	"0.463"	"0.759"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0422837"	"Neurological observations"	"group"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CLINGEN"
"2668"	"GDNF"	"0.463"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0521654"	"Neurologic Deficits"	"group"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2005"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0683357"	"Excessive drinking"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2668"	"GDNF"	"0.463"	"0.759"	"C0746857"	"Focal Neurologic Deficits"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751377"	"Neurologic Dysfunction"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751378"	"Neurologic Signs"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1996"	"1997"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"2668"	"GDNF"	"0.463"	"0.759"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.60"		"1998"	"1998"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2668"	"GDNF"	"0.463"	"0.759"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"1998"	"1998"	"1"	"1"	"CTD_human;UNIPROT"
"2668"	"GDNF"	"0.463"	"0.759"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"1997"	"2012"	"2"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2668"	"GDNF"	"0.463"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2668"	"GDNF"	"0.463"	"0.759"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1997"	"1997"	"1"	"1"	"UNIPROT"
"2668"	"GDNF"	"0.463"	"0.759"	"C3150974"	"HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3"	"disease"		"Finding"	"0.30"		"1996"	"1997"	"3"	"4"	"UNIPROT"
"2668"	"GDNF"	"0.463"	"0.759"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.50"		"1996"	"1997"	"2"	"0"	"CTD_human;ORPHANET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.39"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2670"	"GFAP"	"0.484"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2005"	"2010"	"2"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2015"	"3"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2015"	"3"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.44"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2005"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"2670"	"GFAP"	"0.484"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2005"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"2670"	"GFAP"	"0.484"	"0.759"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0027873"	"Neuromyelitis Optica"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"0.833333333333333"	"1999"	"2015"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2018"	"2"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0037917"	"Spina Bifida Cystica"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"2"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0270726"	"Alexander Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.989690721649485"	"1976"	"2018"	"23"	"89"	"CTD_human;UNIPROT"
"2670"	"GFAP"	"0.484"	"0.759"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2670"	"GFAP"	"0.484"	"0.759"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C0917813"	"Spina Bifida, Open"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"2670"	"GFAP"	"0.484"	"0.759"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2670"	"GFAP"	"0.484"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2670"	"GFAP"	"0.484"	"0.759"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2671"	"GFER"	"0.619"	"0.655"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.52"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2671"	"GFER"	"0.619"	"0.655"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"2671"	"GFER"	"0.619"	"0.655"	"C0392622"	"Toxic effect of carbon tetrachloride"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2017"	"2"	"2"	"GENOMICS_ENGLAND"
"2671"	"GFER"	"0.619"	"0.655"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2671"	"GFER"	"0.619"	"0.655"	"C2751320"	"Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay"	"disease"	"C05;C09;C10;C11;C18;C23;F03"	"Disease or Syndrome"	"0.71"	"1"	"2009"	"2010"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2671"	"GFER"	"0.619"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"2672"	"GFI1"	"0.604"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2002"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"2672"	"GFI1"	"0.604"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C1842930"	"Neutropenia, Nonimmune Chronic Idiopathic, Adult"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"2672"	"GFI1"	"0.604"	"0.345"	"C1859966"	"Neutropenia, Severe Congenital, Autosomal Dominant 1"	"disease"	"C15"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"0"	"0"	"ORPHANET"
"2672"	"GFI1"	"0.604"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2672"	"GFI1"	"0.604"	"0.345"	"C2751288"	"Neutropenia, Severe Congenital, Autosomal Dominant 2"	"disease"	"C15"	"Disease or Syndrome"	"0.80"		"2003"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.57"	"1"	"2011"	"2018"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2673"	"GFPT1"	"0.642"	"0.483"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2673"	"GFPT1"	"0.642"	"0.483"	"C1837091"	"MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2673"	"GFPT1"	"0.642"	"0.483"	"C3552335"	"MYASTHENIC SYNDROME, CONGENITAL, 12"	"disease"		"Disease or Syndrome"	"0.40"		"1996"	"2018"	"1"	"6"	"UNIPROT"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2674"	"GFRA1"	"0.633"	"0.448"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2675"	"GFRA2"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2010"	"2011"	"1"	"0"	"PSYGENET"
"2676"	"GFRA3"	"0.773"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2677"	"GGCX"	"0.696"	"0.345"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.42"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2677"	"GGCX"	"0.696"	"0.345"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1966"	"2009"	"6"	"0"	"GENOMICS_ENGLAND"
"2677"	"GGCX"	"0.696"	"0.345"	"C1835813"	"Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.70"		"1996"	"2009"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"2677"	"GGCX"	"0.696"	"0.345"	"C1848534"	"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.71"	"1"	"1990"	"2009"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2678"	"GGT1"	"0.557"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2003"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0031051"	"Pericementitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0031099"	"Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C0268524"	"gamma-Glutamyltransferase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2678"	"GGT1"	"0.557"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2678"	"GGT1"	"0.557"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2683"	"B4GALT1"	"0.773"	"0.172"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"2683"	"B4GALT1"	"0.773"	"0.172"	"C2931009"	"Congenital disorder of glycosylation type 2D"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2683"	"B4GALT1"	"0.773"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"2688"	"GH1"	"0.438"	"0.793"	"C0001206"	"Acromegaly"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.40"	"0.939393939393939"	"1981"	"2018"	"7"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1991"	"2010"	"5"	"0"	"PSYGENET"
"2688"	"GH1"	"0.438"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.666666666666667"	"1997"	"1999"	"3"	"0"	"PSYGENET"
"2688"	"GH1"	"0.438"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.666666666666667"	"1997"	"1999"	"3"	"0"	"PSYGENET"
"2688"	"GH1"	"0.438"	"0.793"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.31"		"1997"	"2008"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.914285714285714"	"1982"	"2018"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2005"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2688"	"GH1"	"0.438"	"0.793"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.40"	"0.955555555555556"	"1987"	"2017"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.40"	"0.977777777777778"	"1986"	"2016"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0041408"	"Turner Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.40"	"0.883720930232558"	"1992"	"2017"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0242526"	"Gonadal Dysgenesis, 45,X"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0242528"	"Azotemia"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0271567"	"Isolated Growth Hormone Deficiency, Type II"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.75"	"1"	"1994"	"2009"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2688"	"GH1"	"0.438"	"0.793"	"C0342573"	"PITUITARY DWARFISM I"	"disease"	"C05;C10;C19"	"Congenital Abnormality"	"0.62"	"1"	"1993"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"2688"	"GH1"	"0.438"	"0.793"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0346302"	"Growth Hormone-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.40"	"0.916666666666667"	"1991"	"2015"	"2"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C1527168"	"Bonnevie-Ullrich Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2688"	"GH1"	"0.438"	"0.793"	"C1849779"	"Kowarski syndrome"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.71"	"0"	"1996"	"2007"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2688"	"GH1"	"0.438"	"0.793"	"C2748571"	"Isolated Growth Hormone Deficiency, Type IB"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.70"		"1993"	"2003"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2688"	"GH1"	"0.438"	"0.793"	"C3489630"	"Somatotrophinoma, Familial"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"1991"	"1992"	"2"	"0"	"CTD_human"
"2689"	"GH2"	"0.773"	"0.31"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0271568"	"Laron Syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"1.00"	"0.971830985915493"	"1987"	"2018"	"9"	"18"	"CTD_human;ORPHANET;UNIPROT"
"2690"	"GHR"	"0.537"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"0.75"	"2003"	"2014"	"1"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"2690"	"GHR"	"0.537"	"0.621"	"C1858656"	"Short Stature, Idiopathic, Autosomal"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.62"	"0.5"	"1995"	"2000"	"1"	"6"	"ORPHANET;UNIPROT"
"2690"	"GHR"	"0.537"	"0.621"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2691"	"GHRH"	"0.536"	"0.586"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2692"	"GHRHR"	"0.633"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2692"	"GHRHR"	"0.633"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2692"	"GHRHR"	"0.633"	"0.448"	"C2748571"	"Isolated Growth Hormone Deficiency, Type IB"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.74"	"1"	"1996"	"2015"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2693"	"GHSR"	"0.565"	"0.621"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"2693"	"GHSR"	"0.565"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2693"	"GHSR"	"0.565"	"0.621"	"C0012243"	"Digestive System Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2693"	"GHSR"	"0.565"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2693"	"GHSR"	"0.565"	"0.621"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2693"	"GHSR"	"0.565"	"0.621"	"C0751075"	"Cancer of Digestive System"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2693"	"GHSR"	"0.565"	"0.621"	"C1858656"	"Short Stature, Idiopathic, Autosomal"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.60"		"2006"	"2010"	"2"	"3"	"ORPHANET;UNIPROT"
"2694"	"GIF"	"0.565"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2694"	"GIF"	"0.565"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2694"	"GIF"	"0.565"	"0.69"	"C0340957"	"Congenital deficiency of intrinsic factor"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"2694"	"GIF"	"0.565"	"0.69"	"C1394891"	"Intrinsic Factor Deficiency"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.71"	"1"	"2005"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2695"	"GIP"	"0.636"	"0.414"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"CTD_human"
"2696"	"GIPR"	"0.685"	"0.414"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2696"	"GIPR"	"0.685"	"0.414"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0010051"	"Coronary Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0018522"	"Hallermann's Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2013"	"1"	"1"	"UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.45"	"0.8"	"2005"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2006"	"2"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2018"	"1"	"0"	"PSYGENET"
"2697"	"GJA1"	"0.431"	"0.793"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2000"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C0152101"	"Hypoplastic Left Heart Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"				"0"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2006"	"2"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0265292"	"Schwartz-Lelek syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"2697"	"GJA1"	"0.431"	"0.793"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"2697"	"GJA1"	"0.431"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2006"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C0812437"	"Oculo-dento-digital syndrome"	"disease"	"C05;C07;C11;C16"	"Congenital Abnormality"	"1.00"	"0.981481481481482"	"1979"	"2018"	"1"	"13"	"CTD_human;ORPHANET;UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2018"	"1"	"0"	"PSYGENET"
"2697"	"GJA1"	"0.431"	"0.793"	"C1389016"	"ATRIOVENTRICULAR CANAL DEFECT"	"phenotype"	"C14;C16"	"Anatomical Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C1389018"	"Atrioventricular Septal Defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1993"	"2018"	"1"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C1851480"	"Greither Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2003"	"2014"	"10"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C1861366"	"SYNDACTYLY, TYPE III"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"1990"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C1863093"	"Alopecia congenita keratosis palmoplantaris"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"2697"	"GJA1"	"0.431"	"0.793"	"C2749477"	"Oculodentodigital Dysplasia, Autosomal Recessive"	"disease"	"C05;C07;C11;C16"	"Disease or Syndrome"	"0.40"		"2004"	"2006"	"0"	"2"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C2931244"	"Craniometaphyseal dysplasia, autosomal recessive type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2001"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C2931577"	"Basaran Yilmaz syndrome"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2697"	"GJA1"	"0.431"	"0.793"	"C3151468"	"PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"1"	"UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C3275750"	"ATRIOVENTRICULAR SEPTAL DEFECT 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"2"	"UNIPROT"
"2697"	"GJA1"	"0.431"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2697"	"GJA1"	"0.431"	"0.793"	"C4479619"	"ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"2700"	"GJA3"	"0.707"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.39"	"1"	"2004"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"2700"	"GJA3"	"0.707"	"0.276"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2700"	"GJA3"	"0.707"	"0.276"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2700"	"GJA3"	"0.707"	"0.276"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2700"	"GJA3"	"0.707"	"0.276"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"2700"	"GJA3"	"0.707"	"0.276"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2700"	"GJA3"	"0.707"	"0.276"	"C1866078"	"Cataract, Zonular Pulverulent 3"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"1999"	"2017"	"20"	"9"	"CTD_human;UNIPROT"
"2700"	"GJA3"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2701"	"GJA4"	"0.701"	"0.276"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"2701"	"GJA4"	"0.701"	"0.276"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"2701"	"GJA4"	"0.701"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2702"	"GJA5"	"0.59"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2702"	"GJA5"	"0.59"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.11"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2702"	"GJA5"	"0.59"	"0.483"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.62"	"1"	"2003"	"2013"	"0"	"0"	"ORPHANET"
"2702"	"GJA5"	"0.59"	"0.483"	"C1838539"	"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.53"	"1"	"2003"	"2006"	"1"	"2"	"CTD_human;UNIPROT"
"2702"	"GJA5"	"0.59"	"0.483"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2702"	"GJA5"	"0.59"	"0.483"	"C2675897"	"Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb"	"disease"	"C05;C10;C16;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2702"	"GJA5"	"0.59"	"0.483"	"C3279693"	"ATRIAL FIBRILLATION, FAMILIAL, 11"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2013"	"1"	"6"	"CTD_human;UNIPROT"
"2703"	"GJA8"	"0.561"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2703"	"GJA8"	"0.561"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"0.944444444444444"	"1998"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2703"	"GJA8"	"0.561"	"0.621"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2703"	"GJA8"	"0.561"	"0.621"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2703"	"GJA8"	"0.561"	"0.621"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"1998"	"2008"	"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2006"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"2703"	"GJA8"	"0.561"	"0.621"	"C1861828"	"Cataract, Zonular Pulverulent 1"	"disease"	"C11"	"Disease or Syndrome"	"0.84"	"1"	"1963"	"2017"	"9"	"9"	"CTD_human;UNIPROT"
"2703"	"GJA8"	"0.561"	"0.621"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C1866984"	"Sclerocornea, Autosomal Dominant"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2703"	"GJA8"	"0.561"	"0.621"	"C2675897"	"Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb"	"disease"	"C05;C10;C16;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"2703"	"GJA8"	"0.561"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2705"	"GJB1"	"0.527"	"0.621"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.97029702970297"	"1994"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2705"	"GJB1"	"0.527"	"0.621"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"1996"	"2006"	"1"	"1"	"UNIPROT"
"2705"	"GJB1"	"0.527"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"0.875"	"1990"	"2016"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"2"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C0393808"	"Charcot-Marie-Tooth disease, X-linked, 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1979"	"2018"	"58"	"58"	"CTD_human;ORPHANET;UNIPROT"
"2705"	"GJB1"	"0.527"	"0.621"	"C0796205"	"SPINOCEREBELLAR ATAXIA, X-LINKED 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2705"	"GJB1"	"0.527"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"2705"	"GJB1"	"0.527"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2706"	"GJB2"	"0.484"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2004"	"2011"	"0"	"0"	"CGI"
"2706"	"GJB2"	"0.484"	"0.69"	"C0007642"	"Cellulitis"	"phenotype"	"C01;C17;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.45"		"2002"	"2009"	"1"	"1"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.70"	"0.973913043478261"	"1995"	"2018"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0020757"	"Ichthyoses"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.44"	"1"	"1991"	"2014"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0022568"	"Keratitis"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"1989"	"2016"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2706"	"GJB2"	"0.484"	"0.69"	"C0025221"	"Meleda Disease"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0031557"	"Phlegmon"	"phenotype"	"C01;C17;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.34"	"0.75"	"1997"	"2016"	"2"	"1"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0043345"	"Xeroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0162836"	"Hidradenitis Suppurativa"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0265336"	"Senter syndrome"	"disease"	"C09;C10;C11;C16;C17;C23"	"Disease or Syndrome"	"0.90"	"1"	"1991"	"2016"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C0265964"	"Mutilating keratoderma"	"disease"	"C05;C09;C10;C16;C17;C23"	"Congenital Abnormality"	"0.80"	"1"	"1997"	"2015"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C0266004"	"Knuckle pads, leuconychia and sensorineural deafness"	"disease"	"C09;C10;C16;C17;C23"	"Congenital Abnormality"	"0.72"	"1"	"1997"	"2015"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2706"	"GJB2"	"0.484"	"0.69"	"C0473579"	"Porokeratotic eccrine ostial and dermal duct nevus"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"2706"	"GJB2"	"0.484"	"0.69"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C1835672"	"Palmoplantar Keratoderma with Deafness"	"disease"	"C09;C10;C16;C17;C23"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2015"	"7"	"16"	"CTD_human;ORPHANET;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"2706"	"GJB2"	"0.484"	"0.69"	"C1844678"	"Progressive hearing loss stapes fixation"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"8"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.39"	"0.888888888888889"	"1997"	"2016"	"8"	"0"	"CLINGEN"
"2706"	"GJB2"	"0.484"	"0.69"	"C1865234"	"ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS"	"disease"	"C09;C10;C16;C17;C23"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"2015"	"1"	"10"	"CTD_human;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C2673759"	"DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"1964"	"2016"	"7"	"75"	"CTD_human;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C2673760"	"DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"1964"	"2013"	"7"	"16"	"CTD_human;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C2673761"	"DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"1998"	"2009"	"7"	"16"	"CTD_human;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C2675750"	"DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2016"	"7"	"46"	"CTD_human;UNIPROT"
"2706"	"GJB2"	"0.484"	"0.69"	"C3665333"	"Keratitis-Ichthyosis-Deafness Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2017"	"0"	"0"	"ORPHANET"
"2706"	"GJB2"	"0.484"	"0.69"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2706"	"GJB2"	"0.484"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2706"	"GJB2"	"0.484"	"0.69"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.44"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"2707"	"GJB3"	"0.63"	"0.31"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0079153"	"Hyperkeratosis, Epidermolytic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"0.882352941176471"	"1985"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2707"	"GJB3"	"0.63"	"0.31"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1998"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"2707"	"GJB3"	"0.63"	"0.31"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C1851479"	"Keratoderma palmoplantaris transgrediens"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"4"	"UNIPROT"
"2707"	"GJB3"	"0.63"	"0.31"	"C1851480"	"Greither Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.71"	"1"	"1997"	"2007"	"2"	"4"	"CTD_human;UNIPROT"
"2707"	"GJB3"	"0.63"	"0.31"	"C2673759"	"DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C2673760"	"DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C2673761"	"DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"1"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C2675236"	"Deafness, Autosomal Dominant 2B"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"		"1998"	"1998"	"1"	"2"	"CTD_human;UNIPROT"
"2707"	"GJB3"	"0.63"	"0.31"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2707"	"GJB3"	"0.63"	"0.31"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2707"	"GJB3"	"0.63"	"0.31"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2707"	"GJB3"	"0.63"	"0.31"	"C4509933"	"Peripheral neuropathy with sensorineural hearing impairment syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2709"	"GJB5"	"0.886"	"0.138"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2709"	"GJB5"	"0.886"	"0.138"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2710"	"GK"	"0.676"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2710"	"GK"	"0.676"	"0.483"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2710"	"GK"	"0.676"	"0.483"	"C0268418"	"Deficiency of glycerol kinase"	"disease"		"Disease or Syndrome"	"0.69"	"0.888888888888889"	"1988"	"2009"	"2"	"5"	"CTD_human;UNIPROT"
"2710"	"GK"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1996"	"1996"	"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0002985"	"Angiokeratoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"2717"	"GLA"	"0.588"	"0.621"	"C0002986"	"Fabry Disease"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"1.00"	"0.978339350180505"	"1967"	"2018"	"51"	"192"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"2717"	"GLA"	"0.588"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1991"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2717"	"GLA"	"0.588"	"0.621"	"C1970820"	"Fabry Disease, Cardiac Variant"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"		"1967"	"2018"	"48"	"113"	"CLINGEN;UNIPROT"
"2719"	"GPC3"	"0.502"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2719"	"GPC3"	"0.502"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2719"	"GPC3"	"0.502"	"0.724"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"2719"	"GPC3"	"0.502"	"0.724"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.80"	"0.846153846153846"	"1997"	"2018"	"0"	"0"	"CGI;CTD_human;ORPHANET"
"2719"	"GPC3"	"0.502"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2719"	"GPC3"	"0.502"	"0.724"	"C0796154"	"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1"	"disease"	"C05;C10;C14;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"1.00"	"0.970588235294118"	"1996"	"2017"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"2719"	"GPC3"	"0.502"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.975609756097561"	"1997"	"2018"	"1"	"0"	"CTD_human"
"2719"	"GPC3"	"0.502"	"0.724"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2719"	"GPC3"	"0.502"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C0010038"	"Corneal Opacity"	"phenotype"	"C11"	"Finding"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0026707"	"Mucopolysaccharidosis IV"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"		"1991"	"1995"	"2"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"1976"	"1983"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0085131"	"Gangliosidosis GM1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.971428571428571"	"1981"	"2017"	"17"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0086651"	"Mucopolysaccharidosis, MPS-IV-A"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"0"	"1988"	"1995"	"2"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0086652"	"Mucopolysaccharidosis type IVB"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.80"	"1"	"1984"	"2017"	"8"	"31"	"CTD_human;ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C0268271"	"Gangliosidosis, Generalized GM1, Type 1 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.75"	"0.8"	"1981"	"2015"	"17"	"36"	"CTD_human;ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C0268272"	"Gangliosidosis, Generalized GM1, Type 2"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1991"	"2015"	"11"	"26"	"CTD_human;ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C0268273"	"Gangliosidosis, Generalized GM1, Type 3"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1981"	"2015"	"11"	"24"	"CTD_human;ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2720"	"GLB1"	"0.457"	"0.828"	"C1968746"	"Gangliosidosis, Generalized GM1, Late-Infantile Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"2015"	"11"	"0"	"UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C1968748"	"Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2015"	"17"	"2"	"ORPHANET;UNIPROT"
"2720"	"GLB1"	"0.457"	"0.828"	"C2718068"	"beta-Galactosidase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.38"	"0.75"	"1982"	"2011"	"0"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C3179194"	"GALNS Deficiency"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"		"1991"	"1995"	"2"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"2720"	"GLB1"	"0.457"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2729"	"GCLC"	"0.548"	"0.655"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.43"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0010074"	"Coronary Vessel Anomalies"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1996"	"2007"	"5"	"0"	"GENOMICS_ENGLAND"
"2729"	"GCLC"	"0.548"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2002"	"2017"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2011"	"2"	"0"	"PSYGENET"
"2729"	"GCLC"	"0.548"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2007"	"5"	"0"	"GENOMICS_ENGLAND"
"2729"	"GCLC"	"0.548"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C1856603"	"Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1999"	"2003"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2729"	"GCLC"	"0.548"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2729"	"GCLC"	"0.548"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2730"	"GCLM"	"0.624"	"0.517"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2730"	"GCLM"	"0.624"	"0.517"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2730"	"GCLM"	"0.624"	"0.517"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2011"	"2"	"0"	"CTD_human"
"2730"	"GCLM"	"0.624"	"0.517"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2730"	"GCLM"	"0.624"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.04"	"0.666666666666667"	"2006"	"2009"	"3"	"0"	"PSYGENET"
"2730"	"GCLM"	"0.624"	"0.517"	"C0036939"	"Shared Paranoid Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2730"	"GCLM"	"0.624"	"0.517"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2731"	"GLDC"	"0.672"	"0.345"	"C0268560"	"Hyperglycinemia, Transient Neonatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1991"	"2018"	"5"	"12"	"UNIPROT"
"2731"	"GLDC"	"0.672"	"0.345"	"C0268561"	"Hyperglycinemia, Nonketotic, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"3"	"0"	"CTD_human"
"2731"	"GLDC"	"0.672"	"0.345"	"C0268562"	"Hyperglycinemia, Nonketotic, Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"3"	"0"	"CTD_human"
"2731"	"GLDC"	"0.672"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2731"	"GLDC"	"0.672"	"0.345"	"C0751747"	"Hyperglycinemia, Nonketotic, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"3"	"0"	"CTD_human"
"2731"	"GLDC"	"0.672"	"0.345"	"C0751748"	"Nonketotic Hyperglycinemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.962962962962963"	"1979"	"2018"	"8"	"95"	"CTD_human;ORPHANET;UNIPROT"
"2731"	"GLDC"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"		"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"2733"	"GLE1"	"0.681"	"0.448"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"2733"	"GLE1"	"0.681"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2733"	"GLE1"	"0.681"	"0.448"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1985"	"2006"	"4"	"0"	"GENOMICS_ENGLAND"
"2733"	"GLE1"	"0.681"	"0.448"	"C1854664"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"2008"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2733"	"GLE1"	"0.681"	"0.448"	"C2678471"	"Lethal Arthrogryposis With Anterior Horn Cell Disease"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2008"	"2018"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2733"	"GLE1"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2735"	"GLI1"	"0.472"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.956521739130435"	"2007"	"2017"	"0"	"0"	"UNIPROT"
"2735"	"GLI1"	"0.472"	"0.655"	"C0013903"	"Ellis-Van Creveld Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"2735"	"GLI1"	"0.472"	"0.655"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2735"	"GLI1"	"0.472"	"0.655"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2736"	"GLI2"	"0.504"	"0.759"	"C0004779"	"Basal Cell Nevus Syndrome"	"disease"	"C04;C05;C07;C16"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2000"	"2008"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2000"	"2003"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.70"	"0.875"	"2004"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2005"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.52"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"2736"	"GLI2"	"0.504"	"0.759"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"2736"	"GLI2"	"0.504"	"0.759"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"2736"	"GLI2"	"0.504"	"0.759"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C1835819"	"PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.60"		"2004"	"2012"	"3"	"8"	"CTD_human;UNIPROT"
"2736"	"GLI2"	"0.504"	"0.759"	"C1856892"	"Facial Dysmorphism with Multiple Malformations"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2736"	"GLI2"	"0.504"	"0.759"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2736"	"GLI2"	"0.504"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2736"	"GLI2"	"0.504"	"0.759"	"C4014479"	"CULLER-JONES SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2005"	"2013"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C0162835"	"Hypopigmentation disorder"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0220697"	"POLYDACTYLY, POSTAXIAL"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"1997"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0265220"	"Pallister-Hall syndrome"	"disease"	"C04;C05;C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1993"	"2017"	"2"	"31"	"CTD_human;ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C0265306"	"Greig cephalopolysyndactyly syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"0.923076923076923"	"1984"	"2017"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C0265633"	"Congenital absence of tibia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0342418"	"Hypothalamic hamartomas"	"disease"	"C04;C10"	"Congenital Abnormality"	"0.62"	"1"	"1997"	"2008"	"0"	"0"	"CTD_human;ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C0796147"	"Acrocallosal Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C1868111"	"Polydactyly, preaxial 4"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1984"	"2008"	"0"	"1"	"CTD_human;ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C1868120"	"POSTAXIAL POLYDACTYLY, TYPE B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1999"	"1999"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C2931760"	"Acrocallosal syndrome, Schinzel type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2737"	"GLI3"	"0.485"	"0.724"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2737"	"GLI3"	"0.485"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C3887487"	"Postaxial polydactyly type A"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"1999"	"2010"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2737"	"GLI3"	"0.485"	"0.724"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2737"	"GLI3"	"0.485"	"0.724"	"C4282400"	"Polydactyly, Postaxial, Type A1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"1"	"1"	"CTD_human;UNIPROT"
"2739"	"GLO1"	"0.592"	"0.621"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2739"	"GLO1"	"0.592"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2008"	"2"	"0"	"PSYGENET"
"2739"	"GLO1"	"0.592"	"0.621"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2006"	"2012"	"2"	"0"	"CTD_human;PSYGENET"
"2739"	"GLO1"	"0.592"	"0.621"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"2739"	"GLO1"	"0.592"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2739"	"GLO1"	"0.592"	"0.621"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2740"	"GLP1R"	"0.598"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2740"	"GLP1R"	"0.598"	"0.586"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2740"	"GLP1R"	"0.598"	"0.586"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2002"	"2012"	"1"	"0"	"CTD_human"
"2740"	"GLP1R"	"0.598"	"0.586"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2740"	"GLP1R"	"0.598"	"0.586"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2741"	"GLRA1"	"0.642"	"0.379"	"C1835614"	"Hereditary Hyperexplexia"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2017"	"12"	"25"	"CTD_human;ORPHANET;UNIPROT"
"2741"	"GLRA1"	"0.642"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"2741"	"GLRA1"	"0.642"	"0.379"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2742"	"GLRA2"	"0.886"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"2742"	"GLRA2"	"0.886"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"2743"	"GLRB"	"0.735"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2743"	"GLRB"	"0.735"	"0.207"	"C1835614"	"Hereditary Hyperexplexia"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2743"	"GLRB"	"0.735"	"0.207"	"C3553291"	"HYPEREKPLEXIA 2"	"disease"		"Disease or Syndrome"	"0.60"		"1970"	"2013"	"2"	"3"	"UNIPROT"
"2744"	"GLS"	"0.607"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2744"	"GLS"	"0.607"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2744"	"GLS"	"0.607"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2744"	"GLS"	"0.607"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2744"	"GLS"	"0.607"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2007"	"2015"	"1"	"0"	"PSYGENET"
"2744"	"GLS"	"0.607"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2744"	"GLS"	"0.607"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2744"	"GLS"	"0.607"	"0.621"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2746"	"GLUD1"	"0.636"	"0.552"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2746"	"GLUD1"	"0.636"	"0.552"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.59"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2746"	"GLUD1"	"0.636"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.59"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2746"	"GLUD1"	"0.636"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2746"	"GLUD1"	"0.636"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2746"	"GLUD1"	"0.636"	"0.552"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2746"	"GLUD1"	"0.636"	"0.552"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2746"	"GLUD1"	"0.636"	"0.552"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2746"	"GLUD1"	"0.636"	"0.552"	"C1847555"	"Hyperinsulinemic hypoglycemia, familial, 6"	"disease"	"C18"	"Disease or Syndrome"	"0.75"	"1"	"1998"	"2015"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"2746"	"GLUD1"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2747"	"GLUD2"	"0.857"	"0.103"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"1"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2010"	"2"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"1997"	"2011"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.5"	"2003"	"2015"	"4"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2752"	"GLUL"	"0.557"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2752"	"GLUL"	"0.557"	"0.586"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0752107"	"Brain Diseases, Metabolic, Inherited"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0752109"	"Brain Diseases, Metabolic, Inborn"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C0752110"	"Central Nervous System Inborn Metabolic Diseases"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C1864910"	"Glutamine deficiency, congenital"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2005"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2752"	"GLUL"	"0.557"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"2752"	"GLUL"	"0.557"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"2760"	"GM2A"	"0.681"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2760"	"GM2A"	"0.681"	"0.345"	"C0268275"	"Tay-Sachs Disease, AB Variant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"1975"	"2015"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2760"	"GM2A"	"0.681"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2760"	"GM2A"	"0.681"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2766"	"GMPR"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2766"	"GMPR"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2766"	"GMPR"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2767"	"GNA11"	"0.609"	"0.586"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2767"	"GNA11"	"0.609"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1989"	"2016"	"1"	"1"	"CGI;CTD_human"
"2767"	"GNA11"	"0.609"	"0.586"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.42"	"1"	"2014"	"2016"	"0"	"1"	"CGI"
"2767"	"GNA11"	"0.609"	"0.586"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.80"	"1"	"2010"	"2018"	"3"	"1"	"CGI;CTD_human;ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C0346373"	"Malignant melanoma of iris"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C0346388"	"Malignant melanoma of choroid"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C1840347"	"HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"1992"	"2013"	"1"	"2"	"ORPHANET;UNIPROT"
"2767"	"GNA11"	"0.609"	"0.586"	"C3715128"	"HYPOCALCEMIA, AUTOSOMAL DOMINANT 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C3809243"	"HYPOCALCEMIA, AUTOSOMAL DOMINANT 2"	"disease"		"Disease or Syndrome"	"0.40"		"1982"	"2015"	"2"	"5"	"UNIPROT"
"2767"	"GNA11"	"0.609"	"0.586"	"C3838883"	"Phakomatosis cesioflammea"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C3839296"	"Phakomatosis cesiomarmorata"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2767"	"GNA11"	"0.609"	"0.586"	"C4048195"	"Autosomal dominant hypocalcemia"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"2768"	"GNA12"	"0.594"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2017"	"1"	"2"	"CTD_human"
"2768"	"GNA12"	"0.594"	"0.69"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2768"	"GNA12"	"0.594"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2768"	"GNA12"	"0.594"	"0.69"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2770"	"GNAI1"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0001618"	"Tumors of Adrenal Cortex"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0004245"	"Atrioventricular Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0340485"	"Familial ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0346402"	"Malignant neoplasm of adrenal cortex"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2771"	"GNAI2"	"0.656"	"0.414"	"C1332218"	"Adult Type Ovarian Granulosa Cell Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2771"	"GNAI2"	"0.656"	"0.414"	"C1370419"	"Ovarian Granulosa Cell Tumor"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"		"1990"	"1990"	"0"	"2"	"CGI"
"2771"	"GNAI2"	"0.656"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2773"	"GNAI3"	"0.713"	"0.483"	"C1865295"	"Auriculo-condylar syndrome"	"disease"	"C09"	"Disease or Syndrome"	"0.74"	"0.75"	"2000"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2773"	"GNAI3"	"0.713"	"0.483"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2773"	"GNAI3"	"0.713"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2774"	"GNAL"	"0.659"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2005"	"1"	"0"	"PSYGENET"
"2774"	"GNAL"	"0.659"	"0.31"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.39"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"16"	"0"	"GENOMICS_ENGLAND"
"2774"	"GNAL"	"0.659"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2005"	"1"	"0"	"PSYGENET"
"2774"	"GNAL"	"0.659"	"0.31"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2774"	"GNAL"	"0.659"	"0.31"	"C3554447"	"DYSTONIA 25"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1994"	"2015"	"1"	"6"	"ORPHANET;UNIPROT"
"2774"	"GNAL"	"0.659"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2774"	"GNAL"	"0.659"	"0.31"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.5"	"1993"	"2012"	"2"	"0"	"PSYGENET"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2017"	"0"	"2"	"ORPHANET"
"2775"	"GNAO1"	"0.611"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2775"	"GNAO1"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"2775"	"GNAO1"	"0.611"	"0.586"	"C3809606"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2013"	"2017"	"5"	"9"	"CTD_human;UNIPROT"
"2775"	"GNAO1"	"0.611"	"0.586"	"C4479569"	"NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"5"	"6"	"UNIPROT"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1989"	"2016"	"1"	"1"	"CGI;CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0038505"	"Sturge-Weber Syndrome"	"disease"	"C04;C10;C14"	"Congenital Abnormality"	"0.76"	"1"	"2013"	"2018"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.80"	"0.975"	"2008"	"2018"	"3"	"2"	"CGI;CTD_human;ORPHANET"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0235752"	"Port-Wine Stain"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.62"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0340803"	"Capillary malformation (disorder)"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.41"	"1"	"2013"	"2016"	"0"	"1"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0346373"	"Malignant melanoma of iris"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0346388"	"Malignant melanoma of choroid"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2776"	"GNAQ"	"0.586"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2776"	"GNAQ"	"0.586"	"0.483"	"C2931029"	"Nevi flammei, familial multiple"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"2776"	"GNAQ"	"0.586"	"0.483"	"C3838883"	"Phakomatosis cesioflammea"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2778"	"GNAS"	"0.443"	"0.793"	"C0001206"	"Acromegaly"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.43"	"1"	"1991"	"2001"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"2778"	"GNAS"	"0.443"	"0.793"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2778"	"GNAS"	"0.443"	"0.793"	"C0014130"	"Endocrine System Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.37"	"0.857142857142857"	"1991"	"2015"	"2"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0016064"	"Fibrous Dysplasia, Monostotic"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"ORPHANET"
"2778"	"GNAS"	"0.443"	"0.793"	"C0016065"	"Polyostotic fibrous dysplasia"	"disease"	"C05"	"Congenital Abnormality"	"0.75"	"1"	"1991"	"2018"	"5"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C0019087"	"Hemorrhagic Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.46"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"1991"	"1991"	"1"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.47"	"0.857142857142857"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0029396"	"Heterotopic Ossification"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.44"	"1"	"2002"	"2011"	"0"	"0"	"CGI"
"2778"	"GNAS"	"0.443"	"0.793"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0033806"	"Pseudohypoparathyroidism"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.70"	"0.933333333333333"	"1990"	"2017"	"3"	"11"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0033835"	"Pseudopseudohypoparathyroidism"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"1.00"	"0.947368421052632"	"1992"	"2017"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C0034013"	"Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.46"	"0.8"	"1991"	"2018"	"2"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0035204"	"Respiration Disorders"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2778"	"GNAS"	"0.443"	"0.793"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0206724"	"Sex Cord-Stromal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"1986"	"2014"	"0"	"2"	"CGI"
"2778"	"GNAS"	"0.443"	"0.793"	"C0221263"	"Cafe-au-Lait Spots"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"1991"	"1992"	"2"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0221357"	"Brachydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.45"	"1"	"2004"	"2015"	"1"	"1"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0242292"	"McCune-Albright Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.80"	"0.951219512195122"	"1986"	"2018"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0334041"	"Osteoma cutis"	"disease"	"C05;C16;C17;C18;C23"	"Disease or Syndrome"	"0.80"	"0.944444444444444"	"1992"	"2017"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0346302"	"Growth Hormone-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.33"	"0.5"	"2001"	"2013"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2007"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2014"	"0"	"0"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C1841739"	"ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA, SOMATIC"	"phenotype"		"Finding"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C1857451"	"Acth-Independent Macronodular Adrenal Hyperplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.70"		"1986"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C1864100"	"PSEUDOHYPOPARATHYROIDISM, TYPE IB"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.70"	"0.952380952380952"	"1998"	"2017"	"5"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C1969761"	"SEX CORD STROMAL TUMOR, SOMATIC"	"phenotype"		"Finding"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C2675383"	"POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC"	"phenotype"		"Finding"	"0.40"		"1996"	"2004"	"2"	"3"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C2931404"	"Albright's hereditary osteodystrophy"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.40"	"0.925925925925926"	"1990"	"2018"	"4"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C2932715"	"Pseudohypoparathyroidism Type 1B"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.57"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"2778"	"GNAS"	"0.443"	"0.793"	"C2932716"	"Pseudohypoparathyroidism Type 1C"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"2002"	"2014"	"4"	"5"	"ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C3489630"	"Somatotrophinoma, Familial"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C3494506"	"Pseudohypoparathyroidism, Type Ia"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9375"	"1991"	"2018"	"16"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C3697137"	"Fibrous dysplasia of bone with intramuscular myxoma"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2778"	"GNAS"	"0.443"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2778"	"GNAS"	"0.443"	"0.793"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2778"	"GNAS"	"0.443"	"0.793"	"C4016139"	"MCCUNE-ALBRIGHT SYNDROME, SOMATIC, MOSAIC"	"phenotype"		"Finding"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C4016140"	"PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS"	"phenotype"		"Finding"	"0.40"		"1994"	"2004"	"2"	"3"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C4540534"	"PITUITARY ADENOMA 3, MULTIPLE TYPES, SOMATIC"	"disease"		"Neoplastic Process"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C4540535"	"PITUITARY ADENOMA 3, ACTH-SECRETING, SOMATIC"	"phenotype"		"Finding"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C4540536"	"PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC"	"disease"		"Neoplastic Process"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2778"	"GNAS"	"0.443"	"0.793"	"C4540602"	"PITUITARY ADENOMA 3, GROWTH HORMONE-SECRETING, SOMATIC"	"disease"		"Neoplastic Process"	"0.30"		"2002"	"2004"	"2"	"2"	"UNIPROT"
"2779"	"GNAT1"	"0.701"	"0.103"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.62"	"1"	"2007"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"2779"	"GNAT1"	"0.701"	"0.103"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C1864870"	"Night Blindness, Congenital Stationary, Autosomal Dominant 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1996"	"2007"	"2"	"2"	"CTD_human;UNIPROT"
"2779"	"GNAT1"	"0.701"	"0.103"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2779"	"GNAT1"	"0.701"	"0.103"	"C4225345"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"1"	"2"	"UNIPROT"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0009398"	"Color vision defect"	"phenotype"	"C10;C11;C23"	"Disease or Syndrome"	"0.41"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.57"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0155015"	"Color Blindness, Red"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0155016"	"Color Blindness, Red-Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0155017"	"Color Blindness, Blue"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0155018"	"Color Blindness, Acquired"	"phenotype"	"C10;C11;C23"	"Acquired Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0239777"	"Color Blindness, Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0242225"	"Color blindness"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0271092"	"Progressive cone dystrophy (without rod involvement)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0751042"	"Color Blindness, Inherited"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C0751043"	"Monochromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2780"	"GNAT2"	"0.667"	"0.207"	"C1841721"	"ACHROMATOPSIA 4"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2015"	"0"	"3"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2782"	"GNB1"	"0.645"	"0.483"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"2782"	"GNB1"	"0.645"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2782"	"GNB1"	"0.645"	"0.483"	"C4310774"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 42"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"4"	"10"	"CTD_human;UNIPROT"
"2784"	"GNB3"	"0.533"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.39"	"0.75"	"1999"	"2018"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.924528301886792"	"1998"	"2017"	"2"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.848484848484849"	"1999"	"2016"	"2"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.6"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.909090909090909"	"1999"	"2018"	"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.51"	"0"	"2016"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2003"	"2"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.6"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"2784"	"GNB3"	"0.533"	"0.724"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4310758"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"2784"	"GNB3"	"0.533"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2784"	"GNB3"	"0.533"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2787"	"GNG5"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2787"	"GNG5"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2788"	"GNG7"	"0.834"	"0.172"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2788"	"GNG7"	"0.834"	"0.172"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"2791"	"GNG11"	"0.857"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2791"	"GNG11"	"0.857"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2791"	"GNG11"	"0.857"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2791"	"GNG11"	"0.857"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2793"	"GNGT2"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0018681"	"Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0028838"	"Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0034013"	"Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2009"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.64"	"1"	"1977"	"2011"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.58"	"0.875"	"1989"	"2016"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0423618"	"Throbbing Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0423623"	"Bilateral Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0474366"	"Generalized Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0751186"	"Orthostatic Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0751187"	"Periorbital Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0751189"	"Retro-Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0751190"	"Sharp Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0751192"	"Vertex Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0877781"	"Hemicrania"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2796"	"GNRH1"	"0.541"	"0.552"	"C1856897"	"Eunuchoidism, familial hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.60"		"1977"	"2013"	"2"	"1"	"UNIPROT"
"2796"	"GNRH1"	"0.541"	"0.552"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.36"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.70"	"0.96875"	"1999"	"2016"	"1"	"1"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.90"	"0.962962962962963"	"1997"	"2018"	"12"	"22"	"CTD_human;UNIPROT"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2798"	"GNRHR"	"0.559"	"0.517"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.86"	"1"	"1997"	"2015"	"13"	"14"	"CTD_human;UNIPROT"
"2799"	"GNS"	"0.707"	"0.483"	"C0026706"	"Mucopolysaccharidosis III"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.52"		"1988"	"2017"	"1"	"0"	"CTD_human"
"2799"	"GNS"	"0.707"	"0.483"	"C0086647"	"Mucopolysaccharidosis Type IIIA"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.51"	"1"	"1988"	"2017"	"1"	"0"	"CTD_human"
"2799"	"GNS"	"0.707"	"0.483"	"C0086648"	"MPS III B"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1988"	"2017"	"1"	"0"	"CTD_human"
"2799"	"GNS"	"0.707"	"0.483"	"C0086649"	"MPS III C"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"2799"	"GNS"	"0.707"	"0.483"	"C0086650"	"MPS III D"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.76"	"1"	"1980"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"2799"	"GNS"	"0.707"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2803"	"GOLGA4"	"0.701"	"0.586"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2804"	"GOLGB1"	"0.773"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2805"	"GOT1"	"0.672"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2805"	"GOT1"	"0.672"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2810"	"SFN"	"0.621"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"2811"	"GP1BA"	"0.627"	"0.448"	"C0005129"	"Bernard-Soulier Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.90"	"1"	"1992"	"2016"	"5"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2811"	"GP1BA"	"0.627"	"0.448"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2811"	"GP1BA"	"0.627"	"0.448"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2811"	"GP1BA"	"0.627"	"0.448"	"C1280798"	"Von Willebrand disease, platelet type"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2014"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C1847711"	"NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2811"	"GP1BA"	"0.627"	"0.448"	"C1856447"	"Bernard-Soulier Syndrome, Type B"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1998"	"5"	"4"	"UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C1856448"	"Bernard-Soulier Syndrome, Type C"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1998"	"5"	"4"	"UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C2713537"	"Deficiency of Platelet Glycoprotein 1b"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"1992"	"1998"	"5"	"4"	"CTD_human;UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C3277076"	"BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"1992"	"2001"	"1"	"2"	"CTD_human;UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C3278148"	"BERNARD-SOULIER SYNDROME, TYPE A1"	"disease"		"Disease or Syndrome"	"0.40"		"1990"	"2001"	"5"	"6"	"UNIPROT"
"2811"	"GP1BA"	"0.627"	"0.448"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2811"	"GP1BA"	"0.627"	"0.448"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0005129"	"Bernard-Soulier Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.90"	"1"	"1997"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C1856447"	"Bernard-Soulier Syndrome, Type B"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1997"	"2008"	"1"	"5"	"UNIPROT"
"2812"	"GP1BB"	"0.598"	"0.621"	"C1856448"	"Bernard-Soulier Syndrome, Type C"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"2"	"UNIPROT"
"2812"	"GP1BB"	"0.598"	"0.621"	"C2713537"	"Deficiency of Platelet Glycoprotein 1b"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"1997"	"1997"	"1"	"2"	"CTD_human;UNIPROT"
"2812"	"GP1BB"	"0.598"	"0.621"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3278148"	"BERNARD-SOULIER SYNDROME, TYPE A1"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"2"	"UNIPROT"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2812"	"GP1BB"	"0.598"	"0.621"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2813"	"GP2"	"0.743"	"0.241"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2815"	"GP9"	"0.727"	"0.276"	"C0005129"	"Bernard-Soulier Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.972222222222222"	"1983"	"2017"	"6"	"6"	"CTD_human;ORPHANET;UNIPROT"
"2815"	"GP9"	"0.727"	"0.276"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.45"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"2815"	"GP9"	"0.727"	"0.276"	"C1856447"	"Bernard-Soulier Syndrome, Type B"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2002"	"6"	"6"	"UNIPROT"
"2815"	"GP9"	"0.727"	"0.276"	"C1856448"	"Bernard-Soulier Syndrome, Type C"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1957"	"2003"	"6"	"6"	"UNIPROT"
"2815"	"GP9"	"0.727"	"0.276"	"C2713537"	"Deficiency of Platelet Glycoprotein 1b"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"1993"	"2002"	"6"	"6"	"CTD_human;UNIPROT"
"2815"	"GP9"	"0.727"	"0.276"	"C3278148"	"BERNARD-SOULIER SYNDROME, TYPE A1"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2002"	"6"	"6"	"UNIPROT"
"2817"	"GPC1"	"0.667"	"0.586"	"C0005411"	"Biliary Atresia"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.32"	"1"	"2013"	"2017"	"0"	"0"	"ORPHANET"
"2817"	"GPC1"	"0.667"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"UNIPROT"
"2819"	"GPD1"	"0.72"	"0.414"	"C3280953"	"HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2012"	"2018"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"2820"	"GPD2"	"0.707"	"0.414"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.45"	"1"	"1996"	"2005"	"1"	"1"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2820"	"GPD2"	"0.707"	"0.414"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.37"	"1"	"1981"	"2006"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1986"	"1998"	"4"	"0"	"GENOMICS_ENGLAND"
"2821"	"GPI"	"0.527"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1986"	"1998"	"4"	"0"	"GENOMICS_ENGLAND"
"2821"	"GPI"	"0.527"	"0.69"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"2821"	"GPI"	"0.527"	"0.69"	"C3150730"	"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"1998"	"6"	"18"	"CTD_human;ORPHANET;UNIPROT"
"2823"	"GPM6A"	"0.743"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2008"	"2017"	"1"	"2"	"PSYGENET"
"2826"	"CCR10"	"0.659"	"0.379"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2826"	"CCR10"	"0.659"	"0.379"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2831"	"NPBWR1"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2832"	"NPBWR2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2003"	"2004"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2003"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2833"	"CXCR3"	"0.481"	"0.793"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2837"	"UTS2R"	"0.636"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2840"	"GPR17"	"0.752"	"0.138"	"C0393953"	"Anterior Cerebral Circulation Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2840"	"GPR17"	"0.752"	"0.138"	"C0751952"	"Anterior Circulation Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2840"	"GPR17"	"0.752"	"0.138"	"C0751953"	"Brain Infarction, Posterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2840"	"GPR17"	"0.752"	"0.138"	"C0751954"	"Venous Infarction, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2840"	"GPR17"	"0.752"	"0.138"	"C0751955"	"Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2846"	"LPAR4"	"0.928"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"2847"	"MCHR1"	"0.69"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"2847"	"MCHR1"	"0.69"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"2847"	"MCHR1"	"0.69"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"2847"	"MCHR1"	"0.69"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2012"	"3"	"0"	"PSYGENET"
"2847"	"MCHR1"	"0.69"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2010"	"2"	"0"	"PSYGENET"
"2850"	"GPR27"	"1"	"0.069"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2852"	"GPER1"	"0.611"	"0.552"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2852"	"GPER1"	"0.611"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.96875"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2852"	"GPER1"	"0.611"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.970588235294118"	"2001"	"2018"	"1"	"0"	"CTD_human"
"2852"	"GPER1"	"0.611"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2852"	"GPER1"	"0.611"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2857"	"GPR34"	"0.785"	"0.31"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2857"	"GPR34"	"0.785"	"0.31"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2859"	"GPR35"	"0.667"	"0.31"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"2861"	"GPR37"	"0.799"	"0.241"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2869"	"GRK5"	"0.642"	"0.621"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"2869"	"GRK5"	"0.642"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2869"	"GRK5"	"0.642"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2869"	"GRK5"	"0.642"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2870"	"GRK6"	"0.762"	"0.379"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"2870"	"GRK6"	"0.762"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2006"	"2014"	"2"	"0"	"PSYGENET"
"2870"	"GRK6"	"0.762"	"0.379"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2870"	"GRK6"	"0.762"	"0.379"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2873"	"GPS1"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2875"	"GPT"	"0.51"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.875"	"2001"	"2015"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"1978"	"2009"	"2"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"0.942857142857143"	"1993"	"2016"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"1978"	"2014"	"2"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1978"	"2009"	"2"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.892857142857143"	"2001"	"2016"	"1"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1978"	"2009"	"2"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1978"	"2009"	"2"	"0"	"CTD_human"
"2875"	"GPT"	"0.51"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1978"	"2009"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"0.857142857142857"	"2004"	"2014"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"0.888888888888889"	"2004"	"2014"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2876"	"GPX1"	"0.498"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2876"	"GPX1"	"0.498"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2876"	"GPX1"	"0.498"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2011"	"2014"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"0.5"	"1995"	"2008"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.04"	"0.75"	"2005"	"2018"	"3"	"0"	"PSYGENET"
"2876"	"GPX1"	"0.498"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2876"	"GPX1"	"0.498"	"0.759"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"0.875"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"		"2003"	"2008"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C3501647"	"Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2876"	"GPX1"	"0.498"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2877"	"GPX2"	"0.656"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"0.5"	"2013"	"2016"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2877"	"GPX2"	"0.656"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0015624"	"Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"1992"	"2010"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2009"	"2"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0341703"	"Adult Fanconi syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C1857395"	"De Toni-Debre-Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2878"	"GPX3"	"0.575"	"0.586"	"C3495427"	"Fanconi-Bickel Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0006635"	"Cadmium poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2009"	"2"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2007"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1855229"	"Spondylometaphyseal dysplasia, Sedaghatian type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2012"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"2879"	"GPX4"	"0.579"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2879"	"GPX4"	"0.579"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2880"	"GPX5"	"1"	"0.034"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2885"	"GRB2"	"0.602"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"2886"	"GRB7"	"0.63"	"0.414"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1994"	"2018"	"2"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1994"	"2016"	"2"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2886"	"GRB7"	"0.63"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2009"	"2"	"0"	"CTD_human"
"2887"	"GRB10"	"0.701"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"2888"	"GRB14"	"0.834"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2888"	"GRB14"	"0.834"	"0.138"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2888"	"GRB14"	"0.834"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2889"	"RAPGEF1"	"0.752"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2007"	"2012"	"4"	"0"	"PSYGENET"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"5"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6"	"2013"	"2015"	"5"	"0"	"PSYGENET"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6"	"2013"	"2015"	"5"	"0"	"PSYGENET"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"1995"	"2016"	"2"	"1"	"PSYGENET"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2003"	"2"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2001"	"2003"	"2"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2001"	"2003"	"2"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"5"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2008"	"5"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2890"	"GRIA1"	"0.636"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.666666666666667"	"2007"	"2012"	"3"	"0"	"PSYGENET"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"1995"	"2012"	"2"	"0"	"PSYGENET"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2891"	"GRIA2"	"0.639"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"2891"	"GRIA2"	"0.639"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2010"	"5"	"0"	"PSYGENET"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"3"	"0"	"PSYGENET"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2013"	"2"	"0"	"PSYGENET"
"2892"	"GRIA3"	"0.648"	"0.414"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2892"	"GRIA3"	"0.648"	"0.414"	"C2678051"	"MENTAL RETARDATION, X-LINKED 94 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2008"	"2018"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2892"	"GRIA3"	"0.648"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2014"	"9"	"0"	"CLINGEN"
"2892"	"GRIA3"	"0.648"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.48"	"1"	"2005"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.25"	"2003"	"2012"	"4"	"0"	"PSYGENET"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"2893"	"GRIA4"	"0.713"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2893"	"GRIA4"	"0.713"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"2893"	"GRIA4"	"0.713"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2894"	"GRID1"	"0.762"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2894"	"GRID1"	"0.762"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2894"	"GRID1"	"0.762"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2894"	"GRID1"	"0.762"	"0.276"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2013"	"3"	"0"	"PSYGENET"
"2894"	"GRID1"	"0.762"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2013"	"3"	"0"	"PSYGENET"
"2894"	"GRID1"	"0.762"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"2894"	"GRID1"	"0.762"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2895"	"GRID2"	"0.672"	"0.345"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2895"	"GRID2"	"0.672"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2895"	"GRID2"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"2895"	"GRID2"	"0.672"	"0.345"	"C4015505"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18"	"disease"		"Disease or Syndrome"	"0.80"		"2014"	"2017"	"4"	"2"	"ORPHANET;UNIPROT"
"2896"	"GRN"	"0.476"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2896"	"GRN"	"0.476"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"2896"	"GRN"	"0.476"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2012"	"3"	"0"	"PSYGENET"
"2896"	"GRN"	"0.476"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2010"	"2012"	"3"	"0"	"PSYGENET"
"2896"	"GRN"	"0.476"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8"	"1993"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"2896"	"GRN"	"0.476"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2012"	"2"	"0"	"PSYGENET"
"2896"	"GRN"	"0.476"	"0.724"	"C0282513"	"Primary Progressive Aphasia (disorder)"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.90"	"1"	"2006"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"2896"	"GRN"	"0.476"	"0.724"	"C0338451"	"Frontotemporal dementia"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.70"	"0.957142857142857"	"2006"	"2018"	"2"	"6"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2010"	"2015"	"2"	"0"	"CTD_human;ORPHANET"
"2896"	"GRN"	"0.476"	"0.724"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.96551724137931"	"2006"	"2016"	"2"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.977443609022556"	"2006"	"2018"	"1"	"0"	"CTD_human"
"2896"	"GRN"	"0.476"	"0.724"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.875"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"2896"	"GRN"	"0.476"	"0.724"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2896"	"GRN"	"0.476"	"0.724"	"C1843792"	"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED"	"disease"		"Disease or Syndrome"	"0.88"	"1"	"1993"	"2015"	"2"	"10"	"CTD_human;UNIPROT"
"2896"	"GRN"	"0.476"	"0.724"	"C3539123"	"CEROID LIPOFUSCINOSIS, NEURONAL, 11"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"2896"	"GRN"	"0.476"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2896"	"GRN"	"0.476"	"0.724"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.36"	"0.833333333333333"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.5"	"1995"	"2013"	"2"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2001"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0573196"	"Overdose of cocaine"	"disease"		"Injury or Poisoning"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2015"	"2"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"2897"	"GRIK1"	"0.642"	"0.345"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2897"	"GRIK1"	"0.642"	"0.345"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2002"	"2010"	"2"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2007"	"2016"	"3"	"0"	"CTD_human;PSYGENET"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2898"	"GRIK2"	"0.621"	"0.586"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C1970198"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"2898"	"GRIK2"	"0.621"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"2898"	"GRIK2"	"0.621"	"0.586"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2006"	"2013"	"2"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.6"	"2002"	"2010"	"5"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2899"	"GRIK3"	"0.727"	"0.379"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"2899"	"GRIK3"	"0.727"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2006"	"2013"	"4"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"2900"	"GRIK4"	"0.701"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"PSYGENET"
"2901"	"GRIK5"	"0.834"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"2901"	"GRIK5"	"0.834"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2003"	"2012"	"2"	"0"	"PSYGENET"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2902"	"GRIN1"	"0.63"	"0.448"	"C3280282"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 8"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2018"	"5"	"8"	"CTD_human;UNIPROT"
"2902"	"GRIN1"	"0.63"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2016"	"4"	"0"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2003"	"2012"	"5"	"0"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0009090"	"Cluttering"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2013"	"4"	"0"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2013"	"4"	"0"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.941176470588235"	"1998"	"2018"	"2"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.6"	"2003"	"2018"	"5"	"2"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0037822"	"Speech Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0233726"	"Aprosodia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0282512"	"Landau-Kleffner Syndrome"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2012"	"2017"	"11"	"18"	"CTD_human;ORPHANET;UNIPROT"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0376532"	"Epilepsy, Rolandic"	"disease"	"C10"	"Disease or Syndrome"	"0.63"	"1"	"2012"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0751512"	"Dysglossia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0751513"	"Rhinolalia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C0751514"	"Verbal Fluency Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C1832814"	"Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"11"	"30"	"CTD_human;UNIPROT"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C2363129"	"Benign Rolandic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.71"	"0"	"2012"	"2018"	"11"	"19"	"CTD_human;ORPHANET;UNIPROT"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C3495145"	"Dyslalia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C3806402"	"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2017"	"11"	"18"	"CTD_human;UNIPROT"
"2903"	"GRIN2A"	"0.577"	"0.414"	"C3806403"	"Continuous spike and waves during slow sleep"	"disease"		"Disease or Syndrome"	"0.52"	"1"	"2012"	"2017"	"11"	"18"	"CTD_human;UNIPROT"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2005"	"2016"	"5"	"0"	"PSYGENET"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2010"	"2015"	"5"	"0"	"PSYGENET"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2010"	"2015"	"5"	"0"	"PSYGENET"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.61"	"1"	"2004"	"2009"	"1"	"1"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.916666666666667"	"2000"	"2016"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C3151411"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 6"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2006"	"2017"	"7"	"17"	"CTD_human;UNIPROT"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.65"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"2904"	"GRIN2B"	"0.561"	"0.483"	"C4015316"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2018"	"3"	"9"	"CTD_human;UNIPROT"
"2905"	"GRIN2C"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2004"	"2015"	"4"	"0"	"PSYGENET"
"2906"	"GRIN2D"	"0.735"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2906"	"GRIN2D"	"0.735"	"0.31"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2906"	"GRIN2D"	"0.735"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"2906"	"GRIN2D"	"0.735"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2906"	"GRIN2D"	"0.735"	"0.31"	"C4310687"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2000"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1999"	"2018"	"5"	"0"	"PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1999"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.7"	"1993"	"2016"	"2"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0028840"	"Ocular Hypertension"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"0.5"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2000"	"2015"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.909090909090909"	"2000"	"2015"	"2"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2005"	"2017"	"6"	"0"	"CTD_human;PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0238394"	"Female Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2003"	"2016"	"5"	"0"	"PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0600260"	"Lung Diseases, Obstructive"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2006"	"2017"	"5"	"0"	"PSYGENET"
"2908"	"NR3C1"	"0.427"	"0.793"	"C1841972"	"Glucocorticoid Receptor Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.928571428571429"	"1976"	"2017"	"14"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2908"	"NR3C1"	"0.427"	"0.793"	"C1841973"	"Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"0"	"1"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C1841982"	"BODY COMPOSITION, BENEFICIAL"	"phenotype"	"C16;C18"	"Finding"	"0.30"				"0"	"0"	"CTD_human"
"2908"	"NR3C1"	"0.427"	"0.793"	"C2936403"	"46, XX Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2909"	"ARHGAP35"	"0.762"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"2911"	"GRM1"	"0.555"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2014"	"5"	"0"	"PSYGENET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2014"	"5"	"0"	"PSYGENET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.52"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0016045"	"fibroma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0016048"	"Fibromatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2015"	"2"	"0"	"PSYGENET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2017"	"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0205766"	"Myxofibroma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0206639"	"Neoplasms, Bone Tissue"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0221290"	"Chondromyxoid fibroma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"2911"	"GRM1"	"0.555"	"0.586"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2911"	"GRM1"	"0.555"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2911"	"GRM1"	"0.555"	"0.586"	"C3553816"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13"	"disease"		"Disease or Syndrome"	"0.50"		"2006"	"2011"	"0"	"0"	"ORPHANET"
"2911"	"GRM1"	"0.555"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"0.5"	"2016"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"2911"	"GRM1"	"0.555"	"0.586"	"C4521563"	"SPINOCEREBELLAR ATAXIA 44"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"2912"	"GRM2"	"0.645"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2912"	"GRM2"	"0.645"	"0.414"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2912"	"GRM2"	"0.645"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"2912"	"GRM2"	"0.645"	"0.414"	"C0858355"	"Addicted to cocaine"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2913"	"GRM3"	"0.627"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2913"	"GRM3"	"0.627"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"2913"	"GRM3"	"0.627"	"0.414"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.945945945945946"	"2002"	"2018"	"1"	"1"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2913"	"GRM3"	"0.627"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"2913"	"GRM3"	"0.627"	"0.414"	"C0858355"	"Addicted to cocaine"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"2914"	"GRM4"	"0.72"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2007"	"2"	"0"	"PSYGENET"
"2914"	"GRM4"	"0.72"	"0.172"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2914"	"GRM4"	"0.72"	"0.172"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2914"	"GRM4"	"0.72"	"0.172"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2914"	"GRM4"	"0.72"	"0.172"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2013"	"2017"	"1"	"1"	"CTD_human"
"2914"	"GRM4"	"0.72"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.333333333333333"	"2002"	"2014"	"3"	"0"	"PSYGENET"
"2914"	"GRM4"	"0.72"	"0.172"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2914"	"GRM4"	"0.72"	"0.172"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2915"	"GRM5"	"0.559"	"0.483"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2016"	"3"	"0"	"PSYGENET"
"2915"	"GRM5"	"0.559"	"0.483"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"2915"	"GRM5"	"0.559"	"0.483"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2010"	"2016"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"2915"	"GRM5"	"0.559"	"0.483"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2915"	"GRM5"	"0.559"	"0.483"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2916"	"GRM6"	"0.696"	"0.276"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.69"	"1"	"2005"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"2916"	"GRM6"	"0.696"	"0.276"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.81"	"1"	"2002"	"2017"	"2"	"9"	"CTD_human;UNIPROT"
"2916"	"GRM6"	"0.696"	"0.276"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2916"	"GRM6"	"0.696"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2916"	"GRM6"	"0.696"	"0.276"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.666666666666667"	"2007"	"2015"	"3"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2017"	"4"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"2917"	"GRM7"	"0.659"	"0.414"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2917"	"GRM7"	"0.659"	"0.414"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0001957"	"Alcohol Withdrawal Delirium"	"disease"	"C10;C25;F03"	"Disease or Syndrome"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"2918"	"GRM8"	"0.672"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"PSYGENET"
"2918"	"GRM8"	"0.672"	"0.345"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2003"	"2008"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.333333333333333"	"2001"	"2016"	"3"	"0"	"PSYGENET"
"2918"	"GRM8"	"0.672"	"0.345"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2918"	"GRM8"	"0.672"	"0.345"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2919"	"CXCL1"	"0.503"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2920"	"CXCL2"	"0.555"	"0.69"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2921"	"CXCL3"	"0.735"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2922"	"GRP"	"0.527"	"0.586"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2923"	"PDIA3"	"0.633"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2925"	"GRPR"	"0.609"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2925"	"GRPR"	"0.609"	"0.517"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"0.6666667"	"2003"	"2010"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2925"	"GRPR"	"0.609"	"0.517"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2931"	"GSK3A"	"0.667"	"0.345"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9189189"	"2000"	"2016"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"2004"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2008"	"2017"	"3"	"0"	"PSYGENET"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2008"	"2017"	"5"	"0"	"CTD_human;PSYGENET"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0031154"	"Peritonitis"	"disease"	"C01;C06"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2017"	"2"	"0"	"PSYGENET"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0949664"	"Tauopathies"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2017"	"5"	"0"	"PSYGENET"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1449646"	"Primary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1449647"	"Secondary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2932"	"GSK3B"	"0.488"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1997"	"2016"	"0"	"0"	"UNIPROT"
"2934"	"GSN"	"0.498"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"PSYGENET"
"2934"	"GSN"	"0.498"	"0.828"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C0936273"	"Familial Amyloid Polyneuropathy, Type IV"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"1993"	"0"	"0"	"ORPHANET"
"2934"	"GSN"	"0.498"	"0.828"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C1622345"	"Meretoja syndrome"	"disease"	"C11;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1973"	"2002"	"2"	"1"	"CTD_human;UNIPROT"
"2934"	"GSN"	"0.498"	"0.828"	"C1628319"	"Lattice corneal dystrophy Type II"	"disease"	"C11;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1990"	"2011"	"2"	"1"	"CTD_human;UNIPROT"
"2934"	"GSN"	"0.498"	"0.828"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1973"	"1991"	"3"	"0"	"GENOMICS_ENGLAND"
"2934"	"GSN"	"0.498"	"0.828"	"C2751493"	"Cerebral Amyloid Angiopathy, Gsn-Related"	"disease"	"C11;C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"1993"	"2"	"1"	"CTD_human;UNIPROT"
"2934"	"GSN"	"0.498"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"GENOMICS_ENGLAND"
"2934"	"GSN"	"0.498"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2934"	"GSN"	"0.498"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1968"	"1968"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2936"	"GSR"	"0.548"	"0.759"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2010"	"2014"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0033626"	"Protein Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"2936"	"GSR"	"0.548"	"0.759"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C1456865"	"Ureteral Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2011"	"2012"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2936"	"GSR"	"0.548"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1996"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"2937"	"GSS"	"0.648"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2937"	"GSS"	"0.648"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"2937"	"GSS"	"0.648"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C0398746"	"Gluthathione synthetase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1996"	"2016"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"2937"	"GSS"	"0.648"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2937"	"GSS"	"0.648"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2937"	"GSS"	"0.648"	"0.586"	"C1856399"	"Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"1970"	"2001"	"0"	"1"	"CTD_human;ORPHANET"
"2937"	"GSS"	"0.648"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1996"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"0.5"	"2005"	"2010"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"2938"	"GSTA1"	"0.579"	"0.621"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2939"	"GSTA2"	"0.857"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2940"	"GSTA3"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2941"	"GSTA4"	"0.752"	"0.31"	"C0003850"	"Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2010"	"2"	"0"	"CTD_human"
"2941"	"GSTA4"	"0.752"	"0.31"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"2941"	"GSTA4"	"0.752"	"0.31"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2941"	"GSTA4"	"0.752"	"0.31"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2004"	"2010"	"2"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.8888889"	"2001"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2017"	"2"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9418605"	"1993"	"2017"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9166667"	"1997"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8974359"	"1993"	"2015"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8947368"	"1995"	"2017"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.75"	"1993"	"2012"	"4"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.75"	"1993"	"2012"	"4"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.6"	"1999"	"2014"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2012"	"3"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8"	"1999"	"2017"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"		"2001"	"2012"	"3"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0034734"	"Raynaud Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0034735"	"Raynaud Phenomenon"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.75"	"2001"	"2016"	"4"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.01"	"0"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9067797"	"1993"	"2018"	"3"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2018"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"0.75"	"1995"	"2012"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.71875"	"1999"	"2016"	"3"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2005"	"2013"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2010"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8947368"	"1995"	"2017"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8823529"	"1995"	"2015"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2944"	"GSTM1"	"0.403"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2016"	"1"	"0"	"PSYGENET"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2946"	"GSTM2"	"0.517"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2947"	"GSTM3"	"0.592"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2948"	"GSTM4"	"0.727"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2949"	"GSTM5"	"0.834"	"0.172"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2949"	"GSTM5"	"0.834"	"0.172"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2949"	"GSTM5"	"0.834"	"0.172"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2949"	"GSTM5"	"0.834"	"0.172"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2949"	"GSTM5"	"0.834"	"0.172"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9268293"	"2000"	"2016"	"3"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.59"	"0.8888889"	"1995"	"2014"	"3"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.7222222"	"1995"	"2017"	"3"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8947368"	"1994"	"2018"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.7777778"	"2000"	"2014"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2011"	"4"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2011"	"4"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2011"	"4"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.60"	"0"	"2002"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9375"	"1995"	"2017"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"2007"	"2016"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"0.6666667"	"2003"	"2014"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0032230"	"Pleural Rub"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1989"	"2017"	"5"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2013"	"5"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0034642"	"Rales"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0035234"	"Respiratory Sounds"	"phenotype"	"C23"	"Clinical Attribute"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0035508"	"Rhonchi"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.5"	"2003"	"2018"	"2"	"0"	"PSYGENET"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0036939"	"Shared Paranoid Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0038450"	"Stridor"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0043144"	"Wheezing"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.8"	"2006"	"2014"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2011"	"4"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.7878788"	"1999"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0270736"	"Essential Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2008"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"2012"	"5"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8181818"	"1998"	"2017"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9753086"	"1994"	"2016"	"5"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0393615"	"Familial Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8965517"	"1994"	"2018"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1456865"	"Ureteral Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"		"2003"	"2015"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9333333"	"1988"	"2017"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"2950"	"GSTP1"	"0.406"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2013"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"PSYGENET"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2011"	"2016"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9230769"	"1997"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2013"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2001"	"2016"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.39"		"2002"	"2008"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.35"	"0.6"	"2007"	"2008"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"		"2001"	"2012"	"4"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0034734"	"Raynaud Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0034735"	"Raynaud Phenomenon"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2008"	"2016"	"5"	"0"	"PSYGENET"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.92"	"1997"	"2017"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2005"	"2015"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9333333"	"1999"	"2016"	"4"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0403823"	"Asthenozoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2952"	"GSTT1"	"0.419"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"3"	"0"	"CTD_human"
"2953"	"GSTT2"	"0.815"	"0.241"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2953"	"GSTT2"	"0.815"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"2953"	"GSTT2"	"0.815"	"0.241"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"2954"	"GSTZ1"	"0.773"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"2954"	"GSTZ1"	"0.773"	"0.207"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"2954"	"GSTZ1"	"0.773"	"0.207"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"2954"	"GSTZ1"	"0.773"	"0.207"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2954"	"GSTZ1"	"0.773"	"0.207"	"C1291607"	"Deficiency of maleylacetoacetate isomerase"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"4"	"UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9090909"	"2001"	"2011"	"0"	"1"	"UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.40"	"0.9565217"	"1999"	"2013"	"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.44"		"1991"	"2018"	"5"	"107"	"CTD_human"
"2956"	"MSH6"	"0.495"	"0.586"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.32"		"1999"	"2008"	"1"	"0"	"CTD_human"
"2956"	"MSH6"	"0.495"	"0.586"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"1"	"UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"2956"	"MSH6"	"0.495"	"0.586"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C0265325"	"Turcot syndrome (disorder)"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.70"	"0.9230769"	"2000"	"2015"	"0"	"3"	"CTD_human;ORPHANET"
"2956"	"MSH6"	"0.495"	"0.586"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2002"	"2018"	"4"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.80"	"0.9574468"	"1999"	"2017"	"3"	"6"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.60"	"1"	"1998"	"2013"	"12"	"32"	"CGI;UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2956"	"MSH6"	"0.495"	"0.586"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"2956"	"MSH6"	"0.495"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.55"	"1"	"2006"	"2015"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"2956"	"MSH6"	"0.495"	"0.586"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"2956"	"MSH6"	"0.495"	"0.586"	"C1321489"	"Torre-Muir syndrome"	"disease"	"C04;C16;C17"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"0"	"0"	"ORPHANET"
"2956"	"MSH6"	"0.495"	"0.586"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"	"0.9398496"	"1988"	"2018"	"5"	"229"	"CTD_human;ORPHANET"
"2956"	"MSH6"	"0.495"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9620253"	"1988"	"2018"	"12"	"32"	"GENOMICS_ENGLAND;UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"2956"	"MSH6"	"0.495"	"0.586"	"C1833477"	"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"		"1994"	"2017"	"16"	"61"	"CLINGEN;CTD_human;UNIPROT"
"2956"	"MSH6"	"0.495"	"0.586"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"2957"	"GTF2A1"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2959"	"GTF2B"	"0.834"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2961"	"GTF2E2"	"0.785"	"0.345"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2018"	"0"	"0"	"ORPHANET"
"2961"	"GTF2E2"	"0.785"	"0.345"	"C4310785"	"TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"2969"	"GTF2I"	"0.565"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.80"	"0.9666667"	"1998"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"2969"	"GTF2I"	"0.565"	"0.655"	"C1266101"	"Thymic epithelial tumor"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.40"		"2014"	"2017"	"1"	"1"	"CTD_human"
"2969"	"GTF2I"	"0.565"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2971"	"GTF3A"	"0.762"	"0.345"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2971"	"GTF3A"	"0.762"	"0.345"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2972"	"BRF1"	"0.696"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2972"	"BRF1"	"0.696"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"1"	"1"	"UNIPROT"
"2972"	"BRF1"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"2972"	"BRF1"	"0.696"	"0.379"	"C4015495"	"CEREBELLOFACIODENTAL SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"2973"	"GTS"	"0.773"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"1995"	"1"	"0"	"PSYGENET"
"2973"	"GTS"	"0.773"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"1995"	"1"	"0"	"PSYGENET"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"2977"	"GUCY1A2"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2008"	"2011"	"2"	"0"	"CTD_human;UNIPROT"
"2978"	"GUCA1A"	"0.69"	"0.207"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.47"	"1"	"1998"	"2017"	"0"	"1"	"ORPHANET"
"2978"	"GUCA1A"	"0.69"	"0.207"	"C0271092"	"Progressive cone dystrophy (without rod involvement)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2978"	"GUCA1A"	"0.69"	"0.207"	"C1536451"	"Central areolar choroidal sclerosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"2978"	"GUCA1A"	"0.69"	"0.207"	"C1865869"	"CONE DYSTROPHY 3 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.62"	"1"	"1998"	"2015"	"8"	"5"	"CTD_human;UNIPROT"
"2979"	"GUCA1B"	"0.696"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.63"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"2979"	"GUCA1B"	"0.696"	"0.31"	"C3151190"	"RETINITIS PIGMENTOSA 48"	"disease"		"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"2981"	"GUCA2B"	"0.773"	"0.172"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"2981"	"GUCA2B"	"0.773"	"0.172"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0340100"	"High altitude pulmonary edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C0340552"	"High altitude pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"4"	"CTD_human"
"2982"	"GUCY1A1"	"0.713"	"0.31"	"C3810403"	"MOYAMOYA DISEASE 6 WITH ACHALASIA"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"3"	"CTD_human;ORPHANET"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9473684"	"1998"	"2014"	"1"	"0"	"CTD_human"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.42"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9473684"	"1998"	"2014"	"1"	"0"	"CTD_human"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C2939175"	"Meconium ileus"	"disease"	"C06"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C3553270"	"DIARRHEA 6"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"ORPHANET;UNIPROT"
"2984"	"GUCY2C"	"0.642"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2986"	"GUCY2F"	"0.815"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"2986"	"GUCY2F"	"0.815"	"0.207"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2986"	"GUCY2F"	"0.815"	"0.207"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"2986"	"GUCY2F"	"0.815"	"0.207"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"2990"	"GUSB"	"0.619"	"0.655"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2990"	"GUSB"	"0.619"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"2990"	"GUSB"	"0.619"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.41"	"1"	"1998"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"2990"	"GUSB"	"0.619"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"2"	"0"	"CTD_human"
"2990"	"GUSB"	"0.619"	"0.655"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"2990"	"GUSB"	"0.619"	"0.655"	"C0085132"	"Mucopolysaccharidosis VII"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"1977"	"2017"	"13"	"30"	"CTD_human;ORPHANET;UNIPROT"
"2990"	"GUSB"	"0.619"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1997"	"1997"	"0"	"0"	"GENOMICS_ENGLAND"
"2992"	"GYG1"	"0.727"	"0.241"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2992"	"GYG1"	"0.727"	"0.241"	"C0017919"	"Glycogen Storage Disease"	"group"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"2992"	"GYG1"	"0.727"	"0.241"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2010"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"2992"	"GYG1"	"0.727"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"2992"	"GYG1"	"0.727"	"0.241"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"2992"	"GYG1"	"0.727"	"0.241"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2992"	"GYG1"	"0.727"	"0.241"	"C3150754"	"GLYCOGEN STORAGE DISEASE XV"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"2992"	"GYG1"	"0.727"	"0.241"	"C4015452"	"POLYGLUCOSAN BODY MYOPATHY 2"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"5"	"ORPHANET;UNIPROT"
"2993"	"GYPA"	"0.58"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"2993"	"GYPA"	"0.58"	"0.759"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2015"	"0"	"0"	"CTD_human"
"2993"	"GYPA"	"0.58"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"2994"	"GYPB"	"0.676"	"0.655"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"2995"	"GYPC"	"0.735"	"0.414"	"C0013902"	"Elliptocytosis, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2001"	"0"	"0"	"ORPHANET"
"2995"	"GYPC"	"0.735"	"0.414"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2004"	"0"	"0"	"CTD_human"
"2996"	"GYPE"	"0.681"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1989"	"2012"	"2"	"0"	"PSYGENET"
"2996"	"GYPE"	"0.681"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1989"	"2012"	"2"	"0"	"PSYGENET"
"2997"	"GYS1"	"0.743"	"0.276"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2007"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"2997"	"GYS1"	"0.743"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2997"	"GYS1"	"0.743"	"0.276"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2997"	"GYS1"	"0.743"	"0.276"	"C1969054"	"Glycogen Storage Disease 0, Muscle"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2007"	"2010"	"0"	"2"	"CTD_human;ORPHANET"
"2998"	"GYS2"	"0.799"	"0.138"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"2998"	"GYS2"	"0.799"	"0.138"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"2998"	"GYS2"	"0.799"	"0.138"	"C1855861"	"Glycogen Storage Disease 0, Liver"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1977"	"2017"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"2998"	"GYS2"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"0.96"	"1999"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1996"	"2017"	"0"	"0"	"ORPHANET"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C0344297"	"Choroidal sclerosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C1536451"	"Central areolar choroidal sclerosis"	"disease"	"C11"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C1866293"	"Retinal cone dystrophy 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.86"	"1"	"1996"	"2017"	"11"	"6"	"CTD_human;UNIPROT"
"3000"	"GUCY2D"	"0.619"	"0.586"	"C2931258"	"Amaurosis congenita of Leber, type 1"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"0.9512195"	"1993"	"2017"	"7"	"18"	"CTD_human;UNIPROT"
"3001"	"GZMA"	"0.685"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3002"	"GZMB"	"0.524"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"3005"	"H1F0"	"0.707"	"0.483"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3005"	"H1F0"	"0.707"	"0.483"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3005"	"H1F0"	"0.707"	"0.483"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3006"	"HIST1H1C"	"0.815"	"0.172"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3008"	"HIST1H1E"	"0.72"	"0.345"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3008"	"HIST1H1E"	"0.72"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3008"	"HIST1H1E"	"0.72"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3008"	"HIST1H1E"	"0.72"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3009"	"HIST1H1B"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3009"	"HIST1H1B"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3012"	"HIST1H2AE"	"0.857"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3012"	"HIST1H2AE"	"0.857"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3012"	"HIST1H2AE"	"0.857"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0032578"	"Polyploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3014"	"H2AFX"	"0.511"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2014"	"2016"	"0"	"1"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9411765"	"2012"	"2017"	"2"	"1"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2012"	"2016"	"2"	"0"	"CGI;CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0206638"	"Giant Cell Tumor of Bone"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0206725"	"Subependymal Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3020"	"H3F3A"	"0.667"	"0.31"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human;UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C1842010"	"Glioma of Brain, Familial"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C2750850"	"GLIOMA SUSCEPTIBILITY 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"UNIPROT"
"3020"	"H3F3A"	"0.667"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0008441"	"Chondroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3021"	"H3F3B"	"0.762"	"0.207"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3021"	"H3F3B"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3026"	"HABP2"	"0.639"	"0.448"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3026"	"HABP2"	"0.639"	"0.448"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3026"	"HABP2"	"0.639"	"0.448"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"3026"	"HABP2"	"0.639"	"0.448"	"C4225292"	"THYROID CANCER, NONMEDULLARY, 5"	"disease"		"Neoplastic Process"	"0.50"		"2003"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"3028"	"HSD17B10"	"0.645"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3028"	"HSD17B10"	"0.645"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3028"	"HSD17B10"	"0.645"	"0.483"	"C3266731"	"2-methyl-3-hydroxybutyric aciduria"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.60"		"1999"	"2017"	"13"	"9"	"CTD_human;UNIPROT"
"3028"	"HSD17B10"	"0.645"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2008"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"3029"	"HAGH"	"0.735"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3029"	"HAGH"	"0.735"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3030"	"HADHA"	"0.616"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.41"	"1"	"2000"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C1455728"	"Acute fatty liver of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.36"	"1"	"1995"	"2010"	"0"	"0"	"ORPHANET"
"3030"	"HADHA"	"0.616"	"0.552"	"C1969443"	"Trifunctional Protein Deficiency With Myopathy And Neuropathy"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3030"	"HADHA"	"0.616"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C3711645"	"Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"		"1995"	"1997"	"2"	"2"	"CTD_human;UNIPROT"
"3030"	"HADHA"	"0.616"	"0.552"	"C3714237"	"Trifunctional Protein Deficiency, Type 2"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"GENOMICS_ENGLAND"
"3030"	"HADHA"	"0.616"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3030"	"HADHA"	"0.616"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3032"	"HADHB"	"0.685"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"3032"	"HADHB"	"0.685"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3032"	"HADHB"	"0.685"	"0.552"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"3032"	"HADHB"	"0.685"	"0.552"	"C0154251"	"Lipid Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3032"	"HADHB"	"0.685"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C1969443"	"Trifunctional Protein Deficiency With Myopathy And Neuropathy"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.65"	"1"	"1996"	"2016"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"3032"	"HADHB"	"0.685"	"0.552"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C3711645"	"Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3032"	"HADHB"	"0.685"	"0.552"	"C3714237"	"Trifunctional Protein Deficiency, Type 2"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3033"	"HADH"	"0.652"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3033"	"HADH"	"0.652"	"0.414"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3033"	"HADH"	"0.652"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2005"	"2011"	"1"	"0"	"CTD_human"
"3033"	"HADH"	"0.652"	"0.414"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3033"	"HADH"	"0.652"	"0.414"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3033"	"HADH"	"0.652"	"0.414"	"C1291230"	"3-Hydroxyacyl-CoA Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2008"	"2008"	"0"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3033"	"HADH"	"0.652"	"0.414"	"C1864948"	"Hyperinsulinemic Hypoglycemia, Familial, 4"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2001"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"3033"	"HADH"	"0.652"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3034"	"HAL"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3034"	"HAL"	"0.681"	"0.483"	"C0220992"	"Histidinemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1991"	"2005"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3034"	"HAL"	"0.681"	"0.483"	"C0268642"	"Histidinuria renal tubular defect"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3035"	"HARS"	"0.609"	"0.655"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3035"	"HARS"	"0.609"	"0.655"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3035"	"HARS"	"0.609"	"0.655"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN;ORPHANET"
"3035"	"HARS"	"0.609"	"0.655"	"C3281066"	"USHER SYNDROME, TYPE IIIB"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2012"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"3035"	"HARS"	"0.609"	"0.655"	"C4225265"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"3038"	"HAS3"	"0.681"	"0.448"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3038"	"HAS3"	"0.681"	"0.448"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0002312"	"alpha-Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"0.9594595"	"1980"	"2017"	"1"	"2"	"CTD_human;ORPHANET"
"3039"	"HBA1"	"0.508"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3039"	"HBA1"	"0.508"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.35"	"0.6"	"1991"	"2009"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.50"	"0.8571429"	"1976"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"3039"	"HBA1"	"0.508"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0025637"	"Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"3039"	"HBA1"	"0.508"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3039"	"HBA1"	"0.508"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0475813"	"Alpha-thalassemia/mental retardation syndrome (301040) is an allelic disorder"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3039"	"HBA1"	"0.508"	"0.759"	"C0700299"	"Heinz Body Anemias"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1988"	"1988"	"0"	"1"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C0795917"	"Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type"	"disease"	"C10;C15;C16;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"3039"	"HBA1"	"0.508"	"0.759"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C1260396"	"Alpha thalassemia intermedia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3039"	"HBA1"	"0.508"	"0.759"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3039"	"HBA1"	"0.508"	"0.759"	"C3161174"	"Hemoglobin H Disease"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"1980"	"2016"	"0"	"0"	"ORPHANET"
"3039"	"HBA1"	"0.508"	"0.759"	"C3665425"	"Hemoglobin M Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C0002312"	"alpha-Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"0.9620253"	"1971"	"2017"	"2"	"9"	"CTD_human;ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.36"	"0.8333333"	"1983"	"2017"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"0.9548872"	"1981"	"2018"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3040"	"HBA2"	"0.524"	"0.724"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"1982"	"2007"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.50"	"0.8571429"	"1980"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"3040"	"HBA2"	"0.524"	"0.724"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2007"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"2017"	"9"	"0"	"GENOMICS_ENGLAND"
"3040"	"HBA2"	"0.524"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3040"	"HBA2"	"0.524"	"0.724"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"1983"	"2011"	"1"	"0"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0475813"	"Alpha-thalassemia/mental retardation syndrome (301040) is an allelic disorder"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C0700299"	"Heinz Body Anemias"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1968"	"1995"	"0"	"1"	"CTD_human"
"3040"	"HBA2"	"0.524"	"0.724"	"C0795917"	"Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type"	"disease"	"C10;C15;C16;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C1260396"	"Alpha thalassemia intermedia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C3161174"	"Hemoglobin H Disease"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"1980"	"2016"	"0"	"0"	"ORPHANET"
"3040"	"HBA2"	"0.524"	"0.724"	"C3665425"	"Hemoglobin M Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0002312"	"alpha-Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"0.9"	"1985"	"2012"	"0"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"	"1"	"1979"	"2017"	"6"	"0"	"CTD_human;ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.960396"	"1953"	"2018"	"5"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3043"	"HBB"	"0.513"	"0.793"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"0.9638009"	"1961"	"2018"	"12"	"73"	"CTD_human;UNIPROT"
"3043"	"HBB"	"0.513"	"0.793"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"3043"	"HBB"	"0.513"	"0.793"	"C0010520"	"Cyanosis"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3043"	"HBB"	"0.513"	"0.793"	"C0013502"	"Echinococcosis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0019021"	"Hemoglobin C Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"	"1"	"1979"	"2017"	"6"	"0"	"CTD_human;ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0019034"	"Hemoglobin SC Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"1996"	"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0019045"	"Hemoglobinopathies"	"group"	"C15;C16"	"Disease or Syndrome"	"0.50"	"0.9545455"	"1964"	"2015"	"1"	"11"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.47"	"0.6666667"	"2006"	"2018"	"0"	"2"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0024535"	"Malaria, Falciparum"	"disease"	"C03"	"Disease or Syndrome"	"0.32"	"0.5"	"2008"	"2010"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0025637"	"Methemoglobinemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1975"	"1983"	"2"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"1969"	"1969"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"2014"	"6"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2017"	"8"	"0"	"GENOMICS_ENGLAND"
"3043"	"HBB"	"0.513"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3043"	"HBB"	"0.513"	"0.793"	"C0221019"	"Sickle cell-beta-thalassemia"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1988"	"1988"	"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0238159"	"Hemoglobin E disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"1979"	"2014"	"6"	"0"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C0271985"	"Delta-Beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"0.8823529"	"1983"	"1994"	"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0272080"	"Hemoglobin D disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0272084"	"Hemoglobin SD disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0272085"	"Sickle cell-hemoglobin E disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0472767"	"Beta thalassemia intermedia"	"disease"		"Disease or Syndrome"	"0.50"	"0.9090909"	"1982"	"2016"	"0"	"8"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0472777"	"Hemoglobin E/beta thalassemia disease"	"disease"		"Disease or Syndrome"	"0.40"		"1961"	"2009"	"0"	"1"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0700299"	"Heinz Body Anemias"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1964"	"2002"	"0"	"7"	"CTD_human;ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C0857812"	"Sickle cell-beta^+^-thalassemia"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1988"	"1988"	"0"	"0"	"ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.40"		"1975"	"1983"	"2"	"1"	"CTD_human"
"3043"	"HBB"	"0.513"	"0.793"	"C1858990"	"Beta Thalassemia, Dominant Inclusion Body Type"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1974"	"2011"	"0"	"4"	"CTD_human;ORPHANET"
"3043"	"HBB"	"0.513"	"0.793"	"C3665425"	"Hemoglobin M Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3045"	"HBD"	"0.707"	"0.172"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3045"	"HBD"	"0.707"	"0.172"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3045"	"HBD"	"0.707"	"0.172"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3045"	"HBD"	"0.707"	"0.172"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3045"	"HBD"	"0.707"	"0.172"	"C0271985"	"Delta-Beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.35"	"1"	"1982"	"1992"	"0"	"0"	"ORPHANET"
"3047"	"HBG1"	"0.639"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3047"	"HBG1"	"0.639"	"0.448"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"1982"	"2010"	"0"	"0"	"ORPHANET"
"3047"	"HBG1"	"0.639"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3047"	"HBG1"	"0.639"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3047"	"HBG1"	"0.639"	"0.448"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3047"	"HBG1"	"0.639"	"0.448"	"C0271985"	"Delta-Beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.35"	"0.8"	"1982"	"1988"	"0"	"0"	"ORPHANET"
"3047"	"HBG1"	"0.639"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3048"	"HBG2"	"0.636"	"0.552"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3048"	"HBG2"	"0.636"	"0.552"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1977"	"1977"	"2"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C0028961"	"Oliguria"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3048"	"HBG2"	"0.636"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1977"	"1977"	"2"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1977"	"1977"	"2"	"0"	"CTD_human"
"3048"	"HBG2"	"0.636"	"0.552"	"C3151421"	"CYANOSIS, TRANSIENT NEONATAL"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1980"	"2014"	"6"	"4"	"CTD_human;UNIPROT"
"3050"	"HBZ"	"0.727"	"0.276"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.32"	"1"	"1985"	"1997"	"1"	"0"	"GENOMICS_ENGLAND"
"3052"	"HCCS"	"0.577"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"3052"	"HCCS"	"0.577"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3052"	"HCCS"	"0.577"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3052"	"HCCS"	"0.577"	"0.69"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3052"	"HCCS"	"0.577"	"0.69"	"C0796070"	"MICROPHTHALMIA, SYNDROMIC 7"	"disease"	"C11;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.80"	"0.8461538"	"1993"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3052"	"HCCS"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0007274"	"Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0025472"	"Mesenteric Vascular Occlusion"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"1990"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0398626"	"Heparin cofactor II deficiency (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"1989"	"2006"	"3"	"5"	"CTD_human;UNIPROT"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0750988"	"Common Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0750989"	"External Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C0750990"	"Internal Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3053"	"SERPIND1"	"0.659"	"0.379"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3054"	"HCFC1"	"0.681"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3054"	"HCFC1"	"0.681"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3054"	"HCFC1"	"0.681"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3054"	"HCFC1"	"0.681"	"0.448"	"C0796208"	"MENTAL RETARDATION, X-LINKED 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3054"	"HCFC1"	"0.681"	"0.448"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3054"	"HCFC1"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"0.75"	"1996"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3054"	"HCFC1"	"0.681"	"0.448"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3055"	"HCK"	"0.707"	"0.448"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3055"	"HCK"	"0.707"	"0.448"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3055"	"HCK"	"0.707"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3055"	"HCK"	"0.707"	"0.448"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3055"	"HCK"	"0.707"	"0.448"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3059"	"HCLS1"	"0.614"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0007384"	"Cataplexy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.8571429"	"2000"	"2016"	"1"	"1"	"UNIPROT"
"3060"	"HCRT"	"0.579"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9625"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3060"	"HCRT"	"0.579"	"0.724"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9230769"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"3060"	"HCRT"	"0.579"	"0.724"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3060"	"HCRT"	"0.579"	"0.724"	"C1456240"	"Narcolepsy without cataplexy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3060"	"HCRT"	"0.579"	"0.724"	"C1834372"	"Narcolepsy 1"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"1"	"1"	"CTD_human;UNIPROT"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"3"	"0"	"CTD_human"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2008"	"2"	"0"	"PSYGENET"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"3"	"0"	"CTD_human"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3061"	"HCRTR1"	"0.713"	"0.241"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2010"	"3"	"0"	"CTD_human"
"3062"	"HCRTR2"	"0.743"	"0.448"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.59"	"0.8888889"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3062"	"HCRTR2"	"0.743"	"0.448"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0006635"	"Cadmium poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2015"	"4"	"0"	"PSYGENET"
"3064"	"HTT"	"0.579"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2015"	"4"	"0"	"PSYGENET"
"3064"	"HTT"	"0.579"	"0.517"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.90"	"0.9714286"	"1993"	"2018"	"11"	"15"	"CTD_human;ORPHANET"
"3064"	"HTT"	"0.579"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.43"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"3064"	"HTT"	"0.579"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"11"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"3064"	"HTT"	"0.579"	"0.517"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"11"	"0"	"CTD_human"
"3064"	"HTT"	"0.579"	"0.517"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2018"	"11"	"0"	"CTD_human;ORPHANET"
"3064"	"HTT"	"0.579"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"3064"	"HTT"	"0.579"	"0.517"	"C4479491"	"LOPES-MACIEL-RODAN SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"2"	"3"	"UNIPROT"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2008"	"2018"	"2"	"0"	"PSYGENET"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3065"	"HDAC1"	"0.521"	"0.724"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3065"	"HDAC1"	"0.521"	"0.724"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2014"	"2"	"0"	"PSYGENET"
"3066"	"HDAC2"	"0.534"	"0.759"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"3066"	"HDAC2"	"0.534"	"0.759"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3067"	"HDC"	"0.639"	"0.517"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3067"	"HDC"	"0.639"	"0.517"	"C0040517"	"Gilles de la Tourette syndrome"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.64"	"1"	"2001"	"2015"	"0"	"1"	"CTD_human"
"3067"	"HDC"	"0.639"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3068"	"HDGF"	"0.639"	"0.345"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3068"	"HDGF"	"0.639"	"0.345"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3069"	"HDLBP"	"0.773"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3069"	"HDLBP"	"0.773"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"3069"	"HDLBP"	"0.773"	"0.379"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3069"	"HDLBP"	"0.773"	"0.379"	"C2931817"	"Chromosome 2q37 deletion syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3070"	"HELLS"	"0.663"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3070"	"HELLS"	"0.663"	"0.552"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3070"	"HELLS"	"0.663"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"3070"	"HELLS"	"0.663"	"0.552"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3070"	"HELLS"	"0.663"	"0.552"	"C4310798"	"IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2016"	"1"	"6"	"CTD_human;UNIPROT"
"3071"	"NCKAP1L"	"0.886"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3073"	"HEXA"	"0.616"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3073"	"HEXA"	"0.616"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C0039373"	"Tay-Sachs Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1983"	"2017"	"25"	"92"	"CTD_human;UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C0282220"	"Amaurotic Familial Idiocy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3073"	"HEXA"	"0.616"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848913"	"Tay-Sachs Disease, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"1988"	"2016"	"24"	"35"	"UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848914"	"Hexosaminidase A Deficiency, Adult Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1988"	"2016"	"24"	"35"	"ORPHANET;UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848915"	"Gm2-Gangliosidosis, Adult Chronic Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1988"	"2016"	"24"	"35"	"UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848916"	"Tay-Sachs Disease, Variant B1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1988"	"2016"	"24"	"36"	"ORPHANET;UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848917"	"Tay-Sachs Disease, Pseudo-AB Variant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1988"	"2016"	"24"	"35"	"UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C1848922"	"Hexosaminidase alpha-Subunit Deficiency (Variant B)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1985"	"2001"	"1"	"0"	"CTD_human"
"3073"	"HEXA"	"0.616"	"0.517"	"C2749283"	"Gm2-Gangliosidosis, Variant B1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1988"	"2016"	"24"	"36"	"ORPHANET;UNIPROT"
"3073"	"HEXA"	"0.616"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3074"	"HEXB"	"0.648"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3074"	"HEXB"	"0.648"	"0.552"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3074"	"HEXB"	"0.648"	"0.552"	"C0036161"	"Sandhoff Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9354839"	"1989"	"2017"	"10"	"18"	"CTD_human;UNIPROT"
"3074"	"HEXB"	"0.648"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3074"	"HEXB"	"0.648"	"0.552"	"C0751489"	"Adult Sandhoff Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1998"	"2002"	"0"	"0"	"CTD_human;ORPHANET"
"3074"	"HEXB"	"0.648"	"0.552"	"C0751490"	"Infantile Sandhoff Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1992"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"3074"	"HEXB"	"0.648"	"0.552"	"C0751491"	"Juvenile Sandhoff Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"1992"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"3074"	"HEXB"	"0.648"	"0.552"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3074"	"HEXB"	"0.648"	"0.552"	"C1849320"	"Sandhoff Disease, Adult Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1979"	"1998"	"10"	"3"	"ORPHANET;UNIPROT"
"3074"	"HEXB"	"0.648"	"0.552"	"C1849321"	"Sandhoff Disease, Juvenile Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1986"	"1998"	"10"	"3"	"ORPHANET;UNIPROT"
"3074"	"HEXB"	"0.648"	"0.552"	"C1849322"	"Sandhoff Disease, Infantile Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1992"	"1998"	"10"	"2"	"ORPHANET;UNIPROT"
"3074"	"HEXB"	"0.648"	"0.552"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3074"	"HEXB"	"0.648"	"0.552"	"C2713499"	"Total Hexosaminidase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3074"	"HEXB"	"0.648"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3075"	"CFH"	"0.478"	"0.793"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C0017662"	"Glomerulonephritis, Membranoproliferative"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C0025303"	"Meningococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.38"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C0162739"	"HELLP Syndrome"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.9625935"	"2005"	"2018"	"6"	"71"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.70"	"0.9545455"	"1995"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C0398777"	"Complement Factor H Deficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.79"	"0.8888889"	"1987"	"2015"	"8"	"7"	"CTD_human;ORPHANET;UNIPROT"
"3075"	"CFH"	"0.478"	"0.793"	"C0730295"	"BASAL LAMINAR DRUSEN (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.46"	"1"	"2005"	"2016"	"0"	"4"	"CTD_human"
"3075"	"CFH"	"0.478"	"0.793"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"0"	"CTD_human;ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C1832174"	"DOYNE HONEYCOMB RETINAL DYSTROPHY"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C1852020"	"Malattia Leventinese"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C1852021"	"Drusen, Radial, Autosomal Dominant"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3075"	"CFH"	"0.478"	"0.793"	"C1853147"	"MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"1995"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"3075"	"CFH"	"0.478"	"0.793"	"C1856143"	"HEMOLYTIC UREMIC SYNDROME, TYPICAL"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2010"	"8"	"4"	"UNIPROT"
"3075"	"CFH"	"0.478"	"0.793"	"C2749604"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.40"		"1978"	"2015"	"8"	"14"	"UNIPROT"
"3075"	"CFH"	"0.478"	"0.793"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.60"	"0.9711538"	"2000"	"2018"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9583333"	"2001"	"2016"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2014"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9535519"	"1987"	"2018"	"14"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.9583333"	"1998"	"2014"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.7777778"	"2002"	"2017"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3077"	"HFE"	"0.44"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.11"	"1"	"2012"	"2018"	"1"	"1"	"PSYGENET"
"3077"	"HFE"	"0.44"	"0.69"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2016"	"1"	"0"	"PSYGENET"
"3077"	"HFE"	"0.44"	"0.69"	"C0162566"	"Porphyria Cutanea Tarda"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.60"	"0.96"	"1996"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"3077"	"HFE"	"0.44"	"0.69"	"C0162569"	"Hepatoerythropoietic Porphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3077"	"HFE"	"0.44"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0268323"	"Familial porphyria cutanea tarda"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3077"	"HFE"	"0.44"	"0.69"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C0342861"	"Uroporphyrinogen decarboxylase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3077"	"HFE"	"0.44"	"0.69"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"	"0.9368771"	"1993"	"2018"	"30"	"11"	"CTD_human;UNIPROT"
"3077"	"HFE"	"0.44"	"0.69"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3077"	"HFE"	"0.44"	"0.69"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2018"	"1"	"1"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C1867968"	"Porphyria Cutanea Tarda, Type I"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3077"	"HFE"	"0.44"	"0.69"	"C2673520"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)"	"phenotype"		"Finding"	"0.40"		"1996"	"2008"	"0"	"1"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C2936913"	"Porphyria, South African type"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.36"	"0.8333333"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3077"	"HFE"	"0.44"	"0.69"	"C3469186"	"HEMOCHROMATOSIS, TYPE 1"	"disease"		"Disease or Syndrome"	"0.70"	"0.9493243"	"1987"	"2018"	"16"	"15"	"UNIPROT"
"3078"	"CFHR1"	"0.652"	"0.379"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3078"	"CFHR1"	"0.652"	"0.379"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3078"	"CFHR1"	"0.652"	"0.379"	"C1864205"	"Macular Degeneration, Age-Related, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3078"	"CFHR1"	"0.652"	"0.379"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.60"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3078"	"CFHR1"	"0.652"	"0.379"	"C3553720"	"CFHR5 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3081"	"HGD"	"0.69"	"0.414"	"C0002066"	"Alkaptonuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1988"	"2018"	"13"	"62"	"CTD_human;ORPHANET;UNIPROT"
"3081"	"HGD"	"0.69"	"0.414"	"C2931645"	"Ochronosis, hereditary"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3082"	"HGF"	"0.394"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.8333333"	"1998"	"2012"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2000"	"2011"	"7"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9814815"	"1994"	"2018"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.9"	"1997"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0043254"	"Wounds, Penetrating"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"1992"	"2005"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2008"	"2"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C1842342"	"DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"1"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CLINGEN"
"3082"	"HGF"	"0.394"	"0.793"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3082"	"HGF"	"0.394"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9864865"	"1992"	"2017"	"2"	"0"	"CTD_human"
"3083"	"HGFAC"	"0.676"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"3084"	"NRG1"	"0.506"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3084"	"NRG1"	"0.506"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2009"	"2"	"0"	"PSYGENET"
"3084"	"NRG1"	"0.506"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2009"	"2"	"0"	"PSYGENET"
"3084"	"NRG1"	"0.506"	"0.759"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2005"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2005"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2018"	"1"	"2"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.6666667"	"2007"	"2012"	"3"	"0"	"PSYGENET"
"3084"	"NRG1"	"0.506"	"0.759"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9641026"	"2002"	"2018"	"7"	"1"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"0.8333333"	"2004"	"2018"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2017"	"1"	"2"	"CTD_human"
"3084"	"NRG1"	"0.506"	"0.759"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9615385"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3087"	"HHEX"	"0.652"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0032584"	"polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0265219"	"Miller Dieker syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"3090"	"HIC1"	"0.542"	"0.517"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0685938"	"Malignant neoplasm of gastrointestinal tract"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3090"	"HIC1"	"0.542"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0002793"	"Anaplasia"	"disease"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"0.8571429"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9793814"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0007124"	"Noninfiltrating Intraductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9512195"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.57"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.8571429"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2005"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2013"	"2"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0178540"	"Cerebral Hypoxia-Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0206734"	"Hemangioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"0.8571429"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9782609"	"2001"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9850746"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.97"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0751692"	"Multiple Hemangioblastomas"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0752304"	"Hypoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0752305"	"Anoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0752306"	"Anoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0752307"	"Anoxia-Ischemia, Cerebral"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0752308"	"Hypoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1176475"	"Ductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1332347"	"Atypical Ductal Breast Hyperplasia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9285714"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3091"	"HIF1A"	"0.367"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3092"	"HIP1"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3092"	"HIP1"	"0.681"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2008"	"0"	"0"	"CTD_human"
"3092"	"HIP1"	"0.681"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2008"	"0"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3094"	"HINT1"	"0.667"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3094"	"HINT1"	"0.667"	"0.345"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C0242287"	"Isaacs syndrome"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.67"	"1"	"2006"	"2017"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3094"	"HINT1"	"0.667"	"0.345"	"C0751919"	"Acquired Neuromyotonia"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C2932678"	"Inherited Peripheral Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3094"	"HINT1"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3097"	"HIVEP2"	"0.72"	"0.379"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3097"	"HIVEP2"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"3097"	"HIVEP2"	"0.72"	"0.379"	"C4310771"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 43"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"0"	"6"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3098"	"HK1"	"0.572"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1995"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"3098"	"HK1"	"0.572"	"0.586"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"1993"	"2011"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2014"	"1"	"0"	"PSYGENET"
"3098"	"HK1"	"0.572"	"0.586"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3098"	"HK1"	"0.572"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"3098"	"HK1"	"0.572"	"0.586"	"C1854449"	"Neuropathy, hereditary motor and sensory, Russe type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"3098"	"HK1"	"0.572"	"0.586"	"C3150343"	"HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"1995"	"2003"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3098"	"HK1"	"0.572"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3098"	"HK1"	"0.572"	"0.586"	"C4479526"	"RETINITIS PIGMENTOSA 79"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"3099"	"HK2"	"0.584"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.52"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"3099"	"HK2"	"0.584"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3099"	"HK2"	"0.584"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3101"	"HK3"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3101"	"HK3"	"0.815"	"0.138"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3101"	"HK3"	"0.815"	"0.138"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3101"	"HK3"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2018"	"0"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0014799"	"Erythroderma, Maculopapular"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.34"	"0.6666667"	"1982"	"2014"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0030437"	"Parakeratosis Variegata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0030491"	"Parapsoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.5"	"2002"	"2016"	"4"	"0"	"PSYGENET"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1983"	"2006"	"1"	"0"	"PSYGENET"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2018"	"0"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0162442"	"Parapsoriasis en Plaques"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3105"	"HLA-A"	"0.404"	"0.793"	"C1853959"	"Birdshot chorioretinopathy"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"3105"	"HLA-A"	"0.404"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"3105"	"HLA-A"	"0.404"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.70"	"0.9452055"	"1980"	"2017"	"2"	"2"	"CTD_human;ORPHANET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1986"	"2008"	"2"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.37"	"1"	"2002"	"2013"	"4"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1980"	"1988"	"5"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2004"	"2018"	"9"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0015230"	"Exanthema"	"phenotype"	"C17"	"Sign or Symptom"	"0.37"	"0.8571429"	"2006"	"2015"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.41"		"2008"	"2017"	"1"	"1"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.31"	"1"	"1983"	"1999"	"2"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1980"	"1986"	"4"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2006"	"2018"	"2"	"3"	"PSYGENET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"0.9418605"	"1980"	"2018"	"3"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.60"	"1"	"2004"	"2018"	"9"	"0"	"CTD_human;ORPHANET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0039103"	"Synovitis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2003"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0039263"	"Takayasu Arteritis"	"disease"	"C14;C17"	"Disease or Syndrome"	"0.40"	"0.9444444"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1980"	"1988"	"5"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0410574"	"Synovial Hypertrophy"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"2"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"2"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2015"	"9"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2015"	"9"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.35"	"0.8"	"2004"	"2016"	"9"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C3697982"	"Pulmonary arterial hypertension associated with connective tissue disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3106"	"HLA-B"	"0.423"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3106"	"HLA-B"	"0.423"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3106"	"HLA-B"	"0.423"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"	"0.8965517"	"1999"	"2016"	"1"	"1"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"1"	"1"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1988"	"2015"	"0"	"1"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2010"	"2"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.907563"	"1997"	"2018"	"2"	"6"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1994"	"2016"	"2"	"1"	"PSYGENET"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"1"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"3107"	"HLA-C"	"0.419"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3107"	"HLA-C"	"0.419"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3107"	"HLA-C"	"0.419"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3108"	"HLA-DMA"	"0.681"	"0.517"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3108"	"HLA-DMA"	"0.681"	"0.517"	"C0028796"	"Dermatitis, Occupational"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3108"	"HLA-DMA"	"0.681"	"0.517"	"C0086457"	"Industrial Dermatosis"	"disease"	"C17;C24"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3108"	"HLA-DMA"	"0.681"	"0.517"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3110"	"MNX1"	"0.616"	"0.517"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.80"	"0.8333333"	"1995"	"2014"	"4"	"4"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"3110"	"MNX1"	"0.616"	"0.517"	"C1867774"	"Sacral Agenesis Syndrome"	"disease"	"C04;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2012"	"4"	"1"	"UNIPROT"
"3110"	"MNX1"	"0.616"	"0.517"	"C1867775"	"Sacral Agenesis, Hereditary, With Presacral Mass, Anterior Meningocele, And-Or Teratoma, And Anorectal Malformation"	"disease"	"C04;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2012"	"4"	"1"	"UNIPROT"
"3110"	"MNX1"	"0.616"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3113"	"HLA-DPA1"	"0.762"	"0.379"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3113"	"HLA-DPA1"	"0.762"	"0.379"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2014"	"1"	"42"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.9545455"	"1988"	"2015"	"2"	"62"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2015"	"2"	"1"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.50"		"1993"	"2008"	"6"	"0"	"CTD_human;ORPHANET"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.9"	"1988"	"2015"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9130435"	"1988"	"2013"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.34"	"1"	"1993"	"2011"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.38"	"1"	"1996"	"2015"	"3"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"1995"	"2001"	"1"	"0"	"PSYGENET"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0221052"	"Chronic berylliosis"	"disease"		"Disease or Syndrome"	"0.40"	"0.9411765"	"1997"	"2012"	"0"	"0"	"ORPHANET"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2017"	"1"	"70"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2008"	"6"	"0"	"CTD_human"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C3495801"	"Granulomatosis with polyangiitis"	"disease"	"C08;C14;C20"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2015"	"0"	"1"	"ORPHANET"
"3115"	"HLA-DPB1"	"0.484"	"0.862"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"3116"	"HLA-DPB2"	"0.752"	"0.379"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3116"	"HLA-DPB2"	"0.752"	"0.379"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3116"	"HLA-DPB2"	"0.752"	"0.379"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3116"	"HLA-DPB2"	"0.752"	"0.379"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.44"	"1"	"2000"	"2015"	"1"	"4"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.50"	"1"	"1989"	"2016"	"0"	"1"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"0.890625"	"1989"	"2018"	"1"	"2"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0014848"	"Esophageal Achalasia"	"disease"	"C06"	"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.43"	"1"	"2001"	"2017"	"1"	"2"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.47"	"1"	"1995"	"2016"	"1"	"2"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0025164"	"Megaesophagus"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0029295"	"Oropharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0085179"	"Eosinophilia-Myalgia Syndrome"	"disease"	"C05;C10;C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.37"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0751622"	"Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related"	"disease"	"C05;C10;C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C0859976"	"Idiopathic achalasia of esophagus"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C2349952"	"Oropharyngeal Carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C2936833"	"Mycobacterium tuberculosis, susceptibility to infection by"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3117"	"HLA-DQA1"	"0.503"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3118"	"HLA-DQA2"	"0.676"	"0.552"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2007"	"2011"	"1"	"11"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.8888889"	"1996"	"2014"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.9565217"	"1991"	"2015"	"0"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"	"0.9350649"	"1990"	"2018"	"1"	"1"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0014848"	"Esophageal Achalasia"	"disease"	"C06"	"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.35"	"1"	"1991"	"2015"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.40"		"1996"	"2013"	"1"	"1"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0025164"	"Megaesophagus"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.60"	"0.9130435"	"1991"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9666667"	"1997"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0029295"	"Oropharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0030805"	"Bullous pemphigoid"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2018"	"0"	"0"	"ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.48"	"0.5"	"1993"	"2018"	"2"	"4"	"PSYGENET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.32"	"0.5"	"2003"	"2015"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.66"	"0.8333333"	"2004"	"2015"	"1"	"1"	"CTD_human;ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0859976"	"Idiopathic achalasia of esophagus"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C1456240"	"Narcolepsy without cataplexy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C2349952"	"Oropharyngeal Carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"1"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3119"	"HLA-DQB1"	"0.446"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.44"	"1"	"1999"	"2011"	"1"	"10"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.49"	"0.7777778"	"2010"	"2016"	"1"	"1"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"CTD_human"
"3122"	"HLA-DRA"	"0.616"	"0.69"	"C4273658"	"Graham Little Piccardi Lassueur syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.920078"	"1983"	"2018"	"3"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.8636364"	"1997"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8837209"	"1993"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8695652"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"	"0.92"	"1988"	"2018"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.8765432"	"1989"	"2016"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2010"	"2017"	"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.60"	"0.8854167"	"1984"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.7058824"	"1993"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1984"	"2017"	"2"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0029295"	"Oropharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0030805"	"Bullous pemphigoid"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2002"	"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.31"		"1984"	"2008"	"2"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.70"	"0.9047619"	"1994"	"2016"	"1"	"13"	"CTD_human;ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1984"	"2018"	"1"	"6"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0041466"	"Typhoid Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.43"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0085179"	"Eosinophilia-Myalgia Syndrome"	"disease"	"C05;C10;C15"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0751622"	"Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related"	"disease"	"C05;C10;C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1258104"	"Diffuse Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.35"	"1"	"1989"	"2013"	"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1384600"	"Systemic onset juvenile chronic arthritis"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1456240"	"Narcolepsy without cataplexy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C2349952"	"Oropharyngeal Carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3123"	"HLA-DRB1"	"0.347"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"3126"	"HLA-DRB4"	"0.586"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"3126"	"HLA-DRB4"	"0.586"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3126"	"HLA-DRB4"	"0.586"	"0.724"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3126"	"HLA-DRB4"	"0.586"	"0.724"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3126"	"HLA-DRB4"	"0.586"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3127"	"HLA-DRB5"	"0.648"	"0.517"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3131"	"HLF"	"0.681"	"0.483"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"3131"	"HLF"	"0.681"	"0.483"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"3131"	"HLF"	"0.681"	"0.483"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3131"	"HLF"	"0.681"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3131"	"HLF"	"0.681"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3131"	"HLF"	"0.681"	"0.483"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.37"	"1"	"1994"	"2011"	"0"	"0"	"ORPHANET"
"3131"	"HLF"	"0.681"	"0.483"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0014799"	"Erythroderma, Maculopapular"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0030437"	"Parakeratosis Variegata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0030491"	"Parapsoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.8"	"2012"	"2015"	"5"	"0"	"PSYGENET"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0162442"	"Parapsoriasis en Plaques"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3133"	"HLA-E"	"0.602"	"0.586"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3135"	"HLA-G"	"0.511"	"0.759"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2005"	"2016"	"0"	"0"	"CTD_human"
"3135"	"HLA-G"	"0.511"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3137"	"HLA-J"	"0.886"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3141"	"HLCS"	"0.681"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"3141"	"HLCS"	"0.681"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3141"	"HLCS"	"0.681"	"0.345"	"C0268581"	"Holocarboxylase Synthetase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1981"	"2017"	"13"	"19"	"CTD_human;ORPHANET;UNIPROT"
"3141"	"HLCS"	"0.681"	"0.345"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3141"	"HLCS"	"0.681"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3141"	"HLCS"	"0.681"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3141"	"HLCS"	"0.681"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3145"	"HMBS"	"0.6"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3145"	"HMBS"	"0.6"	"0.552"	"C0162565"	"Acute intermittent porphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.992"	"1981"	"2018"	"44"	"38"	"CTD_human;ORPHANET;UNIPROT"
"3145"	"HMBS"	"0.6"	"0.552"	"C0268322"	"Chester-type porphyria"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1990"	"2015"	"42"	"34"	"UNIPROT"
"3145"	"HMBS"	"0.6"	"0.552"	"C1867969"	"Porphyria, Acute Intermittent, Nonerythroid Variant"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.40"		"1990"	"2015"	"42"	"35"	"UNIPROT"
"3145"	"HMBS"	"0.6"	"0.552"	"C2936779"	"Hydroxymethylbilane Synthase Deficiency"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.51"	"1"	"1983"	"2015"	"44"	"34"	"CTD_human;UNIPROT"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.34"		"2002"	"2013"	"5"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0264939"	"Systemic Vasculitis"	"phenotype"	"C14"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0282548"	"Leukostasis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C1850383"	"Neuropathy, Painful"	"disease"	"C10;C23;F02"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3146"	"HMGB1"	"0.433"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3148"	"HMGB2"	"0.681"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3148"	"HMGB2"	"0.681"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"3148"	"HMGB2"	"0.681"	"0.379"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"3149"	"HMGB3"	"0.676"	"0.517"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"1971"	"1971"	"1"	"0"	"GENOMICS_ENGLAND"
"3149"	"HMGB3"	"0.676"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1971"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"3149"	"HMGB3"	"0.676"	"0.517"	"C3806742"	"MICROPHTHALMIA, SYNDROMIC 13"	"disease"		"Disease or Syndrome"	"0.40"		"1971"	"2015"	"0"	"1"	"CTD_human"
"3150"	"HMGN1"	"0.743"	"0.414"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3155"	"HMGCL"	"0.785"	"0.207"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3155"	"HMGCL"	"0.785"	"0.207"	"C0268601"	"HMG CoA lyase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2014"	"10"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3155"	"HMGCL"	"0.785"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"3155"	"HMGCL"	"0.785"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"3155"	"HMGCL"	"0.785"	"0.207"	"C1533587"	"Hydroxymethylglutaric aciduria"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3155"	"HMGCL"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2010"	"2011"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0034362"	"Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C0519066"	"Acute Q fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C1443892"	"Chronic Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1991"	"2015"	"2"	"0"	"CTD_human"
"3156"	"HMGCR"	"0.584"	"0.621"	"C2973787"	"Coxiella burnetii Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2017"	"2"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C2751532"	"3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1997"	"2016"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3158"	"HMGCS2"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0023269"	"leiomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0205815"	"Leiomyosarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0205816"	"Leiomyosarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3159"	"HMGA1"	"0.532"	"0.552"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3161"	"HMMR"	"0.624"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2010"	"4"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.8888889"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2013"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8666667"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2010"	"4"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2017"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0012715"	"Iron Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0019212"	"Hepatorenal Syndrome"	"disease"	"C06;C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2006"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.35"		"2003"	"2013"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.53"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"4"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2006"	"2011"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"2005"	"2017"	"0"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2017"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2002"	"2015"	"6"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"PSYGENET"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2004"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2010"	"4"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2007"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0152020"	"Gastroparesis"	"disease"	"C06;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0221013"	"Mastocytosis, Systemic"	"disease"	"C04;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0272203"	"Indolent Systemic Mastocytosis"	"disease"	"C04;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2015"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1112486"	"Aggressive Systemic Mastocytosis"	"disease"	"C04;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2006"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1841651"	"Heme Oxygenase 1 Deficiency"	"disease"	"C15;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8421053"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3162"	"HMOX1"	"0.403"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"3163"	"HMOX2"	"0.752"	"0.414"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"3164"	"NR4A1"	"0.558"	"0.621"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3166"	"HMX1"	"0.735"	"0.276"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2008"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"3166"	"HMX1"	"0.735"	"0.276"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"3166"	"HMX1"	"0.735"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3166"	"HMX1"	"0.735"	"0.276"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3166"	"HMX1"	"0.735"	"0.276"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2008"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"3166"	"HMX1"	"0.735"	"0.276"	"C2677500"	"Oculoauricular Syndrome"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"2005"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2004"	"2018"	"1"	"0"	"CGI;CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2018"	"3"	"0"	"CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"3"	"0"	"CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2004"	"2018"	"1"	"0"	"CGI;CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3169"	"FOXA1"	"0.59"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3169"	"FOXA1"	"0.59"	"0.586"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3170"	"FOXA2"	"0.592"	"0.483"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3170"	"FOXA2"	"0.592"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3170"	"FOXA2"	"0.592"	"0.483"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"3171"	"FOXA3"	"0.857"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3171"	"FOXA3"	"0.857"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3172"	"HNF4A"	"0.486"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"3172"	"HNF4A"	"0.486"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"0.9302326"	"1992"	"2017"	"4"	"3"	"CTD_human;UNIPROT"
"3172"	"HNF4A"	"0.486"	"0.69"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.47"	"1"	"2007"	"2015"	"1"	"1"	"GENOMICS_ENGLAND"
"3172"	"HNF4A"	"0.486"	"0.69"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9277108"	"1995"	"2017"	"0"	"0"	"ORPHANET"
"3172"	"HNF4A"	"0.486"	"0.69"	"C0431693"	"Renal cysts and diabetes syndrome"	"disease"	"C10;C12;C13;C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"3172"	"HNF4A"	"0.486"	"0.69"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"3172"	"HNF4A"	"0.486"	"0.69"	"C1852093"	"Maturity-Onset Diabetes of the Young, Type 1"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"1"	"1990"	"2013"	"5"	"12"	"CTD_human;UNIPROT"
"3172"	"HNF4A"	"0.486"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3172"	"HNF4A"	"0.486"	"0.69"	"C4014962"	"FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"3172"	"HNF4A"	"0.486"	"0.69"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"3172"	"HNF4A"	"0.486"	"0.69"	"C4274078"	"Hyperinsulinism due to HNF4A deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3176"	"HNMT"	"0.642"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2011"	"3"	"0"	"PSYGENET"
"3176"	"HNMT"	"0.642"	"0.483"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.36"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"3176"	"HNMT"	"0.642"	"0.483"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3176"	"HNMT"	"0.642"	"0.483"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3176"	"HNMT"	"0.642"	"0.483"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"0"	"2006"	"2010"	"1"	"0"	"CTD_human"
"3176"	"HNMT"	"0.642"	"0.483"	"C4225220"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.45"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C1833662"	"INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA"	"disease"	"C05;C10;C16;C18;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C3715156"	"AMYOTROPHIC LATERAL SCLEROSIS 20"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"3178"	"HNRNPA1"	"0.561"	"0.69"	"C3809469"	"INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2015"	"1"	"1"	"UNIPROT"
"3181"	"HNRNPA2B1"	"0.607"	"0.655"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3181"	"HNRNPA2B1"	"0.607"	"0.655"	"C1833662"	"INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA"	"disease"	"C05;C10;C16;C18;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3181"	"HNRNPA2B1"	"0.607"	"0.655"	"C3809468"	"INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2013"	"1"	"1"	"UNIPROT"
"3182"	"HNRNPAB"	"0.857"	"0.172"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3187"	"HNRNPH1"	"0.773"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3187"	"HNRNPH1"	"0.773"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3187"	"HNRNPH1"	"0.773"	"0.379"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3188"	"HNRNPH2"	"0.672"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3188"	"HNRNPH2"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3188"	"HNRNPH2"	"0.672"	"0.345"	"C4310814"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"3190"	"HNRNPK"	"0.604"	"0.724"	"C4225274"	"AU-KLINE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3191"	"HNRNPL"	"0.762"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3192"	"HNRNPU"	"0.676"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2018"	"1"	"4"	"GENOMICS_ENGLAND"
"3192"	"HNRNPU"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3192"	"HNRNPU"	"0.676"	"0.483"	"C4304540"	"1q44 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3192"	"HNRNPU"	"0.676"	"0.483"	"C4479319"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2018"	"0"	"5"	"CTD_human"
"3195"	"TLX1"	"0.727"	"0.138"	"C0002938"	"Aneuploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3195"	"TLX1"	"0.727"	"0.138"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3195"	"TLX1"	"0.727"	"0.138"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1991"	"2008"	"1"	"0"	"CTD_human"
"3195"	"TLX1"	"0.727"	"0.138"	"C0037997"	"Splenic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3195"	"TLX1"	"0.727"	"0.138"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.9302326"	"1989"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8888889"	"2001"	"2012"	"1"	"0"	"CTD_human"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3198"	"HOXA1"	"0.619"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3198"	"HOXA1"	"0.619"	"0.552"	"C1832215"	"Athabaskan brainstem dysgenesis"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.80"		"1999"	"2014"	"1"	"1"	"CTD_human;ORPHANET"
"3198"	"HOXA1"	"0.619"	"0.552"	"C1832216"	"Bosley-Salih-Alorainy Syndrome"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.82"	"1"	"1999"	"2014"	"1"	"1"	"CTD_human;ORPHANET"
"3198"	"HOXA1"	"0.619"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"3199"	"HOXA2"	"0.785"	"0.31"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3199"	"HOXA2"	"0.785"	"0.31"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3199"	"HOXA2"	"0.785"	"0.31"	"C0152423"	"Congenital small ears"	"disease"	"C09;C16"	"Congenital Abnormality"	"0.44"	"1"	"2008"	"2017"	"0"	"0"	"ORPHANET"
"3199"	"HOXA2"	"0.785"	"0.31"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3199"	"HOXA2"	"0.785"	"0.31"	"C2676772"	"Microtia, Hearing Impairment, And Cleft Palate"	"disease"	"C05;C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.70"		"2008"	"2014"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3199"	"HOXA2"	"0.785"	"0.31"	"C3808166"	"MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2014"	"1"	"2"	"UNIPROT"
"3200"	"HOXA3"	"0.799"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3200"	"HOXA3"	"0.799"	"0.345"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3200"	"HOXA3"	"0.799"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3200"	"HOXA3"	"0.799"	"0.345"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3200"	"HOXA3"	"0.799"	"0.345"	"C0398368"	"Lymphatic Abnormalities"	"group"	"C15;C16"	"Anatomical Abnormality"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3201"	"HOXA4"	"0.727"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3202"	"HOXA5"	"0.648"	"0.483"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3202"	"HOXA5"	"0.648"	"0.483"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3202"	"HOXA5"	"0.648"	"0.483"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3202"	"HOXA5"	"0.648"	"0.483"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9811321"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3205"	"HOXA9"	"0.572"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2006"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"3206"	"HOXA10"	"0.596"	"0.586"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3207"	"HOXA11"	"0.59"	"0.586"	"C1854273"	"Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia"	"disease"	"C05;C15;C16"	"Disease or Syndrome"	"0.61"	"1"	"2000"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"3208"	"HPCA"	"0.735"	"0.345"	"C1857093"	"DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1981"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3209"	"HOXA13"	"0.611"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3209"	"HOXA13"	"0.611"	"0.414"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3209"	"HOXA13"	"0.611"	"0.414"	"C1841679"	"Hand foot uterus syndrome"	"disease"	"C05;C12;C13;C16"	"Disease or Syndrome"	"1.00"	"1"	"1970"	"2016"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3209"	"HOXA13"	"0.611"	"0.414"	"C1867801"	"Preaxial deficiency, postaxial polydactyly and hypospadias"	"disease"	"C05;C12;C13;C16"	"Disease or Syndrome"	"0.62"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human;ORPHANET;UNIPROT"
"3209"	"HOXA13"	"0.611"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3209"	"HOXA13"	"0.611"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1997"	"2000"	"2"	"0"	"GENOMICS_ENGLAND"
"3211"	"HOXB1"	"0.713"	"0.414"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3211"	"HOXB1"	"0.713"	"0.414"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3211"	"HOXB1"	"0.713"	"0.414"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3211"	"HOXB1"	"0.713"	"0.414"	"C1858717"	"Facial paresis, hereditary, congenital"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3211"	"HOXB1"	"0.713"	"0.414"	"C3553625"	"FACIAL PARESIS, HEREDITARY CONGENITAL, 3"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"3213"	"HOXB3"	"0.743"	"0.31"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3215"	"HOXB5"	"0.735"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2015"	"1"	"1"	"CTD_human"
"3218"	"HOXB8"	"0.773"	"0.241"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"3218"	"HOXB8"	"0.773"	"0.241"	"C0040953"	"Trichotillomania"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3219"	"HOXB9"	"0.663"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"3225"	"HOXC9"	"0.773"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3229"	"HOXC13"	"0.762"	"0.207"	"C1865951"	"Ectodermal Dysplasia, Pure Hair-Nail Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"3229"	"HOXC13"	"0.762"	"0.207"	"C3554127"	"ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2018"	"2"	"2"	"CTD_human;UNIPROT"
"3229"	"HOXC13"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3231"	"HOXD1"	"0.785"	"0.276"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3232"	"HOXD3"	"0.72"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3232"	"HOXD3"	"0.72"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3233"	"HOXD4"	"0.815"	"0.241"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"3233"	"HOXD4"	"0.815"	"0.241"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3233"	"HOXD4"	"0.815"	"0.241"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C0007130"	"Mucinous Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3235"	"HOXD9"	"0.685"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0016202"	"Flatfoot"	"phenotype"	"C05;C16"	"Anatomical Abnormality"	"0.30"		"2004"	"2014"	"3"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0152237"	"Talipes Calcaneovalgus"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2014"	"3"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0240912"	"Vertical Talus"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.64"	"1"	"2004"	"2016"	"3"	"1"	"CTD_human;UNIPROT"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0431943"	"Lower Extremity Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3236"	"HOXD10"	"0.639"	"0.414"	"C1860446"	"Congenital vertical talus, bilateral"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"3236"	"HOXD10"	"0.639"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1994"	"1996"	"3"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3237"	"HOXD11"	"0.72"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3238"	"HOXD12"	"0.886"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3238"	"HOXD12"	"0.886"	"0.103"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1996"	"2009"	"2"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0039075"	"Syndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.45"	"1"	"2004"	"2015"	"0"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.40"	"0.9285714"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0220664"	"BRACHYDACTYLY, TYPE D"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"		"2003"	"2014"	"2"	"2"	"CTD_human;UNIPROT"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0220708"	"VATER Association"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0265312"	"Brachydactyly syndrome type E"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3239"	"HOXD13"	"0.541"	"0.621"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3239"	"HOXD13"	"0.541"	"0.621"	"C1735591"	"VACTERL Association"	"disease"	"C05;C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"3239"	"HOXD13"	"0.541"	"0.621"	"C1853137"	"BRACHYDACTYLY-SYNDACTYLY SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2007"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3239"	"HOXD13"	"0.541"	"0.621"	"C1861348"	"Syndactyly, type v"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.71"	"1"	"2005"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3239"	"HOXD13"	"0.541"	"0.621"	"C1862102"	"BRACHYDACTYLY, TYPE E1"	"phenotype"	"C05;C16"	"Finding"	"0.60"		"2003"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"3239"	"HOXD13"	"0.541"	"0.621"	"C2699746"	"Syndactyly, type 2"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"0.952381"	"1993"	"2016"	"6"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3239"	"HOXD13"	"0.541"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3239"	"HOXD13"	"0.541"	"0.621"	"C4310807"	"BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"3240"	"HP"	"0.461"	"0.793"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1982"	"1982"	"1"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.35"	"1"	"1987"	"2014"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0003864"	"Arthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.6666667"	"1984"	"1994"	"3"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.6666667"	"1984"	"1994"	"3"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"1"	"1986"	"2018"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0016479"	"Food Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0017416"	"Genital Neoplasms, Female"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.33"	"1"	"1982"	"2011"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1984"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"0.9333333"	"1980"	"2014"	"2"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.8"	"1982"	"2012"	"3"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1985"	"2008"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0041296"	"Tuberculosis"	"disease"	"C01"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"1984"	"1997"	"4"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0085397"	"Pasteurellaceae Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0162323"	"Polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"0"	"2006"	"2012"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0341934"	"Transient hypertension of pregnancy"	"phenotype"	"C13;C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0524910"	"Hepatitis C, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1981"	"1986"	"2"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0679360"	"Foodborne Disease"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C0852036"	"Pregnancy associated hypertension"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1994"	"1997"	"3"	"0"	"PSYGENET"
"3240"	"HP"	"0.461"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C3279786"	"ANHAPTOGLOBINEMIA"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2003"	"2016"	"1"	"1"	"UNIPROT"
"3240"	"HP"	"0.461"	"0.793"	"C3279787"	"HYPOHAPTOGLOBINEMIA (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"3240"	"HP"	"0.461"	"0.793"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3240"	"HP"	"0.461"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3241"	"HPCAL1"	"0.857"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C0268483"	"Tyrosinemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C0268487"	"Tyrosine Transaminase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C0268490"	"Tyrosinemia, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C0268623"	"Tyrosinemia, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.94"	"1"	"1991"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3242"	"HPD"	"0.619"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C2931042"	"Hawkinsinuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"2000"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"3242"	"HPD"	"0.619"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3242"	"HPD"	"0.619"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3242"	"HPD"	"0.619"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0029411"	"Osteoarthropathy, Primary Hypertrophic"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3248"	"HPGD"	"0.557"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0206693"	"Medullary carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0345408"	"Hereditary clubbing"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.70"		"2008"	"2015"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3248"	"HPGD"	"0.557"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3248"	"HPGD"	"0.557"	"0.586"	"C2674695"	"Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"3248"	"HPGD"	"0.557"	"0.586"	"C2678439"	"CRANIOOSTEOARTHROPATHY"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1998"	"2015"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3248"	"HPGD"	"0.557"	"0.586"	"C2930922"	"Reginato Schiapachasse syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3248"	"HPGD"	"0.557"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3249"	"HPN"	"0.681"	"0.448"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"3249"	"HPN"	"0.681"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.38"	"0.8"	"2001"	"2009"	"2"	"0"	"CTD_human"
"3249"	"HPN"	"0.681"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"3251"	"HPRT1"	"0.518"	"0.793"	"C0023374"	"Lesch-Nyhan Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.974359"	"1980"	"2018"	"21"	"22"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"3251"	"HPRT1"	"0.518"	"0.793"	"C0268117"	"Gout, HPRT-Related"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1983"	"2017"	"13"	"16"	"CTD_human;ORPHANET;UNIPROT"
"3251"	"HPRT1"	"0.518"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3251"	"HPRT1"	"0.518"	"0.793"	"C0740394"	"Hyperuricemia"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"1"	"1982"	"2018"	"1"	"0"	"CTD_human"
"3251"	"HPRT1"	"0.518"	"0.793"	"C1845892"	"Lesch-Nyhan Syndrome, Neurologic Variant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1983"	"2017"	"21"	"13"	"CLINGEN;UNIPROT"
"3251"	"HPRT1"	"0.518"	"0.793"	"C1959897"	"Alcohol consumption during pregnancy"	"phenotype"		"Finding"	"0.30"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"3251"	"HPRT1"	"0.518"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3257"	"HPS1"	"0.63"	"0.586"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.42"	"1"	"1995"	"2006"	"4"	"0"	"GENOMICS_ENGLAND"
"3257"	"HPS1"	"0.63"	"0.586"	"C2931875"	"Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.62"	"1"	"1978"	"2015"	"0"	"25"	"CTD_human"
"3257"	"HPS1"	"0.63"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3260"	"HPV18I1"			"C3887947"	"HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3261"	"HPV18I2"	"1"		"C3887948"	"HUMAN PAPILLOMAVIRUS TYPE 18 INTEGRATION SITE 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0009492"	"Compartment syndromes"	"group"	"C05;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3263"	"HPX"	"0.648"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1993"	"1995"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"1"	"1983"	"2015"	"3"	"1"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.95"	"1983"	"2015"	"3"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9583333"	"1986"	"2011"	"4"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1988"	"2016"	"7"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.96875"	"1986"	"2016"	"2"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.53"	"1"	"1988"	"1991"	"1"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2008"	"2014"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007847"	"Malignant tumor of cervix"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"1"	"2"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1994"	"2016"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1994"	"2016"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.49"	"0.7142857"	"1988"	"2016"	"0"	"8"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.39"	"0.8888889"	"1987"	"2009"	"5"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1994"	"2016"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1986"	"2006"	"5"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1989"	"2016"	"2"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1994"	"2001"	"2"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1984"	"2015"	"1"	"2"	"CGI;UNIPROT"
"3265"	"HRAS"	"0.404"	"0.828"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2016"	"3"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1988"	"2015"	"2"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.8333333"	"1992"	"2006"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0030849"	"Penile Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1985"	"2011"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"1990"	"2018"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2007"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"0.8333333"	"1989"	"2016"	"7"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0037999"	"Splenic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2001"	"2016"	"2"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.44"	"0.5"	"1990"	"2016"	"1"	"6"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1994"	"2016"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2016"	"0"	"7"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"9"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.33"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0153470"	"Malignant neoplasm of spleen"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0153601"	"Malignant neoplasm of penis"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2003"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0206682"	"Follicular thyroid carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"1"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0206739"	"Epithelioid and spindle cell nevus"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2014"	"0"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"3265"	"HRAS"	"0.404"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2005"	"5"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0265329"	"Organoid Nevus Phakomatosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.51"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"3265"	"HRAS"	"0.404"	"0.828"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0302592"	"Cervix carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"0"	"1997"	"1997"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0334082"	"NEVUS, EPIDERMAL (disorder)"	"disease"	"C04"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"3"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0343114"	"Woolly hair nevus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3265"	"HRAS"	"0.404"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2008"	"5"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0346099"	"Nevus spilus"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0362030"	"Verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0473574"	"Inflammatory linear verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.54"	"1"	"1988"	"2013"	"1"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"0.9850746"	"1982"	"2018"	"22"	"16"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"3265"	"HRAS"	"0.404"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9642857"	"1986"	"2011"	"4"	"0"	"CGI;CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.70"	"1"	"1983"	"2016"	"0"	"2"	"CGI;UNIPROT"
"3265"	"HRAS"	"0.404"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2003"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2009"	"4"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1983"	"2016"	"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"0.37"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.875"	"1989"	"2016"	"4"	"7"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2001"	"2016"	"2"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1842036"	"GIANT PIGMENTED HAIRY NEVUS"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C1968782"	"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"2005"	"2017"	"19"	"10"	"CLINGEN;UNIPROT"
"3265"	"HRAS"	"0.404"	"0.828"	"C2145472"	"Urothelial Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9"	"1987"	"2016"	"4"	"6"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C2931658"	"Phacomatosis pigmentokeratotica"	"disease"	"C04;C17"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"3265"	"HRAS"	"0.404"	"0.828"	"C3179502"	"Linear Verrucous Epidermal Nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C3714644"	"Thymus Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3265"	"HRAS"	"0.404"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1983"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3265"	"HRAS"	"0.404"	"0.828"	"C3854181"	"Nevus sebaceous"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2018"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3265"	"HRAS"	"0.404"	"0.828"	"C4011754"	"Nevus, Keratinocytic, Nonepidermolytic"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3265"	"HRAS"	"0.404"	"0.828"	"C4225426"	"THYROID CANCER, NONMEDULLARY, 2"	"disease"		"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"1"	"UNIPROT"
"3267"	"AGFG1"	"0.642"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"1991"	"2003"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2004"	"2"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3269"	"HRH1"	"0.685"	"0.414"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3269"	"HRH1"	"0.685"	"0.414"	"C2607914"	"Allergic rhinitis (disorder)"	"disease"	"C08;C09;C20"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3270"	"HRC"	"0.735"	"0.379"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3270"	"HRC"	"0.735"	"0.379"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3270"	"HRC"	"0.735"	"0.379"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3273"	"HRG"	"0.69"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"3273"	"HRG"	"0.69"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"3273"	"HRG"	"0.69"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3273"	"HRG"	"0.69"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2009"	"1"	"0"	"CTD_human"
"3273"	"HRG"	"0.69"	"0.276"	"C2751090"	"Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1998"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3273"	"HRG"	"0.69"	"0.276"	"C2751091"	"Thrombophilia Due To Elevated Histidine-Rich Glycoprotein"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"1998"	"2001"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3274"	"HRH2"	"0.663"	"0.31"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"1997"	"2000"	"1"	"0"	"PSYGENET"
"3274"	"HRH2"	"0.663"	"0.31"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0242231"	"Coronary Stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3274"	"HRH2"	"0.663"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751674"	"Lymphangioleiomyomatosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2010"	"2"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3280"	"HES1"	"0.5"	"0.655"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3283"	"HSD3B1"	"0.656"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.51"		"2004"	"2012"	"1"	"0"	"CTD_human"
"3283"	"HSD3B1"	"0.656"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3283"	"HSD3B1"	"0.656"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3283"	"HSD3B1"	"0.656"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.48"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0342471"	"3 beta-Hydroxysteroid dehydrogenase deficiency"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.78"	"1"	"1979"	"2015"	"17"	"17"	"CTD_human;ORPHANET;UNIPROT"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C0848558"	"Hypospadias"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.42"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3284"	"HSD3B2"	"0.588"	"0.448"	"C2931782"	"Adrenal hyperplasia 2"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2013"	"3"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.9333333"	"2000"	"2015"	"2"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0311277"	"Obesity, Abdominal"	"phenotype"	"C18"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C1291245"	"Cortisone reductase deficiency"	"disease"	"C12;C13;C16;C17;C18;C19;C23"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3290"	"HSD11B1"	"0.577"	"0.655"	"C2936179"	"Obesity, Visceral"	"phenotype"	"C18"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.9"	"1995"	"2016"	"4"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0032962"	"Pregnancy Complications"	"group"	"C13"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C0342488"	"Mineralocorticoid Excess Syndrome, Apparent"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C2936861"	"Cortisol 11-beta-ketoreductase deficiency"	"disease"		"Disease or Syndrome"	"0.60"		"1985"	"2007"	"12"	"12"	"ORPHANET;UNIPROT"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3291"	"HSD11B2"	"0.551"	"0.724"	"C3887949"	"Apparent mineralocorticoid excess"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"0.9705882"	"1995"	"2015"	"16"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.40"	"0.8"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3292"	"HSD17B1"	"0.614"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0019269"	"Hermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0033804"	"Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"1996"	"2007"	"1"	"10"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0266362"	"Ambiguous Genitalia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0268296"	"17-Hydroxysteroid Dehydrogenase Deficiency"	"disease"	"C12;C13;C16;C17;C18;C19"	"Disease or Syndrome"	"0.75"	"1"	"1977"	"2016"	"7"	"16"	"CTD_human;ORPHANET;UNIPROT"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C1849695"	"Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"1994"	"2016"	"6"	"14"	"UNIPROT"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C2930618"	"Intersex Conditions"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3293"	"HSD17B3"	"0.667"	"0.276"	"C2930619"	"Sex Differentiation Disorders"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"3294"	"HSD17B2"	"0.672"	"0.241"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"0.5"	"2011"	"2013"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"GENOMICS_ENGLAND"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0282526"	"Hyperpipecolic Acidemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1997"	"2015"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0342870"	"Bifunctional peroxisomal enzyme deficiency"	"phenotype"	"C09;C10;C12;C13;C16;C19;C23"	"Pathologic Function"	"0.90"		"1998"	"2017"	"5"	"25"	"CTD_human;ORPHANET;UNIPROT"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.63"	"1"	"2010"	"2017"	"8"	"1"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0751708"	"Peroxisomal Dysfunction, General"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0751709"	"Peroxisomal Dysfunction, Multiple"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C0751710"	"Peroxisomal Dysfunction, Single"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3295"	"HSD17B4"	"0.55"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"2002"	"6"	"0"	"GENOMICS_ENGLAND"
"3297"	"HSF1"	"0.552"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"3297"	"HSF1"	"0.552"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"3297"	"HSF1"	"0.552"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3297"	"HSF1"	"0.552"	"0.655"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3297"	"HSF1"	"0.552"	"0.655"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3299"	"HSF4"	"0.69"	"0.31"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"	"0.8888889"	"2002"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3299"	"HSF4"	"0.69"	"0.31"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3299"	"HSF4"	"0.69"	"0.31"	"C1861821"	"CATARACT, MARNER TYPE"	"disease"	"C11"	"Disease or Syndrome"	"0.73"	"1"	"2006"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"3299"	"HSF4"	"0.69"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3299"	"HSF4"	"0.69"	"0.31"	"C3888417"	"CATARACT 5, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.50"		"2006"	"2012"	"1"	"4"	"UNIPROT"
"3300"	"DNAJB2"	"0.735"	"0.172"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2016"	"2"	"2"	"GENOMICS_ENGLAND"
"3300"	"DNAJB2"	"0.735"	"0.172"	"C3553989"	"SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3300"	"DNAJB2"	"0.735"	"0.172"	"C4015635"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"0"	"1"	"CTD_human"
"3301"	"DNAJA1"	"0.799"	"0.276"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2011"	"2"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2005"	"2014"	"5"	"0"	"PSYGENET"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"1999"	"2007"	"3"	"0"	"PSYGENET"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0085592"	"Heat Cramps"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0282507"	"Heat Stress Disorders"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"1999"	"2007"	"3"	"0"	"PSYGENET"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"3303"	"HSPA1A"	"0.516"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.6666667"	"2005"	"2014"	"3"	"0"	"PSYGENET"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"1999"	"2007"	"3"	"0"	"PSYGENET"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"1999"	"2007"	"3"	"0"	"PSYGENET"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3304"	"HSPA1B"	"0.514"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2005"	"2014"	"4"	"0"	"PSYGENET"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3305"	"HSPA1L"	"0.624"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3306"	"HSPA2"	"0.592"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3306"	"HSPA2"	"0.592"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3306"	"HSPA2"	"0.592"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"2"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"1996"	"2004"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C0564408"	"Manic mood"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"1996"	"2004"	"1"	"0"	"PSYGENET"
"3308"	"HSPA4"	"0.441"	"0.793"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0376544"	"Hematopoietic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3309"	"HSPA5"	"0.482"	"0.793"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.962963"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3309"	"HSPA5"	"0.482"	"0.793"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3310"	"HSPA6"	"0.834"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3310"	"HSPA6"	"0.834"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3310"	"HSPA6"	"0.834"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3312"	"HSPA8"	"0.575"	"0.621"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"PSYGENET"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"3313"	"HSPA9"	"0.567"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"3313"	"HSPA9"	"0.567"	"0.724"	"C4225180"	"EVEN-PLUS SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2016"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3313"	"HSPA9"	"0.567"	"0.724"	"C4225428"	"ANEMIA, SIDEROBLASTIC, 4"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"3313"	"HSPA9"	"0.567"	"0.724"	"C4274077"	"Autosomal recessive sideroblastic anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3313"	"HSPA9"	"0.567"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.49"	"1"	"2004"	"2017"	"1"	"1"	"GENOMICS_ENGLAND"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1847823"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.75"	"1"	"2001"	"2017"	"5"	"11"	"CTD_human;ORPHANET;UNIPROT"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3315"	"HSPB1"	"0.468"	"0.69"	"C2608087"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2001"	"2017"	"11"	"12"	"CTD_human;UNIPROT"
"3315"	"HSPB1"	"0.468"	"0.69"	"C3711384"	"Distal Hereditary Motor Neuropathy, Type II"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"3315"	"HSPB1"	"0.468"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0009178"	"Cocaine withdrawal"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0206180"	"Ki-1+ Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3320"	"HSP90AA1"	"0.453"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3321"	"IGSF3"	"0.857"	"0.138"	"C0022906"	"Lacrimal Duct Obstruction"	"phenotype"	"C11"	"Anatomical Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3321"	"IGSF3"	"0.857"	"0.138"	"C1281931"	"Obstruction of nasolacrimal duct"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"3321"	"IGSF3"	"0.857"	"0.138"	"C1835612"	"LACRIMAL DUCT DEFECT"	"phenotype"		"Finding"	"0.40"		"2014"	"2014"	"0"	"1"	"ORPHANET"
"3321"	"IGSF3"	"0.857"	"0.138"	"C1867060"	"Lacrimal Puncta, Absence of"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3326"	"HSP90AB1"	"0.663"	"0.552"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3326"	"HSP90AB1"	"0.663"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3326"	"HSP90AB1"	"0.663"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3326"	"HSP90AB1"	"0.663"	"0.552"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.6666667"	"2005"	"2017"	"2"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2002"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"3329"	"HSPD1"	"0.481"	"0.793"	"C1854467"	"Spastic paraplegia 13, autosomal dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.92"	"0.5"	"2002"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3329"	"HSPD1"	"0.481"	"0.793"	"C2677109"	"Leukodystrophy, Hypomyelinating, 4"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"2008"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3329"	"HSPD1"	"0.481"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3329"	"HSPD1"	"0.481"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3336"	"HSPE1"	"0.701"	"0.414"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3336"	"HSPE1"	"0.701"	"0.414"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3336"	"HSPE1"	"0.701"	"0.414"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3337"	"DNAJB1"	"0.676"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2004"	"2"	"0"	"PSYGENET"
"3337"	"DNAJB1"	"0.676"	"0.552"	"C0334287"	"Fibrolamellar Hepatocellular Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2014"	"2018"	"0"	"0"	"ORPHANET"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"1999"	"2002"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.97"	"1"	"1999"	"2016"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C1857100"	"Dyssegmental dysplasia"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.72"	"1"	"1999"	"2003"	"1"	"0"	"CTD_human;ORPHANET"
"3339"	"HSPG2"	"0.494"	"0.793"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2001"	"2"	"0"	"CTD_human"
"3339"	"HSPG2"	"0.494"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3340"	"NDST1"	"0.701"	"0.517"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3340"	"NDST1"	"0.701"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3340"	"NDST1"	"0.701"	"0.517"	"C4015283"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"3342"	"HTC2"	"0.447"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"3346"	"HTN1"	"0.799"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1999"	"2013"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0003578"	"Apnea"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"1993"	"2014"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2011"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1991"	"2016"	"1"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2016"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"3350"	"HTR1A"	"0.529"	"0.621"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C3553418"	"PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3350"	"HTR1A"	"0.529"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3350"	"HTR1A"	"0.529"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"2006"	"3"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2012"	"5"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2003"	"2004"	"2"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1998"	"2012"	"3"	"0"	"CTD_human;PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.8"	"2003"	"2012"	"5"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2011"	"4"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1998"	"2012"	"4"	"0"	"CTD_human;PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2003"	"2012"	"5"	"0"	"PSYGENET"
"3351"	"HTR1B"	"0.565"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3351"	"HTR1B"	"0.565"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3352"	"HTR1D"	"0.707"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3352"	"HTR1D"	"0.707"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1994"	"2012"	"2"	"0"	"PSYGENET"
"3352"	"HTR1D"	"0.707"	"0.276"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3352"	"HTR1D"	"0.707"	"0.276"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3352"	"HTR1D"	"0.707"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"1993"	"2006"	"1"	"0"	"PSYGENET"
"3355"	"HTR1F"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.5"	"1996"	"2004"	"2"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.59"	"1"	"1999"	"2014"	"5"	"0"	"CTD_human;PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0003125"	"Anorexia Nervosa"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8333333"	"1998"	"2010"	"0"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1991"	"2017"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.80"	"0.6"	"1997"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2009"	"3"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"5"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2004"	"2005"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.38"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9333333"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9259259"	"1992"	"2016"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2000"	"2017"	"5"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1997"	"2010"	"5"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"0.5"	"1998"	"2008"	"2"	"0"	"CTD_human;PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2009"	"3"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1997"	"2012"	"5"	"0"	"PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2013"	"3"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2000"	"2017"	"5"	"0"	"CTD_human;PSYGENET"
"3356"	"HTR2A"	"0.488"	"0.759"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"3356"	"HTR2A"	"0.488"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2005"	"2010"	"3"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2010"	"4"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2002"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2010"	"3"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3357"	"HTR2B"	"0.696"	"0.31"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.2"	"1999"	"2004"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"1996"	"2014"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9411765"	"1997"	"2017"	"2"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1996"	"2016"	"4"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2001"	"2015"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2016"	"3"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2001"	"2015"	"5"	"0"	"PSYGENET"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3358"	"HTR2C"	"0.579"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2001"	"2015"	"5"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2009"	"2013"	"4"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2013"	"2"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2012"	"5"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2012"	"4"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.5"	"2001"	"2013"	"2"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2017"	"2"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2010"	"2"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3359"	"HTR3A"	"0.639"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2017"	"2"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"4"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"4"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.25"	"2003"	"2013"	"4"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2011"	"2"	"0"	"PSYGENET"
"3360"	"HTR4"	"0.645"	"0.552"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3360"	"HTR4"	"0.645"	"0.552"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2010"	"2"	"0"	"PSYGENET"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2000"	"2015"	"4"	"0"	"PSYGENET"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"3361"	"HTR5A"	"0.785"	"0.103"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.3333333"	"2000"	"2010"	"3"	"0"	"PSYGENET"
"3361"	"HTR5A"	"0.785"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3362"	"HTR6"	"0.69"	"0.207"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8181818"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2010"	"3"	"0"	"PSYGENET"
"3362"	"HTR6"	"0.69"	"0.207"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3362"	"HTR6"	"0.69"	"0.207"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2015"	"2"	"0"	"PSYGENET"
"3363"	"HTR7"	"0.607"	"0.379"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2013"	"5"	"0"	"PSYGENET"
"3363"	"HTR7"	"0.607"	"0.379"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2004"	"2013"	"6"	"0"	"CTD_human;PSYGENET"
"3363"	"HTR7"	"0.607"	"0.379"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8333333"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3363"	"HTR7"	"0.607"	"0.379"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.39"	"0.8888889"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1992"	"2013"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0042345"	"Varicosity"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2014"	"3"	"0"	"CLINGEN"
"3371"	"TNC"	"0.475"	"0.759"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2014"	"3"	"0"	"CLINGEN"
"3371"	"TNC"	"0.475"	"0.759"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3371"	"TNC"	"0.475"	"0.759"	"C3810170"	"DEAFNESS, AUTOSOMAL DOMINANT 56"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"3373"	"HYAL1"	"0.648"	"0.483"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3373"	"HYAL1"	"0.648"	"0.483"	"C1291490"	"Hyaluronidase Deficiency"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.90"		"1996"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3373"	"HYAL1"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3375"	"IAPP"	"0.559"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3375"	"IAPP"	"0.559"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3375"	"IAPP"	"0.559"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9315068"	"1989"	"2018"	"2"	"0"	"CTD_human"
"3375"	"IAPP"	"0.559"	"0.655"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3375"	"IAPP"	"0.559"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3376"	"IARS"	"0.642"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3376"	"IARS"	"0.642"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3376"	"IARS"	"0.642"	"0.586"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3376"	"IARS"	"0.642"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3376"	"IARS"	"0.642"	"0.586"	"C4310720"	"GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"3381"	"IBSP"	"0.586"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3381"	"IBSP"	"0.586"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"3381"	"IBSP"	"0.586"	"0.621"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3381"	"IBSP"	"0.586"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3381"	"IBSP"	"0.586"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3381"	"IBSP"	"0.586"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2003"	"2015"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2014"	"3"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2015"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9583333"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0006267"	"Bronchiectasis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2015"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"0.8571429"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1993"	"2006"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2014"	"3"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.60"	"0.8888889"	"1999"	"2017"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"0.5"	"2002"	"2016"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.35"		"2002"	"2014"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.38"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.60"	"0.9411765"	"1992"	"2015"	"0"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.57"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2001"	"2013"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0035235"	"Respiratory Syncytial Virus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2002"	"2010"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2014"	"3"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.33"	"0.6666667"	"2000"	"2014"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2008"	"2017"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0282548"	"Leukostasis"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"2"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3383"	"ICAM1"	"0.386"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3384"	"ICAM2"	"0.707"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3384"	"ICAM2"	"0.707"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"3384"	"ICAM2"	"0.707"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3384"	"ICAM2"	"0.707"	"0.276"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3384"	"ICAM2"	"0.707"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3385"	"ICAM3"	"0.69"	"0.414"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3385"	"ICAM3"	"0.69"	"0.414"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3385"	"ICAM3"	"0.69"	"0.414"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3394"	"IRF8"	"0.579"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3394"	"IRF8"	"0.579"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2013"	"2018"	"0"	"0"	"UNIPROT"
"3394"	"IRF8"	"0.579"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3394"	"IRF8"	"0.579"	"0.724"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.38"	"0.875"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3394"	"IRF8"	"0.579"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"0"	"0"	"CGI"
"3394"	"IRF8"	"0.579"	"0.724"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3394"	"IRF8"	"0.579"	"0.724"	"C3808589"	"IMMUNODEFICIENCY 32A"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3394"	"IRF8"	"0.579"	"0.724"	"C4016741"	"IMMUNODEFICIENCY 32B"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"3397"	"ID1"	"0.572"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3397"	"ID1"	"0.572"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3398"	"ID2"	"0.592"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2013"	"2"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3399"	"ID3"	"0.621"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3400"	"ID4"	"0.627"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9508197"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3416"	"IDE"	"0.627"	"0.483"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8888889"	"2002"	"2012"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3416"	"IDE"	"0.627"	"0.483"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.50"	"1"	"2009"	"2018"	"0"	"2"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3417"	"IDH1"	"0.463"	"0.69"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C0014084"	"Enchondromatosis"	"disease"	"C05"	"Disease or Syndrome"	"0.68"	"1"	"2012"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9404145"	"2008"	"2018"	"8"	"2"	"CGI;CTD_human;UNIPROT"
"3417"	"IDH1"	"0.463"	"0.69"	"C0018916"	"Hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9411765"	"2009"	"2018"	"2"	"2"	"CGI;CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0024454"	"Maffucci Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.58"	"1"	"2012"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.925"	"2009"	"2016"	"1"	"1"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2014"	"0"	"0"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3417"	"IDH1"	"0.463"	"0.69"	"C0205788"	"Histiocytoid hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0205789"	"Hemangioma, Intramuscular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"1"	"2012"	"2017"	"1"	"0"	"CGI;CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"0"	"0"	"ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"5"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3417"	"IDH1"	"0.463"	"0.69"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.36"	"1"	"2010"	"2017"	"0"	"0"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2018"	"5"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0677608"	"Chorioangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9411765"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C0936248"	"Chondroma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2015"	"0"	"1"	"UNIPROT"
"3417"	"IDH1"	"0.463"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8421053"	"2008"	"2016"	"0"	"0"	"CGI"
"3417"	"IDH1"	"0.463"	"0.69"	"C1704356"	"Enchondroma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C1959588"	"Angioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.43"	"0.6666667"	"2012"	"2016"	"1"	"2"	"CTD_human"
"3417"	"IDH1"	"0.463"	"0.69"	"C3553958"	"METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"3417"	"IDH1"	"0.463"	"0.69"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2018"	"2"	"1"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3418"	"IDH2"	"0.469"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0007682"	"CNS disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0014084"	"Enchondromatosis"	"disease"	"C05"	"Disease or Syndrome"	"0.66"	"1"	"2012"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"1"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0018916"	"Hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0020295"	"Hydronephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0020981"	"Angioimmunoblastic Lymphadenopathy"	"disease"	"C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9487179"	"2010"	"2018"	"2"	"5"	"CGI;CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0024454"	"Maffucci Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.55"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9375"	"2009"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.43"	"0.6666667"	"2012"	"2018"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.75"	"2012"	"2016"	"2"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C0205788"	"Histiocytoid hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0205789"	"Hemangioma, Intramuscular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"1"	"2012"	"2017"	"1"	"0"	"CGI;CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0206725"	"Subependymal Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"1"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"0.8"	"2009"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2017"	"0"	"0"	"CGI"
"3418"	"IDH2"	"0.469"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0431108"	"Anaplastic Oligoastrocytoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C0677608"	"Chorioangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9333333"	"2009"	"2016"	"3"	"1"	"CTD_human;UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C0936248"	"Chondroma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"2"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2009"	"2016"	"2"	"1"	"CGI;UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C1704356"	"Enchondroma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C1842010"	"Glioma of Brain, Familial"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"1"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2017"	"2"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C1959588"	"Angioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C2746066"	"Combined D-2- and L-2-hydroxyglutaric aciduria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C2750850"	"GLIOMA SUSCEPTIBILITY 1"	"phenotype"		"Finding"	"0.30"		"2009"	"2016"	"2"	"1"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C3150909"	"D-2-HYDROXYGLUTARIC ACIDURIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2015"	"1"	"2"	"UNIPROT"
"3418"	"IDH2"	"0.469"	"0.655"	"C3152055"	"D-2-HYDROXYGLUTARIC ACIDURIA 1"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2010"	"2011"	"0"	"0"	"ORPHANET"
"3418"	"IDH2"	"0.469"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"3418"	"IDH2"	"0.469"	"0.655"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3418"	"IDH2"	"0.469"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3419"	"IDH3A"	"0.857"	"0.103"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3419"	"IDH3A"	"0.857"	"0.103"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3420"	"IDH3B"	"0.696"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3420"	"IDH3B"	"0.696"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.61"		"2008"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"3420"	"IDH3B"	"0.696"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3420"	"IDH3B"	"0.696"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3420"	"IDH3B"	"0.696"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3420"	"IDH3B"	"0.696"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3420"	"IDH3B"	"0.696"	"0.379"	"C2675496"	"Retinitis Pigmentosa 46"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"3423"	"IDS"	"0.616"	"0.655"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3423"	"IDS"	"0.616"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3423"	"IDS"	"0.616"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3423"	"IDS"	"0.616"	"0.655"	"C0026705"	"Mucopolysaccharidosis II"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"1991"	"2017"	"37"	"64"	"CLINGEN;CTD_human;UNIPROT"
"3423"	"IDS"	"0.616"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3423"	"IDS"	"0.616"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3423"	"IDS"	"0.616"	"0.655"	"C2718304"	"Sulfoiduronate Sulfatase Deficiency"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1992"	"2017"	"8"	"0"	"CLINGEN;CTD_human"
"3423"	"IDS"	"0.616"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3425"	"IDUA"	"0.558"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3425"	"IDUA"	"0.558"	"0.724"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"GENOMICS_ENGLAND"
"3425"	"IDUA"	"0.558"	"0.724"	"C0023786"	"Mucopolysaccharidosis I"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2018"	"5"	"16"	"CTD_human"
"3425"	"IDUA"	"0.558"	"0.724"	"C0026708"	"Mucopolysaccharidosis V"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.73"	"1"	"1993"	"2016"	"13"	"13"	"CTD_human;ORPHANET;UNIPROT"
"3425"	"IDUA"	"0.558"	"0.724"	"C0086431"	"Hurler-Scheie Syndrome"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2014"	"13"	"21"	"CTD_human;ORPHANET;UNIPROT"
"3425"	"IDUA"	"0.558"	"0.724"	"C0086795"	"Pfaundler-Hurler Syndrome"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.80"	"0.96875"	"1965"	"2016"	"19"	"39"	"CTD_human;ORPHANET;UNIPROT"
"3425"	"IDUA"	"0.558"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3425"	"IDUA"	"0.558"	"0.724"	"C2713321"	"alpha-L-Iduronidase Deficiency"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2015"	"5"	"0"	"CTD_human"
"3425"	"IDUA"	"0.558"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"3426"	"CFI"	"0.633"	"0.517"	"C0162739"	"HELLP Syndrome"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"3426"	"CFI"	"0.633"	"0.517"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.9411765"	"2009"	"2017"	"3"	"2"	"CTD_human"
"3426"	"CFI"	"0.633"	"0.517"	"C1832174"	"DOYNE HONEYCOMB RETINAL DYSTROPHY"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3426"	"CFI"	"0.633"	"0.517"	"C1852020"	"Malattia Leventinese"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3426"	"CFI"	"0.633"	"0.517"	"C1852021"	"Drusen, Radial, Autosomal Dominant"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3426"	"CFI"	"0.633"	"0.517"	"C2752039"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.60"		"2004"	"2010"	"4"	"12"	"ORPHANET;UNIPROT"
"3426"	"CFI"	"0.633"	"0.517"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.56"	"1"	"2004"	"2013"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3426"	"CFI"	"0.633"	"0.517"	"C3463916"	"Complement Factor I (C3 inactivator) deficiency"	"disease"	"C16"	"Disease or Syndrome"	"0.62"	"1"	"1996"	"2018"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3426"	"CFI"	"0.633"	"0.517"	"C3809523"	"MACULAR DEGENERATION, AGE-RELATED, 13"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"3429"	"IFI27"	"0.495"	"0.724"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"3430"	"IFI35"	"0.773"	"0.379"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3430"	"IFI35"	"0.773"	"0.379"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3430"	"IFI35"	"0.773"	"0.379"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3430"	"IFI35"	"0.773"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3431"	"SP110"	"0.743"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3431"	"SP110"	"0.743"	"0.448"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3431"	"SP110"	"0.743"	"0.448"	"C1856128"	"Hepatic venoocclusive disease with immunodeficiency"	"disease"	"C06;C14;C20"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2013"	"0"	"7"	"CTD_human;ORPHANET"
"3431"	"SP110"	"0.743"	"0.448"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3433"	"IFIT2"	"0.773"	"0.207"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3434"	"IFIT1"	"0.735"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3434"	"IFIT1"	"0.735"	"0.276"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"3434"	"IFIT1"	"0.735"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3437"	"IFIT3"	"0.752"	"0.414"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0001175"	"Acquired Immunodeficiency Syndrome"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0011993"	"Vipoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.9555556"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.85"	"1998"	"2017"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2005"	"3"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8333333"	"1984"	"2018"	"7"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0042237"	"Malignant Vaginal Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0042258"	"Vaginal Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0086768"	"Pancreatic Cholera"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"PSYGENET"
"3439"	"IFNA1"	"0.403"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3439"	"IFNA1"	"0.403"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9615385"	"2001"	"2016"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0000737"	"Abdominal Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"1991"	"2012"	"5"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2006"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2006"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2006"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2011"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0015672"	"Fatigue"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"1995"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0018681"	"Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"1989"	"2018"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.38"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2018"	"7"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1989"	"2008"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0021845"	"Intestinal Perforation"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2003"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1987"	"2003"	"5"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1989"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9090909"	"1992"	"2017"	"18"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0025287"	"Meningism"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1987"	"1997"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1997"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0028838"	"Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.37"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0033999"	"Pterygium"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0034734"	"Raynaud Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0034735"	"Raynaud Phenomenon"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0037650"	"Somatoform Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0038362"	"Stomatitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.35"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1996"	"2004"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0040264"	"Tinnitus"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0042170"	"Uveomeningoencephalitic Syndrome"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2011"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0042749"	"Viremia"	"disease"	"C02;C23"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2001"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0085593"	"Chills"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0086525"	"Lassitude"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0155305"	"Optic Neuropathy, Ischemic"	"disease"	"C10;C11;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0155533"	"Tinnitus, Subjective"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0155534"	"Tinnitus, Objective"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0206608"	"Flavivirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0206732"	"Epithelioid hemangioendothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2006"	"3"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0395955"	"Tinnitus, Noise Induced"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0395959"	"Tinnitus of Vascular Origin"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0423618"	"Throbbing Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0423623"	"Bilateral Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0474366"	"Generalized Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2006"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0520482"	"Somatization Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0521787"	"Tinnitus, Clicking"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0521788"	"Tinnitus, Leudet"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2018"	"7"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0524910"	"Hepatitis C, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.9741379"	"1992"	"2017"	"10"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751186"	"Orthostatic Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751187"	"Periorbital Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751189"	"Retro-Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751190"	"Sharp Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751192"	"Vertex Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751556"	"Tinnitus, Spontaneous Oto-Acoustic Emission"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751557"	"Tinnitus, Tensor Palatini Induced"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751558"	"Tinnitus, Tensor Tympani Induced"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751559"	"Pulsatile Tinnitus"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751711"	"Anterior Ischemic Optic Neuropathy"	"disease"	"C10;C11;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0751712"	"Posterior Ischemic Optic Neuropathy"	"disease"	"C10;C11;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0877781"	"Hemicrania"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1568868"	"Oral Mucositis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2012"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C3888418"	"Colicky Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3440"	"IFNA2"	"0.459"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3442"	"IFNA5"	"0.785"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3442"	"IFNA5"	"0.785"	"0.172"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3442"	"IFNA5"	"0.785"	"0.172"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3446"	"IFNA10"	"0.928"	"0.069"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3446"	"IFNA10"	"0.928"	"0.069"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3454"	"IFNAR1"	"0.594"	"0.69"	"C0042769"	"Virus Diseases"	"group"	"C02"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"3454"	"IFNAR1"	"0.594"	"0.69"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3454"	"IFNAR1"	"0.594"	"0.69"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3455"	"IFNAR2"	"0.636"	"0.621"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2014"	"0"	"0"	"CTD_human"
"3455"	"IFNAR2"	"0.636"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3455"	"IFNAR2"	"0.636"	"0.621"	"C4225252"	"IMMUNODEFICIENCY 45"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"3455"	"IFNAR2"	"0.636"	"0.621"	"C4225260"	"IMMUNODEFICIENCY 44"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0003463"	"Anus Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0004565"	"Melanoma, B16"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1990"	"2002"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1990"	"2002"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.55"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0009075"	"Melanoma, Cloudman S91"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0018598"	"Melanoma, Harding-Passey"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.36"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2017"	"2"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0025205"	"Melanoma, Experimental"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9679144"	"1996"	"2018"	"5"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0206735"	"Melanoma, Amelanotic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0279637"	"Anal carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1999"	"2016"	"5"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2008"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3456"	"IFNB1"	"0.466"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0001175"	"Acquired Immunodeficiency Syndrome"	"group"	"C02;C20"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2017"	"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0003615"	"Appendicitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0003869"	"Arthritis, Infectious"	"group"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.8846154"	"1990"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0003875"	"Arthritis, Viral"	"disease"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"0.974359"	"1988"	"2017"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0006272"	"Bronchiolitis Obliterans"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0008149"	"Chlamydia Infections"	"group"	"C01;C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8846154"	"1993"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3458"	"IFNG"	"0.323"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.92"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0015423"	"Eyelid Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2008"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1991"	"2002"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.40"	"0.9"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0018790"	"Cardiac Arrest"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"0.5"	"1998"	"2013"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1986"	"2013"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1986"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"0.8333333"	"1986"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.85"	"1992"	"2017"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.925"	"1995"	"2018"	"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"1"	"1986"	"2018"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0020625"	"Hyponatremia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0020951"	"Immune Complex Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.36"		"2003"	"2013"	"3"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1986"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023241"	"Legionnaires' Disease"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.38"	"0.8333333"	"2002"	"2016"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.38"	"1"	"1994"	"2012"	"3"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.39"	"0.8888889"	"1991"	"2018"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"1988"	"2012"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9152542"	"1983"	"2017"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2009"	"3"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0031154"	"Peritonitis"	"disease"	"C01;C06"	"Pathologic Function"	"0.33"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1986"	"1994"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1986"	"2010"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0035235"	"Respiratory Syncytial Virus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.36"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0036118"	"Salmonella Infections, Animal"	"group"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1997"	"2013"	"3"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0040954"	"Infection by Trichuris trichiura"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0041341"	"Tuberous Sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0085593"	"Chills"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"1986"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3458"	"IFNG"	"0.323"	"0.897"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2010"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1986"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.33"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0265319"	"Fibrous skin tumor of tuberous sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0343528"	"Pontiac Fever"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0348890"	"Aplastic anemia, idiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0549463"	"X-Linked Lymphoproliferative Disorder"	"disease"	"C15;C20"	"Neoplastic Process"	"0.33"	"0.6666667"	"1989"	"2012"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0600228"	"Cardiopulmonary Arrest"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0854119"	"Ruptured Appendicitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0857501"	"Acute schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2012"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1328252"	"Mucocutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"1995"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1449646"	"Primary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1449647"	"Secondary Peritonitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1986"	"1994"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1692886"	"Arthritis, Bacterial"	"group"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1860707"	"TUBEROUS SCLEROSIS 2 (disorder)"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1986"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1986"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1968689"	"Hyper-Immunoglobulin E Syndrome, Autosomal Recessive"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C2350875"	"Constrictive Bronchiolitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C2350876"	"Bronchiolitis, Exudative"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C2350988"	"Bronchiolitis, Proliferative"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C2936739"	"Hyper-Immunoglobulin E Syndrome, Autosomal Dominant"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C2939186"	"Disturbance in mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3458"	"IFNG"	"0.323"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3887645"	"Job Syndrome"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C3891815"	"Arthritis, Suppurative"	"disease"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3458"	"IFNG"	"0.323"	"0.897"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3458"	"IFNG"	"0.323"	"0.897"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0026919"	"Mycobacterium Infections, Nontuberculous"	"group"	"C01"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C1608955"	"Mycobacterium abscessus Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"1998"	"1998"	"0"	"1"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C2930924"	"Interferon gamma, receptor 1, deficiency"	"disease"	"C02"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C3266863"	"Atypical Mycobacteriosis, Familial"	"disease"	"C01"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C4011949"	"IMMUNODEFICIENCY 27A"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2018"	"13"	"5"	"UNIPROT"
"3459"	"IFNGR1"	"0.575"	"0.621"	"C4014863"	"IMMUNODEFICIENCY 27B"	"disease"		"Disease or Syndrome"	"0.60"		"1976"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"3460"	"IFNGR2"	"0.652"	"0.448"	"C4013947"	"IMMUNODEFICIENCY 28"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2013"	"4"	"4"	"CTD_human;UNIPROT"
"3475"	"IFRD1"	"0.752"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3475"	"IFRD1"	"0.752"	"0.207"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3475"	"IFRD1"	"0.752"	"0.207"	"C1843884"	"SPINOCEREBELLAR ATAXIA 18"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C1845446"	"Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia"	"disease"	"C05;C07;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3476"	"IGBP1"	"0.696"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3476"	"IGBP1"	"0.696"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3479"	"IGF1"	"0.355"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0001206"	"Acromegaly"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.40"	"0.8571429"	"1991"	"2018"	"4"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2016"	"2"	"0"	"PSYGENET"
"3479"	"IGF1"	"0.355"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9625"	"1986"	"2018"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0010034"	"Corneal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2007"	"2015"	"3"	"0"	"PSYGENET"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1997"	"2015"	"5"	"0"	"PSYGENET"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1997"	"2015"	"5"	"0"	"PSYGENET"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.39"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"1993"	"2013"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2007"	"3"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1998"	"1999"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3479"	"IGF1"	"0.355"	"0.828"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.42"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1998"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.31"	"0"	"1992"	"2004"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.33"	"1"	"1992"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"3"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0034013"	"Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1992"	"1992"	"1"	"0"	"PSYGENET"
"3479"	"IGF1"	"0.355"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9375"	"1993"	"2016"	"3"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"3479"	"IGF1"	"0.355"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9634146"	"1986"	"2018"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C1837475"	"Insulin-Like Growth Factor I Deficiency"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.70"	"0.9"	"1993"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"3479"	"IGF1"	"0.355"	"0.828"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2004"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"3479"	"IGF1"	"0.355"	"0.828"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3479"	"IGF1"	"0.355"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.52"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2011"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2009"	"2010"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.35"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2003"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9876543"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C1849157"	"Resistance to Insulin-Like Growth Factor I"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.77"	"0.8571429"	"2003"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3480"	"IGF1R"	"0.433"	"0.828"	"C1849158"	"Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2003"	"2016"	"3"	"4"	"UNIPROT"
"3480"	"IGF1R"	"0.433"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3480"	"IGF1R"	"0.433"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3480"	"IGF1R"	"0.433"	"0.828"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.55"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.40"	"0.971831"	"1986"	"2016"	"2"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9166667"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1991"	"2012"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2013"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.42"		"2002"	"2008"	"2"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0020224"	"Polyhydramnios"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8"	"1990"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.50"	"0.9104478"	"1985"	"2015"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"0.5"	"2008"	"2017"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0032045"	"Placenta Disorders"	"group"	"C13"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2007"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2015"	"2"	"0"	"PSYGENET"
"3481"	"IGF2"	"0.399"	"0.828"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"1"	"2003"	"2018"	"2"	"2"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"3481"	"IGF2"	"0.399"	"0.828"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9411765"	"1989"	"2013"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.50"	"0.9333333"	"1993"	"2016"	"2"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"1988"	"2008"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0332890"	"Congenital hemihypertrophy"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"3481"	"IGF2"	"0.399"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1988"	"2003"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0678807"	"prenatal alcohol exposure"	"phenotype"		"Finding"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3481"	"IGF2"	"0.399"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C1856184"	"HEMIHYPERPLASIA, ISOLATED"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3481"	"IGF2"	"0.399"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9272727"	"1989"	"2018"	"2"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3481"	"IGF2"	"0.399"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3481"	"IGF2"	"0.399"	"0.828"	"C4225307"	"GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2003"	"2018"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3482"	"IGF2R"	"0.545"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"1"	"1995"	"2014"	"1"	"2"	"CGI;CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.40"		"2004"	"2008"	"2"	"0"	"CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3483"	"IGFALS"	"0.565"	"0.69"	"C3900122"	"Acid-Labile Subunit Deficiency"	"phenotype"		"Laboratory or Test Result"	"0.61"	"1"	"2006"	"2015"	"7"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.37"	"0.8333333"	"2003"	"2012"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"0"	"1994"	"2016"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.32"	"0.5"	"2010"	"2012"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3484"	"IGFBP1"	"0.538"	"0.621"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.6666667"	"2005"	"2007"	"3"	"0"	"PSYGENET"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3485"	"IGFBP2"	"0.521"	"0.69"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9411765"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2005"	"2011"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"3"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9268293"	"1996"	"2016"	"3"	"0"	"CTD_human"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9411765"	"2003"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"3486"	"IGFBP3"	"0.464"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3488"	"IGFBP5"	"0.58"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"		"2003"	"2010"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3489"	"IGFBP6"	"0.633"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"0.8888889"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3490"	"IGFBP7"	"0.525"	"0.655"	"C3280205"	"RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3491"	"CYR61"	"0.514"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.38"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3491"	"CYR61"	"0.514"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2007"	"2017"	"1"	"0"	"CTD_human"
"3491"	"CYR61"	"0.514"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"3491"	"CYR61"	"0.514"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3492"	"IGH"	"0.507"	"0.621"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.36"	"0.8333333"	"2006"	"2014"	"0"	"0"	"ORPHANET"
"3492"	"IGH"	"0.507"	"0.621"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9245283"	"1990"	"2017"	"0"	"0"	"ORPHANET"
"3492"	"IGH"	"0.507"	"0.621"	"C0242647"	"Mucosa-Associated Lymphoid Tissue Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2014"	"0"	"0"	"ORPHANET"
"3492"	"IGH"	"0.507"	"0.621"	"C0555202"	"Malignant lymphoma - lymphocytic, intermediate differentiation"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3492"	"IGH"	"0.507"	"0.621"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"0.9230769"	"1991"	"2017"	"0"	"0"	"ORPHANET"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0027121"	"Myositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0158353"	"Myositis, Infectious"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0544796"	"Myositis, Proliferative"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0751356"	"Idiopathic Inflammatory Myopathies"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0751357"	"Myositis, Focal"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3500"	"IGHG1"	"0.707"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3500"	"IGHG1"	"0.707"	"0.345"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0027121"	"Myositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0158353"	"Myositis, Infectious"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0162539"	"IgG Deficiency disorder"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0544796"	"Myositis, Proliferative"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0751356"	"Idiopathic Inflammatory Myopathies"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3501"	"IGHG2"	"0.762"	"0.172"	"C0751357"	"Myositis, Focal"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3501"	"IGHG2"	"0.762"	"0.172"	"C3279824"	"Kappa-Chain Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3507"	"IGHM"	"0.672"	"0.517"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"3507"	"IGHM"	"0.672"	"0.517"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3507"	"IGHM"	"0.672"	"0.517"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"0"	"0"	"ORPHANET"
"3508"	"IGHMBP2"	"0.672"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"3508"	"IGHMBP2"	"0.672"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2018"	"1"	"6"	"GENOMICS_ENGLAND"
"3508"	"IGHMBP2"	"0.672"	"0.517"	"C1858517"	"SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1"	"disease"	"C08;C10;C16"	"Disease or Syndrome"	"1.00"	"0.9259259"	"1975"	"2018"	"7"	"32"	"CTD_human;ORPHANET;UNIPROT"
"3508"	"IGHMBP2"	"0.672"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3508"	"IGHMBP2"	"0.672"	"0.517"	"C4015349"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S"	"disease"		"Disease or Syndrome"	"0.70"		"1975"	"2017"	"1"	"18"	"CTD_human;ORPHANET;UNIPROT"
"3514"	"IGKC"	"0.707"	"0.345"	"C0013374"	"Dysgammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0027121"	"Myositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0158353"	"Myositis, Infectious"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0162539"	"IgG Deficiency disorder"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3514"	"IGKC"	"0.707"	"0.345"	"C0544796"	"Myositis, Proliferative"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0751356"	"Idiopathic Inflammatory Myopathies"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C0751357"	"Myositis, Focal"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3514"	"IGKC"	"0.707"	"0.345"	"C3279824"	"Kappa-Chain Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.60"		"1985"	"1985"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3516"	"RBPJ"	"0.577"	"0.655"	"C3553748"	"ADAMS-OLIVER SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"3516"	"RBPJ"	"0.577"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"3543"	"IGLL1"	"0.727"	"0.414"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"3543"	"IGLL1"	"0.727"	"0.414"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3543"	"IGLL1"	"0.727"	"0.414"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3543"	"IGLL1"	"0.727"	"0.414"	"C3150750"	"AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"1998"	"1"	"2"	"UNIPROT"
"3547"	"IGSF1"	"0.685"	"0.379"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"		"2013"	"2017"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3547"	"IGSF1"	"0.685"	"0.379"	"C0039584"	"Testicular Diseases"	"group"	"C12;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3547"	"IGSF1"	"0.685"	"0.379"	"C0342200"	"Endemic Cretinism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3547"	"IGSF1"	"0.685"	"0.379"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2013"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"3547"	"IGSF1"	"0.685"	"0.379"	"C1578691"	"Myxedema, Congenital"	"disease"	"C05;C16;C19"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3547"	"IGSF1"	"0.685"	"0.379"	"C3550963"	"HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3547"	"IGSF1"	"0.685"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"3549"	"IHH"	"0.572"	"0.621"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"3549"	"IHH"	"0.572"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3549"	"IHH"	"0.572"	"0.621"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C1843096"	"Acrocapitofemoral Dysplasia"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"2003"	"2010"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3549"	"IHH"	"0.572"	"0.621"	"C1862151"	"BRACHYDACTYLY, TYPE A1 (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.97"	"0.8571429"	"1963"	"2012"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3549"	"IHH"	"0.572"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3549"	"IHH"	"0.572"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3551"	"IKBKB"	"0.57"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2013"	"0"	"0"	"UNIPROT"
"3551"	"IKBKB"	"0.57"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2009"	"2016"	"1"	"0"	"CTD_human"
"3551"	"IKBKB"	"0.57"	"0.621"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3551"	"IKBKB"	"0.57"	"0.621"	"C0857007"	"Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3551"	"IKBKB"	"0.57"	"0.621"	"C1565885"	"Direct Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3551"	"IKBKB"	"0.57"	"0.621"	"C1565886"	"Indirect Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3551"	"IKBKB"	"0.57"	"0.621"	"C3810043"	"IMMUNODEFICIENCY 15"	"disease"		"Disease or Syndrome"	"0.60"		"1999"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"3552"	"IL1A"	"0.366"	"0.931"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2005"	"2010"	"1"	"0"	"PSYGENET"
"3552"	"IL1A"	"0.366"	"0.931"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0002631"	"Infection of amniotic cavity"	"disease"	"C13;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0008495"	"Chorioamnionitis"	"phenotype"	"C13;C16"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"1999"	"2017"	"5"	"0"	"PSYGENET"
"3552"	"IL1A"	"0.366"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"1999"	"2017"	"5"	"0"	"PSYGENET"
"3552"	"IL1A"	"0.366"	"0.931"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.32"	"0"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0022541"	"Kearns-Sayre syndrome"	"disease"	"C05;C10;C11;C14;C18;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.10"	"0.8333333"	"1999"	"2016"	"2"	"0"	"PSYGENET"
"3552"	"IL1A"	"0.366"	"0.931"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0085655"	"Polymyositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"0"	"1994"	"2007"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"0"	"2013"	"2018"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0206637"	"Mesenchymal Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0263984"	"Polymyositis Ossificans"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0343755"	"HIV Wasting Syndrome"	"disease"	"C02;C18;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0554591"	"Polymyositis, Idiopathic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2007"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C1275592"	"Funisitis (disorder)"	"disease"	"C13;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3552"	"IL1A"	"0.366"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3553"	"IL1B"	"0.312"	"0.931"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2005"	"2010"	"4"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9464286"	"1989"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9621212"	"1989"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9428571"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006287"	"Bronchopulmonary Dysplasia"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2015"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1997"	"2007"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.57"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8695652"	"1992"	"2015"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2013"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.75"	"1993"	"2012"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.59"	"0.8"	"1999"	"2017"	"5"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1999"	"2017"	"5"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.37"	"0.8333333"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.32"	"0"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"2014"	"5"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0017154"	"Gastritis, Atrophic"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2002"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2018"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1993"	"2012"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.58"	"0.8571429"	"1994"	"2016"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"		"1991"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1991"	"2005"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.37"		"1999"	"2017"	"9"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0022541"	"Kearns-Sayre syndrome"	"disease"	"C05;C10;C11;C14;C18;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2012"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023380"	"Lethargy"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2004"	"2017"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9275362"	"2000"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0024799"	"Marginal ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.7727273"	"1997"	"2016"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2004"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9230769"	"1995"	"2016"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2000"	"2000"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"0.9736842"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"1999"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0030920"	"Peptic Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2010"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.9545455"	"1990"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2000"	"2010"	"5"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8571429"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"0.7777778"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2014"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.37"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"1994"	"2015"	"5"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0085655"	"Polymyositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.32"	"0.5"	"1994"	"2012"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2008"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0263984"	"Polymyositis Ossificans"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0343755"	"HIV Wasting Syndrome"	"disease"	"C02;C18;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0554591"	"Polymyositis, Idiopathic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2013"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1994"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2011"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2012"	"4"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"1994"	"2015"	"5"	"0"	"PSYGENET"
"3553"	"IL1B"	"0.312"	"0.931"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2017"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"3"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"6"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.39"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"2"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3553"	"IL1B"	"0.312"	"0.931"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3553"	"IL1B"	"0.312"	"0.931"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.40"		"2011"	"2013"	"1"	"14"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3554"	"IL1R1"	"0.564"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3556"	"IL1RAP"	"0.72"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3556"	"IL1RAP"	"0.72"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3556"	"IL1RAP"	"0.72"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3556"	"IL1RAP"	"0.72"	"0.483"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9534884"	"1992"	"2018"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"2"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2013"	"2"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"0"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0015230"	"Exanthema"	"phenotype"	"C17"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2004"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.37"	"0.7142857"	"1996"	"2010"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8125"	"2003"	"2015"	"0"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.7857143"	"1997"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2011"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0027121"	"Myositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1992"	"2011"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.38"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2006"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0036429"	"Sclerosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"2006"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2008"	"0"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0158353"	"Myositis, Infectious"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"2"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0524988"	"Schnitzler Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0544796"	"Myositis, Proliferative"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751356"	"Idiopathic Inflammatory Myopathies"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2001"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751357"	"Myositis, Focal"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"1999"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C2675112"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C2748507"	"INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.64"	"1"	"2009"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"3557"	"IL1RN"	"0.398"	"0.897"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2011"	"4"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3557"	"IL1RN"	"0.398"	"0.897"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"3558"	"IL2"	"0.373"	"0.931"	"C0001175"	"Acquired Immunodeficiency Syndrome"	"group"	"C02;C20"	"Disease or Syndrome"	"0.35"	"1"	"1986"	"1999"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0004093"	"Asthenia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1987"	"2018"	"2"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"1"	"1987"	"2018"	"2"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.35"	"1"	"1984"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1987"	"2009"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2010"	"2"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"0.9210526"	"1986"	"2014"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"1993"	"2009"	"4"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9736842"	"1983"	"2016"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9583333"	"1982"	"2017"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2009"	"3"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2015"	"22"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1987"	"2012"	"3"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"1996"	"2014"	"3"	"0"	"PSYGENET"
"3558"	"IL2"	"0.373"	"0.931"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3558"	"IL2"	"0.373"	"0.931"	"C0042237"	"Malignant Vaginal Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0042258"	"Vaginal Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1984"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"1991"	"2009"	"3"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0242594"	"Residual Cancer"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0242596"	"Neoplasm, Residual"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"1992"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1993"	"1998"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0543478"	"Residual Tumor"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"1992"	"2014"	"4"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1992"	"2003"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1984"	"1990"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"1995"	"2006"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3558"	"IL2"	"0.373"	"0.931"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2016"	"1"	"1"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"1"	"1992"	"2016"	"3"	"2"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.46"	"1"	"2000"	"2018"	"1"	"6"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"0.95"	"1984"	"2017"	"3"	"3"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"0"	"2000"	"2004"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"1"	"1994"	"2018"	"4"	"6"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"3"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2014"	"4"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3559"	"IL2RA"	"0.419"	"0.828"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C1853392"	"Interleukin 2 Receptor, Alpha, Deficiency of"	"disease"	"C20"	"Disease or Syndrome"	"0.71"	"0"	"1997"	"2014"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3559"	"IL2RA"	"0.419"	"0.828"	"C1866040"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 10"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3559"	"IL2RA"	"0.419"	"0.828"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"3559"	"IL2RA"	"0.419"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3559"	"IL2RA"	"0.419"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2014"	"2"	"2"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3560"	"IL2RB"	"0.545"	"0.724"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3560"	"IL2RB"	"0.545"	"0.724"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3561"	"IL2RG"	"0.551"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3561"	"IL2RG"	"0.551"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3561"	"IL2RG"	"0.551"	"0.69"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3561"	"IL2RG"	"0.551"	"0.69"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3561"	"IL2RG"	"0.551"	"0.69"	"C1279481"	"X-Linked Combined Immunodeficiency Diseases"	"disease"	"C16;C20"	"Disease or Syndrome"	"0.80"	"0.9803922"	"1985"	"2017"	"13"	"25"	"CTD_human;ORPHANET;UNIPROT"
"3561"	"IL2RG"	"0.551"	"0.69"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"0"	"0"	"ORPHANET"
"3562"	"IL3"	"0.523"	"0.724"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"1994"	"2003"	"2"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2007"	"2015"	"5"	"0"	"PSYGENET"
"3562"	"IL3"	"0.523"	"0.724"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3562"	"IL3"	"0.523"	"0.724"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3563"	"IL3RA"	"0.663"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2009"	"3"	"0"	"PSYGENET"
"3563"	"IL3RA"	"0.663"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3565"	"IL4"	"0.364"	"0.931"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.9340659"	"1992"	"2017"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2015"	"3"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"0.75"	"2000"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.60"	"0.969697"	"1994"	"2017"	"3"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2005"	"2010"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.31"		"2005"	"2011"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2003"	"2013"	"3"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1988"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.875"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0032230"	"Pleural Rub"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2003"	"2014"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0034642"	"Rales"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0035234"	"Respiratory Sounds"	"phenotype"	"C23"	"Clinical Attribute"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.56"	"1"	"1992"	"2009"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0035508"	"Rhonchi"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.4"	"2003"	"2012"	"5"	"0"	"PSYGENET"
"3565"	"IL4"	"0.364"	"0.931"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3565"	"IL4"	"0.364"	"0.931"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0038450"	"Stridor"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0041307"	"Tuberculosis, Bovine"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0043144"	"Wheezing"	"phenotype"	"C23"	"Sign or Symptom"	"0.34"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2009"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2008"	"3"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.32"		"2004"	"2016"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2011"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"0"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3565"	"IL4"	"0.364"	"0.931"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3566"	"IL4R"	"0.512"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.9677419"	"1991"	"2016"	"2"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1994"	"2008"	"2"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1990"	"2016"	"2"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1991"	"2000"	"2"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2008"	"2"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3567"	"IL5"	"0.463"	"0.828"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3568"	"IL5RA"	"0.69"	"0.552"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2012"	"2"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9786096"	"1989"	"2018"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9555556"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.50"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"2"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9615385"	"1998"	"2018"	"4"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1999"	"2008"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0006435"	"Chemical Burns"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.8571429"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2003"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9333333"	"1989"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007772"	"Intracranial Arteriovenous Malformation"	"disease"	"C10;C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2007"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8965517"	"1992"	"2018"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.6"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1995"	"2018"	"5"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.6"	"1995"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"1995"	"2005"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0017531"	"Angiolymphoid hyperplasia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2007"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0018681"	"Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"0.5"	"1995"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2018"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020500"	"Hyperoxaluria"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020503"	"Hyperparathyroidism, Secondary"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2001"	"2016"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.37"		"2001"	"2016"	"11"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"0.9310345"	"1992"	"2018"	"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0022876"	"Premature Obstetric Labor"	"phenotype"	"C13"	"Pathologic Function"	"0.39"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2012"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0025290"	"Aseptic Meningitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"0.9458333"	"1990"	"2018"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8974359"	"1995"	"2017"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9545455"	"1992"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.9512195"	"2001"	"2018"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0028838"	"Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.34"	"0.75"	"1995"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.9375"	"1993"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0032963"	"Pregnancy Complications, Cardiovascular"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2015"	"5"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2015"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2005"	"2012"	"5"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0036220"	"Kaposi Sarcoma"	"disease"	"C02;C04"	"Neoplastic Process"	"0.40"	"0.9677419"	"1992"	"2016"	"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.7272727"	"1994"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.34"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.875"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.57"	"1"	"1994"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0085655"	"Polymyositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3569"	"IL6"	"0.287"	"0.966"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.32"		"2005"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0162848"	"Lichenoid Eruptions"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"0.75"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0239981"	"Hypoalbuminemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.96875"	"1991"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0263984"	"Polymyositis Ossificans"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C0343755"	"HIV Wasting Syndrome"	"disease"	"C02;C18;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2018"	"5"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0423618"	"Throbbing Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0423623"	"Bilateral Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2013"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0474366"	"Generalized Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.8571429"	"2004"	"2018"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.35"	"0.75"	"1995"	"2004"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0554591"	"Polymyositis, Idiopathic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9615385"	"1998"	"2018"	"4"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.32"	"1"	"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751008"	"Intracranial Arteriovenous Malformation, Ruptured"	"disease"	"C10;C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751186"	"Orthostatic Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751187"	"Periorbital Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751189"	"Retro-Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751190"	"Sharp Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751192"	"Vertex Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0877781"	"Hemicrania"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2009"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0917804"	"Arteriovenous Malformations, Cerebral"	"group"	"C10;C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2004"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.9615385"	"1993"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2009"	"4"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1994"	"2016"	"5"	"0"	"PSYGENET"
"3569"	"IL6"	"0.287"	"0.966"	"C1298681"	"Oxalosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1384600"	"Systemic onset juvenile chronic arthritis"	"disease"		"Disease or Syndrome"	"0.38"	"1"	"1998"	"2016"	"0"	"0"	"ORPHANET"
"3569"	"IL6"	"0.287"	"0.966"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9230769"	"1991"	"2016"	"4"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1858558"	"Rheumatoid Arthritis, Systemic Juvenile"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9626866"	"1988"	"2017"	"4"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"1994"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2008"	"3"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.38"	"1"	"1993"	"2013"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2005"	"2"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3569"	"IL6"	"0.287"	"0.966"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3569"	"IL6"	"0.287"	"0.966"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2016"	"2"	"1"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"3570"	"IL6R"	"0.496"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3570"	"IL6R"	"0.496"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3570"	"IL6R"	"0.496"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.56"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;UNIPROT"
"3572"	"IL6ST"	"0.522"	"0.759"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3572"	"IL6ST"	"0.522"	"0.759"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3574"	"IL7"	"0.503"	"0.724"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"1"	"2"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2017"	"4"	"2"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"4"	"0"	"CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C1837028"	"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.70"		"1998"	"2016"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3575"	"IL7R"	"0.538"	"0.724"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.56"	"1"	"2011"	"2016"	"1"	"0"	"CGI;CTD_human"
"3575"	"IL7R"	"0.538"	"0.724"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"3575"	"IL7R"	"0.538"	"0.724"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0002965"	"Angina, Unstable"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9824561"	"1990"	"2016"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.39"	"0.75"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9818182"	"2001"	"2018"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.33"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8666667"	"1999"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1994"	"2016"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"5"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0014869"	"Peptic Esophagitis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0015404"	"Eye Infections, Bacterial"	"group"	"C01;C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0017168"	"Gastroesophageal reflux disease"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2005"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0019187"	"Hepatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"2003"	"2015"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0022568"	"Keratitis"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.9130435"	"2000"	"2017"	"3"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0030200"	"Pain, Intractable"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0030805"	"Bullous pemphigoid"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0032768"	"Postherpetic neuralgia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"2007"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0038160"	"Staphylococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1992"	"2011"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0086666"	"Myocardial Preinfarction Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0162848"	"Lichenoid Eruptions"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2008"	"2015"	"5"	"0"	"PSYGENET"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9666667"	"2000"	"2015"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0524610"	"Chronic Alcoholic Hepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9824561"	"2001"	"2018"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.9444444"	"1999"	"2017"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1318973"	"Staphylococcus aureus infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2017"	"3"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"1999"	"2"	"0"	"CTD_human"
"3576"	"CXCL8"	"0.342"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3577"	"CXCR1"	"0.555"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3577"	"CXCR1"	"0.555"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2015"	"0"	"0"	"CTD_human"
"3577"	"CXCR1"	"0.555"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3578"	"IL9"	"0.53"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3578"	"IL9"	"0.53"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3578"	"IL9"	"0.53"	"0.69"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3578"	"IL9"	"0.53"	"0.69"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0024894"	"Mastitis"	"disease"	"C13;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C3850148"	"Vascular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3579"	"CXCR2"	"0.482"	"0.828"	"C3852953"	"Pulmonary Arterial Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3581"	"IL9R"	"0.72"	"0.448"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2008"	"2011"	"3"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C0003615"	"Appendicitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.954023"	"1994"	"2018"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.70"	"0.96"	"2007"	"2018"	"2"	"3"	"CTD_human;ORPHANET"
"3586"	"IL10"	"0.32"	"0.931"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"0.9210526"	"1995"	"2017"	"4"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9047619"	"1995"	"2017"	"2"	"1"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9454545"	"1996"	"2018"	"1"	"1"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2016"	"1"	"1"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0014324"	"Entamoebiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0014356"	"Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.40"	"0.9333333"	"1998"	"2013"	"0"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"0.969697"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0020877"	"Ileitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.35"		"2001"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.70"	"0.9868421"	"1995"	"2018"	"2"	"1"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0022104"	"Irritable Bowel Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2016"	"3"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2008"	"9"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.9777778"	"1994"	"2017"	"2"	"1"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9642857"	"1997"	"2018"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.7272727"	"2001"	"2010"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"3"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0033581"	"prostatitis"	"disease"	"C12"	"Disease or Syndrome"	"0.50"		"2002"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.32"		"2002"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"4"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"0.8846154"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.6666667"	"2002"	"2014"	"2"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"0.9189189"	"2000"	"2017"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9473684"	"2001"	"2018"	"3"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0854119"	"Ruptured Appendicitis"	"disease"	"C01;C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.04"	"0.75"	"2002"	"2014"	"2"	"0"	"PSYGENET"
"3586"	"IL10"	"0.32"	"0.931"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1720795"	"Acute Bacterial Prostatitis"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1720796"	"Asymptomatic Inflammatory Prostatitis"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1720797"	"Chronic Bacterial Prostatitis"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C1723764"	"Chronic Prostatitis with Chronic Pelvic Pain Syndrome"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1995"	"2007"	"2"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3586"	"IL10"	"0.32"	"0.931"	"C4316791"	"Entamoeba histolytica Infection"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3586"	"IL10"	"0.32"	"0.931"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3587"	"IL10RA"	"0.652"	"0.621"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3587"	"IL10RA"	"0.652"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"3587"	"IL10RA"	"0.652"	"0.621"	"C2751053"	"INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2009"	"2015"	"3"	"5"	"CTD_human;UNIPROT"
"3588"	"IL10RB"	"0.676"	"0.414"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3588"	"IL10RB"	"0.676"	"0.414"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2015"	"0"	"0"	"CTD_human"
"3588"	"IL10RB"	"0.676"	"0.414"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3588"	"IL10RB"	"0.676"	"0.414"	"C2675508"	"INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2009"	"2011"	"0"	"2"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0010692"	"Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3589"	"IL11"	"0.523"	"0.69"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3589"	"IL11"	"0.523"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3589"	"IL11"	"0.523"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3590"	"IL11RA"	"0.69"	"0.414"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"3590"	"IL11RA"	"0.69"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3590"	"IL11RA"	"0.69"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"3590"	"IL11RA"	"0.69"	"0.414"	"C3280073"	"CRANIOSYNOSTOSIS AND DENTAL ANOMALIES"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2011"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3590"	"IL11RA"	"0.69"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3592"	"IL12A"	"0.547"	"0.759"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"3592"	"IL12A"	"0.547"	"0.759"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.63"	"1"	"2009"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"3592"	"IL12A"	"0.547"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2010"	"2012"	"1"	"3"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3592"	"IL12A"	"0.547"	"0.759"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2016"	"3"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2017"	"2"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"3"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.8918919"	"2003"	"2018"	"3"	"2"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3593"	"IL12B"	"0.506"	"0.793"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0039263"	"Takayasu Arteritis"	"disease"	"C14;C17"	"Disease or Syndrome"	"0.38"	"1"	"2006"	"2018"	"0"	"0"	"ORPHANET"
"3593"	"IL12B"	"0.506"	"0.793"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3593"	"IL12B"	"0.506"	"0.793"	"C4013948"	"IMMUNODEFICIENCY 29"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"3594"	"IL12RB1"	"0.588"	"0.621"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3594"	"IL12RB1"	"0.588"	"0.621"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"3594"	"IL12RB1"	"0.588"	"0.621"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3594"	"IL12RB1"	"0.588"	"0.621"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"3594"	"IL12RB1"	"0.588"	"0.621"	"C4013949"	"IMMUNODEFICIENCY 30"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"1998"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3595"	"IL12RB2"	"0.642"	"0.621"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3595"	"IL12RB2"	"0.642"	"0.621"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3595"	"IL12RB2"	"0.642"	"0.621"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3595"	"IL12RB2"	"0.642"	"0.621"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.70"	"0.971831"	"1995"	"2018"	"1"	"2"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.70"	"1"	"1996"	"2017"	"2"	"4"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.40"		"2011"	"2017"	"1"	"2"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2013"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0025568"	"Metaplasia"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"0.8"	"2002"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.7058824"	"1997"	"2016"	"2"	"2"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2017"	"2"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2013"	"2"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C2607914"	"Allergic rhinitis (disorder)"	"disease"	"C08;C09;C20"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1999"	"2018"	"0"	"0"	"CTD_human"
"3596"	"IL13"	"0.421"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"0.8"	"2002"	"2011"	"1"	"0"	"CTD_human"
"3598"	"IL13RA2"	"0.604"	"0.517"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3598"	"IL13RA2"	"0.604"	"0.517"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3598"	"IL13RA2"	"0.604"	"0.517"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3598"	"IL13RA2"	"0.604"	"0.517"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.952381"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3600"	"IL15"	"0.467"	"0.724"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"3603"	"IL16"	"0.543"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"1"	"UNIPROT"
"3604"	"TNFRSF9"	"0.565"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"3605"	"IL17A"	"0.391"	"0.862"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"0.9793814"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0007682"	"CNS disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.31"		"2008"	"2011"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.35"		"2003"	"2012"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9583333"	"1999"	"2017"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"3605"	"IL17A"	"0.391"	"0.862"	"C0549463"	"X-Linked Lymphoproliferative Disorder"	"disease"	"C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3605"	"IL17A"	"0.391"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3606"	"IL18"	"0.404"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9736842"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2002"	"2005"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2012"	"3"	"0"	"PSYGENET"
"3606"	"IL18"	"0.404"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2012"	"3"	"0"	"PSYGENET"
"3606"	"IL18"	"0.404"	"0.862"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2008"	"2016"	"2"	"0"	"PSYGENET"
"3606"	"IL18"	"0.404"	"0.862"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3606"	"IL18"	"0.404"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3608"	"ILF2"	"0.743"	"0.276"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3608"	"ILF2"	"0.743"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3608"	"ILF2"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3608"	"ILF2"	"0.743"	"0.276"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"3611"	"ILK"	"0.534"	"0.69"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0009376"	"Colonic Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0039978"	"Thoracic Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3611"	"ILK"	"0.534"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3611"	"ILK"	"0.534"	"0.69"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2010"	"2"	"0"	"PSYGENET"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4310619"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3612"	"IMPA1"	"0.642"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2000"	"2011"	"5"	"0"	"PSYGENET"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2005"	"2007"	"1"	"0"	"CTD_human"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2017"	"1"	"0"	"PSYGENET"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2001"	"2007"	"2"	"0"	"PSYGENET"
"3613"	"IMPA2"	"0.696"	"0.276"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3614"	"IMPDH1"	"0.619"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2015"	"2"	"1"	"CTD_human;ORPHANET"
"3614"	"IMPDH1"	"0.619"	"0.448"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"3614"	"IMPDH1"	"0.619"	"0.448"	"C1840284"	"LEBER CONGENITAL AMAUROSIS 11"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"2"	"CTD_human;UNIPROT"
"3614"	"IMPDH1"	"0.619"	"0.448"	"C1867299"	"Retinitis Pigmentosa 10"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.62"	"1"	"2002"	"2016"	"3"	"4"	"CTD_human;UNIPROT"
"3614"	"IMPDH1"	"0.619"	"0.448"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3615"	"IMPDH2"	"0.752"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3617"	"IMPG1"	"0.727"	"0.138"	"C0339510"	"Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"2013"	"2015"	"0"	"0"	"CTD_human"
"3617"	"IMPG1"	"0.727"	"0.138"	"C1842914"	"Adult-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3617"	"IMPG1"	"0.727"	"0.138"	"C2745945"	"Juvenile-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3617"	"IMPG1"	"0.727"	"0.138"	"C4015342"	"MACULAR DYSTROPHY, VITELLIFORM, 4"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"4"	"UNIPROT"
"3619"	"INCENP"	"0.815"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2015"	"4"	"0"	"PSYGENET"
"3620"	"IDO1"	"0.532"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2015"	"4"	"0"	"PSYGENET"
"3620"	"IDO1"	"0.532"	"0.862"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3620"	"IDO1"	"0.532"	"0.862"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0581391"	"Chronic depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3620"	"IDO1"	"0.532"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3620"	"IDO1"	"0.532"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2006"	"2010"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3621"	"ING1"	"0.609"	"0.586"	"C0280302"	"Squamous cell carcinoma of lip"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3621"	"ING1"	"0.609"	"0.586"	"C0280313"	"Squamous cell carcinoma of oropharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3621"	"ING1"	"0.609"	"0.586"	"C0280321"	"Squamous cell carcinoma of the hypopharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3621"	"ING1"	"0.609"	"0.586"	"C0280324"	"Laryngeal Squamous Cell Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3621"	"ING1"	"0.609"	"0.586"	"C0585362"	"Squamous cell carcinoma of mouth"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3621"	"ING1"	"0.609"	"0.586"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.71"	"1"	"2000"	"2000"	"1"	"3"	"CGI;CTD_human;UNIPROT"
"3621"	"ING1"	"0.609"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3623"	"INHA"	"0.602"	"0.448"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3623"	"INHA"	"0.602"	"0.448"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3623"	"INHA"	"0.602"	"0.448"	"C0342549"	"Familial Testotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2003"	"2007"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3624"	"INHBA"	"0.624"	"0.552"	"C0948216"	"Ovarian adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3625"	"INHBB"	"0.72"	"0.345"	"C0342549"	"Familial Testotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3626"	"INHBC"	"0.886"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2005"	"2007"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2001"	"2013"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.37"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0282488"	"Interstitial Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0600040"	"Chronic interstitial cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3627"	"CXCL10"	"0.437"	"0.828"	"C1720830"	"Painful Bladder Syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3627"	"CXCL10"	"0.437"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3628"	"INPP1"	"0.834"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3628"	"INPP1"	"0.834"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1998"	"2006"	"4"	"0"	"PSYGENET"
"3630"	"INS"	"0.458"	"0.828"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.52"	"1"	"1991"	"2007"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"1970"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"3630"	"INS"	"0.458"	"0.828"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1970"	"1970"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0005686"	"Urinary Bladder Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9020979"	"1981"	"2018"	"8"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.70"	"0.9408602"	"1983"	"2018"	"1"	"1"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9"	"1985"	"2016"	"10"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011880"	"Diabetic Ketoacidosis"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.38"	"1"	"1990"	"1999"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0016579"	"Formication"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"1990"	"1995"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0018790"	"Cardiac Arrest"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2016"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.39"	"0.8333333"	"1984"	"2015"	"4"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020461"	"Hyperkalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"1996"	"2010"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.56"	"1"	"1997"	"2008"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"1975"	"2015"	"7"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1975"	"1992"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2001"	"2015"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0022492"	"Kandinsky Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0023213"	"Ventricular Outflow Obstruction, Left"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1970"	"1970"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0028313"	"Organic Brain Syndrome, Nonpsychotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.8095238"	"1989"	"2016"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0029227"	"Delirium, Dementia, Amnestic, Cognitive Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0029230"	"Organic Mental Disorders, Psychotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0030319"	"Panic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0030554"	"Paresthesia"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.40"	"0.7692308"	"1989"	"2015"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0033943"	"Psychoses, Traumatic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1996"	"1999"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0035619"	"Ventricular Outflow Obstruction, Right"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1990"	"2008"	"2"	"0"	"PSYGENET"
"3630"	"INS"	"0.458"	"0.828"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1969"	"1969"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0042512"	"Ventricular Outflow Obstruction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0086769"	"Panic Attacks"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.55"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0235044"	"Paresthesia, Distal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0270730"	"MPTP Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"	"0.8"	"1985"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1975"	"2015"	"7"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1975"	"2015"	"7"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"0"	"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1970"	"1970"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.68"	"0.875"	"1997"	"2017"	"0"	"0"	"ORPHANET"
"3630"	"INS"	"0.458"	"0.828"	"C0342283"	"Hyperproinsulinemia"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9090909"	"1979"	"2014"	"4"	"5"	"CTD_human;UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"2003"	"2015"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0392699"	"Dysesthesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0600228"	"Cardiopulmonary Arrest"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1998"	"2005"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751412"	"Painful Paresthesias"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0751864"	"MPTP-Induced Degeneration of the Striatum"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2001"	"2015"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"1989"	"2006"	"3"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1984"	"1986"	"4"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1984"	"1986"	"4"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1984"	"1986"	"4"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1996"	"1999"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1833102"	"DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES"	"disease"	"C10;C18;C19;C23"	"Disease or Syndrome"	"0.50"		"1998"	"2008"	"2"	"14"	"UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.98"	"1"	"1993"	"2016"	"2"	"20"	"CTD_human;ORPHANET;UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C1852092"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 2"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"2"	"CTD_human;UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C1853490"	"22q13.3 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1853564"	"Developmental Delay, Epilepsy, and Neonatal Diabetes"	"disease"	"C10;C16;C18;C19;C23;F01"	"Disease or Syndrome"	"0.50"		"1998"	"2008"	"2"	"14"	"UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.50"		"1996"	"2008"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C3150617"	"Maturity-onset diabetes of the young, type 10"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2015"	"4"	"4"	"CTD_human;UNIPROT"
"3630"	"INS"	"0.458"	"0.828"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4041080"	"Neurocognitive Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3630"	"INS"	"0.458"	"0.828"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2004"	"2"	"0"	"CTD_human"
"3631"	"INPP4A"	"0.799"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3631"	"INPP4A"	"0.799"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3631"	"INPP4A"	"0.799"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3631"	"INPP4A"	"0.799"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3632"	"INPP5A"	"0.743"	"0.345"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3635"	"INPP5D"	"0.636"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3635"	"INPP5D"	"0.636"	"0.552"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0432194"	"Schneckenbecken dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0432219"	"Opsismodysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.74"	"1"	"2013"	"2018"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3636"	"INPPL1"	"0.63"	"0.517"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3636"	"INPPL1"	"0.63"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3638"	"INSIG1"	"0.707"	"0.379"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3640"	"INSL3"	"0.611"	"0.448"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.90"	"0.7777778"	"1999"	"2017"	"5"	"5"	"CTD_human;UNIPROT"
"3640"	"INSL3"	"0.611"	"0.448"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.35"	"0.8"	"2000"	"2009"	"2"	"0"	"CTD_human"
"3640"	"INSL3"	"0.611"	"0.448"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.41"	"1"	"2004"	"2009"	"2"	"0"	"CTD_human"
"3640"	"INSL3"	"0.611"	"0.448"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3640"	"INSL3"	"0.611"	"0.448"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3642"	"INSM1"	"0.752"	"0.207"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1997"	"2012"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.59"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1997"	"2012"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9318182"	"1985"	"2016"	"3"	"2"	"UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9285714"	"1984"	"2016"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.70"	"0.8695652"	"1989"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3643"	"INSR"	"0.459"	"0.724"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.40"		"1991"	"2014"	"2"	"2"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3643"	"INSR"	"0.459"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1997"	"2012"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0265344"	"Donohue Syndrome"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.80"	"0.9607843"	"1985"	"2018"	"21"	"14"	"CTD_human;ORPHANET;UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.39"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0271689"	"Insulin Receptor, Defect in"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"1988"	"2017"	"20"	"11"	"UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0271695"	"Rabson-Mendenhall Syndrome"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.80"	"1"	"1986"	"2018"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0342278"	"Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans"	"disease"	"C17;C18;C19"	"Disease or Syndrome"	"0.60"		"1988"	"2017"	"20"	"11"	"CTD_human;ORPHANET;UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C0342336"	"Insulin resistance - type A"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1988"	"2017"	"0"	"0"	"ORPHANET"
"3643"	"INSR"	"0.459"	"0.724"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2000"	"2002"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2008"	"2"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1992"	"1995"	"3"	"2"	"UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C1864952"	"Hyperinsulinemic Hypoglycemia, Familial, 5"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1994"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3643"	"INSR"	"0.459"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3643"	"INSR"	"0.459"	"0.724"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1992"	"1995"	"3"	"2"	"UNIPROT"
"3643"	"INSR"	"0.459"	"0.724"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3645"	"INSRR"	"0.707"	"0.448"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3645"	"INSRR"	"0.707"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3645"	"INSRR"	"0.707"	"0.448"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3646"	"EIF3E"	"0.72"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9090909"	"1998"	"2016"	"2"	"4"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2016"	"3"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"1"	"1998"	"2012"	"0"	"0"	"ORPHANET"
"3651"	"PDX1"	"0.557"	"0.483"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"3"	"0"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"3651"	"PDX1"	"0.557"	"0.483"	"C1833382"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.62"	"1"	"1998"	"2015"	"1"	"5"	"CTD_human"
"3651"	"PDX1"	"0.557"	"0.483"	"C1850096"	"Pancreatic Agenesis, Congenital"	"disease"	"C06"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"0"	"4"	"CTD_human;ORPHANET"
"3652"	"IPP"	"0.799"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3652"	"IPP"	"0.799"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3652"	"IPP"	"0.799"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3653"	"IPW"	"0.707"	"0.276"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.36"	"1"	"1997"	"2017"	"0"	"0"	"CTD_human"
"3653"	"IPW"	"0.707"	"0.276"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.44"	"1"	"2008"	"2016"	"0"	"1"	"ORPHANET"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0178540"	"Cerebral Hypoxia-Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0752304"	"Hypoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0752305"	"Anoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0752306"	"Anoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0752307"	"Anoxia-Ischemia, Cerebral"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C0752308"	"Hypoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3654"	"IRAK1"	"0.573"	"0.655"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"3654"	"IRAK1"	"0.573"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"3655"	"ITGA6"	"0.588"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3655"	"ITGA6"	"0.588"	"0.586"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.32"	"1"	"1997"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"3655"	"ITGA6"	"0.588"	"0.586"	"C1856934"	"Epidermolysis bullosa with pyloric atresia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.57"	"1"	"1997"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"3656"	"IRAK2"	"0.799"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3658"	"IREB2"	"0.685"	"0.345"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3659"	"IRF1"	"0.503"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.55"	"1"	"1998"	"2017"	"0"	"0"	"CGI;CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.61"	"1"	"1998"	"2013"	"0"	"1"	"CGI;CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3659"	"IRF1"	"0.503"	"0.724"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3659"	"IRF1"	"0.503"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3659"	"IRF1"	"0.503"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3659"	"IRF1"	"0.503"	"0.724"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.64"	"1"	"1998"	"2017"	"2"	"2"	"CGI;UNIPROT"
"3659"	"IRF1"	"0.503"	"0.724"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3659"	"IRF1"	"0.503"	"0.724"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"2"	"UNIPROT"
"3660"	"IRF2"	"0.607"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2012"	"2013"	"1"	"0"	"CTD_human"
"3661"	"IRF3"	"0.562"	"0.724"	"C0001338"	"Herpetic Acute Necrotizing Encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3661"	"IRF3"	"0.562"	"0.724"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3661"	"IRF3"	"0.562"	"0.724"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"3661"	"IRF3"	"0.562"	"0.724"	"C4225294"	"HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 7"	"phenotype"		"Finding"	"0.40"		"2015"	"2016"	"1"	"2"	"UNIPROT"
"3662"	"IRF4"	"0.547"	"0.517"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2015"	"1"	"3"	"CTD_human"
"3662"	"IRF4"	"0.547"	"0.517"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3662"	"IRF4"	"0.547"	"0.517"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"0.96"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3662"	"IRF4"	"0.547"	"0.517"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3662"	"IRF4"	"0.547"	"0.517"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.8695652"	"2005"	"2016"	"2"	"2"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2015"	"0"	"1"	"ORPHANET"
"3663"	"IRF5"	"0.518"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.9662921"	"2005"	"2018"	"2"	"5"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3663"	"IRF5"	"0.518"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"3663"	"IRF5"	"0.518"	"0.69"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3663"	"IRF5"	"0.518"	"0.69"	"C1258104"	"Diffuse Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"3663"	"IRF5"	"0.518"	"0.69"	"C2677100"	"Inflammatory Bowel Disease 14"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"3664"	"IRF6"	"0.562"	"0.655"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.70"	"0.8888889"	"2003"	"2016"	"3"	"5"	"CTD_human;ORPHANET"
"3664"	"IRF6"	"0.562"	"0.655"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.40"	"0.9166667"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.41"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"3664"	"IRF6"	"0.562"	"0.655"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.40"	"0.9230769"	"2004"	"2017"	"0"	"0"	"ORPHANET"
"3664"	"IRF6"	"0.562"	"0.655"	"C0175697"	"Van der Woude syndrome"	"disease"	"C04;C05;C07;C16;C23"	"Disease or Syndrome"	"1.00"	"0.9574468"	"1999"	"2018"	"11"	"16"	"CTD_human;ORPHANET;UNIPROT"
"3664"	"IRF6"	"0.562"	"0.655"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C0265259"	"Popliteal pterygium syndrome"	"disease"	"C05;C07;C11;C12;C13;C16"	"Disease or Syndrome"	"1.00"	"0.9285714"	"2002"	"2017"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3664"	"IRF6"	"0.562"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C1298692"	"Cleft lip and alveolus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3664"	"IRF6"	"0.562"	"0.655"	"C1837213"	"OROFACIAL CLEFT 6, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.60"		"2002"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"3664"	"IRF6"	"0.562"	"0.655"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.37"	"0.8571429"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3664"	"IRF6"	"0.562"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3664"	"IRF6"	"0.562"	"0.655"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"3665"	"IRF7"	"0.6"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3665"	"IRF7"	"0.6"	"0.69"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3665"	"IRF7"	"0.6"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3665"	"IRF7"	"0.6"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3665"	"IRF7"	"0.6"	"0.69"	"C4225358"	"IMMUNODEFICIENCY 39"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"3665"	"IRF7"	"0.6"	"0.69"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3667"	"IRS1"	"0.532"	"0.621"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.962963"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"0.9411765"	"1993"	"2017"	"9"	"1"	"CTD_human;UNIPROT"
"3667"	"IRS1"	"0.532"	"0.621"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2000"	"2017"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.9428571"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2008"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"1992"	"2004"	"3"	"1"	"UNIPROT"
"3667"	"IRS1"	"0.532"	"0.621"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"1992"	"2017"	"2"	"0"	"CTD_human"
"3667"	"IRS1"	"0.532"	"0.621"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1996"	"2003"	"3"	"0"	"UNIPROT"
"3669"	"ISG20"	"0.451"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3670"	"ISL1"	"0.621"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3670"	"ISL1"	"0.621"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"3670"	"ISL1"	"0.621"	"0.586"	"C0005689"	"Bladder Exstrophy"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"3670"	"ISL1"	"0.621"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"3670"	"ISL1"	"0.621"	"0.586"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3671"	"ISLR"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3672"	"ITGA1"	"0.681"	"0.517"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3672"	"ITGA1"	"0.681"	"0.517"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0035328"	"Retinal Vein Occlusion"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C1527411"	"Thrombosis of retinal vein"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C3280114"	"Glycoprotein IA Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3673"	"ITGA2"	"0.565"	"0.655"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3673"	"ITGA2"	"0.565"	"0.655"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3673"	"ITGA2"	"0.565"	"0.655"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0007274"	"Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.36"	"0.4"	"1997"	"2012"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0040015"	"Thrombasthenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.9245283"	"1988"	"2016"	"20"	"24"	"CTD_human;ORPHANET;UNIPROT"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2004"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0750988"	"Common Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0750989"	"External Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0750990"	"Internal Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C1861195"	"Glanzmann Thrombasthenia, Autosomal Dominant"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"		"1992"	"2012"	"2"	"2"	"CTD_human;UNIPROT"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C3179396"	"Glanzmann Thrombasthenia, Type A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3674"	"ITGA2B"	"0.548"	"0.517"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3675"	"ITGA3"	"0.621"	"0.517"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"3675"	"ITGA3"	"0.621"	"0.517"	"C3553636"	"INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3675"	"ITGA3"	"0.621"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3676"	"ITGA4"	"0.596"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"3676"	"ITGA4"	"0.596"	"0.655"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3676"	"ITGA4"	"0.596"	"0.655"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"3676"	"ITGA4"	"0.596"	"0.655"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"3676"	"ITGA4"	"0.596"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"3676"	"ITGA4"	"0.596"	"0.655"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3678"	"ITGA5"	"0.557"	"0.655"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3679"	"ITGA7"	"0.663"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3679"	"ITGA7"	"0.663"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3679"	"ITGA7"	"0.663"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3679"	"ITGA7"	"0.663"	"0.379"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.51"	"1"	"1997"	"2014"	"0"	"0"	"ORPHANET"
"3679"	"ITGA7"	"0.663"	"0.379"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1998"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"3679"	"ITGA7"	"0.663"	"0.379"	"C2750786"	"Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"1997"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"3679"	"ITGA7"	"0.663"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3680"	"ITGA9"	"0.663"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3680"	"ITGA9"	"0.663"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3680"	"ITGA9"	"0.663"	"0.448"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3683"	"ITGAL"	"0.547"	"0.793"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3683"	"ITGAL"	"0.547"	"0.793"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"CTD_human"
"3683"	"ITGAL"	"0.547"	"0.793"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"3683"	"ITGAL"	"0.547"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3683"	"ITGAL"	"0.547"	"0.793"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0020877"	"Ileitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.96875"	"2008"	"2017"	"2"	"11"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0752332"	"Lupus Vasculitis, Central Nervous System"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0752334"	"Lupus Meningoencephalitis"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3684"	"ITGAM"	"0.491"	"0.69"	"C0752335"	"Neuropsychiatric Systemic Lupus Erythematosus"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3685"	"ITGAV"	"0.551"	"0.655"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3685"	"ITGAV"	"0.551"	"0.655"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3685"	"ITGAV"	"0.551"	"0.655"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3687"	"ITGAX"	"0.562"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1989"	"2007"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3688"	"ITGB1"	"0.536"	"0.655"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0023510"	"Leukocyte Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1987"	"1998"	"2"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"1999"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0037299"	"Skin Ulcer"	"phenotype"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0242597"	"Leukocyte-Adhesion Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0398738"	"Leukocyte adhesion deficiency type 1"	"disease"	"C20"	"Disease or Syndrome"	"1.00"	"0.9705882"	"1990"	"2016"	"11"	"22"	"CTD_human;ORPHANET;UNIPROT"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3689"	"ITGB2"	"0.496"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2006"	"2011"	"3"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0007274"	"Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0010072"	"Coronary Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0019557"	"Hip Fractures"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.8421053"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"		"2002"	"2008"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.8888889"	"1998"	"2017"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0040015"	"Thrombasthenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"1.00"	"1"	"1986"	"2018"	"17"	"20"	"CTD_human;ORPHANET;UNIPROT"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0162385"	"Intertrochanteric Fractures"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0162386"	"Subtrochanteric Fractures"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0162387"	"Trochanteric Fractures"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0750988"	"Common Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0750989"	"External Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0750990"	"Internal Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"0.6666667"	"1999"	"2014"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C1861195"	"Glanzmann Thrombasthenia, Autosomal Dominant"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"		"1999"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"3690"	"ITGB3"	"0.507"	"0.69"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C3179396"	"Glanzmann Thrombasthenia, Type A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"2"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.56"	"1"	"1991"	"2012"	"2"	"0"	"CTD_human;ORPHANET"
"3690"	"ITGB3"	"0.507"	"0.69"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3690"	"ITGB3"	"0.507"	"0.69"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3690"	"ITGB3"	"0.507"	"0.69"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0013575"	"Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.55"	"1"	"1995"	"2014"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079295"	"Epidermolysis Bullosa Herpetiformis Dowling-Meara"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079297"	"Epidermolysis Bullosa Progressiva"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1995"	"2000"	"2"	"1"	"CTD_human;UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079298"	"Epidermolysis Bullosa Simplex"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079299"	"Epidermolysis Bullosa Simplex Kobner"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079301"	"Junctional Epidermolysis Bullosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.76"	"1"	"1995"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0079683"	"Herlitz Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2004"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0080333"	"Weber-Cockayne Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1999"	"2015"	"0"	"1"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0162361"	"Hidrotic Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0266159"	"Pyloric Atresia"	"disease"	"C06"	"Congenital Abnormality"	"0.35"	"1"	"1995"	"2016"	"2"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0268374"	"Adult junctional epidermolysis bullosa (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"1996"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C0282160"	"Aplasia Cutis Congenita"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C1706004"	"Anhydrotic Ectodermal Dysplasias"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3691"	"ITGB4"	"0.551"	"0.621"	"C1856934"	"Epidermolysis bullosa with pyloric atresia"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2017"	"9"	"14"	"CTD_human;ORPHANET;UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C2608084"	"EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1996"	"2000"	"1"	"1"	"CTD_human;UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C2673609"	"Epidermolysis bullosa inversa dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"1996"	"2000"	"1"	"1"	"UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C2673610"	"JEB-I"	"disease"		"Disease or Syndrome"	"0.50"		"1996"	"2000"	"1"	"1"	"UNIPROT"
"3691"	"ITGB4"	"0.551"	"0.621"	"C2677349"	"Epidermolysis Bullosa Simplex With Pyloric Atresia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3691"	"ITGB4"	"0.551"	"0.621"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3692"	"EIF6"	"0.713"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3693"	"ITGB5"	"0.713"	"0.448"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3693"	"ITGB5"	"0.713"	"0.448"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3693"	"ITGB5"	"0.713"	"0.448"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3693"	"ITGB5"	"0.713"	"0.448"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.43"	"1"	"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0399367"	"Amelogenesis imperfecta local hypoplastic form"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0399376"	"Amelogenesis Imperfecta, Type III"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3694"	"ITGB6"	"0.619"	"0.586"	"C0524910"	"Hepatitis C, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3694"	"ITGB6"	"0.619"	"0.586"	"C2931280"	"Perniola Krajewska Carnevale syndrome"	"disease"	"C10;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3694"	"ITGB6"	"0.619"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3694"	"ITGB6"	"0.619"	"0.586"	"C4015557"	"AMELOGENESIS IMPERFECTA, TYPE IH"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"2"	"4"	"CTD_human;UNIPROT"
"3696"	"ITGB8"	"0.815"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3696"	"ITGB8"	"0.815"	"0.138"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3696"	"ITGB8"	"0.815"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3697"	"ITIH1"	"0.752"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2017"	"2"	"3"	"PSYGENET"
"3697"	"ITIH1"	"0.752"	"0.241"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3697"	"ITIH1"	"0.752"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2015"	"1"	"1"	"PSYGENET"
"3697"	"ITIH1"	"0.752"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"6"	"PSYGENET"
"3697"	"ITIH1"	"0.752"	"0.241"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3697"	"ITIH1"	"0.752"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3699"	"ITIH3"	"0.785"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2015"	"4"	"2"	"PSYGENET"
"3699"	"ITIH3"	"0.785"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2011"	"2018"	"1"	"3"	"PSYGENET"
"3699"	"ITIH3"	"0.785"	"0.138"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"3700"	"ITIH4"	"0.6"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3700"	"ITIH4"	"0.6"	"0.621"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3702"	"ITK"	"0.551"	"0.655"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2012"	"0"	"0"	"ORPHANET"
"3702"	"ITK"	"0.551"	"0.655"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"3702"	"ITK"	"0.551"	"0.655"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3702"	"ITK"	"0.551"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3702"	"ITK"	"0.551"	"0.655"	"C2751686"	"Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3702"	"ITK"	"0.551"	"0.655"	"C3552634"	"LYMPHOPROLIFERATIVE SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2012"	"1"	"3"	"UNIPROT"
"3703"	"STT3A"	"0.735"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3703"	"STT3A"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"3703"	"STT3A"	"0.735"	"0.31"	"C3810062"	"Congenital disorder of glycosylation type 1w"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3704"	"ITPA"	"0.642"	"0.345"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2002"	"2010"	"2"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3704"	"ITPA"	"0.642"	"0.345"	"C0342800"	"Inosine Triphosphatase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2002"	"2003"	"2"	"1"	"CTD_human;UNIPROT"
"3704"	"ITPA"	"0.642"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3704"	"ITPA"	"0.642"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"3704"	"ITPA"	"0.642"	"0.345"	"C4225256"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3705"	"ITPK1"	"0.834"	"0.138"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0003132"	"Anoxic Encephalopathy"	"disease"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1994"	"2006"	"2"	"0"	"PSYGENET"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.42"	"1"	"2005"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0431401"	"Gillespie syndrome"	"disease"	"C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.71"	"1"	"1994"	"2017"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C0995195"	"Anoxia of brain"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1140716"	"Hypoxic Brain Damage"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1527348"	"Brain Hypoxia"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1847725"	"SPINOCEREBELLAR ATAXIA 15"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.73"	"1"	"1993"	"2013"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3708"	"ITPR1"	"0.577"	"0.69"	"C1861732"	"SPINOCEREBELLAR ATAXIA 29"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2005"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3708"	"ITPR1"	"0.577"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3708"	"ITPR1"	"0.577"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3708"	"ITPR1"	"0.577"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C0003132"	"Anoxic Encephalopathy"	"disease"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C0995195"	"Anoxia of brain"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C1140716"	"Hypoxic Brain Damage"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C1527348"	"Brain Hypoxia"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3709"	"ITPR2"	"0.676"	"0.517"	"C1862871"	"ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS"	"disease"		"Disease or Syndrome"	"0.90"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3710"	"ITPR3"	"0.636"	"0.586"	"C0001197"	"Acrodermatitis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3710"	"ITPR3"	"0.636"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2011"	"0"	"0"	"CTD_human"
"3710"	"ITPR3"	"0.636"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3710"	"ITPR3"	"0.636"	"0.586"	"C0263372"	"Gianotti-Crosti Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3710"	"ITPR3"	"0.636"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3710"	"ITPR3"	"0.636"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3712"	"IVD"	"0.727"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3712"	"IVD"	"0.727"	"0.414"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"3712"	"IVD"	"0.727"	"0.414"	"C0268575"	"Isovaleryl-CoA dehydrogenase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1985"	"2018"	"6"	"24"	"CTD_human;ORPHANET;UNIPROT"
"3712"	"IVD"	"0.727"	"0.414"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3712"	"IVD"	"0.727"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"3713"	"IVL"	"0.685"	"0.276"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3713"	"IVL"	"0.685"	"0.276"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"0.8"	"1991"	"2009"	"1"	"0"	"CTD_human"
"3713"	"IVL"	"0.685"	"0.276"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3714"	"JAG2"	"0.642"	"0.517"	"C0039075"	"Syndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0751674"	"Lymphangioleiomyomatosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3714"	"JAG2"	"0.642"	"0.517"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3716"	"JAK1"	"0.533"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2011"	"0"	"1"	"CGI"
"3716"	"JAK1"	"0.533"	"0.621"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2017"	"0"	"1"	"CGI"
"3716"	"JAK1"	"0.533"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2018"	"1"	"0"	"CTD_human"
"3716"	"JAK1"	"0.533"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"3716"	"JAK1"	"0.533"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2018"	"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"1.00"	"0.9453125"	"2005"	"2018"	"9"	"1"	"CGI;CTD_human;ORPHANET"
"3717"	"JAK2"	"0.43"	"0.69"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.38"	"0.875"	"2009"	"2016"	"2"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3717"	"JAK2"	"0.43"	"0.69"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0019154"	"Hepatic Vein Thrombosis"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.58"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"3717"	"JAK2"	"0.43"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.90625"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9142857"	"2005"	"2017"	"1"	"2"	"CGI;CTD_human;UNIPROT"
"3717"	"JAK2"	"0.43"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.50"	"0.9615385"	"1997"	"2017"	"0"	"1"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0025472"	"Mesenteric Vascular Occlusion"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0026987"	"Myelofibrosis"	"disease"		"Neoplastic Process"	"0.70"	"0.9423077"	"2005"	"2017"	"0"	"0"	"ORPHANET"
"3717"	"JAK2"	"0.43"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.50"	"0.9571429"	"2005"	"2018"	"1"	"6"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"1.00"	"0.954416"	"2005"	"2018"	"12"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3717"	"JAK2"	"0.43"	"0.69"	"C0032962"	"Pregnancy Complications"	"group"	"C13"	"Pathologic Function"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.80"	"0.9630996"	"2005"	"2018"	"8"	"0"	"CTD_human;ORPHANET"
"3717"	"JAK2"	"0.43"	"0.69"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.41"		"2009"	"2010"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.46"		"2007"	"2010"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2012"	"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2007"	"2017"	"0"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3717"	"JAK2"	"0.43"	"0.69"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"	"0.9565217"	"2005"	"2018"	"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0836924"	"Thrombocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"0.9230769"	"2006"	"2015"	"2"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C0856761"	"Budd-Chiari Syndrome"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.70"	"1"	"2006"	"2016"	"2"	"1"	"CTD_human;ORPHANET"
"3717"	"JAK2"	"0.43"	"0.69"	"C1332201"	"Adult Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C1332967"	"Childhood Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3717"	"JAK2"	"0.43"	"0.69"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"0"	"0"	"CGI"
"3717"	"JAK2"	"0.43"	"0.69"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C3275959"	"LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"3717"	"JAK2"	"0.43"	"0.69"	"C3281125"	"THROMBOCYTHEMIA 3"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2012"	"2"	"1"	"UNIPROT"
"3717"	"JAK2"	"0.43"	"0.69"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2012"	"8"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"3717"	"JAK2"	"0.43"	"0.69"	"C4303761"	"Familial thrombocytosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3718"	"JAK3"	"0.532"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3718"	"JAK3"	"0.532"	"0.621"	"C0023462"	"Acute Megakaryocytic Leukemias"	"disease"	"C04"	"Neoplastic Process"	"0.46"	"1"	"2006"	"2011"	"0"	"4"	"CGI"
"3718"	"JAK3"	"0.532"	"0.621"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"0.6666667"	"2002"	"2014"	"0"	"0"	"CGI"
"3718"	"JAK3"	"0.532"	"0.621"	"C0025063"	"Mediastinal Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.50"	"1"	"1995"	"2018"	"2"	"4"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0153504"	"Malignant tumor of mediastinum"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3718"	"JAK3"	"0.532"	"0.621"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3718"	"JAK3"	"0.532"	"0.621"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C0392788"	"Nasal Type Extranodal NK/T-Cell Lymphoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"2"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C1292778"	"Chronic myeloproliferative disorder"	"disease"		"Neoplastic Process"	"0.40"		"2010"	"2015"	"0"	"1"	"CGI"
"3718"	"JAK3"	"0.532"	"0.621"	"C1833275"	"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.70"		"1995"	"2004"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3718"	"JAK3"	"0.532"	"0.621"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C1955906"	"Lymphoma, Extranodal NK-T-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CGI"
"3718"	"JAK3"	"0.532"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"3718"	"JAK3"	"0.532"	"0.621"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"3718"	"JAK3"	"0.532"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3720"	"JARID2"	"0.672"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"3720"	"JARID2"	"0.672"	"0.414"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2008"	"2"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0021846"	"Intestinal Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2010"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2010"	"2"	"0"	"PSYGENET"
"3725"	"JUN"	"0.473"	"0.828"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0086626"	"Minamata Disease"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.6666667"	"2006"	"2017"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0274859"	"Inorganic Mercury Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0274860"	"Mercury Poisoning, Organic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2014"	"2"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0546127"	"Mercury Poisoning, Nervous System"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751855"	"Mercury Encephalopathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751856"	"Mad Hatter Disease"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751857"	"Mercurial Neuroanesthenia"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0751858"	"Mercury Psychosis"	"disease"	"C10;C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CGI"
"3725"	"JUN"	"0.473"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9375"	"1993"	"2016"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3725"	"JUN"	"0.473"	"0.828"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3726"	"JUNB"	"0.491"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3727"	"JUND"	"0.514"	"0.724"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2000"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2000"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0232347"	"No-Reflow Phenomenon"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.37"	"1"	"2002"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3728"	"JUP"	"0.619"	"0.414"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2000"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"3728"	"JUP"	"0.619"	"0.414"	"C1832600"	"Naxos disease"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.60"		"1993"	"2012"	"0"	"5"	"CTD_human;ORPHANET"
"3728"	"JUP"	"0.619"	"0.414"	"C1864826"	"Epidermolysis bullosa, lethal acantholytic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3728"	"JUP"	"0.619"	"0.414"	"C1969081"	"Arrhythmogenic Right Ventricular Dysplasia, Familial, 12"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2010"	"2"	"2"	"CTD_human;UNIPROT"
"3730"	"ANOS1"	"0.552"	"0.655"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"	"1"	"1987"	"2016"	"15"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3730"	"ANOS1"	"0.552"	"0.655"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.49"	"1"	"2001"	"2016"	"4"	"1"	"GENOMICS_ENGLAND"
"3730"	"ANOS1"	"0.552"	"0.655"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.61"	"1"	"1992"	"2017"	"15"	"17"	"CTD_human;UNIPROT"
"3730"	"ANOS1"	"0.552"	"0.655"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3730"	"ANOS1"	"0.552"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3730"	"ANOS1"	"0.552"	"0.655"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9568966"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2003"	"0"	"0"	"CTD_human"
"3732"	"CD82"	"0.533"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.88"	"1995"	"2017"	"0"	"0"	"CTD_human"
"3735"	"KARS"	"0.701"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"3735"	"KARS"	"0.701"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3735"	"KARS"	"0.701"	"0.379"	"C3150897"	"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2010"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3735"	"KARS"	"0.701"	"0.379"	"C3151351"	"DEAFNESS, AUTOSOMAL RECESSIVE 89"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2018"	"2"	"2"	"CTD_human;UNIPROT"
"3735"	"KARS"	"0.701"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C0242287"	"Isaacs syndrome"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.52"	"1"	"1995"	"2012"	"13"	"12"	"UNIPROT"
"3736"	"KCNA1"	"0.676"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C1719788"	"Episodic ataxia type 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2016"	"13"	"18"	"CTD_human;ORPHANET;UNIPROT"
"3736"	"KCNA1"	"0.676"	"0.483"	"C1834559"	"Continuous Muscle Fiber Activity, Hereditary"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.70"		"1995"	"2012"	"13"	"12"	"ORPHANET;UNIPROT"
"3736"	"KCNA1"	"0.676"	"0.483"	"C1868682"	"Paroxysmal kinesigenic choreoathetosis"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3736"	"KCNA1"	"0.676"	"0.483"	"C2674766"	"Myokymia 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"		"1995"	"2012"	"13"	"12"	"UNIPROT"
"3736"	"KCNA1"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3736"	"KCNA1"	"0.676"	"0.483"	"C4305155"	"Isolated autosomal dominant hypomagnesemia Glaudemans type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"0"	"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0477370"	"Other generalized epilepsy and epileptic syndromes"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2017"	"10"	"0"	"CLINGEN"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2015"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4225350"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3737"	"KCNA2"	"0.656"	"0.276"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3739"	"KCNA4"	"0.815"	"0.138"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3741"	"KCNA5"	"0.648"	"0.414"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.37"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3741"	"KCNA5"	"0.648"	"0.414"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2010"	"2017"	"1"	"0"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3741"	"KCNA5"	"0.648"	"0.414"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C2677106"	"Atrial Fibrillation, Familial, 7"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2006"	"2013"	"0"	"4"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"3741"	"KCNA5"	"0.648"	"0.414"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"0.75"	"2007"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"3741"	"KCNA5"	"0.648"	"0.414"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3741"	"KCNA5"	"0.648"	"0.414"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3744"	"KCNA10"	"0.886"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3745"	"KCNB1"	"0.773"	"0.241"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3745"	"KCNB1"	"0.773"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"3745"	"KCNB1"	"0.773"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3745"	"KCNB1"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"3745"	"KCNB1"	"0.773"	"0.241"	"C4015119"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"3"	"5"	"CTD_human;UNIPROT"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3746"	"KCNC1"	"0.752"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"3746"	"KCNC1"	"0.752"	"0.069"	"C4015420"	"EPILEPSY, PROGRESSIVE MYOCLONIC 7"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"1"	"1"	"ORPHANET;UNIPROT"
"3748"	"KCNC3"	"0.713"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3748"	"KCNC3"	"0.713"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3748"	"KCNC3"	"0.713"	"0.241"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3748"	"KCNC3"	"0.713"	"0.241"	"C1854488"	"Spinocerebellar ataxia 13"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.74"	"1"	"2000"	"2017"	"7"	"9"	"CTD_human;ORPHANET;UNIPROT"
"3748"	"KCNC3"	"0.713"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3749"	"KCNC4"	"0.735"	"0.345"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3749"	"KCNC4"	"0.735"	"0.345"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3749"	"KCNC4"	"0.735"	"0.345"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3749"	"KCNC4"	"0.735"	"0.345"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3750"	"KCND1"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3752"	"KCND3"	"0.676"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3752"	"KCND3"	"0.676"	"0.241"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"3752"	"KCND3"	"0.676"	"0.241"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3752"	"KCND3"	"0.676"	"0.241"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.54"	"1"	"2000"	"2012"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"3752"	"KCND3"	"0.676"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3752"	"KCND3"	"0.676"	"0.241"	"C1846367"	"Spinocerebellar ataxia 19"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2001"	"2018"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3752"	"KCND3"	"0.676"	"0.241"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3752"	"KCND3"	"0.676"	"0.241"	"C2746067"	"Spinocerebellar ataxia 22"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2018"	"3"	"4"	"UNIPROT"
"3752"	"KCND3"	"0.676"	"0.241"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3752"	"KCND3"	"0.676"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3752"	"KCND3"	"0.676"	"0.241"	"C4225340"	"BRUGADA SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2012"	"2"	"3"	"CTD_human;UNIPROT"
"3753"	"KCNE1"	"0.642"	"0.31"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3753"	"KCNE1"	"0.642"	"0.31"	"C0022387"	"Jervell-Lange Nielsen Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"3753"	"KCNE1"	"0.642"	"0.31"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.60"	"0.972973"	"1997"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3753"	"KCNE1"	"0.642"	"0.31"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.36"	"1"	"1999"	"2009"	"0"	"0"	"ORPHANET"
"3753"	"KCNE1"	"0.642"	"0.31"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3753"	"KCNE1"	"0.642"	"0.31"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3753"	"KCNE1"	"0.642"	"0.31"	"C1867904"	"LONG QT SYNDROME 5"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2015"	"7"	"20"	"CTD_human;UNIPROT"
"3753"	"KCNE1"	"0.642"	"0.31"	"C2676723"	"JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2012"	"3"	"4"	"CTD_human;UNIPROT"
"3753"	"KCNE1"	"0.642"	"0.31"	"C3150956"	"LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1997"	"2015"	"7"	"20"	"UNIPROT"
"3753"	"KCNE1"	"0.642"	"0.31"	"C3279092"	"LONG QT SYNDROME 2/5, DIGENIC (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2015"	"7"	"20"	"UNIPROT"
"3753"	"KCNE1"	"0.642"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3753"	"KCNE1"	"0.642"	"0.31"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"2007"	"2017"	"1"	"1"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C0796013"	"Zimmerman Laband syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.63"	"1"	"2015"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3756"	"KCNH1"	"0.607"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3756"	"KCNH1"	"0.607"	"0.655"	"C2678486"	"Temple-Baraitser Syndrome"	"disease"	"C10;C23;F01;F03"	"Congenital Abnormality; Disease or Syndrome"	"0.73"	"1"	"2008"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3756"	"KCNH1"	"0.607"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"3756"	"KCNH1"	"0.607"	"0.655"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.40"		"2004"	"2008"	"3"	"21"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9700599"	"1995"	"2018"	"19"	"67"	"CTD_human;GENOMICS_ENGLAND"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.46"	"1"	"2004"	"2017"	"0"	"2"	"ORPHANET"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2013"	"4"	"0"	"PSYGENET"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0040479"	"Torsades de Pointes"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"	"0.9411765"	"1995"	"2017"	"3"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3757"	"KCNH2"	"0.543"	"0.586"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"3757"	"KCNH2"	"0.543"	"0.586"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"2002"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"3757"	"KCNH2"	"0.543"	"0.586"	"C1865020"	"Short QT Syndrome 1"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.91"	"1"	"1999"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3150943"	"Long Qt Syndrome 2"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9545455"	"1995"	"2017"	"30"	"243"	"CTD_human;UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3276240"	"LONG QT SYNDROME 2/3, DIGENIC"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2017"	"30"	"226"	"UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3277700"	"LONG QT SYNDROME 1/2, DIGENIC (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2017"	"30"	"226"	"UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3279092"	"LONG QT SYNDROME 2/5, DIGENIC (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2017"	"30"	"226"	"UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3279093"	"LONG QT SYNDROME 2/9, DIGENIC"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2017"	"30"	"226"	"UNIPROT"
"3757"	"KCNH2"	"0.543"	"0.586"	"C3888153"	"LONG QT SYNDROME 2, ACQUIRED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"1995"	"2017"	"30"	"227"	"UNIPROT"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C0004775"	"Bartter Disease"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2015"	"3"	"0"	"CTD_human"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C1855849"	"Bartter syndrome, antenatal , type 2"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.81"	"1"	"1996"	"2008"	"3"	"11"	"CTD_human;UNIPROT"
"3758"	"KCNJ1"	"0.627"	"0.483"	"C1866495"	"Bartter syndrome, antenatal type 1"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C1563715"	"Andersen Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.80"	"0.9433962"	"1993"	"2018"	"6"	"21"	"CTD_human;ORPHANET;UNIPROT"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C1865018"	"Short QT Syndrome 3"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"2001"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C1865020"	"Short QT Syndrome 1"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3759"	"KCNJ2"	"0.602"	"0.517"	"C3151431"	"ATRIAL FIBRILLATION, FAMILIAL, 9"	"disease"		"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"3760"	"KCNJ3"	"0.743"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3761"	"KCNJ4"	"0.886"	"0.172"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3761"	"KCNJ4"	"0.886"	"0.172"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0004331"	"Auriculo-Ventricular Dissociation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0018794"	"Heart Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0206667"	"Adrenal Cortical Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C0428908"	"Sinus Node Dysfunction (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C1563715"	"Andersen Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2018"	"0"	"1"	"ORPHANET"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C3150733"	"LONG QT SYNDROME 13"	"disease"		"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"3762"	"KCNJ5"	"0.579"	"0.517"	"C3150933"	"HYPERALDOSTERONISM, FAMILIAL, TYPE III"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2016"	"9"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2014"	"2"	"77"	"PSYGENET"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C3279800"	"KEPPEN-LUBINSKY SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2003"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3763"	"KCNJ6"	"0.659"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"1"	"UNIPROT"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2002"	"2005"	"1"	"0"	"CTD_human"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0340493"	"Paroxysmal familial ventricular fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C0795905"	"Cantu syndrome"	"disease"	"C05;C14;C16;C17;C23"	"Disease or Syndrome"	"0.63"	"1"	"2014"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3764"	"KCNJ8"	"0.676"	"0.483"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2012"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0271829"	"Pendred's syndrome"	"disease"	"C09;C10;C19;C23"	"Disease or Syndrome"	"0.54"	"0.75"	"2009"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C2748572"	"SeSAME syndrome"	"disease"	"C09;C10;C23;F01;F03"	"Disease or Syndrome"	"1.00"	"1"	"2000"	"2014"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C3538946"	"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3766"	"KCNJ10"	"0.607"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.36"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9605263"	"1996"	"2017"	"2"	"3"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.47"	"1"	"2000"	"2011"	"0"	"1"	"GENOMICS_ENGLAND"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0027773"	"Nesidioblastosis"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.40"		"1995"	"2015"	"11"	"13"	"UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.42"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0342277"	"Diabetes mellitus autosomal dominant type II (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C1832386"	"Diabetes Mellitus, Transient Neonatal, 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2008"	"0"	"0"	"ORPHANET"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C1833102"	"DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES"	"disease"	"C10;C18;C19;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2017"	"13"	"8"	"UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"13"	"20"	"CTD_human;ORPHANET;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C1853564"	"Developmental Delay, Epilepsy, and Neonatal Diabetes"	"disease"	"C10;C16;C18;C19;C23;F01"	"Disease or Syndrome"	"0.77"	"1"	"2004"	"2017"	"13"	"0"	"ORPHANET;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C1864623"	"DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"2"	"3"	"CTD_human;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C2931832"	"Hyperinsulinemic hypoglycemia, familial, 1"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C2931833"	"Hyperinsulinemic hypoglycemia, familial, 2"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.50"		"1995"	"2009"	"11"	"1"	"CTD_human;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C3888018"	"Congenital Hyperinsulinism"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9642857"	"1995"	"2016"	"11"	"1"	"CTD_human;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4225365"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2005"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4274081"	"Autosomal dominant hyperinsulinism due to Kir6.2 deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4303593"	"DEND syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3767"	"KCNJ11"	"0.542"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3769"	"KCNJ13"	"0.681"	"0.172"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.42"	"1"	"2016"	"2016"	"0"	"1"	"ORPHANET"
"3769"	"KCNJ13"	"0.681"	"0.172"	"C1860405"	"Snowflake vitreoretinal degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.74"	"1"	"2008"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3769"	"KCNJ13"	"0.681"	"0.172"	"C3280062"	"LEBER CONGENITAL AMAUROSIS 16"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2011"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"3772"	"KCNJ15"	"0.785"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3772"	"KCNJ15"	"0.785"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3772"	"KCNJ15"	"0.785"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3772"	"KCNJ15"	"0.785"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3775"	"KCNK1"	"0.785"	"0.414"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2007"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"3776"	"KCNK2"	"0.667"	"0.276"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.52"	"1"	"2016"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"3777"	"KCNK3"	"0.663"	"0.276"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"3777"	"KCNK3"	"0.663"	"0.276"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1993"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"3777"	"KCNK3"	"0.663"	"0.276"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.69"	"1"	"1993"	"2017"	"7"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3777"	"KCNK3"	"0.663"	"0.276"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3777"	"KCNK3"	"0.663"	"0.276"	"C3809198"	"PULMONARY HYPERTENSION, PRIMARY, 4"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2016"	"1"	"6"	"UNIPROT"
"3777"	"KCNK3"	"0.663"	"0.276"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2017"	"1"	"1"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0410916"	"Neonatal Death"	"disease"	"C13;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0701826"	"Perinatal death"	"phenotype"	"C13;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C1836173"	"Generalized Epilepsy and Paroxysmal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.72"	"1"	"2005"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3778"	"KCNMA1"	"0.572"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"3779"	"KCNMB1"	"0.785"	"0.345"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3779"	"KCNMB1"	"0.785"	"0.345"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3779"	"KCNMB1"	"0.785"	"0.345"	"C1837739"	"Hypertension, Diastolic, Resistance to"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3780"	"KCNN1"	"0.886"	"0.069"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3782"	"KCNN3"	"0.659"	"0.379"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"	"0.8"	"2010"	"2018"	"1"	"4"	"CTD_human"
"3782"	"KCNN3"	"0.659"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2000"	"2005"	"5"	"0"	"PSYGENET"
"3782"	"KCNN3"	"0.659"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6666667"	"1999"	"2011"	"3"	"0"	"PSYGENET"
"3782"	"KCNN3"	"0.659"	"0.379"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3782"	"KCNN3"	"0.659"	"0.379"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3782"	"KCNN3"	"0.659"	"0.379"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3783"	"KCNN4"	"0.707"	"0.379"	"C0272051"	"Xerocytosis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.52"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"3783"	"KCNN4"	"0.707"	"0.379"	"C4225242"	"DEHYDRATED HEREDITARY STOMATOCYTOSIS 2"	"disease"		"Disease or Syndrome"	"0.40"		"1974"	"2015"	"3"	"3"	"UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"	"0.9166667"	"1997"	"2015"	"0"	"1"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CLINGEN"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2017"	"3"	"18"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0022387"	"Jervell-Lange Nielsen Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"1.00"	"0.9666667"	"1997"	"2017"	"6"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.50"	"0.9665072"	"1992"	"2018"	"7"	"75"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"41"	"215"	"CTD_human;ORPHANET;UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CLINGEN"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1837014"	"Atrial Fibrillation, Familial, 3"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1843738"	"LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"1996"	"2015"	"40"	"192"	"UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1865019"	"SHORT QT SYNDROME 2 (disorder)"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.62"	"1"	"2004"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C1865020"	"Short QT Syndrome 1"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3784"	"KCNQ1"	"0.525"	"0.586"	"C3277700"	"LONG QT SYNDROME 1/2, DIGENIC (disorder)"	"disease"		"Disease or Syndrome"	"0.50"		"1996"	"2015"	"40"	"192"	"UNIPROT"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.36"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9772727"	"1998"	"2018"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2013"	"2"	"0"	"PSYGENET"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.9473684"	"2004"	"2018"	"1"	"4"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0220669"	"Familial benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.9019608"	"1994"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0270851"	"Benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.57"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0393693"	"Benign Neonatal Epilepsy, Nonfamilial"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"2003"	"2018"	"0"	"6"	"GENOMICS_ENGLAND"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C1843140"	"SEIZURES, BENIGN FAMILIAL INFANTILE, 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"2"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C2751195"	"Epilepsy, Benign Neonatal, 1, And-Or Myokymia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"1998"	"2017"	"8"	"23"	"CTD_human;UNIPROT"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C3149074"	"SEIZURES, BENIGN FAMILIAL NEONATAL, 1"	"disease"		"Disease or Syndrome"	"0.50"		"1998"	"2017"	"8"	"23"	"CTD_human;UNIPROT"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C3149075"	"SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2017"	"8"	"24"	"CTD_human;UNIPROT"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C3150986"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2017"	"8"	"44"	"CTD_human;ORPHANET;UNIPROT"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.46"	"1"	"2004"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3785"	"KCNQ2"	"0.557"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C0220669"	"Familial benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.9354839"	"1989"	"2017"	"0"	"1"	"ORPHANET"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2003"	"0"	"0"	"ORPHANET"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C1852581"	"EPILEPSY, BENIGN NEONATAL, 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9"	"1991"	"2016"	"5"	"5"	"CTD_human;UNIPROT"
"3786"	"KCNQ3"	"0.648"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"3787"	"KCNS1"	"0.928"	"0.103"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"3790"	"KCNS3"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"3791"	"KDR"	"0.423"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3791"	"KDR"	"0.423"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9444444"	"2007"	"2018"	"0"	"0"	"CGI"
"3791"	"KDR"	"0.423"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2010"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.55"	"1"	"2008"	"2016"	"1"	"0"	"CGI;CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2003"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3791"	"KDR"	"0.423"	"0.724"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"3791"	"KDR"	"0.423"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2017"	"0"	"0"	"UNIPROT"
"3791"	"KDR"	"0.423"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2013"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3791"	"KDR"	"0.423"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8888889"	"1995"	"2016"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.58"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human;UNIPROT"
"3791"	"KDR"	"0.423"	"0.724"	"C1865871"	"HEMANGIOMA, CAPILLARY INFANTILE"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2008"	"3"	"2"	"CTD_human;UNIPROT"
"3791"	"KDR"	"0.423"	"0.724"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3791"	"KDR"	"0.423"	"0.724"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3795"	"KHK"	"0.799"	"0.207"	"C0268160"	"Deficiency of fructokinase"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1995"	"2008"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3796"	"KIF2A"	"0.652"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3796"	"KIF2A"	"0.652"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3796"	"KIF2A"	"0.652"	"0.483"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3796"	"KIF2A"	"0.652"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3796"	"KIF2A"	"0.652"	"0.483"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3796"	"KIF2A"	"0.652"	"0.483"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3796"	"KIF2A"	"0.652"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"3796"	"KIF2A"	"0.652"	"0.483"	"C3809414"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"3796"	"KIF2A"	"0.652"	"0.483"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3797"	"KIF3C"	"0.815"	"0.172"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3797"	"KIF3C"	"0.815"	"0.172"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3798"	"KIF5A"	"0.642"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2014"	"1"	"1"	"CTD_human"
"3798"	"KIF5A"	"0.642"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"3798"	"KIF5A"	"0.642"	"0.483"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3798"	"KIF5A"	"0.642"	"0.483"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"3798"	"KIF5A"	"0.642"	"0.483"	"C1858712"	"Spastic paraplegia 10, autosomal dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.73"	"1"	"2003"	"2014"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3798"	"KIF5A"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3798"	"KIF5A"	"0.642"	"0.483"	"C4310658"	"MYOCLONUS, INTRACTABLE, NEONATAL"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"CTD_human"
"3799"	"KIF5B"	"0.667"	"0.31"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"3799"	"KIF5B"	"0.667"	"0.31"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3800"	"KIF5C"	"0.685"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3800"	"KIF5C"	"0.685"	"0.345"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3800"	"KIF5C"	"0.685"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3800"	"KIF5C"	"0.685"	"0.345"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3800"	"KIF5C"	"0.685"	"0.345"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3800"	"KIF5C"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"3800"	"KIF5C"	"0.685"	"0.345"	"C3809013"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2018"	"4"	"2"	"CTD_human;UNIPROT"
"3800"	"KIF5C"	"0.685"	"0.345"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3811"	"KIR3DL1"	"0.546"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"0.9375"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3811"	"KIR3DL1"	"0.546"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2006"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3814"	"KISS1"	"0.528"	"0.517"	"C3541462"	"HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.80"		"2007"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.46"	"1"	"1997"	"2015"	"1"	"1"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3815"	"KIT"	"0.394"	"0.759"	"C0023461"	"Leukemia, Mast-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1993"	"2016"	"0"	"1"	"CGI;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9224138"	"1989"	"2018"	"0"	"3"	"CGI;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0023479"	"Acute myelomonocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.75"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0024899"	"Mastocytosis"	"disease"	"C04;C17;C20"	"Disease or Syndrome"	"0.90"	"0.9565217"	"1996"	"2016"	"0"	"1"	"CGI;CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.978022"	"1992"	"2018"	"0"	"21"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9375"	"1996"	"2014"	"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2010"	"3"	"1"	"UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0042111"	"Urticaria Pigmentosa"	"disease"	"C04;C17"	"Congenital Abnormality"	"0.36"	"1"	"1996"	"2006"	"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C0080024"	"Piebaldism"	"disease"	"C16;C17;C18"	"Congenital Abnormality"	"1.00"	"1"	"1977"	"2016"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.8928571"	"1991"	"2016"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"2009"	"2016"	"0"	"2"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3815"	"KIT"	"0.394"	"0.759"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"0.7272727"	"2006"	"2014"	"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C0221013"	"Mastocytosis, Systemic"	"disease"	"C04;C20"	"Neoplastic Process"	"0.70"	"0.9893617"	"1998"	"2018"	"1"	"1"	"CGI;CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"1.00"	"0.9402516"	"1998"	"2018"	"7"	"26"	"CGI;CTD_human;ORPHANET;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C0263402"	"Telangiectasia macularis eruptiva perstans"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C0272203"	"Indolent Systemic Mastocytosis"	"disease"	"C04;C20"	"Neoplastic Process"	"0.38"	"0.875"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0343115"	"Skin Mastocytoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1992"	"2012"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C0684337"	"Ewings sarcoma-primitive neuroectodermal tumor (PNET)"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C1112486"	"Aggressive Systemic Mastocytosis"	"disease"	"C04;C20"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C1292778"	"Chronic myeloproliferative disorder"	"disease"		"Neoplastic Process"	"0.48"	"1"	"1994"	"2016"	"0"	"1"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C1301365"	"Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.52"	"1"	"2006"	"2009"	"2"	"2"	"CTD_human;UNIPROT"
"3815"	"KIT"	"0.394"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3815"	"KIT"	"0.394"	"0.759"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3815"	"KIT"	"0.394"	"0.759"	"C2861596"	"AML M4 Eo with inv(16) or t(16;16)"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.56"	"0.8333333"	"2002"	"2016"	"3"	"0"	"CTD_human;ORPHANET"
"3815"	"KIT"	"0.394"	"0.759"	"C3496549"	"Male Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C3714644"	"Thymus Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3815"	"KIT"	"0.394"	"0.759"	"C3898222"	"Mucosal Melanoma"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2008"	"2018"	"0"	"0"	"CGI"
"3815"	"KIT"	"0.394"	"0.759"	"C4509020"	"Isolated bone marrow mastocytosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3816"	"KLK1"	"0.564"	"0.552"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C1835808"	"Kallikrein, Decreased Urinary Activity of"	"phenotype"	"C16;C18"	"Finding"	"0.40"		"2002"	"2005"	"0"	"1"	"CTD_human"
"3816"	"KLK1"	"0.564"	"0.552"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3817"	"KLK2"	"0.735"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"		"2005"	"2009"	"2"	"0"	"CTD_human"
"3817"	"KLK2"	"0.735"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9565217"	"1999"	"2015"	"2"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0007274"	"Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0272339"	"Prekallikrein deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.72"	"1"	"1981"	"2015"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0750988"	"Common Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0750989"	"External Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3818"	"KLKB1"	"0.663"	"0.448"	"C0750990"	"Internal Carotid Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3820"	"KLRB1"	"0.72"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"3822"	"KLRC2"	"0.752"	"0.31"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3822"	"KLRC2"	"0.752"	"0.31"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3822"	"KLRC2"	"0.752"	"0.31"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0002792"	"anaphylaxis"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0010200"	"Coughing"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.36"	"0.8333333"	"2000"	"2012"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1987"	"1992"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0019243"	"Angioedemas, Hereditary"	"group"	"C14;C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.969697"	"1983"	"2018"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1989"	"2013"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020453"	"Hyperesthesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1981"	"2017"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1984"	"2011"	"9"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1980"	"1986"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1991"	"1995"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.38"	"1"	"1986"	"2016"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0272340"	"High molecular weight kininogen deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.64"	"1"	"1975"	"2007"	"0"	"3"	"CTD_human;ORPHANET"
"3827"	"KNG1"	"0.53"	"0.862"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1987"	"1992"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751215"	"Hyperesthesia, Tactile"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751216"	"Hyperesthesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1986"	"2010"	"6"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1980"	"1986"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C1856719"	"Kininogen Deficiency, Total"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"1975"	"1993"	"0"	"1"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1980"	"1986"	"2"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C2931758"	"Acquired angioedema"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"2011"	"17"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3827"	"KNG1"	"0.53"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3832"	"KIF11"	"0.659"	"0.448"	"C0002938"	"Aneuploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3832"	"KIF11"	"0.659"	"0.448"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"3832"	"KIF11"	"0.659"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3832"	"KIF11"	"0.659"	"0.448"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3832"	"KIF11"	"0.659"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"3832"	"KIF11"	"0.659"	"0.448"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3832"	"KIF11"	"0.659"	"0.448"	"C1835265"	"Lymphedema, microcephaly and chorioretinopathy syndrome"	"disease"	"C05;C10;C11;C15;C16;C23"	"Disease or Syndrome"	"0.74"	"1"	"2012"	"2016"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3832"	"KIF11"	"0.659"	"0.448"	"C3501946"	"Microcephaly with Chorioretinopathy, Autosomal Dominant"	"disease"	"C05;C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3832"	"KIF11"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3835"	"KIF22"	"0.607"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3835"	"KIF22"	"0.607"	"0.483"	"C1863732"	"Spondyloepimetaphyseal dysplasia with multiple dislocations"	"disease"	"C05;C16;C26"	"Disease or Syndrome"	"0.63"	"1"	"2009"	"2016"	"2"	"3"	"ORPHANET;UNIPROT"
"3835"	"KIF22"	"0.607"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3836"	"KPNA1"	"0.815"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3837"	"KPNB1"	"0.799"	"0.172"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3837"	"KPNB1"	"0.799"	"0.172"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3838"	"KPNA2"	"0.611"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"3839"	"KPNA3"	"0.815"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3839"	"KPNA3"	"0.815"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2013"	"3"	"0"	"PSYGENET"
"3839"	"KPNA3"	"0.815"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3839"	"KPNA3"	"0.815"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3841"	"KPNA5"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3843"	"IPO5"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2011"	"4"	"0"	"PSYGENET"
"3843"	"IPO5"	"0.886"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9370079"	"1983"	"2018"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9538462"	"1991"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.62"	"1"	"1984"	"2018"	"0"	"1"	"CTD_human;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2018"	"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.952381"	"1988"	"2016"	"0"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2000"	"2018"	"2"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2018"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9622642"	"1990"	"2018"	"6"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007115"	"Malignant neoplasm of thyroid"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2012"	"2015"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.9498328"	"1989"	"2018"	"7"	"11"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2017"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007528"	"Cecal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007772"	"Intracranial Arteriovenous Malformation"	"disease"	"C10;C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007847"	"Malignant tumor of cervix"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9411765"	"1988"	"2015"	"6"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9634146"	"1992"	"2018"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9090909"	"1993"	"2016"	"3"	"12"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1994"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.56"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.64"	"1"	"1994"	"2016"	"4"	"1"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1988"	"2017"	"0"	"4"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"3"	"UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.902439"	"1993"	"2017"	"32"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9615385"	"1989"	"2017"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.45"	"1"	"2001"	"2016"	"0"	"2"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9016393"	"1991"	"2018"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.962963"	"2000"	"2018"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"2016"	"5"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2016"	"4"	"11"	"CTD_human;ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9166667"	"1993"	"2017"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"1"	"1993"	"2016"	"6"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0030849"	"Penile Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.50"		"2018"	"2018"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.46"	"1"	"1993"	"2016"	"2"	"2"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.63"	"1"	"1990"	"2016"	"1"	"8"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2014"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2016"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.42"	"1"	"1984"	"2016"	"0"	"2"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.9396552"	"1990"	"2018"	"5"	"3"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0153437"	"Malignant neoplasm of cecum"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0153601"	"Malignant neoplasm of penis"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"3"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"2016"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2010"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2010"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0206682"	"Follicular thyroid carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8"	"1993"	"2013"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9482759"	"1986"	"2018"	"0"	"1"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.45"	"1"	"2009"	"2015"	"0"	"1"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.9352518"	"1990"	"2018"	"32"	"1"	"CGI;CTD_human;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0265329"	"Organoid Nevus Phakomatosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.52"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0279680"	"Transitional cell carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"1"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0302592"	"Cervix carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.72"	"1"	"2005"	"2013"	"1"	"1"	"CGI;CTD_human;ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"1993"	"2002"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.59"	"0.8888889"	"1997"	"2018"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9512195"	"1992"	"2018"	"6"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"1.00"	"1"	"1987"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0362030"	"Verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.58"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0406612"	"Encephalocraniocutaneous lipomatosis"	"disease"	"C10;C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C0473574"	"Inflammatory linear verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.56"	"1"	"1990"	"2015"	"1"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.58"	"1"	"2007"	"2016"	"2"	"0"	"CLINGEN;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9534884"	"1990"	"2018"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.96"	"1988"	"2016"	"0"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.70"	"0.9596774"	"1983"	"2018"	"3"	"3"	"CGI;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"0.9310345"	"1987"	"2017"	"3"	"5"	"UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0751008"	"Intracranial Arteriovenous Malformation, Ruptured"	"disease"	"C10;C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"		"1987"	"2016"	"0"	"1"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0917804"	"Arteriovenous Malformations, Cerebral"	"group"	"C10;C14;C16"	"Congenital Abnormality"	"0.41"	"1"	"2018"	"2018"	"0"	"1"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"1"	"1991"	"2013"	"1"	"2"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"	"0.8823529"	"1997"	"2017"	"1"	"0"	"CGI;CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"0.70"	"1"	"2006"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.40"	"0.9"	"1993"	"2015"	"0"	"0"	"CGI"
"3845"	"KRAS"	"0.35"	"0.724"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.40"	"0.8"	"1996"	"2014"	"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2013"	"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9643606"	"1993"	"2018"	"4"	"4"	"CTD_human;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"4"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2001"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1838329"	"APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C1860991"	"NOONAN SYNDROME 3"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.90"		"2006"	"2015"	"10"	"11"	"CLINGEN;CTD_human;UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C1968782"	"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"3845"	"KRAS"	"0.35"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9"	"1993"	"2016"	"2"	"2"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C2674723"	"RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER"	"disease"		"Disease or Syndrome"	"0.40"		"1987"	"2016"	"0"	"3"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"3845"	"KRAS"	"0.35"	"0.724"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.33"	"0.6666667"	"2012"	"2015"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"		"1987"	"2003"	"3"	"5"	"UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C3179502"	"Linear Verrucous Epidermal Nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3845"	"KRAS"	"0.35"	"0.724"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"3845"	"KRAS"	"0.35"	"0.724"	"C3809005"	"CARDIOFACIOCUTANEOUS SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2015"	"5"	"8"	"UNIPROT"
"3845"	"KRAS"	"0.35"	"0.724"	"C3854181"	"Nevus sebaceous"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3848"	"KRT1"	"0.616"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3848"	"KRT1"	"0.616"	"0.345"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"3848"	"KRT1"	"0.616"	"0.345"	"C0079153"	"Hyperkeratosis, Epidermolytic"	"disease"	"C16;C17"	"Congenital Abnormality"	"1.00"	"0.9714286"	"1992"	"2018"	"12"	"17"	"CTD_human;ORPHANET;UNIPROT"
"3848"	"KRT1"	"0.616"	"0.345"	"C0343110"	"Epidermolytic palmoplantar keratoderma of Vorner"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C0432307"	"Ichthyosis hystrix of Curth-Macklin"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C1721006"	"Keratoderma, Palmoplantar, Epidermolytic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.66"	"1"	"2001"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C1833030"	"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"1995"	"2001"	"2"	"1"	"CTD_human;UNIPROT"
"3848"	"KRT1"	"0.616"	"0.345"	"C1836681"	"Erythrokeratoderma, Reticular"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C1840296"	"Ichthyosis hystrix, Curth Macklin type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human;ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C1843463"	"Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1999"	"2000"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3848"	"KRT1"	"0.616"	"0.345"	"C1862005"	"Epidermolytic Hyperkeratosis, Late-Onset"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1992"	"2011"	"12"	"14"	"UNIPROT"
"3848"	"KRT1"	"0.616"	"0.345"	"C2931123"	"Keratosis palmoplantaris striata 3"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3848"	"KRT1"	"0.616"	"0.345"	"C2931735"	"Epidermolytic palmoplantar keratoderma Vorner type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3848"	"KRT1"	"0.616"	"0.345"	"C2936837"	"Keratosis of Greither"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3848"	"KRT1"	"0.616"	"0.345"	"C3665704"	"Congenital reticular ichthyosiform erythroderma"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"3849"	"KRT2"	"0.752"	"0.138"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3849"	"KRT2"	"0.752"	"0.138"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3849"	"KRT2"	"0.752"	"0.138"	"C0432306"	"Ichthyosis Bullosa of Siemens"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.80"	"1"	"1991"	"2005"	"15"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3849"	"KRT2"	"0.752"	"0.138"	"C1838440"	"ICHTHYOSIS EXFOLIATIVA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"1991"	"2005"	"15"	"12"	"UNIPROT"
"3849"	"KRT2"	"0.752"	"0.138"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3850"	"KRT3"	"0.762"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3850"	"KRT3"	"0.762"	"0.345"	"C0339277"	"Corneal Dystrophy, Juvenile Epithelial of Meesmann"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.77"	"1"	"1997"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3850"	"KRT3"	"0.762"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3850"	"KRT3"	"0.762"	"0.345"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1997"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"3851"	"KRT4"	"0.743"	"0.31"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3851"	"KRT4"	"0.743"	"0.31"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3851"	"KRT4"	"0.743"	"0.31"	"C1721005"	"Leukokeratosis, Hereditary Mucosal"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.94"	"1"	"1996"	"2013"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3851"	"KRT4"	"0.743"	"0.31"	"C4011926"	"WHITE SPONGE NEVUS 1"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2003"	"2"	"0"	"UNIPROT"
"3852"	"KRT5"	"0.555"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2009"	"2016"	"2"	"1"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.32"	"1"	"2007"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"3852"	"KRT5"	"0.555"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0079295"	"Epidermolysis Bullosa Herpetiformis Dowling-Meara"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.91"	"1"	"1992"	"2017"	"10"	"13"	"CTD_human;ORPHANET;UNIPROT"
"3852"	"KRT5"	"0.555"	"0.552"	"C0079298"	"Epidermolysis Bullosa Simplex"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"0.9824561"	"1991"	"2018"	"0"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0079299"	"Epidermolysis Bullosa Simplex Kobner"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.71"	"1"	"1991"	"2012"	"7"	"11"	"CTD_human;ORPHANET;UNIPROT"
"3852"	"KRT5"	"0.555"	"0.552"	"C0080333"	"Weber-Cockayne Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2015"	"15"	"23"	"CTD_human;ORPHANET;UNIPROT"
"3852"	"KRT5"	"0.555"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0406811"	"Reticulate acropigmentation of Kitamura"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C0432316"	"Epidermolysis bullosa simplex with mottled pigmentation"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.77"	"1"	"1976"	"2012"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3852"	"KRT5"	"0.555"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2003"	"2015"	"1"	"0"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1832926"	"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"0"	"2"	"CTD_human"
"3852"	"KRT5"	"0.555"	"0.552"	"C1836284"	"Epidermolysis Bullosa Simplex with Migratory Circinate Erythema"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2006"	"0"	"1"	"CTD_human;ORPHANET"
"3852"	"KRT5"	"0.555"	"0.552"	"C3714534"	"dowling-degos disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"0.8"	"1998"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"3853"	"KRT6A"	"0.685"	"0.31"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1995"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"3853"	"KRT6A"	"0.685"	"0.31"	"C0265334"	"Pachyonychia Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"0.9230769"	"2003"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"3853"	"KRT6A"	"0.685"	"0.31"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1995"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"3853"	"KRT6A"	"0.685"	"0.31"	"C1706595"	"Pachyonychia Congenita, Jadassohn Lewandowsky Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2007"	"0"	"0"	"CTD_human"
"3853"	"KRT6A"	"0.685"	"0.31"	"C1721007"	"Pachyonychia Congenita, Type 2 (disorder)"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3853"	"KRT6A"	"0.685"	"0.31"	"C3714948"	"PACHYONYCHIA CONGENITA 3"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2013"	"12"	"20"	"UNIPROT"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1999"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0265334"	"Pachyonychia Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"3854"	"KRT6B"	"0.69"	"0.414"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1999"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"3854"	"KRT6B"	"0.69"	"0.414"	"C1706595"	"Pachyonychia Congenita, Jadassohn Lewandowsky Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3854"	"KRT6B"	"0.69"	"0.414"	"C1721007"	"Pachyonychia Congenita, Type 2 (disorder)"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human"
"3854"	"KRT6B"	"0.69"	"0.414"	"C3714949"	"PACHYONYCHIA CONGENITA 4"	"disease"		"Disease or Syndrome"	"0.40"		"1999"	"2011"	"3"	"1"	"UNIPROT"
"3855"	"KRT7"	"0.534"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"0.8571429"	"2004"	"2016"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C0949541"	"Hurthle Cell Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"0.5"	"2004"	"2010"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2013"	"2"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1510502"	"Oxyphilic Adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"3855"	"KRT7"	"0.534"	"0.655"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2002"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"0.75"	"2003"	"2013"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0267809"	"Cirrhosis, Cryptogenic"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"1997"	"2003"	"1"	"6"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C0268074"	"Indian childhood cirrhosis"	"disease"	"C06;C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"5"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"1995"	"2017"	"1"	"1"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3856"	"KRT8"	"0.534"	"0.586"	"C1835713"	"CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"1997"	"2003"	"1"	"5"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C1859088"	"COPPER TOXICOSIS, IDIOPATHIC"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"5"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C1861556"	"Cirrhosis, Familial"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"5"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"5"	"UNIPROT"
"3856"	"KRT8"	"0.534"	"0.586"	"C1876166"	"Endemic Tyrolean Infantile Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"5"	"UNIPROT"
"3857"	"KRT9"	"0.707"	"0.207"	"C0022584"	"Keratoderma, Palmoplantar, Diffuse"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1994"	"2012"	"23"	"14"	"UNIPROT"
"3857"	"KRT9"	"0.707"	"0.207"	"C0343110"	"Epidermolytic palmoplantar keratoderma of Vorner"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3857"	"KRT9"	"0.707"	"0.207"	"C1721006"	"Keratoderma, Palmoplantar, Epidermolytic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"1978"	"2018"	"23"	"14"	"CTD_human;ORPHANET;UNIPROT"
"3857"	"KRT9"	"0.707"	"0.207"	"C1840427"	"PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, WITH KNUCKLE PADS (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1990"	"2012"	"23"	"14"	"UNIPROT"
"3857"	"KRT9"	"0.707"	"0.207"	"C2931735"	"Epidermolytic palmoplantar keratoderma Vorner type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3857"	"KRT9"	"0.707"	"0.207"	"C2936837"	"Keratosis of Greither"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3857"	"KRT9"	"0.707"	"0.207"	"C3489771"	"Keratosis Palmaris et Plantaris Familiaris"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1994"	"2012"	"23"	"14"	"UNIPROT"
"3858"	"KRT10"	"0.636"	"0.379"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.44"	"1"	"2000"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3858"	"KRT10"	"0.636"	"0.379"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0079153"	"Hyperkeratosis, Epidermolytic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.80"	"0.9777778"	"1990"	"2018"	"9"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3858"	"KRT10"	"0.636"	"0.379"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3858"	"KRT10"	"0.636"	"0.379"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3858"	"KRT10"	"0.636"	"0.379"	"C1836681"	"Erythrokeratoderma, Reticular"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"2010"	"2010"	"0"	"4"	"CTD_human;ORPHANET"
"3858"	"KRT10"	"0.636"	"0.379"	"C1843463"	"Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"1999"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3858"	"KRT10"	"0.636"	"0.379"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3858"	"KRT10"	"0.636"	"0.379"	"C1862005"	"Epidermolytic Hyperkeratosis, Late-Onset"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"1992"	"2011"	"9"	"10"	"UNIPROT"
"3858"	"KRT10"	"0.636"	"0.379"	"C3665704"	"Congenital reticular ichthyosiform erythroderma"	"disease"		"Disease or Syndrome"	"0.58"	"1"	"2012"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"3859"	"KRT12"	"0.799"	"0.103"	"C0339277"	"Corneal Dystrophy, Juvenile Epithelial of Meesmann"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.80"	"1"	"1997"	"2016"	"14"	"15"	"CTD_human;ORPHANET;UNIPROT"
"3859"	"KRT12"	"0.799"	"0.103"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1997"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"3860"	"KRT13"	"0.735"	"0.345"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3860"	"KRT13"	"0.735"	"0.345"	"C1721005"	"Leukokeratosis, Hereditary Mucosal"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"1996"	"2001"	"0"	"0"	"CTD_human;ORPHANET"
"3860"	"KRT13"	"0.735"	"0.345"	"C4014321"	"WHITE SPONGE NEVUS 2"	"disease"		"Disease or Syndrome"	"0.40"		"1995"	"2004"	"4"	"5"	"UNIPROT"
"3861"	"KRT14"	"0.572"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.34"	"1"	"1991"	"2010"	"11"	"0"	"GENOMICS_ENGLAND"
"3861"	"KRT14"	"0.572"	"0.586"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"1998"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"3861"	"KRT14"	"0.572"	"0.586"	"C0036305"	"Schamberg Disease"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0079295"	"Epidermolysis Bullosa Herpetiformis Dowling-Meara"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.93"	"1"	"1991"	"2006"	"17"	"14"	"CTD_human;ORPHANET;UNIPROT"
"3861"	"KRT14"	"0.572"	"0.586"	"C0079298"	"Epidermolysis Bullosa Simplex"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"1"	"1991"	"2018"	"0"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0079299"	"Epidermolysis Bullosa Simplex Kobner"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.72"	"1"	"1991"	"2012"	"8"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3861"	"KRT14"	"0.572"	"0.586"	"C0080333"	"Weber-Cockayne Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1993"	"2006"	"13"	"15"	"CTD_human;ORPHANET;UNIPROT"
"3861"	"KRT14"	"0.572"	"0.586"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0343111"	"Naegeli syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"3861"	"KRT14"	"0.572"	"0.586"	"C0406778"	"Dermatopathia pigmentosa reticularis"	"disease"	"C04;C17;C23"	"Congenital Abnormality"	"0.62"	"1"	"1992"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"3861"	"KRT14"	"0.572"	"0.586"	"C0432316"	"Epidermolysis bullosa simplex with mottled pigmentation"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3861"	"KRT14"	"0.572"	"0.586"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"3861"	"KRT14"	"0.572"	"0.586"	"C0549567"	"Pigmentation Disorders"	"group"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C1832926"	"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"1994"	"1997"	"0"	"3"	"CTD_human"
"3861"	"KRT14"	"0.572"	"0.586"	"C3715082"	"EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1"	"disease"		"Disease or Syndrome"	"0.50"		"1995"	"1995"	"1"	"1"	"ORPHANET;UNIPROT"
"3866"	"KRT15"	"0.696"	"0.448"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3866"	"KRT15"	"0.696"	"0.448"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3866"	"KRT15"	"0.696"	"0.448"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3866"	"KRT15"	"0.696"	"0.448"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3868"	"KRT16"	"0.614"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3868"	"KRT16"	"0.614"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3868"	"KRT16"	"0.614"	"0.517"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"1995"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"3868"	"KRT16"	"0.614"	"0.517"	"C0265334"	"Pachyonychia Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.79"	"1"	"2001"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"3868"	"KRT16"	"0.614"	"0.517"	"C0343110"	"Epidermolytic palmoplantar keratoderma of Vorner"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3868"	"KRT16"	"0.614"	"0.517"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1995"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"3868"	"KRT16"	"0.614"	"0.517"	"C1706595"	"Pachyonychia Congenita, Jadassohn Lewandowsky Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.85"	"1"	"1995"	"2014"	"12"	"12"	"CTD_human;UNIPROT"
"3868"	"KRT16"	"0.614"	"0.517"	"C1721006"	"Keratoderma, Palmoplantar, Epidermolytic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"3868"	"KRT16"	"0.614"	"0.517"	"C1721007"	"Pachyonychia Congenita, Type 2 (disorder)"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"2012"	"2012"	"0"	"0"	"CTD_human"
"3868"	"KRT16"	"0.614"	"0.517"	"C2931735"	"Epidermolytic palmoplantar keratoderma Vorner type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3868"	"KRT16"	"0.614"	"0.517"	"C2931923"	"Hyperkeratosis of the palms and soles and esophageal papillomas"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.75"	"1"	"1996"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3872"	"KRT17"	"0.59"	"0.414"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"1995"	"2012"	"5"	"0"	"GENOMICS_ENGLAND"
"3872"	"KRT17"	"0.59"	"0.414"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C0259771"	"Steatocystoma multiplex"	"disease"	"C16;C17"	"Neoplastic Process"	"0.74"	"1"	"1997"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3872"	"KRT17"	"0.59"	"0.414"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C0265334"	"Pachyonychia Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.59"	"1"	"1995"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"3872"	"KRT17"	"0.59"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1995"	"2012"	"5"	"0"	"GENOMICS_ENGLAND"
"3872"	"KRT17"	"0.59"	"0.414"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C1706595"	"Pachyonychia Congenita, Jadassohn Lewandowsky Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3872"	"KRT17"	"0.59"	"0.414"	"C1721007"	"Pachyonychia Congenita, Type 2 (disorder)"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.68"	"1"	"1986"	"2014"	"18"	"13"	"CTD_human;UNIPROT"
"3872"	"KRT17"	"0.59"	"0.414"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"1991"	"1999"	"3"	"0"	"GENOMICS_ENGLAND"
"3872"	"KRT17"	"0.59"	"0.414"	"C3671377"	"Sebocystomatosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3875"	"KRT18"	"0.557"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2015"	"4"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0267809"	"Cirrhosis, Cryptogenic"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C0268074"	"Indian childhood cirrhosis"	"disease"	"C06;C08"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"		"2003"	"2015"	"2"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C1835713"	"CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C1859088"	"COPPER TOXICOSIS, IDIOPATHIC"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C1861556"	"Cirrhosis, Familial"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C1876166"	"Endemic Tyrolean Infantile Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"4"	"UNIPROT"
"3875"	"KRT18"	"0.557"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3875"	"KRT18"	"0.557"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3880"	"KRT19"	"0.51"	"0.621"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3882"	"KRT32"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3887"	"KRT81"	"0.713"	"0.345"	"C0546966"	"Monilethrix"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.72"	"1"	"1995"	"2015"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"3889"	"KRT83"	"0.752"	"0.103"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3889"	"KRT83"	"0.752"	"0.103"	"C0546966"	"Monilethrix"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.72"	"1"	"2005"	"2015"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3891"	"KRT85"	"0.762"	"0.138"	"C1865951"	"Ectodermal Dysplasia, Pure Hair-Nail Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3892"	"KRT86"	"0.773"	"0.207"	"C0546966"	"Monilethrix"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.75"	"1"	"1995"	"2016"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"3895"	"KTN1"	"0.857"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3895"	"KTN1"	"0.857"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0003537"	"Aphasia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1994"	"2005"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0003546"	"Aphasia, Acquired"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9333333"	"1994"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231686"	"Gait, Unsteady"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231687"	"Spastic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231688"	"Gait, Shuffling"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231689"	"Gait, Athetotic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231693"	"Charcot Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231694"	"Gait, Festinating"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231695"	"Cerebellar ataxic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231696"	"Gait, Hemiplegic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231698"	"Gait, Scissors"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0231712"	"Waddling gait"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234462"	"Aphasia, Ageusic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234469"	"Aphasia, Global"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234472"	"Aphasia, Functional"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234474"	"Aphasia, Graphomotor"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234476"	"Aphasia, Intellectual"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234482"	"Aphasia, Semantic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234484"	"Aphasia, Syntactical"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0234996"	"Gait, Rigid"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0235000"	"Gait, Broadened"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0265216"	"X-linked hydrocephalus syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9756098"	"1949"	"2015"	"23"	"18"	"CTD_human;ORPHANET;UNIPROT"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0337210"	"Gait, Stumbling"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0338457"	"Aphasia, Progressive"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0427128"	"Rapid Fatigue of Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0427149"	"Gait, Drop Foot"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0427169"	"Marche a Petit Pas"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0427177"	"Gait, Hysterical"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0454576"	"Aphasia, Mixed"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0750917"	"Aphasia, Auditory Discriminatory"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0750918"	"Aphasia, Commisural"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0750919"	"Aphasia, Post-Ictal"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0750920"	"Aphasia, Post-Traumatic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0750921"	"Dejerine-Lichtheim Phenomenon"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0751829"	"Gait Disorder, Sensorimotor"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0751830"	"Gait Disorders, Neurologic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0751831"	"Gait, Frontal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0751832"	"Gait, Widebased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0795953"	"MASA SYNDROME (disorder)"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"1.00"	"1"	"1986"	"2017"	"21"	"11"	"CTD_human;ORPHANET;UNIPROT"
"3897"	"L1CAM"	"0.5"	"0.655"	"C0973461"	"Dysphasia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1839909"	"CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.70"		"1997"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3897"	"L1CAM"	"0.5"	"0.655"	"C1844006"	"Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2013"	"22"	"12"	"UNIPROT"
"3897"	"L1CAM"	"0.5"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1993"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3899"	"AFF3"	"0.672"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.47"	"1"	"2009"	"2013"	"2"	"1"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3899"	"AFF3"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"3899"	"AFF3"	"0.672"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3903"	"LAIR1"	"0.659"	"0.517"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"3908"	"LAMA2"	"0.598"	"0.621"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.50"	"0.9677419"	"1996"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3908"	"LAMA2"	"0.598"	"0.621"	"C1263858"	"Muscular dystrophy congenital, merosin negative"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"0.9615385"	"1955"	"2017"	"3"	"51"	"CTD_human;ORPHANET;UNIPROT"
"3908"	"LAMA2"	"0.598"	"0.621"	"C1842898"	"Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"2000"	"2016"	"3"	"7"	"UNIPROT"
"3908"	"LAMA2"	"0.598"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.46"	"1"	"2000"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"		"2012"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"1993"	"2004"	"6"	"0"	"GENOMICS_ENGLAND"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0027339"	"Nail Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0037299"	"Skin Ulcer"	"phenotype"	"C17"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0079297"	"Epidermolysis Bullosa Progressiva"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"1999"	"2004"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0079301"	"Junctional Epidermolysis Bullosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0079683"	"Herlitz Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"1992"	"2012"	"1"	"23"	"CTD_human;ORPHANET"
"3909"	"LAMA3"	"0.604"	"0.69"	"C0268374"	"Adult junctional epidermolysis bullosa (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1999"	"2002"	"0"	"1"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C1328355"	"Laryngoonychocutaneous syndrome"	"disease"	"C08;C09;C11"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"3909"	"LAMA3"	"0.604"	"0.69"	"C2608084"	"EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"0"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3909"	"LAMA3"	"0.604"	"0.69"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3910"	"LAMA4"	"0.752"	"0.31"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3910"	"LAMA4"	"0.752"	"0.31"	"C3808935"	"CARDIOMYOPATHY, DILATED, 1JJ"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0266463"	"Lissencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0266483"	"Pachygyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C1879312"	"Agyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"3912"	"LAMB1"	"0.642"	"0.483"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3912"	"LAMB1"	"0.642"	"0.483"	"C3554657"	"LISSENCEPHALY 5"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2015"	"2"	"4"	"CLINGEN;ORPHANET"
"3912"	"LAMB1"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3913"	"LAMB2"	"0.639"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3913"	"LAMB2"	"0.639"	"0.483"	"C0268747"	"Diffuse mesangial sclerosis (disorder)"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.43"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"3913"	"LAMB2"	"0.639"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3913"	"LAMB2"	"0.639"	"0.483"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"3913"	"LAMB2"	"0.639"	"0.483"	"C1836876"	"Pierson syndrome"	"disease"	"C10;C11;C12;C13;C16;C23"	"Disease or Syndrome"	"1.00"	"1"	"1963"	"2017"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"3913"	"LAMB2"	"0.639"	"0.483"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1963"	"2005"	"3"	"0"	"GENOMICS_ENGLAND"
"3913"	"LAMB2"	"0.639"	"0.483"	"C3280113"	"NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.70"		"2006"	"2011"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3913"	"LAMB2"	"0.639"	"0.483"	"C3489732"	"Familial mesangial sclerosis"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3913"	"LAMB2"	"0.639"	"0.483"	"C3501249"	"Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome"	"disease"	"C10;C11;C12;C13;C16;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.42"	"1"	"1995"	"2016"	"7"	"0"	"GENOMICS_ENGLAND"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.33"	"0.6666667"	"1995"	"2010"	"5"	"0"	"GENOMICS_ENGLAND"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0079297"	"Epidermolysis Bullosa Progressiva"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1997"	"2007"	"2"	"3"	"CTD_human;UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0079301"	"Junctional Epidermolysis Bullosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0079683"	"Herlitz Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.92"	"1"	"1993"	"2016"	"1"	"38"	"CTD_human;ORPHANET;UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0268374"	"Adult junctional epidermolysis bullosa (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"1995"	"2013"	"2"	"10"	"CTD_human;UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C0399367"	"Amelogenesis imperfecta local hypoplastic form"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.62"	"1"	"2006"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"3914"	"LAMB3"	"0.614"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C2608084"	"EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"1997"	"2007"	"2"	"3"	"CTD_human;UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C2673609"	"Epidermolysis bullosa inversa dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"1997"	"2007"	"2"	"3"	"UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C2673610"	"JEB-I"	"disease"		"Disease or Syndrome"	"0.50"		"1997"	"2007"	"2"	"3"	"UNIPROT"
"3914"	"LAMB3"	"0.614"	"0.621"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3914"	"LAMB3"	"0.614"	"0.621"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3915"	"LAMC1"	"0.672"	"0.586"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3915"	"LAMC1"	"0.672"	"0.586"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3915"	"LAMC1"	"0.672"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"3915"	"LAMC1"	"0.672"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3915"	"LAMC1"	"0.672"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2006"	"2013"	"1"	"2"	"UNIPROT"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.34"	"1"	"1994"	"2010"	"8"	"0"	"GENOMICS_ENGLAND"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0079297"	"Epidermolysis Bullosa Progressiva"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"0"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0079301"	"Junctional Epidermolysis Bullosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2016"	"0"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0079683"	"Herlitz Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.82"	"1"	"1992"	"2015"	"0"	"25"	"CTD_human;ORPHANET"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C0268374"	"Adult junctional epidermolysis bullosa (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"2002"	"2014"	"1"	"1"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C2608084"	"EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2010"	"2014"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C2673609"	"Epidermolysis bullosa inversa dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"1995"	"2010"	"0"	"0"	"ORPHANET"
"3918"	"LAMC2"	"0.419"	"0.931"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3918"	"LAMC2"	"0.419"	"0.931"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"		"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2005"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2002"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3920"	"LAMP2"	"0.604"	"0.517"	"C0878677"	"Glycogen Storage Disease Type IIb"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1995"	"2018"	"9"	"30"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"3920"	"LAMP2"	"0.604"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2005"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"3921"	"RPSA"	"0.548"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3921"	"RPSA"	"0.548"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"3921"	"RPSA"	"0.548"	"0.655"	"C0685889"	"Splenic Hypoplasia"	"disease"	"C20"	"Congenital Abnormality"	"0.71"	"1"	"1997"	"2013"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"3925"	"STMN1"	"0.497"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2014"	"3"	"0"	"PSYGENET"
"3925"	"STMN1"	"0.497"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2014"	"3"	"0"	"PSYGENET"
"3925"	"STMN1"	"0.497"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.6666667"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3925"	"STMN1"	"0.497"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2008"	"1"	"0"	"CTD_human"
"3927"	"LASP1"	"0.6"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3927"	"LASP1"	"0.6"	"0.483"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3927"	"LASP1"	"0.6"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3927"	"LASP1"	"0.6"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3929"	"LBP"	"0.627"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.53"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"0.8333333"	"1993"	"2012"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"0.8333333"	"1993"	"2012"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3929"	"LBP"	"0.627"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3930"	"LBR"	"0.516"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1988"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"3930"	"LBR"	"0.516"	"0.69"	"C0030779"	"Pelger-Huet Anomaly"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.89"	"1"	"2002"	"2017"	"1"	"8"	"CTD_human;UNIPROT"
"3930"	"LBR"	"0.516"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3930"	"LBR"	"0.516"	"0.69"	"C0478077"	"Other osteochondrodysplasia with defects of growth of tubular bones and spine"	"disease"		"Congenital Abnormality"	"0.30"		"2003"	"2015"	"5"	"0"	"CLINGEN"
"3930"	"LBR"	"0.516"	"0.69"	"C0748397"	"Reynolds syndrome"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2010"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3930"	"LBR"	"0.516"	"0.69"	"C2931048"	"HEM dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.66"	"1"	"2003"	"2015"	"0"	"5"	"CTD_human;ORPHANET"
"3930"	"LBR"	"0.516"	"0.69"	"C3179244"	"Pseudo Pelger-Huet Anomaly"	"phenotype"	"C15;C16"	"Finding"	"0.30"				"0"	"0"	"CTD_human"
"3930"	"LBR"	"0.516"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"3930"	"LBR"	"0.516"	"0.69"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3931"	"LCAT"	"0.639"	"0.448"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"GENOMICS_ENGLAND"
"3931"	"LCAT"	"0.639"	"0.448"	"C0023195"	"Lecithin Acyltransferase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.7931034"	"1967"	"2014"	"15"	"16"	"CTD_human;ORPHANET;UNIPROT"
"3931"	"LCAT"	"0.639"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3931"	"LCAT"	"0.639"	"0.448"	"C0342895"	"Fish-Eye Disease"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.875"	"1987"	"2014"	"7"	"11"	"CTD_human;ORPHANET;UNIPROT"
"3932"	"LCK"	"0.619"	"0.517"	"C4014233"	"IMMUNODEFICIENCY 22"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"3934"	"LCN2"	"0.469"	"0.793"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"0"	"2003"	"2015"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0019188"	"Hepatitis, Animal"	"disease"	"C06;C22"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2016"	"4"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.58"	"1"	"2004"	"2017"	"5"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.952381"	"2005"	"2016"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3934"	"LCN2"	"0.469"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"5"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"5"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3934"	"LCN2"	"0.469"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"3936"	"LCP1"	"0.672"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3936"	"LCP1"	"0.672"	"0.414"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3936"	"LCP1"	"0.672"	"0.414"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3936"	"LCP1"	"0.672"	"0.414"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3936"	"LCP1"	"0.672"	"0.414"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3937"	"LCP2"	"0.785"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3938"	"LCT"	"0.652"	"0.483"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3938"	"LCT"	"0.652"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3938"	"LCT"	"0.652"	"0.483"	"C0268179"	"Lactase Deficiency, Congenital"	"phenotype"	"C16;C18"	"Pathologic Function"	"0.70"		"2007"	"2012"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"3939"	"LDHA"	"0.562"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3939"	"LDHA"	"0.562"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3939"	"LDHA"	"0.562"	"0.655"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C0027080"	"Myoglobinuria"	"phenotype"	"C05"	"Finding"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1991"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"3939"	"LDHA"	"0.562"	"0.655"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3939"	"LDHA"	"0.562"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"		"1984"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"3939"	"LDHA"	"0.562"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3939"	"LDHA"	"0.562"	"0.655"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3939"	"LDHA"	"0.562"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"3939"	"LDHA"	"0.562"	"0.655"	"C2931743"	"Lactate dehydrogenase deficiency type A"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"3945"	"LDHB"	"0.633"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0007124"	"Noninfiltrating Intraductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1332347"	"Atypical Ductal Breast Hyperplasia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3945"	"LDHB"	"0.633"	"0.414"	"C3279904"	"Lactate Dehydrogenase B Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1990"	"2001"	"7"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3948"	"LDHC"	"0.785"	"0.241"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3948"	"LDHC"	"0.785"	"0.241"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3948"	"LDHC"	"0.785"	"0.241"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3948"	"LDHC"	"0.785"	"0.241"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"0.9642857"	"1980"	"2018"	"5"	"1"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9672131"	"1987"	"2017"	"2"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9452055"	"1986"	"2017"	"1"	"2"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9191176"	"1982"	"2017"	"4"	"12"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"	"0.9578313"	"1964"	"2018"	"8"	"1120"	"CTD_human;GENOMICS_ENGLAND"
"3949"	"LDLR"	"0.475"	"0.828"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9545455"	"1990"	"2017"	"2"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0034362"	"Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"3949"	"LDLR"	"0.475"	"0.828"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.37"	"0.7142857"	"1996"	"2016"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"1992"	"2017"	"0"	"0"	"ORPHANET"
"3949"	"LDLR"	"0.475"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2013"	"3"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0519066"	"Acute Q fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"0.9562172"	"1980"	"2018"	"57"	"127"	"CTD_human;UNIPROT"
"3949"	"LDLR"	"0.475"	"0.828"	"C1443892"	"Chronic Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2017"	"5"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2003"	"6"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2002"	"2016"	"2"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9710145"	"1986"	"2018"	"2"	"2"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C2973787"	"Coxiella burnetii Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"0"	"CTD_human"
"3949"	"LDLR"	"0.475"	"0.828"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.50"		"1986"	"2015"	"51"	"127"	"CTD_human;UNIPROT"
"3952"	"LEP"	"0.4"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.58"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9824561"	"2001"	"2018"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"0.8888889"	"2005"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2015"	"5"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2015"	"5"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.8928571"	"1995"	"2015"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"1"	"2003"	"2017"	"5"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.70"	"0.9642857"	"1997"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020505"	"Hyperphagia"	"phenotype"	"C23"	"Finding"	"0.40"		"2015"	"2015"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.9310345"	"1998"	"2017"	"4"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.64"	"1"	"1998"	"2012"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.37"		"2003"	"2017"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2000"	"2001"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2005"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.70"	"0.9169279"	"1973"	"2018"	"14"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9655172"	"1996"	"2018"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.40"	"0.8666667"	"1998"	"2013"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0032617"	"Polyuria"	"phenotype"	"C12;C13;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2003"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2009"	"2"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2016"	"2"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1999"	"2008"	"6"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2004"	"2016"	"5"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0085602"	"Polydipsia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0149745"	"Oral Ulcer"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2005"	"2015"	"3"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2013"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.55"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.60"	"0.9318182"	"1976"	"2017"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0556385"	"Craving for alcohol"	"phenotype"		"Finding"	"0.30"	"1"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9833333"	"2001"	"2018"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2000"	"2001"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1998"	"2004"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1998"	"2017"	"1"	"0"	"PSYGENET"
"3952"	"LEP"	"0.4"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2001"	"2017"	"5"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C3554224"	"LEPTIN DEFICIENCY OR DYSFUNCTION"	"disease"		"Disease or Syndrome"	"0.80"	"0.8888889"	"1997"	"2018"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3952"	"LEP"	"0.4"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3952"	"LEP"	"0.4"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2016"	"9"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9310345"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.39"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2016"	"9"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.875"	"1979"	"2018"	"4"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0018206"	"granulosa cell tumor"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1986"	"2015"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.44"	"1"	"1986"	"2015"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020505"	"Hyperphagia"	"phenotype"	"C23"	"Finding"	"0.40"		"1986"	"2007"	"3"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0021359"	"Infertility"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2017"	"4"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.70"	"0.8719512"	"1979"	"2018"	"8"	"2"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9230769"	"1997"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0032002"	"Pituitary Diseases"	"group"	"C10;C19"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"1999"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0035243"	"Respiratory Tract Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2016"	"9"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0041912"	"Upper Respiratory Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"0.5"	"2000"	"2015"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.55"	"1"	"1999"	"2017"	"3"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0497406"	"Overweight"	"phenotype"	"C23"	"Finding"	"0.40"	"0.9"	"2001"	"2013"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9259259"	"2006"	"2018"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0729353"	"Subfertility"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0751437"	"Adenohypophyseal Diseases"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0751438"	"Posterior pituitary disease"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2017"	"4"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"2015"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"2015"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"2015"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1567257"	"Granulosa Cell Cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"1986"	"2014"	"5"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3953"	"LEPR"	"0.474"	"0.793"	"C3554225"	"LEPTIN RECEPTOR DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2015"	"2"	"0"	"CTD_human;ORPHANET;UNIPROT"
"3953"	"LEPR"	"0.474"	"0.793"	"C4074771"	"Sterility, Reproductive"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.9090909"	"2001"	"2016"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3954"	"LETM1"	"0.555"	"0.586"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.60"	"0.8571429"	"1999"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"3954"	"LETM1"	"0.555"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3954"	"LETM1"	"0.555"	"0.586"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3955"	"LFNG"	"0.799"	"0.138"	"C0265343"	"Jarcho-Levin syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3955"	"LFNG"	"0.799"	"0.138"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"3955"	"LFNG"	"0.799"	"0.138"	"C1837549"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3955"	"LFNG"	"0.799"	"0.138"	"C1853296"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"1"	"1"	"CTD_human;UNIPROT"
"3955"	"LFNG"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3956"	"LGALS1"	"0.496"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3957"	"LGALS2"	"0.727"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3957"	"LGALS2"	"0.727"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3957"	"LGALS2"	"0.727"	"0.31"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.7142857"	"2004"	"2012"	"1"	"0"	"CTD_human"
"3957"	"LGALS2"	"0.727"	"0.31"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2015"	"2"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.7777778"	"2003"	"2016"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3958"	"LGALS3"	"0.466"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3959"	"LGALS3BP"	"0.639"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"3959"	"LGALS3BP"	"0.639"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3963"	"LGALS7"	"0.652"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3965"	"LGALS9"	"0.588"	"0.552"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"1992"	"2012"	"4"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"1980"	"2004"	"3"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0023601"	"Leydig Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0034013"	"Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0271582"	"Isolated lutropin deficiency (disorder)"	"disease"	"C19"	"Disease or Syndrome"	"0.70"		"1979"	"2012"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"3972"	"LHB"	"0.652"	"0.379"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1992"	"2008"	"4"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3972"	"LHB"	"0.652"	"0.379"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"1980"	"2004"	"3"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"1980"	"2004"	"3"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1992"	"2008"	"4"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"2"	"0"	"CTD_human"
"3972"	"LHB"	"0.652"	"0.379"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1992"	"2008"	"4"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2008"	"0"	"0"	"UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0019269"	"Hermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0023601"	"Leydig Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.50"		"1999"	"2002"	"2"	"1"	"CTD_human;UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0033804"	"Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.51"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0238395"	"Male Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.33"	"1"	"1995"	"2010"	"2"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0266362"	"Ambiguous Genitalia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0266432"	"Leydig cell agenesis"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.61"	"1"	"1995"	"2015"	"10"	"13"	"CTD_human;UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0342549"	"Familial Testotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2016"	"15"	"12"	"CTD_human;ORPHANET;UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0860158"	"Leydig Cell Hypoplasia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"	"1"	"1995"	"2016"	"0"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C1504412"	"Testotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2010"	"0"	"0"	"ORPHANET"
"3973"	"LHCGR"	"0.562"	"0.483"	"C2673497"	"Leydig Cell Hypoplasia, Type II"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.52"	"1"	"1995"	"2013"	"10"	"9"	"CTD_human;UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C2674612"	"Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.40"		"1993"	"2002"	"11"	"12"	"UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C2751824"	"46, XY Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2012"	"2"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C2930618"	"Intersex Conditions"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C2930619"	"Sex Differentiation Disorders"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C3489793"	"46,XY Sex Reversal 3"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"1995"	"2010"	"2"	"0"	"CTD_human"
"3973"	"LHCGR"	"0.562"	"0.483"	"C3668935"	"Luteinizing Hormone Resistance, Female"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.50"		"1995"	"2009"	"10"	"9"	"CTD_human;UNIPROT"
"3973"	"LHCGR"	"0.562"	"0.483"	"C3714042"	"46,XY Disorder of Sex Development Due To LH Defects"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3975"	"LHX1"	"0.773"	"0.172"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3975"	"LHX1"	"0.773"	"0.172"	"C3281138"	"CHROMOSOME 17q12 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3976"	"LIF"	"0.528"	"0.655"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.6666667"	"2007"	"2011"	"3"	"0"	"PSYGENET"
"3976"	"LIF"	"0.528"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"3976"	"LIF"	"0.528"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"3976"	"LIF"	"0.528"	"0.655"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3976"	"LIF"	"0.528"	"0.655"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"3977"	"LIFR"	"0.569"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3977"	"LIFR"	"0.569"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3977"	"LIFR"	"0.569"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3977"	"LIFR"	"0.569"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3977"	"LIFR"	"0.569"	"0.621"	"C0349398"	"Paranoid delusion"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"3977"	"LIFR"	"0.569"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3977"	"LIFR"	"0.569"	"0.621"	"C0432240"	"Stuve-Wiedemann dysplasia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3977"	"LIFR"	"0.569"	"0.621"	"C0796176"	"STUVE-WIEDEMANN SYNDROME"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.77"	"1"	"2004"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"3977"	"LIFR"	"0.569"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"3977"	"LIFR"	"0.569"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"3978"	"LIG1"	"0.727"	"0.379"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2007"	"1"	"0"	"CTD_human"
"3978"	"LIG1"	"0.727"	"0.379"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2007"	"1"	"0"	"CTD_human"
"3978"	"LIG1"	"0.727"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"3980"	"LIG3"	"0.713"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"3981"	"LIG4"	"0.524"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2014"	"0"	"1"	"UNIPROT"
"3981"	"LIG4"	"0.524"	"0.724"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.36"	"1"	"2006"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"3981"	"LIG4"	"0.524"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"3981"	"LIG4"	"0.524"	"0.724"	"C0175691"	"Dubowitz syndrome"	"disease"	"C05;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"3981"	"LIG4"	"0.524"	"0.724"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"3981"	"LIG4"	"0.524"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"3981"	"LIG4"	"0.524"	"0.724"	"C1847827"	"LIG4 Syndrome"	"disease"	"C05;C16;C20;C23"	"Disease or Syndrome"	"0.99"	"1"	"1999"	"2017"	"1"	"10"	"CTD_human;ORPHANET;UNIPROT"
"3981"	"LIG4"	"0.524"	"0.724"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"3981"	"LIG4"	"0.524"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3982"	"LIM2"	"0.743"	"0.276"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3982"	"LIM2"	"0.743"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.52"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3982"	"LIM2"	"0.743"	"0.276"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"3982"	"LIM2"	"0.743"	"0.276"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3982"	"LIM2"	"0.743"	"0.276"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"3982"	"LIM2"	"0.743"	"0.276"	"C3809004"	"CATARACT 19, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.80"		"1996"	"2008"	"1"	"2"	"CTD_human;UNIPROT"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3983"	"ABLIM1"	"0.834"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3984"	"LIMK1"	"0.552"	"0.621"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.60"	"0.9230769"	"1998"	"2015"	"0"	"0"	"ORPHANET"
"3984"	"LIMK1"	"0.552"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"3985"	"LIMK2"	"0.752"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3988"	"LIPA"	"0.609"	"0.448"	"C0008384"	"Cholesterol Ester Storage Disease"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1994"	"2015"	"1"	"1"	"CTD_human;ORPHANET"
"3988"	"LIPA"	"0.609"	"0.448"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"3988"	"LIPA"	"0.609"	"0.448"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"3988"	"LIPA"	"0.609"	"0.448"	"C0043208"	"Wolman Disease"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"0.9787234"	"1984"	"2018"	"2"	"7"	"ORPHANET;UNIPROT"
"3988"	"LIPA"	"0.609"	"0.448"	"C0220756"	"Niemann-Pick Disease, Type C"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"3988"	"LIPA"	"0.609"	"0.448"	"C0268247"	"Niemann-Pick Disease, Type D"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"2018"	"8"	"0"	"GENOMICS_ENGLAND"
"3988"	"LIPA"	"0.609"	"0.448"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2003"	"2018"	"1"	"3"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C2936797"	"Acid cholesteryl ester hydrolase deficiency, type 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1998"	"2018"	"0"	"0"	"CTD_human"
"3988"	"LIPA"	"0.609"	"0.448"	"C3179455"	"Niemann-Pick Disease, Type C1"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.47"	"1"	"2001"	"2008"	"2"	"1"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"3990"	"LIPC"	"0.611"	"0.517"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"1991"	"2003"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0020476"	"Hyperlipoproteinemias"	"group"	"C18"	"Disease or Syndrome"	"0.50"		"2003"	"2008"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"2004"	"3"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C2675071"	"HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12"	"phenotype"		"Finding"	"0.40"		"2004"	"2008"	"0"	"1"	"CTD_human"
"3990"	"LIPC"	"0.611"	"0.517"	"C3151466"	"HEPATIC LIPASE DEFICIENCY (disorder)"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"1991"	"2004"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"3991"	"LIPE"	"0.648"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"3991"	"LIPE"	"0.648"	"0.345"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"3991"	"LIPE"	"0.648"	"0.345"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3991"	"LIPE"	"0.648"	"0.345"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3991"	"LIPE"	"0.648"	"0.345"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"3991"	"LIPE"	"0.648"	"0.345"	"C4014869"	"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"0"	"2"	"ORPHANET"
"3992"	"FADS1"	"0.636"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"3992"	"FADS1"	"0.636"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3992"	"FADS1"	"0.636"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"3993"	"LLGL2"	"0.785"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"3993"	"LLGL2"	"0.785"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"3993"	"LLGL2"	"0.785"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"3993"	"LLGL2"	"0.785"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3993"	"LLGL2"	"0.785"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"3996"	"LLGL1"	"0.681"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3996"	"LLGL1"	"0.681"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3996"	"LLGL1"	"0.681"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3996"	"LLGL1"	"0.681"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"3998"	"LMAN1"	"0.707"	"0.379"	"C1856883"	"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1997"	"2014"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0004245"	"Atrioventricular Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0004331"	"Auriculo-Ventricular Dissociation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.9879518"	"1999"	"2018"	"4"	"38"	"CTD_human;GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"1993"	"2007"	"0"	"4"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0011644"	"Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0016508"	"Congenital Foot Deformity"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0018794"	"Heart Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.44"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0033300"	"Progeria"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.9589041"	"1993"	"2018"	"14"	"21"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C0036420"	"Localized scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0037188"	"Sinoatrial Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0263409"	"Linear Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.50"		"2012"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.40"	"0.961039"	"2000"	"2017"	"4"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0406585"	"Lethal tight skin contracture syndrome (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.60"		"2003"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"4000"	"LMNA"	"0.406"	"0.724"	"C0410189"	"Muscular Dystrophy, Emery-Dreifuss"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"0.95"	"1999"	"2017"	"1"	"1"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0410190"	"Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2017"	"3"	"66"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C0432291"	"Mandibuloacral dysostosis"	"disease"	"C05;C17;C18"	"Disease or Syndrome"	"0.80"	"1"	"2002"	"2015"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1996"	"2015"	"1"	"3"	"CTD_human;GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"2004"	"2017"	"3"	"1"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C0796031"	"Malouf syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.71"	"1"	"2003"	"2015"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C0796083"	"Najjar syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2003"	"2009"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C1136321"	"HIV-Associated Lipodystrophy Syndrome"	"disease"	"C02;C17;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"1.00"	"0.9210526"	"1993"	"2018"	"20"	"44"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C1450051"	"Autosomal Recessive Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.53"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4000"	"LMNA"	"0.406"	"0.724"	"C1527383"	"Morphea"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C1720824"	"Sudden Cardiac Arrest"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2009"	"4"	"0"	"CTD_human;ORPHANET"
"4000"	"LMNA"	"0.406"	"0.724"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2018"	"15"	"21"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2009"	"4"	"0"	"CTD_human"
"4000"	"LMNA"	"0.406"	"0.724"	"C1834653"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.9285714"	"2000"	"2016"	"8"	"19"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C1854154"	"Charcot-Marie-Tooth disease, Type 2B1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"		"1993"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C1857829"	"Heart-hand syndrome, Slovenian type"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"4000"	"LMNA"	"0.406"	"0.724"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"4000"	"LMNA"	"0.406"	"0.724"	"C2750035"	"Emery-Dreifuss Muscular Dystrophy 3"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2000"	"2016"	"2"	"4"	"ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C2750285"	"Progeria Syndrome, Childhood-Onset"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2001"	"2014"	"10"	"12"	"UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C2750785"	"MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.91"	"1"	"2004"	"2015"	"1"	"15"	"CTD_human;ORPHANET;UNIPROT"
"4000"	"LMNA"	"0.406"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4000"	"LMNA"	"0.406"	"0.724"	"C4275075"	"Atypical Werner syndrome"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2003"	"2018"	"0"	"0"	"ORPHANET"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.48"	"1"	"2006"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0205711"	"Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0751914"	"Adult Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0751915"	"Pelizaeus-Merzbacher Disease, Atypical"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0751916"	"Classic Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0751917"	"Pelizaeus-Merzbacher Disease, Transitional"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C0751918"	"Cockayne-Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4001"	"LMNB1"	"0.598"	"0.586"	"C1868512"	"Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2014"	"0"	"0"	"ORPHANET"
"4001"	"LMNB1"	"0.598"	"0.586"	"C3164344"	"Adult onset autosomal dominant leukodystrophy"	"disease"		"Disease or Syndrome"	"0.53"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"4004"	"LMO1"	"0.685"	"0.276"	"C0023492"	"Leukemia, T-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"1988"	"1991"	"2"	"0"	"CTD_human"
"4004"	"LMO1"	"0.685"	"0.276"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.67"	"1"	"2011"	"2017"	"0"	"2"	"CGI;ORPHANET"
"4004"	"LMO1"	"0.685"	"0.276"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.58"	"0.875"	"1994"	"2009"	"1"	"0"	"CGI;CTD_human"
"4004"	"LMO1"	"0.685"	"0.276"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4005"	"LMO2"	"0.639"	"0.414"	"C0023492"	"Leukemia, T-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"4005"	"LMO2"	"0.639"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4005"	"LMO2"	"0.639"	"0.414"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9130435"	"1993"	"2016"	"2"	"0"	"CTD_human"
"4007"	"PRICKLE3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4007"	"PRICKLE3"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4008"	"LMO7"	"0.762"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4009"	"LMX1A"	"0.72"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0009081"	"Congenital clubfoot"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0018965"	"Hematuria"	"phenotype"	"C12;C13;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0021603"	"Sleep Initiation and Maintenance Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0027341"	"Nail-Patella Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1998"	"2017"	"7"	"10"	"CTD_human;ORPHANET;UNIPROT"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0033139"	"Primary Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.40"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0270541"	"Rebound Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0349255"	"Nonorganic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0393759"	"Transient Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0541798"	"Early Awakening"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0751249"	"Chronic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0751250"	"Psychophysiological Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0751251"	"Secondary Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0751252"	"Sleep Initiation Dysfunction"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C0917801"	"Sleeplessness"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4010"	"LMX1B"	"0.596"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4010"	"LMX1B"	"0.596"	"0.552"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4012"	"LNPEP"	"0.582"	"0.724"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.31"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"4014"	"LOR"	"0.667"	"0.379"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4014"	"LOR"	"0.667"	"0.379"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"4014"	"LOR"	"0.667"	"0.379"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4014"	"LOR"	"0.667"	"0.379"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"4014"	"LOR"	"0.667"	"0.379"	"C1858805"	"Vohwinkel Syndrome, Variant Form"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.59"	"0.8888889"	"1998"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"4015"	"LOX"	"0.488"	"0.793"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4015"	"LOX"	"0.488"	"0.793"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2016"	"5"	"0"	"CLINGEN"
"4015"	"LOX"	"0.488"	"0.793"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4015"	"LOX"	"0.488"	"0.793"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4015"	"LOX"	"0.488"	"0.793"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4015"	"LOX"	"0.488"	"0.793"	"C4284414"	"AORTIC ANEURYSM, FAMILIAL THORACIC 10"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"6"	"CTD_human;UNIPROT"
"4016"	"LOXL1"	"0.648"	"0.483"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4016"	"LOXL1"	"0.648"	"0.483"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4016"	"LOXL1"	"0.648"	"0.483"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4016"	"LOXL1"	"0.648"	"0.483"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.9466667"	"2007"	"2018"	"2"	"11"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"4017"	"LOXL2"	"0.607"	"0.448"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9210526"	"1987"	"2016"	"3"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9672131"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.968254"	"1986"	"2018"	"2"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.969697"	"1986"	"2018"	"1"	"2"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1991"	"2016"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0020623"	"Hypolipoproteinemias"	"group"	"C16;C18"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.50"	"0.962963"	"1989"	"2014"	"1"	"1"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1993"	"2007"	"3"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C1720772"	"Hypoprebetalipoproteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4018"	"LPA"	"0.489"	"0.655"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9357798"	"1986"	"2018"	"2"	"7"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9545455"	"1993"	"2016"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.46"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4023"	"LPL"	"0.504"	"0.724"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0020474"	"Hyperlipidemia, Familial Combined"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.9615385"	"1987"	"2016"	"0"	"2"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0020481"	"Hyperlipoproteinemia Type V"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"4023"	"LPL"	"0.504"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.8823529"	"1998"	"2018"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"	"0.9767442"	"1984"	"2018"	"2"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0023817"	"Hyperlipoproteinemia Type I"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.956044"	"1981"	"2018"	"55"	"46"	"CTD_human;ORPHANET;UNIPROT"
"4023"	"LPL"	"0.504"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.9565217"	"1993"	"2016"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"PSYGENET"
"4023"	"LPL"	"0.504"	"0.724"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.39"	"1"	"1993"	"2005"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2005"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4023"	"LPL"	"0.504"	"0.724"	"C1720779"	"Apolipoprotein C-II Deficiency (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4026"	"LPP"	"0.588"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4026"	"LPP"	"0.588"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"0.5"	"2009"	"2013"	"1"	"0"	"CTD_human"
"4026"	"LPP"	"0.588"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4035"	"LRP1"	"0.533"	"0.724"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.46"	"1"	"2011"	"2017"	"1"	"1"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0263428"	"Burnett Schwartz Berberian syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"4035"	"LRP1"	"0.533"	"0.724"	"C0263429"	"Atrophoderma vermiculatum"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"1"	"ORPHANET"
"4035"	"LRP1"	"0.533"	"0.724"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"1"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0343057"	"Keratosis pilaris decalvans"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4035"	"LRP1"	"0.533"	"0.724"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4035"	"LRP1"	"0.533"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4035"	"LRP1"	"0.533"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"1"	"UNIPROT"
"4035"	"LRP1"	"0.533"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4036"	"LRP2"	"0.552"	"0.69"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"4036"	"LRP2"	"0.552"	"0.69"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2012"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"PSYGENET"
"4036"	"LRP2"	"0.552"	"0.69"	"C0042870"	"Vitamin D Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4036"	"LRP2"	"0.552"	"0.69"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C1857277"	"Donnai-Barrow syndrome"	"disease"	"C09;C10;C11;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.95"	"1"	"1993"	"2016"	"1"	"16"	"CTD_human;ORPHANET;UNIPROT"
"4036"	"LRP2"	"0.552"	"0.69"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4036"	"LRP2"	"0.552"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4038"	"LRP4"	"0.609"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4038"	"LRP4"	"0.609"	"0.552"	"C0039075"	"Syndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4038"	"LRP4"	"0.609"	"0.552"	"C0265301"	"Sclerosteosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"4038"	"LRP4"	"0.609"	"0.552"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.53"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4038"	"LRP4"	"0.609"	"0.552"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4038"	"LRP4"	"0.609"	"0.552"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4038"	"LRP4"	"0.609"	"0.552"	"C1859309"	"Syndactyly Cenani Lenz type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"1997"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4038"	"LRP4"	"0.609"	"0.552"	"C3280402"	"SCLEROSTEOSIS 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1994"	"2014"	"2"	"2"	"UNIPROT"
"4038"	"LRP4"	"0.609"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4038"	"LRP4"	"0.609"	"0.552"	"C4225377"	"MYASTHENIC SYNDROME, CONGENITAL, 17"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"4040"	"LRP6"	"0.588"	"0.724"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4040"	"LRP6"	"0.588"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4040"	"LRP6"	"0.588"	"0.724"	"C1970440"	"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2 (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2007"	"2014"	"2"	"4"	"CTD_human;UNIPROT"
"4040"	"LRP6"	"0.588"	"0.724"	"C3539878"	"Triple Negative Breast Neoplasms"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"4040"	"LRP6"	"0.588"	"0.724"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4040"	"LRP6"	"0.588"	"0.724"	"C4225231"	"TOOTH AGENESIS, SELECTIVE, 7"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"4041"	"LRP5"	"0.532"	"0.793"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4041"	"LRP5"	"0.532"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.70"	"0.96875"	"2004"	"2016"	"0"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0035344"	"Retinopathy of Prematurity"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2017"	"1"	"2"	"ORPHANET;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4041"	"LRP5"	"0.532"	"0.793"	"C0158683"	"Polycystic liver disease"	"disease"	"C04;C06;C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"4041"	"LRP5"	"0.532"	"0.793"	"C0242852"	"Proliferative vitreoretinopathy"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.50"	"1"	"2000"	"2017"	"0"	"2"	"ORPHANET"
"4041"	"LRP5"	"0.532"	"0.793"	"C0432252"	"Osteoporosis with pseudoglioma"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"2002"	"2017"	"6"	"26"	"CTD_human;ORPHANET;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"4041"	"LRP5"	"0.532"	"0.793"	"C0432273"	"Worth disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2003"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4041"	"LRP5"	"0.532"	"0.793"	"C1277579"	"At risk of osteoporosis"	"phenotype"		"Finding"	"0.30"		"2002"	"2007"	"5"	"1"	"UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1843323"	"Van Buchem disease type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1843330"	"OSTEOPETROSIS, AUTOSOMAL DOMINANT 1"	"disease"	"C05"	"Disease or Syndrome"	"0.70"		"1999"	"2003"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.62"	"1"	"2004"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1866079"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.40"		"2002"	"2015"	"5"	"2"	"UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1866080"	"HIGH BONE MASS"	"phenotype"		"Finding"	"0.40"		"2002"	"2007"	"5"	"1"	"UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C1866176"	"EXUDATIVE VITREORETINOPATHY 4 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2004"	"2014"	"8"	"18"	"CTD_human;UNIPROT"
"4041"	"LRP5"	"0.532"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4043"	"LRPAP1"	"0.6"	"0.621"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"0"	"1"	"ORPHANET"
"4043"	"LRPAP1"	"0.6"	"0.621"	"C3809482"	"MYOPIA 23, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"3"	"CTD_human"
"4045"	"LSAMP"	"0.636"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4045"	"LSAMP"	"0.636"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4045"	"LSAMP"	"0.636"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4046"	"LSP1"	"0.713"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2017"	"2"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.49"	"1"	"2007"	"2018"	"2"	"3"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"4046"	"LSP1"	"0.713"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C0034362"	"Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4047"	"LSS"	"0.676"	"0.448"	"C0519066"	"Acute Q fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C1443892"	"Chronic Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C2973787"	"Coxiella burnetii Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4047"	"LSS"	"0.676"	"0.448"	"C4225300"	"CATARACT 44"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"4048"	"LTA4H"	"0.636"	"0.483"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"4048"	"LTA4H"	"0.636"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4048"	"LTA4H"	"0.636"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4048"	"LTA4H"	"0.636"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4048"	"LTA4H"	"0.636"	"0.483"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"0.8571429"	"1998"	"2010"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9047619"	"2002"	"2014"	"2"	"2"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"PSYGENET"
"4049"	"LTA"	"0.463"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"4049"	"LTA"	"0.463"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.37"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"4049"	"LTA"	"0.463"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.35"	"0.8"	"1999"	"2013"	"1"	"0"	"CTD_human"
"4049"	"LTA"	"0.463"	"0.862"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8333333"	"1998"	"2011"	"1"	"0"	"CTD_human"
"4050"	"LTB"	"0.596"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4051"	"CYP4F3"	"0.572"	"0.655"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4052"	"LTBP1"	"0.72"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.45"	"0.8"	"2009"	"2016"	"2"	"0"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C0020302"	"Hydrophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.32"	"0.5"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"4053"	"LTBP2"	"0.611"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4053"	"LTBP2"	"0.611"	"0.552"	"C0265313"	"Weill-Marchesani syndrome"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"4053"	"LTBP2"	"0.611"	"0.552"	"C1832977"	"GLAUCOMA 3, PRIMARY INFANTILE, B"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4053"	"LTBP2"	"0.611"	"0.552"	"C1869114"	"Weill-Marchesani Syndrome, Autosomal Recessive"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C1869115"	"Weill-Marchesani Syndrome, Autosomal Dominant"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C2751316"	"Glaucoma 3, Primary Congenital, D"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2009"	"2011"	"0"	"2"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C3538951"	"MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4053"	"LTBP2"	"0.611"	"0.552"	"C3553785"	"WEILL-MARCHESANI SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4053"	"LTBP2"	"0.611"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.61"	"1"	"2016"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2016"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0022821"	"Kyphosis deformity of spine"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0026267"	"Mitral Valve Prolapse Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0029464"	"Osteosclerosis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0265287"	"Acromicric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0399352"	"Developmental absence of tooth"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C0432228"	"Brachyolmia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C1832594"	"Verloes Bourguignon syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2016"	"0"	"7"	"ORPHANET"
"4054"	"LTBP3"	"0.63"	"0.621"	"C2751297"	"Tooth Agenesis, Selective, 6"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C3489529"	"Tooth Agenesis, Familial"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"4054"	"LTBP3"	"0.63"	"0.621"	"C3489726"	"Geleophysic dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4054"	"LTBP3"	"0.63"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4055"	"LTBR"	"0.53"	"0.793"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4056"	"LTC4S"	"0.656"	"0.483"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4056"	"LTC4S"	"0.656"	"0.483"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2012"	"4"	"0"	"CTD_human"
"4056"	"LTC4S"	"0.656"	"0.483"	"C3279662"	"Leukotriene C4 Synthase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0006849"	"Oral candidiasis"	"disease"	"C01;C07"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0006852"	"Candidiasis of vagina"	"disease"	"C01;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"		"2007"	"2011"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0017181"	"Gastrointestinal Hemorrhage"	"phenotype"	"C06;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0018932"	"Hematochezia"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0022408"	"Arthropathy"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0392622"	"Toxic effect of carbon tetrachloride"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0700345"	"Candidiasis, Vulvovaginal"	"disease"	"C01;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0860029"	"Vaginal Yeast Infections"	"disease"	"C01;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4057"	"LTF"	"0.573"	"0.69"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4058"	"LTK"	"0.857"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4058"	"LTK"	"0.857"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4060"	"LUM"	"0.59"	"0.586"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4061"	"LY6E"	"0.611"	"0.621"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4061"	"LY6E"	"0.611"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4061"	"LY6E"	"0.611"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2013"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4066"	"LYL1"	"0.72"	"0.138"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4067"	"LYN"	"0.659"	"0.345"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4067"	"LYN"	"0.659"	"0.345"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4068"	"SH2D1A"	"0.57"	"0.69"	"C0024314"	"Lymphoproliferative Disorders"	"group"	"C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"4068"	"SH2D1A"	"0.57"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4068"	"SH2D1A"	"0.57"	"0.69"	"C0549463"	"X-Linked Lymphoproliferative Disorder"	"disease"	"C15;C20"	"Neoplastic Process"	"1.00"	"0.9579832"	"1998"	"2017"	"12"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4069"	"LYZ"	"0.609"	"0.69"	"C0268389"	"Amyloidosis, familial visceral"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1992"	"2006"	"1"	"5"	"CTD_human;UNIPROT"
"4069"	"LYZ"	"0.609"	"0.69"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"4070"	"TACSTD2"	"0.584"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4070"	"TACSTD2"	"0.584"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4070"	"TACSTD2"	"0.584"	"0.552"	"C0339273"	"Corneal dystrophy, Lattice type 3"	"disease"	"C11;C16;C18"	"Disease or Syndrome"	"0.70"	"0.952381"	"1999"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"4070"	"TACSTD2"	"0.584"	"0.552"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1995"	"1999"	"2"	"0"	"GENOMICS_ENGLAND"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.31"		"2009"	"2016"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"				"0"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"1987"	"2016"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2004"	"2011"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4072"	"EPCAM"	"0.499"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.38"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"	"1"	"2009"	"2018"	"1"	"7"	"CTD_human;ORPHANET"
"4072"	"EPCAM"	"0.499"	"0.69"	"C2750471"	"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.50"		"2006"	"2015"	"6"	"0"	"CLINGEN;CTD_human"
"4072"	"EPCAM"	"0.499"	"0.69"	"C2750737"	"DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL"	"disease"	"C06;C18;C23"	"Disease or Syndrome"	"0.96"	"1"	"2008"	"2018"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4072"	"EPCAM"	"0.499"	"0.69"	"C2931459"	"Lynch syndrome I (site-specific colonic cancer)"	"disease"	"C04;C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4074"	"M6PR"	"0.727"	"0.207"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4074"	"M6PR"	"0.727"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4074"	"M6PR"	"0.727"	"0.207"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4074"	"M6PR"	"0.727"	"0.207"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4074"	"M6PR"	"0.727"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4076"	"CAPRIN1"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4082"	"MARCKS"	"0.6"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"4084"	"MXD1"	"0.614"	"0.483"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4085"	"MAD2L1"	"0.621"	"0.414"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4085"	"MAD2L1"	"0.621"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4085"	"MAD2L1"	"0.621"	"0.414"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4086"	"SMAD1"	"0.572"	"0.552"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"4086"	"SMAD1"	"0.572"	"0.552"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"0"	"0"	"UNIPROT"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2016"	"6"	"0"	"CLINGEN"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0265287"	"Acromicric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1998"	"2004"	"2"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0600519"	"Ventricular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C0600520"	"Left Ventricle Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9285714"	"1997"	"2016"	"0"	"0"	"UNIPROT"
"4087"	"SMAD2"	"0.496"	"0.724"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4087"	"SMAD2"	"0.496"	"0.724"	"C3489726"	"Geleophysic dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0002949"	"Aneurysm, Dissecting"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0003486"	"Aortic Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2017"	"1"	"3"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"5"	"0"	"CLINGEN"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2014"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0340643"	"Dissection of aorta"	"disease"	"C14"	"Pathologic Function"	"0.42"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2011"	"2"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0600519"	"Ventricular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0600520"	"Left Ventricle Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"0"	"0"	"UNIPROT"
"4088"	"SMAD3"	"0.462"	"0.862"	"C1836635"	"Loeys-Dietz Aortic Aneurysm Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C2697932"	"Loeys-Dietz Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.44"	"1"	"2012"	"2016"	"1"	"2"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C3151087"	"LOEYS-DIETZ SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.76"	"1"	"2001"	"2016"	"6"	"9"	"CLINGEN;ORPHANET;UNIPROT"
"4088"	"SMAD3"	"0.462"	"0.862"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4088"	"SMAD3"	"0.462"	"0.862"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"1"	"1"	"CTD_human"
"4088"	"SMAD3"	"0.462"	"0.862"	"C4277533"	"Dissection, Blood Vessel"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9811321"	"1996"	"2018"	"3"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"1996"	"2016"	"3"	"8"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9230769"	"1998"	"2015"	"0"	"0"	"CGI;CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2011"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.58"	"0.875"	"2004"	"2018"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0221357"	"Brachydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9850746"	"1996"	"2018"	"1"	"4"	"CGI;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"1996"	"2015"	"2"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0345832"	"Neoplasm of small intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0345893"	"Juvenile polyposis syndrome"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"1.00"	"0.96875"	"1993"	"2017"	"9"	"69"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9647059"	"1996"	"2018"	"0"	"0"	"CGI;CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C0796081"	"Myhre syndrome"	"disease"	"C05;C10;C12;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.77"	"1"	"1993"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.9636364"	"1996"	"2018"	"4"	"1"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1832940"	"JUVENILE POLYPOSIS OF STOMACH"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.80"		"1998"	"2015"	"9"	"3"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1832942"	"JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)"	"disease"	"C06;C14;C15;C16"	"Disease or Syndrome"	"0.64"	"1"	"1983"	"2016"	"1"	"20"	"CTD_human;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C1868081"	"Juvenile Polyposis Coli"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.80"		"1998"	"2015"	"9"	"3"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4089"	"SMAD4"	"0.43"	"0.759"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"4089"	"SMAD4"	"0.43"	"0.759"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3714239"	"Bmpr1a-Related Juvenile Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3714240"	"Smad4-Related Juvenile Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"4089"	"SMAD4"	"0.43"	"0.759"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4089"	"SMAD4"	"0.43"	"0.759"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4090"	"SMAD5"	"0.681"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4090"	"SMAD5"	"0.681"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0003507"	"Aortic Valve Stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"2"	"CTD_human;UNIPROT"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0149630"	"Bicuspid aortic valve"	"disease"	"C14"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"4091"	"SMAD6"	"0.639"	"0.379"	"C1260873"	"Aortic valve disorder"	"group"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4091"	"SMAD6"	"0.639"	"0.379"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4091"	"SMAD6"	"0.639"	"0.379"	"C3542024"	"AORTIC VALVE DISEASE 2"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"2"	"CTD_human;UNIPROT"
"4091"	"SMAD6"	"0.639"	"0.379"	"C3887892"	"Aortic Valve Disease 1"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4091"	"SMAD6"	"0.639"	"0.379"	"C4479496"	"CRANIOSYNOSTOSIS 7"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"4092"	"SMAD7"	"0.52"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"4092"	"SMAD7"	"0.52"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4092"	"SMAD7"	"0.52"	"0.621"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4092"	"SMAD7"	"0.52"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4092"	"SMAD7"	"0.52"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2018"	"1"	"6"	"CTD_human"
"4092"	"SMAD7"	"0.52"	"0.621"	"C2931434"	"Paraquat lung"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4093"	"SMAD9"	"0.735"	"0.172"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4093"	"SMAD9"	"0.735"	"0.172"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2012"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"4093"	"SMAD9"	"0.735"	"0.172"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4093"	"SMAD9"	"0.735"	"0.172"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4093"	"SMAD9"	"0.735"	"0.172"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4093"	"SMAD9"	"0.735"	"0.172"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2016"	"7"	"0"	"GENOMICS_ENGLAND"
"4093"	"SMAD9"	"0.735"	"0.172"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.63"	"0.6666667"	"1993"	"2016"	"7"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4093"	"SMAD9"	"0.735"	"0.172"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4093"	"SMAD9"	"0.735"	"0.172"	"C3888002"	"PULMONARY HYPERTENSION, PRIMARY, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2012"	"1"	"3"	"UNIPROT"
"4094"	"MAF"	"0.624"	"0.621"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4094"	"MAF"	"0.624"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"4094"	"MAF"	"0.624"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.44"	"1"	"2002"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"4094"	"MAF"	"0.624"	"0.621"	"C0344523"	"Cataract, congenital, cerulean type 1"	"disease"	"C11"	"Congenital Abnormality"	"0.43"	"0.6666667"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"4094"	"MAF"	"0.624"	"0.621"	"C1832812"	"Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation"	"disease"	"C09;C10;C11;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"1996"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"4094"	"MAF"	"0.624"	"0.621"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"4094"	"MAF"	"0.624"	"0.621"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4094"	"MAF"	"0.624"	"0.621"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2002"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"4094"	"MAF"	"0.624"	"0.621"	"C1857768"	"Cataract, Pulverulent, Juvenile-Onset"	"disease"	"C11"	"Congenital Abnormality"	"0.70"		"2002"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"4094"	"MAF"	"0.624"	"0.621"	"C1861829"	"Cataract microcornea syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4094"	"MAF"	"0.624"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4094"	"MAF"	"0.624"	"0.621"	"C3888097"	"CATARACT 21, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2015"	"3"	"4"	"UNIPROT"
"4097"	"MAFG"	"0.785"	"0.138"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4099"	"MAG"	"0.621"	"0.552"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4099"	"MAG"	"0.621"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"2004"	"2011"	"5"	"0"	"PSYGENET"
"4099"	"MAG"	"0.621"	"0.552"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4099"	"MAG"	"0.621"	"0.552"	"C4225250"	"SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4100"	"MAGEA1"	"0.633"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"UNIPROT"
"4100"	"MAGEA1"	"0.633"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9230769"	"1992"	"2015"	"1"	"0"	"CTD_human"
"4103"	"MAGEA4"	"0.762"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4108"	"MAGEA9"	"0.928"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4108"	"MAGEA9"	"0.928"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4110"	"MAGEA11"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4112"	"MAGEB1"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4113"	"MAGEB2"	"0.785"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4117"	"MAK"	"0.676"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.45"	"1"	"2011"	"2016"	"0"	"3"	"ORPHANET"
"4117"	"MAK"	"0.676"	"0.448"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4117"	"MAK"	"0.676"	"0.448"	"C3280042"	"RETINITIS PIGMENTOSA 62"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"2"	"6"	"CTD_human;UNIPROT"
"4118"	"MAL"	"0.609"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4118"	"MAL"	"0.609"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4124"	"MAN2A1"	"0.752"	"0.31"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C0024748"	"alpha-Mannosidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1973"	"2016"	"5"	"69"	"CTD_human;UNIPROT"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4125"	"MAN2B1"	"0.656"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4126"	"MANBA"	"0.707"	"0.483"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4126"	"MANBA"	"0.707"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4126"	"MANBA"	"0.707"	"0.483"	"C2931893"	"Lysosomal beta-mannosidase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4126"	"MANBA"	"0.707"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4126"	"MANBA"	"0.707"	"0.483"	"C4048196"	"beta-Mannosidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1983"	"2009"	"0"	"3"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2016"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0003431"	"Antisocial Personality Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1993"	"2016"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"1999"	"2015"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"1998"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"1995"	"2013"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"4128"	"MAOA"	"0.497"	"0.655"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2016"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2016"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0013409"	"Dyssocial Behavior"	"phenotype"	"F03"	"Individual Behavior"	"0.30"		"1993"	"2008"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1999"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"1999"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.7333333"	"1994"	"2017"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2015"	"1"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1996"	"2015"	"2"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2015"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2012"	"2"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0158850"	"Fetal Malnutrition"	"phenotype"	"C13;C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"1997"	"2015"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C0745744"	"End Stage Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1999"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1999"	"3"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C0796275"	"Brunner Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.81"	"1"	"1993"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"4128"	"MAOA"	"0.497"	"0.655"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C1285261"	"Fetal Nutrition Disorders"	"disease"	"C13;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"4128"	"MAOA"	"0.497"	"0.655"	"C2936476"	"Chronic Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4128"	"MAOA"	"0.497"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4128"	"MAOA"	"0.497"	"0.655"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"1994"	"2015"	"5"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.38"	"1"	"1995"	"2018"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0002888"	"Anemia, Megaloblastic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.6666667"	"1995"	"2000"	"3"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"1999"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.974359"	"1993"	"2016"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9333333"	"1996"	"2015"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0333463"	"Senile Plaques"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"1997"	"2000"	"3"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1995"	"2011"	"2"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"4129"	"MAOB"	"0.575"	"0.724"	"C2936349"	"Plaque, Amyloid"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"4129"	"MAOB"	"0.575"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1996"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"4131"	"MAP1B"	"0.701"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"4133"	"MAP2"	"0.598"	"0.483"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4133"	"MAP2"	"0.598"	"0.483"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4133"	"MAP2"	"0.598"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4133"	"MAP2"	"0.598"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.5"	"2002"	"2009"	"1"	"0"	"PSYGENET"
"4133"	"MAP2"	"0.598"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4133"	"MAP2"	"0.598"	"0.483"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4133"	"MAP2"	"0.598"	"0.483"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4133"	"MAP2"	"0.598"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4133"	"MAP2"	"0.598"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"4133"	"MAP2"	"0.598"	"0.483"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4133"	"MAP2"	"0.598"	"0.483"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4134"	"MAP4"	"0.834"	"0.276"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4135"	"MAP6"	"0.727"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2002"	"2015"	"4"	"0"	"PSYGENET"
"4135"	"MAP6"	"0.727"	"0.414"	"C0085633"	"Mood swings"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4135"	"MAP6"	"0.727"	"0.414"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4135"	"MAP6"	"0.727"	"0.414"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4135"	"MAP6"	"0.727"	"0.414"	"C2678117"	"Schizophrenia-like symptoms (uncommon)"	"phenotype"		"Finding"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4137"	"MAPT"	"0.492"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9793103"	"1988"	"2018"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"4137"	"MAPT"	"0.492"	"0.724"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9090909"	"2001"	"2018"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9833333"	"1998"	"2018"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2018"	"4"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.979798"	"1999"	"2018"	"2"	"24"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.80"	"0.9478261"	"1995"	"2018"	"9"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4137"	"MAPT"	"0.492"	"0.724"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2002"	"2018"	"4"	"1"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0236642"	"Pick Disease of the Brain"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9663462"	"1998"	"2018"	"6"	"4"	"CTD_human;UNIPROT"
"4137"	"MAPT"	"0.492"	"0.724"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.9868421"	"1998"	"2018"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2016"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0338451"	"Frontotemporal dementia"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.70"	"0.9683908"	"1992"	"2018"	"27"	"15"	"CTD_human;UNIPROT"
"4137"	"MAPT"	"0.492"	"0.724"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"1998"	"2011"	"6"	"0"	"CTD_human;ORPHANET"
"4137"	"MAPT"	"0.492"	"0.724"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2012"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0392156"	"Akathisia"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2003"	"2016"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9863014"	"1998"	"2018"	"2"	"1"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0520716"	"Pallidopontonigral degeneration"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2015"	"24"	"11"	"UNIPROT"
"4137"	"MAPT"	"0.492"	"0.724"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.989011"	"1998"	"2018"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2016"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2016"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2016"	"7"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2002"	"2012"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2018"	"4"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2018"	"4"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2018"	"4"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.43"	"1"	"2002"	"2018"	"4"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2011"	"0"	"0"	"ORPHANET"
"4137"	"MAPT"	"0.492"	"0.724"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C0949664"	"Tauopathies"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.9813084"	"1998"	"2018"	"5"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C1838313"	"Pick Complex"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2015"	"24"	"11"	"UNIPROT"
"4137"	"MAPT"	"0.492"	"0.724"	"C1850077"	"Supranuclear Palsy, Progressive, 1, Atypical"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human;ORPHANET"
"4137"	"MAPT"	"0.492"	"0.724"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"2000"	"2014"	"0"	"1"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"4137"	"MAPT"	"0.492"	"0.724"	"C3887612"	"Psychomotor Agitation"	"phenotype"	"C10;C23;F01"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4137"	"MAPT"	"0.492"	"0.724"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"4139"	"MARK1"	"0.735"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"4139"	"MARK1"	"0.735"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4139"	"MARK1"	"0.735"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4139"	"MARK1"	"0.735"	"0.345"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4139"	"MARK1"	"0.735"	"0.345"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4139"	"MARK1"	"0.735"	"0.345"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4141"	"MARS"	"0.707"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"0"	"1"	"GENOMICS_ENGLAND"
"4141"	"MARS"	"0.707"	"0.414"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4141"	"MARS"	"0.707"	"0.414"	"C4084821"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4141"	"MARS"	"0.707"	"0.414"	"C4225400"	"INTERSTITIAL LUNG AND LIVER DISEASE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2014"	"2018"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4142"	"MAS1"	"0.609"	"0.586"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4142"	"MAS1"	"0.609"	"0.586"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"1996"	"2"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0268621"	"Hepatic methionine adenosyltransferase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.79"	"1"	"1974"	"2017"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"4143"	"MAT1A"	"0.614"	"0.517"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"1996"	"2"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C1847720"	"Glycine N-Methyltransferase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2014"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C3151058"	"S-adenosylhomocysteine hydrolase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4143"	"MAT1A"	"0.614"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4143"	"MAT1A"	"0.614"	"0.517"	"C4048705"	"Hypermethioninemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.45"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human"
"4144"	"MAT2A"	"0.713"	"0.448"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"4144"	"MAT2A"	"0.713"	"0.448"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4145"	"MATK"	"0.707"	"0.414"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4145"	"MATK"	"0.707"	"0.414"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4148"	"MATN3"	"0.685"	"0.172"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.70"	"1"	"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"4148"	"MATN3"	"0.685"	"0.172"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.49"	"1"	"2002"	"2012"	"0"	"0"	"CTD_human"
"4148"	"MATN3"	"0.685"	"0.172"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4148"	"MATN3"	"0.685"	"0.172"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4148"	"MATN3"	"0.685"	"0.172"	"C1837481"	"Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2004"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4148"	"MATN3"	"0.685"	"0.172"	"C1846843"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 5"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1959"	"2012"	"7"	"10"	"CTD_human;ORPHANET;UNIPROT"
"4149"	"MAX"	"0.604"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4149"	"MAX"	"0.604"	"0.586"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4149"	"MAX"	"0.604"	"0.586"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4149"	"MAX"	"0.604"	"0.586"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"1"	"2011"	"2016"	"3"	"1"	"CGI;CTD_human;UNIPROT"
"4149"	"MAX"	"0.604"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1995"	"2015"	"7"	"0"	"CLINGEN"
"4149"	"MAX"	"0.604"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1995"	"2015"	"7"	"0"	"CLINGEN"
"4149"	"MAX"	"0.604"	"0.586"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4149"	"MAX"	"0.604"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1995"	"2015"	"7"	"0"	"CLINGEN"
"4149"	"MAX"	"0.604"	"0.586"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4149"	"MAX"	"0.604"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1995"	"2015"	"7"	"0"	"CLINGEN"
"4149"	"MAX"	"0.604"	"0.586"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4149"	"MAX"	"0.604"	"0.586"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"CGI"
"4149"	"MAX"	"0.604"	"0.586"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4149"	"MAX"	"0.604"	"0.586"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4149"	"MAX"	"0.604"	"0.586"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2011"	"2016"	"3"	"4"	"UNIPROT"
"4150"	"MAZ"	"0.672"	"0.448"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4150"	"MAZ"	"0.672"	"0.448"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4152"	"MBD1"	"0.701"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4152"	"MBD1"	"0.701"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4153"	"MBL2"	"0.415"	"0.828"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C3280586"	"Mannose-Binding Protein Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.8709677"	"1991"	"2016"	"0"	"2"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.40"		"1995"	"2009"	"1"	"0"	"CTD_human"
"4153"	"MBL2"	"0.415"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4154"	"MBNL1"	"0.701"	"0.345"	"C0027125"	"Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4154"	"MBNL1"	"0.701"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4154"	"MBNL1"	"0.701"	"0.345"	"C0751358"	"Myotonic Phenomenon"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4154"	"MBNL1"	"0.701"	"0.345"	"C0751359"	"Percussion Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4154"	"MBNL1"	"0.701"	"0.345"	"C3250443"	"MYOTONIC DYSTROPHY 1"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"2"	"1"	"UNIPROT"
"4155"	"MBP"	"0.542"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4155"	"MBP"	"0.542"	"0.793"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.56"	"1"	"1985"	"2008"	"1"	"0"	"CTD_human"
"4155"	"MBP"	"0.542"	"0.793"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"4155"	"MBP"	"0.542"	"0.793"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2001"	"2014"	"3"	"0"	"CTD_human"
"4155"	"MBP"	"0.542"	"0.793"	"C0027873"	"Neuromyelitis Optica"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4155"	"MBP"	"0.542"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.75"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"4155"	"MBP"	"0.542"	"0.793"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"		"2006"	"2016"	"1"	"1"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4157"	"MC1R"	"0.57"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4157"	"MC1R"	"0.57"	"0.586"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9591837"	"1997"	"2018"	"3"	"1"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0268495"	"Oculocutaneous albinism type 2"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.53"	"1"	"2003"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"4157"	"MC1R"	"0.57"	"0.586"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C1318558"	"Congenital melanocytic nevus"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"4157"	"MC1R"	"0.57"	"0.586"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4157"	"MC1R"	"0.57"	"0.586"	"C1842036"	"GIANT PIGMENTED HAIRY NEVUS"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"4157"	"MC1R"	"0.57"	"0.586"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4157"	"MC1R"	"0.57"	"0.586"	"C2751295"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5"	"phenotype"		"Finding"	"0.50"		"2007"	"2009"	"2"	"4"	"CTD_human;UNIPROT"
"4157"	"MC1R"	"0.57"	"0.586"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4158"	"MC2R"	"0.611"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1995"	"1998"	"2"	"0"	"PSYGENET"
"4158"	"MC2R"	"0.611"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4158"	"MC2R"	"0.611"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4158"	"MC2R"	"0.611"	"0.483"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4158"	"MC2R"	"0.611"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4158"	"MC2R"	"0.611"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4158"	"MC2R"	"0.611"	"0.483"	"C4049650"	"Familial Glucocorticoid Deficiency Type 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.70"		"1993"	"2008"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"4159"	"MC3R"	"0.743"	"0.276"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"4159"	"MC3R"	"0.743"	"0.276"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4159"	"MC3R"	"0.743"	"0.276"	"C2677162"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9"	"phenotype"		"Finding"	"0.40"		"2002"	"2011"	"0"	"2"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"4160"	"MC4R"	"0.58"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4160"	"MC4R"	"0.58"	"0.586"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.37"	"0.7142857"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0020505"	"Hyperphagia"	"phenotype"	"C23"	"Finding"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.90"	"0.9484127"	"1997"	"2018"	"14"	"33"	"CTD_human;UNIPROT"
"4160"	"MC4R"	"0.58"	"0.586"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.962963"	"1999"	"2018"	"2"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C0039870"	"Thinness"	"phenotype"	"C23"	"Finding"	"0.30"		"1999"	"2005"	"8"	"22"	"UNIPROT"
"4160"	"MC4R"	"0.58"	"0.586"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4160"	"MC4R"	"0.58"	"0.586"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4160"	"MC4R"	"0.58"	"0.586"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4160"	"MC4R"	"0.58"	"0.586"	"C4273958"	"Obesity due to melanocortin 4 receptor deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4161"	"MC5R"	"0.799"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4161"	"MC5R"	"0.799"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4162"	"MCAM"	"0.572"	"0.621"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"		"2013"	"2014"	"2"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0751871"	"Autoimmune Diseases of the Nervous System"	"group"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C0751872"	"Immune Disorders, Nervous System"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4162"	"MCAM"	"0.572"	"0.621"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2014"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4163"	"MCC"	"0.604"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9166667"	"1991"	"2017"	"3"	"4"	"UNIPROT"
"4163"	"MCC"	"0.604"	"0.552"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4163"	"MCC"	"0.604"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4166"	"CHST6"	"0.785"	"0.172"	"C0024439"	"Macular corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"0"	"0"	"ORPHANET"
"4166"	"CHST6"	"0.785"	"0.172"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"4166"	"CHST6"	"0.785"	"0.172"	"C1636149"	"Macular dystrophy, corneal type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"0.84"	"2000"	"2016"	"16"	"34"	"CTD_human;ORPHANET;UNIPROT"
"4166"	"CHST6"	"0.785"	"0.172"	"C1691013"	"Macular corneal dystrophy Type II (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"2001"	"2016"	"16"	"33"	"UNIPROT"
"4166"	"CHST6"	"0.785"	"0.172"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2000"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"4170"	"MCL1"	"0.477"	"0.793"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"0.98"	"2000"	"2017"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"2"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4170"	"MCL1"	"0.477"	"0.793"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4171"	"MCM2"	"0.6"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"4171"	"MCM2"	"0.6"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2009"	"2013"	"1"	"0"	"CTD_human"
"4171"	"MCM2"	"0.6"	"0.621"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4171"	"MCM2"	"0.6"	"0.621"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4171"	"MCM2"	"0.6"	"0.621"	"C4310775"	"DEAFNESS, AUTOSOMAL DOMINANT 70"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"4173"	"MCM4"	"0.713"	"0.448"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"4173"	"MCM4"	"0.713"	"0.448"	"C1864947"	"Natural Killer Cell Deficiency, Familial Isolated"	"disease"	"C20"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4174"	"MCM5"	"0.676"	"0.621"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4174"	"MCM5"	"0.676"	"0.621"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4174"	"MCM5"	"0.676"	"0.621"	"C4479655"	"MEIER-GORLIN SYNDROME 8"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"4175"	"MCM6"	"0.773"	"0.448"	"C0268181"	"Lactose Intolerance, Adult Type"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4179"	"CD46"	"0.529"	"0.828"	"C0025007"	"Measles"	"disease"	"C02"	"Disease or Syndrome"	"0.40"	"0.9318182"	"1993"	"2015"	"1"	"0"	"CTD_human"
"4179"	"CD46"	"0.529"	"0.828"	"C0162739"	"HELLP Syndrome"	"disease"	"C13"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2013"	"0"	"0"	"ORPHANET"
"4179"	"CD46"	"0.529"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4179"	"CD46"	"0.529"	"0.828"	"C2752040"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.60"		"2004"	"2010"	"4"	"6"	"ORPHANET;UNIPROT"
"4179"	"CD46"	"0.529"	"0.828"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.70"	"0.9166667"	"2004"	"2017"	"3"	"1"	"CTD_human;GENOMICS_ENGLAND"
"4185"	"ADAM11"	"0.713"	"0.414"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4189"	"DNAJB9"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"PSYGENET"
"4190"	"MDH1"	"0.735"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4190"	"MDH1"	"0.735"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"4191"	"MDH2"	"0.627"	"0.483"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"4191"	"MDH2"	"0.627"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"4191"	"MDH2"	"0.627"	"0.483"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"4191"	"MDH2"	"0.627"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4191"	"MDH2"	"0.627"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4191"	"MDH2"	"0.627"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4191"	"MDH2"	"0.627"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4191"	"MDH2"	"0.627"	"0.483"	"C4479208"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"4192"	"MDK"	"0.524"	"0.655"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2018"	"1"	"1"	"PSYGENET"
"4192"	"MDK"	"0.524"	"0.655"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4192"	"MDK"	"0.524"	"0.655"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9701493"	"1994"	"2018"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"4193"	"MDM2"	"0.396"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"2"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"0"	"0"	"CGI"
"4193"	"MDM2"	"0.396"	"0.759"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2004"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0085390"	"Li-Fraumeni Syndrome"	"disease"	"C04;C16;C18"	"Neoplastic Process"	"0.40"	"0.8666667"	"2001"	"2015"	"0"	"0"	"ORPHANET"
"4193"	"MDM2"	"0.396"	"0.759"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"0"	"0"	"ORPHANET"
"4193"	"MDM2"	"0.396"	"0.759"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9354839"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.9767442"	"1993"	"2018"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0745730"	"Multiple lipomata"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4193"	"MDM2"	"0.396"	"0.759"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9444444"	"1992"	"2016"	"0"	"0"	"CGI"
"4193"	"MDM2"	"0.396"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"CGI"
"4193"	"MDM2"	"0.396"	"0.759"	"C1370889"	"Liposarcoma, well differentiated"	"disease"		"Neoplastic Process"	"0.40"	"0.8421053"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"4193"	"MDM2"	"0.396"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"4193"	"MDM2"	"0.396"	"0.759"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8095238"	"1995"	"2017"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0035335"	"Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2017"	"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4194"	"MDM4"	"0.501"	"0.724"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.875"	"1995"	"2016"	"1"	"2"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.37"	"0.8571429"	"2002"	"2016"	"0"	"0"	"CGI"
"4194"	"MDM4"	"0.501"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4194"	"MDM4"	"0.501"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4194"	"MDM4"	"0.501"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"1"	"2002"	"2014"	"1"	"0"	"CGI;CTD_human"
"4199"	"ME1"	"0.727"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4199"	"ME1"	"0.727"	"0.345"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4199"	"ME1"	"0.727"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"4200"	"ME2"	"0.735"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4200"	"ME2"	"0.735"	"0.172"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4200"	"ME2"	"0.735"	"0.172"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4200"	"ME2"	"0.735"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4200"	"ME2"	"0.735"	"0.172"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4200"	"ME2"	"0.735"	"0.172"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4204"	"MECP2"	"0.463"	"0.862"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9206349"	"2000"	"2017"	"3"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0008074"	"Child Development Disorders, Pervasive"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0021712"	"Myoclonus, Intention"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.35"	"1"	"1999"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"4204"	"MECP2"	"0.463"	"0.862"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0027066"	"Myoclonus"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0030214"	"Myoclonus, Palatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0035372"	"Rett Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.954023"	"1966"	"2018"	"48"	"278"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.9375"	"2002"	"2016"	"1"	"1"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2002"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0524528"	"Pervasive Development Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4204"	"MECP2"	"0.463"	"0.862"	"C0585540"	"Myoclonus, Oculopalatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751348"	"Myoclonus Simplex"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751349"	"Myoclonus, Eyelid"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751350"	"Myoclonus, Lower Extremity"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751351"	"Myoclonus, Segmental"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751352"	"Myoclonus, Nocturnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751353"	"Myoclonus, Upper Extremity"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751354"	"Myoclonus, Action"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751355"	"Polymyoclonus"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C0796222"	"Mental Retardation, X-Linked 16"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2007"	"10"	"8"	"UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.984127"	"1999"	"2018"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C1839332"	"Rett Syndrome, Preserved Speech Variant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2018"	"32"	"35"	"CLINGEN;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C1846058"	"Lubs X-linked mental retardation syndrome"	"disease"	"C10;C16"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"2009"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"4204"	"MECP2"	"0.463"	"0.862"	"C1848211"	"Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism"	"disease"	"C05;C10;C16;C23;F03"	"Disease or Syndrome"	"0.30"		"2000"	"2007"	"10"	"8"	"UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C1968550"	"Mental Retardation, X-Linked, Syndromic 13"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2017"	"10"	"30"	"CTD_human;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C1968551"	"Mental Retardation, X-Linked 79"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2007"	"10"	"8"	"UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C1968552"	"Mental Retardation, X-Linked, With Spasticity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2007"	"10"	"8"	"UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C1968556"	"ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2017"	"1"	"20"	"CTD_human;ORPHANET;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C2677682"	"Rett Syndrome, Zappella Variant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2018"	"32"	"36"	"CLINGEN;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9166667"	"1999"	"2018"	"32"	"36"	"CLINGEN;ORPHANET;UNIPROT"
"4204"	"MECP2"	"0.463"	"0.862"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"ORPHANET"
"4204"	"MECP2"	"0.463"	"0.862"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C3713418"	"Ppm-X Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"4204"	"MECP2"	"0.463"	"0.862"	"C3714043"	"Trisomy Xq28"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4204"	"MECP2"	"0.463"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.70"	"0.943662"	"1999"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4204"	"MECP2"	"0.463"	"0.862"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4204"	"MECP2"	"0.463"	"0.862"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4205"	"MEF2A"	"0.648"	"0.483"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4205"	"MEF2A"	"0.648"	"0.483"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4205"	"MEF2A"	"0.648"	"0.483"	"C1842247"	"CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"0.5"	"2006"	"2011"	"0"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0005899"	"Body Rocking"	"phenotype"	"F03"	"Individual Behavior"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0018672"	"Head Banging"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0038273"	"Stereotypic Movement Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C3150700"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 20"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2017"	"0"	"10"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2010"	"2015"	"6"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4208"	"MEF2C"	"0.57"	"0.483"	"C4225434"	"CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4208"	"MEF2C"	"0.57"	"0.483"	"C4304529"	"5q14.3 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4209"	"MEF2D"	"0.667"	"0.31"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2012"	"2017"	"1"	"0"	"CTD_human"
"4210"	"MEFV"	"0.494"	"0.724"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4210"	"MEFV"	"0.494"	"0.724"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2016"	"0"	"3"	"ORPHANET"
"4210"	"MEFV"	"0.494"	"0.724"	"C0031069"	"Familial Mediterranean Fever"	"disease"	"C16"	"Disease or Syndrome"	"1.00"	"0.9540636"	"1993"	"2018"	"19"	"49"	"CTD_human;ORPHANET;UNIPROT"
"4210"	"MEFV"	"0.494"	"0.724"	"C0149910"	"Intermittent joint effusion"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"4210"	"MEFV"	"0.494"	"0.724"	"C0585274"	"Periodic syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"4210"	"MEFV"	"0.494"	"0.724"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"4210"	"MEFV"	"0.494"	"0.724"	"C1851347"	"Familial Mediterranean Fever, Autosomal Dominant"	"disease"	"C16"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"2"	"7"	"CTD_human;UNIPROT"
"4210"	"MEFV"	"0.494"	"0.724"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0021603"	"Sleep Initiation and Maintenance Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0033139"	"Primary Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0035258"	"Restless Legs Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.8181818"	"2007"	"2017"	"2"	"3"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0270541"	"Rebound Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0349255"	"Nonorganic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0393759"	"Transient Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0541798"	"Early Awakening"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0751249"	"Chronic Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0751250"	"Psychophysiological Insomnia"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0751251"	"Secondary Insomnia"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0751252"	"Sleep Initiation Dysfunction"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C0917801"	"Sleeplessness"	"phenotype"	"C10;F03"	"Sign or Symptom"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4211"	"MEIS1"	"0.614"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4212"	"MEIS2"	"0.696"	"0.483"	"C1832950"	"Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies"	"disease"	"C05;C07;C10;C14;C16"	"Disease or Syndrome"	"0.40"		"2016"	"2017"	"0"	"2"	"CTD_human"
"4212"	"MEIS2"	"0.696"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4212"	"MEIS2"	"0.696"	"0.483"	"C4225666"	"CHROMOSOME 15q14 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.88"	"2007"	"2017"	"1"	"0"	"CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2002"	"2018"	"1"	"0"	"CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.88"	"2007"	"2017"	"1"	"6"	"CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.53"		"2007"	"2009"	"1"	"0"	"CGI;CTD_human"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C3151064"	"46,XY SEX REVERSAL 6"	"disease"		"Disease or Syndrome"	"0.60"		"1970"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4214"	"MAP3K1"	"0.569"	"0.586"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4215"	"MAP3K3"	"0.701"	"0.379"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4215"	"MAP3K3"	"0.701"	"0.379"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4216"	"MAP3K4"	"0.743"	"0.276"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4216"	"MAP3K4"	"0.743"	"0.276"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4216"	"MAP3K4"	"0.743"	"0.276"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4216"	"MAP3K4"	"0.743"	"0.276"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4216"	"MAP3K4"	"0.743"	"0.276"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"0.75"	"2006"	"2012"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4217"	"MAP3K5"	"0.551"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4218"	"RAB8A"	"0.667"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C0011993"	"Vipoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0017150"	"Gastrinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.7777778"	"1991"	"2013"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0017689"	"Glucagonoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.43"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0021670"	"insulinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.70"	"0.9565217"	"1991"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"4221"	"MEN1"	"0.463"	"0.724"	"C0025267"	"Multiple Endocrine Neoplasia Type 1"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"1.00"	"0.9454545"	"1980"	"2018"	"45"	"85"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4221"	"MEN1"	"0.463"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.39"	"0.8888889"	"1991"	"2011"	"2"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0030521"	"Parathyroid Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.9130435"	"1989"	"2013"	"0"	"1"	"UNIPROT"
"4221"	"MEN1"	"0.463"	"0.724"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.50"	"0.9375"	"1990"	"2018"	"0"	"0"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.70"	"0.7272727"	"1996"	"2016"	"0"	"0"	"ORPHANET"
"4221"	"MEN1"	"0.463"	"0.724"	"C0086768"	"Pancreatic Cholera"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.31"	"0"	"1999"	"1999"	"0"	"0"	"GENOMICS_ENGLAND"
"4221"	"MEN1"	"0.463"	"0.724"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9615385"	"1999"	"2018"	"1"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0242363"	"Islet Cell Tumor"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2007"	"0"	"0"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C0262587"	"Parathyroid Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.50"	"0.9545455"	"1997"	"2015"	"0"	"1"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C0338078"	"Non-Functioning Pituitary Gland Neoplasm"	"disease"		"Neoplastic Process"	"0.41"	"1"	"1996"	"1996"	"0"	"0"	"ORPHANET"
"4221"	"MEN1"	"0.463"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"4221"	"MEN1"	"0.463"	"0.724"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"4221"	"MEN1"	"0.463"	"0.724"	"C1328479"	"Pancreatic Endocrine Carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4221"	"MEN1"	"0.463"	"0.724"	"C1840402"	"HYPERPARATHYROIDISM 1"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"0.9473684"	"1994"	"2012"	"0"	"1"	"ORPHANET"
"4221"	"MEN1"	"0.463"	"0.724"	"C3149237"	"MEN1 SOMATIC MUTATIONS"	"disease"		"Disease or Syndrome"	"0.50"		"1997"	"2015"	"44"	"18"	"CLINGEN;UNIPROT"
"4222"	"MEOX1"	"0.72"	"0.414"	"C0022738"	"Klippel-Feil Syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"4222"	"MEOX1"	"0.72"	"0.414"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4222"	"MEOX1"	"0.72"	"0.414"	"C1859209"	"Klippel Feil syndrome recessive type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"4223"	"MEOX2"	"0.743"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4223"	"MEOX2"	"0.743"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4224"	"MEP1A"	"0.886"	"0.069"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4224"	"MEP1A"	"0.886"	"0.069"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4232"	"MEST"	"0.713"	"0.448"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9444444"	"1993"	"2018"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.41"	"1"	"1998"	"2017"	"1"	"6"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.9719626"	"2002"	"2018"	"4"	"0"	"CGI;CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"0.96875"	"1996"	"2017"	"1"	"7"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8125"	"1997"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"1"	"1997"	"2018"	"4"	"2"	"CGI;CTD_human;UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.8977273"	"1995"	"2017"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2014"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.56"	"1"	"1991"	"2016"	"2"	"0"	"CGI;CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4233"	"MET"	"0.405"	"0.793"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4233"	"MET"	"0.405"	"0.793"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"3"	"UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.969697"	"2000"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0279606"	"Childhood Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.40"		"1999"	"1999"	"0"	"3"	"ORPHANET"
"4233"	"MET"	"0.405"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.57"	"1"	"2003"	"2018"	"1"	"0"	"CGI;CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4233"	"MET"	"0.405"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2012"	"1"	"3"	"UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4233"	"MET"	"0.405"	"0.793"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1989"	"2018"	"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"1997"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4233"	"MET"	"0.405"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C0879257"	"Hereditary Papillary Renal Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1998"	"2009"	"0"	"0"	"ORPHANET"
"4233"	"MET"	"0.405"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2003"	"2011"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.38"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2017"	"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.80"	"1"	"2002"	"2016"	"1"	"0"	"CGI;CTD_human;ORPHANET"
"4233"	"MET"	"0.405"	"0.793"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4233"	"MET"	"0.405"	"0.793"	"C1336839"	"Type 1 Papillary Renal Cell Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"1997"	"2017"	"5"	"11"	"UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1709353"	"Osteofibrous Dysplasia"	"disease"	"C05"	"Disease or Syndrome"	"0.41"	"1"	"1976"	"2016"	"0"	"2"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1836723"	"Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum"	"disease"	"C05;C16;C26"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4233"	"MET"	"0.405"	"0.793"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4233"	"MET"	"0.405"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.80"	"0.972973"	"1991"	"2018"	"1"	"3"	"CGI;CTD_human;UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C2676033"	"Hepatoblastoma Caused By Somatic Mutation"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"3"	"UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C2931899"	"Papillary renal cell carcinoma, familial"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4233"	"MET"	"0.405"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4233"	"MET"	"0.405"	"0.793"	"C4084709"	"DEAFNESS, AUTOSOMAL RECESSIVE 97"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"4233"	"MET"	"0.405"	"0.793"	"C4085248"	"OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"4237"	"MFAP2"	"0.886"	"0.172"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4237"	"MFAP2"	"0.886"	"0.172"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4239"	"MFAP4"	"0.773"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4240"	"MFGE8"	"0.616"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1991"	"2011"	"1"	"0"	"CTD_human"
"4241"	"MELTF"	"0.72"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9166667"	"1986"	"2009"	"1"	"0"	"CTD_human"
"4247"	"MGAT2"	"0.642"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4247"	"MGAT2"	"0.642"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4247"	"MGAT2"	"0.642"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"4247"	"MGAT2"	"0.642"	"0.414"	"C2931008"	"Congenital disorder of glycosylation type 2A"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"1996"	"2012"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4247"	"MGAT2"	"0.642"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4249"	"MGAT5"	"0.685"	"0.276"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4249"	"MGAT5"	"0.685"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4253"	"MIA2"	"0.752"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4254"	"KITLG"	"0.491"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0027430"	"Nasal Polyps"	"disease"	"C08;C09;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.32"		"2004"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"4254"	"KITLG"	"0.491"	"0.759"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"4254"	"KITLG"	"0.491"	"0.759"	"C1835039"	"Melanosis, Universal"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4254"	"KITLG"	"0.491"	"0.759"	"C1840392"	"HYPERPIGMENTATION, FAMILIAL PROGRESSIVE"	"disease"	"C17"	"Disease or Syndrome"	"0.71"	"1"	"2004"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4254"	"KITLG"	"0.491"	"0.759"	"C2700265"	"Waardenburg Syndrome Type 2"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4254"	"KITLG"	"0.491"	"0.759"	"C4225241"	"DEAFNESS, AUTOSOMAL DOMINANT 69"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.9545455"	"1992"	"2017"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9584906"	"1992"	"2018"	"2"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9793103"	"1991"	"2018"	"3"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"4255"	"MGMT"	"0.438"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"3"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2010"	"2012"	"2"	"0"	"CTD_human;ORPHANET"
"4255"	"MGMT"	"0.438"	"0.759"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"3"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.875"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9454545"	"1999"	"2018"	"2"	"0"	"CTD_human"
"4255"	"MGMT"	"0.438"	"0.759"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4256"	"MGP"	"0.57"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0042345"	"Varicosity"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C0342649"	"Vascular calcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"4256"	"MGP"	"0.57"	"0.724"	"C1855607"	"Keutel syndrome"	"disease"	"C05;C14;C16;C17;C18"	"Disease or Syndrome"	"0.63"	"1"	"1999"	"2016"	"1"	"4"	"CTD_human;ORPHANET"
"4256"	"MGP"	"0.57"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"4257"	"MGST1"	"0.752"	"0.207"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4257"	"MGST1"	"0.752"	"0.207"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4257"	"MGST1"	"0.752"	"0.207"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4261"	"CIITA"	"0.564"	"0.724"	"C0001403"	"Addison Disease"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"4261"	"CIITA"	"0.564"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.6428571"	"2005"	"2017"	"0"	"1"	"CTD_human"
"4261"	"CIITA"	"0.564"	"0.724"	"C1859534"	"Bare Lymphocyte Syndrome, Type II, Complementation Group A"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.40"		"1993"	"2002"	"5"	"3"	"UNIPROT"
"4261"	"CIITA"	"0.564"	"0.724"	"C1859535"	"Bare Lymphocyte Syndrome, Type II, Complementation Group B"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1993"	"2002"	"5"	"0"	"UNIPROT"
"4261"	"CIITA"	"0.564"	"0.724"	"C1859536"	"Bare Lymphocyte Syndrome, Type II, Complementation Group C"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1993"	"2002"	"5"	"0"	"UNIPROT"
"4261"	"CIITA"	"0.564"	"0.724"	"C1859537"	"Bare Lymphocyte Syndrome, Type II, Complementation Group D"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1993"	"2002"	"5"	"0"	"UNIPROT"
"4261"	"CIITA"	"0.564"	"0.724"	"C1859538"	"Bare Lymphocyte Syndrome, Type II, Complementation Group E"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1993"	"2002"	"5"	"0"	"UNIPROT"
"4261"	"CIITA"	"0.564"	"0.724"	"C2931418"	"Bare lymphocyte syndrome 2"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.73"	"1"	"1993"	"2017"	"5"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4267"	"CD99"	"0.562"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"1994"	"2004"	"1"	"0"	"PSYGENET"
"4267"	"CD99"	"0.562"	"0.621"	"C0206637"	"Mesenchymal Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4267"	"CD99"	"0.562"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4277"	"MICB"	"0.592"	"0.655"	"C0019100"	"Severe Dengue"	"disease"	"C02"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2017"	"1"	"1"	"CTD_human"
"4277"	"MICB"	"0.592"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4277"	"MICB"	"0.592"	"0.655"	"C0376300"	"Dengue Shock Syndrome"	"disease"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4281"	"MID1"	"0.659"	"0.517"	"C0175696"	"Congenital cleft larynx and Opitz-Frias syndrome"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2015"	"5"	"8"	"CLINGEN"
"4281"	"MID1"	"0.659"	"0.517"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4281"	"MID1"	"0.659"	"0.517"	"C2936904"	"Opitz GBBB Syndrome, X-Linked"	"disease"	"C05;C07;C12;C13;C16"	"Disease or Syndrome"	"0.90"	"1"	"1997"	"2017"	"8"	"2"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4281"	"MID1"	"0.659"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4282"	"MIF"	"0.457"	"0.862"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.8666667"	"1999"	"2013"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.36"		"2003"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4282"	"MIF"	"0.457"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4282"	"MIF"	"0.457"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1384600"	"Systemic onset juvenile chronic arthritis"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2001"	"2003"	"0"	"0"	"ORPHANET"
"4282"	"MIF"	"0.457"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C1858558"	"Rheumatoid Arthritis, Systemic Juvenile"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4282"	"MIF"	"0.457"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0282488"	"Interstitial Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0600040"	"Chronic interstitial cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C1720830"	"Painful Bladder Syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4283"	"CXCL9"	"0.532"	"0.69"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4284"	"MIP"	"0.54"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.70"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4284"	"MIP"	"0.54"	"0.759"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C0344523"	"Cataract, congenital, cerulean type 1"	"disease"	"C11"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4284"	"MIP"	"0.54"	"0.759"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4284"	"MIP"	"0.54"	"0.759"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4284"	"MIP"	"0.54"	"0.759"	"C3809001"	"CATARACT 15, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.80"		"1968"	"2017"	"10"	"7"	"CTD_human;UNIPROT"
"4285"	"MIPEP"	"0.762"	"0.207"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4285"	"MIPEP"	"0.762"	"0.207"	"C4310661"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4286"	"MITF"	"0.526"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4286"	"MITF"	"0.526"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.38"	"0.875"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9689441"	"1996"	"2018"	"1"	"0"	"CGI;CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0036305"	"Schamberg Disease"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"4286"	"MITF"	"0.526"	"0.69"	"C0078918"	"Albinism, Oculocutaneous"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.31"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0078921"	"Albinism, Tyrosinase-Negative"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0078922"	"Albinism, Tyrosinase-Positive"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0078923"	"Albinism, Yellow-Mutant"	"phenotype"	"C11;C16;C17;C18"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.61"	"1"	"2012"	"2015"	"1"	"0"	"CGI;CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CLINGEN"
"4286"	"MITF"	"0.526"	"0.69"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CLINGEN"
"4286"	"MITF"	"0.526"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CLINGEN"
"4286"	"MITF"	"0.526"	"0.69"	"C0391816"	"Tietz syndrome"	"disease"	"C09;C10;C11;C16;C17;C18;C23"	"Disease or Syndrome"	"0.93"	"1"	"1963"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4286"	"MITF"	"0.526"	"0.69"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CLINGEN"
"4286"	"MITF"	"0.526"	"0.69"	"C0549567"	"Pigmentation Disorders"	"group"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"4286"	"MITF"	"0.526"	"0.69"	"C1845069"	"ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)"	"disease"	"C09;C10;C11;C16;C17;C18;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C1860339"	"WAARDENBURG SYNDROME, TYPE IIA"	"disease"	"C16"	"Disease or Syndrome"	"0.90"	"1"	"1967"	"2018"	"2"	"8"	"CTD_human;UNIPROT"
"4286"	"MITF"	"0.526"	"0.69"	"C1863198"	"ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)"	"disease"		"Disease or Syndrome"	"0.50"		"1967"	"2002"	"0"	"0"	"ORPHANET"
"4286"	"MITF"	"0.526"	"0.69"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4286"	"MITF"	"0.526"	"0.69"	"C2700265"	"Waardenburg Syndrome Type 2"	"disease"	"C16"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"4286"	"MITF"	"0.526"	"0.69"	"C2700405"	"WAARDENBURG SYNDROME, TYPE IIE"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C3152204"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8"	"phenotype"		"Finding"	"0.60"		"2012"	"2012"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4286"	"MITF"	"0.526"	"0.69"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4286"	"MITF"	"0.526"	"0.69"	"C4310625"	"COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"4286"	"MITF"	"0.526"	"0.69"	"C4518333"	"Clear cell papillary renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"GENOMICS_ENGLAND"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1993"	"2015"	"5"	"0"	"PSYGENET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1993"	"2015"	"5"	"0"	"PSYGENET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0024408"	"Machado-Joseph Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.9727273"	"1994"	"2018"	"0"	"0"	"CTD_human"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2003"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0751668"	"Machado-Joseph Disease Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0751669"	"Machado-Joseph Disease Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0751670"	"Machado-Joseph Disease Type III"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4287"	"ATXN3"	"0.579"	"0.517"	"C0751671"	"Machado-Joseph Disease Type IV"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4287"	"ATXN3"	"0.579"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4288"	"MKI67"	"0.475"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"0.8333333"	"1996"	"2018"	"3"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2008"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0206637"	"Mesenchymal Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"1995"	"2018"	"3"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"3"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2009"	"3"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4288"	"MKI67"	"0.475"	"0.655"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4291"	"MLF1"	"0.727"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"4291"	"MLF1"	"0.727"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4291"	"MLF1"	"0.727"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9897959"	"1988"	"2018"	"1"	"1"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.40"	"0.9230769"	"1996"	"2018"	"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9671533"	"1993"	"2018"	"3"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9375"	"1997"	"2014"	"3"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.90"		"1994"	"2017"	"14"	"95"	"CLINGEN;CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.47"	"0.8333333"	"1997"	"2005"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9210526"	"1997"	"2018"	"1"	"3"	"UNIPROT"
"4292"	"MLH1"	"0.424"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.75"	"2000"	"2016"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1995"	"2016"	"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2003"	"2008"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0085136"	"Central Nervous System Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0265325"	"Turcot syndrome (disorder)"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.80"	"0.92"	"1994"	"2017"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"4292"	"MLH1"	"0.424"	"0.759"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.52"	"1"	"2001"	"2017"	"6"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0348374"	"Malignant Central Nervous System Neoplasm"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"0.7142857"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.44"	"1"	"1997"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.60"	"0.9390244"	"1993"	"2018"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.60"	"0.9855072"	"1994"	"2018"	"11"	"14"	"CGI;UNIPROT"
"4292"	"MLH1"	"0.424"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.59"	"0.8333333"	"1997"	"2009"	"1"	"0"	"CGI;CTD_human"
"4292"	"MLH1"	"0.424"	"0.759"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.50"		"1994"	"2016"	"9"	"0"	"CLINGEN;ORPHANET"
"4292"	"MLH1"	"0.424"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"1"	"1995"	"2016"	"1"	"0"	"CGI;CTD_human;GENOMICS_ENGLAND"
"4292"	"MLH1"	"0.424"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"4292"	"MLH1"	"0.424"	"0.759"	"C1321489"	"Torre-Muir syndrome"	"disease"	"C04;C16;C17"	"Neoplastic Process"	"0.70"	"0.9285714"	"1995"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"4292"	"MLH1"	"0.424"	"0.759"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"1.00"	"0.9503546"	"1992"	"2018"	"14"	"479"	"CLINGEN;CTD_human;ORPHANET"
"4292"	"MLH1"	"0.424"	"0.759"	"C1333991"	"Hereditary Non-Polyposis Colon Cancer Type 2"	"disease"	"C04;C16"	"Neoplastic Process"	"0.61"	"1"	"1991"	"2017"	"61"	"136"	"CTD_human;UNIPROT"
"4292"	"MLH1"	"0.424"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.9634465"	"1993"	"2018"	"14"	"14"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"4292"	"MLH1"	"0.424"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4293"	"MAP3K9"	"0.799"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"4293"	"MAP3K9"	"0.799"	"0.138"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4293"	"MAP3K9"	"0.799"	"0.138"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"4294"	"MAP3K10"	"0.701"	"0.345"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4295"	"MLN"	"0.773"	"0.414"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2008"	"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9710983"	"1987"	"2018"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9615385"	"1996"	"2018"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023464"	"Acute biphenotypic leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"1992"	"2016"	"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023465"	"Acute monocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1994"	"2007"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9761905"	"1993"	"2018"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0023479"	"Acute myelomonocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0280141"	"Acute Undifferentiated Leukemia"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2008"	"2017"	"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0349680"	"Acute bilineal leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"0.8"	"2011"	"2018"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C0856823"	"Undifferentiated type acute leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1292775"	"Acute myeloid leukemia, 11q23 abnormalities"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1854630"	"Growth Deficiency and Mental Retardation with Facial Dysmorphism"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.66"	"1"	"2008"	"2017"	"0"	"23"	"CTD_human;ORPHANET"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9880952"	"1994"	"2018"	"2"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"4297"	"KMT2A"	"0.46"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4298"	"MLLT1"	"0.69"	"0.276"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"4298"	"MLLT1"	"0.69"	"0.276"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4299"	"AFF1"	"0.685"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4299"	"AFF1"	"0.685"	"0.31"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4299"	"AFF1"	"0.685"	"0.31"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1994"	"1994"	"0"	"0"	"ORPHANET"
"4300"	"MLLT3"	"0.72"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2012"	"1"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2005"	"2011"	"1"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2001"	"2016"	"5"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2001"	"2016"	"5"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2006"	"2013"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"1992"	"2015"	"0"	"1"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2015"	"4"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2015"	"0"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2017"	"4"	"0"	"PSYGENET"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1998"	"2015"	"4"	"13"	"CTD_human;ORPHANET;UNIPROT"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1995"	"1998"	"0"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1854631"	"Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2000"	"2005"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4306"	"NR3C2"	"0.52"	"0.69"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4308"	"TRPM1"	"0.648"	"0.379"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.67"	"1"	"2009"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"4308"	"TRPM1"	"0.648"	"0.379"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C2750747"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2017"	"3"	"18"	"UNIPROT"
"4308"	"TRPM1"	"0.648"	"0.379"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4308"	"TRPM1"	"0.648"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4308"	"TRPM1"	"0.648"	"0.379"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"4311"	"MME"	"0.461"	"0.69"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0017665"	"Membranous glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0086445"	"Idiopathic Membranous Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"		"2004"	"2016"	"0"	"1"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0268390"	"Muckle-Wells Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0343068"	"Familial cold urticaria"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0409818"	"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2002"	"2013"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C1704378"	"Heymann Nephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C2316212"	"Cryopyrin-Associated Periodic Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4311"	"MME"	"0.461"	"0.69"	"C4015635"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"2"	"10"	"CTD_human;UNIPROT"
"4311"	"MME"	"0.461"	"0.69"	"C4310763"	"SPINOCEREBELLAR ATAXIA 43"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"4312"	"MMP1"	"0.415"	"0.793"	"C0002940"	"Aneurysm"	"phenotype"	"C14"	"Anatomical Abnormality"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.6666667"	"2005"	"2013"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"		"2002"	"2013"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"4312"	"MMP1"	"0.415"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.70"	"0.8181818"	"2003"	"2016"	"0"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.31"		"2003"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9692308"	"1993"	"2017"	"4"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0028840"	"Ocular Hypertension"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0079136"	"Cockayne-Touraine Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0079294"	"Epidermolysis Bullosa Dystrophica"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0079474"	"Hallopeau-Siemens Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.55"	"1"	"1982"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"4312"	"MMP1"	"0.415"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.8666667"	"2001"	"2018"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0333099"	"Fusiform Aneurysm"	"phenotype"	"C14"	"Anatomical Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"		"2013"	"2015"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C2673611"	"Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4312"	"MMP1"	"0.415"	"0.793"	"C2673612"	"Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4312"	"MMP1"	"0.415"	"0.793"	"C2713497"	"Saccular Aneurysm"	"disease"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4312"	"MMP1"	"0.415"	"0.793"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4313"	"MMP2"	"0.373"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0003496"	"Aortic Rupture"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.8333333"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9591837"	"1992"	"2017"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2018"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2012"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.31"		"2007"	"2017"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9677419"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2006"	"2015"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0022682"	"Kienbock Disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2005"	"2016"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0024143"	"Lupus Nephritis"	"disease"	"C12;C13;C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0024689"	"Mandibular Diseases"	"group"	"C05;C07"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0024950"	"Maxillary Diseases"	"group"	"C05;C07"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"2000"	"2014"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0027543"	"Avascular necrosis of bone"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2008"	"2013"	"4"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9791667"	"1993"	"2018"	"5"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0028433"	"Nose Neoplasms"	"group"	"C04;C05;C08;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0029445"	"Bone necrosis"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2007"	"2014"	"1"	"0"	"PSYGENET"
"4313"	"MMP2"	"0.373"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"1997"	"2018"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0520474"	"Aseptic Necrosis of Bone"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9642857"	"1992"	"2017"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0741160"	"Aortic Aneurysm, Ruptured"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0751394"	"Cancer of Nose"	"disease"	"C04;C05;C08;C09"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"1"	"2003"	"2018"	"3"	"3"	"CTD_human;UNIPROT"
"4313"	"MMP2"	"0.373"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C1850155"	"TORG-WINCHESTER SYNDROME"	"disease"	"C05"	"Disease or Syndrome"	"0.78"	"0.875"	"1984"	"2016"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4313"	"MMP2"	"0.373"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9387755"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.40"	"0.8571429"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C2936380"	"Neointima"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C2936381"	"Neointima Formation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4313"	"MMP2"	"0.373"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.6666667"	"1997"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4314"	"MMP3"	"0.439"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"1996"	"2006"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"1996"	"2010"	"0"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4314"	"MMP3"	"0.439"	"0.793"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0948480"	"Coronary Restenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"0.5"	"1996"	"2011"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1996"	"2014"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4314"	"MMP3"	"0.439"	"0.793"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2007"	"2015"	"1"	"0"	"CTD_human"
"4316"	"MMP7"	"0.47"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4317"	"MMP8"	"0.552"	"0.724"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4317"	"MMP8"	"0.552"	"0.724"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4317"	"MMP8"	"0.552"	"0.724"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2010"	"3"	"0"	"PSYGENET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0003486"	"Aortic Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0003496"	"Aortic Rupture"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.9130435"	"1997"	"2017"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.8888889"	"2000"	"2012"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.875"	"1996"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.96"	"2000"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2012"	"3"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.52"		"2004"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.34"		"2003"	"2015"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0024143"	"Lupus Nephritis"	"disease"	"C12;C13;C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.31"		"2003"	"2014"	"7"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9738806"	"1996"	"2018"	"5"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2005"	"2018"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"0.5"	"2007"	"2012"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4318"	"MMP9"	"0.339"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0031051"	"Pericementitis"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0031099"	"Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.35"	"0.8"	"2004"	"2017"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2004"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2009"	"2018"	"2"	"0"	"PSYGENET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.90625"	"1995"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0340288"	"Stable angina"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9375"	"1995"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9795918"	"1998"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0432226"	"Metaphyseal anadysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2018"	"0"	"0"	"ORPHANET"
"4318"	"MMP9"	"0.339"	"0.862"	"C0432291"	"Mandibuloacral dysostosis"	"disease"	"C05;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9893617"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2009"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0741160"	"Aortic Aneurysm, Ruptured"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.37"	"0.7142857"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2002"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2004"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.96875"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2751322"	"Metaphyseal Anadysplasia 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"1"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2936380"	"Neointima"	"phenotype"	"C23"	"Acquired Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2936381"	"Neointima Formation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2009"	"5"	"0"	"CTD_human"
"4318"	"MMP9"	"0.339"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4319"	"MMP10"	"0.58"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"1990"	"2009"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4319"	"MMP10"	"0.58"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"4319"	"MMP10"	"0.58"	"0.759"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.5"	"2005"	"2012"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"0.6666667"	"2006"	"2018"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2013"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"4319"	"MMP10"	"0.58"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4320"	"MMP11"	"0.57"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4320"	"MMP11"	"0.57"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4320"	"MMP11"	"0.57"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2000"	"1"	"0"	"CTD_human"
"4320"	"MMP11"	"0.57"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2016"	"0"	"0"	"UNIPROT"
"4321"	"MMP12"	"0.516"	"0.862"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2014"	"2"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2014"	"2"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4321"	"MMP12"	"0.516"	"0.862"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2014"	"2"	"0"	"CTD_human"
"4322"	"MMP13"	"0.479"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4322"	"MMP13"	"0.479"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4322"	"MMP13"	"0.479"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4322"	"MMP13"	"0.479"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"4322"	"MMP13"	"0.479"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4322"	"MMP13"	"0.479"	"0.759"	"C0432225"	"Metaphyseal chondrodysplasia Spahr type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2009"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4322"	"MMP13"	"0.479"	"0.759"	"C0432226"	"Metaphyseal anadysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"4322"	"MMP13"	"0.479"	"0.759"	"C1865832"	"Spondyloepimetaphyseal Dysplasia, Missouri Type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2009"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4322"	"MMP13"	"0.479"	"0.759"	"C2748495"	"Metaphyseal Anadysplasia 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2009"	"2"	"4"	"UNIPROT"
"4322"	"MMP13"	"0.479"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4323"	"MMP14"	"0.466"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0432289"	"Winchester syndrome (disorder)"	"disease"	"C05;C11;C16;C18;C23"	"Disease or Syndrome"	"0.60"		"1969"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"4323"	"MMP14"	"0.466"	"0.724"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9655172"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4323"	"MMP14"	"0.466"	"0.724"	"C1850155"	"TORG-WINCHESTER SYNDROME"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4324"	"MMP15"	"0.685"	"0.345"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4324"	"MMP15"	"0.685"	"0.345"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4324"	"MMP15"	"0.685"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4327"	"MMP19"	"0.656"	"0.517"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4327"	"MMP19"	"0.656"	"0.517"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4327"	"MMP19"	"0.656"	"0.517"	"C1969063"	"Cavitary Optic Disc Anomalies"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4329"	"ALDH6A1"	"0.72"	"0.276"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4329"	"ALDH6A1"	"0.72"	"0.276"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4329"	"ALDH6A1"	"0.72"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4329"	"ALDH6A1"	"0.72"	"0.276"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4329"	"ALDH6A1"	"0.72"	"0.276"	"C3279840"	"Methylmalonate Semialdehyde Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1987"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4330"	"MN1"	"0.72"	"0.276"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4330"	"MN1"	"0.72"	"0.276"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4330"	"MN1"	"0.72"	"0.276"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4330"	"MN1"	"0.72"	"0.276"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4330"	"MN1"	"0.72"	"0.276"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C0265219"	"Miller Dieker syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C0431375"	"Classical Lissencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C1848199"	"X-Linked Lissencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C1848201"	"Subcortical Band Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4335"	"MNT"	"0.752"	"0.31"	"C1955870"	"Classical Lissencephalies and Subcortical Band Heterotopias"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4336"	"MOBP"	"0.707"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4336"	"MOBP"	"0.707"	"0.379"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"4336"	"MOBP"	"0.707"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4336"	"MOBP"	"0.707"	"0.379"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"4336"	"MOBP"	"0.707"	"0.379"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4336"	"MOBP"	"0.707"	"0.379"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4337"	"MOCS1"	"0.696"	"0.345"	"C0268119"	"Combined molybdoflavoprotein enzyme deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1998"	"2005"	"4"	"7"	"CTD_human;UNIPROT"
"4337"	"MOCS1"	"0.696"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4337"	"MOCS1"	"0.696"	"0.345"	"C1854988"	"Molybdenum Cofactor Deficiency, Complementation Group A"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1994"	"2005"	"4"	"10"	"ORPHANET;UNIPROT"
"4337"	"MOCS1"	"0.696"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4338"	"MOCS2"	"0.735"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4338"	"MOCS2"	"0.735"	"0.345"	"C1854989"	"Molybdenum Cofactor Deficiency, Complementation Group B"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1992"	"2013"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"4338"	"MOCS2"	"0.735"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4340"	"MOG"	"0.621"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4340"	"MOG"	"0.621"	"0.655"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2003"	"2013"	"11"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.63"	"0.6666667"	"2007"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"4340"	"MOG"	"0.621"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.3333333"	"2005"	"2012"	"3"	"0"	"PSYGENET"
"4340"	"MOG"	"0.621"	"0.655"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4340"	"MOG"	"0.621"	"0.655"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"CTD_human"
"4340"	"MOG"	"0.621"	"0.655"	"C3280266"	"NARCOLEPSY 7"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4342"	"MOS"	"0.639"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4351"	"MPI"	"0.656"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4351"	"MPI"	"0.656"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.9090909"	"1998"	"2015"	"1"	"1"	"GENOMICS_ENGLAND"
"4351"	"MPI"	"0.656"	"0.345"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4351"	"MPI"	"0.656"	"0.345"	"C1865145"	"Congenital disorder of glycosylation type 1B"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.79"	"0.8888889"	"1986"	"2017"	"6"	"21"	"CTD_human;ORPHANET;UNIPROT"
"4351"	"MPI"	"0.656"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1986"	"1998"	"3"	"0"	"GENOMICS_ENGLAND"
"4352"	"MPL"	"0.554"	"0.655"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"1.00"	"1"	"1996"	"2018"	"0"	"1"	"CGI;CTD_human;ORPHANET"
"4352"	"MPL"	"0.554"	"0.655"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C0026987"	"Myelofibrosis"	"disease"		"Neoplastic Process"	"0.90"	"1"	"2007"	"2018"	"2"	"2"	"ORPHANET;UNIPROT"
"4352"	"MPL"	"0.554"	"0.655"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"0.95"	"1996"	"2017"	"0"	"0"	"ORPHANET"
"4352"	"MPL"	"0.554"	"0.655"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2017"	"0"	"1"	"ORPHANET"
"4352"	"MPL"	"0.554"	"0.655"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.41"	"1"	"2007"	"2015"	"0"	"1"	"CGI"
"4352"	"MPL"	"0.554"	"0.655"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C0836924"	"Thrombocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"0.9473684"	"2000"	"2015"	"2"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4352"	"MPL"	"0.554"	"0.655"	"C1292778"	"Chronic myeloproliferative disorder"	"disease"		"Neoplastic Process"	"0.50"	"0.9761905"	"2003"	"2017"	"0"	"2"	"CGI"
"4352"	"MPL"	"0.554"	"0.655"	"C1327915"	"Congenital amegakaryocytic thrombocytopenia"	"disease"	"C15"	"Congenital Abnormality"	"1.00"	"1"	"1999"	"2017"	"2"	"14"	"CTD_human;ORPHANET;UNIPROT"
"4352"	"MPL"	"0.554"	"0.655"	"C3275998"	"THROMBOCYTHEMIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2015"	"4"	"3"	"UNIPROT"
"4352"	"MPL"	"0.554"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.46"	"1"	"1998"	"2012"	"0"	"0"	"CGI"
"4352"	"MPL"	"0.554"	"0.655"	"C4303761"	"Familial thrombocytosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4353"	"MPO"	"0.435"	"0.931"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4353"	"MPO"	"0.435"	"0.931"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4353"	"MPO"	"0.435"	"0.931"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2010"	"2016"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"3"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.33"		"1999"	"2014"	"5"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0022593"	"Keratosis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0022594"	"Keratosis Blennorrhagica"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2010"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.37"		"2002"	"2008"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1996"	"2011"	"6"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0040954"	"Infection by Trichuris trichiura"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0086501"	"Keratoma"	"phenotype"	"C17"	"Acquired Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.8846154"	"1997"	"2015"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4353"	"MPO"	"0.435"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0398595"	"Myeloperoxidase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"0.8"	"1981"	"2013"	"5"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4353"	"MPO"	"0.435"	"0.931"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"4353"	"MPO"	"0.435"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4353"	"MPO"	"0.435"	"0.931"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4354"	"MPP1"	"0.713"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4357"	"MPST"	"0.707"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4358"	"MPV17"	"0.611"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4358"	"MPV17"	"0.611"	"0.483"	"C0009197"	"Cochlear Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0036305"	"Schamberg Disease"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1976"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"4358"	"MPV17"	"0.611"	"0.483"	"C0549567"	"Pigmentation Disorders"	"group"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4358"	"MPV17"	"0.611"	"0.483"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4358"	"MPV17"	"0.611"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"4358"	"MPV17"	"0.611"	"0.483"	"C1850406"	"NAVAJO NEUROHEPATOPATHY"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2016"	"4"	"24"	"CTD_human;ORPHANET;UNIPROT"
"4358"	"MPV17"	"0.611"	"0.483"	"C1850407"	"Navajo Familial Neurogenic Arthropathy"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2006"	"2016"	"4"	"7"	"CTD_human;UNIPROT"
"4358"	"MPV17"	"0.611"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4359"	"MPZ"	"0.535"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4359"	"MPZ"	"0.535"	"0.793"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9917355"	"1988"	"2018"	"39"	"24"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2016"	"12"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0019816"	"Hereditary, Type VII, Motor and Sensory Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0027888"	"Hereditary Motor and Sensory Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.9333333"	"1992"	"2017"	"0"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"		"1992"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"1994"	"2001"	"0"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2018"	"39"	"43"	"CTD_human;ORPHANET;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"0.5"	"1998"	"2007"	"0"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0393818"	"Congenital hypomyelinating neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1998"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1992"	"2017"	"39"	"28"	"CTD_human;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C1843075"	"Charcot-Marie-Tooth Disease, Dominant Intermediate D"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C1843153"	"Charcot-Marie-Tooth disease, Type 2J"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"1999"	"2014"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4359"	"MPZ"	"0.535"	"0.793"	"C3551756"	"NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2004"	"1"	"2"	"UNIPROT"
"4359"	"MPZ"	"0.535"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4359"	"MPZ"	"0.535"	"0.793"	"C3888087"	"Charcot-Marie-Tooth disease, Type 2I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1998"	"2014"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"4360"	"MRC1"	"0.473"	"0.759"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4361"	"MRE11"	"0.554"	"0.724"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2008"	"2016"	"0"	"0"	"UNIPROT"
"4361"	"MRE11"	"0.554"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"3"	"UNIPROT"
"4361"	"MRE11"	"0.554"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"1983"	"1990"	"3"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2017"	"5"	"0"	"CLINGEN"
"4361"	"MRE11"	"0.554"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4361"	"MRE11"	"0.554"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"		"1998"	"2017"	"6"	"1"	"CLINGEN;UNIPROT"
"4361"	"MRE11"	"0.554"	"0.724"	"C1858391"	"ATAXIA-TELANGIECTASIA-LIKE DISORDER"	"disease"	"C10;C14;C16;C18;C20"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"4361"	"MRE11"	"0.554"	"0.724"	"C1859598"	"ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA"	"disease"	"C10;C15;C23;F01"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4361"	"MRE11"	"0.554"	"0.724"	"C2751318"	"Nijmegen Breakage Syndrome-Like Disorder"	"disease"	"C05;C10;C16;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4361"	"MRE11"	"0.554"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"4361"	"MRE11"	"0.554"	"0.724"	"C4012790"	"Ataxia-Telangiectasisa-Like Disorder 1"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4363"	"ABCC1"	"0.479"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4397"	"MS"	"0.663"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4397"	"MS"	"0.663"	"0.448"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4430"	"MYO1B"	"0.799"	"0.241"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4430"	"MYO1B"	"0.799"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4430"	"MYO1B"	"0.799"	"0.241"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4430"	"MYO1B"	"0.799"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.40"	"0.9375"	"1994"	"2017"	"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9529412"	"1993"	"2017"	"1"	"0"	"CTD_human"
"4436"	"MSH2"	"0.437"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9285714"	"1995"	"2018"	"1"	"0"	"CTD_human"
"4436"	"MSH2"	"0.437"	"0.69"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"		"1991"	"2018"	"4"	"84"	"CTD_human"
"4436"	"MSH2"	"0.437"	"0.69"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"1997"	"2015"	"2"	"1"	"UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"1999"	"2012"	"1"	"5"	"UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9473684"	"1994"	"2014"	"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0265325"	"Turcot syndrome (disorder)"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.70"	"0.9545455"	"1994"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"4436"	"MSH2"	"0.437"	"0.69"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2003"	"2017"	"2"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.43"	"1"	"2002"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.60"	"0.9272727"	"1993"	"2017"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.60"	"0.9655172"	"1995"	"2018"	"4"	"9"	"CGI;UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.54"	"1"	"1994"	"2016"	"1"	"0"	"CGI;CTD_human"
"4436"	"MSH2"	"0.437"	"0.69"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4436"	"MSH2"	"0.437"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.9411765"	"1994"	"2014"	"1"	"0"	"CGI;CTD_human;GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4436"	"MSH2"	"0.437"	"0.69"	"C1321489"	"Torre-Muir syndrome"	"disease"	"C04;C16;C17"	"Neoplastic Process"	"0.70"	"0.92"	"1995"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"4436"	"MSH2"	"0.437"	"0.69"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.90"	"0.9625"	"1993"	"2018"	"4"	"442"	"CTD_human;ORPHANET"
"4436"	"MSH2"	"0.437"	"0.69"	"C1333991"	"Hereditary Non-Polyposis Colon Cancer Type 2"	"disease"	"C04;C16"	"Neoplastic Process"	"0.51"	"1"	"1994"	"2016"	"57"	"81"	"CLINGEN;UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.9475983"	"1993"	"2018"	"5"	"9"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"4436"	"MSH2"	"0.437"	"0.69"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4436"	"MSH2"	"0.437"	"0.69"	"C2931459"	"Lynch syndrome I (site-specific colonic cancer)"	"disease"	"C04;C06;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4436"	"MSH2"	"0.437"	"0.69"	"C2936783"	"Colorectal cancer, hereditary nonpolyposis, type 1"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.60"		"1993"	"2017"	"57"	"120"	"CLINGEN;UNIPROT"
"4437"	"MSH3"	"0.507"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4437"	"MSH3"	"0.507"	"0.621"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"1996"	"2017"	"6"	"0"	"CLINGEN"
"4437"	"MSH3"	"0.507"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4437"	"MSH3"	"0.507"	"0.621"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.45"	"0.8"	"1996"	"2002"	"0"	"1"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"1996"	"2017"	"6"	"0"	"CLINGEN"
"4437"	"MSH3"	"0.507"	"0.621"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.34"	"0.75"	"1996"	"2017"	"6"	"0"	"CLINGEN"
"4437"	"MSH3"	"0.507"	"0.621"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4437"	"MSH3"	"0.507"	"0.621"	"C4310719"	"FAMILIAL ADENOMATOUS POLYPOSIS 4"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"ORPHANET"
"4439"	"MSH5"	"0.667"	"0.483"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4439"	"MSH5"	"0.667"	"0.483"	"C4479510"	"PREMATURE OVARIAN FAILURE 13"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"4440"	"MSI1"	"0.592"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"0"	"0"	"UNIPROT"
"4477"	"MSMB"	"0.548"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.56"	"1"	"1998"	"2011"	"3"	"0"	"CTD_human"
"4477"	"MSMB"	"0.548"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"0.9795918"	"1994"	"2018"	"3"	"0"	"CTD_human"
"4477"	"MSMB"	"0.548"	"0.724"	"C2677821"	"Prostate Cancer, Hereditary, 13"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"				"0"	"1"	"CTD_human"
"4477"	"MSMB"	"0.548"	"0.724"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"4478"	"MSN"	"0.573"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4478"	"MSN"	"0.573"	"0.586"	"C4310812"	"IMMUNODEFICIENCY 50"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4481"	"MSR1"	"0.621"	"0.552"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"4481"	"MSR1"	"0.621"	"0.552"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4481"	"MSR1"	"0.621"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"		"2002"	"2008"	"1"	"0"	"CTD_human"
"4481"	"MSR1"	"0.621"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.9615385"	"2002"	"2016"	"1"	"0"	"CTD_human"
"4481"	"MSR1"	"0.621"	"0.552"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4481"	"MSR1"	"0.621"	"0.552"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.57"	"1"	"2002"	"2017"	"5"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"4482"	"MSRA"	"0.636"	"0.517"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2017"	"2"	"3"	"PSYGENET"
"4482"	"MSRA"	"0.636"	"0.517"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4482"	"MSRA"	"0.636"	"0.517"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.49"	"1"	"2008"	"2017"	"2"	"1"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2017"	"1"	"1"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"4485"	"MST1"	"0.525"	"0.724"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4485"	"MST1"	"0.525"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4486"	"MST1R"	"0.582"	"0.483"	"C4310729"	"NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"4487"	"MSX1"	"0.559"	"0.586"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.50"	"1"	"2003"	"2016"	"0"	"0"	"ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.40"	"1"	"1994"	"2016"	"3"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.70"	"0.9375"	"1994"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.39"	"1"	"2003"	"2012"	"0"	"0"	"ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2002"	"2004"	"4"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0399352"	"Developmental absence of tooth"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.53"	"0.3333333"	"1994"	"2014"	"0"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0406716"	"Hypodontia and nail dysgenesis"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C0406735"	"Hypoplastic enamel-onycholysis-hypohidrosis syndrome"	"disease"	"C07;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2001"	"0"	"1"	"CTD_human;ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C1298692"	"Cleft lip and alveolus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4487"	"MSX1"	"0.559"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C1837210"	"OROFACIAL CLEFT 5"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.80"		"1994"	"2006"	"1"	"5"	"CTD_human;UNIPROT"
"4487"	"MSX1"	"0.559"	"0.586"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.38"	"1"	"1994"	"2012"	"3"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.32"	"1"	"1990"	"2004"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C1970117"	"Tooth Agenesis, Selective, With Orofacial Cleft"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2002"	"2"	"2"	"UNIPROT"
"4487"	"MSX1"	"0.559"	"0.586"	"C1970118"	"Hypodontia Oligodontia with Orofacial Cleft"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2002"	"2"	"2"	"UNIPROT"
"4487"	"MSX1"	"0.559"	"0.586"	"C3489529"	"Tooth Agenesis, Familial"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.60"		"1996"	"2015"	"2"	"5"	"CTD_human;UNIPROT"
"4487"	"MSX1"	"0.559"	"0.586"	"C3711374"	"Nonsyndromic Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4487"	"MSX1"	"0.559"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4487"	"MSX1"	"0.559"	"0.586"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.50"	"0.9545455"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"4488"	"MSX2"	"0.57"	"0.586"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.56"	"1"	"1993"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"4488"	"MSX2"	"0.57"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"1995"	"2001"	"1"	"0"	"CTD_human"
"4488"	"MSX2"	"0.57"	"0.586"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4488"	"MSX2"	"0.57"	"0.586"	"C1858160"	"CRANIOSYNOSTOSIS, TYPE 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2014"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4488"	"MSX2"	"0.57"	"0.586"	"C1868597"	"Parietal Foramina With Cleidocranial Dysplasia"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human;ORPHANET"
"4488"	"MSX2"	"0.57"	"0.586"	"C1868598"	"PARIETAL FORAMINA"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.85"	"1"	"2000"	"2004"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4488"	"MSX2"	"0.57"	"0.586"	"C1868599"	"PARIETAL FORAMINA 1"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.40"		"2000"	"2000"	"2"	"3"	"UNIPROT"
"4488"	"MSX2"	"0.57"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4489"	"MT1A"	"0.579"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4489"	"MT1A"	"0.579"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"4495"	"MT1G"	"0.642"	"0.552"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4495"	"MT1G"	"0.642"	"0.552"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"2006"	"2"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1995"	"2006"	"2"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2003"	"2007"	"2"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0349218"	"Recurrent depressive disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4502"	"MT2A"	"0.588"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"0.6666667"	"2002"	"2013"	"2"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4502"	"MT2A"	"0.588"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1991"	"2015"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"0"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"0"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4504"	"MT3"	"0.624"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4507"	"MTAP"	"0.554"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9166667"	"1994"	"2018"	"1"	"3"	"CTD_human"
"4507"	"MTAP"	"0.554"	"0.586"	"C0027960"	"Nevus"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2009"	"2012"	"1"	"7"	"CTD_human"
"4507"	"MTAP"	"0.554"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4507"	"MTAP"	"0.554"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"4507"	"MTAP"	"0.554"	"0.586"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"4507"	"MTAP"	"0.554"	"0.586"	"C1300202"	"Diaphyseal medullary stenosis with bone malignancy"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4507"	"MTAP"	"0.554"	"0.586"	"C1862177"	"Diaphyseal medullary stenosis with malignant fibrous histiocytoma"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4508"	"ATP6"	"0.596"	"0.483"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4508"	"ATP6"	"0.596"	"0.483"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4508"	"ATP6"	"0.596"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2014"	"7"	"7"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4508"	"ATP6"	"0.596"	"0.483"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"4508"	"ATP6"	"0.596"	"0.483"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"4508"	"ATP6"	"0.596"	"0.483"	"C0795996"	"STRIATONIGRAL DEGENERATION, INFANTILE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4508"	"ATP6"	"0.596"	"0.483"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1995"	"2014"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1328349"	"Neuropathy ataxia and retinis pigmentosa"	"disease"	"C05;C10;C11;C16;C18"	"Disease or Syndrome"	"0.69"	"1"	"1990"	"2016"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1838916"	"ATAXIA AND POLYNEUROPATHY, ADULT-ONSET"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"1"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1839022"	"Striatonigral Degeneration, Infantile, Mitochondrial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1995"	"2008"	"3"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C2748884"	"CARDIOMYOPATHY, INFANTILE HYPERTROPHIC"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"2"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"4508"	"ATP6"	"0.596"	"0.483"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"2007"	"5"	"3"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C3275684"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"1"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C4016603"	"SEIZURES AND LACTIC ACIDOSIS"	"phenotype"		"Finding"	"0.30"		"2005"	"2008"	"2"	"2"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C4225415"	"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"4508"	"ATP6"	"0.596"	"0.483"	"C4225591"	"MITOCHONDRIAL MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3 (1 patient)"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"1"	"UNIPROT"
"4509"	"ATP8"	"0.707"	"0.517"	"C0022541"	"Kearns-Sayre syndrome"	"disease"	"C05;C10;C11;C14;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4509"	"ATP8"	"0.707"	"0.517"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4509"	"ATP8"	"0.707"	"0.517"	"C2748884"	"CARDIOMYOPATHY, INFANTILE HYPERTROPHIC"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"UNIPROT"
"4509"	"ATP8"	"0.707"	"0.517"	"C3275685"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 2"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"UNIPROT"
"4509"	"ATP8"	"0.707"	"0.517"	"C3275686"	"CARDIOMYOPATHY, APICAL HYPERTROPHIC, AND NEUROPATHY"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"UNIPROT"
"4509"	"ATP8"	"0.707"	"0.517"	"C3888025"	"BRAIN PSEUDOATROPHY, REVERSIBLE, VALPROATE-INDUCED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"4511"	"TRNC"	"0.713"	"0.345"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4512"	"COX1"	"0.494"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.53"	"1"	"1999"	"2011"	"2"	"4"	"ORPHANET;UNIPROT"
"4512"	"COX1"	"0.494"	"0.862"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2000"	"2010"	"2"	"2"	"UNIPROT"
"4512"	"COX1"	"0.494"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"1"	"ORPHANET"
"4512"	"COX1"	"0.494"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4512"	"COX1"	"0.494"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.6666667"	"1994"	"2014"	"2"	"2"	"UNIPROT"
"4512"	"COX1"	"0.494"	"0.862"	"C1838854"	"DEAFNESS, AMINOGLYCOSIDE-INDUCED"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4512"	"COX1"	"0.494"	"0.862"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4512"	"COX1"	"0.494"	"0.862"	"C4274324"	"Genetic recurrent myoglobinuria"	"disease"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"4513"	"COX2"	"0.397"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4513"	"COX2"	"0.397"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2014"	"5"	"0"	"PSYGENET"
"4513"	"COX2"	"0.397"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2003"	"2014"	"5"	"0"	"PSYGENET"
"4513"	"COX2"	"0.397"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4513"	"COX2"	"0.397"	"0.862"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"4513"	"COX2"	"0.397"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4513"	"COX2"	"0.397"	"0.862"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1993"	"1993"	"0"	"0"	"CTD_human;ORPHANET"
"4513"	"COX2"	"0.397"	"0.862"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.54"	"1"	"1999"	"2016"	"1"	"4"	"ORPHANET;UNIPROT"
"4513"	"COX2"	"0.397"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.971831"	"1994"	"2018"	"1"	"1"	"UNIPROT"
"4514"	"COX3"	"0.592"	"0.517"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4514"	"COX3"	"0.592"	"0.517"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4514"	"COX3"	"0.592"	"0.517"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.51"		"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"4514"	"COX3"	"0.592"	"0.517"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"4"	"ORPHANET"
"4514"	"COX3"	"0.592"	"0.517"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4514"	"COX3"	"0.592"	"0.517"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4514"	"COX3"	"0.592"	"0.517"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"1995"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4514"	"COX3"	"0.592"	"0.517"	"C4274324"	"Genetic recurrent myoglobinuria"	"disease"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"4519"	"CYTB"	"0.569"	"0.724"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4519"	"CYTB"	"0.569"	"0.724"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"1998"	"2014"	"0"	"0"	"ORPHANET"
"4519"	"CYTB"	"0.569"	"0.724"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1992"	"2007"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4519"	"CYTB"	"0.569"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"2"	"UNIPROT"
"4519"	"CYTB"	"0.569"	"0.724"	"C1708371"	"Histiocytoid Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2001"	"1"	"1"	"ORPHANET;UNIPROT"
"4520"	"MTF1"	"0.857"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4520"	"MTF1"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"4521"	"NUDT1"	"0.701"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4521"	"NUDT1"	"0.701"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0000832"	"Abruptio Placentae"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.40"	"0.9285714"	"1998"	"2016"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"PSYGENET"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C1866558"	"Neural tube defect, folate-sensitive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"1998"	"2006"	"3"	"2"	"CTD_human;UNIPROT"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C1866559"	"Spina Bifida, Folate-Sensitive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"3"	"2"	"UNIPROT"
"4522"	"MTHFD1"	"0.602"	"0.621"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2014"	"5"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2002"	"2010"	"5"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.8484848"	"1999"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2014"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0002902"	"Anencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.44"	"1"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.95"	"2001"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9272727"	"2002"	"2018"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.875"	"1999"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9493671"	"1996"	"2017"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"		"2004"	"2005"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.37"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0009081"	"Congenital clubfoot"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9142857"	"1997"	"2018"	"8"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"8"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.8627451"	"1991"	"2018"	"1"	"1"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011057"	"Hearing Loss, Sudden"	"phenotype"	"C09;C10;C23"	"Finding"	"0.31"		"2005"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8333333"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2017"	"5"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1997"	"2017"	"6"	"0"	"CTD_human;PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.8837209"	"1999"	"2016"	"4"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2017"	"11"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.40"	"0.8666667"	"2004"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.6666667"	"1999"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.8846154"	"2002"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"		"2006"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.8571429"	"2003"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8928571"	"2001"	"2017"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0025312"	"Meningomyelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.37"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"0"	"2004"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.40"	"0.8977273"	"1996"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"		"2004"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.37"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.8679245"	"1997"	"2018"	"3"	"1"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0037198"	"Sinus Thrombosis, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0037928"	"Spinal Cord Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2012"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.50"	"0.9058824"	"1997"	"2017"	"3"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0040156"	"Thyrotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"1997"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2017"	"11"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9215686"	"1995"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.33"		"2007"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0086664"	"Myelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"0.75"	"1997"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0162429"	"Malnutrition"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0206064"	"Microvascular Angina"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0206708"	"Cervical Intraepithelial Neoplasia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9375"	"2000"	"2015"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9230769"	"2005"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0266452"	"Hemicephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0266672"	"Amyelencephalus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0302356"	"incomplete anencephaly, hemicrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.8958333"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"4"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"4"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0524948"	"Maxillofacial Abnormalities"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1998"	"2014"	"4"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9083665"	"1995"	"2018"	"11"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9272727"	"2002"	"2018"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0685896"	"Acephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"4"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751316"	"Acquired Meningomyelocele"	"phenotype"	"C10;C16"	"Acquired Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751500"	"Petrous Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751501"	"Intracranial Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751502"	"Petrous Sinus Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2009"	"3"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0852077"	"Blood Coagulation Disorders, Inherited"	"group"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0948480"	"Coronary Restenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1148477"	"Deafness, Sudden"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"5"	"0"	"PSYGENET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0"	"2004"	"2009"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9166667"	"1997"	"2018"	"8"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1856058"	"HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY"	"disease"		"Disease or Syndrome"	"0.49"	"1"	"1987"	"2017"	"7"	"70"	"UNIPROT"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1856059"	"Mthfr Deficiency, Thermolabile Type"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2016"	"7"	"45"	"UNIPROT"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1856061"	"Methylenetetrahydrofolate reductase deficiency"	"disease"	"C05;C10;C16;C17;C18;C23;F03"	"Disease or Syndrome"	"0.51"	"1"	"1995"	"1995"	"0"	"0"	"CTD_human;ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1866558"	"Neural tube defect, folate-sensitive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2001"	"0"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4524"	"MTHFR"	"0.354"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.969697"	"1999"	"2018"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C2751584"	"Neurodegeneration Due To Cerebral Folate Transport Deficiency"	"phenotype"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4524"	"MTHFR"	"0.354"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"4524"	"MTHFR"	"0.354"	"0.828"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4524"	"MTHFR"	"0.354"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4534"	"MTM1"	"0.621"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2000"	"2"	"0"	"GENOMICS_ENGLAND"
"4534"	"MTM1"	"0.621"	"0.517"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1996"	"2000"	"3"	"0"	"GENOMICS_ENGLAND"
"4534"	"MTM1"	"0.621"	"0.517"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"	"0.9459459"	"1992"	"2016"	"1"	"1"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.32"	"1"	"1996"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"4534"	"MTM1"	"0.621"	"0.517"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.80"	"1"	"1995"	"2017"	"14"	"142"	"CTD_human;ORPHANET;UNIPROT"
"4534"	"MTM1"	"0.621"	"0.517"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.962963"	"1992"	"2016"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2011"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C1846169"	"Myotubular Myopathy with Abnormal Genital Development"	"disease"	"C05;C10;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4534"	"MTM1"	"0.621"	"0.517"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4534"	"MTM1"	"0.621"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4535"	"ND1"	"0.557"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4535"	"ND1"	"0.557"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4535"	"ND1"	"0.557"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4535"	"ND1"	"0.557"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4535"	"ND1"	"0.557"	"0.655"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1996"	"2014"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4535"	"ND1"	"0.557"	"0.655"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2017"	"9"	"12"	"CTD_human;ORPHANET;UNIPROT"
"4535"	"ND1"	"0.557"	"0.655"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"4535"	"ND1"	"0.557"	"0.655"	"C1838990"	"ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL"	"disease"		"Finding"	"0.30"		"1993"	"1993"	"1"	"1"	"UNIPROT"
"4535"	"ND1"	"0.557"	"0.655"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4535"	"ND1"	"0.557"	"0.655"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"4536"	"ND2"	"0.681"	"0.379"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.70"		"1991"	"1992"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4536"	"ND2"	"0.681"	"0.379"	"C1838990"	"ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL"	"disease"		"Finding"	"0.30"				"0"	"0"	"UNIPROT"
"4536"	"ND2"	"0.681"	"0.379"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4536"	"ND2"	"0.681"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4537"	"ND3"	"0.696"	"0.379"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"2004"	"2016"	"1"	"5"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2010"	"2"	"3"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"4537"	"ND3"	"0.696"	"0.379"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"2004"	"2010"	"2"	"3"	"ORPHANET;UNIPROT"
"4537"	"ND3"	"0.696"	"0.379"	"C4304725"	"Leber plus disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4538"	"ND4"	"0.592"	"0.621"	"C0029125"	"Optic Atrophies, Hereditary"	"group"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2002"	"2"	"0"	"CTD_human"
"4538"	"ND4"	"0.592"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4538"	"ND4"	"0.592"	"0.621"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1992"	"2003"	"1"	"1"	"ORPHANET;UNIPROT"
"4538"	"ND4"	"0.592"	"0.621"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9615385"	"1989"	"2017"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4538"	"ND4"	"0.592"	"0.621"	"C1838854"	"DEAFNESS, AMINOGLYCOSIDE-INDUCED"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"4538"	"ND4"	"0.592"	"0.621"	"C1839040"	"LEBER OPTIC ATROPHY AND DYSTONIA"	"disease"	"C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"1"	"UNIPROT"
"4538"	"ND4"	"0.592"	"0.621"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4538"	"ND4"	"0.592"	"0.621"	"C4304725"	"Leber plus disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4539"	"ND4L"	"0.799"	"0.241"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.74"	"0.5"	"1996"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4539"	"ND4L"	"0.799"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.36"	"1"	"2002"	"2011"	"3"	"4"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.64"	"1"	"1997"	"2009"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"1"	"ORPHANET"
"4540"	"ND5"	"0.561"	"0.552"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.76"	"1"	"1991"	"2012"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"5"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2010"	"4"	"4"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"2"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"2"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"2"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"2"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4540"	"ND5"	"0.561"	"0.552"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"3"	"2"	"UNIPROT"
"4540"	"ND5"	"0.561"	"0.552"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2010"	"4"	"4"	"UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C0029125"	"Optic Atrophies, Hereditary"	"group"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4541"	"ND6"	"0.59"	"0.552"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2002"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2016"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2010"	"2"	"2"	"UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C1839040"	"LEBER OPTIC ATROPHY AND DYSTONIA"	"disease"	"C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.30"		"1994"	"1996"	"2"	"2"	"UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4541"	"ND6"	"0.59"	"0.552"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2010"	"2"	"2"	"UNIPROT"
"4541"	"ND6"	"0.59"	"0.552"	"C4304725"	"Leber plus disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4542"	"MYO1F"	"0.857"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4543"	"MTNR1A"	"0.663"	"0.586"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4543"	"MTNR1A"	"0.663"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"PSYGENET"
"4543"	"MTNR1A"	"0.663"	"0.586"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2018"	"5"	"1"	"CTD_human"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.6666667"	"2011"	"2017"	"1"	"0"	"PSYGENET"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4544"	"MTNR1B"	"0.642"	"0.586"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4547"	"MTTP"	"0.526"	"0.69"	"C0000744"	"Abetalipoproteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.9487179"	"1992"	"2017"	"7"	"7"	"CTD_human;ORPHANET;UNIPROT"
"4547"	"MTTP"	"0.526"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4547"	"MTTP"	"0.526"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4547"	"MTTP"	"0.526"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"2000"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4547"	"MTTP"	"0.526"	"0.69"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2014"	"0"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C1854178"	"ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C1970051"	"METABOLIC SYNDROME, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9130435"	"2001"	"2017"	"1"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C2930930"	"Abdominal obesity metabolic syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4547"	"MTTP"	"0.526"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"		"2007"	"2011"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"		"2007"	"2011"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1988"	"2009"	"2"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1988"	"2009"	"2"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.34"	"0.75"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C0162429"	"Malnutrition"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4548"	"MTR"	"0.493"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"0"	"2007"	"2009"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1855128"	"Methylcobalamin Deficiency, CblG Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1997"	"2014"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4548"	"MTR"	"0.493"	"0.724"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1866558"	"Neural tube defect, folate-sensitive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4548"	"MTR"	"0.493"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4548"	"MTR"	"0.493"	"0.724"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4549"	"RNR1"	"0.672"	"0.448"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0040264"	"Tinnitus"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0155533"	"Tinnitus, Subjective"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0155534"	"Tinnitus, Objective"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4549"	"RNR1"	"0.672"	"0.448"	"C0395955"	"Tinnitus, Noise Induced"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0395959"	"Tinnitus of Vascular Origin"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0521787"	"Tinnitus, Clicking"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0521788"	"Tinnitus, Leudet"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0751556"	"Tinnitus, Spontaneous Oto-Acoustic Emission"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0751557"	"Tinnitus, Tensor Palatini Induced"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0751558"	"Tinnitus, Tensor Tympani Induced"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C0751559"	"Pulsatile Tinnitus"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C1838854"	"DEAFNESS, AMINOGLYCOSIDE-INDUCED"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"4549"	"RNR1"	"0.672"	"0.448"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4549"	"RNR1"	"0.672"	"0.448"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4549"	"RNR1"	"0.672"	"0.448"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2005"	"4"	"0"	"CTD_human"
"4550"	"RNR2"	"0.752"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4552"	"MTRR"	"0.51"	"0.655"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2012"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1998"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"4552"	"MTRR"	"0.51"	"0.655"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0019880"	"Homocystinuria"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.46"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4552"	"MTRR"	"0.51"	"0.655"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2015"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0751202"	"Cystathionine beta-Synthase Deficiency Disease"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2012"	"2"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C1856057"	"Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type"	"disease"	"C10;C15;C16;C17;C18"	"Disease or Syndrome"	"0.70"		"1998"	"2006"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4552"	"MTRR"	"0.51"	"0.655"	"C1866558"	"Neural tube defect, folate-sensitive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4552"	"MTRR"	"0.51"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4556"	"TRNE"	"0.735"	"0.414"	"C0342289"	"Diabetes-deafness syndrome maternally transmitted (disorder)"	"disease"	"C09;C10;C18;C19;C23"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"4556"	"TRNE"	"0.735"	"0.414"	"C1839028"	"Mitochondrial Myopathy with Diabetes"	"disease"	"C05;C10;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4556"	"TRNE"	"0.735"	"0.414"	"C3151898"	"MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4558"	"TRNF"	"0.616"	"0.517"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4558"	"TRNF"	"0.616"	"0.517"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4564"	"TRNH"	"0.656"	"0.483"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4564"	"TRNH"	"0.656"	"0.483"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4564"	"TRNH"	"0.656"	"0.483"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4565"	"TRNI"	"0.773"	"0.276"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4566"	"TRNK"	"0.611"	"0.552"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2013"	"0"	"0"	"CTD_human"
"4566"	"TRNK"	"0.611"	"0.552"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.57"	"0.8571429"	"1993"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"4566"	"TRNK"	"0.611"	"0.552"	"C0342289"	"Diabetes-deafness syndrome maternally transmitted (disorder)"	"disease"	"C09;C10;C18;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4566"	"TRNK"	"0.611"	"0.552"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0001125"	"Acidosis, Lactic"	"phenotype"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0022541"	"Kearns-Sayre syndrome"	"disease"	"C05;C10;C11;C14;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human;ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C0342289"	"Diabetes-deafness syndrome maternally transmitted (disorder)"	"disease"	"C09;C10;C18;C19;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"4567"	"TRNL1"	"0.58"	"0.552"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4568"	"TRNL2"	"0.886"	"0.207"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4570"	"TRNN"	"0.713"	"0.448"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4570"	"TRNN"	"0.713"	"0.448"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4571"	"TRNP"	"0.752"	"0.345"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4572"	"TRNQ"	"0.624"	"0.517"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2001"	"0"	"0"	"CTD_human;ORPHANET"
"4572"	"TRNQ"	"0.624"	"0.517"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4574"	"TRNS1"	"0.584"	"0.586"	"C1835672"	"Palmoplantar Keratoderma with Deafness"	"disease"	"C09;C10;C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C1838854"	"DEAFNESS, AMINOGLYCOSIDE-INDUCED"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4574"	"TRNS1"	"0.584"	"0.586"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4575"	"TRNS2"	"0.611"	"0.517"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4575"	"TRNS2"	"0.611"	"0.517"	"C0162672"	"MERRF Syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4575"	"TRNS2"	"0.611"	"0.517"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4576"	"TRNT"	"0.815"	"0.276"	"C1838867"	"PARKINSON DISEASE, MITOCHONDRIAL (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4576"	"TRNT"	"0.815"	"0.276"	"C1838876"	"MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"4577"	"TRNV"	"0.713"	"0.345"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4577"	"TRNV"	"0.713"	"0.345"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4578"	"TRNW"	"0.633"	"0.483"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4578"	"TRNW"	"0.633"	"0.483"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4578"	"TRNW"	"0.633"	"0.483"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"4578"	"TRNW"	"0.633"	"0.483"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"4578"	"TRNW"	"0.633"	"0.483"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4578"	"TRNW"	"0.633"	"0.483"	"C2931092"	"Maternally Inherited Leigh Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4582"	"MUC1"	"0.429"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2005"	"2015"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4582"	"MUC1"	"0.429"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4582"	"MUC1"	"0.429"	"0.828"	"C1868139"	"Medullary cystic kidney disease 1"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.60"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"4582"	"MUC1"	"0.429"	"0.828"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4582"	"MUC1"	"0.429"	"0.828"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4582"	"MUC1"	"0.429"	"0.828"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9444444"	"1993"	"2017"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"1994"	"2011"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4583"	"MUC2"	"0.505"	"0.724"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2007"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4585"	"MUC4"	"0.533"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4588"	"MUC6"	"0.594"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4588"	"MUC6"	"0.594"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4588"	"MUC6"	"0.594"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4589"	"MUC7"	"0.752"	"0.483"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2011"	"0"	"0"	"CTD_human"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0016063"	"Osteitis Fibrosa Disseminata"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4591"	"TRIM37"	"0.627"	"0.586"	"C0524582"	"Mulibrey Nanism"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"1"	"1999"	"2016"	"9"	"13"	"CTD_human;ORPHANET;UNIPROT"
"4591"	"TRIM37"	"0.627"	"0.586"	"C2931895"	"Pericardial constriction with growth failure"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4591"	"TRIM37"	"0.627"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4593"	"MUSK"	"0.609"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2005"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"4593"	"MUSK"	"0.609"	"0.621"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.34"		"2007"	"2017"	"2"	"0"	"CTD_human"
"4593"	"MUSK"	"0.609"	"0.621"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.31"	"0"	"2008"	"2017"	"2"	"0"	"CTD_human"
"4593"	"MUSK"	"0.609"	"0.621"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"4593"	"MUSK"	"0.609"	"0.621"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"4593"	"MUSK"	"0.609"	"0.621"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4593"	"MUSK"	"0.609"	"0.621"	"C1276035"	"Pena-Shokeir syndrome type I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"2009"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4593"	"MUSK"	"0.609"	"0.621"	"C1837092"	"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4593"	"MUSK"	"0.609"	"0.621"	"C4225368"	"MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2014"	"5"	"8"	"UNIPROT"
"4594"	"MUT"	"0.616"	"0.655"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4594"	"MUT"	"0.616"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4594"	"MUT"	"0.616"	"0.655"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.9375"	"1990"	"2017"	"1"	"8"	"CTD_human"
"4594"	"MUT"	"0.616"	"0.655"	"C1855114"	"Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"		"1989"	"2018"	"23"	"108"	"CTD_human;ORPHANET;UNIPROT"
"4594"	"MUT"	"0.616"	"0.655"	"C1855115"	"Methylmalonic Aciduria, mut(0) Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"		"1987"	"2018"	"23"	"75"	"CTD_human;UNIPROT"
"4594"	"MUT"	"0.616"	"0.655"	"C1855116"	"Methylmalonic Aciduria, mut(-) Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"		"1990"	"2018"	"23"	"75"	"CTD_human;UNIPROT"
"4594"	"MUT"	"0.616"	"0.655"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"0.95"	"1991"	"2016"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2006"	"2015"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.54"	"1"	"2004"	"2011"	"0"	"0"	"CGI;CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.40"	"0.8767123"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.61"		"2002"	"2015"	"0"	"5"	"CGI;CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0206711"	"Pilomatrixoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"0"	"4"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.46"	"1"	"1993"	"2015"	"0"	"9"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.64"	"1"	"2004"	"2016"	"2"	"2"	"CGI;UNIPROT"
"4595"	"MUTYH"	"0.551"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2000"	"2017"	"4"	"0"	"CLINGEN"
"4595"	"MUTYH"	"0.551"	"0.621"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4595"	"MUTYH"	"0.551"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.974359"	"2003"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"4595"	"MUTYH"	"0.551"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C1837991"	"Colorectal Adenomatous Polyposis, Autosomal Recessive"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.71"	"1"	"1987"	"2018"	"29"	"75"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4595"	"MUTYH"	"0.551"	"0.621"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4595"	"MUTYH"	"0.551"	"0.621"	"C3150911"	"GASTRIC CANCER, INTESTINAL"	"disease"		"Neoplastic Process"	"0.30"		"2004"	"2016"	"2"	"2"	"UNIPROT"
"4597"	"MVD"	"0.642"	"0.448"	"C0265970"	"Porokeratosis, Disseminated Superficial Actinic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2011"	"2016"	"0"	"2"	"ORPHANET"
"4597"	"MVD"	"0.642"	"0.448"	"C3553549"	"POROKERATOSIS 7, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.50"		"2008"	"2016"	"2"	"8"	"CTD_human;UNIPROT"
"4598"	"MVK"	"0.594"	"0.655"	"C0003862"	"Arthralgia"	"phenotype"	"C05;C23"	"Sign or Symptom"	"0.41"	"1"	"1999"	"2001"	"1"	"0"	"CTD_human"
"4598"	"MVK"	"0.594"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4598"	"MVK"	"0.594"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4598"	"MVK"	"0.594"	"0.655"	"C0015230"	"Exanthema"	"phenotype"	"C17"	"Sign or Symptom"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4598"	"MVK"	"0.594"	"0.655"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"		"1999"	"2004"	"1"	"0"	"CTD_human"
"4598"	"MVK"	"0.594"	"0.655"	"C0162296"	"Polyarthralgia"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4598"	"MVK"	"0.594"	"0.655"	"C0265970"	"Porokeratosis, Disseminated Superficial Actinic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.35"	"0.8"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"4598"	"MVK"	"0.594"	"0.655"	"C0342731"	"Deficiency of mevalonate kinase"	"disease"	"C10;C15;C16;C18;C20"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2017"	"3"	"0"	"CTD_human;ORPHANET"
"4598"	"MVK"	"0.594"	"0.655"	"C0398691"	"Hyperimmunoglobulinemia D"	"disease"	"C10;C15;C16;C18;C20"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2017"	"7"	"32"	"CTD_human;ORPHANET;UNIPROT"
"4598"	"MVK"	"0.594"	"0.655"	"C0949506"	"Porokeratosis of Mibelli"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"4598"	"MVK"	"0.594"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4598"	"MVK"	"0.594"	"0.655"	"C1867981"	"POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1999"	"2017"	"2"	"10"	"CTD_human;UNIPROT"
"4598"	"MVK"	"0.594"	"0.655"	"C1959626"	"Mevalonic Aciduria"	"disease"	"C10;C15;C16;C18;C20"	"Disease or Syndrome"	"0.80"	"1"	"1992"	"2017"	"8"	"14"	"CTD_human;ORPHANET;UNIPROT"
"4598"	"MVK"	"0.594"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"4598"	"MVK"	"0.594"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1999"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"4598"	"MVK"	"0.594"	"0.655"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"1999"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"4599"	"MX1"	"0.63"	"0.621"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.40"	"0.9230769"	"1992"	"2015"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4599"	"MX1"	"0.63"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4600"	"MX2"	"0.834"	"0.172"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4600"	"MX2"	"0.834"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"4601"	"MXI1"	"0.592"	"0.448"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4601"	"MXI1"	"0.592"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"1995"	"2001"	"0"	"0"	"CTD_human"
"4601"	"MXI1"	"0.592"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.66"	"0.8333333"	"1995"	"2001"	"1"	"2"	"CTD_human;UNIPROT"
"4602"	"MYB"	"0.53"	"0.552"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"4602"	"MYB"	"0.53"	"0.552"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.96875"	"2009"	"2017"	"2"	"0"	"CTD_human"
"4602"	"MYB"	"0.53"	"0.552"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2016"	"2"	"0"	"CTD_human"
"4602"	"MYB"	"0.53"	"0.552"	"C0023437"	"Acute Basophilic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4602"	"MYB"	"0.53"	"0.552"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"4602"	"MYB"	"0.53"	"0.552"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"4602"	"MYB"	"0.53"	"0.552"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.57"	"1"	"2007"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"4602"	"MYB"	"0.53"	"0.552"	"C2363903"	"Angiocentric glioma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4603"	"MYBL1"	"0.743"	"0.276"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"4603"	"MYBL1"	"0.743"	"0.276"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"4603"	"MYBL1"	"0.743"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4603"	"MYBL1"	"0.743"	"0.276"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4603"	"MYBL1"	"0.743"	"0.276"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4603"	"MYBL1"	"0.743"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C1969655"	"LETHAL CONGENITAL CONTRACTURAL SYNDROME 3"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C3280526"	"ARTHROGRYPOSIS, DISTAL, TYPE 1B"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C3554046"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"1"	"CTD_human"
"4604"	"MYBPC1"	"0.752"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2007"	"2016"	"0"	"4"	"GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"0.9761905"	"1996"	"2018"	"4"	"111"	"CTD_human;GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2014"	"3"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2014"	"3"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2006"	"2017"	"1"	"16"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"	"0.9090909"	"1986"	"2017"	"3"	"205"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C1720824"	"Sudden Cardiac Arrest"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C1861862"	"Familial Hypertrophic Cardiomyopathy Type 4"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.90"		"1990"	"2017"	"34"	"113"	"CLINGEN;CTD_human;UNIPROT"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C2751427"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.80"		"1995"	"2017"	"34"	"52"	"CLINGEN;UNIPROT"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C3715165"	"LEFT VENTRICULAR NONCOMPACTION 10"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"2016"	"2"	"13"	"CTD_human;UNIPROT"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C3809346"	"CARDIOMYOPATHY, DILATED, 1MM"	"disease"		"Disease or Syndrome"	"0.50"		"2010"	"2012"	"2"	"4"	"CTD_human;UNIPROT"
"4607"	"MYBPC3"	"0.621"	"0.31"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4609"	"MYC"	"0.382"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"1.00"	"0.9166667"	"1983"	"2018"	"1"	"4"	"CGI;CTD_human;ORPHANET;UNIPROT"
"4609"	"MYC"	"0.382"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2001"	"2018"	"1"	"0"	"CGI;CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8888889"	"1984"	"2016"	"4"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4609"	"MYC"	"0.382"	"0.724"	"C0007129"	"Merkel cell carcinoma"	"disease"	"C02;C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2018"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9230769"	"1990"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"		"2004"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1985"	"2011"	"4"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2004"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1986"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9411765"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"2008"	"3"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"2008"	"3"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1983"	"2016"	"0"	"0"	"CGI"
"4609"	"MYC"	"0.382"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9787234"	"1988"	"2018"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1985"	"2015"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"2008"	"3"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"0.8"	"1994"	"2016"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9387755"	"1990"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"	"0.9655172"	"1988"	"2018"	"0"	"0"	"CGI"
"4609"	"MYC"	"0.382"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9375"	"1990"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.49"	"1"	"2001"	"2018"	"1"	"6"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.70"	"0.9782609"	"1985"	"2018"	"1"	"3"	"CGI;CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2006"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2013"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1993"	"1994"	"0"	"0"	"ORPHANET"
"4609"	"MYC"	"0.382"	"0.724"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"2008"	"3"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"2008"	"2016"	"2"	"3"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0206093"	"Neuroectodermal Tumors"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1986"	"1996"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2016"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1984"	"2017"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.875"	"2009"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"1989"	"2016"	"0"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2017"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"1987"	"2010"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.39"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1986"	"2012"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2012"	"2"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.8888889"	"1998"	"2017"	"0"	"0"	"ORPHANET"
"4609"	"MYC"	"0.382"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9782609"	"1985"	"2017"	"3"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.37"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"4609"	"MYC"	"0.382"	"0.724"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2012"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4610"	"MYCL"	"0.616"	"0.586"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2006"	"2016"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"1989"	"2016"	"1"	"1"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.35"	"1"	"1991"	"2017"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.80"	"0.9528178"	"1985"	"2018"	"13"	"1"	"CGI;CTD_human;ORPHANET"
"4613"	"MYCN"	"0.481"	"0.759"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4613"	"MYCN"	"0.481"	"0.759"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C0751483"	"Familial Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4613"	"MYCN"	"0.481"	"0.759"	"C0796068"	"Oculodigitoesophagoduodenal syndrome"	"disease"	"C05;C06;C08;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2015"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4613"	"MYCN"	"0.481"	"0.759"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4613"	"MYCN"	"0.481"	"0.759"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4613"	"MYCN"	"0.481"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4615"	"MYD88"	"0.47"	"0.828"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4615"	"MYD88"	"0.47"	"0.828"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.50"	"1"	"2011"	"2017"	"0"	"0"	"CGI"
"4615"	"MYD88"	"0.47"	"0.828"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0024419"	"Waldenstrom Macroglobulinemia"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.80"	"0.98"	"2012"	"2018"	"0"	"0"	"CGI;CTD_human;ORPHANET"
"4615"	"MYD88"	"0.47"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2013"	"2018"	"1"	"0"	"CGI;CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4615"	"MYD88"	"0.47"	"0.828"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4615"	"MYD88"	"0.47"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C2677092"	"MYD88 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.71"	"1"	"2008"	"2014"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4615"	"MYD88"	"0.47"	"0.828"	"C2936755"	"Familial Waldenstrom's Macroglobulinaemia"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"4615"	"MYD88"	"0.47"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4616"	"GADD45B"	"0.627"	"0.621"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4618"	"MYF6"	"0.72"	"0.207"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"4618"	"MYF6"	"0.72"	"0.207"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4618"	"MYF6"	"0.72"	"0.207"	"C3280703"	"MYOPATHY, CENTRONUCLEAR, 3"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"4618"	"MYF6"	"0.72"	"0.207"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4618"	"MYF6"	"0.72"	"0.207"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4619"	"MYH1"	"0.834"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"4620"	"MYH2"	"0.639"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4620"	"MYH2"	"0.639"	"0.586"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.32"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"4620"	"MYH2"	"0.639"	"0.586"	"C1854106"	"INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT"	"disease"	"C05;C10;C11;C23"	"Disease or Syndrome"	"0.60"		"2001"	"2017"	"1"	"11"	"CTD_human;UNIPROT"
"4621"	"MYH3"	"0.63"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.43"	"1"	"2006"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4621"	"MYH3"	"0.63"	"0.448"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"1997"	"2013"	"0"	"0"	"ORPHANET"
"4621"	"MYH3"	"0.63"	"0.448"	"C0265224"	"Freeman-Sheldon syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.79"	"1"	"1997"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"4621"	"MYH3"	"0.63"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2008"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4621"	"MYH3"	"0.63"	"0.448"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.74"	"1"	"2006"	"2013"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"4621"	"MYH3"	"0.63"	"0.448"	"C1848934"	"SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4621"	"MYH3"	"0.63"	"0.448"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4621"	"MYH3"	"0.63"	"0.448"	"C1867440"	"Multiple Pterygium Syndrome, Autosomal Dominant"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2015"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4621"	"MYH3"	"0.63"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4624"	"MYH6"	"0.621"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.84"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4624"	"MYH6"	"0.621"	"0.552"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.74"	"1"	"1984"	"2017"	"6"	"0"	"CLINGEN;CTD_human;GENOMICS_ENGLAND"
"4624"	"MYH6"	"0.621"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4624"	"MYH6"	"0.621"	"0.552"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.42"	"1"	"2011"	"2017"	"1"	"1"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0018817"	"Atrial Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0031192"	"Persistent Ostium Primum"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.53"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"4624"	"MYH6"	"0.621"	"0.552"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4624"	"MYH6"	"0.621"	"0.552"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4624"	"MYH6"	"0.621"	"0.552"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"		"2005"	"2005"	"1"	"0"	"CTD_human;ORPHANET"
"4624"	"MYH6"	"0.621"	"0.552"	"C0428908"	"Sinus Node Dysfunction (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"1984"	"2017"	"5"	"0"	"CLINGEN;CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4624"	"MYH6"	"0.621"	"0.552"	"C2750466"	"Cardiomyopathy, Dilated, 1EE"	"disease"	"C14"	"Disease or Syndrome"	"0.80"		"2006"	"2006"	"1"	"4"	"CTD_human;UNIPROT"
"4624"	"MYH6"	"0.621"	"0.552"	"C2750467"	"Cardiomyopathy, Familial Hypertrophic, 14"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.80"		"1996"	"2010"	"2"	"2"	"CTD_human;UNIPROT"
"4624"	"MYH6"	"0.621"	"0.552"	"C3279790"	"Atrial Septal Defect 3"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"4624"	"MYH6"	"0.621"	"0.552"	"C3279791"	"SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4624"	"MYH6"	"0.621"	"0.552"	"C3495498"	"Cardiomyopathy, Familial Hypertrophic, 1 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.40"		"2006"	"2014"	"0"	"1"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"2000"	"2018"	"1"	"20"	"CTD_human;GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9310345"	"1990"	"2018"	"0"	"63"	"GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0013481"	"Ebstein Anomaly"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.43"	"1"	"2011"	"2018"	"0"	"1"	"ORPHANET"
"4625"	"MYH7"	"0.564"	"0.483"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2002"	"2004"	"1"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0205700"	"Asymmetric Septal Hypertrophy"	"disease"		"Disease or Syndrome"	"0.60"		"1990"	"2017"	"66"	"113"	"CLINGEN;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C0221054"	"Welander Distal Myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"2004"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C0242231"	"Coronary Stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"4625"	"MYH7"	"0.564"	"0.483"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.42"	"1"	"1993"	"2016"	"0"	"6"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.50"		"1990"	"2015"	"57"	"113"	"CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.58"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4625"	"MYH7"	"0.564"	"0.483"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.80"	"0.8571429"	"1990"	"2018"	"67"	"147"	"CLINGEN;CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C1450052"	"Tibial Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C1834481"	"CARDIOMYOPATHY, DILATED, 1S"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"6"	"27"	"CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C1838244"	"TIBIAL MUSCULAR DYSTROPHY, TARDIVE"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C1842160"	"MYOPATHY, MYOSIN STORAGE (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"	"1"	"1971"	"2016"	"4"	"9"	"CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C1850709"	"Myopathy, Hyaline Body, Autosomal Recessive"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.36"	"1"	"2010"	"2015"	"0"	"0"	"ORPHANET"
"4625"	"MYH7"	"0.564"	"0.483"	"C3150690"	"LEFT VENTRICULAR NONCOMPACTION 5"	"disease"		"Disease or Syndrome"	"0.40"		"1971"	"2012"	"6"	"19"	"UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C3495498"	"Cardiomyopathy, Familial Hypertrophic, 1 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"1961"	"2017"	"66"	"130"	"CLINGEN;CTD_human;UNIPROT"
"4625"	"MYH7"	"0.564"	"0.483"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4625"	"MYH7"	"0.564"	"0.483"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2009"	"2016"	"0"	"3"	"GENOMICS_ENGLAND"
"4626"	"MYH8"	"0.735"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"1996"	"2008"	"2"	"0"	"GENOMICS_ENGLAND"
"4626"	"MYH8"	"0.735"	"0.276"	"C0265226"	"Hecht syndrome (disorder)"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.73"	"1"	"1974"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4626"	"MYH8"	"0.735"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"4626"	"MYH8"	"0.735"	"0.276"	"C1837245"	"Carney Complex Variant"	"disease"	"C04;C14;C16"	"Disease or Syndrome"	"0.70"		"1974"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4626"	"MYH8"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4627"	"MYH9"	"0.53"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.53"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human;UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4627"	"MYH9"	"0.53"	"0.724"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0020544"	"Renal hypertension"	"disease"	"C12;C13;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.9545455"	"2008"	"2016"	"2"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0027706"	"Hereditary nephritis"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2010"	"1"	"0"	"PSYGENET"
"4627"	"MYH9"	"0.53"	"0.724"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.45"	"1"	"2000"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"4627"	"MYH9"	"0.53"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4627"	"MYH9"	"0.53"	"0.724"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C0340978"	"May-Hegglin anomaly"	"phenotype"		"Finding"	"0.60"		"1972"	"2017"	"6"	"15"	"UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C0398641"	"Epstein syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.54"	"1"	"2001"	"2012"	"6"	"7"	"UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C0403445"	"Fechtner syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.56"	"1"	"2000"	"2013"	"5"	"7"	"UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C0410005"	"Nodular fasciitis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4627"	"MYH9"	"0.53"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2000"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"4627"	"MYH9"	"0.53"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1567741"	"Alport Syndrome"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2003"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1567742"	"Alport Syndrome, X-Linked"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1567743"	"Alport Syndrome, Autosomal Dominant"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1567744"	"Alport Syndrome, Autosomal Recessive"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C1834478"	"MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS"	"disease"	"C09;C10;C15;C23"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C1854520"	"SEBASTIAN SYNDROME"	"disease"	"C09;C10;C15;C23"	"Disease or Syndrome"	"0.90"	"0.9791667"	"2000"	"2016"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C1863659"	"DEAFNESS, AUTOSOMAL DOMINANT 17"	"disease"	"C09;C10;C15;C23"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C1863660"	"COCHLEOSACCULAR DEGENERATION"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"4627"	"MYH9"	"0.53"	"0.724"	"C2931716"	"Deafness, autosomal dominant nonsyndromic sensorineural 17"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C2931861"	"Hemorrhagic hereditary nephritis"	"disease"	"C12;C13;C16;C17"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4627"	"MYH9"	"0.53"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4628"	"MYH10"	"0.799"	"0.207"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4628"	"MYH10"	"0.799"	"0.207"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4628"	"MYH10"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"4629"	"MYH11"	"0.567"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4629"	"MYH11"	"0.567"	"0.483"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9770115"	"1995"	"2017"	"2"	"0"	"CTD_human"
"4629"	"MYH11"	"0.567"	"0.483"	"C0023479"	"Acute myelomonocytic leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.57"	"0.8571429"	"1995"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"4629"	"MYH11"	"0.567"	"0.483"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2015"	"10"	"0"	"CLINGEN"
"4629"	"MYH11"	"0.567"	"0.483"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"4629"	"MYH11"	"0.567"	"0.483"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4629"	"MYH11"	"0.567"	"0.483"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.34"	"1"	"2007"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4629"	"MYH11"	"0.567"	"0.483"	"C0392775"	"Cystic medial necrosis of aorta"	"disease"	"C04;C14;C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"4629"	"MYH11"	"0.567"	"0.483"	"C1608393"	"Megacystis microcolon intestinal hypoperistalsis syndrome"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4629"	"MYH11"	"0.567"	"0.483"	"C1851504"	"Aortic aneurysm, familial thoracic 4"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"4629"	"MYH11"	"0.567"	"0.483"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2016"	"2"	"0"	"CTD_human"
"4629"	"MYH11"	"0.567"	"0.483"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4629"	"MYH11"	"0.567"	"0.483"	"C2861596"	"AML M4 Eo with inv(16) or t(16;16)"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4632"	"MYL1"	"0.886"	"0.103"	"C0007172"	"Heart Rupture, Traumatic"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4632"	"MYL1"	"0.886"	"0.103"	"C0018805"	"Heart Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4632"	"MYL1"	"0.886"	"0.103"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"4633"	"MYL2"	"0.72"	"0.31"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4633"	"MYL2"	"0.72"	"0.31"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.65"	"0.8"	"1998"	"2015"	"1"	"1"	"CTD_human;GENOMICS_ENGLAND"
"4633"	"MYL2"	"0.72"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4633"	"MYL2"	"0.72"	"0.31"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4633"	"MYL2"	"0.72"	"0.31"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4633"	"MYL2"	"0.72"	"0.31"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4633"	"MYL2"	"0.72"	"0.31"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4633"	"MYL2"	"0.72"	"0.31"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1996"	"2017"	"1"	"9"	"CTD_human"
"4633"	"MYL2"	"0.72"	"0.31"	"C1834460"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"1980"	"2017"	"18"	"10"	"CLINGEN;CTD_human;UNIPROT"
"4634"	"MYL3"	"0.773"	"0.172"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4634"	"MYL3"	"0.773"	"0.172"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2001"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"4634"	"MYL3"	"0.773"	"0.172"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4634"	"MYL3"	"0.773"	"0.172"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4634"	"MYL3"	"0.773"	"0.172"	"C1837471"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"1982"	"2017"	"21"	"6"	"CLINGEN;CTD_human;UNIPROT"
"4635"	"MYL4"	"0.815"	"0.172"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"4635"	"MYL4"	"0.815"	"0.172"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"ORPHANET"
"4635"	"MYL4"	"0.815"	"0.172"	"C4310636"	"ATRIAL FIBRILLATION, FAMILIAL, 18"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"4638"	"MYLK"	"0.565"	"0.621"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"4638"	"MYLK"	"0.565"	"0.621"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"6"	"0"	"CLINGEN"
"4638"	"MYLK"	"0.565"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"1999"	"2004"	"2"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2008"	"2"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4638"	"MYLK"	"0.565"	"0.621"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4638"	"MYLK"	"0.565"	"0.621"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4638"	"MYLK"	"0.565"	"0.621"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4638"	"MYLK"	"0.565"	"0.621"	"C1608393"	"Megacystis microcolon intestinal hypoperistalsis syndrome"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"4638"	"MYLK"	"0.565"	"0.621"	"C3151077"	"AORTIC ANEURYSM, FAMILIAL THORACIC 7"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"4638"	"MYLK"	"0.565"	"0.621"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4640"	"MYO1A"	"0.735"	"0.241"	"C1842939"	"Deafness, Autosomal Dominant 48"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4641"	"MYO1C"	"0.799"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4641"	"MYO1C"	"0.799"	"0.207"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2011"	"3"	"0"	"CLINGEN"
"4641"	"MYO1C"	"0.799"	"0.207"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"3"	"0"	"CLINGEN"
"4642"	"MYO1D"	"0.928"	"0.069"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4642"	"MYO1D"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4643"	"MYO1E"	"0.743"	"0.172"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human"
"4643"	"MYO1E"	"0.743"	"0.172"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4643"	"MYO1E"	"0.743"	"0.172"	"C3279905"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"2"	"1"	"UNIPROT"
"4644"	"MYO5A"	"0.696"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4644"	"MYO5A"	"0.696"	"0.379"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4644"	"MYO5A"	"0.696"	"0.379"	"C1836573"	"GRISCELLI SYNDROME, TYPE 3"	"disease"	"C16;C17;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4644"	"MYO5A"	"0.696"	"0.379"	"C1859194"	"GRISCELLI SYNDROME, TYPE 1"	"disease"	"C09;C10;C16;C17;C18;C23"	"Disease or Syndrome"	"0.70"		"1998"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"4644"	"MYO5A"	"0.696"	"0.379"	"C1860157"	"Elejalde Disease"	"disease"	"C10;C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4644"	"MYO5A"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0268312"	"Progressive intrahepatic cholestasis (disorder)"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0341306"	"Microvillus inclusion disease"	"disease"	"C05;C06;C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"2008"	"2018"	"6"	"8"	"CTD_human;ORPHANET;UNIPROT"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4645"	"MYO5B"	"0.642"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4645"	"MYO5B"	"0.642"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4645"	"MYO5B"	"0.642"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4646"	"MYO6"	"0.659"	"0.517"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4646"	"MYO6"	"0.659"	"0.517"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2017"	"7"	"0"	"CLINGEN"
"4646"	"MYO6"	"0.659"	"0.517"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4646"	"MYO6"	"0.659"	"0.517"	"C1843028"	"Deafness, Autosomal Recessive 37"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"1996"	"2005"	"1"	"3"	"CTD_human;UNIPROT"
"4646"	"MYO6"	"0.659"	"0.517"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2017"	"7"	"0"	"CLINGEN"
"4646"	"MYO6"	"0.659"	"0.517"	"C2931767"	"Deafness, autosomal dominant nonsyndromic sensorineural 22"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.70"		"1996"	"2005"	"2"	"1"	"CTD_human;UNIPROT"
"4646"	"MYO6"	"0.659"	"0.517"	"C3149009"	"DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY"	"disease"		"Disease or Syndrome"	"0.70"		"1996"	"2005"	"2"	"1"	"CTD_human;UNIPROT"
"4646"	"MYO6"	"0.659"	"0.517"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C0271097"	"Usher Syndrome"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2018"	"1"	"7"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C0339534"	"Usher syndrome type 2"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"1.00"	"0.9615385"	"1956"	"2018"	"23"	"122"	"CLINGEN;ORPHANET;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2006"	"1"	"0"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1832475"	"Deafness, Autosomal Dominant 11"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.62"	"1"	"1997"	"2015"	"4"	"5"	"CTD_human;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1838701"	"DEAFNESS, AUTOSOMAL RECESSIVE 2"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.82"	"0.5"	"1994"	"2017"	"3"	"17"	"CTD_human;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1848638"	"USHER SYNDROME, TYPE IB (disorder)"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.90"	"1"	"1956"	"2017"	"23"	"37"	"CLINGEN;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1848639"	"USHER SYNDROME, TYPE IA, FORMERLY"	"disease"		"Disease or Syndrome"	"0.70"		"1956"	"2017"	"23"	"31"	"CLINGEN;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C1848640"	"USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY"	"disease"		"Disease or Syndrome"	"0.70"		"1956"	"2017"	"23"	"31"	"CLINGEN;UNIPROT"
"4647"	"MYO7A"	"0.639"	"0.31"	"C2931205"	"Usher syndrome, type 1A"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C2931206"	"Usher syndrome, type 1B"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2016"	"0"	"0"	"CTD_human"
"4647"	"MYO7A"	"0.639"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4649"	"MYO9A"	"0.857"	"0.103"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"1998"	"2016"	"4"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"4649"	"MYO9A"	"0.857"	"0.103"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4649"	"MYO9A"	"0.857"	"0.103"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4650"	"MYO9B"	"0.707"	"0.517"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.8636364"	"2006"	"2013"	"0"	"0"	"CTD_human"
"4650"	"MYO9B"	"0.707"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.3333333"	"2008"	"2015"	"3"	"0"	"PSYGENET"
"4651"	"MYO10"	"0.762"	"0.276"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4653"	"MYOC"	"0.639"	"0.379"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4653"	"MYOC"	"0.639"	"0.379"	"C0020302"	"Hydrophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.60"	"1"	"1996"	"2013"	"1"	"1"	"ORPHANET;UNIPROT"
"4653"	"MYOC"	"0.639"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4653"	"MYOC"	"0.639"	"0.379"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4653"	"MYOC"	"0.639"	"0.379"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.9529412"	"1996"	"2017"	"1"	"2"	"CTD_human"
"4653"	"MYOC"	"0.639"	"0.379"	"C1842028"	"GLAUCOMA 1, OPEN ANGLE, A"	"disease"	"C11"	"Disease or Syndrome"	"0.62"	"1"	"1964"	"2016"	"36"	"34"	"CTD_human;UNIPROT"
"4653"	"MYOC"	"0.639"	"0.379"	"C1856439"	"GLAUCOMA 3, PRIMARY CONGENITAL, A"	"disease"	"C11"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"4653"	"MYOC"	"0.639"	"0.379"	"C2981140"	"Glaucoma of childhood"	"disease"		"Disease or Syndrome"	"0.39"	"1"	"1996"	"2012"	"0"	"0"	"ORPHANET"
"4653"	"MYOC"	"0.639"	"0.379"	"C3278152"	"GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"4653"	"MYOC"	"0.639"	"0.379"	"C3278153"	"GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"1"	"UNIPROT"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9285714"	"1990"	"2015"	"0"	"0"	"CGI"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0206656"	"Embryonal Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4654"	"MYOD1"	"0.604"	"0.621"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4654"	"MYOD1"	"0.604"	"0.621"	"C1276035"	"Pena-Shokeir syndrome type I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4660"	"PPP1R12B"	"0.815"	"0.241"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4665"	"NAB2"	"0.701"	"0.379"	"C0018922"	"hemangiopericytoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2017"	"0"	"0"	"ORPHANET"
"4665"	"NAB2"	"0.701"	"0.379"	"C1266119"	"Solitary fibrous tumor"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9047619"	"2013"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"4668"	"NAGA"	"0.621"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4668"	"NAGA"	"0.621"	"0.448"	"C0270724"	"Infantile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1990"	"1991"	"1"	"0"	"CTD_human"
"4668"	"NAGA"	"0.621"	"0.448"	"C0338473"	"Neuroaxonal Dystrophies"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1990"	"2004"	"1"	"0"	"CTD_human"
"4668"	"NAGA"	"0.621"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4668"	"NAGA"	"0.621"	"0.448"	"C0751716"	"Adult Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4668"	"NAGA"	"0.621"	"0.448"	"C0751717"	"Juvenile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4668"	"NAGA"	"0.621"	"0.448"	"C0751718"	"Late Infantile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4668"	"NAGA"	"0.621"	"0.448"	"C1836522"	"Schindler Disease, Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1989"	"2015"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4668"	"NAGA"	"0.621"	"0.448"	"C1836544"	"Schindler Disease, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.76"	"1"	"1990"	"2015"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4668"	"NAGA"	"0.621"	"0.448"	"C1836545"	"Schindler Disease, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1990"	"2009"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4668"	"NAGA"	"0.621"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4668"	"NAGA"	"0.621"	"0.448"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0026706"	"Mucopolysaccharidosis III"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.62"	"1"	"1996"	"2016"	"0"	"3"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0086647"	"Mucopolysaccharidosis Type IIIA"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.55"	"1"	"1999"	"2012"	"0"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0086648"	"MPS III B"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.962963"	"1982"	"2018"	"15"	"44"	"CTD_human;ORPHANET;UNIPROT"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0086649"	"MPS III C"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0086650"	"MPS III D"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2012"	"0"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4669"	"NAGLU"	"0.633"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4669"	"NAGLU"	"0.633"	"0.552"	"C4225306"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4671"	"NAIP"	"0.672"	"0.448"	"C0043116"	"HMN (Hereditary Motor Neuropathy) Proximal Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"1999"	"0"	"0"	"ORPHANET"
"4671"	"NAIP"	"0.672"	"0.448"	"C0152109"	"Juvenile Spinal Muscular Atrophy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"4671"	"NAIP"	"0.672"	"0.448"	"C0393538"	"Muscular Atrophy, Spinal, Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4671"	"NAIP"	"0.672"	"0.448"	"C2931358"	"Muscular atrophy, spinal, infantile chronic form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4676"	"NAP1L4"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4680"	"CEACAM6"	"0.619"	"0.586"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4680"	"CEACAM6"	"0.619"	"0.586"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.42"	"1"	"2004"	"2015"	"0"	"1"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8947368"	"2002"	"2017"	"1"	"1"	"UNIPROT"
"4683"	"NBN"	"0.502"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"4683"	"NBN"	"0.502"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"4683"	"NBN"	"0.502"	"0.759"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.55"	"1"	"2001"	"2014"	"2"	"3"	"CTD_human;UNIPROT"
"4683"	"NBN"	"0.502"	"0.759"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2015"	"0"	"0"	"CGI"
"4683"	"NBN"	"0.502"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2008"	"2012"	"0"	"0"	"CGI"
"4683"	"NBN"	"0.502"	"0.759"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2008"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2004"	"2015"	"2"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"CGI"
"4683"	"NBN"	"0.502"	"0.759"	"C0038362"	"Stomatitis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.63"	"0.6666667"	"2000"	"2015"	"5"	"1"	"CLINGEN;GENOMICS_ENGLAND;UNIPROT"
"4683"	"NBN"	"0.502"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"2004"	"2015"	"2"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0398791"	"Nijmegen Breakage Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.90"	"0.9405941"	"1987"	"2017"	"3"	"68"	"CTD_human;ORPHANET"
"4683"	"NBN"	"0.502"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"1998"	"2"	"0"	"GENOMICS_ENGLAND"
"4683"	"NBN"	"0.502"	"0.759"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"4683"	"NBN"	"0.502"	"0.759"	"C1568868"	"Oral Mucositis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"4683"	"NBN"	"0.502"	"0.759"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2011"	"0"	"0"	"CTD_human"
"4683"	"NBN"	"0.502"	"0.759"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"4683"	"NBN"	"0.502"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2013"	"4"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2001"	"2014"	"5"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.75"	"2004"	"2013"	"4"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.75"	"2004"	"2013"	"4"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1992"	"2016"	"3"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2007"	"2"	"0"	"PSYGENET"
"4684"	"NCAM1"	"0.445"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4688"	"NCF2"	"0.642"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4688"	"NCF2"	"0.642"	"0.586"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"4688"	"NCF2"	"0.642"	"0.586"	"C1856245"	"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.60"		"1994"	"2017"	"10"	"20"	"CTD_human;UNIPROT"
"4689"	"NCF4"	"0.69"	"0.345"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.45"	"0.6"	"2008"	"2017"	"1"	"1"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.48"	"1"	"1993"	"2016"	"0"	"2"	"ORPHANET"
"4689"	"NCF4"	"0.69"	"0.345"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4689"	"NCF4"	"0.69"	"0.345"	"C3151409"	"GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"4690"	"NCK1"	"0.743"	"0.414"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4690"	"NCK1"	"0.743"	"0.414"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4690"	"NCK1"	"0.743"	"0.414"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4691"	"NCL"	"0.579"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4691"	"NCL"	"0.579"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9285714"	"1997"	"2015"	"0"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4692"	"NDN"	"0.614"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4693"	"NDP"	"0.602"	"0.517"	"C0035344"	"Retinopathy of Prematurity"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2013"	"0"	"0"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4693"	"NDP"	"0.602"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4693"	"NDP"	"0.602"	"0.517"	"C0154832"	"Exudative retinopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2014"	"0"	"0"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C0266526"	"Norrie disease"	"disease"	"C10;C11;C16;C23"	"Congenital Abnormality"	"1.00"	"1"	"1993"	"2018"	"36"	"21"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4693"	"NDP"	"0.602"	"0.517"	"C0266568"	"Persistent Hyperplastic Primary Vitreous"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2009"	"2015"	"0"	"1"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.40"	"1"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4693"	"NDP"	"0.602"	"0.517"	"C1844579"	"Exudative Vitreoretinopathy, Familial, X-Linked Recessive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1979"	"2014"	"7"	"6"	"CTD_human;UNIPROT"
"4693"	"NDP"	"0.602"	"0.517"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C1857299"	"RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL"	"disease"	"C11"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4693"	"NDP"	"0.602"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4694"	"NDUFA1"	"0.63"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4694"	"NDUFA1"	"0.63"	"0.414"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"4694"	"NDUFA1"	"0.63"	"0.414"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4695"	"NDUFA2"	"0.636"	"0.483"	"C2751843"	"Leukoencephalopathy, Cystic, Without Megalencephaly"	"disease"	"C04;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4696"	"NDUFA3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4696"	"NDUFA3"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4697"	"NDUFA4"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"4698"	"NDUFA5"	"0.928"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4700"	"NDUFA6"	"0.928"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4701"	"NDUFA7"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4702"	"NDUFA8"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4702"	"NDUFA8"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4703"	"NEB"	"0.72"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"4703"	"NEB"	"0.72"	"0.448"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2016"	"0"	"5"	"ORPHANET"
"4703"	"NEB"	"0.72"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"4703"	"NEB"	"0.72"	"0.448"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4703"	"NEB"	"0.72"	"0.448"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4703"	"NEB"	"0.72"	"0.448"	"C1850569"	"Nemaline Myopathy 2"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.63"	"1"	"1993"	"2017"	"0"	"39"	"CTD_human"
"4703"	"NEB"	"0.72"	"0.448"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"4703"	"NEB"	"0.72"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"4704"	"NDUFA9"	"0.659"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"4705"	"NDUFA10"	"0.648"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"4706"	"NDUFAB1"	"0.762"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4708"	"NDUFB2"	"0.834"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4709"	"NDUFB3"	"0.663"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4709"	"NDUFB3"	"0.663"	"0.552"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2012"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"4709"	"NDUFB3"	"0.663"	"0.552"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2012"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4710"	"NDUFB4"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4711"	"NDUFB5"	"1"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4712"	"NDUFB6"	"0.857"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4713"	"NDUFB7"	"0.928"	"0.138"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4713"	"NDUFB7"	"0.928"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4713"	"NDUFB7"	"0.928"	"0.138"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4714"	"NDUFB8"	"0.815"	"0.103"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4715"	"NDUFB9"	"0.656"	"0.448"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4715"	"NDUFB9"	"0.656"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"4715"	"NDUFB9"	"0.656"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"4715"	"NDUFB9"	"0.656"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4716"	"NDUFB10"	"1"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4716"	"NDUFB10"	"1"	"0.034"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4717"	"NDUFC1"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4718"	"NDUFC2"	"0.928"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"PSYGENET"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C1656427"	"Early onset schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2016"	"2"	"0"	"PSYGENET"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.62"	"1"	"2001"	"2011"	"1"	"8"	"CTD_human;UNIPROT"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4719"	"NDUFS1"	"0.624"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.61"	"1"	"2001"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4720"	"NDUFS2"	"0.636"	"0.414"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0029124"	"Optic Atrophy"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2004"	"2015"	"0"	"2"	"CTD_human"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4722"	"NDUFS3"	"0.602"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2013"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.62"	"1"	"1999"	"2016"	"1"	"6"	"CTD_human;UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2001"	"2001"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4723"	"NDUFV1"	"0.616"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"2001"	"2017"	"4"	"3"	"CTD_human;UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"2000"	"2014"	"3"	"3"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"2000"	"2014"	"0"	"4"	"CTD_human"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"1"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"1"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"1"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"1"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"3"	"1"	"UNIPROT"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"4724"	"NDUFS4"	"0.59"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4725"	"NDUFS5"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4726"	"NDUFS6"	"0.639"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4726"	"NDUFS6"	"0.639"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4726"	"NDUFS6"	"0.639"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.61"	"1"	"2004"	"2012"	"2"	"1"	"CTD_human;UNIPROT"
"4726"	"NDUFS6"	"0.639"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.80"		"2004"	"2012"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1999"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"2"	"UNIPROT"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4728"	"NDUFS8"	"0.636"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2004"	"2016"	"5"	"0"	"CTD_human;PSYGENET"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8333333"	"2006"	"2016"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4729"	"NDUFV2"	"0.633"	"0.414"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4731"	"NDUFV3"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"4731"	"NDUFV3"	"1"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"UNIPROT"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.42"	"1"	"2010"	"2015"	"1"	"1"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4734"	"NEDD4"	"0.609"	"0.69"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4735"	"SEPT2"	"0.735"	"0.276"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4735"	"SEPT2"	"0.735"	"0.276"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4735"	"SEPT2"	"0.735"	"0.276"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4735"	"SEPT2"	"0.735"	"0.276"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4736"	"RPL10A"	"0.886"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4741"	"NEFM"	"0.667"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4741"	"NEFM"	"0.667"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4741"	"NEFM"	"0.667"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4741"	"NEFM"	"0.667"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4741"	"NEFM"	"0.667"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4744"	"NEFH"	"0.616"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"1"	"1993"	"2018"	"0"	"0"	"ORPHANET"
"4744"	"NEFH"	"0.616"	"0.586"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4744"	"NEFH"	"0.616"	"0.586"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4744"	"NEFH"	"0.616"	"0.586"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4744"	"NEFH"	"0.616"	"0.586"	"C4310790"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.53"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4745"	"NELL1"	"0.614"	"0.483"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4745"	"NELL1"	"0.614"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4745"	"NELL1"	"0.614"	"0.483"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4745"	"NELL1"	"0.614"	"0.483"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"1999"	"2004"	"1"	"0"	"CTD_human"
"4747"	"NEFL"	"0.577"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4747"	"NEFL"	"0.577"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2007"	"3"	"0"	"PSYGENET"
"4747"	"NEFL"	"0.577"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.9545455"	"2001"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"4747"	"NEFL"	"0.577"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"4747"	"NEFL"	"0.577"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2006"	"2"	"0"	"PSYGENET"
"4747"	"NEFL"	"0.577"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4747"	"NEFL"	"0.577"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2006"	"2"	"0"	"PSYGENET"
"4747"	"NEFL"	"0.577"	"0.483"	"C1843164"	"Charcot-Marie-Tooth disease, demyelinating, Type 1F"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2010"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"4747"	"NEFL"	"0.577"	"0.483"	"C1843225"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.94"	"1"	"1993"	"2017"	"5"	"13"	"CTD_human;ORPHANET;UNIPROT"
"4747"	"NEFL"	"0.577"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4750"	"NEK1"	"0.619"	"0.621"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.61"	"1"	"2016"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"4750"	"NEK1"	"0.619"	"0.621"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2011"	"2018"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"4750"	"NEK1"	"0.619"	"0.621"	"C0026363"	"Mohr Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4750"	"NEK1"	"0.619"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4750"	"NEK1"	"0.619"	"0.621"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"4750"	"NEK1"	"0.619"	"0.621"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"CTD_human"
"4750"	"NEK1"	"0.619"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4750"	"NEK1"	"0.619"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"4750"	"NEK1"	"0.619"	"0.621"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4750"	"NEK1"	"0.619"	"0.621"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"4750"	"NEK1"	"0.619"	"0.621"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"4750"	"NEK1"	"0.619"	"0.621"	"C2931889"	"Oral-facial-digital syndrome, type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4750"	"NEK1"	"0.619"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4750"	"NEK1"	"0.619"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4751"	"NEK2"	"0.609"	"0.655"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"4751"	"NEK2"	"0.609"	"0.655"	"C3809954"	"RETINITIS PIGMENTOSA 67"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2013"	"0"	"1"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"4758"	"NEU1"	"0.533"	"0.621"	"C0023806"	"Lipomucopolysaccharidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1997"	"2015"	"8"	"18"	"ORPHANET;UNIPROT"
"4758"	"NEU1"	"0.533"	"0.621"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4758"	"NEU1"	"0.533"	"0.621"	"C0268226"	"Type I Mucolipidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1984"	"2015"	"8"	"23"	"ORPHANET;UNIPROT"
"4758"	"NEU1"	"0.533"	"0.621"	"C0268228"	"Neuraminidase 1 deficiency"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.65"	"1"	"1997"	"2015"	"8"	"19"	"CTD_human;UNIPROT"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4758"	"NEU1"	"0.533"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4758"	"NEU1"	"0.533"	"0.621"	"C3888317"	"Sialidosis, type 2"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1997"	"2015"	"8"	"18"	"CTD_human;UNIPROT"
"4758"	"NEU1"	"0.533"	"0.621"	"C4282398"	"Sialidase deficiency"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1997"	"2015"	"8"	"18"	"CTD_human;UNIPROT"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.8421053"	"1999"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.8181818"	"1999"	"2015"	"0"	"0"	"ORPHANET"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C1853371"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"		"1999"	"2016"	"3"	"3"	"CTD_human;UNIPROT"
"4760"	"NEUROD1"	"0.572"	"0.69"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"4761"	"NEUROD2"	"0.799"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4762"	"NEUROG1"	"0.72"	"0.276"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4762"	"NEUROG1"	"0.72"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"2"	"0"	"PSYGENET"
"4763"	"NF1"	"0.458"	"0.724"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.49"	"0.875"	"1994"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2014"	"0"	"0"	"UNIPROT"
"4763"	"NF1"	"0.458"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"4763"	"NF1"	"0.458"	"0.724"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"4763"	"NF1"	"0.458"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1994"	"1996"	"3"	"0"	"GENOMICS_ENGLAND"
"4763"	"NF1"	"0.458"	"0.724"	"C0016057"	"Fibrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"0.6"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1994"	"2015"	"1"	"0"	"CGI;CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"1983"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"4763"	"NF1"	"0.458"	"0.724"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1993"	"2008"	"0"	"0"	"CGI"
"4763"	"NF1"	"0.458"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1994"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1993"	"2017"	"2"	"0"	"CGI;CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"0.875"	"1996"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0027830"	"neurofibroma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.9545455"	"1992"	"2016"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"1.00"	"0.9512195"	"1988"	"2018"	"44"	"358"	"CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"4763"	"NF1"	"0.458"	"0.724"	"C0027962"	"Melanocytic nevus"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9230769"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"4763"	"NF1"	"0.458"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"1996"	"3"	"0"	"GENOMICS_ENGLAND"
"4763"	"NF1"	"0.458"	"0.724"	"C0162678"	"Neurofibromatoses"	"group"	"C04;C10;C16"	"Neoplastic Process"	"0.90"	"0.9259259"	"1983"	"2016"	"1"	"3"	"CGI;CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205825"	"Liposarcoma, Pleomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0206727"	"Nerve Sheath Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.9411765"	"1992"	"2016"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0278622"	"Adult Malignant Peripheral Nerve Sheath Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4763"	"NF1"	"0.458"	"0.724"	"C0279987"	"Childhood Malignant Peripheral Nerve Sheath Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4763"	"NF1"	"0.458"	"0.724"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.90"	"0.9230769"	"1995"	"2016"	"3"	"3"	"CTD_human;ORPHANET"
"4763"	"NF1"	"0.458"	"0.724"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4763"	"NF1"	"0.458"	"0.724"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0553586"	"Cafe-au-lait macules with pulmonary stenosis"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"1992"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"4763"	"NF1"	"0.458"	"0.724"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751374"	"Schwannomatosis, Plexiform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751689"	"Peripheral Nerve Sheath Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1991"	"2018"	"1"	"0"	"CGI;CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0751691"	"Perineurioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C0917817"	"Neurofibromatosis 3"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CLINGEN"
"4763"	"NF1"	"0.458"	"0.724"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4763"	"NF1"	"0.458"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C1834235"	"NEUROFIBROMATOSIS, FAMILIAL SPINAL"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"1992"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"4763"	"NF1"	"0.458"	"0.724"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"4763"	"NF1"	"0.458"	"0.724"	"C2931482"	"Neurofibromatosis-Noonan syndrome"	"disease"	"C04;C05;C10;C14;C16;C17"	"Disease or Syndrome"	"0.78"	"1"	"1992"	"2017"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"4763"	"NF1"	"0.458"	"0.724"	"C3150928"	"NF1 Microdeletion Syndrome"	"disease"	"C04;C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2012"	"0"	"0"	"ORPHANET"
"4763"	"NF1"	"0.458"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.63"	"1"	"1992"	"2018"	"7"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4771"	"NF2"	"0.511"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.51"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4771"	"NF2"	"0.511"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.70"	"0.9493671"	"1993"	"2016"	"1"	"2"	"CGI;CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2009"	"6"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9166667"	"1992"	"2018"	"0"	"0"	"CGI"
"4771"	"NF2"	"0.511"	"0.621"	"C0027832"	"Neurofibromatosis 2"	"disease"	"C04;C09;C10;C16"	"Neoplastic Process"	"1.00"	"0.9537037"	"1985"	"2018"	"23"	"23"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C0027859"	"Acoustic Neuroma"	"disease"	"C04;C09;C10"	"Neoplastic Process"	"0.60"	"0.9333333"	"1994"	"2016"	"9"	"0"	"CLINGEN;ORPHANET"
"4771"	"NF2"	"0.511"	"0.621"	"C0032229"	"Pleural Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4771"	"NF2"	"0.511"	"0.621"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2017"	"5"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4771"	"NF2"	"0.511"	"0.621"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C0917817"	"Neurofibromatosis 3"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4771"	"NF2"	"0.511"	"0.621"	"C1136041"	"Familial Acoustic Neuroma"	"disease"	"C04;C09;C10;C16"	"Neoplastic Process"	"0.60"		"1994"	"2015"	"10"	"0"	"CLINGEN;CTD_human;ORPHANET"
"4771"	"NF2"	"0.511"	"0.621"	"C1136042"	"Neuroma, Acoustic, Bilateral"	"disease"	"C04;C09;C10;C16"	"Neoplastic Process"	"0.61"	"1"	"1993"	"2015"	"23"	"6"	"CLINGEN;CTD_human;UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C1136043"	"Schwannoma, Acoustic, Bilateral"	"disease"	"C04;C09;C10;C16"	"Neoplastic Process"	"0.60"		"1993"	"2015"	"23"	"6"	"CLINGEN;CTD_human;UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1300127"	"Perivascular Epithelioid Cell Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4771"	"NF2"	"0.511"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1335929"	"Schwannomatosis"	"disease"	"C04;C10;C16;C17"	"Neoplastic Process"	"0.57"	"0.8571429"	"1998"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"4771"	"NF2"	"0.511"	"0.621"	"C1378703"	"Renal carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4771"	"NF2"	"0.511"	"0.621"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1527349"	"Ductal Breast Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4771"	"NF2"	"0.511"	"0.621"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4771"	"NF2"	"0.511"	"0.621"	"C2931480"	"Neurofibromatosis, Type 3, mixed central and peripheral"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4771"	"NF2"	"0.511"	"0.621"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4772"	"NFATC1"	"0.586"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"4773"	"NFATC2"	"0.588"	"0.517"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2007"	"2017"	"1"	"0"	"CTD_human"
"4773"	"NFATC2"	"0.588"	"0.517"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4774"	"NFIA"	"0.633"	"0.621"	"C3151036"	"CHROMOSOME 1p32-p31 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"4774"	"NFIA"	"0.633"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"4774"	"NFIA"	"0.633"	"0.621"	"C4478940"	"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.9642857"	"2007"	"2018"	"2"	"0"	"CGI;CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"4"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0022593"	"Keratosis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0022594"	"Keratosis Blennorrhagica"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2014"	"2015"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2009"	"2013"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0086501"	"Keratoma"	"phenotype"	"C17"	"Acquired Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.45"	"1"	"2010"	"2017"	"1"	"5"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.8333333"	"2014"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9516129"	"2006"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2017"	"4"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2013"	"2016"	"0"	"5"	"CGI"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"4"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9411765"	"2005"	"2018"	"1"	"3"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"4"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"4"	"0"	"CTD_human"
"4780"	"NFE2L2"	"0.42"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"4"	"0"	"CTD_human"
"4781"	"NFIB"	"0.624"	"0.414"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9565217"	"2009"	"2018"	"1"	"0"	"CTD_human"
"4782"	"NFIC"	"0.696"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4782"	"NFIC"	"0.696"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0393770"	"Delayed Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0494410"	"Nonorganic Sleep Wake Cycle Disorders"	"group"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0751758"	"Advanced Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0751759"	"Non-24 Hour Sleep-Wake Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0751760"	"Shift-Work Sleep Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4783"	"NFIL3"	"0.727"	"0.414"	"C0877792"	"Sleep Disorders, Circadian Rhythm"	"group"	"C10;C24;F03"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4784"	"NFIX"	"0.588"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2018"	"1"	"1"	"PSYGENET"
"4784"	"NFIX"	"0.588"	"0.621"	"C0265211"	"Marshall-Smith syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.63"	"1"	"2010"	"2016"	"0"	"10"	"CTD_human;ORPHANET"
"4784"	"NFIX"	"0.588"	"0.621"	"C3553660"	"SOTOS SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2010"	"2018"	"4"	"6"	"ORPHANET;UNIPROT"
"4784"	"NFIX"	"0.588"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2008"	"2016"	"4"	"0"	"PSYGENET"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9473684"	"2009"	"2017"	"2"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2017"	"1"	"2"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2014"	"2"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.53"	"1"	"2013"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0020500"	"Hyperoxaluria"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4790"	"NFKB1"	"0.365"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C1298681"	"Oxalosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4790"	"NFKB1"	"0.365"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"4791"	"NFKB2"	"0.542"	"0.759"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.74"	"1"	"1998"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"4791"	"NFKB2"	"0.542"	"0.759"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4791"	"NFKB2"	"0.542"	"0.759"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"4791"	"NFKB2"	"0.542"	"0.759"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4791"	"NFKB2"	"0.542"	"0.759"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"4791"	"NFKB2"	"0.542"	"0.759"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4791"	"NFKB2"	"0.542"	"0.759"	"C3809991"	"IMMUNODEFICIENCY, COMMON VARIABLE, 10"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2012"	"2017"	"2"	"5"	"UNIPROT"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"0.875"	"1999"	"2010"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0153392"	"Malignant neoplasm of nasopharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C1846006"	"Ectodermal dysplasia, hypohidrotic, with immune deficiency"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C2677481"	"Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.60"		"2003"	"2008"	"2"	"3"	"CTD_human;UNIPROT"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"4792"	"NFKBIA"	"0.509"	"0.724"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4794"	"NFKBIE"	"0.762"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2013"	"1"	"2"	"CTD_human"
"4794"	"NFKBIE"	"0.762"	"0.31"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4794"	"NFKBIE"	"0.762"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4794"	"NFKBIE"	"0.762"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4795"	"NFKBIL1"	"0.735"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.47"	"1"	"2001"	"2011"	"0"	"4"	"CTD_human"
"4796"	"TONSL"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4796"	"TONSL"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4800"	"NFYA"	"0.707"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4800"	"NFYA"	"0.707"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4802"	"NFYC"	"0.799"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4803"	"NGF"	"0.426"	"0.862"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"4803"	"NGF"	"0.426"	"0.862"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4803"	"NGF"	"0.426"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0010043"	"Corneal Ulcer"	"disease"	"C01;C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0010692"	"Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2004"	"2013"	"1"	"0"	"PSYGENET"
"4803"	"NGF"	"0.426"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2013"	"1"	"0"	"PSYGENET"
"4803"	"NGF"	"0.426"	"0.862"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"0.5"	"1984"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"4803"	"NGF"	"0.426"	"0.862"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0020074"	"HSAN Type IV"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2014"	"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.77"	"1"	"2002"	"2014"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"4803"	"NGF"	"0.426"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2000"	"2003"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0027889"	"Hereditary Sensory and Autonomic Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2009"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"1992"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0037299"	"Skin Ulcer"	"phenotype"	"C17"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0086405"	"Hereditary Sensory Radicular Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4803"	"NGF"	"0.426"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0268849"	"Overactive Detrusor"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"4803"	"NGF"	"0.426"	"0.862"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0699739"	"Sensory Neuropathy, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2007"	"0"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C0878773"	"Overactive Bladder"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4803"	"NGF"	"0.426"	"0.862"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4803"	"NGF"	"0.426"	"0.862"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4804"	"NGFR"	"0.508"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"2"	"0"	"PSYGENET"
"4804"	"NGFR"	"0.508"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2008"	"2"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"PSYGENET"
"4804"	"NGFR"	"0.508"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"1999"	"2003"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2009"	"2"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4804"	"NGFR"	"0.508"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4808"	"NHLH2"	"0.886"	"0.138"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"4810"	"NHS"	"0.6"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"UNIPROT"
"4810"	"NHS"	"0.6"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"4810"	"NHS"	"0.6"	"0.759"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4810"	"NHS"	"0.6"	"0.759"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4810"	"NHS"	"0.6"	"0.759"	"C0796085"	"Nance-Horan syndrome"	"disease"	"C07;C11;C16"	"Disease or Syndrome"	"1.00"	"1"	"1979"	"2018"	"4"	"8"	"CLINGEN;CTD_human;ORPHANET"
"4810"	"NHS"	"0.6"	"0.759"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4810"	"NHS"	"0.6"	"0.759"	"C2930878"	"Cataract, congenital, with microcornea or slight microphthalmia"	"disease"	"C11;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4810"	"NHS"	"0.6"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4810"	"NHS"	"0.6"	"0.759"	"C4049005"	"Cataract, total congenital with posterior sutural opacities in Heterozygotes"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"4811"	"NID1"	"0.69"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4811"	"NID1"	"0.69"	"0.379"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4811"	"NID1"	"0.69"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4814"	"NINJ1"	"0.834"	"0.172"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4824"	"NKX3-1"	"0.727"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.60"	"1"	"1999"	"2013"	"4"	"0"	"CTD_human"
"4824"	"NKX3-1"	"0.727"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.54"	"1"	"1999"	"2016"	"4"	"0"	"CTD_human"
"4825"	"NKX6-1"	"0.857"	"0.069"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4825"	"NKX6-1"	"0.857"	"0.069"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4825"	"NKX6-1"	"0.857"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4825"	"NKX6-1"	"0.857"	"0.069"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4826"	"NNAT"	"0.681"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4826"	"NNAT"	"0.681"	"0.448"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"4829"	"NMBR"	"0.785"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"4829"	"NMBR"	"0.785"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"4829"	"NMBR"	"0.785"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4829"	"NMBR"	"0.785"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.85"	"1991"	"2005"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2005"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9146341"	"1989"	"2017"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.50"	"1"	"1991"	"2015"	"0"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8181818"	"1991"	"2005"	"1"	"0"	"CTD_human"
"4830"	"NME1"	"0.47"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2005"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2005"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"1993"	"2005"	"1"	"0"	"CTD_human"
"4831"	"NME2"	"0.604"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1996"	"2005"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0001824"	"Agranulocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4835"	"NQO2"	"0.624"	"0.448"	"C0005956"	"Bone Marrow Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"0"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4835"	"NQO2"	"0.624"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2005"	"2010"	"2"	"0"	"PSYGENET"
"4835"	"NQO2"	"0.624"	"0.448"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4835"	"NQO2"	"0.624"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"0"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4835"	"NQO2"	"0.624"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4837"	"NNMT"	"0.604"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4837"	"NNMT"	"0.604"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"4838"	"NODAL"	"0.659"	"0.31"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.70"		"1997"	"2009"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4838"	"NODAL"	"0.659"	"0.31"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4838"	"NODAL"	"0.659"	"0.31"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.52"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4838"	"NODAL"	"0.659"	"0.31"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"4838"	"NODAL"	"0.659"	"0.31"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4838"	"NODAL"	"0.659"	"0.31"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4838"	"NODAL"	"0.659"	"0.31"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4838"	"NODAL"	"0.659"	"0.31"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"4838"	"NODAL"	"0.659"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"4838"	"NODAL"	"0.659"	"0.31"	"C3495537"	"Heterotaxy, Visceral, 5, Autosomal"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.60"		"1997"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"4838"	"NODAL"	"0.659"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4838"	"NODAL"	"0.659"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4841"	"NONO"	"0.663"	"0.483"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4841"	"NONO"	"0.663"	"0.483"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4841"	"NONO"	"0.663"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"4841"	"NONO"	"0.663"	"0.483"	"C4225417"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC 34"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2016"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"4841"	"NONO"	"0.663"	"0.483"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4842"	"NOS1"	"0.445"	"0.793"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0014848"	"Esophageal Achalasia"	"disease"	"C06"	"Disease or Syndrome"	"0.62"	"0.5"	"1994"	"2015"	"0"	"0"	"ORPHANET"
"4842"	"NOS1"	"0.445"	"0.793"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.50"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;PSYGENET"
"4842"	"NOS1"	"0.445"	"0.793"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.50"		"1999"	"2009"	"2"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0021845"	"Intestinal Perforation"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"0.875"	"1998"	"2017"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9375"	"1995"	"2017"	"1"	"2"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"1996"	"1999"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0042035"	"Urination Disorders"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0476201"	"Axonotmesis"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0600519"	"Ventricular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0600520"	"Left Ventricle Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0745744"	"End Stage Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751792"	"Trauma, Nervous System"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0751793"	"Craniocervical Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0814154"	"Alcohol Related Neurodevelopmental Disorder"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C0859976"	"Idiopathic achalasia of esophagus"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4842"	"NOS1"	"0.445"	"0.793"	"C1142379"	"Neurotmesis"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C2936476"	"Chronic Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C3146244"	"Alcohol Related Birth Defect"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C3661483"	"Partial Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4842"	"NOS1"	"0.445"	"0.793"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0003510"	"Aortitis Syndrome"	"disease"	"C14;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.50"		"2002"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.9130435"	"1996"	"2017"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1999"	"2014"	"1"	"1"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.57"	"0.8571429"	"1998"	"2018"	"2"	"1"	"CTD_human;UNIPROT"
"4843"	"NOS2"	"0.385"	"0.931"	"C0006261"	"Bronchial Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2003"	"2017"	"1"	"2"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2010"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"4843"	"NOS2"	"0.385"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"4843"	"NOS2"	"0.385"	"0.931"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.53"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0014476"	"Eperythrozoonosis"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"0.8"	"1996"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"0.8571429"	"1996"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.58"	"1"	"1999"	"2016"	"3"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2001"	"2014"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"0.6666667"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2003"	"2012"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"0"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0026936"	"Mycoplasma Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2015"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2011"	"5"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0032290"	"Aspiration Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.45"	"1"	"1996"	"2017"	"1"	"3"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1999"	"2013"	"4"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0036330"	"Schistosomiasis mansoni"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"1999"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"		"2004"	"2008"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.31"		"2003"	"2009"	"3"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038525"	"Subarachnoid Hemorrhage"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0039263"	"Takayasu Arteritis"	"disease"	"C14;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0041408"	"Turner Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0042029"	"Urinary tract infection"	"group"	"C01;C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2001"	"0"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0085740"	"Mendelson Syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0178540"	"Cerebral Hypoxia-Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0206145"	"Stunned Myocardium"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0206146"	"Myocardial Stunning"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0242497"	"Intestinal schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0242526"	"Gonadal Dysgenesis, 45,X"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0270192"	"Perinatal Subarachnoid Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0376416"	"Hibernation, Myocardial"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0472383"	"Subarachnoid Hemorrhage, Spontaneous"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.50"		"1996"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2004"	"2012"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751530"	"Subarachnoid Hemorrhage, Aneurysmal"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0752304"	"Hypoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0752305"	"Anoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0752306"	"Anoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0752307"	"Anoxia-Ischemia, Cerebral"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0752308"	"Hypoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0795688"	"Subarachnoid Hemorrhage, Intracranial"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2007"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1527168"	"Bonnevie-Ullrich Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4843"	"NOS2"	"0.385"	"0.931"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4843"	"NOS2"	"0.385"	"0.931"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0000832"	"Abruptio Placentae"	"phenotype"	"C13"	"Pathologic Function"	"0.31"		"2001"	"2005"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2001"	"2013"	"8"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9411765"	"1999"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2000"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0003850"	"Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9423077"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9795918"	"1999"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"PSYGENET"
"4846"	"NOS3"	"0.401"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9285714"	"1997"	"2018"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2017"	"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9642857"	"1996"	"2018"	"4"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0010073"	"Coronary Artery Vasospasm"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0010398"	"Cruveilhier-Baumgarten Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1999"	"2011"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2001"	"2013"	"8"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.8636364"	"1999"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.53"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9583333"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0018036"	"Hypertension, Goldblatt"	"disease"	"C12;C13;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2002"	"2009"	"4"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8461538"	"2008"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.875"	"2003"	"2016"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"1995"	"1997"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.37"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.9243697"	"1996"	"2018"	"5"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020541"	"Hypertension, Portal"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"0"	"2000"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"2006"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0020545"	"Hypertension, Renovascular"	"disease"	"C12;C13;C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2001"	"2009"	"4"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0021845"	"Intestinal Perforation"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1998"	"2017"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"0.9583333"	"1998"	"2018"	"2"	"1"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.38"		"2002"	"2009"	"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2012"	"3"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2004"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.33"	"0.3333333"	"2009"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2009"	"2017"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2001"	"2013"	"8"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.8571429"	"1995"	"2017"	"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0151636"	"Premature ventricular contractions"	"phenotype"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.60"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.33"	"0.3333333"	"2009"	"2015"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0341934"	"Transient hypertension of pregnancy"	"phenotype"	"C13;C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"3"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1999"	"2010"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.60"	"1"	"2003"	"2018"	"3"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0852036"	"Pregnancy associated hypertension"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.31"		"2002"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2001"	"2009"	"4"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2007"	"4"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2011"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"0"	"2010"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.94"	"1996"	"2018"	"4"	"1"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4846"	"NOS3"	"0.401"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4849"	"CNOT3"	"0.815"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"4849"	"CNOT3"	"0.815"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"4849"	"CNOT3"	"0.815"	"0.276"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.61"	"1"	"2013"	"2013"	"1"	"0"	"CGI;CTD_human;ORPHANET"
"4849"	"CNOT3"	"0.815"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.38"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2017"	"2"	"0"	"CGI;CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"2008"	"2018"	"1"	"0"	"CGI;CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"2011"	"2016"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0023492"	"Leukemia, T-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2016"	"4"	"0"	"CLINGEN"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0036439"	"Scoliosis, unspecified"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0149630"	"Bicuspid aortic valve"	"disease"	"C14"	"Congenital Abnormality"	"0.50"	"0.8"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"2014"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2012"	"2016"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2005"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.63"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2017"	"2"	"0"	"CGI;CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2011"	"2016"	"0"	"0"	"CGI"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1260873"	"Aortic valve disorder"	"group"		"Disease or Syndrome"	"0.44"	"1"	"2005"	"2017"	"0"	"6"	"ORPHANET"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.9705882"	"1999"	"2018"	"5"	"0"	"CGI;CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C3887892"	"Aortic Valve Disease 1"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C4014970"	"ADAMS-OLIVER SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"1992"	"2018"	"1"	"13"	"UNIPROT"
"4851"	"NOTCH1"	"0.415"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2001"	"2014"	"6"	"0"	"CTD_human;PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.55"	"0.6"	"2000"	"2016"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2002"	"2016"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9615385"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2002"	"2007"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0008677"	"Bronchitis, Chronic"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1998"	"2015"	"7"	"0"	"CTD_human;PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2010"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0026837"	"Muscle Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0027429"	"Nasal obstruction present finding"	"phenotype"	"C08;C09"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2014"	"2"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.39"	"1"	"1999"	"2016"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"1998"	"2013"	"7"	"0"	"CTD_human;PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1997"	"1997"	"1"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.71"	"1"	"2003"	"2010"	"3"	"0"	"CTD_human;PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2010"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.32"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0151564"	"Cogwheel Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0231519"	"Gegenhalten"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0233608"	"Catatonic Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"1997"	"2010"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0236664"	"Alcohol-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0239325"	"Extensor Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2012"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0277821"	"Extrapyramidal Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1988"	"2014"	"5"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2009"	"2009"	"2"	"0"	"CTD_human;PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2010"	"2"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2013"	"5"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C1320474"	"Nuchal Rigidity"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C2350170"	"Unilateral Nasal Obstruction"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C2350171"	"Bilateral Nasal Obstruction"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1992"	"1992"	"1"	"0"	"PSYGENET"
"4852"	"NPY"	"0.469"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4852"	"NPY"	"0.469"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"3"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.56"	"1"	"2007"	"2017"	"1"	"0"	"CGI;CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2004"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2014"	"1"	"1"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2015"	"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0085280"	"Alagille Syndrome"	"disease"	"C06;C14;C16"	"Congenital Abnormality"	"0.39"	"0.8888889"	"2006"	"2015"	"0"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.66"	"1"	"2007"	"2018"	"1"	"1"	"CGI;CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C0917715"	"Hajdu-Cheney Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.90"	"1"	"1996"	"2017"	"2"	"6"	"CTD_human;ORPHANET"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2011"	"2013"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1857761"	"Alagille Syndrome 2"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2006"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1956125"	"Alagille Syndrome 1"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C2930797"	"Hepatic ductular hypoplasia"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C2930971"	"Acroosteolysis dominant type"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"4853"	"NOTCH2"	"0.474"	"0.724"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"0"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.42"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0344487"	"Lateral meningocele"	"phenotype"		"Anatomical Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0432284"	"Infantile myofibromatosis"	"disease"	"C04"	"Disease or Syndrome"	"0.61"	"1"	"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0751587"	"CADASIL Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"1.00"	"0.9776536"	"1993"	"2018"	"22"	"21"	"CTD_human;ORPHANET;UNIPROT"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C1449626"	"CADASILM"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C1851710"	"LATERAL MENINGOCELE SYNDROME"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C3809084"	"MYOFIBROMATOSIS, INFANTILE, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"1"	"UNIPROT"
"4854"	"NOTCH3"	"0.469"	"0.69"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2002"	"2013"	"4"	"0"	"PSYGENET"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2010"	"2017"	"2"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.75"	"2000"	"2018"	"4"	"4"	"PSYGENET"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2017"	"2"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2012"	"2"	"0"	"CTD_human"
"4855"	"NOTCH4"	"0.564"	"0.655"	"C3544321"	"Treatment-resistant schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"4860"	"PNP"	"0.545"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0268125"	"Purine-nucleoside phosphorylase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.93"	"1"	"1987"	"2014"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"4860"	"PNP"	"0.545"	"0.793"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4860"	"PNP"	"0.545"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4861"	"NPAS1"	"0.928"	"0.034"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4861"	"NPAS1"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2005"	"2"	"0"	"PSYGENET"
"4861"	"NPAS1"	"0.928"	"0.034"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2016"	"5"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"4862"	"NPAS2"	"0.659"	"0.345"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2016"	"4"	"0"	"PSYGENET"
"4864"	"NPC1"	"0.536"	"0.69"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0006309"	"Brucellosis"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C0013362"	"Dysarthria"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1989"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.47"	"0.8571429"	"2009"	"2014"	"1"	"1"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0029089"	"Ophthalmoplegia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0162292"	"External Ophthalmoplegia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0220756"	"Niemann-Pick Disease, Type C"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9848485"	"1997"	"2018"	"21"	"76"	"CTD_human;UNIPROT"
"4864"	"NPC1"	"0.536"	"0.69"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0240952"	"Dysarthria, Scanning"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0268247"	"Niemann-Pick Disease, Type D"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2012"	"21"	"73"	"CTD_human;UNIPROT"
"4864"	"NPC1"	"0.536"	"0.69"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0339693"	"Internal Ophthalmoplegia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0454596"	"Dysarthria, Spastic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0454597"	"Dysarthria, Flaccid"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0454598"	"Dysarthria, Mixed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C0751401"	"Ophthalmoparesis"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2013"	"8"	"0"	"GENOMICS_ENGLAND"
"4864"	"NPC1"	"0.536"	"0.69"	"C1563666"	"Dysarthria, Guttural"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C1850363"	"Niemann-Pick Disease, Nova Scotian Type"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2007"	"19"	"73"	"UNIPROT"
"4864"	"NPC1"	"0.536"	"0.69"	"C2231324"	"Brucellosis, Pulmonary"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4864"	"NPC1"	"0.536"	"0.69"	"C3179455"	"Niemann-Pick Disease, Type C1"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.96"	"1973"	"2018"	"21"	"132"	"CTD_human;UNIPROT"
"4864"	"NPC1"	"0.536"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1997"	"2003"	"8"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.42"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"4867"	"NPHP1"	"0.619"	"0.552"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"4867"	"NPHP1"	"0.619"	"0.552"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"4867"	"NPHP1"	"0.619"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C1846790"	"JOUBERT SYNDROME 4 (disorder)"	"disease"	"C10;C11;C12;C13"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4867"	"NPHP1"	"0.619"	"0.552"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.80"	"0.9375"	"1995"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4867"	"NPHP1"	"0.619"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"4867"	"NPHP1"	"0.619"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0027721"	"Lipoid nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.41"		"2002"	"2010"	"3"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0403399"	"Finnish congenital nephrotic syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2017"	"17"	"151"	"CTD_human;ORPHANET;UNIPROT"
"4868"	"NPHS1"	"0.614"	"0.517"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C1704320"	"Glomerulonephritis, Minimal Change"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C1704321"	"Nephrotic Syndrome, Minimal Change"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C1853124"	"NEPHROTIC SYNDROME, TYPE 3"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C3496337"	"Idiopathic Nephrotic Syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2009"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C3501848"	"Nephrosis, congenital"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"0.9782609"	"1996"	"2017"	"2"	"0"	"CTD_human"
"4868"	"NPHS1"	"0.614"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4869"	"NPM1"	"0.496"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4869"	"NPM1"	"0.496"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9661017"	"1996"	"2018"	"4"	"2"	"CGI;CTD_human"
"4869"	"NPM1"	"0.496"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.952381"	"1996"	"2016"	"2"	"0"	"CGI;CTD_human;ORPHANET"
"4869"	"NPM1"	"0.496"	"0.69"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"0.875"	"1994"	"2008"	"0"	"0"	"CGI"
"4869"	"NPM1"	"0.496"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"4869"	"NPM1"	"0.496"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2010"	"2017"	"4"	"0"	"CTD_human;ORPHANET"
"4869"	"NPM1"	"0.496"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"4869"	"NPM1"	"0.496"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4869"	"NPM1"	"0.496"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4869"	"NPM1"	"0.496"	"0.69"	"C0206182"	"Lymphomatoid Papulosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"1996"	"1998"	"0"	"0"	"ORPHANET"
"4869"	"NPM1"	"0.496"	"0.69"	"C1301362"	"Primary Cutaneous Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"4869"	"NPM1"	"0.496"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"4869"	"NPM1"	"0.496"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2010"	"2017"	"4"	"0"	"CTD_human;ORPHANET"
"4878"	"NPPA"	"0.546"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2011"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"1989"	"2013"	"2"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2003"	"2011"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.59"	"0.8888889"	"1989"	"2015"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9"	"1989"	"2015"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0020440"	"Hypercapnia"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.952381"	"1989"	"2018"	"7"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0020544"	"Renal hypertension"	"disease"	"C12;C13;C14"	"Disease or Syndrome"	"0.50"		"1996"	"2010"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1987"	"1988"	"2"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1987"	"2012"	"3"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"2005"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0042035"	"Urination Disorders"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.37"	"0.8"	"1998"	"2014"	"2"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"2005"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0242231"	"Coronary Stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0541782"	"Atrial standstill"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"ORPHANET"
"4878"	"NPPA"	"0.546"	"0.69"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2011"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1989"	"2006"	"2"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1987"	"2009"	"3"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C1838539"	"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4878"	"NPPA"	"0.546"	"0.69"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4878"	"NPPA"	"0.546"	"0.69"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"2005"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1991"	"2005"	"4"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1987"	"2009"	"3"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C2677294"	"Atrial Fibrillation, Familial, 6"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2008"	"2009"	"0"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"4878"	"NPPA"	"0.546"	"0.69"	"C3810401"	"ATRIAL STANDSTILL 2"	"disease"		"Disease or Syndrome"	"0.40"		"1983"	"2013"	"1"	"1"	"UNIPROT"
"4879"	"NPPB"	"0.567"	"0.552"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2006"	"2008"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"0.8333333"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0013404"	"Dyspnea"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.31"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2011"	"4"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9166667"	"1991"	"2016"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9090909"	"1991"	"2016"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.875"	"1997"	"2016"	"3"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.53"		"2005"	"2011"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1997"	"2010"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2014"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0032787"	"Postoperative Complications"	"group"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0085128"	"Cardiac Output, High"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"0"	"1999"	"2005"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2014"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.38"		"2003"	"2009"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0242707"	"Ventricular Dysfunction, Right"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"2005"	"2009"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2011"	"4"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2014"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2014"	"12"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4879"	"NPPB"	"0.567"	"0.552"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0007302"	"Cartilage Diseases"	"group"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0085700"	"Chondromalacia"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4880"	"NPPC"	"0.663"	"0.448"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.59"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0236664"	"Alcohol-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"4881"	"NPR1"	"0.672"	"0.414"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4881"	"NPR1"	"0.672"	"0.414"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4882"	"NPR2"	"0.624"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4882"	"NPR2"	"0.624"	"0.552"	"C1864356"	"ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE"	"disease"	"C05"	"Disease or Syndrome"	"0.96"	"1"	"1998"	"2017"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"4882"	"NPR2"	"0.624"	"0.552"	"C2930970"	"Acromesomelic dysplasia Hunter-Thompson type"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.54"	"1"	"2004"	"2016"	"3"	"4"	"UNIPROT"
"4882"	"NPR2"	"0.624"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4882"	"NPR2"	"0.624"	"0.552"	"C4014690"	"EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4882"	"NPR2"	"0.624"	"0.552"	"C4225399"	"SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2014"	"2"	"6"	"UNIPROT"
"4882"	"NPR2"	"0.624"	"0.552"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4883"	"NPR3"	"0.727"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4883"	"NPR3"	"0.727"	"0.414"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4883"	"NPR3"	"0.727"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4883"	"NPR3"	"0.727"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4883"	"NPR3"	"0.727"	"0.414"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"4885"	"NPTX2"	"0.681"	"0.448"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4885"	"NPTX2"	"0.681"	"0.448"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4885"	"NPTX2"	"0.681"	"0.448"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2001"	"2010"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2004"	"2012"	"2"	"0"	"PSYGENET"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0040460"	"Toothache"	"phenotype"	"C07;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4886"	"NPY1R"	"0.63"	"0.345"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2009"	"2011"	"2"	"0"	"CTD_human;PSYGENET"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2007"	"2"	"0"	"PSYGENET"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"4887"	"NPY2R"	"0.645"	"0.379"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4889"	"NPY5R"	"0.701"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"4889"	"NPY5R"	"0.701"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.54"	"0.75"	"1996"	"2007"	"1"	"0"	"CTD_human"
"4889"	"NPY5R"	"0.701"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2005"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"0.75"	"1998"	"2007"	"1"	"0"	"CTD_human"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0162316"	"Iron deficiency anemia"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.8461538"	"1999"	"2013"	"1"	"0"	"CTD_human"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C2673913"	"Anemia, Hypochromic Microcytic, With Iron Overload"	"disease"	"C15"	"Disease or Syndrome"	"0.63"	"1"	"2005"	"2012"	"0"	"3"	"CTD_human;ORPHANET"
"4891"	"SLC11A2"	"0.619"	"0.517"	"C3806153"	"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2006"	"3"	"3"	"UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.51"	"1"	"1987"	"2014"	"1"	"0"	"CGI;CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0007115"	"Malignant neoplasm of thyroid"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.43"	"1"	"1984"	"2015"	"0"	"5"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2018"	"0"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.41"	"1"	"2006"	"2016"	"0"	"7"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9473684"	"1984"	"2015"	"1"	"1"	"UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9642857"	"1985"	"2017"	"1"	"7"	"CGI;CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.44"	"1"	"1990"	"2015"	"0"	"1"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.34"	"1"	"1988"	"2015"	"1"	"2"	"UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0023518"	"Leukocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.43"	"0.6666667"	"1993"	"2013"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9563492"	"1988"	"2018"	"5"	"10"	"CGI;CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.49"	"0.8888889"	"1995"	"2016"	"0"	"7"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0027019"	"Myelomonocytic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.47"	"1"	"2002"	"2017"	"1"	"1"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.77"	"1"	"2004"	"2015"	"4"	"2"	"CLINGEN;CTD_human;ORPHANET"
"4893"	"NRAS"	"0.42"	"0.69"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.45"	"1"	"2003"	"2017"	"0"	"2"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.44"	"1"	"1993"	"2014"	"1"	"4"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0149978"	"Adenocarcinoma of rectum"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.8421053"	"2000"	"2018"	"0"	"7"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0151857"	"Pleocytosis"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"3"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0206682"	"Follicular thyroid carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.45"	"1"	"1995"	"2016"	"0"	"1"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0206729"	"Neurofibrosarcoma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0206739"	"Epithelioid and spindle cell nevus"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2005"	"2013"	"2"	"3"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"4893"	"NRAS"	"0.42"	"0.69"	"C0265329"	"Organoid Nevus Phakomatosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4893"	"NRAS"	"0.42"	"0.69"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"7"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C0334082"	"NEVUS, EPIDERMAL (disorder)"	"disease"	"C04"	"Disease or Syndrome"	"0.60"		"2003"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0343114"	"Woolly hair nevus"	"disease"		"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"3"	"UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0346099"	"Nevus spilus"	"disease"		"Neoplastic Process"	"0.50"		"2009"	"2013"	"2"	"3"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.80"	"1"	"1985"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0362030"	"Verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0473574"	"Inflammatory linear verrucous epidermal nevus"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C0544862"	"Neurocutaneous melanosis"	"phenotype"	"C10;C16;C17"	"Pathologic Function"	"0.60"		"2003"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2017"	"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C1318558"	"Congenital melanocytic nevus"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"4893"	"NRAS"	"0.42"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4893"	"NRAS"	"0.42"	"0.69"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9545455"	"1993"	"2018"	"0"	"1"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C1842036"	"GIANT PIGMENTED HAIRY NEVUS"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"		"1987"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C1846545"	"Autoimmune Lymphoproliferative Syndrome Type 2B"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C2674723"	"RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER"	"disease"		"Disease or Syndrome"	"0.60"		"1985"	"2011"	"1"	"1"	"ORPHANET;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C2717884"	"Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C2750732"	"Noonan Syndrome 6"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.60"		"1985"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C3179502"	"Linear Verrucous Epidermal Nevus"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4893"	"NRAS"	"0.42"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4893"	"NRAS"	"0.42"	"0.69"	"C3854181"	"Nevus sebaceous"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C4011754"	"Nevus, Keratinocytic, Nonepidermolytic"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2012"	"2012"	"1"	"3"	"CTD_human;UNIPROT"
"4893"	"NRAS"	"0.42"	"0.69"	"C4225426"	"THYROID CANCER, NONMEDULLARY, 2"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human;UNIPROT"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"4897"	"NRCAM"	"0.685"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4898"	"NRDC"	"0.762"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"4899"	"NRF1"	"0.659"	"0.586"	"C0006079"	"Bowen's Disease"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4900"	"NRGN"	"0.696"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"4900"	"NRGN"	"0.696"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4900"	"NRGN"	"0.696"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9444444"	"2008"	"2018"	"1"	"1"	"CTD_human"
"4901"	"NRL"	"0.659"	"0.345"	"C0028077"	"Night Blindness"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2003"	"2005"	"2"	"0"	"CTD_human"
"4901"	"NRL"	"0.659"	"0.345"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4901"	"NRL"	"0.659"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.66"	"0.5"	"1999"	"2013"	"2"	"1"	"CTD_human;ORPHANET"
"4901"	"NRL"	"0.659"	"0.345"	"C1834329"	"RETINITIS PIGMENTOSA 27"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2014"	"8"	"7"	"CTD_human;UNIPROT"
"4901"	"NRL"	"0.659"	"0.345"	"C1834330"	"Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"1999"	"2013"	"8"	"8"	"UNIPROT"
"4902"	"NRTN"	"0.743"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4902"	"NRTN"	"0.743"	"0.31"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.44"	"1"	"1998"	"2011"	"0"	"0"	"ORPHANET"
"4902"	"NRTN"	"0.743"	"0.31"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4904"	"YBX1"	"0.582"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9545455"	"2002"	"2018"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4904"	"YBX1"	"0.582"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4905"	"NSF"	"0.707"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4905"	"NSF"	"0.707"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4907"	"NT5E"	"0.542"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4907"	"NT5E"	"0.542"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4907"	"NT5E"	"0.542"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4907"	"NT5E"	"0.542"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4907"	"NT5E"	"0.542"	"0.69"	"C1859372"	"Calcification of Joints and Arteries"	"disease"	"C05;C14;C18"	"Disease or Syndrome"	"0.72"	"1"	"2011"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"4908"	"NTF3"	"0.525"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2004"	"2013"	"2"	"0"	"PSYGENET"
"4908"	"NTF3"	"0.525"	"0.621"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1997"	"1997"	"2"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8333333"	"1994"	"2008"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"PSYGENET"
"4908"	"NTF3"	"0.525"	"0.621"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"PSYGENET"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2015"	"1"	"0"	"PSYGENET"
"4908"	"NTF3"	"0.525"	"0.621"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4908"	"NTF3"	"0.525"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2006"	"2"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4909"	"NTF4"	"0.69"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.50"		"1997"	"1997"	"1"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4909"	"NTF4"	"0.69"	"0.483"	"C2751294"	"GLAUCOMA 1, OPEN ANGLE, O"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2009"	"2010"	"1"	"5"	"CTD_human;UNIPROT"
"4909"	"NTF4"	"0.69"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4913"	"NTHL1"	"0.676"	"0.276"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4913"	"NTHL1"	"0.676"	"0.276"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"4913"	"NTHL1"	"0.676"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"4913"	"NTHL1"	"0.676"	"0.276"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4913"	"NTHL1"	"0.676"	"0.276"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4913"	"NTHL1"	"0.676"	"0.276"	"C4225157"	"FAMILIAL ADENOMATOUS POLYPOSIS 3"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"4"	"1"	"CLINGEN;ORPHANET"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2018"	"0"	"0"	"ORPHANET"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2014"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0020074"	"HSAN Type IV"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9722222"	"1978"	"2018"	"14"	"21"	"CTD_human;ORPHANET;UNIPROT"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2001"	"2002"	"0"	"0"	"CTD_human;ORPHANET"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0027889"	"Hereditary Sensory and Autonomic Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0086405"	"Hereditary Sensory Radicular Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.9473684"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0699739"	"Sensory Neuropathy, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4914"	"NTRK1"	"0.443"	"0.759"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4914"	"NTRK1"	"0.443"	"0.759"	"C1833921"	"Familial medullary thyroid carcinoma"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.56"	"1"	"1995"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"4914"	"NTRK1"	"0.443"	"0.759"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4914"	"NTRK1"	"0.443"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1996"	"2000"	"4"	"0"	"GENOMICS_ENGLAND"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2009"	"2016"	"3"	"0"	"CTD_human;PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2010"	"2018"	"5"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0020505"	"Hyperphagia"	"phenotype"	"C23"	"Finding"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9166667"	"1994"	"2015"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.43"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.5"	"2003"	"2015"	"2"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0678807"	"prenatal alcohol exposure"	"phenotype"		"Finding"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2013"	"2017"	"0"	"0"	"UNIPROT"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"2"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4915"	"NTRK2"	"0.514"	"0.586"	"C3146244"	"Alcohol Related Birth Defect"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4915"	"NTRK2"	"0.514"	"0.586"	"C3151303"	"Obesity, Hyperphagia, and Developmental Delay"	"disease"	"C18;C23;F03"	"Disease or Syndrome"	"0.60"		"2005"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0016057"	"Fibrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1999"	"2016"	"3"	"2"	"PSYGENET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"4916"	"NTRK3"	"0.547"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"4916"	"NTRK3"	"0.547"	"0.586"	"C1332965"	"Congenital Mesoblastic Nephroma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"0.8571429"	"1998"	"2004"	"0"	"0"	"ORPHANET"
"4919"	"ROR1"	"0.616"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4919"	"ROR1"	"0.616"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.54"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human;UNIPROT"
"4919"	"ROR1"	"0.616"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"4919"	"ROR1"	"0.616"	"0.552"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4919"	"ROR1"	"0.616"	"0.552"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4919"	"ROR1"	"0.616"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"4919"	"ROR1"	"0.616"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4919"	"ROR1"	"0.616"	"0.552"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4919"	"ROR1"	"0.616"	"0.552"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4919"	"ROR1"	"0.616"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4919"	"ROR1"	"0.616"	"0.552"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"4919"	"ROR1"	"0.616"	"0.552"	"C4539997"	"DEAFNESS, AUTOSOMAL RECESSIVE 108"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"UNIPROT"
"4920"	"ROR2"	"0.534"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4920"	"ROR2"	"0.534"	"0.69"	"C1300267"	"Brachydactyly syndrome type B"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4920"	"ROR2"	"0.534"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"4920"	"ROR2"	"0.534"	"0.69"	"C1849334"	"Robinow syndrome, autosomal recessive"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.99"	"1"	"2000"	"2016"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"4920"	"ROR2"	"0.534"	"0.69"	"C1862112"	"BRACHYDACTYLY, TYPE B1"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"	"0.9285714"	"1978"	"2014"	"0"	"7"	"CTD_human"
"4920"	"ROR2"	"0.534"	"0.69"	"C3151609"	"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS"	"disease"		"Disease or Syndrome"	"0.60"		"2000"	"2011"	"2"	"3"	"UNIPROT"
"4920"	"ROR2"	"0.534"	"0.69"	"C3151610"	"ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.60"		"2000"	"2011"	"2"	"3"	"UNIPROT"
"4920"	"ROR2"	"0.534"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2000"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"4921"	"DDR2"	"0.579"	"0.621"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.48"	"1"	"2008"	"2018"	"0"	"1"	"CGI"
"4921"	"DDR2"	"0.579"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4921"	"DDR2"	"0.579"	"0.621"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.48"	"1"	"2012"	"2018"	"0"	"5"	"CGI"
"4921"	"DDR2"	"0.579"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"4921"	"DDR2"	"0.579"	"0.621"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4921"	"DDR2"	"0.579"	"0.621"	"C1849011"	"SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.72"	"1"	"1996"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"4921"	"DDR2"	"0.579"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4922"	"NTS"	"0.557"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2014"	"2"	"0"	"PSYGENET"
"4922"	"NTS"	"0.557"	"0.621"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4922"	"NTS"	"0.557"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4922"	"NTS"	"0.557"	"0.621"	"C0026837"	"Muscle Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1999"	"2015"	"4"	"0"	"PSYGENET"
"4922"	"NTS"	"0.557"	"0.621"	"C0151564"	"Cogwheel Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0231519"	"Gegenhalten"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0233608"	"Catatonic Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0239325"	"Extensor Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0277821"	"Extrapyramidal Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1983"	"1986"	"2"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4922"	"NTS"	"0.557"	"0.621"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1983"	"1986"	"2"	"0"	"CTD_human"
"4922"	"NTS"	"0.557"	"0.621"	"C1320474"	"Nuchal Rigidity"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"PSYGENET"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4923"	"NTSR1"	"0.598"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4924"	"NUCB1"	"0.799"	"0.241"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4924"	"NUCB1"	"0.799"	"0.241"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4924"	"NUCB1"	"0.799"	"0.241"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4924"	"NUCB1"	"0.799"	"0.241"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4924"	"NUCB1"	"0.799"	"0.241"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4925"	"NUCB2"	"0.681"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4925"	"NUCB2"	"0.681"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"4926"	"NUMA1"	"0.701"	"0.448"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.61"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human;ORPHANET"
"4926"	"NUMA1"	"0.701"	"0.448"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4927"	"NUP88"	"0.752"	"0.207"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4927"	"NUP88"	"0.752"	"0.207"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"4928"	"NUP98"	"0.586"	"0.414"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9876543"	"1996"	"2018"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4928"	"NUP98"	"0.586"	"0.414"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2000"	"2006"	"1"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.9642857"	"1999"	"2018"	"8"	"0"	"GENOMICS_ENGLAND"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"1999"	"2015"	"5"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4929"	"NR4A2"	"0.559"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4929"	"NR4A2"	"0.559"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4935"	"GPR143"	"0.727"	"0.241"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.50"	"1"	"2002"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"4935"	"GPR143"	"0.727"	"0.241"	"C0342684"	"Ocular albinism, type I"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.99"	"1"	"1996"	"2017"	"12"	"24"	"CTD_human;ORPHANET;UNIPROT"
"4935"	"GPR143"	"0.727"	"0.241"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2011"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"4935"	"GPR143"	"0.727"	"0.241"	"C3151752"	"NYSTAGMUS 6, CONGENITAL, X-LINKED"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"4938"	"OAS1"	"0.642"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2010"	"0"	"0"	"CTD_human"
"4938"	"OAS1"	"0.642"	"0.586"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"0"	"2013"	"2015"	"1"	"0"	"CTD_human"
"4938"	"OAS1"	"0.642"	"0.586"	"C0042769"	"Virus Diseases"	"group"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"4938"	"OAS1"	"0.642"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4938"	"OAS1"	"0.642"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4938"	"OAS1"	"0.642"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4939"	"OAS2"	"0.69"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4939"	"OAS2"	"0.69"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4939"	"OAS2"	"0.69"	"0.414"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4939"	"OAS2"	"0.69"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4939"	"OAS2"	"0.69"	"0.414"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4939"	"OAS2"	"0.69"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4940"	"OAS3"	"0.713"	"0.379"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4942"	"OAT"	"0.652"	"0.448"	"C0018425"	"Gyrate Atrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"1.00"	"0.972973"	"1981"	"2017"	"7"	"29"	"CTD_human;ORPHANET;UNIPROT"
"4942"	"OAT"	"0.652"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4942"	"OAT"	"0.652"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4942"	"OAT"	"0.652"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"4942"	"OAT"	"0.652"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4942"	"OAT"	"0.652"	"0.448"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4942"	"OAT"	"0.652"	"0.448"	"C0599035"	"Hyperornithinemia"	"phenotype"	"C11;C16"	"Disease or Syndrome"	"0.77"	"1"	"1981"	"2013"	"7"	"61"	"CTD_human;ORPHANET;UNIPROT"
"4943"	"TBC1D25"	"0.857"	"0.207"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4948"	"OCA2"	"0.57"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2018"	"0"	"0"	"UNIPROT"
"4948"	"OCA2"	"0.57"	"0.586"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.31"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"4948"	"OCA2"	"0.57"	"0.586"	"C0268495"	"Oculocutaneous albinism type 2"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2017"	"10"	"44"	"CTD_human;ORPHANET;UNIPROT"
"4948"	"OCA2"	"0.57"	"0.586"	"C0268497"	"Brown oculocutaneous albinism"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.50"		"1995"	"2013"	"10"	"28"	"UNIPROT"
"4948"	"OCA2"	"0.57"	"0.586"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4952"	"OCRL"	"0.577"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4952"	"OCRL"	"0.577"	"0.586"	"C0028860"	"Oculocerebrorenal Syndrome"	"disease"	"C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9384615"	"1993"	"2018"	"11"	"42"	"CTD_human;ORPHANET;UNIPROT"
"4952"	"OCRL"	"0.577"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.43"	"0.6666667"	"2005"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"4952"	"OCRL"	"0.577"	"0.586"	"C1845167"	"Dent Disease 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2015"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"4952"	"OCRL"	"0.577"	"0.586"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4952"	"OCRL"	"0.577"	"0.586"	"C2713392"	"Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency"	"disease"	"C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"1997"	"2011"	"11"	"33"	"CTD_human;UNIPROT"
"4952"	"OCRL"	"0.577"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1999"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"4953"	"ODC1"	"0.532"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1987"	"2009"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1990"	"1995"	"2"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1985"	"2003"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2012"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.5"	"1990"	"2012"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"1995"	"2007"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1990"	"2008"	"2"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"1990"	"2012"	"1"	"0"	"CTD_human"
"4953"	"ODC1"	"0.532"	"0.759"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4967"	"OGDH"	"0.743"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4967"	"OGDH"	"0.743"	"0.276"	"C2752074"	"ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"4968"	"OGG1"	"0.476"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.62"	"1"	"2004"	"2011"	"0"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.38"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2009"	"2"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2002"	"2004"	"2"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9459459"	"1998"	"2016"	"2"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.61"	"1"	"2000"	"2009"	"0"	"1"	"CGI;CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"4968"	"OGG1"	"0.476"	"0.759"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"4969"	"OGN"	"0.785"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.48"	"0.8571429"	"2003"	"2014"	"2"	"2"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4973"	"OLR1"	"0.59"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4976"	"OPA1"	"0.555"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4976"	"OPA1"	"0.555"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"4976"	"OPA1"	"0.555"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"4976"	"OPA1"	"0.555"	"0.621"	"C0221061"	"Behr syndrome"	"disease"	"C09;C10;C11;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"1998"	"2015"	"3"	"5"	"CTD_human;UNIPROT"
"4976"	"OPA1"	"0.555"	"0.621"	"C0338508"	"Optic Atrophy, Autosomal Dominant"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.80"	"0.984"	"1993"	"2018"	"22"	"54"	"CTD_human;ORPHANET;UNIPROT"
"4976"	"OPA1"	"0.555"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2017"	"0"	"4"	"GENOMICS_ENGLAND"
"4976"	"OPA1"	"0.555"	"0.621"	"C1832466"	"CAPOS syndrome"	"disease"	"C05;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4976"	"OPA1"	"0.555"	"0.621"	"C1847730"	"GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"4976"	"OPA1"	"0.555"	"0.621"	"C1852267"	"OPTIC ATROPHY 1 AND DEAFNESS"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"		"1984"	"2014"	"0"	"10"	"CTD_human"
"4976"	"OPA1"	"0.555"	"0.621"	"C3276549"	"OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2001"	"2018"	"8"	"7"	"UNIPROT"
"4976"	"OPA1"	"0.555"	"0.621"	"C4225163"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"4977"	"OPA2"	"0.928"	"0.103"	"C1839576"	"OPTIC ATROPHY 2 (disorder)"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"4978"	"OPCML"	"0.663"	"0.517"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2003"	"2014"	"0"	"0"	"CGI"
"4978"	"OPCML"	"0.663"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2016"	"1"	"1"	"PSYGENET"
"4978"	"OPCML"	"0.663"	"0.517"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"4978"	"OPCML"	"0.663"	"0.517"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2013"	"1"	"1"	"UNIPROT"
"4978"	"OPCML"	"0.663"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.63"	"0"	"2003"	"2007"	"0"	"1"	"CGI;CTD_human"
"4978"	"OPCML"	"0.663"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.63"	"1"	"2003"	"2014"	"1"	"1"	"CGI;CTD_human;UNIPROT"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2005"	"2013"	"3"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2013"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.50"	"0.9807692"	"1997"	"2018"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0268414"	"Hyperphosphatasemia with bone disease"	"disease"	"C05"	"Disease or Syndrome"	"0.70"	"0.9473684"	"2002"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4982"	"TNFRSF11B"	"0.467"	"0.69"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"4983"	"OPHN1"	"0.656"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4983"	"OPHN1"	"0.656"	"0.414"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4983"	"OPHN1"	"0.656"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.49"	"1"	"1999"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"4983"	"OPHN1"	"0.656"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"4983"	"OPHN1"	"0.656"	"0.414"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"4983"	"OPHN1"	"0.656"	"0.414"	"C1845366"	"Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"		"2003"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"4983"	"OPHN1"	"0.656"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9285714"	"1999"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2007"	"2009"	"4"	"0"	"PSYGENET"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2018"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0020651"	"Hypotension, Orthostatic"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2013"	"2"	"0"	"PSYGENET"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"2"	"0"	"CTD_human"
"4985"	"OPRD1"	"0.672"	"0.414"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.37"	"0.8571429"	"1998"	"2017"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2010"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1998"	"2010"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.31"	"1"	"1998"	"2014"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2012"	"4"	"0"	"PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"1997"	"2014"	"7"	"0"	"CTD_human;PSYGENET"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4986"	"OPRK1"	"0.596"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2008"	"3"	"0"	"PSYGENET"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0086439"	"Hypokinesia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0233565"	"Bradykinesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"4987"	"OPRL1"	"0.743"	"0.379"	"C0751701"	"Hypokinesia, Antiorthostatic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0001849"	"AIDS Dementia Complex"	"disease"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2014"	"5"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1998"	"2017"	"6"	"0"	"CTD_human;PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2009"	"3"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0009806"	"Constipation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"4"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"4"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0020651"	"Hypotension, Orthostatic"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0026552"	"Morphine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1986"	"2015"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.33"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.34"	"1"	"1997"	"2015"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.32"	"0.5"	"2008"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2006"	"2"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9090909"	"1998"	"2017"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2004"	"2014"	"3"	"0"	"CTD_human;PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0206019"	"HIV Encephalopathy"	"disease"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2009"	"3"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0237326"	"Dyschezia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0243010"	"Viral Encephalitis"	"group"	"C02;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2006"	"2"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0600272"	"Morphine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2001"	"2013"	"6"	"0"	"CTD_human;PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C0936243"	"HIV-1-Associated Cognitive Motor Complex"	"phenotype"	"C02;C10;C20;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C1257861"	"Colonic Inertia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C1837893"	"SCHIZOPHRENIA 12"	"disease"		"Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"4988"	"OPRM1"	"0.479"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"4988"	"OPRM1"	"0.479"	"0.759"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"2007"	"2"	"0"	"CTD_human"
"4990"	"SIX6"	"0.609"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"0.5"	"2004"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"4990"	"SIX6"	"0.609"	"0.552"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"4990"	"SIX6"	"0.609"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4990"	"SIX6"	"0.609"	"0.552"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4990"	"SIX6"	"0.609"	"0.552"	"C1859311"	"Microphthalmia, Isolated, with Cataract 2"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"2"	"CTD_human"
"4990"	"SIX6"	"0.609"	"0.552"	"C1859773"	"Microphthalmia, Syndromic 3"	"disease"	"C06;C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"4990"	"SIX6"	"0.609"	"0.552"	"C4225424"	"OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"4998"	"ORC1"	"0.609"	"0.621"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.45"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"4998"	"ORC1"	"0.609"	"0.621"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4998"	"ORC1"	"0.609"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.52"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"4998"	"ORC1"	"0.609"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"4998"	"ORC1"	"0.609"	"0.621"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.75"	"1"	"2011"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"4998"	"ORC1"	"0.609"	"0.621"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"4998"	"ORC1"	"0.609"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"4998"	"ORC1"	"0.609"	"0.621"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5000"	"ORC4"	"0.645"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5000"	"ORC4"	"0.645"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"5000"	"ORC4"	"0.645"	"0.517"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"5000"	"ORC4"	"0.645"	"0.517"	"C3151097"	"MEIER-GORLIN SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2015"	"2"	"4"	"UNIPROT"
"5000"	"ORC4"	"0.645"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2011"	"0"	"0"	"CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2015"	"1"	"1"	"UNIPROT"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"UNIPROT"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0206656"	"Embryonal Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.45"	"1"	"1997"	"2011"	"0"	"0"	"CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.60"		"1998"	"1998"	"1"	"1"	"CGI;UNIPROT"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"0"	"0"	"CTD_human"
"5002"	"SLC22A18"	"0.621"	"0.483"	"C1849385"	"Rhabdomyosarcoma 1"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C0085605"	"Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5004"	"ORM1"	"0.696"	"0.483"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5007"	"OSBP"	"0.773"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5008"	"OSM"	"0.552"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"5008"	"OSM"	"0.552"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.70"	"1"	"1980"	"2018"	"11"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5009"	"OTC"	"0.627"	"0.552"	"C0268542"	"Ornithine carbamoyltransferase deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1983"	"2017"	"33"	"123"	"CTD_human;ORPHANET;UNIPROT"
"5009"	"OTC"	"0.627"	"0.552"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5009"	"OTC"	"0.627"	"0.552"	"C1839530"	"VALPROATE SENSITIVITY"	"phenotype"		"Finding"	"0.50"		"1988"	"2002"	"30"	"107"	"CTD_human;UNIPROT"
"5009"	"OTC"	"0.627"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5010"	"CLDN11"	"0.713"	"0.414"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"5010"	"CLDN11"	"0.713"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5010"	"CLDN11"	"0.713"	"0.414"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"		"2005"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0022360"	"Jaw Abnormalities"	"group"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0242343"	"Panhypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2012"	"0"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0265242"	"Otocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5015"	"OTX2"	"0.54"	"0.69"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C1864690"	"Microphthalmia, Syndromic 5"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"2005"	"2015"	"6"	"10"	"CTD_human;ORPHANET;UNIPROT"
"5015"	"OTX2"	"0.54"	"0.69"	"C1876185"	"Dysgnathia complex"	"disease"	"C05;C07;C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5015"	"OTX2"	"0.54"	"0.69"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5015"	"OTX2"	"0.54"	"0.69"	"C3151380"	"SCHIZOPHRENIA 15"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5015"	"OTX2"	"0.54"	"0.69"	"C3151440"	"PITUITARY HORMONE DEFICIENCY, COMBINED, 6"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2012"	"2"	"2"	"UNIPROT"
"5015"	"OTX2"	"0.54"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2010"	"6"	"0"	"GENOMICS_ENGLAND"
"5015"	"OTX2"	"0.54"	"0.69"	"C4225436"	"RETINAL DYSTROPHY, EARLY-ONSET, WITH OR WITHOUT PITUITARY DYSFUNCTION"	"phenotype"		"Finding"	"0.30"		"2005"	"2015"	"6"	"4"	"UNIPROT"
"5015"	"OTX2"	"0.54"	"0.69"	"C4511237"	"Butterfly-shaped pigmentary macular dystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5016"	"OVGP1"	"0.834"	"0.207"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5016"	"OVGP1"	"0.834"	"0.207"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5016"	"OVGP1"	"0.834"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5017"	"OVOL1"	"0.834"	"0.207"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2018"	"1"	"1"	"CTD_human"
"5017"	"OVOL1"	"0.834"	"0.207"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5017"	"OVOL1"	"0.834"	"0.207"	"C0206711"	"Pilomatrixoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5018"	"OXA1L"	"0.656"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0342792"	"Succinyl-CoA:3-oxoacid CoA transferase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1992"	"2011"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5019"	"OXCT1"	"0.735"	"0.276"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5019"	"OXCT1"	"0.735"	"0.276"	"C1291422"	"Deficiency of 3-oxoacid CoA-transferase"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5019"	"OXCT1"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5020"	"OXT"	"0.528"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0009421"	"Comatose"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1972"	"2009"	"3"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2010"	"2018"	"5"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2010"	"2018"	"5"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0013390"	"Dysmenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1971"	"1972"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1970"	"1983"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0015927"	"Fetal Death"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"1972"	"1972"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0015930"	"Fetal Distress"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0018681"	"Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2012"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0020625"	"Hyponatremia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1983"	"2009"	"3"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"2004"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0026826"	"Muscle Hypertonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0028838"	"Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"1985"	"2018"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0032617"	"Polyuria"	"phenotype"	"C12;C13;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0033575"	"Prostatic Diseases"	"group"	"C12"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0037763"	"Spasm"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1969"	"1996"	"4"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0039338"	"Taste Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"3"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0043049"	"Water Intoxication"	"disease"	"C18;C25"	"Disease or Syndrome"	"0.30"		"1970"	"1985"	"8"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1971"	"1972"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0151911"	"Generalized Spasms"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1969"	"1996"	"4"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234297"	"Taste Disorder, Primary"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234298"	"Taste Disorder, Primary, Sweet"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234299"	"Taste Disorder, Primary, Salt"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234300"	"Taste Disorder, Primary, Bitter"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234302"	"Taste Disorder, Anterior Tongue"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234303"	"Taste Disorder, Secondary"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234304"	"Taste Disorder, Secondary, Sweet"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234305"	"Taste Disorder, Secondary, Salt"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234306"	"Taste Disorder, Secondary, Bitter"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234319"	"Taste Disorder, Posterior Tongue"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0235229"	"Ciliary Body Spasm"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1969"	"1996"	"4"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0240327"	"Taste, Metallic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0423618"	"Throbbing Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0423623"	"Bilateral Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0474366"	"Generalized Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2018"	"1"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1970"	"1983"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1970"	"1983"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1970"	"1983"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751186"	"Orthostatic Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751187"	"Periorbital Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751189"	"Retro-Ocular Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751190"	"Sharp Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751192"	"Vertex Headache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751325"	"Hypertonia, Detrusor Muscle"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751326"	"Hypertonia, Infantile"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751327"	"Hypertonia, Neonatal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751328"	"Hypertonia, Sphincter"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751329"	"Hypertonia, Transient"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1985"	"2007"	"2"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0860634"	"Psychogenic coma"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1972"	"2009"	"3"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C0877781"	"Hemicrania"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"3"	"0"	"PSYGENET"
"5020"	"OXT"	"0.528"	"0.621"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5020"	"OXT"	"0.528"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"2009"	"6"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.952381"	"2005"	"2018"	"6"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"5021"	"OXTR"	"0.582"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"5021"	"OXTR"	"0.582"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"2"	"0"	"PSYGENET"
"5021"	"OXTR"	"0.582"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"2"	"0"	"PSYGENET"
"5021"	"OXTR"	"0.582"	"0.621"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9375"	"2008"	"2018"	"1"	"0"	"CTD_human"
"5021"	"OXTR"	"0.582"	"0.621"	"C2931337"	"Chromosome 3, monosomy 3p25"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5023"	"P2RX1"	"0.696"	"0.414"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5023"	"P2RX1"	"0.696"	"0.414"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5023"	"P2RX1"	"0.696"	"0.414"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5023"	"P2RX1"	"0.696"	"0.414"	"C1853278"	"Bleeding Disorder Due To P2RY12 Defect"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0476201"	"Axonotmesis"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751792"	"Trauma, Nervous System"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C0751793"	"Craniocervical Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C1142379"	"Neurotmesis"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5024"	"P2RX3"	"0.672"	"0.448"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5025"	"P2RX4"	"0.645"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0020630"	"Hypophosphatasia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.58"	"0.375"	"2000"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2006"	"2017"	"5"	"0"	"PSYGENET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5027"	"P2RX7"	"0.503"	"0.759"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5027"	"P2RX7"	"0.503"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5027"	"P2RX7"	"0.503"	"0.759"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5028"	"P2RY1"	"0.642"	"0.586"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5028"	"P2RY1"	"0.642"	"0.586"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5030"	"P2RY4"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5032"	"P2RY11"	"0.752"	"0.31"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.55"	"0.8"	"2011"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"5032"	"P2RY11"	"0.752"	"0.31"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2017"	"1"	"2"	"CTD_human;ORPHANET"
"5033"	"P4HA1"	"0.799"	"0.241"	"C1866294"	"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5034"	"P4HB"	"0.57"	"0.759"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5034"	"P4HB"	"0.57"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5034"	"P4HB"	"0.57"	"0.759"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5034"	"P4HB"	"0.57"	"0.759"	"C1862178"	"Cole Carpenter syndrome"	"disease"	"C05;C10;C11;C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"5034"	"P4HB"	"0.57"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5034"	"P4HB"	"0.57"	"0.759"	"C4317154"	"COLE-CARPENTER SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2015"	"2018"	"1"	"1"	"UNIPROT"
"5036"	"PA2G4"	"0.69"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5036"	"PA2G4"	"0.69"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5036"	"PA2G4"	"0.69"	"0.345"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5036"	"PA2G4"	"0.69"	"0.345"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5037"	"PEBP1"	"0.525"	"0.724"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5045"	"FURIN"	"0.685"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"1998"	"2018"	"1"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9230769"	"1998"	"2018"	"1"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5047"	"PAEP"	"0.505"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2008"	"1"	"0"	"PSYGENET"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0265219"	"Miller Dieker syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.96"	"1994"	"2017"	"0"	"0"	"ORPHANET"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0266463"	"Lissencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.70"	"1"	"1984"	"2016"	"0"	"0"	"CTD_human"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0266483"	"Pachygyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.64"	"1"	"1998"	"2014"	"0"	"0"	"CTD_human"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0431375"	"Classical Lissencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9333333"	"1993"	"2017"	"7"	"94"	"ORPHANET;UNIPROT"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C1848201"	"Subcortical Band Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1997"	"2014"	"7"	"8"	"ORPHANET;UNIPROT"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C1879312"	"Agyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C2750748"	"Chromosome 17p13.3 Duplication Syndrome"	"disease"	"C10;C16;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5048"	"PAFAH1B1"	"0.516"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"0.3333333"	"2008"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2003"	"2012"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0036323"	"Schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C1848561"	"Methylmalonic acidemia with homocystinuria"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"1"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2005"	"2016"	"1"	"0"	"CTD_human"
"5052"	"PRDX1"	"0.577"	"0.69"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5053"	"PAH"	"0.575"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5053"	"PAH"	"0.575"	"0.552"	"C0031485"	"Phenylketonurias"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9846154"	"1975"	"2018"	"0"	"207"	"CTD_human;ORPHANET"
"5053"	"PAH"	"0.575"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5053"	"PAH"	"0.575"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1993"	"2014"	"2"	"0"	"PSYGENET"
"5053"	"PAH"	"0.575"	"0.552"	"C0085547"	"Phenylketonuria, Maternal"	"disease"	"C10;C13;C16;C18"	"Disease or Syndrome"	"0.78"	"0.75"	"1987"	"2014"	"43"	"183"	"ORPHANET;UNIPROT"
"5053"	"PAH"	"0.575"	"0.552"	"C0268465"	"Phenylketonuria II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5053"	"PAH"	"0.575"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5053"	"PAH"	"0.575"	"0.552"	"C0751434"	"Classical phenylketonuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9875776"	"1982"	"2017"	"43"	"183"	"CTD_human;ORPHANET;UNIPROT"
"5053"	"PAH"	"0.575"	"0.552"	"C0751435"	"Hyperphenylalaninaemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.990099"	"1990"	"2018"	"0"	"16"	"CTD_human;ORPHANET"
"5053"	"PAH"	"0.575"	"0.552"	"C0751436"	"Hyperphenylalaninemia, Non-Phenylketonuric"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"5053"	"PAH"	"0.575"	"0.552"	"C2678416"	"Hyperphenylalaninemia, Non-Pku Mild"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1988"	"2014"	"43"	"183"	"UNIPROT"
"5053"	"PAH"	"0.575"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"1995"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2003"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.6666667"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2009"	"2011"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.96"	"1998"	"2015"	"2"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9166667"	"1991"	"2011"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9538462"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.33"		"2003"	"2008"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2006"	"2009"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.34"		"2002"	"2012"	"2"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2012"	"2"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"0.75"	"1998"	"2015"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5054"	"SERPINE1"	"0.384"	"0.793"	"C2750067"	"Plasminogen Activator Inhibitor-1 Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"0.75"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5055"	"SERPINB2"	"0.535"	"0.621"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"0"	"0"	"CGI"
"5058"	"PAK1"	"0.532"	"0.655"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5058"	"PAK1"	"0.532"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5058"	"PAK1"	"0.532"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"5062"	"PAK2"	"0.735"	"0.31"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5062"	"PAK2"	"0.735"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"5063"	"PAK3"	"0.633"	"0.552"	"C0796237"	"Mental Retardation, X-Linked 30"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1996"	"2015"	"3"	"5"	"CTD_human;UNIPROT"
"5063"	"PAK3"	"0.633"	"0.552"	"C0796249"	"Mental Retardation, X-Linked 47"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2004"	"3"	"2"	"UNIPROT"
"5063"	"PAK3"	"0.633"	"0.552"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5063"	"PAK3"	"0.633"	"0.552"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2005"	"0"	"0"	"ORPHANET"
"5063"	"PAK3"	"0.633"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9166667"	"1999"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5066"	"PAM"	"0.594"	"0.621"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5066"	"PAM"	"0.594"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5067"	"CNTN3"	"0.857"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5067"	"CNTN3"	"0.857"	"0.138"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5067"	"CNTN3"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0002965"	"Angina, Unstable"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0086666"	"Myocardial Preinfarction Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"5069"	"PAPPA"	"0.614"	"0.448"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"0"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2004"	"2015"	"2"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"0.9642857"	"1998"	"2018"	"13"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5071"	"PRKN"	"0.464"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2015"	"2"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.9428571"	"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"2016"	"8"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.45"	"1"	"1999"	"2016"	"8"	"2"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2004"	"0"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"5071"	"PRKN"	"0.464"	"0.793"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2017"	"37"	"25"	"CTD_human;UNIPROT"
"5071"	"PRKN"	"0.464"	"0.793"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.40"	"0.7692308"	"1999"	"2016"	"3"	"4"	"UNIPROT"
"5071"	"PRKN"	"0.464"	"0.793"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1998"	"2018"	"0"	"0"	"ORPHANET"
"5073"	"PARN"	"0.627"	"0.517"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5073"	"PARN"	"0.627"	"0.517"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.44"	"1"	"2015"	"2016"	"0"	"2"	"ORPHANET"
"5073"	"PARN"	"0.627"	"0.517"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5073"	"PARN"	"0.627"	"0.517"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"5073"	"PARN"	"0.627"	"0.517"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"5073"	"PARN"	"0.627"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5073"	"PARN"	"0.627"	"0.517"	"C4225347"	"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"5073"	"PARN"	"0.627"	"0.517"	"C4225356"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"5074"	"PAWR"	"0.562"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2008"	"2"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9444444"	"1998"	"2018"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"5074"	"PAWR"	"0.562"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"5074"	"PAWR"	"0.562"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"5075"	"PAX1"	"0.627"	"0.517"	"C1833691"	"Otofaciocervical Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"5075"	"PAX1"	"0.627"	"0.517"	"C2931416"	"Fara Chlupackova syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5075"	"PAX1"	"0.627"	"0.517"	"C3714942"	"OTOFACIOCERVICAL SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5076"	"PAX2"	"0.516"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5076"	"PAX2"	"0.516"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.35"	"1"	"1995"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5076"	"PAX2"	"0.516"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.43"	"1"	"2014"	"2016"	"0"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C0431692"	"Bilateral renal hypoplasia"	"disease"		"Congenital Abnormality"	"0.50"		"1995"	"2010"	"0"	"0"	"ORPHANET"
"5076"	"PAX2"	"0.516"	"0.69"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C1852759"	"Papillorenal syndrome"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"1.00"	"1"	"1988"	"2018"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"5076"	"PAX2"	"0.516"	"0.69"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5076"	"PAX2"	"0.516"	"0.69"	"C2608080"	"RENAL HYPOPLASIA, ISOLATED (disorder)"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5076"	"PAX2"	"0.516"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5076"	"PAX2"	"0.516"	"0.69"	"C4014925"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"1"	"5"	"UNIPROT"
"5077"	"PAX3"	"0.521"	"0.655"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.40"	"0.9230769"	"1988"	"2018"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5077"	"PAX3"	"0.521"	"0.655"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1984"	"2007"	"4"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0079661"	"Klein's Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2008"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5077"	"PAX3"	"0.521"	"0.655"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.37"	"1"	"1984"	"2015"	"4"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0206655"	"Alveolar rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.90"	"0.9519231"	"1993"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"5077"	"PAX3"	"0.521"	"0.655"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1984"	"2007"	"4"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0599973"	"Waardenburg Anophthalmia Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5077"	"PAX3"	"0.521"	"0.655"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1988"	"2004"	"3"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C1710096"	"Sinonasal undifferentiated carcinoma"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C1847800"	"Waardenburg Syndrome Type 1"	"disease"	"C16"	"Disease or Syndrome"	"1.00"	"0.9756098"	"1964"	"2018"	"20"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5077"	"PAX3"	"0.521"	"0.655"	"C1852510"	"Craniofacial deafness hand syndrome"	"disease"	"C05;C09;C10;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"1983"	"2008"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5077"	"PAX3"	"0.521"	"0.655"	"C3266898"	"Waardenburg Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"	"0.9761905"	"1992"	"2016"	"1"	"1"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5077"	"PAX3"	"0.521"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"5077"	"PAX3"	"0.521"	"0.655"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5078"	"PAX4"	"0.707"	"0.207"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2004"	"2015"	"0"	"0"	"CTD_human"
"5078"	"PAX4"	"0.707"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"0.9285714"	"1999"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"5078"	"PAX4"	"0.707"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5078"	"PAX4"	"0.707"	"0.207"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5078"	"PAX4"	"0.707"	"0.207"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.45"	"0.8"	"1999"	"2013"	"0"	"0"	"ORPHANET"
"5078"	"PAX4"	"0.707"	"0.207"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5078"	"PAX4"	"0.707"	"0.207"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"1"	"UNIPROT"
"5078"	"PAX4"	"0.707"	"0.207"	"C2677132"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.61"	"1"	"2007"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"5078"	"PAX4"	"0.707"	"0.207"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"5078"	"PAX4"	"0.707"	"0.207"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"1"	"UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2007"	"0"	"0"	"ORPHANET"
"5079"	"PAX5"	"0.507"	"0.621"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"0.8"	"2001"	"2017"	"1"	"0"	"CTD_human"
"5079"	"PAX5"	"0.507"	"0.621"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5079"	"PAX5"	"0.507"	"0.621"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"5079"	"PAX5"	"0.507"	"0.621"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"CGI"
"5079"	"PAX5"	"0.507"	"0.621"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5079"	"PAX5"	"0.507"	"0.621"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"5079"	"PAX5"	"0.507"	"0.621"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5079"	"PAX5"	"0.507"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"0.9333333"	"2001"	"2016"	"2"	"1"	"CGI;CTD_human;UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C2751594"	"LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C2751595"	"LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C2751596"	"LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C2751597"	"LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5079"	"PAX5"	"0.507"	"0.621"	"C2751598"	"LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0003076"	"Aniridia"	"disease"	"C11;C16"	"Congenital Abnormality"	"1.00"	"0.9722222"	"1978"	"2018"	"18"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5080"	"PAX6"	"0.479"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.62"	"1"	"2002"	"2015"	"1"	"1"	"GENOMICS_ENGLAND;UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0029132"	"Disorder of the optic nerve"	"group"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1999"	"2014"	"1"	"0"	"PSYGENET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5080"	"PAX6"	"0.479"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"1995"	"1997"	"2"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.44"	"1"	"2000"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"5080"	"PAX6"	"0.479"	"0.655"	"C0152112"	"Foster-Kennedy Syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0155299"	"Coloboma of optic disc"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"2003"	"2003"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C0206115"	"WAGR Syndrome"	"disease"	"C04;C10;C11;C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"0.9230769"	"1989"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0266551"	"Congenital coloboma of iris"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0338502"	"Hypoplasia of the optic nerve"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0344516"	"Coloboma of lens"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0344559"	"Irido-corneo-trabecular dysgenesis (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.90"	"0.9"	"1983"	"2018"	"0"	"10"	"CTD_human;ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1995"	"1997"	"3"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0431401"	"Gillespie syndrome"	"disease"	"C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.52"	"1"	"1994"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0521573"	"Coloboma of eyelid"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"1995"	"1997"	"2"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0549307"	"Morning glory syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C0751402"	"Optic Disk Disorders"	"group"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C1833797"	"Optic Nerve Hypoplasia, Bilateral"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.60"		"2003"	"2003"	"1"	"2"	"CTD_human;UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C1833798"	"Optic Nerve Aplasia, Bilateral"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"1"	"1"	"UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C1835698"	"Keratitis, hereditary"	"disease"	"C11"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C1852767"	"Hereditary macular coloboma"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1970"	"1988"	"3"	"0"	"GENOMICS_ENGLAND"
"5080"	"PAX6"	"0.479"	"0.655"	"C2931644"	"O'Donnell Pappas syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C2931803"	"Deletion 11p13"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5080"	"PAX6"	"0.479"	"0.655"	"C3554721"	"Morning glory anomaly"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"1"	"UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5080"	"PAX6"	"0.479"	"0.655"	"C3714873"	"Axenfeld-Rieger Syndrome, Type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5080"	"PAX6"	"0.479"	"0.655"	"C3805349"	"CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY"	"disease"		"Congenital Abnormality"	"0.40"		"1993"	"2015"	"17"	"9"	"UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C3805604"	"FOVEAL HYPOPLASIA 1"	"disease"		"Disease or Syndrome"	"0.40"		"1996"	"2005"	"2"	"2"	"UNIPROT"
"5080"	"PAX6"	"0.479"	"0.655"	"C4310809"	"ANTERIOR SEGMENT DYSGENESIS 5"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"2003"	"3"	"1"	"UNIPROT"
"5081"	"PAX7"	"0.707"	"0.345"	"C0206655"	"Alveolar rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9767442"	"1994"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"5081"	"PAX7"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5083"	"PAX9"	"0.681"	"0.345"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"	"1"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"5083"	"PAX9"	"0.681"	"0.345"	"C1970291"	"Tooth Agenesis, Selective, 3"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2009"	"1"	"8"	"CTD_human;UNIPROT"
"5083"	"PAX9"	"0.681"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5083"	"PAX9"	"0.681"	"0.345"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.50"	"1"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"5087"	"PBX1"	"0.577"	"0.655"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.51"	"1"	"1990"	"2007"	"2"	"0"	"CTD_human;ORPHANET"
"5087"	"PBX1"	"0.577"	"0.655"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"1990"	"2007"	"2"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C0431692"	"Bilateral renal hypoplasia"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5087"	"PBX1"	"0.577"	"0.655"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"0.9333333"	"1993"	"2015"	"0"	"0"	"ORPHANET"
"5087"	"PBX1"	"0.577"	"0.655"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5087"	"PBX1"	"0.577"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"5087"	"PBX1"	"0.577"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5087"	"PBX1"	"0.577"	"0.655"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5091"	"PC"	"0.565"	"0.724"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5091"	"PC"	"0.565"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5091"	"PC"	"0.565"	"0.724"	"C0034341"	"Pyruvate Carboxylase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.8888889"	"1983"	"2016"	"3"	"15"	"CTD_human;UNIPROT"
"5091"	"PC"	"0.565"	"0.724"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5091"	"PC"	"0.565"	"0.724"	"C2931141"	"Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2009"	"3"	"7"	"UNIPROT"
"5092"	"PCBD1"	"0.676"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5092"	"PCBD1"	"0.676"	"0.552"	"C1849700"	"Hyperphenylalaninemia with primapterinuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2014"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5092"	"PCBD1"	"0.676"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1998"	"2"	"0"	"GENOMICS_ENGLAND"
"5095"	"PCCA"	"0.672"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5095"	"PCCA"	"0.672"	"0.448"	"C0268579"	"Propionic acidemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"4"	"38"	"CTD_human;ORPHANET;UNIPROT"
"5095"	"PCCA"	"0.672"	"0.448"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5095"	"PCCA"	"0.672"	"0.448"	"C0311298"	"Propionic acidemia, type II"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5095"	"PCCA"	"0.672"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5095"	"PCCA"	"0.672"	"0.448"	"C2717876"	"Propionicaciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5095"	"PCCA"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2011"	"10"	"0"	"GENOMICS_ENGLAND"
"5096"	"PCCB"	"0.672"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5096"	"PCCB"	"0.672"	"0.448"	"C0268579"	"Propionic acidemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1990"	"2017"	"8"	"38"	"CTD_human;ORPHANET;UNIPROT"
"5096"	"PCCB"	"0.672"	"0.448"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5096"	"PCCB"	"0.672"	"0.448"	"C0311298"	"Propionic acidemia, type II"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5096"	"PCCB"	"0.672"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5096"	"PCCB"	"0.672"	"0.448"	"C2717876"	"Propionicaciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5096"	"PCCB"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5100"	"PCDH8"	"0.707"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"5100"	"PCDH8"	"0.707"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5100"	"PCDH8"	"0.707"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"5100"	"PCDH8"	"0.707"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"5101"	"PCDH9"	"0.834"	"0.172"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5104"	"SERPINA5"	"0.598"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5104"	"SERPINA5"	"0.598"	"0.517"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5104"	"SERPINA5"	"0.598"	"0.517"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5104"	"SERPINA5"	"0.598"	"0.517"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5105"	"PCK1"	"0.642"	"0.414"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C0268194"	"Phosphoenolpyruvate carboxykinase deficiency"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2015"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5105"	"PCK1"	"0.642"	"0.414"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5105"	"PCK1"	"0.642"	"0.414"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C0268194"	"Phosphoenolpyruvate carboxykinase deficiency"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5106"	"PCK2"	"0.701"	"0.31"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5106"	"PCK2"	"0.701"	"0.31"	"C2931278"	"Phosphoenolpyruvate carboxykinase 2 deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5108"	"PCM1"	"0.681"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"5108"	"PCM1"	"0.681"	"0.31"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"5110"	"PCMT1"	"0.743"	"0.276"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5110"	"PCMT1"	"0.743"	"0.276"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"5110"	"PCMT1"	"0.743"	"0.276"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.8666667"	"1992"	"2018"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2012"	"2"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"1999"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C1858391"	"ATAXIA-TELANGIECTASIA-LIKE DISORDER"	"disease"	"C10;C14;C16;C18;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5111"	"PCNA"	"0.417"	"0.759"	"C4014676"	"ATAXIA-TELANGIECTASIA-LIKE DISORDER 2"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"5116"	"PCNT"	"0.577"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2009"	"3"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"5116"	"PCNT"	"0.577"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5116"	"PCNT"	"0.577"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5116"	"PCNT"	"0.577"	"0.69"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.55"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5116"	"PCNT"	"0.577"	"0.69"	"C0432246"	"Microcephalic Osteodysplastic Primordial Dwarfism, Type II"	"disease"	"C05;C10;C13;C16;C19;C23"	"Congenital Abnormality"	"0.69"	"1"	"2003"	"2016"	"0"	"20"	"CTD_human;ORPHANET"
"5116"	"PCNT"	"0.577"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"5116"	"PCNT"	"0.577"	"0.69"	"C1847572"	"SECKEL SYNDROME 2"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5116"	"PCNT"	"0.577"	"0.69"	"C3502214"	"Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities"	"disease"	"C05;C10;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5116"	"PCNT"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5118"	"PCOLCE"	"0.762"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5119"	"CHMP1A"	"0.685"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5119"	"CHMP1A"	"0.685"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5119"	"CHMP1A"	"0.685"	"0.414"	"C3554209"	"Congenital pontocerebellar hypoplasia type 8"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"5119"	"CHMP1A"	"0.685"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5121"	"PCP4"	"0.743"	"0.276"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5121"	"PCP4"	"0.743"	"0.276"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5122"	"PCSK1"	"0.621"	"0.483"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5122"	"PCSK1"	"0.621"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.70"	"0.9444444"	"1997"	"2016"	"1"	"0"	"CTD_human"
"5122"	"PCSK1"	"0.621"	"0.483"	"C1833053"	"Proprotein Convertase 1 3 Deficiency"	"disease"	"C18;C19;C23"	"Disease or Syndrome"	"0.70"		"1997"	"2007"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5122"	"PCSK1"	"0.621"	"0.483"	"C2676498"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 (disorder)"	"phenotype"		"Finding"	"0.40"		"2008"	"2008"	"0"	"1"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0003466"	"Anus, Imperforate"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0018816"	"Heart Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0022360"	"Jaw Abnormalities"	"group"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0026633"	"Mouth Abnormalities"	"group"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0040588"	"Tracheoesophageal Fistula"	"phenotype"	"C06;C08;C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0220708"	"VATER Association"	"disease"	"C06;C14;C16"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0344490"	"Sacral agenesis"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0431415"	"Lumbosacral agenesis"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0431943"	"Lower Extremity Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C0795690"	"Congenital omphalocele"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C1306503"	"Congenital exomphalos"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5125"	"PCSK5"	"0.696"	"0.241"	"C1838568"	"Sacral defect and anterior sacral meningocele"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5125"	"PCSK5"	"0.696"	"0.241"	"C1838569"	"Caudal Dysgenesis Syndrome"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5126"	"PCSK2"	"0.681"	"0.345"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5126"	"PCSK2"	"0.681"	"0.345"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5126"	"PCSK2"	"0.681"	"0.345"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.36"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5126"	"PCSK2"	"0.681"	"0.345"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5126"	"PCSK2"	"0.681"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"5127"	"CDK16"	"0.696"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2011"	"2"	"0"	"PSYGENET"
"5127"	"CDK16"	"0.696"	"0.414"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5127"	"CDK16"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C1837073"	"Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.71"	"1"	"2004"	"2014"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5130"	"PCYT1A"	"0.573"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5133"	"PDCD1"	"0.535"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.8888889"	"1996"	"2017"	"1"	"0"	"CTD_human"
"5134"	"PDCD2"	"0.743"	"0.345"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5137"	"PDE1C"	"0.799"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5138"	"PDE2A"	"0.773"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5138"	"PDE2A"	"0.773"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5138"	"PDE2A"	"0.773"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5138"	"PDE2A"	"0.773"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5139"	"PDE3A"	"0.752"	"0.345"	"C1862170"	"Brachydactyly with hypertension"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.72"	"1"	"1973"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5140"	"PDE3B"	"0.659"	"0.448"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5140"	"PDE3B"	"0.659"	"0.448"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2012"	"5"	"0"	"PSYGENET"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2013"	"5"	"0"	"PSYGENET"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"5141"	"PDE4A"	"0.607"	"0.621"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2007"	"2010"	"4"	"0"	"CTD_human;PSYGENET"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2012"	"5"	"0"	"PSYGENET"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2012"	"5"	"0"	"PSYGENET"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9473684"	"2005"	"2017"	"2"	"1"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5142"	"PDE4B"	"0.609"	"0.517"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.48"	"0.75"	"2001"	"2016"	"2"	"4"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2002"	"2012"	"2"	"0"	"PSYGENET"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2013"	"3"	"0"	"PSYGENET"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2018"	"2"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2011"	"1"	"1"	"PSYGENET"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.9375"	"2002"	"2017"	"0"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0220659"	"Acrodysostosis"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.59"	"0.8888889"	"2012"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"2"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C3276228"	"ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5144"	"PDE4D"	"0.572"	"0.69"	"C3553250"	"ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"2001"	"2018"	"4"	"9"	"CTD_human;UNIPROT"
"5144"	"PDE4D"	"0.572"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"5145"	"PDE6A"	"0.685"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.84"	"1"	"1996"	"2017"	"2"	"3"	"CTD_human;ORPHANET"
"5145"	"PDE6A"	"0.685"	"0.31"	"C3151139"	"RETINITIS PIGMENTOSA 43"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2016"	"2"	"12"	"CTD_human;UNIPROT"
"5146"	"PDE6C"	"0.701"	"0.207"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.64"	"1"	"2009"	"2017"	"0"	"1"	"ORPHANET"
"5146"	"PDE6C"	"0.701"	"0.207"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5146"	"PDE6C"	"0.701"	"0.207"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5146"	"PDE6C"	"0.701"	"0.207"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5146"	"PDE6C"	"0.701"	"0.207"	"C0271092"	"Progressive cone dystrophy (without rod involvement)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5146"	"PDE6C"	"0.701"	"0.207"	"C2751308"	"CONE DYSTROPHY 4 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2018"	"3"	"7"	"CTD_human;UNIPROT"
"5146"	"PDE6C"	"0.701"	"0.207"	"C2751309"	"Achromatopsia 5"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2018"	"3"	"14"	"UNIPROT"
"5147"	"PDE6D"	"0.743"	"0.207"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5147"	"PDE6D"	"0.743"	"0.207"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5147"	"PDE6D"	"0.743"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"5148"	"PDE6G"	"0.685"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.82"	"1"	"1996"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"5148"	"PDE6G"	"0.685"	"0.345"	"C3150821"	"RETINITIS PIGMENTOSA 57"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5148"	"PDE6G"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0009398"	"Color vision defect"	"phenotype"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0155015"	"Color Blindness, Red"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0155016"	"Color Blindness, Red-Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0155017"	"Color Blindness, Blue"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0155018"	"Color Blindness, Acquired"	"phenotype"	"C10;C11;C23"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0239777"	"Color Blindness, Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0242225"	"Color blindness"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0751042"	"Color Blindness, Inherited"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C0751043"	"Monochromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5149"	"PDE6H"	"0.681"	"0.241"	"C1864900"	"Retinal Cone Dystrophy 3A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2016"	"0"	"1"	"CTD_human"
"5152"	"PDE9A"	"0.815"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5153"	"PDE1B"	"0.762"	"0.379"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5153"	"PDE1B"	"0.762"	"0.379"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0005942"	"Bone Diseases, Endocrine"	"group"	"C05;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2001"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"1989"	"2006"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5154"	"PDGFA"	"0.542"	"0.621"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0017566"	"Gingival Hyperplasia"	"phenotype"	"C07"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0206647"	"Dermatofibrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0334454"	"Dermatofibrosarcoma Protuberans, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0334464"	"Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0392784"	"Dermatofibrosarcoma Protuberans"	"disease"		"Neoplastic Process"	"0.40"	"0.9777778"	"1997"	"2018"	"0"	"0"	"ORPHANET"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0393590"	"Fahr's syndrome (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C3665732"	"Metastatic Dermatofibrosarcoma Protuberans"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2007"	"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C3693482"	"Giant Cell Fibroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9705882"	"1997"	"2018"	"0"	"0"	"CTD_human"
"5155"	"PDGFB"	"0.514"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5155"	"PDGFB"	"0.514"	"0.69"	"C3809645"	"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"2"	"5"	"CTD_human;UNIPROT"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0015927"	"Fetal Death"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"0"	"0"	"CGI"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.46"	"1"	"2007"	"2015"	"0"	"5"	"CGI"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0035238"	"Congenital abnormality of respiratory system"	"group"	"C08;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.35"	"0.8"	"1998"	"2011"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0206141"	"Idiopathic Hypereosinophilic Syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.969697"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0206142"	"Eosinophilic leukemia"	"disease"	"C15"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0206143"	"Loeffler's Endocarditis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0206637"	"Mesenchymal Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.80"	"0.9437086"	"2003"	"2018"	"3"	"15"	"CGI;CTD_human;ORPHANET;UNIPROT"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2007"	"2012"	"1"	"1"	"UNIPROT"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0346421"	"Chronic eosinophilic leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.49"	"1"	"2002"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1540912"	"Hypereosinophilic syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.60"	"0.9285714"	"2003"	"2017"	"1"	"0"	"CGI;CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2016"	"0"	"0"	"UNIPROT"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.51"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"5156"	"PDGFRA"	"0.456"	"0.69"	"C4545381"	"Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5157"	"PDGFRL"	"0.762"	"0.31"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5157"	"PDGFRL"	"0.762"	"0.31"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.40"		"1995"	"1995"	"1"	"1"	"UNIPROT"
"5157"	"PDGFRL"	"0.762"	"0.31"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5157"	"PDGFRL"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2010"	"1"	"1"	"UNIPROT"
"5157"	"PDGFRL"	"0.762"	"0.31"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"				"0"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"1996"	"2015"	"4"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.89"	"1"	"1992"	"2017"	"1"	"14"	"CTD_human;ORPHANET"
"5158"	"PDE6B"	"0.621"	"0.379"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.62"	"1"	"1994"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"5158"	"PDE6B"	"0.621"	"0.379"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C1876182"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"1924"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"5158"	"PDE6B"	"0.621"	"0.379"	"C3151107"	"RETINITIS PIGMENTOSA 40 (disorder)"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2017"	"7"	"18"	"CTD_human;UNIPROT"
"5158"	"PDE6B"	"0.621"	"0.379"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5158"	"PDE6B"	"0.621"	"0.379"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2009"	"0"	"0"	"ORPHANET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0393590"	"Fahr's syndrome (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.71"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0432284"	"Infantile myofibromatosis"	"disease"	"C04"	"Disease or Syndrome"	"0.94"	"1"	"2004"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C1333046"	"Myeloproliferative Neoplasm, Unclassifiable"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C1851585"	"MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA"	"disease"	"C15"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C1866182"	"Penttinen-Aula syndrome"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C3472621"	"Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C3554321"	"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2016"	"3"	"3"	"CTD_human;UNIPROT"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5159"	"PDGFRB"	"0.457"	"0.655"	"C4225270"	"KOSAKI OVERGROWTH SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0001125"	"Acidosis, Lactic"	"phenotype"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2018"	"2"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0034345"	"Pyruvate Dehydrogenase Complex Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"1"	"1990"	"2017"	"19"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0034350"	"Pyruvate Metabolism, Inborn Errors"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2018"	"2"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0751595"	"Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0751596"	"Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0751597"	"Ataxia with Lactic Acidosis, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1990"	"2017"	"19"	"12"	"CTD_human;UNIPROT"
"5160"	"PDHA1"	"0.639"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5160"	"PDHA1"	"0.639"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5160"	"PDHA1"	"0.639"	"0.414"	"C1839413"	"Pyruvate Dehydrogenase E1 Alpha Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"1987"	"2017"	"18"	"29"	"ORPHANET;UNIPROT"
"5160"	"PDHA1"	"0.639"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5162"	"PDHB"	"0.735"	"0.241"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0034345"	"Pyruvate Dehydrogenase Complex Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0751595"	"Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0751596"	"Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0751597"	"Ataxia with Lactic Acidosis, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5162"	"PDHB"	"0.735"	"0.241"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5162"	"PDHB"	"0.735"	"0.241"	"C3279841"	"Pyruvate Dehydrogenase E1-Beta Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"		"2004"	"2004"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5163"	"PDK1"	"0.582"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5164"	"PDK2"	"0.857"	"0.138"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5164"	"PDK2"	"0.857"	"0.138"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5164"	"PDK2"	"0.857"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5164"	"PDK2"	"0.857"	"0.138"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5164"	"PDK2"	"0.857"	"0.138"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2007"	"2"	"1"	"UNIPROT"
"5165"	"PDK3"	"0.857"	"0.103"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5165"	"PDK3"	"0.857"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5165"	"PDK3"	"0.857"	"0.103"	"C3806702"	"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2013"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"5166"	"PDK4"	"0.652"	"0.31"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5166"	"PDK4"	"0.652"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5166"	"PDK4"	"0.652"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.8"	"2000"	"2017"	"0"	"0"	"CTD_human"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.862069"	"2000"	"2013"	"0"	"0"	"CTD_human"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0033847"	"Pseudoxanthoma Elasticum"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.37"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0264955"	"Idiopathic arterial calcification of infancy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0342643"	"Autosomal recessive hypophosphatemic vitamin D refractory rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5167"	"ENPP1"	"0.54"	"0.69"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5167"	"ENPP1"	"0.54"	"0.69"	"C1859727"	"Arterial calcification of infancy"	"disease"	"C18"	"Disease or Syndrome"	"0.98"	"1"	"2001"	"2016"	"7"	"23"	"CTD_human;ORPHANET;UNIPROT"
"5167"	"ENPP1"	"0.54"	"0.69"	"C1859728"	"Coronary Sclerosis, Medial, of Infancy"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2016"	"7"	"19"	"UNIPROT"
"5167"	"ENPP1"	"0.54"	"0.69"	"C1865343"	"OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.50"		"1981"	"1999"	"1"	"1"	"UNIPROT"
"5167"	"ENPP1"	"0.54"	"0.69"	"C2750078"	"Hypophosphatemic Rickets, Autosomal Recessive, 2"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2003"	"2016"	"3"	"4"	"CTD_human;UNIPROT"
"5167"	"ENPP1"	"0.54"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5167"	"ENPP1"	"0.54"	"0.69"	"C3809781"	"Cole disease"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2009"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5168"	"ENPP2"	"0.639"	"0.586"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.53"	"1"	"2006"	"2014"	"1"	"0"	"CGI;CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.53"	"1"	"2006"	"2014"	"1"	"0"	"CGI;CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5170"	"PDPK1"	"0.639"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5170"	"PDPK1"	"0.639"	"0.31"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0018021"	"Goiter"	"phenotype"	"C19"	"Pathologic Function"	"0.40"		"2005"	"2007"	"3"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2016"	"3"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0151516"	"Thyroid Hypoplasia"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0271829"	"Pendred's syndrome"	"disease"	"C09;C10;C19;C23"	"Disease or Syndrome"	"1.00"	"0.9831933"	"1993"	"2018"	"20"	"116"	"CTD_human;ORPHANET;UNIPROT"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.60"		"1997"	"2002"	"2"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.34"		"2007"	"2012"	"1"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C3538946"	"DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.52"	"1"	"1998"	"2017"	"12"	"27"	"CTD_human;UNIPROT"
"5172"	"SLC26A4"	"0.554"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5173"	"PDYN"	"0.528"	"0.414"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1997"	"2018"	"7"	"0"	"CTD_human;PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"5173"	"PDYN"	"0.528"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2001"	"2002"	"2"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"4"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2015"	"5"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2015"	"5"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"2012"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0020440"	"Hypercapnia"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1983"	"1991"	"4"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.33"	"1"	"1998"	"2013"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0035204"	"Respiration Disorders"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.3333333"	"2001"	"2005"	"3"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1991"	"2010"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0036659"	"Sensation Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2014"	"4"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0152027"	"Sensory Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2009"	"4"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1991"	"3"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2000"	"2012"	"5"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"1997"	"2015"	"7"	"0"	"CTD_human;PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"2012"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2010"	"2"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0751497"	"Special Senses Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2014"	"4"	"0"	"PSYGENET"
"5173"	"PDYN"	"0.528"	"0.414"	"C1853250"	"SPINOCEREBELLAR ATAXIA 23"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2011"	"2014"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5173"	"PDYN"	"0.528"	"0.414"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5173"	"PDYN"	"0.528"	"0.414"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5173"	"PDYN"	"0.528"	"0.414"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5174"	"PDZK1"	"0.681"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5175"	"PECAM1"	"0.492"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5175"	"PECAM1"	"0.492"	"0.69"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"5175"	"PECAM1"	"0.492"	"0.69"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"5175"	"PECAM1"	"0.492"	"0.69"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"5175"	"PECAM1"	"0.492"	"0.69"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"1"	"2003"	"2018"	"1"	"1"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0010043"	"Corneal Ulcer"	"disease"	"C01;C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.57"	"1"	"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5176"	"SERPINF1"	"0.507"	"0.724"	"C3279564"	"Osteogenesis Imperfecta, Type VI"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.69"	"1"	"2011"	"2017"	"0"	"6"	"CTD_human"
"5178"	"PEG3"	"0.645"	"0.414"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5178"	"PEG3"	"0.645"	"0.414"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5178"	"PEG3"	"0.645"	"0.414"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5178"	"PEG3"	"0.645"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5178"	"PEG3"	"0.645"	"0.414"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5179"	"PENK"	"0.59"	"0.655"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"PSYGENET"
"5179"	"PENK"	"0.59"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.75"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"5179"	"PENK"	"0.59"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.75"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"5179"	"PENK"	"0.59"	"0.655"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2013"	"3"	"0"	"PSYGENET"
"5179"	"PENK"	"0.59"	"0.655"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2002"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.36"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"1999"	"2007"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5179"	"PENK"	"0.59"	"0.655"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2016"	"1"	"1"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0037299"	"Skin Ulcer"	"phenotype"	"C17"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0268532"	"Deficiency of prolidase"	"disease"	"C16"	"Disease or Syndrome"	"0.76"	"1"	"1983"	"2013"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"5184"	"PEPD"	"0.633"	"0.69"	"C0353676"	"Organophosphorus Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C0700359"	"Organophosphate poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C3494247"	"Organothiophosphonate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C3494248"	"Organothiophosphate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5184"	"PEPD"	"0.633"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1983"	"2010"	"8"	"0"	"GENOMICS_ENGLAND"
"5187"	"PER1"	"0.596"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2015"	"0"	"0"	"UNIPROT"
"5187"	"PER1"	"0.596"	"0.655"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5187"	"PER1"	"0.596"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"5187"	"PER1"	"0.596"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5187"	"PER1"	"0.596"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5188"	"GATB"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"		"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1991"	"2018"	"6"	"64"	"CTD_human;ORPHANET;UNIPROT"
"5189"	"PEX1"	"0.554"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5189"	"PEX1"	"0.554"	"0.655"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1997"	"2011"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5189"	"PEX1"	"0.554"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"3"	"0"	"CTD_human"
"5189"	"PEX1"	"0.554"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2016"	"3"	"4"	"CTD_human"
"5189"	"PEX1"	"0.554"	"0.655"	"C1856186"	"Deafness enamel hypoplasia nail defects"	"disease"	"C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"1991"	"2017"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5189"	"PEX1"	"0.554"	"0.655"	"C1865803"	"Peroxisome Biogenesis Disorder, Complementation Group 1"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2009"	"4"	"4"	"UNIPROT"
"5189"	"PEX1"	"0.554"	"0.655"	"C1865804"	"Peroxisome Biogenesis Disorder, Complementation Group E"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2009"	"4"	"4"	"UNIPROT"
"5189"	"PEX1"	"0.554"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5189"	"PEX1"	"0.554"	"0.655"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human"
"5189"	"PEX1"	"0.554"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.56"	"1"	"1997"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"5190"	"PEX6"	"0.562"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5190"	"PEX6"	"0.562"	"0.655"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"1999"	"0"	"0"	"ORPHANET"
"5190"	"PEX6"	"0.562"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"1996"	"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1999"	"2"	"0"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.46"	"1"	"1996"	"2011"	"2"	"2"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C1832230"	"Peroxisome Biogenesis Disorder, Complementation Group 4"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2016"	"4"	"6"	"CTD_human;UNIPROT"
"5190"	"PEX6"	"0.562"	"0.655"	"C1832231"	"Peroxisome Biogenesis Disorder, Complementation Group 6"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2016"	"4"	"6"	"CTD_human;UNIPROT"
"5190"	"PEX6"	"0.562"	"0.655"	"C1832232"	"Peroxisome Biogenesis Disorder, Complementation Group C"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2016"	"4"	"6"	"CTD_human;UNIPROT"
"5190"	"PEX6"	"0.562"	"0.655"	"C1849094"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5190"	"PEX6"	"0.562"	"0.655"	"C1856186"	"Deafness enamel hypoplasia nail defects"	"disease"	"C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5190"	"PEX6"	"0.562"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C3553936"	"PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2016"	"4"	"12"	"CTD_human;UNIPROT"
"5190"	"PEX6"	"0.562"	"0.655"	"C3553937"	"PEROXISOME BIOGENESIS DISORDER 4B"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2018"	"0"	"3"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2018"	"2"	"0"	"CTD_human"
"5190"	"PEX6"	"0.562"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5190"	"PEX6"	"0.562"	"0.655"	"C4225267"	"HEIMLER SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2016"	"3"	"10"	"UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0008445"	"Chondrodysplasia Punctata"	"disease"	"C05"	"Congenital Abnormality"	"0.58"	"0.875"	"1997"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0034960"	"Refsum Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.66"	"1"	"1997"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"5191"	"PEX7"	"0.592"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C0282529"	"Chondrodysplasia Punctata, Rhizomelic"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C1720802"	"Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5191"	"PEX7"	"0.592"	"0.655"	"C1859133"	"RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.98"	"0.875"	"1991"	"2018"	"3"	"29"	"CTD_human;ORPHANET;UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C1866351"	"Peroxisome Biogenesis Disorder, Complementation Group 11"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C1866352"	"Peroxisome Biogenesis Disorder, Complementation Group R"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5191"	"PEX7"	"0.592"	"0.655"	"C2749346"	"Refsum Disease, Adult, 2"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"1"	"CTD_human;UNIPROT"
"5191"	"PEX7"	"0.592"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1998"	"2017"	"4"	"1"	"CTD_human;ORPHANET"
"5192"	"PEX10"	"0.582"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2017"	"0"	"0"	"ORPHANET"
"5192"	"PEX10"	"0.582"	"0.552"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"5192"	"PEX10"	"0.582"	"0.552"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"4"	"0"	"CTD_human"
"5192"	"PEX10"	"0.582"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.46"	"1"	"1998"	"2017"	"3"	"1"	"CTD_human"
"5192"	"PEX10"	"0.582"	"0.552"	"C1864399"	"Peroxisome Biogenesis Disorder, Complementation Group 7"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"1998"	"2017"	"0"	"1"	"CTD_human"
"5192"	"PEX10"	"0.582"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5192"	"PEX10"	"0.582"	"0.552"	"C3553947"	"PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2015"	"0"	"6"	"CTD_human"
"5192"	"PEX10"	"0.582"	"0.552"	"C3553948"	"PEROXISOME BIOGENESIS DISORDER 6B"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2015"	"1"	"10"	"CTD_human;UNIPROT"
"5192"	"PEX10"	"0.582"	"0.552"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"4"	"0"	"CTD_human"
"5192"	"PEX10"	"0.582"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"5193"	"PEX12"	"0.586"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5193"	"PEX12"	"0.586"	"0.621"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.43"	"1"	"1997"	"2017"	"0"	"4"	"ORPHANET"
"5193"	"PEX12"	"0.586"	"0.621"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"		"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2016"	"2"	"0"	"CTD_human"
"5193"	"PEX12"	"0.586"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"1997"	"2"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.43"	"1"	"1997"	"2016"	"1"	"2"	"CTD_human"
"5193"	"PEX12"	"0.586"	"0.621"	"C1866340"	"Peroxisome Biogenesis Disorder, Complementation Group 3"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"5193"	"PEX12"	"0.586"	"0.621"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5193"	"PEX12"	"0.586"	"0.621"	"C3550693"	"PEROXISOME BIOGENESIS DISORDER 3B"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2009"	"2"	"1"	"UNIPROT"
"5193"	"PEX12"	"0.586"	"0.621"	"C3553929"	"PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"2016"	"1"	"10"	"CTD_human;UNIPROT"
"5193"	"PEX12"	"0.586"	"0.621"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2016"	"2"	"0"	"CTD_human"
"5193"	"PEX12"	"0.586"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1999"	"2009"	"2"	"0"	"CTD_human;ORPHANET"
"5194"	"PEX13"	"0.579"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"1999"	"1999"	"0"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5194"	"PEX13"	"0.579"	"0.621"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"ORPHANET"
"5194"	"PEX13"	"0.579"	"0.621"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2009"	"2"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2009"	"3"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C1866259"	"Peroxisome Biogenesis Disorder, Complementation Group 13"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C1866260"	"Peroxisome Biogenesis Disorder, Complementation Group H"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5194"	"PEX13"	"0.579"	"0.621"	"C3554000"	"PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.40"		"1999"	"1999"	"0"	"1"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C3554001"	"PEROXISOME BIOGENESIS DISORDER 11B"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2006"	"2"	"2"	"CTD_human;UNIPROT"
"5194"	"PEX13"	"0.579"	"0.621"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2014"	"2"	"0"	"CTD_human"
"5194"	"PEX13"	"0.579"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2008"	"2"	"0"	"CTD_human;ORPHANET"
"5195"	"PEX14"	"0.588"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5195"	"PEX14"	"0.588"	"0.621"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"5195"	"PEX14"	"0.588"	"0.621"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2010"	"3"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C1866257"	"Peroxisome Biogenesis Disorder, Complementation Group K"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5195"	"PEX14"	"0.588"	"0.621"	"C3554004"	"PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2004"	"0"	"1"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"5195"	"PEX14"	"0.588"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5196"	"PF4"	"0.607"	"0.517"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.39"	"1"	"1994"	"2016"	"7"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"1994"	"2005"	"4"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"2005"	"4"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5196"	"PF4"	"0.607"	"0.517"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5199"	"CFP"	"0.656"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C0025294"	"Meningococcal meningitis"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C0398762"	"Properdin deficiency disease"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"5199"	"CFP"	"0.656"	"0.448"	"C1135745"	"Meningitis, Meningococcal, Serogroup A"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C1135746"	"Meningitis, Meningococcal, Serogroup B"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C1135747"	"Meningitis, Meningococcal, Serogroup C"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C1136209"	"Meningitis, Meningococcal, Serogroup Y"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C1136210"	"Meningitis, Meningococcal, Serogroup W-135"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"1996"	"2000"	"2"	"0"	"CTD_human"
"5199"	"CFP"	"0.656"	"0.448"	"C1839454"	"PROPERDIN DEFICIENCY, X-LINKED"	"disease"	"C16"	"Disease or Syndrome"	"0.70"		"1983"	"2000"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5199"	"CFP"	"0.656"	"0.448"	"C1839455"	"Properdin Deficiency, Type II"	"disease"	"C16;C20"	"Disease or Syndrome"	"0.40"		"1988"	"2000"	"3"	"3"	"UNIPROT"
"5199"	"CFP"	"0.656"	"0.448"	"C1839456"	"Properdin Deficiency, Type III"	"disease"	"C16;C20"	"Disease or Syndrome"	"0.40"		"1996"	"2000"	"3"	"3"	"UNIPROT"
"5199"	"CFP"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.46"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C0268312"	"Progressive intrahepatic cholestasis (disorder)"	"disease"	"C06"	"Disease or Syndrome"	"0.80"	"0.9444444"	"1969"	"2016"	"6"	"19"	"CTD_human;ORPHANET;UNIPROT"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.66"	"0.8333333"	"2003"	"2013"	"0"	"2"	"CTD_human;ORPHANET"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C3549845"	"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2009"	"3"	"3"	"UNIPROT"
"5205"	"ATP8B1"	"0.63"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5209"	"PFKFB3"	"0.639"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5210"	"PFKFB4"	"0.701"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"5211"	"PFKL"	"0.735"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1995"	"2001"	"5"	"0"	"PSYGENET"
"5211"	"PFKL"	"0.735"	"0.241"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5211"	"PFKL"	"0.735"	"0.241"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1996"	"1996"	"1"	"0"	"PSYGENET"
"5213"	"PFKM"	"0.69"	"0.448"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5213"	"PFKM"	"0.69"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5213"	"PFKM"	"0.69"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1994"	"1997"	"3"	"0"	"GENOMICS_ENGLAND"
"5213"	"PFKM"	"0.69"	"0.448"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5213"	"PFKM"	"0.69"	"0.448"	"C0017926"	"Glycogen Storage Disease Type VII"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.94"	"1"	"1990"	"2015"	"7"	"6"	"CTD_human;ORPHANET;UNIPROT"
"5213"	"PFKM"	"0.69"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1994"	"2018"	"3"	"1"	"GENOMICS_ENGLAND"
"5213"	"PFKM"	"0.69"	"0.448"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5213"	"PFKM"	"0.69"	"0.448"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5213"	"PFKM"	"0.69"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1994"	"1997"	"3"	"0"	"GENOMICS_ENGLAND"
"5213"	"PFKM"	"0.69"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5213"	"PFKM"	"0.69"	"0.448"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5214"	"PFKP"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5216"	"PFN1"	"0.6"	"0.621"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.9090909"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"5216"	"PFN1"	"0.6"	"0.621"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5216"	"PFN1"	"0.6"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5216"	"PFN1"	"0.6"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5216"	"PFN1"	"0.6"	"0.621"	"C3553719"	"AMYOTROPHIC LATERAL SCLEROSIS 18"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"4"	"CTD_human;UNIPROT"
"5218"	"CDK14"	"0.713"	"0.241"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5218"	"CDK14"	"0.713"	"0.241"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.44"	"1"	"2007"	"2018"	"1"	"1"	"CTD_human"
"5222"	"PGA5"	"0.834"	"0.103"	"C0014868"	"Esophagitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5223"	"PGAM1"	"0.663"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5224"	"PGAM2"	"0.857"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5224"	"PGAM2"	"0.857"	"0.172"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5224"	"PGAM2"	"0.857"	"0.172"	"C0268149"	"Glycogen storage disease type X"	"disease"	"C05;C10;C12;C13"	"Disease or Syndrome"	"0.73"	"1"	"1983"	"2014"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5224"	"PGAM2"	"0.857"	"0.172"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5224"	"PGAM2"	"0.857"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5226"	"PGD"	"0.676"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5228"	"PGF"	"0.52"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5228"	"PGF"	"0.52"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5229"	"PGGT1B"	"0.857"	"0.172"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5229"	"PGGT1B"	"0.857"	"0.172"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1992"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5230"	"PGK1"	"0.6"	"0.69"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5230"	"PGK1"	"0.6"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C0684324"	"Deficiency of phosphoglycerate kinase"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2006"	"2008"	"0"	"0"	"ORPHANET"
"5230"	"PGK1"	"0.6"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C1970848"	"Phosphoglycerate Kinase 1 Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1969"	"2015"	"9"	"14"	"CTD_human;ORPHANET;UNIPROT"
"5230"	"PGK1"	"0.6"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.6666667"	"1998"	"2012"	"1"	"0"	"CTD_human"
"5230"	"PGK1"	"0.6"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"5236"	"PGM1"	"0.735"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5236"	"PGM1"	"0.735"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5236"	"PGM1"	"0.735"	"0.414"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5236"	"PGM1"	"0.735"	"0.414"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5236"	"PGM1"	"0.735"	"0.414"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5236"	"PGM1"	"0.735"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5236"	"PGM1"	"0.735"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5236"	"PGM1"	"0.735"	"0.414"	"C2752015"	"Glycogen Storage Disease XIV"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2009"	"2016"	"6"	"12"	"ORPHANET;UNIPROT"
"5236"	"PGM1"	"0.735"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5238"	"PGM3"	"0.667"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"5238"	"PGM3"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5238"	"PGM3"	"0.667"	"0.448"	"C4014371"	"IMMUNODEFICIENCY 23"	"disease"		"Disease or Syndrome"	"0.70"		"1987"	"2017"	"3"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5239"	"PGM5"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5239"	"PGM5"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5239"	"PGM5"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.6666667"	"1992"	"2010"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.956743"	"1985"	"2018"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.38"		"2002"	"2013"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.60"	"0.9512195"	"1995"	"2018"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.9230769"	"1990"	"2014"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2005"	"2015"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"0"	"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.9756098"	"1992"	"2016"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9608355"	"1985"	"2018"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9714286"	"1988"	"2017"	"2"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C1849699"	"Progesterone Resistance"	"disease"	"C13"	"Disease or Syndrome"	"0.36"	"1"	"2000"	"2014"	"0"	"0"	"CTD_human"
"5241"	"PGR"	"0.467"	"0.69"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9285714"	"1995"	"2018"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9927536"	"1987"	"2018"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9268293"	"1989"	"2017"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"1990"	"2018"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.50"		"2008"	"2017"	"4"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8939394"	"1995"	"2017"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0014836"	"Escherichia coli Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0020651"	"Hypotension, Orthostatic"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.50"		"2006"	"2007"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027609"	"Neonatal Abstinence Syndrome"	"disease"	"C16;C25;F03"	"Disease or Syndrome"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9615385"	"1991"	"2013"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2011"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9655172"	"1989"	"2015"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2007"	"2016"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0030201"	"Pain, Postoperative"	"phenotype"	"C23"	"Sign or Symptom"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8823529"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.75"	"2006"	"2016"	"4"	"1"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0040715"	"Chromosomal translocation"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2017"	"5"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.50"		"2008"	"2017"	"4"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1995"	"2010"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"1991"	"2002"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"1995"	"2010"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0376544"	"Hematopoietic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9815951"	"1987"	"2018"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1995"	"2010"	"2"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2017"	"5"	"0"	"PSYGENET"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"1990"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1996"	"2018"	"2"	"0"	"CTD_human;UNIPROT"
"5243"	"ABCB1"	"0.371"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.8947368"	"1993"	"2014"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.962963"	"1991"	"2018"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C2677101"	"Inflammatory Bowel Disease 13"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"1998"	"1998"	"0"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"5243"	"ABCB1"	"0.371"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.38"	"0.75"	"1997"	"2015"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"1"	"1996"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0022354"	"Jaundice, Obstructive"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.44"	"0.75"	"1996"	"2011"	"2"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2010"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"1996"	"2015"	"2"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0268312"	"Progressive intrahepatic cholestasis (disorder)"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.969697"	"1996"	"2017"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.60"	"0.9285714"	"2000"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"0.5"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C0745744"	"End Stage Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5244"	"ABCB4"	"0.555"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C1865643"	"Cholestasis, progressive familial intrahepatic 3"	"disease"	"C06"	"Disease or Syndrome"	"0.73"	"1"	"1996"	"2017"	"11"	"31"	"CTD_human;ORPHANET;UNIPROT"
"5244"	"ABCB4"	"0.555"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.57"	"0.8571429"	"1993"	"2016"	"1"	"0"	"CGI;CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C2609268"	"Low phospholipid-associated cholelithiasis"	"disease"		"Disease or Syndrome"	"0.69"	"0.8888889"	"2001"	"2017"	"6"	"17"	"CTD_human;ORPHANET;UNIPROT"
"5244"	"ABCB4"	"0.555"	"0.517"	"C2936476"	"Chronic Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5244"	"ABCB4"	"0.555"	"0.517"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5244"	"ABCB4"	"0.555"	"0.517"	"C3554241"	"CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3"	"disease"		"Disease or Syndrome"	"0.40"		"1996"	"2009"	"3"	"8"	"UNIPROT"
"5245"	"PHB"	"0.572"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2005"	"2009"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"1992"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"5245"	"PHB"	"0.572"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2011"	"2"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2018"	"0"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2007"	"0"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"5245"	"PHB"	"0.572"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"5250"	"SLC25A3"	"0.602"	"0.621"	"C1835845"	"Mitochondrial Phosphate Carrier Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5251"	"PHEX"	"0.609"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"5251"	"PHEX"	"0.609"	"0.69"	"C0027709"	"Nephrocalcinosis"	"disease"	"C12;C13;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5251"	"PHEX"	"0.609"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5251"	"PHEX"	"0.609"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5251"	"PHEX"	"0.609"	"0.69"	"C0733682"	"Hypophosphatemic Rickets, X-Linked Dominant"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"1.00"	"0.9772727"	"1977"	"2018"	"10"	"44"	"CTD_human;ORPHANET;UNIPROT"
"5251"	"PHEX"	"0.609"	"0.69"	"C1845168"	"Hypophosphatemic Rickets, X-Linked Recessive"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1988"	"2015"	"2"	"0"	"CTD_human"
"5251"	"PHEX"	"0.609"	"0.69"	"C3536983"	"Familial Hypophosphatemic Rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"	"0.9787234"	"1997"	"2018"	"2"	"0"	"CTD_human"
"5251"	"PHEX"	"0.609"	"0.69"	"C3536984"	"Vitamin D-Resistant Rickets, X-Linked"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"	"0.9736842"	"1990"	"2018"	"10"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5251"	"PHEX"	"0.609"	"0.69"	"C3540852"	"Rickets, X-Linked Hypophosphatemic"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9545455"	"1988"	"2013"	"2"	"0"	"CTD_human;ORPHANET"
"5253"	"PHF2"	"0.773"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5255"	"PHKA1"	"0.815"	"0.172"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2004"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"5255"	"PHKA1"	"0.815"	"0.172"	"C1845151"	"Glycogen Storage Disease, Type IXD"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"		"1970"	"2008"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5255"	"PHKA1"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5256"	"PHKA2"	"0.727"	"0.138"	"C0017919"	"Glycogen Storage Disease"	"group"	"C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"5256"	"PHKA2"	"0.727"	"0.138"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5256"	"PHKA2"	"0.727"	"0.138"	"C1844412"	"Liver Glycogenosis, X-Linked, Type II"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"1995"	"2007"	"6"	"11"	"CTD_human;UNIPROT"
"5256"	"PHKA2"	"0.727"	"0.138"	"C2748941"	"Glycogen Storage Disease, Type IXA2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1995"	"2007"	"6"	"12"	"CTD_human;UNIPROT"
"5256"	"PHKA2"	"0.727"	"0.138"	"C2751643"	"Glycogen Storage Disease IXC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5256"	"PHKA2"	"0.727"	"0.138"	"C3694531"	"GLYCOGEN STORAGE DISEASE IXa1"	"disease"		"Disease or Syndrome"	"0.50"		"1995"	"2007"	"6"	"11"	"CTD_human;UNIPROT"
"5256"	"PHKA2"	"0.727"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5257"	"PHKB"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5257"	"PHKB"	"0.799"	"0.172"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5257"	"PHKB"	"0.799"	"0.172"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5257"	"PHKB"	"0.799"	"0.172"	"C0543514"	"Glycogen Storage Disease IXB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1997"	"1998"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5260"	"PHKG1"	"0.928"	"0.138"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5260"	"PHKG1"	"0.928"	"0.138"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5260"	"PHKG1"	"0.928"	"0.138"	"C1845151"	"Glycogen Storage Disease, Type IXD"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5261"	"PHKG2"	"0.773"	"0.207"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5261"	"PHKG2"	"0.773"	"0.207"	"C2751643"	"Glycogen Storage Disease IXC"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1995"	"2004"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5261"	"PHKG2"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5264"	"PHYH"	"0.667"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5264"	"PHYH"	"0.667"	"0.517"	"C0034960"	"Refsum Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"0.9375"	"1985"	"2015"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5264"	"PHYH"	"0.667"	"0.517"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5264"	"PHYH"	"0.667"	"0.517"	"C1720802"	"Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5264"	"PHYH"	"0.667"	"0.517"	"C2749345"	"Refsum Disease, Adult, 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1987"	"2004"	"5"	"9"	"UNIPROT"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0003850"	"Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human;PSYGENET"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0006267"	"Bronchiectasis"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"1973"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1981"	"2017"	"3"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"0.9518072"	"1971"	"2018"	"6"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.40"	"0.9756098"	"1982"	"2018"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.50"	"0.9846154"	"1981"	"2017"	"2"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0030328"	"Panniculitis, Nodular Nonsuppurative"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"1982"	"1988"	"2"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.50"	"0.979798"	"1981"	"2018"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"1978"	"2012"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0039841"	"Thiamine Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0042384"	"Vasculitis"	"group"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"1971"	"2007"	"6"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0221757"	"alpha 1-Antitrypsin Deficiency"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9622642"	"1977"	"2018"	"2"	"32"	"CTD_human;ORPHANET"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1984"	"2016"	"3"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1986"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1981"	"2014"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2007"	"2"	"0"	"PSYGENET"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"2"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"1981"	"2012"	"2"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C3501835"	"alpha-1-Antitrypsin Deficiency, Autosomal Recessive"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.40"	"0.9677419"	"1981"	"2018"	"0"	"0"	"ORPHANET"
"5265"	"SERPINA1"	"0.453"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5266"	"PI3"	"0.707"	"0.414"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5266"	"PI3"	"0.707"	"0.414"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5267"	"SERPINA4"	"0.652"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5267"	"SERPINA4"	"0.652"	"0.586"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5267"	"SERPINA4"	"0.652"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.39"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"5268"	"SERPINB5"	"0.609"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5269"	"SERPINB6"	"0.621"	"0.655"	"C3150704"	"DEAFNESS, AUTOSOMAL RECESSIVE 91"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"1"	"CTD_human"
"5270"	"SERPINE2"	"0.639"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"5271"	"SERPINB8"	"0.815"	"0.069"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5271"	"SERPINB8"	"0.815"	"0.069"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"1"	"CTD_human"
"5271"	"SERPINB8"	"0.815"	"0.069"	"C1838440"	"ICHTHYOSIS EXFOLIATIVA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5271"	"SERPINB8"	"0.815"	"0.069"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5272"	"SERPINB9"	"0.743"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5272"	"SERPINB9"	"0.743"	"0.31"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5273"	"SERPINB10"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5273"	"SERPINB10"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5274"	"SERPINI1"	"0.642"	"0.31"	"C1858680"	"Familial encephalopathy with neuroserpin inclusion bodies"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.93"	"1"	"2002"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5277"	"PIGA"	"0.59"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5277"	"PIGA"	"0.59"	"0.552"	"C0019050"	"Hemoglobinuria, Paroxysmal"	"disease"	"C15"	"Disease or Syndrome"	"0.32"		"2002"	"2007"	"2"	"0"	"CTD_human"
"5277"	"PIGA"	"0.59"	"0.552"	"C0024790"	"Paroxysmal nocturnal hemoglobinuria"	"disease"	"C15"	"Disease or Syndrome"	"0.70"	"0.9618321"	"1983"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"5277"	"PIGA"	"0.59"	"0.552"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5277"	"PIGA"	"0.59"	"0.552"	"C0086774"	"Cold paroxysmal hemoglobinuria"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"5277"	"PIGA"	"0.59"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5277"	"PIGA"	"0.59"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5277"	"PIGA"	"0.59"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5277"	"PIGA"	"0.59"	"0.552"	"C3275508"	"MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.70"		"1996"	"2017"	"5"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5277"	"PIGA"	"0.59"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5277"	"PIGA"	"0.59"	"0.552"	"C3806670"	"PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2002"	"5"	"10"	"UNIPROT"
"5279"	"PIGC"	"0.886"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5279"	"PIGC"	"0.886"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5283"	"PIGH"	"1"		"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"5287"	"PIK3C2B"	"0.752"	"0.241"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"5289"	"PIK3C3"	"0.773"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5289"	"PIK3C3"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2004"	"2009"	"3"	"0"	"PSYGENET"
"5289"	"PIK3C3"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.9679487"	"2001"	"2018"	"9"	"5"	"CGI;CTD_human;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2018"	"0"	"7"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"1"	"2006"	"2017"	"1"	"7"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9772727"	"2001"	"2018"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"0"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.47"	"1"	"2004"	"2016"	"0"	"32"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2016"	"1"	"7"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.43"	"1"	"2005"	"2017"	"0"	"2"	"ORPHANET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"		"2013"	"2015"	"0"	"1"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0022603"	"Seborrheic keratosis"	"disease"	"C17"	"Neoplastic Process"	"0.66"	"1"	"2004"	"2012"	"1"	"4"	"CTD_human;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.60"	"1"	"2004"	"2016"	"0"	"0"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2018"	"1"	"0"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.969697"	"2006"	"2018"	"0"	"1"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9541284"	"2004"	"2018"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9615385"	"1999"	"2018"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0030849"	"Penile Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2018"	"2"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.64"	"1"	"2003"	"2016"	"1"	"3"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"11"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2017"	"1"	"19"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0153601"	"Malignant neoplasm of penis"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2009"	"1"	"1"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"0.9782609"	"2002"	"2018"	"0"	"0"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2017"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0334082"	"NEVUS, EPIDERMAL (disorder)"	"disease"	"C04"	"Disease or Syndrome"	"0.44"	"1"	"2004"	"2016"	"0"	"1"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0341823"	"Epithelial tumor of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2014"	"1"	"1"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2006"	"2006"	"1"	"5"	"CLINGEN;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.952381"	"2000"	"2018"	"2"	"1"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0431391"	"Hemimegalencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.95"	"2005"	"2016"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0585362"	"Squamous cell carcinoma of mouth"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.50"	"1"	"2000"	"2018"	"1"	"3"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9737705"	"2000"	"2018"	"8"	"0"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.50"	"0.9705882"	"2002"	"2018"	"0"	"1"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"1"	"2000"	"2017"	"2"	"8"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"1"	"2003"	"2018"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.40"		"2004"	"2012"	"0"	"3"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.67"	"1"	"2001"	"2013"	"0"	"5"	"CGI;CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.9615385"	"1999"	"2018"	"1"	"2"	"CGI;CLINGEN;CTD_human;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.972973"	"2001"	"2017"	"1"	"29"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2015"	"8"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.48"	"0.875"	"2007"	"2017"	"1"	"1"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2014"	"0"	"0"	"ORPHANET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9555556"	"2005"	"2018"	"8"	"34"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9875"	"2003"	"2018"	"2"	"6"	"CTD_human;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9411765"	"2005"	"2017"	"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"5"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1863924"	"Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1865285"	"Megalencephaly cutis marmorata telangiectatica congenita"	"disease"	"C05;C10;C14;C16;C17"	"Disease or Syndrome"	"0.63"	"1"	"1993"	"2016"	"2"	"12"	"ORPHANET;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.80"	"0.9647059"	"2002"	"2018"	"1"	"11"	"CGI;CTD_human;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2676033"	"Hepatoblastoma Caused By Somatic Mutation"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2752042"	"Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi"	"disease"	"C04;C05;C14;C16"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C3554518"	"COWDEN SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"7"	"UNIPROT"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5290"	"PIK3CA"	"0.341"	"0.897"	"C4011754"	"Nevus, Keratinocytic, Nonepidermolytic"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9894737"	"2001"	"2018"	"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2016"	"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9672131"	"2000"	"2018"	"1"	"0"	"CTD_human"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9888268"	"2000"	"2018"	"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5291"	"PIK3CB"	"0.389"	"0.862"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5292"	"PIM1"	"0.532"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0034186"	"Pyelonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5292"	"PIM1"	"0.532"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5292"	"PIM1"	"0.532"	"0.621"	"C1704315"	"Pyelonephritis acute necrotizing"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2017"	"1"	"0"	"CGI;CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9672131"	"2000"	"2018"	"1"	"0"	"CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5293"	"PIK3CD"	"0.386"	"0.862"	"C3714976"	"ACTIVATED PI3K-DELTA SYNDROME"	"disease"	"C20"	"Disease or Syndrome"	"0.73"	"1"	"2006"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5294"	"PIK3CG"	"0.385"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"0.6666667"	"2010"	"2018"	"2"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0878684"	"SHORT syndrome"	"disease"	"C12;C13;C18;C23"	"Disease or Syndrome"	"0.76"	"1"	"1983"	"2017"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C3554689"	"AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2015"	"0"	"2"	"CTD_human"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C3714976"	"ACTIVATED PI3K-DELTA SYNDROME"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5295"	"PIK3R1"	"0.515"	"0.793"	"C4014934"	"IMMUNODEFICIENCY 36"	"disease"		"Disease or Syndrome"	"0.40"		"1995"	"2017"	"0"	"2"	"CTD_human"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C1153706"	"Endometrial adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C1863924"	"Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2016"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5296"	"PIK3R2"	"0.594"	"0.655"	"C4012727"	"MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2016"	"4"	"4"	"UNIPROT"
"5297"	"PI4KA"	"0.707"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5297"	"PI4KA"	"0.707"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2009"	"2015"	"4"	"0"	"PSYGENET"
"5297"	"PI4KA"	"0.707"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5297"	"PI4KA"	"0.707"	"0.379"	"C1845668"	"Perisylvian syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5297"	"PI4KA"	"0.707"	"0.379"	"C4225295"	"POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"5300"	"PIN1"	"0.536"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9428571"	"2001"	"2016"	"2"	"0"	"CTD_human"
"5300"	"PIN1"	"0.536"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9411765"	"2001"	"2016"	"2"	"0"	"CTD_human"
"5300"	"PIN1"	"0.536"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"5300"	"PIN1"	"0.536"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2012"	"2"	"0"	"CTD_human"
"5303"	"PIN4"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5304"	"PIP"	"0.645"	"0.655"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5305"	"PIP4K2A"	"0.672"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2005"	"2007"	"3"	"0"	"PSYGENET"
"5305"	"PIP4K2A"	"0.672"	"0.414"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5305"	"PIP4K2A"	"0.672"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5305"	"PIP4K2A"	"0.672"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.75"	"2005"	"2016"	"4"	"0"	"PSYGENET"
"5305"	"PIP4K2A"	"0.672"	"0.414"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"		"2014"	"2014"	"0"	"1"	"ORPHANET"
"5307"	"PITX1"	"0.614"	"0.448"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5307"	"PITX1"	"0.614"	"0.448"	"C0009081"	"Congenital clubfoot"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.88"	"0.875"	"2009"	"2014"	"2"	"2"	"CTD_human;UNIPROT"
"5307"	"PITX1"	"0.614"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"5307"	"PITX1"	"0.614"	"0.448"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"5307"	"PITX1"	"0.614"	"0.448"	"C1851100"	"LAURIN-SANDROW SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"5307"	"PITX1"	"0.614"	"0.448"	"C1861313"	"Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"5307"	"PITX1"	"0.614"	"0.448"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5308"	"PITX2"	"0.51"	"0.724"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.40"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5308"	"PITX2"	"0.51"	"0.724"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"GENOMICS_ENGLAND"
"5308"	"PITX2"	"0.51"	"0.724"	"C0265341"	"Rieger syndrome"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2011"	"0"	"0"	"ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C0266548"	"Axenfeld anomaly (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.33"	"1"	"2000"	"2011"	"0"	"0"	"ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C0344559"	"Irido-corneo-trabecular dysgenesis (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human;ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"2004"	"2"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5308"	"PITX2"	"0.51"	"0.724"	"C1842031"	"IRIDOGONIODYSGENESIS, TYPE 2"	"disease"	"C07;C11;C16"	"Disease or Syndrome"	"0.63"	"1"	"1995"	"2011"	"4"	"2"	"CTD_human;UNIPROT"
"5308"	"PITX2"	"0.51"	"0.724"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5308"	"PITX2"	"0.51"	"0.724"	"C1867155"	"RING DERMOID OF CORNEA"	"disease"	"C04;C11"	"Disease or Syndrome"	"0.70"		"2005"	"2012"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5308"	"PITX2"	"0.51"	"0.724"	"C3495488"	"Axenfeld-Rieger syndrome"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2017"	"0"	"0"	"ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C3495489"	"Rieger eye malformation sequence"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"5308"	"PITX2"	"0.51"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5308"	"PITX2"	"0.51"	"0.724"	"C3714873"	"Axenfeld-Rieger Syndrome, Type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.81"	"1"	"1997"	"2008"	"10"	"11"	"CTD_human;UNIPROT"
"5309"	"PITX3"	"0.636"	"0.483"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5309"	"PITX3"	"0.636"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5309"	"PITX3"	"0.636"	"0.483"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.44"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0027854"	"Neurologic Manifestations"	"group"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5309"	"PITX3"	"0.636"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.68"	"1"	"1998"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5309"	"PITX3"	"0.636"	"0.483"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5309"	"PITX3"	"0.636"	"0.483"	"C0235031"	"Neurologic Symptoms"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0422837"	"Neurological observations"	"group"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0521654"	"Neurologic Deficits"	"group"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"2"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0746857"	"Focal Neurologic Deficits"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0751377"	"Neurologic Dysfunction"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0751378"	"Neurologic Signs"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5309"	"PITX3"	"0.636"	"0.483"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"1998"	"2006"	"2"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C1862839"	"Anterior segment mesenchymal dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.75"	"1"	"1968"	"2012"	"2"	"0"	"CTD_human;ORPHANET"
"5309"	"PITX3"	"0.636"	"0.483"	"C1864567"	"CATARACT, POSTERIOR POLAR, 4 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1998"	"2004"	"2"	"1"	"CTD_human;UNIPROT"
"5309"	"PITX3"	"0.636"	"0.483"	"C1970386"	"Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5309"	"PITX3"	"0.636"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5309"	"PITX3"	"0.636"	"0.483"	"C3808029"	"CATARACT 11 WITH MICROPHTHALMIA AND NEURODEVELOPMENTAL ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2004"	"2"	"1"	"UNIPROT"
"5309"	"PITX3"	"0.636"	"0.483"	"C4305131"	"Cataract glaucoma syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5310"	"PKD1"	"0.537"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5310"	"PKD1"	"0.537"	"0.621"	"C0010709"	"Cyst"	"phenotype"	"C04;C23"	"Disease or Syndrome"	"0.40"	"0.96"	"1990"	"2014"	"1"	"0"	"CTD_human"
"5310"	"PKD1"	"0.537"	"0.621"	"C0022680"	"Polycystic Kidney Diseases"	"group"	"C12;C13;C16"	"Disease or Syndrome"	"0.50"	"0.94"	"1990"	"2018"	"3"	"7"	"CTD_human"
"5310"	"PKD1"	"0.537"	"0.621"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"1.00"	"0.9721254"	"1989"	"2018"	"44"	"64"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"5310"	"PKD1"	"0.537"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5310"	"PKD1"	"0.537"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2009"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"5310"	"PKD1"	"0.537"	"0.621"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1994"	"2017"	"6"	"0"	"CTD_human"
"5310"	"PKD1"	"0.537"	"0.621"	"C1567435"	"Polycystic Kidney - body part"	"phenotype"	"C12;C13;C16"	"Anatomical Abnormality"	"0.46"	"1"	"1998"	"2017"	"3"	"0"	"CTD_human"
"5310"	"PKD1"	"0.537"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"5310"	"PKD1"	"0.537"	"0.621"	"C1838327"	"Polycystic kidneys, severe infantile with tuberous sclerosis"	"disease"	"C04;C10;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5310"	"PKD1"	"0.537"	"0.621"	"C1868148"	"Potter Type III Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"1994"	"2012"	"7"	"0"	"CLINGEN"
"5310"	"PKD1"	"0.537"	"0.621"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.34"	"1"	"1994"	"2017"	"6"	"0"	"CTD_human"
"5310"	"PKD1"	"0.537"	"0.621"	"C3149841"	"POLYCYSTIC KIDNEY DISEASE 1"	"disease"		"Disease or Syndrome"	"0.80"	"0.9230769"	"1992"	"2013"	"39"	"40"	"CLINGEN;UNIPROT"
"5310"	"PKD1"	"0.537"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.60"	"0.978836"	"1994"	"2018"	"5"	"0"	"CTD_human;ORPHANET"
"5311"	"PKD2"	"0.575"	"0.655"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2002"	"2017"	"5"	"0"	"CTD_human"
"5311"	"PKD2"	"0.575"	"0.655"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"5311"	"PKD2"	"0.575"	"0.655"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.84"	"1"	"1995"	"2017"	"16"	"12"	"CTD_human;UNIPROT"
"5311"	"PKD2"	"0.575"	"0.655"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5313"	"PKLR"	"0.537"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5313"	"PKLR"	"0.537"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1991"	"2008"	"8"	"0"	"GENOMICS_ENGLAND"
"5313"	"PKLR"	"0.537"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5313"	"PKLR"	"0.537"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5313"	"PKLR"	"0.537"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5313"	"PKLR"	"0.537"	"0.759"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"5313"	"PKLR"	"0.537"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1991"	"2008"	"8"	"0"	"GENOMICS_ENGLAND"
"5313"	"PKLR"	"0.537"	"0.759"	"C0340968"	"Deficiency of pyruvate kinase"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1963"	"2017"	"16"	"47"	"CTD_human;ORPHANET;UNIPROT"
"5313"	"PKLR"	"0.537"	"0.759"	"C1863224"	"Adenosine Triphosphate, Elevated, Of Erythrocytes"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"1965"	"1997"	"1"	"1"	"CTD_human;UNIPROT"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0008340"	"Choledochal Cyst"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0009439"	"Choledochal Cyst, Type I"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0009714"	"Hepatic Fibrosis, Congenital"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.45"	"1"	"2002"	"2015"	"9"	"49"	"UNIPROT"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"1.00"	"1"	"1998"	"2018"	"13"	"175"	"CTD_human;ORPHANET;UNIPROT"
"5314"	"PKHD1"	"0.614"	"0.448"	"C0162510"	"Caroli Disease"	"disease"	"C06;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.34"	"1"	"2004"	"2018"	"0"	"0"	"ORPHANET"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1257796"	"Choledochal Cyst, Type II"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1257797"	"Choledochal Cyst, Type III"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1257798"	"Choledochal Cyst, Type IV"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1257799"	"Choledochal Cyst, Type V"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1988"	"2011"	"1"	"1"	"UNIPROT"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5314"	"PKHD1"	"0.614"	"0.448"	"C1833541"	"Caroli disease isolated"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5314"	"PKHD1"	"0.614"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5314"	"PKHD1"	"0.614"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5315"	"PKM"	"0.552"	"0.586"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5315"	"PKM"	"0.552"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5316"	"PKNOX1"	"0.727"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5317"	"PKP1"	"0.676"	"0.448"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2010"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"5317"	"PKP1"	"0.676"	"0.448"	"C1858302"	"Ectodermal dysplasia/ skin fragility syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.68"	"1"	"1997"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"5317"	"PKP1"	"0.676"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5318"	"PKP2"	"0.681"	"0.241"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5318"	"PKP2"	"0.681"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5318"	"PKP2"	"0.681"	"0.241"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5318"	"PKP2"	"0.681"	"0.241"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.50"	"1"	"1985"	"2018"	"0"	"46"	"GENOMICS_ENGLAND"
"5318"	"PKP2"	"0.681"	"0.241"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.53"	"1"	"2008"	"2015"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"5318"	"PKP2"	"0.681"	"0.241"	"C1836906"	"Arrhythmogenic Right Ventricular Dysplasia, Familial, 9"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"1997"	"2017"	"12"	"40"	"CLINGEN;CTD_human;UNIPROT"
"5318"	"PKP2"	"0.681"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5319"	"PLA2G1B"	"0.502"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6"	"1996"	"2006"	"5"	"0"	"PSYGENET"
"5319"	"PLA2G1B"	"0.502"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2018"	"3"	"0"	"PSYGENET"
"5319"	"PLA2G1B"	"0.502"	"0.793"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5319"	"PLA2G1B"	"0.502"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2005"	"2"	"0"	"PSYGENET"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9285714"	"1999"	"2015"	"1"	"0"	"CTD_human"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2004"	"2011"	"2"	"0"	"PSYGENET"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"PSYGENET"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C0349218"	"Recurrent depressive disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5320"	"PLA2G2A"	"0.509"	"0.69"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2004"	"2011"	"2"	"0"	"PSYGENET"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0005818"	"Blood Platelet Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.53"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human;UNIPROT"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1997"	"2010"	"5"	"0"	"PSYGENET"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5321"	"PLA2G4A"	"0.538"	"0.655"	"C4302263"	"Cryptogenic multifocal ulcerous stenosing enteritis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5322"	"PLA2G5"	"0.799"	"0.276"	"C1856718"	"Fleck Retina, Familial Benign"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"1996"	"2012"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5324"	"PLAG1"	"0.586"	"0.586"	"C0334475"	"Lipoblastomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5324"	"PLAG1"	"0.586"	"0.586"	"C1260965"	"Lipoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"5324"	"PLAG1"	"0.586"	"0.586"	"C1519176"	"Salivary Gland Pleomorphic Adenoma"	"disease"	"C04;C07"	"Neoplastic Process"	"0.57"	"0.8571429"	"1996"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"5325"	"PLAGL1"	"0.592"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5325"	"PLAGL1"	"0.592"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5325"	"PLAGL1"	"0.592"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5325"	"PLAGL1"	"0.592"	"0.552"	"C1832386"	"Diabetes Mellitus, Transient Neonatal, 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.56"	"0.8333333"	"2000"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"5327"	"PLAT"	"0.459"	"0.828"	"C0001125"	"Acidosis, Lactic"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0001883"	"Airway Obstruction"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"2006"	"2010"	"3"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0003537"	"Aphasia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0003546"	"Aphasia, Acquired"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0003838"	"Arterial Occlusive Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1995"	"2010"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0004604"	"Back Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0004610"	"Bacteremia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0007177"	"Cardiac Tamponade"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0007781"	"Intracranial Embolism and Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1995"	"2"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"1991"	"2017"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"25"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0008301"	"Choking"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0010072"	"Coronary Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1988"	"2004"	"3"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0013922"	"Embolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0018946"	"Hematoma, Subdural"	"phenotype"	"C10;C14;C23;C26"	"Pathologic Function"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0018989"	"Hemiparesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0019064"	"Hemopericardium"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1990"	"2012"	"8"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0024031"	"Low Back Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0025309"	"Meningoencephalitis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1986"	"2015"	"35"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0030552"	"Paresis"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0031039"	"Pericardial effusion"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2009"	"9"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5327"	"PLAT"	"0.459"	"0.828"	"C0036980"	"Shock, Cardiogenic"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0037926"	"Compression of spinal cord"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.6923077"	"1990"	"2015"	"59"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"1991"	"2012"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2009"	"3"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0079102"	"Cerebral Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0085307"	"Embolism and Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1991"	"2012"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0149649"	"Cholesterol Embolism"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2009"	"3"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0151699"	"Intracranial Hemorrhages"	"group"	"C10;C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"1988"	"2012"	"14"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234462"	"Aphasia, Ageusic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234469"	"Aphasia, Global"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234472"	"Aphasia, Functional"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234474"	"Aphasia, Graphomotor"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234476"	"Aphasia, Intellectual"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234482"	"Aphasia, Semantic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0234484"	"Aphasia, Syntactical"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0242426"	"Chylopericardium"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0265110"	"Cerebral Vasospasm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0270795"	"Monoparesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0338457"	"Aphasia, Progressive"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0393953"	"Anterior Cerebral Circulation Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0423682"	"Low Back Pain, Mechanical"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0423689"	"Low Back Pain, Posterior Compartment"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0438921"	"Back Pain without Radiation"	"phenotype"	"C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0454576"	"Aphasia, Mixed"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0475059"	"Subdural Hematoma, Traumatic"	"disease"	"C10;C14;C23;C26"	"Injury or Poisoning"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1987"	"2009"	"9"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0553692"	"Brain hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1988"	"2012"	"14"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0577660"	"Low Back Pain, Postural"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0740363"	"Back Pain with Radiation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0742803"	"Conus Medullaris Syndrome"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750917"	"Aphasia, Auditory Discriminatory"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750918"	"Aphasia, Commisural"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750919"	"Aphasia, Post-Ictal"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750920"	"Aphasia, Post-Traumatic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750921"	"Dejerine-Lichtheim Phenomenon"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0750949"	"Vertebrogenic Pain Syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1991"	"2008"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1991"	"2008"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1991"	"2008"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1991"	"2008"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751409"	"Upper Extremity Paresis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751410"	"Lower Extremity Paresis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751648"	"Recurrent Low Back Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2010"	"4"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751893"	"Posterior Fossa Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1988"	"2012"	"14"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751895"	"Vasospasm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751952"	"Anterior Circulation Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751953"	"Brain Infarction, Posterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751954"	"Venous Infarction, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751955"	"Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2015"	"59"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0752143"	"Intracranial Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0752144"	"Brain Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0877172"	"Hematoma, Epidural, Spinal"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2000"	"2002"	"2"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0877855"	"Cerebral Embolism and Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1995"	"2"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1991"	"2008"	"6"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"1995"	"2012"	"25"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0936247"	"Brain Embolism and Thrombosis"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1995"	"2"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0936261"	"Brain Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0936263"	"Cerebral Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C0973461"	"Dysphasia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1704212"	"Embolus"	"phenotype"	"C14"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C2676721"	"Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C2676722"	"Hyperfibrinolysis, Familial, Due To Increased Release Of Tissue Plasminogen Activator"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1991"	"2011"	"21"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5327"	"PLAT"	"0.459"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1991"	"2011"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.58"	"1"	"1994"	"2014"	"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0002962"	"Angina Pectoris"	"phenotype"	"C14;C23"	"Sign or Symptom"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0002965"	"Angina, Unstable"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0003460"	"Anuria"	"phenotype"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0003838"	"Arterial Occlusive Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"2004"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007781"	"Intracranial Embolism and Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"2007"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1976"	"2007"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"2015"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0018128"	"Graft Occlusion, Vascular"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1993"	"2001"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0018814"	"Heart Rupture, Post-Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0018965"	"Hematuria"	"phenotype"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1993"	"2005"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1996"	"2004"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1985"	"2011"	"6"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2016"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9583333"	"1993"	"2017"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0027697"	"Nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.36"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1969"	"2001"	"6"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0034152"	"Henoch-Schoenlein Purpura"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.50"		"1969"	"2010"	"6"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0042386"	"Vasculitis, Hemorrhagic"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1984"	"2004"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0086666"	"Myocardial Preinfarction Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0086922"	"Rheumatoid Purpura"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1969"	"2004"	"6"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0149649"	"Cholesterol Embolism"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"2004"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0151699"	"Intracranial Hemorrhages"	"group"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2017"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0241832"	"Cerebrovascular Insufficiency"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1976"	"2007"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0242461"	"Purpura, Nonthrombocytopenic"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0338575"	"Sagittal Sinus Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2013"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0376362"	"Purpura Hemorrhagica"	"disease"	"C14;C15;C20;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0403823"	"Asthenozoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2008"	"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1969"	"2001"	"6"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0553692"	"Brain hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0596298"	"Cerebrovascular Occlusion"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1976"	"2007"	"2"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751823"	"Septic Phlebitis, Sagittal Sinus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751824"	"Sagittal Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2007"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751893"	"Posterior Fossa Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1999"	"2007"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0877855"	"Cerebral Embolism and Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"2007"	"4"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C0936247"	"Brain Embolism and Thrombosis"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2001"	"2008"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5328"	"PLAU"	"0.434"	"0.69"	"C1866423"	"Quebec platelet disorder"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.55"	"1"	"2001"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"5328"	"PLAU"	"0.434"	"0.69"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1976"	"2007"	"5"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2012"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2004"	"2008"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5329"	"PLAUR"	"0.561"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5332"	"PLCB4"	"0.69"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5332"	"PLCB4"	"0.69"	"0.448"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5332"	"PLCB4"	"0.69"	"0.448"	"C1865295"	"Auriculo-condylar syndrome"	"disease"	"C09"	"Disease or Syndrome"	"0.64"	"0.75"	"2012"	"2014"	"0"	"5"	"CTD_human;ORPHANET"
"5332"	"PLCB4"	"0.69"	"0.448"	"C3553404"	"AURICULOCONDYLAR SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2013"	"1"	"8"	"UNIPROT"
"5333"	"PLCD1"	"0.667"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5333"	"PLCD1"	"0.667"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5333"	"PLCD1"	"0.667"	"0.517"	"C0263532"	"Leukonychia punctata"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"5333"	"PLCD1"	"0.667"	"0.517"	"C0544855"	"Leukonychia totalis"	"phenotype"	"C17"	"Pathologic Function"	"0.70"		"2011"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5333"	"PLCD1"	"0.667"	"0.517"	"C3276977"	"LEUKONYCHIA STRIATUS"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"1"	"2014"	"2016"	"1"	"0"	"CGI;CTD_human"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"5335"	"PLCG1"	"0.611"	"0.517"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.66"	"1"	"2007"	"2017"	"1"	"2"	"CGI;CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0268390"	"Muckle-Wells Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0343068"	"Familial cold urticaria"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0409818"	"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C2316212"	"Cryopyrin-Associated Periodic Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5336"	"PLCG2"	"0.636"	"0.621"	"C3280914"	"FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5336"	"PLCG2"	"0.636"	"0.621"	"C3553961"	"AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5337"	"PLD1"	"0.607"	"0.552"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5337"	"PLD1"	"0.607"	"0.552"	"C1859330"	"Cardiac Valvular Defect, Developmental"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"5338"	"PLD2"	"0.652"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"0.75"	"2010"	"2014"	"0"	"0"	"UNIPROT"
"5338"	"PLD2"	"0.652"	"0.483"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5338"	"PLD2"	"0.652"	"0.483"	"C0029342"	"Orthomyxoviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5338"	"PLD2"	"0.652"	"0.483"	"C0276357"	"Swine influenza"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5338"	"PLD2"	"0.652"	"0.483"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5339"	"PLEC"	"0.569"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"	"1"	"1996"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C0432317"	"Epidermolysis bullosa simplex, Ogna type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.90"		"1993"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5339"	"PLEC"	"0.569"	"0.655"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"0.5"	"1999"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C1856934"	"Epidermolysis bullosa with pyloric atresia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.43"	"1"	"2005"	"2017"	"0"	"1"	"CTD_human"
"5339"	"PLEC"	"0.569"	"0.655"	"C2677349"	"Epidermolysis Bullosa Simplex With Pyloric Atresia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.63"	"1"	"2004"	"2013"	"0"	"5"	"CTD_human;ORPHANET"
"5339"	"PLEC"	"0.569"	"0.655"	"C2931072"	"Epidermolysa bullosa simplex and limb girdle muscular dystrophy"	"disease"	"C05;C10;C16;C17"	"Disease or Syndrome"	"0.90"	"1"	"1996"	"2015"	"0"	"10"	"CTD_human;ORPHANET"
"5339"	"PLEC"	"0.569"	"0.655"	"C3150989"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2016"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5339"	"PLEC"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5339"	"PLEC"	"0.569"	"0.655"	"C4225309"	"EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1997"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"5340"	"PLG"	"0.419"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"1984"	"2010"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5340"	"PLG"	"0.419"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5340"	"PLG"	"0.419"	"0.862"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"1981"	"2018"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C0398621"	"Hypoplasminogenemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"1"	"1989"	"2013"	"0"	"0"	"ORPHANET"
"5340"	"PLG"	"0.419"	"0.862"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"5340"	"PLG"	"0.419"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5340"	"PLG"	"0.419"	"0.862"	"C1274789"	"Ligneous conjunctivitis"	"disease"	"C11;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1982"	"2017"	"8"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5340"	"PLG"	"0.419"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C1968804"	"Plasminogen Deficiency, Type I"	"disease"	"C11;C16;C17"	"Disease or Syndrome"	"0.79"	"1"	"1982"	"2017"	"8"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5340"	"PLG"	"0.419"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C4225445"	"PLASMINOGEN DEFICIENCY, TYPE II"	"disease"		"Disease or Syndrome"	"0.30"		"1982"	"1999"	"8"	"7"	"UNIPROT"
"5340"	"PLG"	"0.419"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5340"	"PLG"	"0.419"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5341"	"PLEK"	"0.614"	"0.621"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5345"	"SERPINF2"	"0.681"	"0.552"	"C2752081"	"ALPHA-2-PLASMIN INHIBITOR DEFICIENCY"	"disease"	"C15"	"Disease or Syndrome"	"0.90"		"1978"	"2000"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5345"	"SERPINF2"	"0.681"	"0.552"	"C3489734"	"Anti-plasmin deficiency, congenital"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9032258"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"0"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5346"	"PLIN1"	"0.656"	"0.379"	"C3151268"	"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5347"	"PLK1"	"0.503"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"5347"	"PLK1"	"0.503"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5347"	"PLK1"	"0.503"	"0.69"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5347"	"PLK1"	"0.503"	"0.69"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5347"	"PLK1"	"0.503"	"0.69"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5348"	"FXYD1"	"0.857"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"5349"	"FXYD3"	"0.707"	"0.241"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5349"	"FXYD3"	"0.707"	"0.241"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.9545455"	"1996"	"2017"	"0"	"3"	"GENOMICS_ENGLAND"
"5350"	"PLN"	"0.627"	"0.379"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5350"	"PLN"	"0.627"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5350"	"PLN"	"0.627"	"0.379"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2017"	"18"	"0"	"CLINGEN"
"5350"	"PLN"	"0.627"	"0.379"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1993"	"2017"	"18"	"0"	"CLINGEN"
"5350"	"PLN"	"0.627"	"0.379"	"C0206145"	"Stunned Myocardium"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0206146"	"Myocardial Stunning"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5350"	"PLN"	"0.627"	"0.379"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"5350"	"PLN"	"0.627"	"0.379"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5350"	"PLN"	"0.627"	"0.379"	"C0376416"	"Hibernation, Myocardial"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5350"	"PLN"	"0.627"	"0.379"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.9411765"	"1993"	"2018"	"18"	"1"	"CLINGEN"
"5350"	"PLN"	"0.627"	"0.379"	"C1835928"	"CARDIOMYOPATHY, DILATED, 1P"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2003"	"2017"	"4"	"4"	"CTD_human;UNIPROT"
"5350"	"PLN"	"0.627"	"0.379"	"C3151265"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2011"	"0"	"1"	"CTD_human"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"1994"	"2017"	"8"	"0"	"GENOMICS_ENGLAND"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0022821"	"Kyphosis deformity of spine"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0268342"	"Ehlers-Danlos syndrome type 6"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.79"	"1"	"1978"	"2017"	"6"	"13"	"CTD_human;ORPHANET;UNIPROT"
"5351"	"PLOD1"	"0.609"	"0.448"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"5351"	"PLOD1"	"0.609"	"0.448"	"C2936777"	"Nevo syndrome (disorder)"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"1994"	"2006"	"6"	"3"	"CTD_human;UNIPROT"
"5351"	"PLOD1"	"0.609"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C0432253"	"Bruck syndrome"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"1999"	"2015"	"0"	"0"	"ORPHANET"
"5352"	"PLOD2"	"0.621"	"0.517"	"C1836602"	"Bruck syndrome 2"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.70"		"2003"	"2005"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5352"	"PLOD2"	"0.621"	"0.517"	"C1850168"	"Bruck syndrome 1"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5352"	"PLOD2"	"0.621"	"0.517"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5352"	"PLOD2"	"0.621"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5352"	"PLOD2"	"0.621"	"0.517"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5354"	"PLP1"	"0.577"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5354"	"PLP1"	"0.577"	"0.517"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"2"	"0"	"PSYGENET"
"5354"	"PLP1"	"0.577"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"1999"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5354"	"PLP1"	"0.577"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.75"	"2004"	"2010"	"4"	"0"	"PSYGENET"
"5354"	"PLP1"	"0.577"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"1995"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5354"	"PLP1"	"0.577"	"0.517"	"C0205711"	"Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9496403"	"1985"	"2017"	"31"	"18"	"CTD_human;UNIPROT"
"5354"	"PLP1"	"0.577"	"0.517"	"C0751914"	"Adult Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5354"	"PLP1"	"0.577"	"0.517"	"C0751915"	"Pelizaeus-Merzbacher Disease, Atypical"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1997"	"2008"	"1"	"1"	"CTD_human"
"5354"	"PLP1"	"0.577"	"0.517"	"C0751916"	"Classic Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1986"	"2018"	"10"	"0"	"CLINGEN;CTD_human;ORPHANET"
"5354"	"PLP1"	"0.577"	"0.517"	"C0751917"	"Pelizaeus-Merzbacher Disease, Transitional"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"5354"	"PLP1"	"0.577"	"0.517"	"C0751918"	"Cockayne-Pelizaeus-Merzbacher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5354"	"PLP1"	"0.577"	"0.517"	"C1839264"	"SPASTIC PARAPLEGIA 2, X-LINKED (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9375"	"1962"	"2017"	"10"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5354"	"PLP1"	"0.577"	"0.517"	"C2673482"	"Increased susceptibility to schizophrenia"	"phenotype"		"Finding"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"5354"	"PLP1"	"0.577"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5357"	"PLS1"	"0.834"	"0.241"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5357"	"PLS1"	"0.834"	"0.241"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5358"	"PLS3"	"0.685"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"5358"	"PLS3"	"0.685"	"0.414"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5358"	"PLS3"	"0.685"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5358"	"PLS3"	"0.685"	"0.414"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5358"	"PLS3"	"0.685"	"0.414"	"C3806712"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18"	"phenotype"		"Finding"	"0.40"		"2013"	"2013"	"0"	"3"	"CTD_human"
"5359"	"PLSCR1"	"0.72"	"0.448"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5359"	"PLSCR1"	"0.72"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5360"	"PLTP"	"0.676"	"0.414"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5362"	"PLXNA2"	"0.614"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"5362"	"PLXNA2"	"0.614"	"0.621"	"C0338908"	"Mixed anxiety and depressive disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5364"	"PLXNB1"	"0.701"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2017"	"0"	"0"	"UNIPROT"
"5364"	"PLXNB1"	"0.701"	"0.31"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5365"	"PLXNB3"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5366"	"PMAIP1"	"0.598"	"0.724"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5367"	"PMCH"	"0.652"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1995"	"1995"	"1"	"0"	"PSYGENET"
"5367"	"PMCH"	"0.652"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5367"	"PMCH"	"0.652"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5367"	"PMCH"	"0.652"	"0.448"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2002"	"2010"	"1"	"0"	"CTD_human"
"5367"	"PMCH"	"0.652"	"0.448"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5368"	"PNOC"	"0.672"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2009"	"3"	"0"	"PSYGENET"
"5368"	"PNOC"	"0.672"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2009"	"3"	"0"	"PSYGENET"
"5368"	"PNOC"	"0.672"	"0.414"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1998"	"2009"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2001"	"2001"	"2"	"0"	"PSYGENET"
"5368"	"PNOC"	"0.672"	"0.414"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5368"	"PNOC"	"0.672"	"0.414"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5368"	"PNOC"	"0.672"	"0.414"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9713024"	"1990"	"2018"	"20"	"0"	"CTD_human;ORPHANET"
"5371"	"PML"	"0.519"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2018"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5371"	"PML"	"0.519"	"0.759"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"5"	"0"	"GENOMICS_ENGLAND"
"5373"	"PMM2"	"0.557"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"1993"	"2016"	"3"	"5"	"GENOMICS_ENGLAND"
"5373"	"PMM2"	"0.557"	"0.621"	"C0349653"	"Congenital disorder of glycosylation type 1A"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"14"	"59"	"CTD_human;ORPHANET;UNIPROT"
"5373"	"PMM2"	"0.557"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5373"	"PMM2"	"0.557"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5373"	"PMM2"	"0.557"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5375"	"PMP2"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"5376"	"PMP22"	"0.506"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9640719"	"1990"	"2018"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5376"	"PMP22"	"0.506"	"0.69"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1994"	"2016"	"16"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5376"	"PMP22"	"0.506"	"0.69"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0016579"	"Formication"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0018378"	"Guillain-Barre Syndrome"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0019816"	"Hereditary, Type VII, Motor and Sensory Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0023944"	"Locked-In Syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0027888"	"Hereditary Motor and Sensory Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.8181818"	"1994"	"2017"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0030554"	"Paresthesia"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2018"	"2"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0034372"	"Quadriplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0034933"	"Reflex, Abnormal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0151572"	"Reflex, Corneal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.43"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0151888"	"Hyporeflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0151889"	"Hyperreflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1997"	"2009"	"3"	"0"	"CTD_human;ORPHANET"
"5376"	"PMP22"	"0.506"	"0.69"	"C0234146"	"Absent reflex"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0234784"	"Reflex, Gag, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0235044"	"Paresthesia, Distal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0241772"	"Reflex, Deep Tendon, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0270790"	"Quadriparesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9859155"	"1992"	"2016"	"17"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5376"	"PMP22"	"0.506"	"0.69"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"3"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"0"	"2004"	"2009"	"3"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0277839"	"Hoffman's Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0277850"	"Reflex, Pendular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0278211"	"Reflex, Corneal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0392699"	"Dysesthesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0393814"	"Hereditary liability to pressure palsies"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"0.983871"	"1993"	"2018"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"5376"	"PMP22"	"0.506"	"0.69"	"C0426970"	"Spastic Quadriplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0522345"	"Reflex, Acoustic, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0558845"	"Reflex, Ankle, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0558846"	"Reflex, Triceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0558847"	"Reflex, Biceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0576612"	"Reflex, Anal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0743002"	"Abnormal Deep Tendon Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"1993"	"2017"	"3"	"5"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751412"	"Painful Paresthesias"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751460"	"Flaccid Quadriplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751461"	"Paralysis, Spinal, Quadriplegic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751468"	"Bulbocavernosus Reflex, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751469"	"Bulbocavernousus Reflex Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751470"	"Palmo-Mental Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751471"	"Reflex, Anal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751472"	"Reflex, Ankle, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751473"	"Reflex, Ankle, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751474"	"Reflex, Biceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751475"	"Reflex, Biceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751476"	"Reflex, Gag, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751477"	"Reflex, Knee, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751478"	"Reflex, Knee, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751479"	"Reflex, Moro, Asymmetric"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751480"	"Reflex, Triceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0751481"	"Reflex, Triceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C1861669"	"Charcot-Marie-Tooth disease and deafness"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"1982"	"2003"	"0"	"6"	"ORPHANET"
"5376"	"PMP22"	"0.506"	"0.69"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5376"	"PMP22"	"0.506"	"0.69"	"C2931686"	"Charcot-Marie-Tooth disease, Type 1E"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"ORPHANET"
"5376"	"PMP22"	"0.506"	"0.69"	"C3495591"	"Charcot-Marie-Tooth Disease, Demyelinating, Type 1e"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.82"	"1"	"1999"	"2013"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5376"	"PMP22"	"0.506"	"0.69"	"C3542501"	"Acute inflammatory demyelinating polyneuropathy"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"5376"	"PMP22"	"0.506"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5376"	"PMP22"	"0.506"	"0.69"	"C4083008"	"Guillain-Barre Syndrome, Familial"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5378"	"PMS1"	"0.6"	"0.552"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5378"	"PMS1"	"0.6"	"0.552"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"5378"	"PMS1"	"0.6"	"0.552"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"1994"	"2001"	"4"	"0"	"CLINGEN;ORPHANET"
"5378"	"PMS1"	"0.6"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5378"	"PMS1"	"0.6"	"0.552"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2005"	"4"	"0"	"CLINGEN;ORPHANET"
"5378"	"PMS1"	"0.6"	"0.552"	"C2931459"	"Lynch syndrome I (site-specific colonic cancer)"	"disease"	"C04;C06;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2010"	"2016"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.44"		"1986"	"2017"	"3"	"57"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2007"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2009"	"2013"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.33"	"0.6666667"	"2008"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.35"	"1"	"2006"	"2016"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0038874"	"Supratentorial Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0221263"	"Cafe-au-Lait Spots"	"phenotype"	"C17;C23"	"Finding"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0265325"	"Turcot syndrome (disorder)"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2017"	"6"	"24"	"CTD_human;ORPHANET;UNIPROT"
"5395"	"PMS2"	"0.526"	"0.586"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"1995"	"2018"	"4"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.70"	"1"	"1999"	"2016"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.37"	"1"	"2011"	"2016"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0751588"	"Benign Supratentorial Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0751589"	"Cancer, Supratentorial"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0751590"	"Primary Supratentorial Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5395"	"PMS2"	"0.526"	"0.586"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"		"2006"	"2006"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5395"	"PMS2"	"0.526"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.65"	"1"	"2006"	"2016"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"5395"	"PMS2"	"0.526"	"0.586"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"	"0.9759036"	"1995"	"2018"	"3"	"76"	"CTD_human;ORPHANET"
"5395"	"PMS2"	"0.526"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5395"	"PMS2"	"0.526"	"0.586"	"C1838333"	"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4"	"disease"	"C04;C06;C16;C18"	"Disease or Syndrome"	"0.70"		"1994"	"2017"	"17"	"33"	"CLINGEN;CTD_human;UNIPROT"
"5395"	"PMS2"	"0.526"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.42"	"0.5"	"2012"	"2017"	"1"	"1"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0035353"	"Congenital retrognathism"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0265242"	"Otocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"		"2011"	"2011"	"1"	"1"	"ORPHANET;UNIPROT"
"5396"	"PRRX1"	"0.582"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C1876185"	"Dysgnathia complex"	"disease"	"C05;C07;C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2002"	"2013"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5396"	"PRRX1"	"0.582"	"0.552"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3494422"	"Retrognathia"	"phenotype"	"C05;C07;C16"	"Anatomical Abnormality"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3494423"	"Maxillary Retroposition"	"phenotype"	"C05;C07;C16"	"Anatomical Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3494424"	"Maxillary Retrusion"	"phenotype"	"C05;C07;C16"	"Anatomical Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3494425"	"Mandibular Retroposition"	"phenotype"	"C05;C07;C16"	"Anatomical Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5396"	"PRRX1"	"0.582"	"0.552"	"C3494426"	"Mandibular Retrusion"	"phenotype"	"C05;C07;C16"	"Anatomical Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5406"	"PNLIP"	"0.72"	"0.276"	"C0268241"	"Pancreatic colipase deficiency"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"5406"	"PNLIP"	"0.72"	"0.276"	"C3280527"	"PANCREATIC LIPASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"5406"	"PNLIP"	"0.72"	"0.276"	"C3280528"	"COLIPASE, CONGENITAL ABSENCE OF PANCREATIC"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"5406"	"PNLIP"	"0.72"	"0.276"	"C3280529"	"LIPASE AND COLIPASE, DEFICIENCY OF"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"5406"	"PNLIP"	"0.72"	"0.276"	"C3280530"	"LIPASE AND COLIPASE, CONGENITAL ABSENCE OF PANCREATIC"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"5407"	"PNLIPRP1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5413"	"SEPT5"	"0.707"	"0.414"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5413"	"SEPT5"	"0.707"	"0.414"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5413"	"SEPT5"	"0.707"	"0.414"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5413"	"SEPT5"	"0.707"	"0.414"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5420"	"PODXL"	"0.633"	"0.414"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5420"	"PODXL"	"0.633"	"0.414"	"C4510873"	"Atypical juvenile parkinsonism"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5422"	"POLA1"	"0.676"	"0.621"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2005"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5422"	"POLA1"	"0.676"	"0.621"	"C0796250"	"PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5422"	"POLA1"	"0.676"	"0.621"	"C1845050"	"PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS"	"disease"	"C16;C17;C18;C23"	"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"5422"	"POLA1"	"0.676"	"0.621"	"C2936859"	"N syndrome"	"disease"	"C04;C10;C15;C18;C20;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5422"	"POLA1"	"0.676"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1997"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5423"	"POLB"	"0.63"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"0.6666667"	"1996"	"2009"	"1"	"0"	"CTD_human"
"5423"	"POLB"	"0.63"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"0.6666667"	"1996"	"2009"	"1"	"0"	"CTD_human"
"5423"	"POLB"	"0.63"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"5423"	"POLB"	"0.63"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"5423"	"POLB"	"0.63"	"0.586"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0004991"	"Benign neoplasm of colon"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2016"	"12"	"0"	"CLINGEN"
"5424"	"POLD1"	"0.546"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5424"	"POLD1"	"0.546"	"0.655"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0022360"	"Jaw Abnormalities"	"group"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0023787"	"Lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.38"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5424"	"POLD1"	"0.546"	"0.655"	"C2675481"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, 10"	"phenotype"		"Finding"	"0.40"		"2006"	"2017"	"2"	"2"	"UNIPROT"
"5424"	"POLD1"	"0.546"	"0.655"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5424"	"POLD1"	"0.546"	"0.655"	"C3715192"	"ANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2013"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"5424"	"POLD1"	"0.546"	"0.655"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5426"	"POLE"	"0.616"	"0.345"	"C0004991"	"Benign neoplasm of colon"	"disease"		"Neoplastic Process"	"0.30"		"2009"	"2016"	"8"	"0"	"CLINGEN"
"5426"	"POLE"	"0.616"	"0.345"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.37"	"1"	"2013"	"2017"	"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2013"	"2018"	"2"	"0"	"CTD_human"
"5426"	"POLE"	"0.616"	"0.345"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"2"	"3"	"CTD_human"
"5426"	"POLE"	"0.616"	"0.345"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5426"	"POLE"	"0.616"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"2013"	"2017"	"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5426"	"POLE"	"0.616"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"2013"	"2018"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5426"	"POLE"	"0.616"	"0.345"	"C3554460"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, 12"	"phenotype"		"Finding"	"0.40"		"2003"	"2018"	"4"	"2"	"UNIPROT"
"5426"	"POLE"	"0.616"	"0.345"	"C3554576"	"FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2013"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"5428"	"POLG"	"0.477"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0004712"	"Balo's Concentric Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2018"	"2"	"0"	"PSYGENET"
"5428"	"POLG"	"0.477"	"0.724"	"C0007795"	"Diffuse Cerebral Sclerosis of Schilder"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9583333"	"2005"	"2015"	"3"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.37"	"0.5714286"	"2004"	"2014"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.45"	"0.8"	"2008"	"2015"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.50"	"0.9655172"	"2002"	"2017"	"1"	"1"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0205710"	"Alpers Syndrome (disorder)"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.80"	"0.9285714"	"1978"	"2017"	"9"	"19"	"CTD_human;ORPHANET;UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"PSYGENET"
"5428"	"POLG"	"0.477"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.70"	"0.9428571"	"1993"	"2018"	"1"	"7"	"CTD_human;GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0872218"	"MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"5428"	"POLG"	"0.477"	"0.724"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C1834846"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"	"disease"	"C10;C11;C18;C23"	"Disease or Syndrome"	"0.70"		"1962"	"2015"	"7"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1843851"	"Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.76"	"1"	"1978"	"2016"	"11"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1843852"	"SPINOCEREBELLAR ATAXIA WITH EPILEPSY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"1978"	"2016"	"10"	"9"	"ORPHANET;UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1850303"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.62"	"1"	"1978"	"2016"	"0"	"6"	"CTD_human;ORPHANET"
"5428"	"POLG"	"0.477"	"0.724"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"2"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C3150914"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2015"	"2"	"9"	"CTD_human;UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5428"	"POLG"	"0.477"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4225153"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2006"	"14"	"22"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C4225409"	"EPILEPSY, PROGRESSIVE MYOCLONIC, 5, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2016"	"10"	"9"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C4225440"	"EPILEPSY, PROGRESSIVE MYOCLONIC, WITH SENSORY ATAXIC NEUROPATHY"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2016"	"10"	"9"	"UNIPROT"
"5428"	"POLG"	"0.477"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5428"	"POLG"	"0.477"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5429"	"POLH"	"0.667"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5429"	"POLH"	"0.667"	"0.414"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.60"	"0.9583333"	"1999"	"2017"	"1"	"0"	"CTD_human"
"5429"	"POLH"	"0.667"	"0.414"	"C0432328"	"Xeroderma pigmentosum, variant form"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5429"	"POLH"	"0.667"	"0.414"	"C1848410"	"Xeroderma pigmentosum, variant type"	"disease"	"C04;C16;C17;C18"	"Disease or Syndrome"	"0.94"	"1"	"1993"	"2016"	"6"	"13"	"CTD_human;ORPHANET;UNIPROT"
"5435"	"POLR2F"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5443"	"POMC"	"0.382"	"0.862"	"C0001231"	"ACTH Syndrome, Ectopic"	"disease"	"C04"	"Disease or Syndrome"	"0.40"	"0.8666667"	"1974"	"2010"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0001614"	"Adrenal Cortex Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1974"	"2009"	"5"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1989"	"2015"	"5"	"0"	"PSYGENET"
"5443"	"POMC"	"0.382"	"0.862"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2014"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2014"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0003868"	"Arthritis, Gouty"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"1985"	"1998"	"3"	"0"	"CTD_human;PSYGENET"
"5443"	"POMC"	"0.382"	"0.862"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1998"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2004"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1988"	"1996"	"5"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1984"	"1986"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0007789"	"Cerebral Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0009806"	"Constipation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0010481"	"Cushing Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"0.9516129"	"1984"	"2016"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0010692"	"Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"5443"	"POMC"	"0.382"	"0.862"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2003"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"5443"	"POMC"	"0.382"	"0.862"	"C0011848"	"Diabetes Insipidus"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.35"	"0.8"	"1997"	"2017"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1971"	"1996"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0015397"	"Disorder of eye"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"1972"	"1972"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0015469"	"Facial paralysis"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0015814"	"Femur Head Necrosis"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1974"	"1983"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1984"	"2009"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2005"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1987"	"1994"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0018965"	"Hematuria"	"phenotype"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1976"	"1992"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1976"	"1986"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0019572"	"Hirsutism"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020438"	"Hypercalciuria"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1986"	"1992"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020488"	"Hypernatremia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1982"	"2002"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.8461538"	"1974"	"2016"	"68"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020598"	"Hypocalcemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"1971"	"1999"	"9"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1989"	"1991"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0021053"	"Immune System Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0022672"	"Acute Kidney Tubular Necrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1974"	"1981"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1987"	"1994"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0023882"	"Little's Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1998"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2018"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"1988"	"2004"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0026896"	"Myasthenia Gravis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0027709"	"Nephrocalcinosis"	"disease"	"C12;C13;C18"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.70"	"0.9402985"	"1992"	"2017"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0028961"	"Oliguria"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.32"	"1"	"1974"	"2009"	"5"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1974"	"2009"	"5"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.39"	"1"	"1973"	"2014"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0030846"	"Penile Diseases"	"group"	"C12"	"Disease or Syndrome"	"0.30"		"1987"	"1992"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1981"	"2017"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0032787"	"Postoperative Complications"	"group"	"C23"	"Pathologic Function"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1974"	"1974"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0035258"	"Restless Legs Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0035411"	"Rhabdomyoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.39"	"1"	"1982"	"2016"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1981"	"2018"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1979"	"2012"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0039103"	"Synovitis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0042029"	"Urinary tract infection"	"group"	"C01;C12;C13"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"1974"	"1984"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2005"	"3"	"0"	"PSYGENET"
"5443"	"POMC"	"0.382"	"0.862"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1979"	"2010"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.31"	"1"	"1979"	"2012"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1971"	"1996"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0151827"	"Eye pain"	"phenotype"	"C11;C23"	"Sign or Symptom"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0154695"	"Diplegic Infantile Cerebral Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0154697"	"Cerebral Palsy, Quadriplegic, Infantile"	"disease"	"C10"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0154698"	"Monoplegic Infantile Cerebral Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0221406"	"Pituitary-dependent Cushing's disease"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.40"	"0.952381"	"1990"	"2016"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1984"	"1986"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1987"	"1994"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0237326"	"Dyschezia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2014"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0242217"	"Calcium Pyrophosphate Dihydrate Deposition"	"phenotype"	"C05"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0270742"	"Athetoid cerebral palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0270807"	"Monoplegic Cerebral Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0338596"	"Spastic cerebral palsy"	"disease"	"C10"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1998"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0340375"	"Subaortic stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"5443"	"POMC"	"0.382"	"0.862"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393626"	"Opsoclonus-Myoclonus Syndrome"	"disease"	"C04;C10;C11"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0394003"	"Cerebral Palsy, Dystonic-Rigid"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0394007"	"Cerebral Palsy, Atonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0410480"	"Avascular Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0410574"	"Synovial Hypertrophy"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0427055"	"Facial Paresis"	"phenotype"	"C07;C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0428908"	"Sinus Node Dysfunction (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1990"	"2009"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0524595"	"Aseptic Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0553730"	"Calcium pyrophosphate deposition disease"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0553767"	"Congenital Cerebral Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0574960"	"Sacroiliitis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2009"	"4"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2014"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751024"	"Cerebral Palsy, Mixed"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751025"	"Cerebral Palsy, Rolandic Type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751141"	"Facial Palsy, Upper Motor Neuron"	"phenotype"	"C07;C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751142"	"Facial Palsy, Lower Motor Neuron"	"phenotype"	"C07;C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751143"	"Hemifacial Paralysis"	"phenotype"	"C07;C10;C23"	"Sign or Symptom"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751220"	"Inappropriate ACTH Secretion Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1988"	"1998"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751339"	"Myasthenia Gravis, Generalized"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751340"	"Myasthenia Gravis, Ocular"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"1971"	"1971"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1974"	"2009"	"5"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1973"	"2010"	"3"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1096154"	"Kinsbourne Syndrome"	"disease"	"C04;C10;C11"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1257861"	"Colonic Inertia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"1993"	"2001"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1984"	"2009"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"2010"	"20"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1974"	"1983"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1721017"	"Paraneoplastic Opsoclonus-Myoclonus Ataxia"	"disease"	"C04;C10;C11"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1857854"	"Proopiomelanocortin Deficiency"	"disease"	"C18;C19;C23"	"Disease or Syndrome"	"0.60"		"1998"	"2003"	"0"	"5"	"CTD_human;ORPHANET"
"5443"	"POMC"	"0.382"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1987"	"1994"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1987"	"1994"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C2936444"	"Pyogenic Sacroiliitis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C2936445"	"Septic Sacroiliitis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.31"		"1981"	"2004"	"2"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5443"	"POMC"	"0.382"	"0.862"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1982"	"1991"	"6"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0001828"	"Agricultural Workers' Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"5444"	"PON1"	"0.443"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.8181818"	"2007"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"5444"	"PON1"	"0.443"	"0.828"	"C0003860"	"Arteritis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9494949"	"1998"	"2018"	"6"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2005"	"2012"	"3"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2015"	"2015"	"3"	"0"	"PSYGENET"
"5444"	"PON1"	"0.443"	"0.828"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0009806"	"Constipation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8085106"	"1996"	"2018"	"3"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8928571"	"1997"	"2018"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0010073"	"Coronary Artery Vasospasm"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"0.75"	"2007"	"2015"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9393939"	"1998"	"2016"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2014"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0017662"	"Glomerulonephritis, Membranoproliferative"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0019112"	"Hemorrhoids"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"0.75"	"2000"	"2008"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2005"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0020476"	"Hyperlipoproteinemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0031090"	"Periodontal Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2003"	"2012"	"3"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0034219"	"Alveolar pyorrhea"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2002"	"2009"	"2"	"0"	"PSYGENET"
"5444"	"PON1"	"0.443"	"0.828"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0237326"	"Dyschezia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0282550"	"Persian Gulf Syndrome"	"disease"	"C24"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.31"		"2006"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0353676"	"Organophosphorus Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2000"	"2017"	"7"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2018"	"3"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0376544"	"Hematopoietic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2018"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2007"	"2"	"0"	"PSYGENET"
"5444"	"PON1"	"0.443"	"0.828"	"C0700359"	"Organophosphate poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2000"	"2017"	"7"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2005"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5444"	"PON1"	"0.443"	"0.828"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1257861"	"Colonic Inertia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2016"	"6"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.34"	"0.75"	"2007"	"2013"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9032258"	"1996"	"2018"	"3"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C2674665"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)"	"phenotype"		"Finding"	"0.40"		"1997"	"2002"	"0"	"1"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C3494247"	"Organothiophosphonate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2000"	"2017"	"7"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C3494248"	"Organothiophosphate Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2000"	"2017"	"7"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5444"	"PON1"	"0.443"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5445"	"PON2"	"0.596"	"0.621"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"5445"	"PON2"	"0.596"	"0.621"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"5445"	"PON2"	"0.596"	"0.621"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2006"	"1"	"0"	"CTD_human"
"5445"	"PON2"	"0.596"	"0.621"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2006"	"1"	"0"	"CTD_human"
"5445"	"PON2"	"0.596"	"0.621"	"C1704417"	"Hyperlipoproteinemia Type IIb"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5445"	"PON2"	"0.596"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5446"	"PON3"	"0.701"	"0.345"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"5447"	"POR"	"0.554"	"0.586"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.44"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"5447"	"POR"	"0.554"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2004"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"5447"	"POR"	"0.554"	"0.586"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"5447"	"POR"	"0.554"	"0.586"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C1860042"	"Antley-Bixler Syndrome with Disordered Steroidogenesis"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2016"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5447"	"POR"	"0.554"	"0.586"	"C2350233"	"Antley-Bixler Syndrome Phenotype"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.31"		"2004"	"2016"	"4"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C2936791"	"Antley-Bixler Syndrome, Autosomal Dominant"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2016"	"4"	"0"	"CTD_human"
"5447"	"POR"	"0.554"	"0.586"	"C3150099"	"ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2005"	"3"	"0"	"CTD_human;UNIPROT"
"5449"	"POU1F1"	"0.598"	"0.414"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"5449"	"POU1F1"	"0.598"	"0.414"	"C0013338"	"Pituitary dwarfism"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"5449"	"POU1F1"	"0.598"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5449"	"POU1F1"	"0.598"	"0.414"	"C0271567"	"Isolated Growth Hormone Deficiency, Type II"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5449"	"POU1F1"	"0.598"	"0.414"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2001"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"5449"	"POU1F1"	"0.598"	"0.414"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.70"		"1990"	"2016"	"12"	"19"	"CTD_human;ORPHANET;UNIPROT"
"5449"	"POU1F1"	"0.598"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"5450"	"POU2AF1"	"0.652"	"0.345"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"5451"	"POU2F1"	"0.596"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"5453"	"POU3F1"	"0.752"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5453"	"POU3F1"	"0.752"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"5453"	"POU3F1"	"0.752"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"5454"	"POU3F2"	"0.735"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5455"	"POU3F3"	"0.857"	"0.207"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5455"	"POU3F3"	"0.857"	"0.207"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5456"	"POU3F4"	"0.773"	"0.241"	"C1844678"	"Progressive hearing loss stapes fixation"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.75"	"1"	"1992"	"2015"	"4"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5457"	"POU4F1"	"0.672"	"0.276"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C0206708"	"Cervical Intraepithelial Neoplasia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5457"	"POU4F1"	"0.672"	"0.276"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"5459"	"POU4F3"	"0.752"	"0.414"	"C1865366"	"Deafness, Autosomal Dominant 15"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2017"	"8"	"6"	"CTD_human;UNIPROT"
"5459"	"POU4F3"	"0.752"	"0.414"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2003"	"2005"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C1135868"	"Gestational Trophoblastic Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5460"	"POU5F1"	"0.485"	"0.69"	"C2931618"	"Gestational trophoblastic disease"	"disease"	"C04;C13"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5464"	"PPA1"	"0.752"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"5465"	"PPARA"	"0.465"	"0.793"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9302326"	"2000"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0015696"	"Fatty Liver, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2004"	"2012"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0020476"	"Hyperlipoproteinemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"2002"	"2010"	"2"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.36"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2012"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0022672"	"Acute Kidney Tubular Necrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.8717949"	"1997"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2012"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2002"	"2015"	"3"	"0"	"PSYGENET"
"5465"	"PPARA"	"0.465"	"0.793"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"0.9583333"	"2000"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8823529"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.96"	"2005"	"2018"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C2718067"	"Alcoholic Steatohepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C2930930"	"Abdominal obesity metabolic syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5465"	"PPARA"	"0.465"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5467"	"PPARD"	"0.551"	"0.621"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0023896"	"Alcoholic Liver Diseases"	"group"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5467"	"PPARD"	"0.551"	"0.621"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9090909"	"1998"	"2014"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.8928571"	"2000"	"2017"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9756098"	"1998"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"5468"	"PPARG"	"0.388"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.75"	"2003"	"2010"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8823529"	"2000"	"2015"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2005"	"2013"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9367089"	"1999"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011859"	"Lipoatrophic Diabetes Mellitus"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9528796"	"1998"	"2018"	"6"	"5"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2009"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.9259259"	"1999"	"2016"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2006"	"2011"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.40"		"2006"	"2011"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2014"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2014"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2003"	"2018"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2018"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.90"	"0.9681529"	"1997"	"2018"	"3"	"1"	"CTD_human;UNIPROT"
"5468"	"PPARG"	"0.388"	"0.828"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.39"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2006"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2002"	"2014"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2003"	"2009"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0039870"	"Thinness"	"phenotype"	"C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"5468"	"PPARG"	"0.388"	"0.828"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0085278"	"Antiphospholipid Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0221032"	"Familial generalized lipodystrophy"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0221406"	"Pituitary-dependent Cushing's disease"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0236811"	"Chronobiology Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2015"	"0"	"0"	"ORPHANET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0282548"	"Leukostasis"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5468"	"PPARG"	"0.388"	"0.828"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.50"	"0.9767442"	"1998"	"2017"	"0"	"4"	"CGI"
"5468"	"PPARG"	"0.388"	"0.828"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0751220"	"Inappropriate ACTH Secretion Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0813142"	"Circadian Rhythm Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0887800"	"Psychogenic Inversion of Circadian Rhythm"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2011"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.90625"	"2001"	"2015"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.50"		"2007"	"2009"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.94"	"1"	"2000"	"2016"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5468"	"PPARG"	"0.388"	"0.828"	"C1836302"	"Carotid Intimal Medial Thickness 1"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.95"	"2003"	"2018"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2014"	"3"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5468"	"PPARG"	"0.388"	"0.828"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5469"	"MED1"	"0.607"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5471"	"PPAT"	"0.799"	"0.172"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"5471"	"PPAT"	"0.799"	"0.172"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"5471"	"PPAT"	"0.799"	"0.172"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"5471"	"PPAT"	"0.799"	"0.172"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"5471"	"PPAT"	"0.799"	"0.172"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5473"	"PPBP"	"0.609"	"0.655"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5473"	"PPBP"	"0.609"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1983"	"2005"	"2"	"0"	"CTD_human"
"5473"	"PPBP"	"0.609"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5473"	"PPBP"	"0.609"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5473"	"PPBP"	"0.609"	"0.655"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5476"	"CTSA"	"0.696"	"0.552"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1995"	"2009"	"3"	"0"	"GENOMICS_ENGLAND"
"5476"	"CTSA"	"0.696"	"0.552"	"C0268233"	"GALACTOSIALIDOSIS"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1992"	"2018"	"4"	"14"	"CTD_human;ORPHANET;UNIPROT"
"5476"	"CTSA"	"0.696"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5478"	"PPIA"	"0.57"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5478"	"PPIA"	"0.57"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5478"	"PPIA"	"0.57"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5479"	"PPIB"	"0.69"	"0.379"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"0"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5479"	"PPIB"	"0.69"	"0.379"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.56"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5479"	"PPIB"	"0.69"	"0.379"	"C0268358"	"Osteogenesis imperfecta, dominant perinatal lethal"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5479"	"PPIB"	"0.69"	"0.379"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5479"	"PPIB"	"0.69"	"0.379"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5479"	"PPIB"	"0.69"	"0.379"	"C1850169"	"OSTEOGENESIS IMPERFECTA, TYPE IX (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.83"	"1"	"2009"	"2018"	"2"	"6"	"CTD_human;UNIPROT"
"5479"	"PPIB"	"0.69"	"0.379"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5480"	"PPIC"	"0.886"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5480"	"PPIC"	"0.886"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5480"	"PPIC"	"0.886"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5481"	"PPID"	"0.69"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5493"	"PPL"	"0.707"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5493"	"PPL"	"0.707"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5495"	"PPM1B"	"0.735"	"0.414"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5495"	"PPM1B"	"0.735"	"0.414"	"C1848030"	"Hypotonia-Cystinuria Syndrome"	"disease"	"C05;C10;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5495"	"PPM1B"	"0.735"	"0.414"	"C4304537"	"2p21 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5496"	"PPM1G"	"0.886"	"0.069"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5498"	"PPOX"	"0.707"	"0.241"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5498"	"PPOX"	"0.707"	"0.241"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5498"	"PPOX"	"0.707"	"0.241"	"C0162532"	"Variegate Porphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.90"	"0.9428571"	"1982"	"2015"	"29"	"19"	"ORPHANET;UNIPROT"
"5498"	"PPOX"	"0.707"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5498"	"PPOX"	"0.707"	"0.241"	"C2936913"	"Porphyria, South African type"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2014"	"29"	"18"	"CTD_human;UNIPROT"
"5498"	"PPOX"	"0.707"	"0.241"	"C3149848"	"VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2014"	"29"	"18"	"UNIPROT"
"5498"	"PPOX"	"0.707"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5500"	"PPP1CB"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"5500"	"PPP1CB"	"0.69"	"0.448"	"C4479577"	"NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"4"	"5"	"UNIPROT"
"5501"	"PPP1CC"	"0.815"	"0.172"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5501"	"PPP1CC"	"0.815"	"0.172"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5502"	"PPP1R1A"	"0.6"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"0.9166667"	"1994"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"1994"	"1995"	"1"	"2"	"UNIPROT"
"5506"	"PPP1R3A"	"0.681"	"0.379"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1994"	"1994"	"1"	"1"	"UNIPROT"
"5507"	"PPP1R3C"	"0.799"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5515"	"PPP2CA"	"0.672"	"0.586"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5515"	"PPP2CA"	"0.672"	"0.586"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5515"	"PPP2CA"	"0.672"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C3544205"	"Ovarian clear cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5518"	"PPP2R1A"	"0.59"	"0.517"	"C4225352"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 36"	"disease"		"Mental or Behavioral Dysfunction"	"0.70"		"2015"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5519"	"PPP2R1B"	"0.696"	"0.276"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human"
"5519"	"PPP2R1B"	"0.696"	"0.276"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.52"	"1"	"2000"	"2000"	"0"	"3"	"CTD_human;UNIPROT"
"5519"	"PPP2R1B"	"0.696"	"0.276"	"C0338106"	"Adenocarcinoma of colon"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5519"	"PPP2R1B"	"0.696"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"0"	"0"	"UNIPROT"
"5520"	"PPP2R2A"	"0.72"	"0.379"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5520"	"PPP2R2A"	"0.72"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2018"	"1"	"0"	"CTD_human"
"5520"	"PPP2R2A"	"0.72"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5520"	"PPP2R2A"	"0.72"	"0.379"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.12"	"0.5"	"2003"	"2012"	"1"	"2"	"PSYGENET"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C1858501"	"Spinocerebellar Ataxia 12"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.56"	"1"	"2001"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"5521"	"PPP2R2B"	"0.609"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5522"	"PPP2R2C"	"0.762"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"5522"	"PPP2R2C"	"0.762"	"0.172"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5524"	"PTPA"	"0.54"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5524"	"PTPA"	"0.54"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"5524"	"PTPA"	"0.54"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5524"	"PTPA"	"0.54"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5524"	"PTPA"	"0.54"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5524"	"PTPA"	"0.54"	"0.655"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5525"	"PPP2R5A"	"0.815"	"0.207"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5527"	"PPP2R5C"	"0.785"	"0.207"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5527"	"PPP2R5C"	"0.785"	"0.207"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5527"	"PPP2R5C"	"0.785"	"0.207"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5527"	"PPP2R5C"	"0.785"	"0.207"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5527"	"PPP2R5C"	"0.785"	"0.207"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5528"	"PPP2R5D"	"0.707"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5528"	"PPP2R5D"	"0.707"	"0.414"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5528"	"PPP2R5D"	"0.707"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5528"	"PPP2R5D"	"0.707"	"0.414"	"C4225354"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 35"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5529"	"PPP2R5E"	"0.773"	"0.138"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0039584"	"Testicular Diseases"	"group"	"C12;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5530"	"PPP3CA"	"0.569"	"0.724"	"C4540199"	"EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"5532"	"PPP3CB"	"0.815"	"0.207"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5532"	"PPP3CB"	"0.815"	"0.207"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2015"	"4"	"0"	"PSYGENET"
"5533"	"PPP3CC"	"0.815"	"0.103"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5534"	"PPP3R1"	"0.743"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2008"	"1"	"1"	"PSYGENET"
"5534"	"PPP3R1"	"0.743"	"0.276"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"5534"	"PPP3R1"	"0.743"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5537"	"PPP6C"	"0.743"	"0.172"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5537"	"PPP6C"	"0.743"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"1"	"2012"	"2015"	"1"	"0"	"CGI;CTD_human"
"5537"	"PPP6C"	"0.743"	"0.172"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"1"	"CGI"
"5537"	"PPP6C"	"0.743"	"0.172"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5538"	"PPT1"	"0.627"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5538"	"PPT1"	"0.627"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5538"	"PPT1"	"0.627"	"0.448"	"C0268281"	"Infantile neuronal ceroid lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9166667"	"1995"	"2018"	"7"	"22"	"UNIPROT"
"5538"	"PPT1"	"0.627"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5538"	"PPT1"	"0.627"	"0.448"	"C1850451"	"CEROID LIPOFUSCINOSIS, NEURONAL, 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.94"	"1"	"1989"	"2018"	"7"	"75"	"CTD_human;ORPHANET;UNIPROT"
"5538"	"PPT1"	"0.627"	"0.448"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"8"	"22"	"CTD_human;UNIPROT"
"5538"	"PPT1"	"0.627"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5546"	"PRCC"	"0.762"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2003"	"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.42"	"1"	"1997"	"2002"	"0"	"0"	"CTD_human"
"5546"	"PRCC"	"0.762"	"0.103"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5550"	"PREP"	"0.627"	"0.552"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0002624"	"Retrograde amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5550"	"PREP"	"0.627"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"5550"	"PREP"	"0.627"	"0.552"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0750908"	"Pre-Ictal Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0750909"	"Retrograde Memory Loss"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C0750910"	"Pre-Ictal Memory Loss"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5550"	"PREP"	"0.627"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"0"	"1"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2011"	"0"	"0"	"CGI"
"5551"	"PRF1"	"0.475"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5551"	"PRF1"	"0.475"	"0.69"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.49"	"0.8888889"	"1995"	"2016"	"0"	"0"	"CGI"
"5551"	"PRF1"	"0.475"	"0.69"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"		"1999"	"2006"	"0"	"1"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C0272199"	"Familial Hemophagocytic Lymphocytosis"	"phenotype"	"C15"	"Disease or Syndrome"	"0.41"	"1"	"1999"	"2017"	"0"	"1"	"ORPHANET"
"5551"	"PRF1"	"0.475"	"0.69"	"C0348890"	"Aplastic anemia, idiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5551"	"PRF1"	"0.475"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"5551"	"PRF1"	"0.475"	"0.69"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C1863727"	"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2"	"disease"	"C15"	"Disease or Syndrome"	"0.85"	"1"	"1995"	"2017"	"2"	"18"	"CTD_human;UNIPROT"
"5551"	"PRF1"	"0.475"	"0.69"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5551"	"PRF1"	"0.475"	"0.69"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5552"	"SRGN"	"0.735"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5553"	"PRG2"	"0.707"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2018"	"1"	"1"	"UNIPROT"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5562"	"PRKAA1"	"0.54"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2013"	"2018"	"0"	"0"	"UNIPROT"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5563"	"PRKAA2"	"0.546"	"0.655"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5564"	"PRKAB1"	"0.551"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"5564"	"PRKAB1"	"0.551"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5564"	"PRKAB1"	"0.551"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5564"	"PRKAB1"	"0.551"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C0334287"	"Fibrolamellar Hepatocellular Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"5566"	"PRKACA"	"0.616"	"0.552"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5566"	"PRKACA"	"0.616"	"0.552"	"C4014425"	"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"4"	"2"	"CTD_human;UNIPROT"
"5566"	"PRKACA"	"0.616"	"0.552"	"C4016748"	"CUSHING SYNDROME, ACTH-INDEPENDENT ADRENAL, SOMATIC"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"4"	"1"	"CTD_human;UNIPROT"
"5566"	"PRKACA"	"0.616"	"0.552"	"C4304832"	"Primary pigmented nodular adrenocortical disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0005426"	"Biliary Tract Neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C0750952"	"Biliary Tract Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5567"	"PRKACB"	"0.685"	"0.414"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5568"	"PRKACG"	"0.701"	"0.414"	"C4015405"	"BLEEDING DISORDER, PLATELET-TYPE, 19"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0001618"	"Tumors of Adrenal Cortex"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0007115"	"Malignant neoplasm of thyroid"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2002"	"2014"	"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0010481"	"Cushing Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"0.8235294"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0014132"	"Endocrine Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0027149"	"Myxoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2016"	"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2010"	"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0220659"	"Acrodysostosis"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.58"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0346402"	"Malignant neoplasm of adrenal cortex"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2012"	"0"	"0"	"CGI"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0406810"	"Carney Complex"	"disease"	"C04;C14;C16"	"Disease or Syndrome"	"0.90"	"0.9489796"	"2000"	"2018"	"1"	"3"	"CTD_human;ORPHANET"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.63"	"1"	"1993"	"2014"	"2"	"0"	"CGI;GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C1850635"	"Atrial myxoma, familial"	"disease"	"C04;C14"	"Neoplastic Process"	"0.60"		"1976"	"2000"	"0"	"1"	"CTD_human;ORPHANET"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C1854540"	"Carney Complex, Type 2"	"disease"	"C04;C14;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2017"	"1"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C1864846"	"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (disorder)"	"disease"	"C19"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"0"	"2"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C2607929"	"Carney Complex, Type 1"	"disease"	"C04;C14;C16"	"Disease or Syndrome"	"0.92"	"1"	"1993"	"2017"	"6"	"24"	"CTD_human;ORPHANET;UNIPROT"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C2931787"	"Intracardiac myxoma"	"disease"	"C04;C14"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C3276228"	"ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2001"	"2017"	"8"	"4"	"CTD_human;UNIPROT"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C3553250"	"ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C3887949"	"Apparent mineralocorticoid excess"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5573"	"PRKAR1A"	"0.466"	"0.69"	"C4304832"	"Primary pigmented nodular adrenocortical disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5577"	"PRKAR2B"	"0.762"	"0.345"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0032617"	"Polyuria"	"phenotype"	"C12;C13;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2011"	"2"	"0"	"PSYGENET"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0162283"	"Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0268443"	"Acquired Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5578"	"PRKCA"	"0.535"	"0.655"	"C0677501"	"Congenital Nephrogenic Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5578"	"PRKCA"	"0.535"	"0.655"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C1563705"	"Nephrogenic Diabetes Insipidus, Type I"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C1563706"	"Nephrogenic Diabetes Insipidus, Type II"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5578"	"PRKCA"	"0.535"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"5578"	"PRKCA"	"0.535"	"0.655"	"C3542500"	"ADH-Resistant Diabetes Insipidus"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"2005"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5579"	"PRKCB"	"0.564"	"0.69"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2014"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C1328840"	"Autoimmune Lymphoproliferative Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"5580"	"PRKCD"	"0.524"	"0.586"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C3280742"	"SYSTEMIC LUPUS ERYTHEMATOSUS 16"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5580"	"PRKCD"	"0.524"	"0.586"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C3809928"	"AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"3"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5580"	"PRKCD"	"0.524"	"0.586"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0242231"	"Coronary Stenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"1995"	"2006"	"2"	"1"	"CTD_human;UNIPROT"
"5581"	"PRKCE"	"0.604"	"0.552"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2011"	"3"	"0"	"CTD_human"
"5581"	"PRKCE"	"0.604"	"0.552"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C1854369"	"Spinocerebellar ataxia 14"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2015"	"1"	"25"	"CTD_human;ORPHANET;UNIPROT"
"5582"	"PRKCG"	"0.642"	"0.345"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"5582"	"PRKCG"	"0.642"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2004"	"2012"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2012"	"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5583"	"PRKCH"	"0.676"	"0.483"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5583"	"PRKCH"	"0.676"	"0.483"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5584"	"PRKCI"	"0.63"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"5584"	"PRKCI"	"0.63"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5584"	"PRKCI"	"0.63"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5584"	"PRKCI"	"0.63"	"0.414"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5585"	"PKN1"	"0.681"	"0.517"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5585"	"PKN1"	"0.681"	"0.517"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5585"	"PKN1"	"0.681"	"0.517"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5587"	"PRKD1"	"0.569"	"0.655"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5587"	"PRKD1"	"0.569"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"5587"	"PRKD1"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5587"	"PRKD1"	"0.569"	"0.655"	"C4479250"	"CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2014"	"3"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"		"2008"	"2010"	"1"	"1"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5588"	"PRKCQ"	"0.645"	"0.483"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5589"	"PRKCSH"	"0.735"	"0.517"	"C0022680"	"Polycystic Kidney Diseases"	"group"	"C12;C13;C16"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"5589"	"PRKCSH"	"0.735"	"0.517"	"C0158683"	"Polycystic liver disease"	"disease"	"C04;C06;C23"	"Disease or Syndrome"	"0.70"	"0.9375"	"2003"	"2014"	"2"	"0"	"CTD_human;ORPHANET"
"5589"	"PRKCSH"	"0.735"	"0.517"	"C1567435"	"Polycystic Kidney - body part"	"phenotype"	"C12;C13;C16"	"Anatomical Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5589"	"PRKCSH"	"0.735"	"0.517"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5589"	"PRKCSH"	"0.735"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5590"	"PRKCZ"	"0.619"	"0.483"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0001364"	"Massive Hepatic Necrosis"	"phenotype"	"C06"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"5591"	"PRKDC"	"0.552"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C4014833"	"IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2013"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5591"	"PRKDC"	"0.552"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5591"	"PRKDC"	"0.552"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"1998"	"2017"	"3"	"0"	"CLINGEN"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5592"	"PRKG1"	"0.575"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5592"	"PRKG1"	"0.575"	"0.724"	"C3809513"	"AORTIC ANEURYSM, FAMILIAL THORACIC 8"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"5593"	"PRKG2"	"0.785"	"0.31"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"PSYGENET"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.31"	"0"	"2013"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9772727"	"2003"	"2018"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"PSYGENET"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2005"	"2008"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2018"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2011"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C2678480"	"Chromosome 22q11.2 Deletion Syndrome, Distal"	"disease"	"C05;C14;C15;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5594"	"MAPK1"	"0.387"	"0.862"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5594"	"MAPK1"	"0.387"	"0.862"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2012"	"5"	"0"	"PSYGENET"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2012"	"5"	"0"	"PSYGENET"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9583333"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9642857"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2015"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2017"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"2005"	"2007"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5595"	"MAPK3"	"0.429"	"0.828"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5597"	"MAPK6"	"0.762"	"0.241"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5598"	"MAPK7"	"0.614"	"0.448"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2011"	"2"	"0"	"PSYGENET"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2011"	"2"	"0"	"PSYGENET"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"5599"	"MAPK8"	"0.458"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5599"	"MAPK8"	"0.458"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5600"	"MAPK11"	"0.799"	"0.31"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5600"	"MAPK11"	"0.799"	"0.31"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5600"	"MAPK11"	"0.799"	"0.31"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5601"	"MAPK9"	"0.607"	"0.586"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5601"	"MAPK9"	"0.607"	"0.586"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5601"	"MAPK9"	"0.607"	"0.586"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5602"	"MAPK10"	"0.69"	"0.414"	"C0238111"	"Lennox-Gastaut syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5602"	"MAPK10"	"0.69"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5602"	"MAPK10"	"0.69"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5603"	"MAPK13"	"0.773"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"1"	"1995"	"2016"	"0"	"3"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0023443"	"Hairy Cell Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.8928571"	"2003"	"2018"	"1"	"14"	"CGI;CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.34"	"1"	"2003"	"2015"	"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"6"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.63"	"1"	"2008"	"2016"	"1"	"6"	"CGI;CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.54"	"1"	"2007"	"2016"	"1"	"0"	"CLINGEN;CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2015"	"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"0.70"	"1"	"1993"	"2017"	"2"	"10"	"CTD_human;ORPHANET"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C1968782"	"MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5604"	"MAP2K1"	"0.459"	"0.759"	"C3809006"	"CARDIOFACIOCUTANEOUS SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2016"	"7"	"6"	"CLINGEN;UNIPROT"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.66"	"1"	"2011"	"2015"	"1"	"5"	"CGI;CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2016"	"0"	"2"	"CGI"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0553586"	"Cafe-au-lait macules with pulmonary stenosis"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"0.80"	"0.9285714"	"1993"	"2017"	"6"	"6"	"CLINGEN;CTD_human;ORPHANET"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C2931482"	"Neurofibromatosis-Noonan syndrome"	"disease"	"C04;C05;C10;C14;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5605"	"MAP2K2"	"0.559"	"0.586"	"C3809007"	"CARDIOFACIOCUTANEOUS SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2015"	"3"	"6"	"UNIPROT"
"5606"	"MAP2K3"	"0.69"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5607"	"MAP2K5"	"0.659"	"0.448"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5607"	"MAP2K5"	"0.659"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5607"	"MAP2K5"	"0.659"	"0.448"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5607"	"MAP2K5"	"0.659"	"0.448"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5607"	"MAP2K5"	"0.659"	"0.448"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5608"	"MAP2K6"	"0.707"	"0.448"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5609"	"MAP2K7"	"0.462"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2000"	"2013"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5610"	"EIF2AK2"	"0.562"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5611"	"DNAJC3"	"0.707"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5611"	"DNAJC3"	"0.707"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5611"	"DNAJC3"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5611"	"DNAJC3"	"0.707"	"0.379"	"C4015436"	"ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5617"	"PRL"	"0.454"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9473684"	"1981"	"2018"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0002453"	"Amenorrhea"	"phenotype"	"C23"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1981"	"2014"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0005001"	"Benign prostatic hypertrophy"	"phenotype"	"C12"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0008909"	"Claustrophobia"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0015951"	"Fetal Resorption"	"disease"	"C13;C23"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0016722"	"Frigidity"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0018418"	"Gynecomastia"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1997"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.60"	"0.9655172"	"1983"	"2018"	"4"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0020594"	"Hypoactive Sexual Desire Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0020635"	"Hypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"1998"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1977"	"1983"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0021308"	"Infarction"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0023601"	"Leydig Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1982"	"2006"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0029261"	"Orgasmic Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.40"	"0.962963"	"1980"	"2018"	"3"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0032019"	"Pituitary Neoplasms"	"group"	"C04;C10;C19"	"Neoplastic Process"	"0.40"	"0.9756098"	"1980"	"2015"	"3"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0032796"	"Postpartum Amenorrhea"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0032963"	"Pregnancy Complications, Cardiovascular"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.60"	"0.8571429"	"1979"	"2016"	"4"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0033953"	"Psychosexual Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0034040"	"Puerperal Disorders"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2004"	"2018"	"1"	"0"	"PSYGENET"
"5617"	"PRL"	"0.454"	"0.793"	"C0036902"	"Sexual Arousal Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1991"	"2002"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0237873"	"Physiological Sexual Disorders"	"group"	"C12;C13"	"Pathologic Function"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0242342"	"Sheehan Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.31"	"1"	"1980"	"2011"	"5"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.31"	"0"	"2002"	"2012"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0344452"	"Microprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"1979"	"1998"	"4"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0344453"	"Macroprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.32"	"0.5"	"1979"	"2014"	"4"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0346300"	"Pituitary carcinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.33"	"1"	"1980"	"2011"	"3"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0346302"	"Growth Hormone-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.33"	"1"	"1991"	"2010"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0349231"	"Phobic anxiety disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0520477"	"Prostatic Adenoma"	"disease"	"C12"	"Neoplastic Process"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"PSYGENET"
"5617"	"PRL"	"0.454"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1982"	"2006"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1449720"	"Adolescent Gynecomastia"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1997"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1449721"	"Infant Gynecomastia"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1997"	"2"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1704272"	"Benign Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.32"	"1"	"1990"	"2002"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1739363"	"Prostatic Hypertrophy"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1975"	"1975"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C2937421"	"Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2002"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C3489630"	"Somatotrophinoma, Familial"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"5617"	"PRL"	"0.454"	"0.793"	"C3665358"	"Galactorrhea"	"disease"	"C13;C17"	"Disease or Syndrome"	"0.31"	"0"	"1993"	"2010"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0020514"	"Hyperprolactinemia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.73"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5618"	"PRLR"	"0.621"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"5618"	"PRLR"	"0.621"	"0.379"	"C3809918"	"MULTIPLE FIBROADENOMAS OF THE BREAST"	"disease"		"Neoplastic Process"	"0.60"		"2008"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9104478"	"1986"	"2016"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5621"	"PRNP"	"0.474"	"0.897"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"5621"	"PRNP"	"0.474"	"0.897"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9032258"	"1990"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5621"	"PRNP"	"0.474"	"0.897"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1992"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"5621"	"PRNP"	"0.474"	"0.897"	"C0017495"	"Gerstmann-Straussler-Scheinker Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9826087"	"1989"	"2017"	"12"	"13"	"CTD_human;ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"1.00"	"0.9463602"	"1988"	"2018"	"12"	"10"	"CTD_human;ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0022802"	"Kuru"	"disease"	"C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5621"	"PRNP"	"0.474"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0036457"	"Scrapie"	"disease"	"C10;C22"	"Disease or Syndrome"	"0.35"	"1"	"1994"	"2011"	"4"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2006"	"2008"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0162534"	"Prion Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.9562363"	"1988"	"2018"	"4"	"15"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0206042"	"Fatal Familial Insomnia"	"disease"	"C10"	"Disease or Syndrome"	"1.00"	"0.9577465"	"1989"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"0.5"	"2000"	"2012"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.875"	"1990"	"2016"	"12"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"5621"	"PRNP"	"0.474"	"0.897"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5621"	"PRNP"	"0.474"	"0.897"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2018"	"12"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751645"	"Human Transmissible Spongiform Encephalopathies, Inherited"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2007"	"4"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5621"	"PRNP"	"0.474"	"0.897"	"C1847650"	"SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.60"		"1997"	"2006"	"2"	"3"	"CTD_human;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C1852467"	"Creutzfeldt-Jakob Disease, Sporadic"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9722222"	"1990"	"2016"	"10"	"8"	"ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C1864112"	"HUNTINGTON DISEASE-LIKE 1"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.60"		"1989"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"5621"	"PRNP"	"0.474"	"0.897"	"C1969957"	"Creutzfeldt-Jakob Disease, Heidenhain Variant"	"disease"	"C10;C11;C23;F03"	"Disease or Syndrome"	"0.50"		"1990"	"2010"	"10"	"8"	"ORPHANET;UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5621"	"PRNP"	"0.474"	"0.897"	"C2931022"	"Amyloidosis, Cerebral, with Spongiform Encephalopathy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1989"	"2010"	"11"	"8"	"UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C3805618"	"CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED"	"disease"		"Disease or Syndrome"	"0.40"		"1989"	"2011"	"11"	"11"	"UNIPROT"
"5621"	"PRNP"	"0.474"	"0.897"	"C4303482"	"Familial Alzheimer-like prion disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5623"	"PSPN"	"0.743"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5624"	"PROC"	"0.645"	"0.586"	"C0003860"	"Arteritis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.34"		"1996"	"2008"	"4"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.43"		"2004"	"2015"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0085650"	"Purpura Fulminans"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1996"	"2008"	"4"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2004"	"2016"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"		"2002"	"2007"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C0398625"	"Protein C Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2012"	"3"	"0"	"CTD_human;ORPHANET"
"5624"	"PROC"	"0.645"	"0.586"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.33"		"1997"	"2011"	"2"	"0"	"CTD_human"
"5624"	"PROC"	"0.645"	"0.586"	"C2674321"	"Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1987"	"2017"	"16"	"26"	"UNIPROT"
"5624"	"PROC"	"0.645"	"0.586"	"C2674322"	"Protein C Deficiency, Acquired"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1987"	"2016"	"16"	"18"	"UNIPROT"
"5624"	"PROC"	"0.645"	"0.586"	"C2676759"	"THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1988"	"2016"	"7"	"12"	"CTD_human;UNIPROT"
"5624"	"PROC"	"0.645"	"0.586"	"C2930896"	"Congenital thrombotic disease, due to Protein C deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5625"	"PRODH"	"0.614"	"0.586"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5625"	"PRODH"	"0.614"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2006"	"2007"	"2"	"0"	"PSYGENET"
"5625"	"PRODH"	"0.614"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"5625"	"PRODH"	"0.614"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5625"	"PRODH"	"0.614"	"0.586"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5625"	"PRODH"	"0.614"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9444444"	"2004"	"2018"	"1"	"0"	"CTD_human"
"5625"	"PRODH"	"0.614"	"0.586"	"C0268529"	"Proline dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.77"	"1"	"1996"	"2008"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"5625"	"PRODH"	"0.614"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5625"	"PRODH"	"0.614"	"0.586"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5625"	"PRODH"	"0.614"	"0.586"	"C1833247"	"SCHIZOPHRENIA 4 (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2005"	"1"	"9"	"UNIPROT"
"5625"	"PRODH"	"0.614"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"		"2003"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"5626"	"PROP1"	"0.609"	"0.483"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"1998"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"5626"	"PROP1"	"0.609"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5626"	"PROP1"	"0.609"	"0.483"	"C0242343"	"Panhypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.70"	"0.9772727"	"1998"	"2018"	"7"	"7"	"ORPHANET;UNIPROT"
"5626"	"PROP1"	"0.609"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5626"	"PROP1"	"0.609"	"0.483"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1998"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"5626"	"PROP1"	"0.609"	"0.483"	"C0878683"	"Pituitary Dwarfism Type 3"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.60"		"1967"	"2012"	"7"	"23"	"CTD_human;UNIPROT"
"5626"	"PROP1"	"0.609"	"0.483"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5626"	"PROP1"	"0.609"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5627"	"PROS1"	"0.562"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"2001"	"2005"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0338575"	"Sagittal Sinus Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0600433"	"Activated Protein C Resistance"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"		"2001"	"2008"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0751823"	"Septic Phlebitis, Sagittal Sinus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C0751824"	"Sagittal Sinus Thrombophlebitis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5627"	"PROS1"	"0.562"	"0.621"	"C3278211"	"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.40"		"1994"	"2017"	"26"	"31"	"UNIPROT"
"5627"	"PROS1"	"0.562"	"0.621"	"C3281092"	"THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"1995"	"2017"	"1"	"3"	"UNIPROT"
"5627"	"PROS1"	"0.562"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C3502051"	"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C3502052"	"Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5627"	"PROS1"	"0.562"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5629"	"PROX1"	"0.596"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2018"	"1"	"2"	"CTD_human"
"5629"	"PROX1"	"0.596"	"0.448"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5630"	"PRPH"	"0.639"	"0.379"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2016"	"0"	"0"	"ORPHANET"
"5630"	"PRPH"	"0.639"	"0.379"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5630"	"PRPH"	"0.639"	"0.379"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"5631"	"PRPS1"	"0.614"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"5631"	"PRPS1"	"0.614"	"0.655"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5631"	"PRPS1"	"0.614"	"0.655"	"C0796028"	"ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.77"	"1"	"1993"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C1839566"	"CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5"	"disease"	"C05;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C1844677"	"DEAFNESS, X-LINKED 1 (disorder)"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.44"	"1"	"1997"	"2016"	"1"	"7"	"UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C1970827"	"Phosphoribosylpyrophosphate Synthetase Superactivity"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1975"	"2012"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"5631"	"PRPS1"	"0.614"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5638"	"PRRG1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5638"	"PRRG1"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5641"	"LGMN"	"0.652"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5644"	"PRSS1"	"0.592"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.70"	"0.9268293"	"1997"	"2014"	"1"	"1"	"CTD_human"
"5644"	"PRSS1"	"0.592"	"0.621"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9672131"	"1997"	"2017"	"1"	"0"	"CTD_human"
"5644"	"PRSS1"	"0.592"	"0.621"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.80"	"0.9333333"	"1967"	"2017"	"11"	"16"	"CTD_human;ORPHANET;UNIPROT"
"5644"	"PRSS1"	"0.592"	"0.621"	"C0268417"	"Pancreatic trypsinogen deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5644"	"PRSS1"	"0.592"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5644"	"PRSS1"	"0.592"	"0.621"	"C1832108"	"PANCREATITIS, CHRONIC, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1996"	"2006"	"11"	"9"	"UNIPROT"
"5644"	"PRSS1"	"0.592"	"0.621"	"C1868653"	"Pancreatitis, Calcific"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1996"	"2006"	"11"	"9"	"UNIPROT"
"5644"	"PRSS1"	"0.592"	"0.621"	"C1969419"	"PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1996"	"2006"	"11"	"9"	"UNIPROT"
"5644"	"PRSS1"	"0.592"	"0.621"	"C4080064"	"Autosomal Dominant Hereditary Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"5645"	"PRSS2"	"0.69"	"0.448"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"5645"	"PRSS2"	"0.69"	"0.448"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.8888889"	"2006"	"2016"	"2"	"0"	"CTD_human"
"5645"	"PRSS2"	"0.69"	"0.448"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"5645"	"PRSS2"	"0.69"	"0.448"	"C4080064"	"Autosomal Dominant Hereditary Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5646"	"PRSS3"	"0.639"	"0.448"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"5646"	"PRSS3"	"0.639"	"0.448"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0036305"	"Schamberg Disease"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0549567"	"Pigmentation Disorders"	"group"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0796032"	"Malpuech facial clefting syndrome"	"disease"	"C05;C14;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0796059"	"Oculopalatoskeletal syndrome"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2016"	"1"	"4"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C0796279"	"Carnevale syndrome"	"disease"	"C05;C10;C11;C12;C16;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5648"	"MASP1"	"0.607"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"5648"	"MASP1"	"0.607"	"0.69"	"C4303860"	"Craniofacial ulnar renal syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5649"	"RELN"	"0.547"	"0.655"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9259259"	"2001"	"2017"	"3"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2001"	"2015"	"8"	"0"	"CTD_human;PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2005"	"3"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2014"	"4"	"0"	"PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2005"	"2014"	"4"	"0"	"CTD_human;PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2005"	"3"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9411765"	"1999"	"2017"	"4"	"1"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2005"	"2014"	"3"	"0"	"CTD_human;PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2005"	"3"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C0796089"	"LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"5649"	"RELN"	"0.547"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2001"	"2014"	"3"	"0"	"CTD_human;PSYGENET"
"5649"	"RELN"	"0.547"	"0.655"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8571429"	"2003"	"2018"	"2"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5649"	"RELN"	"0.547"	"0.655"	"C1838062"	"EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.51"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"5649"	"RELN"	"0.547"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5649"	"RELN"	"0.547"	"0.655"	"C4225327"	"EPILEPSY, FAMILIAL TEMPORAL LOBE, 7"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"1"	"7"	"CTD_human;UNIPROT"
"5651"	"TMPRSS15"	"0.857"	"0.172"	"C0268416"	"Enterokinase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1971"	"2013"	"0"	"4"	"CTD_human;ORPHANET"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0013949"	"Embryopathies"	"disease"	"C13;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0015929"	"Fetal Diseases"	"group"	"C13;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0032045"	"Placenta Disorders"	"group"	"C13"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"5652"	"PRSS8"	"0.639"	"0.414"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2017"	"1"	"0"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0206729"	"Neurofibrosarcoma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0751587"	"CADASIL Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5654"	"HTRA1"	"0.572"	"0.621"	"C1449626"	"CADASILM"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C1838577"	"Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy"	"disease"	"C05;C10;C14;C17;C23"	"Disease or Syndrome"	"0.80"	"0.9"	"1993"	"2018"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"5654"	"HTRA1"	"0.572"	"0.621"	"C1857813"	"Macular Degeneration, Age-Related, 7"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2006"	"2010"	"0"	"1"	"CTD_human"
"5654"	"HTRA1"	"0.572"	"0.621"	"C4225211"	"CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"6"	"UNIPROT"
"5655"	"KLK10"	"0.63"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2013"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"5655"	"KLK10"	"0.63"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5657"	"PRTN3"	"0.58"	"0.586"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"5657"	"PRTN3"	"0.58"	"0.586"	"C3495801"	"Granulomatosis with polyangiitis"	"disease"	"C08;C14;C20"	"Disease or Syndrome"	"0.60"	"0.9583333"	"1996"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5660"	"PSAP"	"0.577"	"0.69"	"C0268262"	"Metachromatic Leukodystrophy due to Saposin B Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1971"	"2009"	"5"	"4"	"CTD_human;UNIPROT"
"5660"	"PSAP"	"0.577"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5660"	"PSAP"	"0.577"	"0.69"	"C0751273"	"Infantile Globoid Cell Leukodystrophy"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C0751276"	"Metachromatic leukodystrophy, juvenile type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C0751278"	"Metachromatic Leukodystrophy, Infant"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C0751279"	"Metachromatic Leukodystrophy, Adult-Type (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C1864651"	"GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"		"1986"	"2008"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5660"	"PSAP"	"0.577"	"0.69"	"C2673266"	"KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"5660"	"PSAP"	"0.577"	"0.69"	"C2673635"	"Combined Saposin Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1990"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"5660"	"PSAP"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5662"	"PSD"	"0.743"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2006"	"2014"	"1"	"0"	"PSYGENET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9385246"	"1990"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9230769"	"1996"	"2018"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.62"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9736842"	"1990"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2012"	"5"	"0"	"PSYGENET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2000"	"2012"	"5"	"0"	"PSYGENET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9285714"	"2002"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0236642"	"Pick Disease of the Brain"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"1"	"1995"	"2017"	"2"	"9"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9615385"	"1989"	"2018"	"13"	"0"	"CTD_human;ORPHANET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0338451"	"Frontotemporal dementia"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2017"	"1"	"9"	"CTD_human;UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2001"	"2001"	"1"	"0"	"CTD_human;ORPHANET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9333333"	"1995"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0520716"	"Pallidopontonigral degeneration"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"1"	"UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9880952"	"1995"	"2018"	"13"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.43"	"1"	"2008"	"2018"	"2"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"5663"	"PSEN1"	"0.49"	"0.69"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1838313"	"Pick Complex"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"1"	"UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1843013"	"Alzheimer disease, familial, type 3"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2017"	"39"	"88"	"UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1843014"	"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.50"		"1995"	"2016"	"39"	"80"	"UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C1843015"	"Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.80"		"1995"	"2016"	"39"	"81"	"CTD_human;UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C3160720"	"Cardiomyopathy, Dilated, 1u"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"5663"	"PSEN1"	"0.49"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5663"	"PSEN1"	"0.49"	"0.69"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.9781022"	"1995"	"2018"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2010"	"2"	"0"	"PSYGENET"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9"	"1997"	"2011"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2004"	"2013"	"3"	"0"	"PSYGENET"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"	"0.9466667"	"1995"	"2017"	"3"	"0"	"CTD_human;ORPHANET"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1997"	"2016"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2006"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2006"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"3"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5664"	"PSEN2"	"0.567"	"0.517"	"C1847200"	"ALZHEIMER DISEASE 4"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"6"	"11"	"CTD_human;UNIPROT"
"5664"	"PSEN2"	"0.567"	"0.517"	"C3150958"	"Cardiomyopathy, Dilated, 1V"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"5673"	"PSG5"	"0.72"	"0.379"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5683"	"PSMA2"	"0.815"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5685"	"PSMA4"	"0.743"	"0.276"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5686"	"PSMA5"	"0.663"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5687"	"PSMA6"	"0.69"	"0.379"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5687"	"PSMA6"	"0.69"	"0.379"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2006"	"2013"	"1"	"1"	"CTD_human"
"5687"	"PSMA6"	"0.69"	"0.379"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5688"	"PSMA7"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5689"	"PSMB1"	"0.815"	"0.207"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5689"	"PSMB1"	"0.815"	"0.207"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"5689"	"PSMB1"	"0.815"	"0.207"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5689"	"PSMB1"	"0.815"	"0.207"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5690"	"PSMB2"	"0.886"	"0.138"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5690"	"PSMB2"	"0.886"	"0.138"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5692"	"PSMB4"	"0.834"	"0.172"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5692"	"PSMB4"	"0.834"	"0.172"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5692"	"PSMB4"	"0.834"	"0.172"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5692"	"PSMB4"	"0.834"	"0.172"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5693"	"PSMB5"	"0.762"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5696"	"PSMB8"	"0.586"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5696"	"PSMB8"	"0.586"	"0.759"	"C1850568"	"Nakajo syndrome"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.76"	"1"	"1993"	"2017"	"6"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5696"	"PSMB8"	"0.586"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5696"	"PSMB8"	"0.586"	"0.759"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"5697"	"PYY"	"0.639"	"0.414"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1996"	"2011"	"2"	"0"	"PSYGENET"
"5697"	"PYY"	"0.639"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1996"	"2011"	"2"	"0"	"PSYGENET"
"5697"	"PYY"	"0.639"	"0.414"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9444444"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5697"	"PYY"	"0.639"	"0.414"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5698"	"PSMB9"	"0.579"	"0.69"	"C0001197"	"Acrodermatitis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5698"	"PSMB9"	"0.579"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5698"	"PSMB9"	"0.579"	"0.69"	"C0263372"	"Gianotti-Crosti Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5699"	"PSMB10"	"0.762"	"0.31"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5699"	"PSMB10"	"0.762"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5699"	"PSMB10"	"0.762"	"0.31"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5702"	"PSMC3"	"0.886"	"0.138"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5702"	"PSMC3"	"0.886"	"0.138"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5705"	"PSMC5"	"0.762"	"0.31"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5705"	"PSMC5"	"0.762"	"0.31"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5709"	"PSMD3"	"0.799"	"0.172"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5709"	"PSMD3"	"0.799"	"0.172"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5714"	"PSMD8"	"0.743"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5714"	"PSMD8"	"0.743"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5716"	"PSMD10"	"0.614"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5718"	"PSMD12"	"0.743"	"0.448"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5718"	"PSMD12"	"0.743"	"0.448"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5718"	"PSMD12"	"0.743"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5719"	"PSMD13"	"0.886"	"0.103"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5719"	"PSMD13"	"0.886"	"0.103"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5720"	"PSME1"	"0.773"	"0.345"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5721"	"PSME2"	"0.815"	"0.207"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5721"	"PSME2"	"0.815"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5721"	"PSME2"	"0.815"	"0.207"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5721"	"PSME2"	"0.815"	"0.207"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5723"	"PSPH"	"0.72"	"0.414"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5723"	"PSPH"	"0.72"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5723"	"PSPH"	"0.72"	"0.414"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5723"	"PSPH"	"0.72"	"0.414"	"C1291463"	"Deficiency of phosphoserine phosphatase"	"disease"		"Disease or Syndrome"	"0.70"		"1997"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5723"	"PSPH"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"5724"	"PTAFR"	"0.639"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5724"	"PTAFR"	"0.639"	"0.552"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5724"	"PTAFR"	"0.639"	"0.552"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5725"	"PTBP1"	"0.499"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.54"	"0.75"	"1992"	"2011"	"4"	"0"	"CTD_human;PSYGENET"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C0455383"	"FH: Depression"	"phenotype"		"Finding"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C1868397"	"THIOUREA TASTING"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C1868398"	"PHENYLTHIOCARBAMIDE TASTING"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C1868399"	"PTC TASTING"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C1868400"	"PROPYLTHIOURACIL TASTING"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5726"	"TAS2R38"	"0.592"	"0.655"	"C1868401"	"PROP TASTING"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0004779"	"Basal Cell Nevus Syndrome"	"disease"	"C04;C05;C07;C16"	"Neoplastic Process"	"1.00"	"0.9736842"	"1996"	"2018"	"20"	"49"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2000"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.90"		"1998"	"2016"	"3"	"0"	"CGI;CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2012"	"1"	"2"	"UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.41"	"1"	"2006"	"2017"	"1"	"1"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.90"	"1"	"1997"	"2016"	"3"	"0"	"CGI;CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"1998"	"2008"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2002"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2009"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C0812437"	"Oculo-dento-digital syndrome"	"disease"	"C05;C07;C11;C16"	"Congenital Abnormality"	"0.60"	"1"	"1996"	"2016"	"9"	"0"	"CLINGEN;ORPHANET"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2016"	"3"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1835820"	"HOLOPROSENCEPHALY 7"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2009"	"3"	"6"	"CTD_human;UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C1854245"	"Basal cell carcinoma, multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"		"1996"	"1998"	"2"	"1"	"UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C2751544"	"BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1"	"disease"		"Finding"	"0.30"		"1996"	"1998"	"2"	"1"	"UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C2751545"	"Basal Cell Carcinoma, Nonsyndromic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1998"	"2"	"1"	"UNIPROT"
"5727"	"PTCH1"	"0.435"	"0.759"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5727"	"PTCH1"	"0.435"	"0.759"	"C3711390"	"9q22.3 Microdeletion"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5727"	"PTCH1"	"0.435"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5727"	"PTCH1"	"0.435"	"0.759"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9714286"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0003081"	"Anisometropia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"0.96"	"2001"	"2018"	"4"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.50"	"1"	"1999"	"2015"	"0"	"4"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9714286"	"1997"	"2018"	"4"	"0"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.60"	"0.9756098"	"1999"	"2016"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.43"	"1"	"2009"	"2017"	"0"	"2"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"0.9818182"	"1998"	"2018"	"0"	"1"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"1"	"1998"	"2017"	"1"	"2"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2009"	"3"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0013403"	"Dysplastic Nevus Syndrome"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.60"	"1"	"1997"	"2014"	"4"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0014173"	"Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.38"	"0.875"	"1998"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1993"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9285714"	"1997"	"2017"	"4"	"4"	"UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9527559"	"1997"	"2018"	"3"	"1"	"CGI;CTD_human;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"1.00"	"0.947619"	"1997"	"2018"	"31"	"20"	"CTD_human;ORPHANET;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0018916"	"Hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2002"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2009"	"5"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023798"	"Lipoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023801"	"Lipomatosis"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.44"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.59"	"1"	"1998"	"2017"	"2"	"0"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9230769"	"1998"	"2018"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.954023"	"1997"	"2017"	"3"	"3"	"CGI;CTD_human;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.44"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2009"	"5"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9745763"	"1997"	"2018"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9142857"	"1998"	"2018"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.60"	"0.96"	"1997"	"2018"	"14"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0085261"	"Proteus Syndrome"	"disease"	"C04;C05;C16"	"Neoplastic Process"	"0.60"	"0.8888889"	"2001"	"2015"	"3"	"0"	"CTD_human;ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"3"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"3"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"0.9"	"1985"	"2017"	"1"	"2"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.63"	"1"	"2000"	"2016"	"0"	"2"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2017"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205788"	"Histiocytoid hemangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205789"	"Hemangioma, Intramuscular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205822"	"Hibernoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205823"	"Pleomorphic Lipoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"1"	"1998"	"2017"	"2"	"0"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0265326"	"Bannayan-Riley-Ruvalcaba Syndrome"	"disease"	"C04;C16"	"Disease or Syndrome"	"1.00"	"0.9811321"	"1997"	"2016"	"15"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.39"	"1"	"2002"	"2018"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0280302"	"Squamous cell carcinoma of lip"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0280313"	"Squamous cell carcinoma of oropharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0280321"	"Squamous cell carcinoma of the hypopharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0280324"	"Laryngeal Squamous Cell Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0345893"	"Juvenile polyposis syndrome"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.40"	"0.9333333"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9090909"	"2002"	"2014"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0349578"	"Complex Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0349579"	"Atypical Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.80"	"0.9695652"	"1997"	"2018"	"16"	"0"	"CTD_human;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2009"	"6"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0391826"	"Lhermitte-Duclos disease"	"disease"	"C04;C16"	"Neoplastic Process"	"1.00"	"0.9166667"	"1997"	"2016"	"31"	"14"	"CTD_human;ORPHANET;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0456483"	"Simple Endometrial Hyperplasia"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.80"	"0.9685039"	"1995"	"2016"	"4"	"2"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.9411765"	"1993"	"2017"	"2"	"0"	"CGI;GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9285714"	"1998"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0585362"	"Squamous cell carcinoma of mouth"	"disease"		"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0677608"	"Chorioangioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2014"	"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.964497"	"1997"	"2018"	"4"	"0"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2000"	"2009"	"5"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.66"	"0.8"	"1998"	"2011"	"1"	"0"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.9333333"	"1998"	"2018"	"1"	"0"	"CGI;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9230769"	"1998"	"2016"	"2"	"3"	"CGI;CTD_human;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2010"	"4"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1266181"	"Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos)"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5728"	"PTEN"	"0.334"	"0.828"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"1999"	"2017"	"4"	"5"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9347826"	"2000"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1834711"	"CEREBELLOPARENCHYMAL DISORDER VI"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2008"	"20"	"13"	"UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C1834712"	"Cerebellar Granule Cell Hypertrophy and Megalencephaly"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2008"	"20"	"13"	"UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C1835047"	"MELANOMA, CUTANEOUS MALIGNANT, 1"	"disease"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1848599"	"VACTERL Association With Hydrocephalus"	"disease"	"C05;C06;C10;C14;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1854416"	"MACROCEPHALY/AUTISM SYNDROME"	"disease"	"C05;C10;C16;C23;F03"	"Disease or Syndrome"	"0.90"		"1998"	"2017"	"3"	"17"	"CTD_human;ORPHANET;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C1866398"	"Proteus-Like Syndrome (disorder)"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.75"	"1"	"1997"	"2016"	"23"	"15"	"CTD_human;ORPHANET;UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C1959582"	"PTEN Hamartoma Tumor Syndrome"	"disease"	"C04;C16"	"Neoplastic Process"	"0.70"	"0.9473684"	"1997"	"2018"	"21"	"90"	"CLINGEN;CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C1959588"	"Angioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C2751642"	"GLIOMA SUSCEPTIBILITY 2"	"disease"		"Finding"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"5728"	"PTEN"	"0.334"	"0.828"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C3489413"	"Lipomatosis, Multiple"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.63"	"1"	"2001"	"2013"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5728"	"PTEN"	"0.334"	"0.828"	"C3714976"	"ACTIVATED PI3K-DELTA SYNDROME"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5728"	"PTEN"	"0.334"	"0.828"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5728"	"PTEN"	"0.334"	"0.828"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.40"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"5729"	"PTGDR"	"0.713"	"0.414"	"C1846534"	"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5730"	"PTGDS"	"0.536"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"5730"	"PTGDS"	"0.536"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0237873"	"Physiological Sexual Disorders"	"group"	"C12;C13"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5731"	"PTGER1"	"0.676"	"0.414"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0021359"	"Infertility"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0237873"	"Physiological Sexual Disorders"	"group"	"C12;C13"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C0729353"	"Subfertility"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C1859648"	"Asthma, Nasal Polyps, And Aspirin Intolerance"	"disease"	"C08;C09;C20;C23;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5732"	"PTGER2"	"0.607"	"0.621"	"C4074771"	"Sterility, Reproductive"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0030804"	"Pemphigoid, Benign Mucous Membrane"	"disease"	"C11;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C1282359"	"Ocular Cicatricial Pemphigoid"	"disease"	"C11;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5733"	"PTGER3"	"0.645"	"0.552"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0237873"	"Physiological Sexual Disorders"	"group"	"C12;C13"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5734"	"PTGER4"	"0.58"	"0.517"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5737"	"PTGFR"	"0.752"	"0.207"	"C0001883"	"Airway Obstruction"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"5737"	"PTGFR"	"0.752"	"0.207"	"C0008301"	"Choking"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1976"	"1976"	"1"	"0"	"CTD_human"
"5737"	"PTGFR"	"0.752"	"0.207"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5737"	"PTGFR"	"0.752"	"0.207"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5739"	"PTGIR"	"0.752"	"0.241"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5739"	"PTGIR"	"0.752"	"0.241"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2001"	"2004"	"0"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5740"	"PTGIS"	"0.624"	"0.552"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"5"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2010"	"2"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0004779"	"Basal Cell Nevus Syndrome"	"disease"	"C04;C05;C07;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0005942"	"Bone Diseases, Endocrine"	"group"	"C05;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.60"	"0.9431818"	"1980"	"2017"	"6"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020438"	"Hypercalciuria"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"	"0.9375"	"1985"	"2017"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020492"	"Hyperostosis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020503"	"Hyperparathyroidism, Secondary"	"disease"	"C19"	"Disease or Syndrome"	"0.60"	"1"	"1980"	"2017"	"3"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1991"	"1992"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0020598"	"Hypocalcemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.50"	"0.921875"	"1980"	"2017"	"2"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1985"	"2007"	"6"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"5"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2011"	"5"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0035579"	"Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.37"	"0.8571429"	"1999"	"2013"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.53"	"1"	"1991"	"2013"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0085681"	"Hyperphosphatemia (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.70"	"0.9705882"	"1992"	"2017"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C0342345"	"Hypoparathyroidism - autosomal dominant"	"disease"	"C18;C19;C23"	"Disease or Syndrome"	"0.38"	"1"	"1990"	"2015"	"3"	"2"	"UNIPROT"
"5741"	"PTH"	"0.457"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"5"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C1832648"	"Hypoparathyroidism familial isolated"	"disease"	"C19"	"Disease or Syndrome"	"0.65"	"0.6"	"1986"	"2017"	"3"	"2"	"CTD_human;UNIPROT"
"5741"	"PTH"	"0.457"	"0.793"	"C1840334"	"Hypoparathyroidism, Autosomal Recessive"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"1990"	"2017"	"3"	"2"	"UNIPROT"
"5741"	"PTH"	"0.457"	"0.793"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5741"	"PTH"	"0.457"	"0.793"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"1994"	"2004"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"1998"	"2009"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0021846"	"Intestinal Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2000"	"2002"	"2"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0037316"	"Sleep Deprivation"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2009"	"2"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"1998"	"2009"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751505"	"Insufficient Sleep Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751506"	"REM Sleep Deprivation"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C0751507"	"Sleep Fragmentation"	"phenotype"	"C10;C23;F03"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5742"	"PTGS1"	"0.495"	"0.828"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2017"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9333333"	"2000"	"2017"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.60"	"0.9375"	"2000"	"2014"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0005694"	"Bladder neck obstruction"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.962406"	"1998"	"2018"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007099"	"Carcinoma in Situ"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9578947"	"1996"	"2018"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1998"	"2014"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.59"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.962963"	"1997"	"2017"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2010"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.7"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.57"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9714286"	"1998"	"2018"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2003"	"2014"	"5"	"0"	"PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2003"	"2014"	"6"	"0"	"CTD_human;PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.60"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"2000"	"2016"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0017168"	"Gastroesophageal reflux disease"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2002"	"2014"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0019064"	"Hemopericardium"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020295"	"Hydronephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2014"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2012"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.59"	"1"	"2002"	"2016"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.37"		"2001"	"2009"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0021846"	"Intestinal Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.33"	"1"	"1999"	"2003"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0023269"	"leiomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0023532"	"Leukoplakia, Oral"	"disease"	"C04;C07;C23"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9880952"	"1999"	"2018"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9583333"	"2001"	"2018"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.32"		"2003"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9313725"	"1998"	"2018"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"0.6666667"	"1999"	"2013"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.5"	"2002"	"2014"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0031039"	"Pericardial effusion"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.40"	"0.9655172"	"1997"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9047619"	"2000"	"2011"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2012"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0034013"	"Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2000"	"2010"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2004"	"2012"	"4"	"0"	"PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.8333333"	"1998"	"2017"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.57"	"0.8"	"1997"	"2009"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2008"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"0.5"	"2009"	"2011"	"3"	"0"	"CTD_human;PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2011"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2005"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205815"	"Leiomyosarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205816"	"Leiomyosarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2005"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2005"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0242426"	"Chylopericardium"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2011"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2011"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.95"	"2000"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0339143"	"Thyroid associated opthalmopathies"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9545455"	"1999"	"2016"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0376323"	"Congestive Ophthalmopathy"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9803922"	"1998"	"2017"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2005"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2011"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2005"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.962406"	"1998"	"2018"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0878500"	"Intraepithelial Neoplasia"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2010"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2009"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.96"	"1999"	"2016"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2009"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2011"	"3"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.31"	"0"	"2006"	"2010"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2017"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9855072"	"1994"	"2018"	"6"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1563709"	"Myopathic Ophthalmopathy"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1999"	"2012"	"4"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9677419"	"2000"	"2017"	"5"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5743"	"PTGS2"	"0.338"	"0.897"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0005974"	"Bone Resorption"	"phenotype"	"C05"	"Organ or Tissue Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9423077"	"1992"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0016508"	"Congenital Foot Deformity"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9636364"	"1987"	"2017"	"4"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1987"	"2002"	"4"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"1994"	"2002"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0038833"	"Superior Vena Cava Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0038834"	"Superior Vena Cava Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1990"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0265312"	"Brachydactyly syndrome type E"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0267941"	"Pancreatitis, Acute Necrotizing"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0376670"	"Pancreatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9615385"	"1992"	"2016"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2013"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5744"	"PTHLH"	"0.472"	"0.793"	"C3150644"	"BRACHYDACTYLY, TYPE E2"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"4"	"CTD_human;UNIPROT"
"5744"	"PTHLH"	"0.472"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0014084"	"Enchondromatosis"	"disease"	"C05"	"Disease or Syndrome"	"0.65"	"0.8"	"2002"	"2011"	"1"	"1"	"ORPHANET;UNIPROT"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0020502"	"Hyperparathyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0035579"	"Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5745"	"PTH1R"	"0.579"	"0.586"	"C0265295"	"Jansen type metaphyseal chondrodysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1995"	"2018"	"5"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5745"	"PTH1R"	"0.579"	"0.586"	"C1838779"	"Eiken Skeletal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2005"	"2005"	"0"	"1"	"CTD_human;ORPHANET"
"5745"	"PTH1R"	"0.579"	"0.586"	"C1852222"	"Failure of Tooth Eruption, Primary"	"disease"	"C07"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"0"	"1"	"CTD_human;ORPHANET"
"5745"	"PTH1R"	"0.579"	"0.586"	"C1859148"	"Chondrodysplasia, blomstrand type"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1985"	"2007"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5745"	"PTH1R"	"0.579"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5747"	"PTK2"	"0.545"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2015"	"2"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2003"	"2015"	"2"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5747"	"PTK2"	"0.545"	"0.655"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5747"	"PTK2"	"0.545"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2003"	"2003"	"1"	"0"	"CTD_human;UNIPROT"
"5747"	"PTK2"	"0.545"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5754"	"PTK7"	"0.639"	"0.379"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5754"	"PTK7"	"0.639"	"0.379"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5756"	"TWF1"	"0.928"	"0.069"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5757"	"PTMA"	"0.648"	"0.621"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5764"	"PTN"	"0.565"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5768"	"QSOX1"	"0.681"	"0.345"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.95"	"1999"	"2017"	"0"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0025063"	"Mediastinal Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.962963"	"1999"	"2016"	"2"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0035372"	"Rett Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0153504"	"Malignant tumor of mediastinum"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5770"	"PTPN1"	"0.569"	"0.621"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.45"	"1"	"2012"	"2014"	"1"	"2"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.47"	"1"	"2008"	"2017"	"1"	"3"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2017"	"1"	"4"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0023492"	"Leukemia, T-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"5771"	"PTPN2"	"0.616"	"0.483"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5774"	"PTPN3"	"0.685"	"0.414"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"5774"	"PTPN3"	"0.685"	"0.414"	"C0740277"	"Bile duct carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5777"	"PTPN6"	"0.535"	"0.724"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2004"	"2016"	"1"	"2"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0014084"	"Enchondromatosis"	"disease"	"C05"	"Disease or Syndrome"	"0.41"	"0"	"2010"	"2011"	"2"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0015306"	"Hereditary Multiple Exostoses"	"disease"	"C04;C05;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2009"	"9"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9310345"	"1991"	"2017"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"1"	"1989"	"2017"	"1"	"2"	"CGI;CTD_human;UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2016"	"2"	"9"	"UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0024454"	"Maffucci Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"0"	"2010"	"2011"	"2"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0027019"	"Myelomonocytic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.46"	"1"	"2005"	"2017"	"1"	"4"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"1.00"	"0.9567901"	"2001"	"2018"	"27"	"54"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0029423"	"Cartilaginous exostosis"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.90"	"0.9680851"	"1993"	"2018"	"19"	"44"	"CTD_human;UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"1.00"	"0.9622642"	"2002"	"2017"	"19"	"10"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0265261"	"Multiple pterygium syndrome"	"disease"	"C16;C17;C23"	"Congenital Abnormality"	"0.50"		"2001"	"2018"	"15"	"37"	"UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"1.00"	"0.9555556"	"2003"	"2017"	"4"	"17"	"CTD_human;ORPHANET;UNIPROT"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0410530"	"Metachondromatosis"	"disease"	"C04;C05;C16"	"Disease or Syndrome"	"0.64"	"1"	"2010"	"2016"	"0"	"20"	"CTD_human;ORPHANET"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0587248"	"Costello syndrome (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C1275081"	"Cardio-facio-cutaneous syndrome"	"disease"	"C14;C16;C17;C23"	"Congenital Abnormality"	"0.36"	"0.8333333"	"2002"	"2010"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2004"	"2007"	"4"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5781"	"PTPN11"	"0.429"	"0.828"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2009"	"0"	"0"	"CGI"
"5781"	"PTPN11"	"0.429"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5782"	"PTPN12"	"0.681"	"0.552"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1994"	"1994"	"1"	"1"	"UNIPROT"
"5782"	"PTPN12"	"0.681"	"0.552"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"GENOMICS_ENGLAND"
"5782"	"PTPN12"	"0.681"	"0.552"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.42"	"1"	"1994"	"2014"	"0"	"1"	"CGI"
"5784"	"PTPN14"	"0.701"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"5784"	"PTPN14"	"0.701"	"0.379"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5784"	"PTPN14"	"0.701"	"0.379"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5784"	"PTPN14"	"0.701"	"0.379"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5784"	"PTPN14"	"0.701"	"0.379"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5784"	"PTPN14"	"0.701"	"0.379"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5784"	"PTPN14"	"0.701"	"0.379"	"C3150875"	"CHOANAL ATRESIA AND LYMPHEDEMA"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"5786"	"PTPRA"	"0.624"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"5786"	"PTPRA"	"0.624"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5787"	"PTPRB"	"0.928"	"0.034"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.53"	"1"	"2014"	"2016"	"1"	"0"	"CGI;CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.46"	"0.8333333"	"1991"	"2016"	"2"	"1"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"5788"	"PTPRC"	"0.488"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"1994"	"2018"	"1"	"0"	"CTD_human"
"5788"	"PTPRC"	"0.488"	"0.759"	"C1837028"	"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.60"		"2012"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"5788"	"PTPRC"	"0.488"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"0.6666667"	"2006"	"2014"	"0"	"0"	"CGI"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0035258"	"Restless Legs Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.46"	"1"	"2008"	"2017"	"1"	"5"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2018"	"1"	"1"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5789"	"PTPRD"	"0.607"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2008"	"2011"	"2"	"0"	"CTD_human;UNIPROT"
"5792"	"PTPRF"	"0.659"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5792"	"PTPRF"	"0.659"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5792"	"PTPRF"	"0.659"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5792"	"PTPRF"	"0.659"	"0.448"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5792"	"PTPRF"	"0.659"	"0.448"	"C0432357"	"Congenital absence of breast with absent nipple"	"disease"	"C17"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"5792"	"PTPRF"	"0.659"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5792"	"PTPRF"	"0.659"	"0.448"	"C4014918"	"BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"5793"	"PTPRG"	"0.639"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5793"	"PTPRG"	"0.639"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"5793"	"PTPRG"	"0.639"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5795"	"PTPRJ"	"0.636"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2010"	"2"	"2"	"UNIPROT"
"5795"	"PTPRJ"	"0.636"	"0.379"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.45"	"1"	"2002"	"2010"	"0"	"2"	"CGI"
"5796"	"PTPRK"	"0.743"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"5796"	"PTPRK"	"0.743"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5796"	"PTPRK"	"0.743"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"5799"	"PTPRN2"	"0.735"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5800"	"PTPRO"	"0.676"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5800"	"PTPRO"	"0.676"	"0.31"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"5800"	"PTPRO"	"0.676"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5800"	"PTPRO"	"0.676"	"0.31"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"5800"	"PTPRO"	"0.676"	"0.31"	"C3280100"	"NEPHROTIC SYNDROME, TYPE 6"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5801"	"PTPRR"	"0.799"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"PSYGENET"
"5801"	"PTPRR"	"0.799"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"PSYGENET"
"5802"	"PTPRS"	"0.815"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5803"	"PTPRZ1"	"0.656"	"0.448"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5803"	"PTPRZ1"	"0.656"	"0.448"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5803"	"PTPRZ1"	"0.656"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2008"	"2013"	"3"	"0"	"PSYGENET"
"5803"	"PTPRZ1"	"0.656"	"0.448"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5805"	"PTS"	"0.681"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5805"	"PTS"	"0.681"	"0.345"	"C0878676"	"6-pyruvoyl-tetrahydropterin synthase deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"		"1994"	"2017"	"12"	"16"	"CTD_human;ORPHANET;UNIPROT"
"5805"	"PTS"	"0.681"	"0.345"	"C2678415"	"Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"2001"	"12"	"14"	"UNIPROT"
"5805"	"PTS"	"0.681"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1999"	"3"	"0"	"GENOMICS_ENGLAND"
"5806"	"PTX3"	"0.543"	"0.69"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5806"	"PTX3"	"0.543"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5806"	"PTX3"	"0.543"	"0.69"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5806"	"PTX3"	"0.543"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"5813"	"PURA"	"0.713"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5813"	"PURA"	"0.713"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5813"	"PURA"	"0.713"	"0.276"	"C4015357"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 31"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2017"	"2"	"16"	"CTD_human;ORPHANET;UNIPROT"
"5816"	"PVALB"	"0.588"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"0"	"2003"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C0949541"	"Hurthle Cell Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2001"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C1510502"	"Oxyphilic Adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5816"	"PVALB"	"0.588"	"0.448"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5817"	"PVR"	"0.604"	"0.448"	"C0032371"	"Poliomyelitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.39"	"1"	"1986"	"2017"	"2"	"0"	"CTD_human"
"5817"	"PVR"	"0.604"	"0.448"	"C0751445"	"Encephalitis, Polio"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"		"1986"	"2017"	"2"	"0"	"CTD_human"
"5817"	"PVR"	"0.604"	"0.448"	"C0751446"	"Poliomyelitis, Nonpoliovirus"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"		"1986"	"2017"	"2"	"0"	"CTD_human"
"5817"	"PVR"	"0.604"	"0.448"	"C0751447"	"Poliomyelitis, Preparalytic"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"		"1986"	"2017"	"2"	"0"	"CTD_human"
"5817"	"PVR"	"0.604"	"0.448"	"C1527258"	"Infantile paralysis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"		"1986"	"2017"	"2"	"0"	"CTD_human"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.44"	"1"	"2006"	"2014"	"0"	"0"	"ORPHANET"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C0019372"	"Herpesviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C0037140"	"B Virus Infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.36"	"1"	"2000"	"2016"	"0"	"0"	"ORPHANET"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C1298692"	"Cleft lip and alveolus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C2931488"	"Zlotogora-Ogur syndrome"	"disease"	"C05;C07;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.63"	"1"	"1987"	"2016"	"1"	"3"	"CTD_human;ORPHANET"
"5818"	"NECTIN1"	"0.575"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5819"	"NECTIN2"	"0.701"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"		"2010"	"2014"	"1"	"4"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C0162538"	"Immunoglobulin A deficiency (disorder)"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5820"	"PVT1"	"0.555"	"0.552"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5824"	"PEX19"	"0.577"	"0.655"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"5824"	"PEX19"	"0.577"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5824"	"PEX19"	"0.577"	"0.655"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5824"	"PEX19"	"0.577"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5824"	"PEX19"	"0.577"	"0.655"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C1838299"	"Peroxisome Biogenesis Disorder, Complementation Group 14"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C1838300"	"Peroxisome Biogenesis Disorder, Complementation Group J"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5824"	"PEX19"	"0.577"	"0.655"	"C3554002"	"PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5824"	"PEX19"	"0.577"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5825"	"ABCD3"	"0.752"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"1996"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5825"	"ABCD3"	"0.752"	"0.31"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"5825"	"ABCD3"	"0.752"	"0.31"	"C4225390"	"BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5"	"disease"		"Congenital Abnormality"	"0.50"		"2015"	"2015"	"0"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C0042847"	"Vitamin B 12 Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5826"	"ABCD4"	"0.773"	"0.276"	"C3553915"	"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5826"	"ABCD4"	"0.773"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5828"	"PEX2"	"0.575"	"0.621"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"1992"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5828"	"PEX2"	"0.575"	"0.621"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5828"	"PEX2"	"0.575"	"0.621"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"1997"	"2004"	"1"	"0"	"CTD_human;ORPHANET"
"5828"	"PEX2"	"0.575"	"0.621"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"1992"	"2017"	"2"	"2"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C3539010"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C3542026"	"PEROXISOME BIOGENESIS DISORDER 5B"	"disease"		"Disease or Syndrome"	"0.60"		"1992"	"2012"	"1"	"6"	"CTD_human;UNIPROT"
"5828"	"PEX2"	"0.575"	"0.621"	"C3553940"	"PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.40"		"1992"	"2011"	"0"	"5"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C3553941"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 5"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C3553942"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 10"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5828"	"PEX2"	"0.575"	"0.621"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0004565"	"Melanoma, B16"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0009075"	"Melanoma, Cloudman S91"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0018598"	"Melanoma, Harding-Passey"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0025205"	"Melanoma, Experimental"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5829"	"PXN"	"0.604"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9375"	"1997"	"2016"	"1"	"0"	"CTD_human"
"5830"	"PEX5"	"0.555"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1995"	"2007"	"0"	"0"	"ORPHANET"
"5830"	"PEX5"	"0.555"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1995"	"1995"	"0"	"1"	"ORPHANET"
"5830"	"PEX5"	"0.555"	"0.69"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"5830"	"PEX5"	"0.555"	"0.69"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C3550234"	"PEROXISOME BIOGENESIS DISORDER 2B"	"disease"		"Disease or Syndrome"	"0.50"		"1995"	"1995"	"1"	"1"	"CTD_human;UNIPROT"
"5830"	"PEX5"	"0.555"	"0.69"	"C3550273"	"PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5830"	"PEX5"	"0.555"	"0.69"	"C3550274"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5830"	"PEX5"	"0.555"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5830"	"PEX5"	"0.555"	"0.69"	"C4225237"	"RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0010495"	"Cutis Laxa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1986"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0033300"	"Progeria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0432255"	"Geroderma osteodysplastica"	"disease"	"C05;C16;C17;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"5831"	"PYCR1"	"0.611"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5831"	"PYCR1"	"0.611"	"0.621"	"C2751987"	"Cutis Laxa, Autosomal Recessive, Type IIB"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.74"	"1"	"2005"	"2015"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5831"	"PYCR1"	"0.611"	"0.621"	"C3280799"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB"	"disease"		"Disease or Syndrome"	"0.70"		"1986"	"2012"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5831"	"PYCR1"	"0.611"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2010"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2001"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0268350"	"Cutis Laxa, Autosomal Dominant"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2018"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0268354"	"De Barsy syndrome"	"disease"	"C10;C11;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2001"	"2015"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C1832669"	"SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.70"		"1996"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C4225268"	"CUTIS LAXA, AUTOSOMAL DOMINANT 3"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2015"	"1"	"2"	"UNIPROT"
"5832"	"ALDH18A1"	"0.594"	"0.586"	"C4225272"	"SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5834"	"PYGB"	"0.857"	"0.138"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5834"	"PYGB"	"0.857"	"0.138"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5834"	"PYGB"	"0.857"	"0.138"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5834"	"PYGB"	"0.857"	"0.138"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5836"	"PYGL"	"0.735"	"0.276"	"C0017925"	"Glycogen Storage Disease Type VI"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2017"	"2"	"18"	"CTD_human;ORPHANET;UNIPROT"
"5836"	"PYGL"	"0.735"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5836"	"PYGL"	"0.735"	"0.276"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5836"	"PYGL"	"0.735"	"0.276"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"5836"	"PYGL"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5837"	"PYGM"	"0.707"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5837"	"PYGM"	"0.707"	"0.414"	"C0017924"	"Glycogen Storage Disease Type V"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.9787234"	"1976"	"2018"	"15"	"54"	"CTD_human;ORPHANET;UNIPROT"
"5837"	"PYGM"	"0.707"	"0.414"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5837"	"PYGM"	"0.707"	"0.414"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"5837"	"PYGM"	"0.707"	"0.414"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5837"	"PYGM"	"0.707"	"0.414"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5858"	"PZP"	"0.762"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5858"	"PZP"	"0.762"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5858"	"PZP"	"0.762"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5858"	"PZP"	"0.762"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5858"	"PZP"	"0.762"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5858"	"PZP"	"0.762"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5858"	"PZP"	"0.762"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5859"	"QARS"	"0.72"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5859"	"QARS"	"0.72"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5859"	"QARS"	"0.72"	"0.241"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"5859"	"QARS"	"0.72"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5859"	"QARS"	"0.72"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5859"	"QARS"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"5859"	"QARS"	"0.72"	"0.241"	"C4014239"	"MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5860"	"QDPR"	"0.72"	"0.276"	"C0031485"	"Phenylketonurias"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"5860"	"QDPR"	"0.72"	"0.276"	"C0268465"	"Phenylketonuria II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1987"	"2015"	"6"	"10"	"CTD_human;ORPHANET;UNIPROT"
"5860"	"QDPR"	"0.72"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5860"	"QDPR"	"0.72"	"0.276"	"C0751434"	"Classical phenylketonuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"5860"	"QDPR"	"0.72"	"0.276"	"C0751435"	"Hyperphenylalaninaemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.48"	"1"	"1981"	"2015"	"1"	"0"	"CTD_human"
"5860"	"QDPR"	"0.72"	"0.276"	"C0751436"	"Hyperphenylalaninemia, Non-Phenylketonuric"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"5860"	"QDPR"	"0.72"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1990"	"2012"	"5"	"0"	"GENOMICS_ENGLAND"
"5862"	"RAB2A"	"0.752"	"0.207"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5862"	"RAB2A"	"0.752"	"0.207"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5864"	"RAB3A"	"0.735"	"0.241"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5864"	"RAB3A"	"0.735"	"0.241"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5864"	"RAB3A"	"0.735"	"0.241"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5864"	"RAB3A"	"0.735"	"0.241"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5864"	"RAB3A"	"0.735"	"0.241"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5868"	"RAB5A"	"0.621"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5873"	"RAB27A"	"0.627"	"0.483"	"C1868679"	"GRISCELLI SYNDROME, TYPE 2"	"disease"	"C15;C16;C17;C18;C20"	"Disease or Syndrome"	"0.80"	"1"	"2000"	"2018"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5873"	"RAB27A"	"0.627"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5878"	"RAB5C"	"0.857"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5879"	"RAC1"	"0.47"	"0.931"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2013"	"2"	"0"	"PSYGENET"
"5879"	"RAC1"	"0.47"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2013"	"2"	"0"	"PSYGENET"
"5879"	"RAC1"	"0.47"	"0.931"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2003"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2003"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2004"	"2017"	"1"	"1"	"CGI;CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5879"	"RAC1"	"0.47"	"0.931"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.42"	"1"	"2015"	"2016"	"0"	"2"	"CGI"
"5879"	"RAC1"	"0.47"	"0.931"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5879"	"RAC1"	"0.47"	"0.931"	"C0876994"	"Cardiotoxicity"	"disease"	"C23;C25;C26"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"5879"	"RAC1"	"0.47"	"0.931"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5879"	"RAC1"	"0.47"	"0.931"	"C4540321"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"5880"	"RAC2"	"0.621"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5880"	"RAC2"	"0.621"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5880"	"RAC2"	"0.621"	"0.586"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5880"	"RAC2"	"0.621"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5880"	"RAC2"	"0.621"	"0.586"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"5880"	"RAC2"	"0.621"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5880"	"RAC2"	"0.621"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5880"	"RAC2"	"0.621"	"0.586"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5880"	"RAC2"	"0.621"	"0.586"	"C1842398"	"Neutrophil Immunodeficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.71"	"1"	"2000"	"2000"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5883"	"RAD9A"	"0.713"	"0.241"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"5883"	"RAD9A"	"0.713"	"0.241"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5883"	"RAD9A"	"0.713"	"0.241"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"5885"	"RAD21"	"0.559"	"0.759"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"5885"	"RAD21"	"0.559"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2013"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"5885"	"RAD21"	"0.559"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"5885"	"RAD21"	"0.559"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5885"	"RAD21"	"0.559"	"0.759"	"C1802395"	"Congenital muscular hypertrophy-cerebral syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C1853099"	"Cornelia de Lange Syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5885"	"RAD21"	"0.559"	"0.759"	"C3553517"	"CORNELIA DE LANGE SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1993"	"2015"	"1"	"6"	"UNIPROT"
"5885"	"RAD21"	"0.559"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5885"	"RAD21"	"0.559"	"0.759"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"5886"	"RAD23A"	"0.857"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5886"	"RAD23A"	"0.857"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5886"	"RAD23A"	"0.857"	"0.172"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5886"	"RAD23A"	"0.857"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5887"	"RAD23B"	"0.663"	"0.552"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9701493"	"1998"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"5888"	"RAD51"	"0.517"	"0.724"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2018"	"0"	"0"	"ORPHANET"
"5888"	"RAD51"	"0.517"	"0.724"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2006"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.46"	"1"	"1999"	"2015"	"1"	"1"	"UNIPROT"
"5888"	"RAD51"	"0.517"	"0.724"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"5888"	"RAD51"	"0.517"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.9615385"	"1998"	"2016"	"0"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2015"	"0"	"0"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"5888"	"RAD51"	"0.517"	"0.724"	"C3281089"	"MIRROR MOVEMENTS 2"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2016"	"0"	"2"	"CTD_human"
"5888"	"RAD51"	"0.517"	"0.724"	"C4284093"	"FANCONI ANEMIA, COMPLEMENTATION GROUP R"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8823529"	"2010"	"2018"	"2"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"1988"	"2015"	"6"	"0"	"CLINGEN"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.47"	"1"	"2011"	"2017"	"0"	"5"	"ORPHANET"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.8823529"	"2010"	"2018"	"2"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"0"	"2010"	"2012"	"1"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.80"	"0.9655172"	"2010"	"2018"	"8"	"0"	"CLINGEN;CTD_human;GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5889"	"RAD51C"	"0.614"	"0.517"	"C3150653"	"FANCONI ANEMIA, COMPLEMENTATION GROUP O"	"disease"		"Disease or Syndrome"	"0.70"		"2003"	"2017"	"3"	"38"	"CLINGEN;CTD_human;UNIPROT"
"5889"	"RAD51C"	"0.614"	"0.517"	"C3150659"	"BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.60"		"2003"	"2017"	"3"	"22"	"CTD_human;UNIPROT"
"5889"	"RAD51C"	"0.614"	"0.517"	"C3150660"	"BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.50"		"2010"	"2014"	"3"	"4"	"CTD_human;UNIPROT"
"5889"	"RAD51C"	"0.614"	"0.517"	"C3150661"	"OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.50"		"2010"	"2014"	"3"	"4"	"CTD_human;UNIPROT"
"5889"	"RAD51C"	"0.614"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"5889"	"RAD51C"	"0.614"	"0.517"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8181818"	"2009"	"2014"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0238033"	"Carcinoma of Male Breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0242788"	"Breast Neoplasms, Male"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.8181818"	"2009"	"2018"	"1"	"57"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5890"	"RAD51B"	"0.616"	"0.621"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5891"	"MOK"	"0.554"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"5892"	"RAD51D"	"0.707"	"0.31"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5892"	"RAD51D"	"0.707"	"0.31"	"C0008628"	"Chromosome Deletion"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5892"	"RAD51D"	"0.707"	"0.31"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"0"	"2000"	"2017"	"8"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"5892"	"RAD51D"	"0.707"	"0.31"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.40"		"2011"	"2017"	"0"	"3"	"ORPHANET"
"5892"	"RAD51D"	"0.707"	"0.31"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5892"	"RAD51D"	"0.707"	"0.31"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.80"	"1"	"2000"	"2017"	"10"	"0"	"CLINGEN;CTD_human;GENOMICS_ENGLAND"
"5892"	"RAD51D"	"0.707"	"0.31"	"C2930745"	"Partial Monosomy"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5892"	"RAD51D"	"0.707"	"0.31"	"C3280345"	"BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.40"		"2000"	"2017"	"0"	"30"	"CTD_human"
"5893"	"RAD52"	"0.659"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"5893"	"RAD52"	"0.659"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5893"	"RAD52"	"0.659"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"2007"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2003"	"2017"	"0"	"2"	"CGI"
"5894"	"RAF1"	"0.462"	"0.793"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2016"	"11"	"18"	"CLINGEN;CTD_human;ORPHANET"
"5894"	"RAF1"	"0.462"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2014"	"2"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"2005"	"2016"	"0"	"1"	"CGI"
"5894"	"RAF1"	"0.462"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.42"	"1"	"2014"	"2018"	"0"	"1"	"UNIPROT"
"5894"	"RAF1"	"0.462"	"0.793"	"C0175704"	"LEOPARD Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2012"	"1"	"4"	"CTD_human;ORPHANET"
"5894"	"RAF1"	"0.462"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"5894"	"RAF1"	"0.462"	"0.793"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5894"	"RAF1"	"0.462"	"0.793"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5894"	"RAF1"	"0.462"	"0.793"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1990"	"2011"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C1969056"	"LEOPARD SYNDROME 2"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.60"		"2007"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"5894"	"RAF1"	"0.462"	"0.793"	"C1969057"	"Noonan Syndrome 5"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.81"	"1"	"2007"	"2016"	"3"	"10"	"CTD_human;UNIPROT"
"5894"	"RAF1"	"0.462"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5894"	"RAF1"	"0.462"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5894"	"RAF1"	"0.462"	"0.793"	"C4014656"	"CARDIOMYOPATHY, DILATED, 1NN"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"5896"	"RAG1"	"0.528"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5896"	"RAG1"	"0.528"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5896"	"RAG1"	"0.528"	"0.69"	"C1832322"	"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive"	"disease"	"C20"	"Disease or Syndrome"	"0.70"		"1996"	"2017"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"5896"	"RAG1"	"0.528"	"0.69"	"C1835931"	"ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY"	"disease"	"C02;C15;C20"	"Disease or Syndrome"	"0.70"		"2001"	"2006"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5896"	"RAG1"	"0.528"	"0.69"	"C2673536"	"Combined Cellular And Humoral Immune Defects With Granulomas"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.70"		"2001"	"2017"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5896"	"RAG1"	"0.528"	"0.69"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.60"	"0.9642857"	"1998"	"2016"	"6"	"24"	"ORPHANET;UNIPROT"
"5896"	"RAG1"	"0.528"	"0.69"	"C2931884"	"Reticuloendotheliosis, familial, with eosinophilia"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.50"		"1998"	"2011"	"6"	"24"	"CTD_human;UNIPROT"
"5897"	"RAG2"	"0.525"	"0.759"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0025568"	"Metaplasia"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5897"	"RAG2"	"0.525"	"0.759"	"C1832322"	"Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive"	"disease"	"C20"	"Disease or Syndrome"	"0.90"		"1992"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5897"	"RAG2"	"0.525"	"0.759"	"C2673536"	"Combined Cellular And Humoral Immune Defects With Granulomas"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.70"		"2008"	"2008"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5897"	"RAG2"	"0.525"	"0.759"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.80"	"1"	"1998"	"2016"	"1"	"2"	"ORPHANET;UNIPROT"
"5897"	"RAG2"	"0.525"	"0.759"	"C2931884"	"Reticuloendotheliosis, familial, with eosinophilia"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.70"		"1998"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"5897"	"RAG2"	"0.525"	"0.759"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5900"	"RALGDS"	"0.762"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5900"	"RALGDS"	"0.762"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5900"	"RALGDS"	"0.762"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5900"	"RALGDS"	"0.762"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5900"	"RALGDS"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5901"	"RAN"	"0.6"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"5901"	"RAN"	"0.6"	"0.621"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5902"	"RANBP1"	"0.735"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5902"	"RANBP1"	"0.735"	"0.517"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5902"	"RANBP1"	"0.735"	"0.517"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5902"	"RANBP1"	"0.735"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5902"	"RANBP1"	"0.735"	"0.517"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5902"	"RANBP1"	"0.735"	"0.517"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5903"	"RANBP2"	"0.659"	"0.517"	"C0018199"	"Granuloma, Plasma Cell"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5903"	"RANBP2"	"0.659"	"0.517"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.56"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5903"	"RANBP2"	"0.659"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"5903"	"RANBP2"	"0.659"	"0.517"	"C2675556"	"ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.70"		"1989"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5905"	"RANGAP1"	"0.663"	"0.448"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"5906"	"RAP1A"	"0.546"	"0.724"	"C0796004"	"Kabuki make-up syndrome"	"disease"	"C09;C15;C16"	"Congenital Abnormality"	"0.51"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"5908"	"RAP1B"	"0.624"	"0.621"	"C0796004"	"Kabuki make-up syndrome"	"disease"	"C09;C15;C16"	"Congenital Abnormality"	"0.51"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2013"	"2"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2006"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5909"	"RAP1GAP"	"0.642"	"0.483"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"0.6666667"	"2010"	"2013"	"1"	"0"	"CTD_human"
"5911"	"RAP2A"	"0.752"	"0.276"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5913"	"RAPSN"	"0.614"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"5913"	"RAPSN"	"0.614"	"0.586"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"5913"	"RAPSN"	"0.614"	"0.586"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.40"		"1998"	"2015"	"1"	"1"	"CTD_human"
"5913"	"RAPSN"	"0.614"	"0.586"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2011"	"4"	"2"	"GENOMICS_ENGLAND"
"5913"	"RAPSN"	"0.614"	"0.586"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5913"	"RAPSN"	"0.614"	"0.586"	"C1276035"	"Pena-Shokeir syndrome type I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"2008"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5913"	"RAPSN"	"0.614"	"0.586"	"C1837092"	"Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5913"	"RAPSN"	"0.614"	"0.586"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5913"	"RAPSN"	"0.614"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"5913"	"RAPSN"	"0.614"	"0.586"	"C4225367"	"MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2015"	"9"	"11"	"UNIPROT"
"5914"	"RARA"	"0.515"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9655172"	"1993"	"2017"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0010701"	"Phyllodes Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9791123"	"1990"	"2018"	"23"	"0"	"CTD_human;ORPHANET"
"5914"	"RARA"	"0.515"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2005"	"2014"	"3"	"0"	"PSYGENET"
"5914"	"RARA"	"0.515"	"0.724"	"C0085183"	"Neoplasms, Second Primary"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0086696"	"Neoplasms, Therapy-Associated"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0149940"	"Sciatic Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0154748"	"Lesion of Sciatic Nerve"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0206650"	"Fibroadenoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0242013"	"Sciatic Neuritis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5914"	"RARA"	"0.515"	"0.724"	"C0600066"	"Malignant Cystosarcoma Phyllodes"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9677419"	"1993"	"2017"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0751924"	"Neuralgia-Neuritis, Sciatic Nerve"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0751925"	"Sciatic Nerve Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C0877578"	"Treatment related secondary malignancy"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.875"	"1994"	"2016"	"1"	"0"	"CTD_human"
"5914"	"RARA"	"0.515"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"1990"	"2014"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9411765"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"1991"	"2016"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"5915"	"RARB"	"0.506"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0149940"	"Sciatic Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0154748"	"Lesion of Sciatic Nerve"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0242013"	"Sciatic Neuritis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9411765"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0751924"	"Neuralgia-Neuritis, Sciatic Nerve"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0751925"	"Sciatic Nerve Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"UNIPROT"
"5915"	"RARB"	"0.506"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5915"	"RARB"	"0.506"	"0.759"	"C1832661"	"ANOPHTHALMIA AND PULMONARY HYPOPLASIA"	"disease"	"C08;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5915"	"RARB"	"0.506"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"5915"	"RARB"	"0.506"	"0.759"	"C3809803"	"MICROPHTHALMIA, SYNDROMIC 12"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2016"	"2"	"5"	"CTD_human;UNIPROT"
"5915"	"RARB"	"0.506"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5916"	"RARG"	"0.636"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2015"	"0"	"0"	"UNIPROT"
"5916"	"RARG"	"0.636"	"0.552"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5916"	"RARG"	"0.636"	"0.552"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5916"	"RARG"	"0.636"	"0.552"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"5916"	"RARG"	"0.636"	"0.552"	"C0876994"	"Cardiotoxicity"	"disease"	"C23;C25;C26"	"Injury or Poisoning"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"5916"	"RARG"	"0.636"	"0.552"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5917"	"RARS"	"0.614"	"0.414"	"C4015323"	"LEUKODYSTROPHY, HYPOMYELINATING, 9"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"5918"	"RARRES1"	"0.676"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5918"	"RARRES1"	"0.676"	"0.31"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"5918"	"RARRES1"	"0.676"	"0.31"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"5918"	"RARRES1"	"0.676"	"0.31"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5919"	"RARRES2"	"0.639"	"0.414"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0003857"	"Congenital arteriovenous malformation"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.46"	"0.8333333"	"2004"	"2014"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"		"1994"	"1994"	"1"	"3"	"CGI;CTD_human;UNIPROT"
"5921"	"RASA1"	"0.534"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"5921"	"RASA1"	"0.534"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CLINGEN"
"5921"	"RASA1"	"0.534"	"0.655"	"C0038505"	"Sturge-Weber Syndrome"	"disease"	"C04;C10;C14"	"Congenital Abnormality"	"0.55"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"5921"	"RASA1"	"0.534"	"0.655"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"5921"	"RASA1"	"0.534"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C0235752"	"Port-Wine Stain"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.41"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5921"	"RASA1"	"0.534"	"0.655"	"C1842180"	"CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.80"	"0.9333333"	"2004"	"2017"	"2"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5921"	"RASA1"	"0.534"	"0.655"	"C2675370"	"Capillary Malformation Without Arteriovenous Malformation"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.60"		"2004"	"2014"	"2"	"4"	"CTD_human;UNIPROT"
"5921"	"RASA1"	"0.534"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"5922"	"RASA2"	"0.667"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2016"	"2"	"0"	"CTD_human"
"5922"	"RASA2"	"0.667"	"0.483"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"0.5"	"2013"	"2018"	"1"	"0"	"CTD_human"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C0034951"	"Refractive Errors"	"group"	"C11"	"Disease or Syndrome"	"0.40"		"2010"	"2013"	"1"	"1"	"CTD_human"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5923"	"RASGRF1"	"0.573"	"0.655"	"C1527310"	"Ametropia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5924"	"RASGRF2"	"0.773"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5925"	"RB1"	"0.467"	"0.828"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.54"	"1"	"1997"	"2009"	"0"	"0"	"CGI;CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9444444"	"1992"	"2016"	"3"	"0"	"CGI;CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1987"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"5925"	"RB1"	"0.467"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2004"	"2018"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0035335"	"Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.80"	"0.9555556"	"1984"	"2018"	"13"	"110"	"CGI;CTD_human;UNIPROT"
"5925"	"RB1"	"0.467"	"0.828"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"		"1990"	"2015"	"2"	"2"	"CGI;CTD_human;ORPHANET"
"5925"	"RB1"	"0.467"	"0.828"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.6666667"	"1999"	"2014"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.95"	"1989"	"2016"	"3"	"0"	"CGI;CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1989"	"1989"	"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0751483"	"Familial Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.60"	"0.9090909"	"1992"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"5925"	"RB1"	"0.467"	"0.828"	"C0751484"	"Sporadic Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2014"	"0"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2011"	"3"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1989"	"2002"	"0"	"0"	"CGI"
"5925"	"RB1"	"0.467"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2016"	"3"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.8"	"1994"	"2014"	"2"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C3151302"	"Chromosome 13q14 deletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5925"	"RB1"	"0.467"	"0.828"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5925"	"RB1"	"0.467"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5926"	"ARID4A"	"0.762"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5926"	"ARID4A"	"0.762"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"5927"	"KDM5A"	"0.652"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5927"	"KDM5A"	"0.652"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5927"	"KDM5A"	"0.652"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5927"	"KDM5A"	"0.652"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5932"	"RBBP8"	"0.611"	"0.586"	"C0796063"	"microcephaly-digital anomalies syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"2008"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"5932"	"RBBP8"	"0.611"	"0.586"	"C1847572"	"SECKEL SYNDROME 2"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.60"		"2002"	"2014"	"2"	"3"	"CTD_human;UNIPROT"
"5932"	"RBBP8"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2002"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"5934"	"RBL2"	"0.63"	"0.483"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"5934"	"RBL2"	"0.63"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5934"	"RBL2"	"0.63"	"0.483"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5934"	"RBL2"	"0.63"	"0.483"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5935"	"RBM3"	"0.735"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"5935"	"RBM3"	"0.735"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5935"	"RBM3"	"0.735"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"5935"	"RBM3"	"0.735"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5935"	"RBM3"	"0.735"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2010"	"1"	"0"	"CTD_human"
"5940"	"RBMY1A1"	"0.735"	"0.379"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"5940"	"RBMY1A1"	"0.735"	"0.379"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5940"	"RBMY1A1"	"0.735"	"0.379"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5947"	"RBP1"	"0.58"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"5947"	"RBP1"	"0.58"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5947"	"RBP1"	"0.58"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5949"	"RBP3"	"0.624"	"0.517"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2011"	"2"	"0"	"CTD_human"
"5949"	"RBP3"	"0.624"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.66"	"1"	"1990"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"5949"	"RBP3"	"0.624"	"0.517"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.39"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"5949"	"RBP3"	"0.624"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5949"	"RBP3"	"0.624"	"0.517"	"C3715216"	"RETINITIS PIGMENTOSA 66"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2013"	"2"	"1"	"CTD_human;UNIPROT"
"5950"	"RBP4"	"0.534"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"5950"	"RBP4"	"0.534"	"0.724"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0023896"	"Alcoholic Liver Diseases"	"group"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0042842"	"Vitamin A Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0152455"	"Keratomalacia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0271271"	"Xerotic keratitis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C0856901"	"Retinol Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5950"	"RBP4"	"0.534"	"0.724"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5950"	"RBP4"	"0.534"	"0.724"	"C3554593"	"RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"1999"	"2013"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"5950"	"RBP4"	"0.534"	"0.724"	"C4225330"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"5954"	"RCN1"	"0.762"	"0.172"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5954"	"RCN1"	"0.762"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5955"	"RCN2"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C0155015"	"Color Blindness, Red"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.60"		"2002"	"2002"	"1"	"1"	"CTD_human;UNIPROT"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C0339537"	"Cone monochromatism"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.72"	"1"	"1991"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C2931753"	"Achromatopsia incomplete, X-linked"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C3887937"	"CONE DYSTROPHY 5, X-LINKED"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"1996"	"2"	"0"	"UNIPROT"
"5956"	"OPN1LW"	"0.559"	"0.655"	"C3887980"	"COLORBLINDNESS, PARTIAL, PROTAN SERIES"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2002"	"1"	"0"	"CTD_human;UNIPROT"
"5959"	"RDH5"	"0.681"	"0.31"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"0"	"2013"	"2015"	"1"	"0"	"CTD_human"
"5959"	"RDH5"	"0.681"	"0.31"	"C0311338"	"Fundus Albipunctatus"	"disease"	"C11"	"Disease or Syndrome"	"0.80"	"1"	"1999"	"2015"	"10"	"14"	"CTD_human;ORPHANET;UNIPROT"
"5959"	"RDH5"	"0.681"	"0.31"	"C1405854"	"Retinitis punctata albescens (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.61"	"1"	"1999"	"2015"	"10"	"12"	"CTD_human;ORPHANET;UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"0.9459459"	"1991"	"2017"	"0"	"4"	"ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C0271093"	"Stargardt's disease"	"phenotype"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C0311338"	"Fundus Albipunctatus"	"disease"	"C11"	"Disease or Syndrome"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C0339510"	"Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2015"	"0"	"0"	"CTD_human"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1405854"	"Retinitis punctata albescens (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.54"	"1"	"1993"	"1997"	"0"	"0"	"CTD_human;ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1536451"	"Central areolar choroidal sclerosis"	"disease"	"C11"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2009"	"0"	"0"	"ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1837029"	"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1842475"	"Retinitis Pigmentosa 7"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.81"	"1"	"1985"	"2016"	"10"	"9"	"CTD_human;UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1842914"	"Adult-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2016"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1855465"	"STARGARDT DISEASE 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C1868569"	"Patterned dystrophy of retinal pigment epithelium"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1992"	"2016"	"4"	"7"	"CTD_human;UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C2675552"	"Retinitis Pigmentosa 7, Digenic"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1985"	"2016"	"10"	"2"	"UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C2745945"	"Juvenile-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"5961"	"PRPH2"	"0.588"	"0.379"	"C2751290"	"CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1993"	"2016"	"4"	"4"	"CTD_human;UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C4013102"	"LEBER CONGENITAL AMAUROSIS 18"	"phenotype"		"Finding"	"0.60"		"1985"	"2016"	"10"	"3"	"UNIPROT"
"5961"	"PRPH2"	"0.588"	"0.379"	"C4509881"	"Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5961"	"PRPH2"	"0.588"	"0.379"	"C4511237"	"Butterfly-shaped pigmentary macular dystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"5962"	"RDX"	"0.652"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2016"	"1"	"0"	"CTD_human"
"5962"	"RDX"	"0.652"	"0.483"	"C1970239"	"DEAFNESS, AUTOSOMAL RECESSIVE, 24"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"5965"	"RECQL"	"0.659"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"5965"	"RECQL"	"0.659"	"0.552"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"5"	"0"	"CLINGEN"
"5965"	"RECQL"	"0.659"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"5965"	"RECQL"	"0.659"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CLINGEN"
"5965"	"RECQL"	"0.659"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5965"	"RECQL"	"0.659"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2009"	"2015"	"3"	"2"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.56"	"1"	"2001"	"2010"	"1"	"0"	"CGI;CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2007"	"2016"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5966"	"REL"	"0.588"	"0.655"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5970"	"RELA"	"0.456"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0010692"	"Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"2014"	"2017"	"0"	"0"	"ORPHANET"
"5970"	"RELA"	"0.456"	"0.828"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2006"	"2016"	"2"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2010"	"2013"	"2"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5970"	"RELA"	"0.456"	"0.828"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"		"2002"	"2010"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5970"	"RELA"	"0.456"	"0.828"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"5971"	"RELB"	"0.681"	"0.517"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2002"	"2009"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1997"	"1998"	"2"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"1991"	"2010"	"2"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.46"	"1"	"1986"	"2018"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0004775"	"Bartter Disease"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"1978"	"2006"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.96875"	"1982"	"2017"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9677419"	"1982"	"2017"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1980"	"1980"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.9551821"	"1975"	"2018"	"17"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0020540"	"Malignant Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"1989"	"2009"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.40"		"1980"	"2001"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"0.9583333"	"1980"	"2018"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1982"	"2011"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9354839"	"1992"	"2014"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1984"	"1991"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1979"	"1991"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1987"	"2014"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2017"	"3"	"0"	"PSYGENET"
"5972"	"REN"	"0.423"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1978"	"1978"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2018"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0221043"	"Liddle Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1982"	"2011"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0242528"	"Azotemia"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C0266313"	"Allanson Pantzar McLeod syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.78"	"1"	"2005"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"5972"	"REN"	"0.423"	"0.759"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1982"	"2011"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1982"	"2011"	"3"	"0"	"CTD_human"
"5972"	"REN"	"0.423"	"0.759"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5972"	"REN"	"0.423"	"0.759"	"C2678367"	"Renal Tubular Dysgenesis With Choanal Atresia And Athelia"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"5972"	"REN"	"0.423"	"0.759"	"C2751310"	"Hyperuricemic Nephropathy, Familial Juvenile 2"	"disease"	"C12;C13;C15;C23"	"Disease or Syndrome"	"0.71"	"1"	"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5973"	"RENBP"	"0.588"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5973"	"RENBP"	"0.588"	"0.655"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5973"	"RENBP"	"0.588"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5977"	"DPF2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"5978"	"REST"	"0.584"	"0.517"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5978"	"REST"	"0.584"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.61"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"5978"	"REST"	"0.584"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5978"	"REST"	"0.584"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0399440"	"Hereditary gingival fibromatosis"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"5978"	"REST"	"0.584"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"5978"	"REST"	"0.584"	"0.517"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C3891301"	"WILMS TUMOR, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"5978"	"REST"	"0.584"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5978"	"REST"	"0.584"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"5979"	"RET"	"0.418"	"0.724"	"C0007115"	"Malignant neoplasm of thyroid"	"disease"		"Neoplastic Process"	"0.40"	"0.9818182"	"1992"	"2018"	"0"	"0"	"CGI"
"5979"	"RET"	"0.418"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2018"	"0"	"0"	"CGI"
"5979"	"RET"	"0.418"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"	"0.9537815"	"1993"	"2018"	"2"	"14"	"CTD_human;ORPHANET"
"5979"	"RET"	"0.418"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"0"	"0"	"CGI"
"5979"	"RET"	"0.418"	"0.724"	"C0025268"	"Multiple Endocrine Neoplasia Type 2a"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.80"	"0.9491018"	"1988"	"2018"	"13"	"30"	"CTD_human;ORPHANET;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C0025269"	"Multiple Endocrine Neoplasia Type 2b"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"1.00"	"1"	"1988"	"2018"	"7"	"13"	"CTD_human;ORPHANET;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C0027662"	"Multiple Endocrine Neoplasia"	"disease"	"C04;C16;C19"	"Disease or Syndrome"	"0.50"	"0.976378"	"1987"	"2018"	"1"	"1"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"1.00"	"0.9710145"	"1988"	"2018"	"1"	"6"	"CGI;CTD_human;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.70"	"0.9166667"	"1993"	"2018"	"1"	"2"	"CGI;CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.35"	"1"	"1994"	"2015"	"2"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"1991"	"2010"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CGI"
"5979"	"RET"	"0.418"	"0.724"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1993"	"2017"	"12"	"0"	"CLINGEN"
"5979"	"RET"	"0.418"	"0.724"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1993"	"2017"	"12"	"0"	"CLINGEN"
"5979"	"RET"	"0.418"	"0.724"	"C0206693"	"Medullary carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.8571429"	"1991"	"2015"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"5979"	"RET"	"0.418"	"0.724"	"C0238462"	"Medullary carcinoma of thyroid"	"disease"	"C04;C19"	"Neoplastic Process"	"0.70"	"0.9458763"	"1992"	"2018"	"1"	"16"	"CGI;CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.9485981"	"1990"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"5979"	"RET"	"0.418"	"0.724"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"5979"	"RET"	"0.418"	"0.724"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0279680"	"Transitional cell carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1993"	"2017"	"12"	"0"	"CLINGEN"
"5979"	"RET"	"0.418"	"0.724"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1993"	"2017"	"12"	"0"	"CLINGEN"
"5979"	"RET"	"0.418"	"0.724"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.70"	"0.9807692"	"1990"	"2018"	"3"	"1"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"5979"	"RET"	"0.418"	"0.724"	"C0740340"	"Amyloidosis, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.64"	"1"	"1997"	"2015"	"3"	"5"	"CTD_human;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"1"	"UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.58"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.55"	"0.8"	"2001"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"5979"	"RET"	"0.418"	"0.724"	"C1833921"	"Familial medullary thyroid carcinoma"	"disease"	"C04;C16;C19"	"Neoplastic Process"	"0.80"	"0.974359"	"1986"	"2016"	"28"	"26"	"CTD_human;ORPHANET;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"1998"	"2004"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.50"		"2000"	"2009"	"1"	"4"	"UNIPROT"
"5979"	"RET"	"0.418"	"0.724"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"0.5"	"1999"	"2017"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"5979"	"RET"	"0.418"	"0.724"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.61"	"1"	"1994"	"2017"	"2"	"4"	"CTD_human;ORPHANET"
"5979"	"RET"	"0.418"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"5979"	"RET"	"0.418"	"0.724"	"C3888239"	"HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1"	"disease"		"Finding"	"0.30"		"1994"	"2012"	"15"	"34"	"UNIPROT"
"5980"	"REV3L"	"0.648"	"0.517"	"C0221060"	"Mobius Syndrome"	"disease"	"C07;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"5980"	"REV3L"	"0.648"	"0.517"	"C0853240"	"Mobius II syndrome"	"disease"	"C07;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"5981"	"RFC1"	"0.614"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"5981"	"RFC1"	"0.614"	"0.552"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5981"	"RFC1"	"0.614"	"0.552"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5981"	"RFC1"	"0.614"	"0.552"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"5982"	"RFC2"	"0.59"	"0.655"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2012"	"0"	"0"	"ORPHANET"
"5984"	"RFC4"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"5984"	"RFC4"	"0.857"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"5986"	"RFNG"	"1"	"0.034"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"5987"	"TRIM27"	"0.645"	"0.448"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"5990"	"RFX2"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"5991"	"RFX3"	"0.735"	"0.241"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5991"	"RFX3"	"0.735"	"0.241"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5991"	"RFX3"	"0.735"	"0.241"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5991"	"RFX3"	"0.735"	"0.241"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5991"	"RFX3"	"0.735"	"0.241"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5991"	"RFX3"	"0.735"	"0.241"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5992"	"RFX4"	"0.928"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"5992"	"RFX4"	"0.928"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2008"	"2"	"0"	"PSYGENET"
"5993"	"RFX5"	"0.681"	"0.517"	"C1859534"	"Bare Lymphocyte Syndrome, Type II, Complementation Group A"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"5993"	"RFX5"	"0.681"	"0.517"	"C1859535"	"Bare Lymphocyte Syndrome, Type II, Complementation Group B"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"5993"	"RFX5"	"0.681"	"0.517"	"C1859536"	"Bare Lymphocyte Syndrome, Type II, Complementation Group C"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"5993"	"RFX5"	"0.681"	"0.517"	"C1859537"	"Bare Lymphocyte Syndrome, Type II, Complementation Group D"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"5993"	"RFX5"	"0.681"	"0.517"	"C1859538"	"Bare Lymphocyte Syndrome, Type II, Complementation Group E"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.40"		"2000"	"2002"	"1"	"1"	"UNIPROT"
"5993"	"RFX5"	"0.681"	"0.517"	"C2931418"	"Bare lymphocyte syndrome 2"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"2000"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"5994"	"RFXAP"	"0.701"	"0.517"	"C2931418"	"Bare lymphocyte syndrome 2"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.64"	"0.75"	"2000"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"5995"	"RGR"	"0.681"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.62"	"1"	"1999"	"2011"	"2"	"0"	"CTD_human;ORPHANET"
"5995"	"RGR"	"0.681"	"0.448"	"C3151068"	"RETINITIS PIGMENTOSA 44"	"disease"		"Disease or Syndrome"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;UNIPROT"
"5996"	"RGS1"	"0.685"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"5996"	"RGS1"	"0.685"	"0.448"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5996"	"RGS1"	"0.685"	"0.448"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9444444"	"1992"	"2016"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"5997"	"RGS2"	"0.598"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"5997"	"RGS2"	"0.598"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"5998"	"RGS3"	"0.857"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"5999"	"RGS4"	"0.685"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"5999"	"RGS4"	"0.685"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2005"	"2010"	"5"	"0"	"PSYGENET"
"5999"	"RGS4"	"0.685"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5999"	"RGS4"	"0.685"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"5999"	"RGS4"	"0.685"	"0.345"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6000"	"RGS7"	"0.785"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6000"	"RGS7"	"0.785"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6000"	"RGS7"	"0.785"	"0.276"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6000"	"RGS7"	"0.785"	"0.276"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6000"	"RGS7"	"0.785"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6000"	"RGS7"	"0.785"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6001"	"RGS10"	"0.773"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6001"	"RGS10"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"6002"	"RGS12"	"0.799"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6005"	"RHAG"	"0.727"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1985"	"2012"	"7"	"0"	"GENOMICS_ENGLAND"
"6005"	"RHAG"	"0.727"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1985"	"2012"	"7"	"0"	"GENOMICS_ENGLAND"
"6005"	"RHAG"	"0.727"	"0.276"	"C0272052"	"Rh Deficiency Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"1996"	"1998"	"3"	"4"	"ORPHANET;UNIPROT"
"6005"	"RHAG"	"0.727"	"0.276"	"C1849387"	"Rh-Null, Regulator Type"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1996"	"1999"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6005"	"RHAG"	"0.727"	"0.276"	"C1861455"	"STOMATOCYTOSIS I"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1961"	"2013"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6006"	"RHCE"	"0.762"	"0.207"	"C0002881"	"Anemia, Hemolytic, Congenital"	"disease"	"C15;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6006"	"RHCE"	"0.762"	"0.207"	"C0272052"	"Rh Deficiency Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6006"	"RHCE"	"0.762"	"0.207"	"C1849387"	"Rh-Null, Regulator Type"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6007"	"RHD"	"0.659"	"0.448"	"C0002881"	"Anemia, Hemolytic, Congenital"	"disease"	"C15;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6007"	"RHD"	"0.659"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6007"	"RHD"	"0.659"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2009"	"3"	"0"	"PSYGENET"
"6007"	"RHD"	"0.659"	"0.448"	"C0272052"	"Rh Deficiency Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6007"	"RHD"	"0.659"	"0.448"	"C1849387"	"Rh-Null, Regulator Type"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6009"	"RHEB"	"0.696"	"0.379"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6009"	"RHEB"	"0.696"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6009"	"RHEB"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6010"	"RHO"	"0.564"	"0.69"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"1996"	"2017"	"2"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"0.9774436"	"1981"	"2017"	"8"	"10"	"CTD_human;ORPHANET"
"6010"	"RHO"	"0.564"	"0.69"	"C0311338"	"Fundus Albipunctatus"	"disease"	"C11"	"Disease or Syndrome"	"0.61"	"1"	"1988"	"1988"	"0"	"0"	"CTD_human;ORPHANET"
"6010"	"RHO"	"0.564"	"0.69"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6010"	"RHO"	"0.564"	"0.69"	"C1405854"	"Retinitis punctata albescens (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.62"	"1"	"1991"	"2006"	"0"	"1"	"CTD_human;ORPHANET"
"6010"	"RHO"	"0.564"	"0.69"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C1864869"	"Night Blindness, Congenital Stationary, Autosomal Dominant 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2011"	"4"	"4"	"CTD_human;UNIPROT"
"6010"	"RHO"	"0.564"	"0.69"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C3151001"	"Retinitis Pigmentosa 4"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"1990"	"2017"	"26"	"36"	"CTD_human;UNIPROT"
"6010"	"RHO"	"0.564"	"0.69"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6010"	"RHO"	"0.564"	"0.69"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6011"	"GRK1"	"0.707"	"0.31"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"1997"	"1998"	"0"	"0"	"ORPHANET"
"6011"	"GRK1"	"0.707"	"0.31"	"C1306122"	"Oguchi disease"	"disease"	"C11"	"Disease or Syndrome"	"0.69"	"1"	"1997"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"6011"	"GRK1"	"0.707"	"0.31"	"C3150678"	"OGUCHI DISEASE 2"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"2007"	"2"	"2"	"UNIPROT"
"6013"	"RLN1"	"0.799"	"0.207"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6016"	"RIT1"	"0.619"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6016"	"RIT1"	"0.619"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"6016"	"RIT1"	"0.619"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6016"	"RIT1"	"0.619"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6016"	"RIT1"	"0.619"	"0.621"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.47"	"1"	"2013"	"2017"	"0"	"13"	"ORPHANET"
"6016"	"RIT1"	"0.619"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6016"	"RIT1"	"0.619"	"0.621"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6016"	"RIT1"	"0.619"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6016"	"RIT1"	"0.619"	"0.621"	"C3809233"	"NOONAN SYNDROME 8"	"disease"		"Disease or Syndrome"	"0.70"		"1987"	"2017"	"6"	"8"	"CLINGEN;CTD_human;UNIPROT"
"6017"	"RLBP1"	"0.642"	"0.379"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6017"	"RLBP1"	"0.642"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.44"	"1"	"1990"	"2017"	"0"	"1"	"ORPHANET"
"6017"	"RLBP1"	"0.642"	"0.379"	"C0311338"	"Fundus Albipunctatus"	"disease"	"C11"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6017"	"RLBP1"	"0.642"	"0.379"	"C1405854"	"Retinitis punctata albescens (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.80"	"1"	"1997"	"2018"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6017"	"RLBP1"	"0.642"	"0.379"	"C1843815"	"Newfoundland Rod-Cone Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"6017"	"RLBP1"	"0.642"	"0.379"	"C1843816"	"Bothnia Retinal Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.90"		"1999"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6019"	"RLN2"	"0.785"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2007"	"1"	"0"	"CTD_human"
"6019"	"RLN2"	"0.785"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6023"	"RMRP"	"0.586"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"6023"	"RMRP"	"0.586"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"6023"	"RMRP"	"0.586"	"0.655"	"C0220748"	"Cartilage-hair hypoplasia"	"disease"	"C05;C06;C16;C20"	"Congenital Abnormality; Disease or Syndrome"	"0.60"	"1"	"1982"	"2018"	"0"	"8"	"CTD_human;ORPHANET"
"6023"	"RMRP"	"0.586"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6023"	"RMRP"	"0.586"	"0.655"	"C1834821"	"METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"1991"	"2007"	"0"	"2"	"CTD_human"
"6023"	"RMRP"	"0.586"	"0.655"	"C1846796"	"Anauxetic dysplasia"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2011"	"0"	"2"	"CTD_human;ORPHANET"
"6023"	"RMRP"	"0.586"	"0.655"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6023"	"RMRP"	"0.586"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6037"	"RNASE3"	"0.545"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.8461538"	"1996"	"2013"	"3"	"0"	"CTD_human"
"6037"	"RNASE3"	"0.545"	"0.793"	"C0085423"	"Gram-Negative Bacterial Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6037"	"RNASE3"	"0.545"	"0.793"	"C0085426"	"Gram-Positive Bacterial Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6038"	"RNASE4"	"0.834"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6038"	"RNASE4"	"0.834"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6038"	"RNASE4"	"0.834"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6039"	"RNASE6"	"0.928"	"0.069"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6039"	"RNASE6"	"0.928"	"0.069"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6039"	"RNASE6"	"0.928"	"0.069"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6039"	"RNASE6"	"0.928"	"0.069"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6039"	"RNASE6"	"0.928"	"0.069"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6041"	"RNASEL"	"0.607"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6041"	"RNASEL"	"0.607"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"3"	"0"	"CTD_human"
"6041"	"RNASEL"	"0.607"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.9444444"	"2002"	"2016"	"3"	"0"	"CTD_human"
"6041"	"RNASEL"	"0.607"	"0.552"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.80"	"0.8695652"	"2002"	"2017"	"1"	"2"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"6046"	"BRD2"	"0.488"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2000"	"2016"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6046"	"BRD2"	"0.488"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6046"	"BRD2"	"0.488"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"6049"	"RNF6"	"0.707"	"0.31"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2014"	"2017"	"1"	"1"	"CTD_human"
"6049"	"RNF6"	"0.707"	"0.31"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"6049"	"RNF6"	"0.707"	"0.31"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"6049"	"RNF6"	"0.707"	"0.31"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6049"	"RNF6"	"0.707"	"0.31"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6049"	"RNF6"	"0.707"	"0.31"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"6049"	"RNF6"	"0.707"	"0.31"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"6051"	"RNPEP"	"0.785"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6059"	"ABCE1"	"0.785"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6059"	"ABCE1"	"0.785"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6059"	"ABCE1"	"0.785"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6079"	"SNORD15A"	"0.696"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"2"	"UNIPROT"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"6091"	"ROBO1"	"0.575"	"0.586"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0042580"	"Vesico-Ureteral Reflux"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.46"	"1"	"2005"	"2014"	"0"	"0"	"ORPHANET"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6092"	"ROBO2"	"0.701"	"0.241"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6092"	"ROBO2"	"0.701"	"0.241"	"C1970483"	"Vesicoureteral Reflux 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"6092"	"ROBO2"	"0.701"	"0.241"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6093"	"ROCK1"	"0.579"	"0.517"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6094"	"ROM1"	"0.639"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.68"	"1"	"1992"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"6094"	"ROM1"	"0.639"	"0.483"	"C1842475"	"Retinitis Pigmentosa 7"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6095"	"RORA"	"0.645"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2011"	"2"	"0"	"CTD_human"
"6095"	"RORA"	"0.645"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"6095"	"RORA"	"0.645"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"6095"	"RORA"	"0.645"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"3"	"0"	"PSYGENET"
"6095"	"RORA"	"0.645"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6095"	"RORA"	"0.645"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6095"	"RORA"	"0.645"	"0.552"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6095"	"RORA"	"0.645"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6096"	"RORB"	"0.857"	"0.103"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6096"	"RORB"	"0.857"	"0.103"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6096"	"RORB"	"0.857"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6097"	"RORC"	"0.609"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0393770"	"Delayed Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0494410"	"Nonorganic Sleep Wake Cycle Disorders"	"group"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0751758"	"Advanced Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0751759"	"Non-24 Hour Sleep-Wake Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0751760"	"Shift-Work Sleep Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C0877792"	"Sleep Disorders, Circadian Rhythm"	"group"	"C10;C24;F03"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6097"	"RORC"	"0.609"	"0.655"	"C4225266"	"IMMUNODEFICIENCY 42"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6098"	"ROS1"	"0.493"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9594595"	"2008"	"2018"	"4"	"0"	"CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"1"	"2012"	"2018"	"1"	"1"	"CGI;CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"UNIPROT"
"6098"	"ROS1"	"0.493"	"0.759"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6098"	"ROS1"	"0.493"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6098"	"ROS1"	"0.493"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6100"	"RP9"	"0.672"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"		"2002"	"2002"	"0"	"0"	"ORPHANET"
"6100"	"RP9"	"0.672"	"0.414"	"C1867300"	"RETINITIS PIGMENTOSA 9"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2008"	"1"	"2"	"CTD_human;UNIPROT"
"6101"	"RP1"	"0.659"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"1999"	"2017"	"0"	"7"	"ORPHANET"
"6101"	"RP1"	"0.659"	"0.483"	"C0220701"	"RETINITIS PIGMENTOSA 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"1992"	"2016"	"9"	"20"	"CTD_human;UNIPROT"
"6102"	"RP2"	"0.667"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6102"	"RP2"	"0.667"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.47"	"1"	"1999"	"2006"	"0"	"0"	"ORPHANET"
"6102"	"RP2"	"0.667"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6102"	"RP2"	"0.667"	"0.379"	"C2681923"	"RETINITIS PIGMENTOSA 2 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.83"	"1"	"1998"	"2017"	"13"	"7"	"CTD_human;UNIPROT"
"6103"	"RPGR"	"0.577"	"0.621"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2013"	"0"	"0"	"ORPHANET"
"6103"	"RPGR"	"0.577"	"0.621"	"C0035243"	"Respiratory Tract Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.31"		"2002"	"2010"	"1"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"0.9833333"	"1995"	"2017"	"3"	"7"	"CTD_human;ORPHANET"
"6103"	"RPGR"	"0.577"	"0.621"	"C0041912"	"Upper Respiratory Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6103"	"RPGR"	"0.577"	"0.621"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C0854723"	"Retinal Dystrophies"	"group"	"C11"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2002"	"2017"	"1"	"2"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C1844776"	"CONE-ROD DYSTROPHY, X-LINKED, 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2000"	"2014"	"0"	"5"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C1844777"	"CONE DYSTROPHY, X-LINKED, 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2003"	"0"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C1845667"	"RETINITIS PIGMENTOSA 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.77"	"1"	"1996"	"2015"	"14"	"19"	"CTD_human;UNIPROT"
"6103"	"RPGR"	"0.577"	"0.621"	"C2749137"	"Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness"	"disease"	"C01;C08;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2004"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6103"	"RPGR"	"0.577"	"0.621"	"C3151784"	"MACULAR DEGENERATION, X-LINKED ATROPHIC"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6103"	"RPGR"	"0.577"	"0.621"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6117"	"RPA1"	"0.713"	"0.448"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.40"		"2014"	"2015"	"1"	"1"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.69"	"1"	"1998"	"2016"	"3"	"2"	"CTD_human;ORPHANET"
"6121"	"RPE65"	"0.479"	"0.759"	"C0155003"	"Blindness, Transient"	"phenotype"	"C10;C11;C23"	"Pathologic Function"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0221473"	"Blindness, Hysterical"	"disease"	"C10;C11;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0271215"	"Blindness, Legal"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.40"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.60"	"0.9833333"	"1997"	"2018"	"3"	"0"	"CTD_human;ORPHANET"
"6121"	"RPE65"	"0.479"	"0.759"	"C0339730"	"Blindness, Acquired"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0376288"	"Amaurosis"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0456909"	"Blindness"	"phenotype"	"C10;C11;C23"	"Finding"	"0.45"		"2001"	"2008"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0750958"	"Blindness, Monocular"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0854723"	"Retinal Dystrophies"	"group"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2017"	"1"	"2"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"6121"	"RPE65"	"0.479"	"0.759"	"C1859844"	"LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.94"	"0.75"	"1959"	"2017"	"27"	"28"	"CLINGEN;CTD_human;UNIPROT"
"6121"	"RPE65"	"0.479"	"0.759"	"C1879328"	"Blindness both eyes NOS (disorder)"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C3151086"	"Retinitis Pigmentosa 20"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.90"		"1959"	"2017"	"11"	"19"	"CLINGEN;CTD_human;UNIPROT"
"6121"	"RPE65"	"0.479"	"0.759"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1997"	"2009"	"3"	"0"	"CTD_human"
"6121"	"RPE65"	"0.479"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6122"	"RPL3"	"0.799"	"0.31"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6122"	"RPL3"	"0.799"	"0.31"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6123"	"RPL3L"			"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6125"	"RPL5"	"0.663"	"0.586"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6125"	"RPL5"	"0.663"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6125"	"RPL5"	"0.663"	"0.586"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6125"	"RPL5"	"0.663"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6125"	"RPL5"	"0.663"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6125"	"RPL5"	"0.663"	"0.586"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.46"	"1"	"2009"	"2017"	"0"	"1"	"ORPHANET"
"6125"	"RPL5"	"0.663"	"0.586"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.51"	"1"	"2013"	"2013"	"1"	"0"	"CGI;CTD_human"
"6125"	"RPL5"	"0.663"	"0.586"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6125"	"RPL5"	"0.663"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"6128"	"RPL6"	"0.785"	"0.172"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6128"	"RPL6"	"0.785"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6133"	"RPL9"	"0.857"	"0.172"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6133"	"RPL9"	"0.857"	"0.172"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6134"	"RPL10"	"0.659"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6134"	"RPL10"	"0.659"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6134"	"RPL10"	"0.659"	"0.621"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6134"	"RPL10"	"0.659"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6134"	"RPL10"	"0.659"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6134"	"RPL10"	"0.659"	"0.621"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.52"	"1"	"2013"	"2016"	"1"	"0"	"CGI;CTD_human"
"6134"	"RPL10"	"0.659"	"0.621"	"C3275438"	"AUTISM, SUSCEPTIBILITY TO, X-LINKED 5"	"phenotype"		"Finding"	"0.40"		"2007"	"2015"	"3"	"1"	"UNIPROT"
"6134"	"RPL10"	"0.659"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6134"	"RPL10"	"0.659"	"0.621"	"C4478383"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2016"	"3"	"2"	"UNIPROT"
"6135"	"RPL11"	"0.633"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"6135"	"RPL11"	"0.633"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6135"	"RPL11"	"0.633"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"6135"	"RPL11"	"0.633"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6135"	"RPL11"	"0.633"	"0.517"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6135"	"RPL11"	"0.633"	"0.517"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2018"	"0"	"0"	"ORPHANET"
"6135"	"RPL11"	"0.633"	"0.517"	"C2675512"	"Diamond-Blackfan Anemia 7"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2013"	"2"	"3"	"CTD_human;UNIPROT"
"6135"	"RPL11"	"0.633"	"0.517"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6135"	"RPL11"	"0.633"	"0.517"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"6136"	"RPL12"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6136"	"RPL12"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6137"	"RPL13"	"0.762"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6137"	"RPL13"	"0.762"	"0.31"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6137"	"RPL13"	"0.762"	"0.31"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6137"	"RPL13"	"0.762"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6137"	"RPL13"	"0.762"	"0.31"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6137"	"RPL13"	"0.762"	"0.31"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6138"	"RPL15"	"0.727"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2011"	"1"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6138"	"RPL15"	"0.727"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6138"	"RPL15"	"0.727"	"0.379"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"6138"	"RPL15"	"0.727"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6138"	"RPL15"	"0.727"	"0.379"	"C3809888"	"DIAMOND-BLACKFAN ANEMIA 12"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6138"	"RPL15"	"0.727"	"0.379"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6139"	"RPL17"	"0.727"	"0.414"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6141"	"RPL18"	"0.752"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6141"	"RPL18"	"0.752"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6141"	"RPL18"	"0.752"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6141"	"RPL18"	"0.752"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6141"	"RPL18"	"0.752"	"0.345"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6141"	"RPL18"	"0.752"	"0.345"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6141"	"RPL18"	"0.752"	"0.345"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6141"	"RPL18"	"0.752"	"0.345"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6143"	"RPL19"	"0.735"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6143"	"RPL19"	"0.735"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6144"	"RPL21"	"0.834"	"0.103"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"6144"	"RPL21"	"0.834"	"0.103"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"6144"	"RPL21"	"0.834"	"0.103"	"C4014563"	"HYPOTRICHOSIS 12"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2011"	"1"	"1"	"UNIPROT"
"6147"	"RPL23A"	"0.834"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6147"	"RPL23A"	"0.834"	"0.138"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6147"	"RPL23A"	"0.834"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6147"	"RPL23A"	"0.834"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6147"	"RPL23A"	"0.834"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6152"	"RPL24"	"0.857"	"0.172"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6152"	"RPL24"	"0.857"	"0.172"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6154"	"RPL26"	"0.69"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6154"	"RPL26"	"0.69"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6154"	"RPL26"	"0.69"	"0.414"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6154"	"RPL26"	"0.69"	"0.414"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"6154"	"RPL26"	"0.69"	"0.414"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6154"	"RPL26"	"0.69"	"0.414"	"C3554042"	"DIAMOND-BLACKFAN ANEMIA 11"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"6154"	"RPL26"	"0.69"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6155"	"RPL27"	"0.762"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6155"	"RPL27"	"0.762"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6155"	"RPL27"	"0.762"	"0.31"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6155"	"RPL27"	"0.762"	"0.31"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"6155"	"RPL27"	"0.762"	"0.31"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6155"	"RPL27"	"0.762"	"0.31"	"C4479424"	"DIAMOND-BLACKFAN ANEMIA 16"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0007758"	"Cerebellar Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0162834"	"Hyperpigmentation"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0234162"	"Cerebellar Dysmetria"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0234357"	"Adiadochokinesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C0750994"	"Cerebellar Hemiataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6157"	"RPL27A"	"0.928"	"0.103"	"C3668822"	"Hypermetria (finding)"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6158"	"RPL28"	"1"	"0.069"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6160"	"RPL31"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6160"	"RPL31"	"0.815"	"0.172"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6160"	"RPL31"	"0.815"	"0.172"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6160"	"RPL31"	"0.815"	"0.172"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6160"	"RPL31"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6160"	"RPL31"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6160"	"RPL31"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6165"	"RPL35A"	"0.713"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6165"	"RPL35A"	"0.713"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6165"	"RPL35A"	"0.713"	"0.345"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6165"	"RPL35A"	"0.713"	"0.345"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2008"	"2012"	"0"	"0"	"ORPHANET"
"6165"	"RPL35A"	"0.713"	"0.345"	"C2675859"	"Diamond-Blackfan Anemia 5"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2008"	"1"	"3"	"CTD_human;UNIPROT"
"6165"	"RPL35A"	"0.713"	"0.345"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6165"	"RPL35A"	"0.713"	"0.345"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"6168"	"RPL37A"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6168"	"RPL37A"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6173"	"RPL36A"	"0.645"	"0.345"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"6182"	"MRPL12"	"0.928"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6182"	"MRPL12"	"0.928"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6183"	"MRPS12"	"1"	"0.034"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6185"	"RPN2"	"0.713"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6185"	"RPN2"	"0.713"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6187"	"RPS2"	"0.815"	"0.31"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6187"	"RPS2"	"0.815"	"0.31"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6187"	"RPS2"	"0.815"	"0.31"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6187"	"RPS2"	"0.815"	"0.31"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6188"	"RPS3"	"0.762"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"6188"	"RPS3"	"0.762"	"0.207"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6191"	"RPS4X"	"0.743"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6191"	"RPS4X"	"0.743"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"6191"	"RPS4X"	"0.743"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6191"	"RPS4X"	"0.743"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6194"	"RPS6"	"0.602"	"0.414"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6195"	"RPS6KA1"	"0.69"	"0.414"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6196"	"RPS6KA2"	"0.685"	"0.276"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"6196"	"RPS6KA2"	"0.685"	"0.276"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2017"	"1"	"1"	"UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"0.8"	"2010"	"2018"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0265252"	"Coffin-Lowry syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1996"	"2016"	"7"	"13"	"CTD_human;ORPHANET;UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C0796225"	"Mental Retardation, X-Linked 19"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1996"	"2015"	"2"	"5"	"CTD_human;UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6197"	"RPS6KA3"	"0.541"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2002"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6198"	"RPS6KB1"	"0.555"	"0.621"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6199"	"RPS6KB2"	"0.785"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"6199"	"RPS6KB2"	"0.785"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"6199"	"RPS6KB2"	"0.785"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6199"	"RPS6KB2"	"0.785"	"0.207"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"6199"	"RPS6KB2"	"0.785"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"6201"	"RPS7"	"0.72"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"6201"	"RPS7"	"0.72"	"0.379"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6201"	"RPS7"	"0.72"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"6201"	"RPS7"	"0.72"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C2675511"	"Diamond-Blackfan Anemia 8"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2017"	"0"	"2"	"CTD_human"
"6201"	"RPS7"	"0.72"	"0.379"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6201"	"RPS7"	"0.72"	"0.379"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"6202"	"RPS8"	"0.834"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6202"	"RPS8"	"0.834"	"0.172"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6202"	"RPS8"	"0.834"	"0.172"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6202"	"RPS8"	"0.834"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6202"	"RPS8"	"0.834"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6202"	"RPS8"	"0.834"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6203"	"RPS9"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6204"	"RPS10"	"0.727"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6204"	"RPS10"	"0.727"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6204"	"RPS10"	"0.727"	"0.414"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6204"	"RPS10"	"0.727"	"0.414"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.53"	"1"	"2010"	"2015"	"5"	"0"	"CLINGEN;ORPHANET"
"6204"	"RPS10"	"0.727"	"0.414"	"C2750081"	"Diamond-Blackfan Anemia 9"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"2010"	"2013"	"0"	"2"	"CTD_human"
"6204"	"RPS10"	"0.727"	"0.414"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"2010"	"2015"	"5"	"0"	"CLINGEN;ORPHANET"
"6204"	"RPS10"	"0.727"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"6208"	"RPS14"	"0.667"	"0.345"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6208"	"RPS14"	"0.667"	"0.345"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6208"	"RPS14"	"0.667"	"0.345"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C0740302"	"5q-syndrome"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.60"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"6208"	"RPS14"	"0.667"	"0.345"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6208"	"RPS14"	"0.667"	"0.345"	"C1292779"	"Myelodysplastic Syndrome with Isolated del(5q)"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"6209"	"RPS15"	"0.735"	"0.241"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"6209"	"RPS15"	"0.735"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6209"	"RPS15"	"0.735"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6209"	"RPS15"	"0.735"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6209"	"RPS15"	"0.735"	"0.241"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6209"	"RPS15"	"0.735"	"0.241"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6209"	"RPS15"	"0.735"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6209"	"RPS15"	"0.735"	"0.241"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6218"	"RPS17"	"0.743"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"6218"	"RPS17"	"0.743"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"6218"	"RPS17"	"0.743"	"0.276"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6218"	"RPS17"	"0.743"	"0.276"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.58"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"6218"	"RPS17"	"0.743"	"0.276"	"C2675860"	"Diamond-Blackfan Anemia 4"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2013"	"0"	"3"	"CTD_human"
"6218"	"RPS17"	"0.743"	"0.276"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6218"	"RPS17"	"0.743"	"0.276"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2008"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"6223"	"RPS19"	"0.527"	"0.793"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"6223"	"RPS19"	"0.527"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"6223"	"RPS19"	"0.527"	"0.793"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6223"	"RPS19"	"0.527"	"0.793"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"0.9550562"	"1992"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"6223"	"RPS19"	"0.527"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6223"	"RPS19"	"0.527"	"0.793"	"C2676137"	"Diamond-Blackfan Anemia 1"	"disease"	"C15;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.47"	"0.8571429"	"1985"	"2014"	"8"	"8"	"UNIPROT"
"6223"	"RPS19"	"0.527"	"0.793"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6223"	"RPS19"	"0.527"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6223"	"RPS19"	"0.527"	"0.793"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1992"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"6224"	"RPS20"	"0.773"	"0.172"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2014"	"2017"	"2"	"0"	"CLINGEN"
"6224"	"RPS20"	"0.773"	"0.172"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2017"	"2"	"0"	"CLINGEN"
"6224"	"RPS20"	"0.773"	"0.172"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2014"	"2017"	"2"	"0"	"CLINGEN"
"6224"	"RPS20"	"0.773"	"0.172"	"C3896578"	"Familial Colorectal Cancer Type X"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6227"	"RPS21"	"0.886"	"0.138"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6227"	"RPS21"	"0.886"	"0.138"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6227"	"RPS21"	"0.886"	"0.138"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6227"	"RPS21"	"0.886"	"0.138"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6228"	"RPS23"	"0.773"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6228"	"RPS23"	"0.773"	"0.31"	"C4479431"	"BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"6229"	"RPS24"	"0.752"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1990"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"6229"	"RPS24"	"0.752"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1990"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"6229"	"RPS24"	"0.752"	"0.31"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6229"	"RPS24"	"0.752"	"0.31"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.49"	"1"	"2007"	"2017"	"0"	"2"	"ORPHANET"
"6229"	"RPS24"	"0.752"	"0.31"	"C1857719"	"Anemia, Diamond-Blackfan, 3"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"6"	"3"	"CLINGEN;CTD_human"
"6229"	"RPS24"	"0.752"	"0.31"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6229"	"RPS24"	"0.752"	"0.31"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1990"	"2010"	"5"	"0"	"GENOMICS_ENGLAND"
"6231"	"RPS26"	"0.727"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"6231"	"RPS26"	"0.727"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6231"	"RPS26"	"0.727"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6231"	"RPS26"	"0.727"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"6231"	"RPS26"	"0.727"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6231"	"RPS26"	"0.727"	"0.448"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6231"	"RPS26"	"0.727"	"0.448"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2010"	"2014"	"0"	"0"	"ORPHANET"
"6231"	"RPS26"	"0.727"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6231"	"RPS26"	"0.727"	"0.448"	"C2750080"	"Diamond-Blackfan Anemia 10"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2007"	"2017"	"2"	"7"	"CTD_human;UNIPROT"
"6231"	"RPS26"	"0.727"	"0.448"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6231"	"RPS26"	"0.727"	"0.448"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"6232"	"RPS27"	"0.652"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6232"	"RPS27"	"0.652"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6232"	"RPS27"	"0.652"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6232"	"RPS27"	"0.652"	"0.552"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"6232"	"RPS27"	"0.652"	"0.552"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6232"	"RPS27"	"0.652"	"0.552"	"C4479428"	"DIAMOND-BLACKFAN ANEMIA 17"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"6233"	"RPS27A"	"0.707"	"0.483"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2014"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"6234"	"RPS28"	"0.713"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1993"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6234"	"RPS28"	"0.713"	"0.345"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6234"	"RPS28"	"0.713"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6234"	"RPS28"	"0.713"	"0.345"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6234"	"RPS28"	"0.713"	"0.345"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6234"	"RPS28"	"0.713"	"0.345"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6234"	"RPS28"	"0.713"	"0.345"	"C4225411"	"DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6235"	"RPS29"	"0.743"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6235"	"RPS29"	"0.743"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6235"	"RPS29"	"0.743"	"0.345"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6235"	"RPS29"	"0.743"	"0.345"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6235"	"RPS29"	"0.743"	"0.345"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6235"	"RPS29"	"0.743"	"0.345"	"C4014641"	"DIAMOND-BLACKFAN ANEMIA 13"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"6235"	"RPS29"	"0.743"	"0.345"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"6236"	"RRAD"	"0.681"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6236"	"RRAD"	"0.681"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6237"	"RRAS"	"0.636"	"0.552"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"6237"	"RRAS"	"0.636"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6237"	"RRAS"	"0.636"	"0.552"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.51"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6237"	"RRAS"	"0.636"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"6239"	"RREB1"	"0.536"	"0.759"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6239"	"RREB1"	"0.536"	"0.759"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6239"	"RREB1"	"0.536"	"0.759"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6239"	"RREB1"	"0.536"	"0.759"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6239"	"RREB1"	"0.536"	"0.759"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6239"	"RREB1"	"0.536"	"0.759"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6240"	"RRM1"	"0.584"	"0.483"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6240"	"RRM1"	"0.584"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"6241"	"RRM2"	"0.604"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"6247"	"RS1"	"0.707"	"0.276"	"C0152439"	"Retinoschisis"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"6247"	"RS1"	"0.707"	"0.276"	"C0271091"	"Retinoschisis, Juvenile, X-Linked"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"1"	"1997"	"2016"	"2"	"18"	"CTD_human;ORPHANET"
"6247"	"RS1"	"0.707"	"0.276"	"C1137478"	"Retinoschisis, Degenerative"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"6247"	"RS1"	"0.707"	"0.276"	"C3714753"	"RETINOSCHISIS 1, X-LINKED, JUVENILE"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"1997"	"2017"	"13"	"56"	"UNIPROT"
"6249"	"CLIP1"	"0.667"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2016"	"0"	"0"	"UNIPROT"
"6251"	"RSU1"	"0.743"	"0.276"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6251"	"RSU1"	"0.743"	"0.276"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6251"	"RSU1"	"0.743"	"0.276"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6251"	"RSU1"	"0.743"	"0.276"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6251"	"RSU1"	"0.743"	"0.276"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6252"	"RTN1"	"0.72"	"0.483"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6253"	"RTN2"	"0.743"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"6253"	"RTN2"	"0.743"	"0.276"	"C1858106"	"SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2012"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6253"	"RTN2"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"6256"	"RXRA"	"0.584"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0149940"	"Sciatic Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0154748"	"Lesion of Sciatic Nerve"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0242013"	"Sciatic Neuritis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0751924"	"Neuralgia-Neuritis, Sciatic Nerve"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C0751925"	"Sciatic Nerve Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6256"	"RXRA"	"0.584"	"0.621"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2003"	"2013"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2003"	"2013"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6257"	"RXRB"	"0.752"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6258"	"RXRG"	"0.752"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6259"	"RYK"	"0.743"	"0.276"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2006"	"1"	"0"	"CTD_human"
"6259"	"RYK"	"0.743"	"0.276"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6259"	"RYK"	"0.743"	"0.276"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6259"	"RYK"	"0.743"	"0.276"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6259"	"RYK"	"0.743"	"0.276"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"GENOMICS_ENGLAND"
"6261"	"RYR1"	"0.545"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0024591"	"Malignant hyperpyrexia due to anesthesia"	"disease"	"C23"	"Disease or Syndrome"	"1.00"	"0.9536082"	"1990"	"2018"	"50"	"89"	"CTD_human;ORPHANET;UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.40"	"0.9411765"	"2000"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6261"	"RYR1"	"0.545"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.42"	"1"	"1993"	"2011"	"1"	"7"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"GENOMICS_ENGLAND"
"6261"	"RYR1"	"0.545"	"0.621"	"C0751951"	"Central Core Myopathy (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"1.00"	"0.9886364"	"1993"	"2018"	"28"	"97"	"CTD_human;ORPHANET;UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"6261"	"RYR1"	"0.545"	"0.621"	"C1840365"	"King Denborough syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.62"	"1"	"1992"	"2016"	"44"	"89"	"ORPHANET;UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C1850674"	"MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)"	"disease"	"C05;C10;C11;C23"	"Disease or Syndrome"	"0.80"	"1"	"1982"	"2017"	"3"	"17"	"CTD_human;ORPHANET;UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C1854678"	"MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"6261"	"RYR1"	"0.545"	"0.621"	"C1861751"	"Minicore Myopathy, Moderate, with Hand Involvement"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1993"	"2016"	"26"	"53"	"UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C1861752"	"Multicore Myopathy, Moderate, with Hand Involvement"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1993"	"2016"	"26"	"53"	"UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C1861753"	"Multiminicore Disease, Moderate, with Hand Involvement"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"		"1993"	"2016"	"26"	"53"	"ORPHANET;UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C2674259"	"NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"		"1993"	"2016"	"26"	"55"	"UNIPROT"
"6261"	"RYR1"	"0.545"	"0.621"	"C2930980"	"Malignant hyperthermia susceptibility type 1"	"disease"	"C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6261"	"RYR1"	"0.545"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2016"	"2"	"0"	"CLINGEN"
"6262"	"RYR2"	"0.575"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.49"	"1"	"2005"	"2016"	"1"	"2"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0340485"	"Familial ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"2"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0340493"	"Paroxysmal familial ventricular fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.39"	"1"	"2001"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6262"	"RYR2"	"0.575"	"0.414"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2016"	"2"	"0"	"CLINGEN"
"6262"	"RYR2"	"0.575"	"0.414"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"1.00"	"0.9690722"	"1990"	"2018"	"23"	"27"	"CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"6262"	"RYR2"	"0.575"	"0.414"	"C1832931"	"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.81"	"1"	"2001"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"6262"	"RYR2"	"0.575"	"0.414"	"C2677794"	"Stress-induced polymorphic ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"6262"	"RYR2"	"0.575"	"0.414"	"C4053736"	"Catecholaminergic Polymorphic Ventricular Tachycardia Type 1"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"1990"	"2017"	"9"	"18"	"CLINGEN"
"6263"	"RYR3"	"0.701"	"0.241"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6263"	"RYR3"	"0.701"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6263"	"RYR3"	"0.701"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"6271"	"S100A1"	"0.479"	"0.759"	"C0265110"	"Cerebral Vasospasm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6271"	"S100A1"	"0.479"	"0.759"	"C0751895"	"Vasospasm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6272"	"SORT1"	"0.624"	"0.448"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"6272"	"SORT1"	"0.624"	"0.448"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6272"	"SORT1"	"0.624"	"0.448"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9469697"	"1992"	"2017"	"2"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0265110"	"Cerebral Vasospasm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C0751895"	"Vasospasm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6275"	"S100A4"	"0.483"	"0.621"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6276"	"S100A5"	"0.785"	"0.069"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0265110"	"Cerebral Vasospasm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C0751895"	"Vasospasm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6277"	"S100A6"	"0.533"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6278"	"S100A7"	"0.609"	"0.517"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6278"	"S100A7"	"0.609"	"0.517"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.9285714"	"1996"	"2017"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6279"	"S100A8"	"0.481"	"0.828"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6280"	"S100A9"	"0.488"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"2"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"2006"	"2015"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"2006"	"2012"	"3"	"0"	"CTD_human;PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2008"	"2012"	"3"	"0"	"CTD_human;PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0349217"	"Depressive episode, unspecified"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"6281"	"S100A10"	"0.598"	"0.552"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6281"	"S100A10"	"0.598"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6282"	"S100A11"	"0.611"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6283"	"S100A12"	"0.564"	"0.552"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.71"	"1"	"2005"	"2012"	"6"	"0"	"CTD_human;PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"1996"	"2011"	"5"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1996"	"2011"	"5"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0012734"	"Disruptive Behavior Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.95"	"1988"	"2013"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0018944"	"Hematoma"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0029121"	"Oppositional Defiant Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2012"	"3"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.75"	"2009"	"2011"	"4"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0236964"	"Attention Deficit and Disruptive Behavior Disorders"	"phenotype"	"F03"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0265110"	"Cerebral Vasospasm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C0751895"	"Vasospasm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.75"	"2009"	"2011"	"4"	"0"	"PSYGENET"
"6285"	"S100B"	"0.443"	"0.862"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6285"	"S100B"	"0.443"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.31"		"2006"	"2009"	"1"	"0"	"CTD_human"
"6286"	"S100P"	"0.815"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6286"	"S100P"	"0.815"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6288"	"SAA1"	"0.602"	"0.655"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6288"	"SAA1"	"0.602"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6288"	"SAA1"	"0.602"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6288"	"SAA1"	"0.602"	"0.655"	"C0221014"	"Reactive systemic amyloidosis"	"disease"		"Disease or Syndrome"	"0.40"	"0.875"	"1986"	"2015"	"0"	"0"	"ORPHANET"
"6288"	"SAA1"	"0.602"	"0.655"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6288"	"SAA1"	"0.602"	"0.655"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6293"	"VPS52"	"0.785"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6293"	"VPS52"	"0.785"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.67"	"0.8333333"	"1985"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"6295"	"SAG"	"0.598"	"0.724"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"6295"	"SAG"	"0.598"	"0.724"	"C1306122"	"Oguchi disease"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2015"	"2"	"5"	"CTD_human;ORPHANET"
"6295"	"SAG"	"0.598"	"0.724"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C3151061"	"RETINITIS PIGMENTOSA 47"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6295"	"SAG"	"0.598"	"0.724"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6296"	"ACSM3"	"0.762"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6296"	"ACSM3"	"0.762"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6297"	"SALL2"	"0.72"	"0.345"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6297"	"SALL2"	"0.72"	"0.345"	"C0155299"	"Coloboma of optic disc"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6297"	"SALL2"	"0.72"	"0.345"	"C0266551"	"Congenital coloboma of iris"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6297"	"SALL2"	"0.72"	"0.345"	"C0344516"	"Coloboma of lens"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6297"	"SALL2"	"0.72"	"0.345"	"C0521573"	"Coloboma of eyelid"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6297"	"SALL2"	"0.72"	"0.345"	"C1852767"	"Hereditary macular coloboma"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6297"	"SALL2"	"0.72"	"0.345"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6299"	"SALL1"	"0.619"	"0.69"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6299"	"SALL1"	"0.619"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6299"	"SALL1"	"0.619"	"0.69"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1998"	"2008"	"2"	"0"	"CTD_human"
"6299"	"SALL1"	"0.619"	"0.69"	"C0265246"	"Townes syndrome"	"disease"	"C06;C09;C10;C16;C23"	"Disease or Syndrome"	"0.90"	"1"	"1998"	"2017"	"2"	"1"	"CTD_human;ORPHANET"
"6299"	"SALL1"	"0.619"	"0.69"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6299"	"SALL1"	"0.619"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1984"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"6299"	"SALL1"	"0.619"	"0.69"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6301"	"SARS"	"0.639"	"0.414"	"C4540188"	"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"UNIPROT"
"6303"	"SAT1"	"0.546"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2014"	"2"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6303"	"SAT1"	"0.546"	"0.759"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6303"	"SAT1"	"0.546"	"0.759"	"C0343057"	"Keratosis pilaris decalvans"	"disease"		"Congenital Abnormality"	"0.32"	"1"	"2002"	"2014"	"0"	"0"	"ORPHANET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"PSYGENET"
"6303"	"SAT1"	"0.546"	"0.759"	"C3887525"	"Keratosis Follicularis Spinulosa Decalvans, X-Linked"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2002"	"2014"	"0"	"0"	"CTD_human"
"6304"	"SATB1"	"0.577"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6305"	"SBF1"	"0.752"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2001"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"6305"	"SBF1"	"0.752"	"0.31"	"C3695063"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6307"	"MSMO1"	"0.69"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6307"	"MSMO1"	"0.69"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6307"	"MSMO1"	"0.69"	"0.414"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6307"	"MSMO1"	"0.69"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"6307"	"MSMO1"	"0.69"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6307"	"MSMO1"	"0.69"	"0.414"	"C4225189"	"MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6309"	"SC5D"	"0.63"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6309"	"SC5D"	"0.63"	"0.517"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6309"	"SC5D"	"0.63"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6309"	"SC5D"	"0.63"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6309"	"SC5D"	"0.63"	"0.517"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6309"	"SC5D"	"0.63"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6309"	"SC5D"	"0.63"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6309"	"SC5D"	"0.63"	"0.517"	"C1846421"	"Lathosterolosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2002"	"2007"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6309"	"SC5D"	"0.63"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.9428571"	"1989"	"2016"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9772727"	"1980"	"2017"	"4"	"0"	"CTD_human;ORPHANET"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.39"	"0.8888889"	"1993"	"2008"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2008"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2008"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2008"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2014"	"4"	"0"	"CTD_human"
"6310"	"ATXN1"	"0.55"	"0.517"	"C2362914"	"clinical depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.9555556"	"2006"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8"	"2003"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.9166667"	"1994"	"2018"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"1996"	"2010"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9710145"	"1997"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"0.5"	"1998"	"2010"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2010"	"2"	"0"	"CTD_human"
"6311"	"ATXN2"	"0.534"	"0.621"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0034933"	"Reflex, Abnormal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0151572"	"Reflex, Corneal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0151888"	"Hyporeflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0151889"	"Hyperreflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0231691"	"Cerebellar Gait Ataxia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0234146"	"Absent reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0234784"	"Reflex, Gag, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0241772"	"Reflex, Deep Tendon, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0277839"	"Hoffman's Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0277850"	"Reflex, Pendular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0278211"	"Reflex, Corneal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0522345"	"Reflex, Acoustic, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0558845"	"Reflex, Ankle, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0558846"	"Reflex, Triceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0558847"	"Reflex, Biceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0576612"	"Reflex, Anal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0743002"	"Abnormal Deep Tendon Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751468"	"Bulbocavernosus Reflex, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751469"	"Bulbocavernousus Reflex Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751470"	"Palmo-Mental Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751471"	"Reflex, Anal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751472"	"Reflex, Ankle, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751473"	"Reflex, Ankle, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751474"	"Reflex, Biceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751475"	"Reflex, Biceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751476"	"Reflex, Gag, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751477"	"Reflex, Knee, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751478"	"Reflex, Knee, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751479"	"Reflex, Moro, Asymmetric"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751480"	"Reflex, Triceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751481"	"Reflex, Triceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751836"	"Gait Ataxia, Sensory"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751837"	"Gait Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9787234"	"1998"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"6314"	"ATXN7"	"0.609"	"0.517"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6314"	"ATXN7"	"0.609"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"GENOMICS_ENGLAND"
"6315"	"ATXN8OS"	"0.707"	"0.207"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6315"	"ATXN8OS"	"0.707"	"0.207"	"C1837454"	"SPINOCEREBELLAR ATAXIA 8"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6317"	"SERPINB3"	"0.59"	"0.483"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6318"	"SERPINB4"	"0.636"	"0.379"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6318"	"SERPINB4"	"0.636"	"0.379"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6318"	"SERPINB4"	"0.636"	"0.379"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6318"	"SERPINB4"	"0.636"	"0.379"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.50"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0339143"	"Thyroid associated opthalmopathies"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C0376323"	"Congestive Ophthalmopathy"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C1563709"	"Myopathic Ophthalmopathy"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6319"	"SCD"	"0.538"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6320"	"CLEC11A"	"0.72"	"0.414"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"	"0.972973"	"2002"	"2017"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9415584"	"2001"	"2018"	"3"	"1"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0014548"	"Epilepsy, Generalized"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"2003"	"2016"	"1"	"1"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.6666667"	"2002"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0017332"	"Generalized Nonconvulsive Seizure Disorder"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0086236"	"Epilepsy, Atonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0086241"	"Epilepsy, Tonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2017"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2013"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0238111"	"Lennox-Gastaut syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2017"	"0"	"0"	"ORPHANET"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0270854"	"Symptomatic Generalized Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0270862"	"Hemiplegic migraine"	"disease"		"Disease or Syndrome"	"0.36"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0311334"	"Generalized convulsive epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0347869"	"Epilepsy, Akinetic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"2008"	"2018"	"0"	"2"	"GENOMICS_ENGLAND"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2013"	"3"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"1.00"	"0.968254"	"2001"	"2018"	"44"	"378"	"CTD_human;ORPHANET;UNIPROT"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C1858672"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"		"2010"	"2010"	"0"	"11"	"CTD_human"
"6323"	"SCN1A"	"0.506"	"0.517"	"C1858673"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2015"	"30"	"68"	"CTD_human;UNIPROT"
"6323"	"SCN1A"	"0.506"	"0.517"	"C1864987"	"Migraine, Familial Hemiplegic, 3"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"4"	"5"	"CTD_human;UNIPROT"
"6323"	"SCN1A"	"0.506"	"0.517"	"C2751756"	"Febrile Convulsions, Familial, 3a"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2001"	"2012"	"30"	"32"	"UNIPROT"
"6323"	"SCN1A"	"0.506"	"0.517"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6323"	"SCN1A"	"0.506"	"0.517"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"6323"	"SCN1A"	"0.506"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.47"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"1"	"2002"	"2013"	"0"	"0"	"ORPHANET"
"6324"	"SCN1B"	"0.598"	"0.276"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.63"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"6324"	"SCN1B"	"0.598"	"0.276"	"C1721096"	"Brugada ECG Pattern"	"phenotype"	"C14;C16"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6324"	"SCN1B"	"0.598"	"0.276"	"C1858672"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.80"		"1998"	"2015"	"3"	"4"	"CTD_human;UNIPROT"
"6324"	"SCN1B"	"0.598"	"0.276"	"C1879286"	"Hereditary bundle branch system defect"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6324"	"SCN1B"	"0.598"	"0.276"	"C2748541"	"Brugada Syndrome 5"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.40"		"1970"	"2017"	"0"	"2"	"CTD_human"
"6324"	"SCN1B"	"0.598"	"0.276"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.49"	"1"	"2000"	"2012"	"0"	"1"	"ORPHANET"
"6324"	"SCN1B"	"0.598"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"6324"	"SCN1B"	"0.598"	"0.276"	"C3809311"	"ATRIAL FIBRILLATION, FAMILIAL, 13"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"3"	"CTD_human;UNIPROT"
"6324"	"SCN1B"	"0.598"	"0.276"	"C4479236"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2013"	"2"	"2"	"CTD_human;UNIPROT"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.47"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9189189"	"2003"	"2017"	"2"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0220669"	"Familial benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"2013"	"2018"	"0"	"7"	"GENOMICS_ENGLAND"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"6326"	"SCN2A"	"0.586"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C1842382"	"Epilepsy, Benign Neonatal, 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6326"	"SCN2A"	"0.586"	"0.276"	"C1843140"	"SEIZURES, BENIGN FAMILIAL INFANTILE, 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.47"	"0.8571429"	"1989"	"2017"	"13"	"23"	"UNIPROT"
"6326"	"SCN2A"	"0.586"	"0.276"	"C3150987"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2018"	"21"	"34"	"CTD_human;UNIPROT"
"6326"	"SCN2A"	"0.586"	"0.276"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2009"	"0"	"0"	"ORPHANET"
"6326"	"SCN2A"	"0.586"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6327"	"SCN2B"	"0.752"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6327"	"SCN2B"	"0.752"	"0.172"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"6327"	"SCN2B"	"0.752"	"0.172"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6327"	"SCN2B"	"0.752"	"0.172"	"C3809312"	"ATRIAL FIBRILLATION, FAMILIAL, 14"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"6328"	"SCN3A"	"0.752"	"0.207"	"C0085417"	"Epilepsy, Complex Partial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6328"	"SCN3A"	"0.752"	"0.207"	"C0751640"	"Cryptogenic Partial Complex Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6328"	"SCN3A"	"0.752"	"0.207"	"C0751641"	"Epilepsy, Symptomatic, Partial Complex"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6328"	"SCN3A"	"0.752"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0027125"	"Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.42"		"1994"	"2008"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0027127"	"Myotonia Congenita"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"0.75"	"1992"	"2016"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0221055"	"Paramyotonia Congenita (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"	"1"	"1992"	"2016"	"16"	"14"	"CTD_human;ORPHANET;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0238357"	"Hyperkalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2018"	"6"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0238358"	"Hypokalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0270959"	"Myotonia Levior"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0553604"	"Myotonic Disorders"	"group"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2008"	"0"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751358"	"Myotonic Phenomenon"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751359"	"Percussion Myotonia"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751360"	"Becker Generalized Myotonia"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2016"	"1"	"2"	"CTD_human;GENOMICS_ENGLAND"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"0"	"CTD_human;ORPHANET"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C0752355"	"Myotonia Fluctuans (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"		"1992"	"2017"	"13"	"12"	"CTD_human;ORPHANET;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C1868433"	"Normokalemic Periodic Paralysis, Potassium-Sensitive"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"1992"	"2011"	"6"	"7"	"UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C1868619"	"Paramyotonia Congenita Without Cold Paralysis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"		"1992"	"2011"	"16"	"12"	"CTD_human;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C2750061"	"Hypokalemic Periodic Paralysis, Type 2"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2017"	"12"	"8"	"CTD_human;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C2931826"	"Potassium aggravated myotonia"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.67"	"1"	"1994"	"2017"	"13"	"10"	"CTD_human;ORPHANET;UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C2936781"	"Generalized Myotonia of Thomsen"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"0.8"	"1992"	"2016"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C3149517"	"LARYNGOSPASM, SEVERE NEONATAL EPISODIC"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"1994"	"2017"	"13"	"10"	"UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C3280112"	"MYASTHENIC SYNDROME, CONGENITAL, 16"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2016"	"3"	"3"	"UNIPROT"
"6329"	"SCN4A"	"0.58"	"0.483"	"C3489447"	"Hyperkalemic Periodic Paralysis Type 2"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C3714580"	"Hypokalemic periodic paralysis type 1"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"1993"	"2016"	"0"	"4"	"CTD_human"
"6329"	"SCN4A"	"0.58"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6329"	"SCN4A"	"0.58"	"0.483"	"C4275008"	"Acetazolamide responsive myotonia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6330"	"SCN4B"	"0.752"	"0.172"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6330"	"SCN4B"	"0.752"	"0.172"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6330"	"SCN4B"	"0.752"	"0.172"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6330"	"SCN4B"	"0.752"	"0.172"	"C2678484"	"Long Qt Syndrome 10"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.70"		"2007"	"2013"	"2"	"3"	"CLINGEN;CTD_human;UNIPROT"
"6330"	"SCN4B"	"0.752"	"0.172"	"C4013560"	"ATRIAL FIBRILLATION, FAMILIAL, 17"	"phenotype"		"Finding"	"0.40"		"2007"	"2013"	"2"	"3"	"UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"	"0.9285714"	"2005"	"2017"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"2005"	"2018"	"1"	"3"	"GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9831933"	"1995"	"2018"	"10"	"3"	"CTD_human;GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.44"	"1"	"1999"	"2011"	"0"	"2"	"ORPHANET"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.47"	"1"	"2003"	"2015"	"0"	"2"	"ORPHANET"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.60"	"0.9565217"	"2001"	"2016"	"2"	"4"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0040479"	"Torsades de Pointes"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.49"	"0.8888889"	"2002"	"2015"	"2"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0340493"	"Paroxysmal familial ventricular fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.60"	"0.9285714"	"1998"	"2015"	"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"6331"	"SCN5A"	"0.527"	"0.552"	"C0541782"	"Atrial standstill"	"phenotype"		"Pathologic Function"	"0.40"				"0"	"0"	"ORPHANET"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"1.00"	"0.9742268"	"1996"	"2018"	"49"	"263"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1721096"	"Brugada ECG Pattern"	"phenotype"	"C14;C16"	"Finding"	"0.30"		"2000"	"2013"	"15"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1832680"	"CARDIOMYOPATHY, DILATED, 1E"	"disease"	"C14"	"Disease or Syndrome"	"0.80"		"1986"	"2013"	"2"	"4"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1837845"	"SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2013"	"3"	"6"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1838527"	"LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.50"		"1995"	"2016"	"28"	"141"	"UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1838539"	"CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.56"	"1"	"2003"	"2015"	"2"	"1"	"ORPHANET;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1859062"	"LONG QT SYNDROME 3"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2018"	"28"	"146"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1861983"	"Heart Block, Nonprogressive"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.80"		"1999"	"2013"	"6"	"11"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1861984"	"Cardiac Conduction Defect, Nonprogressive"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.80"		"2001"	"2013"	"6"	"10"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C1879286"	"Hereditary bundle branch system defect"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.96"	"1"	"1999"	"2013"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C2748542"	"CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1998"	"2016"	"33"	"216"	"UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C2751898"	"Ventricular Fibrillation, Paroxysmal Familial, 1"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"1"	"1"	"ORPHANET;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C2931401"	"Long QT syndrome type 3"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C3151464"	"ATRIAL FIBRILLATION, FAMILIAL, 10"	"disease"		"Disease or Syndrome"	"0.60"		"1986"	"2008"	"2"	"12"	"CTD_human;UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C3276240"	"LONG QT SYNDROME 2/3, DIGENIC"	"disease"		"Disease or Syndrome"	"0.50"		"1995"	"2016"	"28"	"141"	"UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C3276241"	"LONG QT SYNDROME 3/6, DIGENIC Disorder"	"disease"		"Disease or Syndrome"	"0.60"		"1995"	"2016"	"28"	"141"	"UNIPROT"
"6331"	"SCN5A"	"0.527"	"0.552"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6331"	"SCN5A"	"0.527"	"0.552"	"C4017668"	"VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.50"		"2000"	"2000"	"1"	"1"	"ORPHANET;UNIPROT"
"6332"	"SCN7A"	"0.727"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.34"	"1"	"1998"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0007758"	"Cerebellar Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.44"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"0.9473684"	"2008"	"2017"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0019372"	"Herpesviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0032768"	"Postherpetic neuralgia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0037140"	"B Virus Infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0220669"	"Familial benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234162"	"Cerebellar Dysmetria"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234357"	"Adiadochokinesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0477370"	"Other generalized epilepsy and epileptic syndromes"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2015"	"8"	"0"	"CLINGEN"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"2012"	"2018"	"0"	"4"	"GENOMICS_ENGLAND"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0750994"	"Cerebellar Hemiataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C1865926"	"Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6334"	"SCN8A"	"0.557"	"0.552"	"C3280415"	"COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2006"	"0"	"1"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C3281191"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2018"	"15"	"46"	"CTD_human;UNIPROT"
"6334"	"SCN8A"	"0.557"	"0.552"	"C3668822"	"Hypermetria (finding)"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6334"	"SCN8A"	"0.557"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.64"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6334"	"SCN8A"	"0.557"	"0.552"	"C4310728"	"SEIZURES, BENIGN FAMILIAL INFANTILE, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0014804"	"Erythromelalgia"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2005"	"2017"	"3"	"0"	"CTD_human;ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0014805"	"Primary Erythermalgia"	"disease"	"C14"	"Disease or Syndrome"	"0.80"	"1"	"1992"	"2014"	"13"	"12"	"CTD_human;ORPHANET;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0019372"	"Herpesviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0032768"	"Postherpetic neuralgia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0037140"	"B Virus Infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0150055"	"Chronic pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1992"	"2018"	"15"	"0"	"GENOMICS_ENGLAND"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.53"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0751540"	"Morvan's Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C1833661"	"PAROXYSMAL EXTREME PAIN DISORDER"	"disease"	"C23;F02"	"Disease or Syndrome"	"0.80"	"1"	"2007"	"2015"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C1855739"	"Indifference to Pain, Congenital, Autosomal Recessive"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.66"	"0.8333333"	"1993"	"2015"	"1"	"7"	"CTD_human;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C2751778"	"Generalized Epilepsy With Febrile Seizures Plus, 7"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"4"	"CTD_human;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C2752089"	"Neuropathy, Hereditary Sensory And Autonomic, Type IIA"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2017"	"0"	"7"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C3151229"	"FEBRILE SEIZURES, FAMILIAL, 3B"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"4"	"CTD_human;UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C3178789"	"Widespread Chronic Pain"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2013"	"1"	"0"	"CTD_human"
"6335"	"SCN9A"	"0.569"	"0.552"	"C3276706"	"Small Fiber Neuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2017"	"10"	"9"	"UNIPROT"
"6335"	"SCN9A"	"0.569"	"0.552"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6335"	"SCN9A"	"0.569"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6335"	"SCN9A"	"0.569"	"0.552"	"C4012054"	"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID"	"phenotype"		"Finding"	"0.40"		"2010"	"2013"	"1"	"2"	"UNIPROT"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0004331"	"Auriculo-Ventricular Dissociation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0014805"	"Primary Erythermalgia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0018794"	"Heart Block"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2018"	"9"	"0"	"GENOMICS_ENGLAND"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.76"	"1"	"2013"	"2016"	"2"	"1"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"6336"	"SCN10A"	"0.642"	"0.414"	"C1721096"	"Brugada ECG Pattern"	"phenotype"	"C14;C16"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C1833661"	"PAROXYSMAL EXTREME PAIN DISORDER"	"disease"	"C23;F02"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6336"	"SCN10A"	"0.642"	"0.414"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6336"	"SCN10A"	"0.642"	"0.414"	"C3809893"	"EPISODIC PAIN SYNDROME, FAMILIAL, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.37"	"0.8333333"	"2004"	"2016"	"2"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.44"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0221043"	"Liddle Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0339985"	"Idiopathic bronchiectasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1996"	"2013"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"2"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6337"	"SCNN1A"	"0.639"	"0.483"	"C2751666"	"BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"1998"	"2009"	"1"	"3"	"CTD_human;UNIPROT"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.60"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.75"	"1996"	"2015"	"3"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2010"	"0"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0221043"	"Liddle Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1994"	"2018"	"8"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2013"	"0"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0339985"	"Idiopathic bronchiectasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"		"1996"	"1997"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6338"	"SCNN1B"	"0.645"	"0.483"	"C2749757"	"BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"2006"	"2009"	"3"	"7"	"CTD_human;UNIPROT"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.49"	"0.75"	"1996"	"2015"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.42"	"1"	"1996"	"2010"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0221043"	"Liddle Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2018"	"0"	"1"	"CTD_human;ORPHANET"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0339985"	"Idiopathic bronchiectasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"1996"	"1"	"0"	"CTD_human;ORPHANET"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6340"	"SCNN1G"	"0.639"	"0.448"	"C2751324"	"BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6341"	"SCO1"	"0.645"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.32"	"0.5"	"2009"	"2014"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.84"	"1"	"2000"	"2014"	"4"	"3"	"CTD_human;UNIPROT"
"6341"	"SCO1"	"0.645"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6341"	"SCO1"	"0.645"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6341"	"SCO1"	"0.645"	"0.621"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6341"	"SCO1"	"0.645"	"0.621"	"C1858424"	"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6341"	"SCO1"	"0.645"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6342"	"SCP2"	"0.69"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"6342"	"SCP2"	"0.69"	"0.31"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6342"	"SCP2"	"0.69"	"0.31"	"C0152025"	"Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0271683"	"Polyneuropathy, Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6342"	"SCP2"	"0.69"	"0.31"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0393851"	"Polyneuropathy, Critical Illness"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0751448"	"Polyneuropathy, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C0751449"	"Acquired Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6342"	"SCP2"	"0.69"	"0.31"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6342"	"SCP2"	"0.69"	"0.31"	"C3150990"	"LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY"	"disease"		"Disease or Syndrome"	"0.60"				"0"	"1"	"CTD_human;ORPHANET"
"6343"	"SCT"	"0.557"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"1999"	"2006"	"4"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C0008340"	"Choledochal Cyst"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C0009439"	"Choledochal Cyst, Type I"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C1257796"	"Choledochal Cyst, Type II"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C1257797"	"Choledochal Cyst, Type III"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C1257798"	"Choledochal Cyst, Type IV"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6343"	"SCT"	"0.557"	"0.621"	"C1257799"	"Choledochal Cyst, Type V"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6346"	"CCL1"	"0.663"	"0.483"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1999"	"2001"	"1"	"0"	"CTD_human"
"6346"	"CCL1"	"0.663"	"0.483"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6346"	"CCL1"	"0.663"	"0.483"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6346"	"CCL1"	"0.663"	"0.483"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6346"	"CCL1"	"0.663"	"0.483"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.59"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9821429"	"1996"	"2016"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6347"	"CCL2"	"0.353"	"0.897"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2005"	"2008"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.58"	"0.75"	"2001"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"0.8333333"	"1995"	"2017"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2000"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.37"	"1"	"1994"	"2013"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2016"	"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0020500"	"Hyperoxaluria"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.50"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.58"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.50"		"1998"	"2008"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.34"		"2003"	"2011"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.36"	"0.8"	"2003"	"2014"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"	"0.8"	"1997"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0022876"	"Premature Obstetric Labor"	"phenotype"	"C13"	"Pathologic Function"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.32"	"0.5"	"1996"	"2010"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.34"	"0.75"	"1994"	"2012"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.53"	"1"	"2005"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"6347"	"CCL2"	"0.353"	"0.897"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.52"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"1994"	"2016"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2002"	"2005"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0037926"	"Compression of spinal cord"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"		"2009"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0041327"	"Tuberculosis, Pulmonary"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.40"	"0.7857143"	"2006"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6347"	"CCL2"	"0.353"	"0.897"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2016"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6347"	"CCL2"	"0.353"	"0.897"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2004"	"2010"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.33"	"1"	"2001"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0742803"	"Conus Medullaris Syndrome"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6347"	"CCL2"	"0.353"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0917713"	"Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6347"	"CCL2"	"0.353"	"0.897"	"C1298681"	"Oxalosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.50"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2011"	"3"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.7826087"	"2001"	"2016"	"2"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C3542021"	"Duchenne and Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6347"	"CCL2"	"0.353"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6347"	"CCL2"	"0.353"	"0.897"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.37"	"0.8333333"	"2004"	"2016"	"0"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2014"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2013"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2014"	"2"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6348"	"CCL3"	"0.522"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6349"	"CCL3L1"	"0.681"	"0.586"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2007"	"2014"	"0"	"0"	"CTD_human"
"6349"	"CCL3L1"	"0.681"	"0.586"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6351"	"CCL4"	"0.526"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6352"	"CCL5"	"0.429"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.8"	"1996"	"2015"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9"	"1996"	"2016"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2006"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0019187"	"Hepatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0020500"	"Hyperoxaluria"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C0524610"	"Chronic Alcoholic Hepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C1298681"	"Oxalosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6352"	"CCL5"	"0.429"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6354"	"CCL7"	"0.573"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1999"	"2001"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6354"	"CCL7"	"0.573"	"0.621"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C1619692"	"Nephrogenic Fibrosing Dermopathy"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6355"	"CCL8"	"0.6"	"0.621"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.9"	"1998"	"2016"	"0"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2002"	"2010"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2008"	"2"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"6356"	"CCL11"	"0.586"	"0.655"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9333333"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2005"	"2011"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6361"	"CCL17"	"0.579"	"0.655"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"6362"	"CCL18"	"0.557"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6362"	"CCL18"	"0.557"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6362"	"CCL18"	"0.557"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6363"	"CCL19"	"0.575"	"0.586"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6364"	"CCL20"	"0.535"	"0.655"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6366"	"CCL21"	"0.55"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.38"	"0.5714286"	"2003"	"2016"	"3"	"2"	"CTD_human"
"6367"	"CCL22"	"0.564"	"0.69"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.38"	"1"	"2001"	"2014"	"2"	"0"	"CTD_human"
"6367"	"CCL22"	"0.564"	"0.69"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2012"	"2"	"0"	"CTD_human"
"6368"	"CCL23"	"0.785"	"0.345"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6369"	"CCL24"	"0.69"	"0.448"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6369"	"CCL24"	"0.69"	"0.448"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6369"	"CCL24"	"0.69"	"0.448"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"6372"	"CXCL6"	"0.659"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6372"	"CXCL6"	"0.659"	"0.448"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"6372"	"CXCL6"	"0.659"	"0.448"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6373"	"CXCL11"	"0.582"	"0.724"	"C0282488"	"Interstitial Cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6373"	"CXCL11"	"0.582"	"0.724"	"C0600040"	"Chronic interstitial cystitis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6373"	"CXCL11"	"0.582"	"0.724"	"C1720830"	"Painful Bladder Syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6374"	"CXCL5"	"0.567"	"0.655"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6376"	"CX3CL1"	"0.533"	"0.759"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6382"	"SDC1"	"0.497"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"6385"	"SDC4"	"0.667"	"0.276"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6386"	"SDCBP"	"0.713"	"0.31"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6386"	"SDCBP"	"0.713"	"0.31"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9821429"	"2003"	"2018"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.40"	"0.9615385"	"1997"	"2016"	"0"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2016"	"3"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9776119"	"2001"	"2018"	"2"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0266929"	"Chronic Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9827586"	"2003"	"2018"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.7"	"1995"	"2016"	"1"	"0"	"CTD_human"
"6387"	"CXCL12"	"0.421"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6389"	"SDHA"	"0.55"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.60"				"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.52"	"0.5"	"1995"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"6389"	"SDHA"	"0.55"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2013"	"8"	"0"	"CLINGEN"
"6389"	"SDHA"	"0.55"	"0.621"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2013"	"8"	"0"	"CLINGEN"
"6389"	"SDHA"	"0.55"	"0.621"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"2005"	"2017"	"0"	"0"	"ORPHANET"
"6389"	"SDHA"	"0.55"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6389"	"SDHA"	"0.55"	"0.621"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2013"	"8"	"0"	"CLINGEN"
"6389"	"SDHA"	"0.55"	"0.621"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2005"	"2013"	"8"	"0"	"CLINGEN"
"6389"	"SDHA"	"0.55"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"6389"	"SDHA"	"0.55"	"0.621"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C1855008"	"Mitochondrial Complex II Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2000"	"2017"	"0"	"13"	"CTD_human;ORPHANET;UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"3"	"2"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C3150898"	"CARDIOMYOPATHY, DILATED, 1GG"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6389"	"SDHA"	"0.55"	"0.621"	"C3279992"	"PARAGANGLIOMAS 5"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"17"	"CTD_human;UNIPROT"
"6389"	"SDHA"	"0.55"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6389"	"SDHA"	"0.55"	"0.621"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6390"	"SDHB"	"0.513"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"6390"	"SDHB"	"0.513"	"0.69"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"6390"	"SDHB"	"0.513"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6390"	"SDHB"	"0.513"	"0.69"	"C0030421"	"Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.943662"	"2001"	"2018"	"1"	"0"	"CGI;CTD_human"
"6390"	"SDHB"	"0.513"	"0.69"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9784946"	"1992"	"2018"	"7"	"43"	"CGI;CTD_human;UNIPROT"
"6390"	"SDHB"	"0.513"	"0.69"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2001"	"2013"	"8"	"0"	"CLINGEN"
"6390"	"SDHB"	"0.513"	"0.69"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2001"	"2013"	"8"	"0"	"CLINGEN"
"6390"	"SDHB"	"0.513"	"0.69"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6390"	"SDHB"	"0.513"	"0.69"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.875"	"1992"	"2017"	"0"	"32"	"CTD_human;ORPHANET"
"6390"	"SDHB"	"0.513"	"0.69"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2001"	"2013"	"8"	"0"	"CLINGEN"
"6390"	"SDHB"	"0.513"	"0.69"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2001"	"2013"	"8"	"0"	"CLINGEN"
"6390"	"SDHB"	"0.513"	"0.69"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"6390"	"SDHB"	"0.513"	"0.69"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6390"	"SDHB"	"0.513"	"0.69"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.45"	"1"	"2005"	"2008"	"0"	"0"	"CTD_human"
"6390"	"SDHB"	"0.513"	"0.69"	"C1847319"	"PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.65"	"1"	"2004"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"6390"	"SDHB"	"0.513"	"0.69"	"C1855008"	"Mitochondrial Complex II Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"6390"	"SDHB"	"0.513"	"0.69"	"C1861848"	"PARAGANGLIOMAS 4"	"disease"	"C04;C16"	"Neoplastic Process"	"0.61"	"1"	"1979"	"2017"	"5"	"40"	"CTD_human;UNIPROT"
"6390"	"SDHB"	"0.513"	"0.69"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6390"	"SDHB"	"0.513"	"0.69"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2001"	"2007"	"7"	"10"	"UNIPROT"
"6390"	"SDHB"	"0.513"	"0.69"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6390"	"SDHB"	"0.513"	"0.69"	"C3552552"	"COWDEN SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"2"	"UNIPROT"
"6391"	"SDHC"	"0.547"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6391"	"SDHC"	"0.547"	"0.69"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6391"	"SDHC"	"0.547"	"0.69"	"C0030421"	"Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9772727"	"1999"	"2017"	"0"	"0"	"CGI"
"6391"	"SDHC"	"0.547"	"0.69"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2016"	"0"	"0"	"CGI"
"6391"	"SDHC"	"0.547"	"0.69"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2013"	"8"	"0"	"CLINGEN"
"6391"	"SDHC"	"0.547"	"0.69"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2013"	"8"	"0"	"CLINGEN"
"6391"	"SDHC"	"0.547"	"0.69"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6391"	"SDHC"	"0.547"	"0.69"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.69"	"1"	"2003"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"6391"	"SDHC"	"0.547"	"0.69"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2013"	"8"	"0"	"CLINGEN"
"6391"	"SDHC"	"0.547"	"0.69"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2000"	"2013"	"8"	"0"	"CLINGEN"
"6391"	"SDHC"	"0.547"	"0.69"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6391"	"SDHC"	"0.547"	"0.69"	"C1847319"	"PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.62"	"1"	"2007"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"6391"	"SDHC"	"0.547"	"0.69"	"C1854336"	"PARAGANGLIOMAS 3"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.43"	"1"	"2000"	"2017"	"0"	"7"	"CTD_human"
"6391"	"SDHC"	"0.547"	"0.69"	"C1861848"	"PARAGANGLIOMAS 4"	"disease"	"C04;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6391"	"SDHC"	"0.547"	"0.69"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6392"	"SDHD"	"0.499"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"6392"	"SDHD"	"0.499"	"0.793"	"C0007129"	"Merkel cell carcinoma"	"disease"	"C02;C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6392"	"SDHD"	"0.499"	"0.793"	"C0007279"	"Carotid Body Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.47"	"1"	"2001"	"2015"	"4"	"6"	"UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C0017671"	"Glomus Jugulare Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2001"	"2004"	"4"	"5"	"UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"ORPHANET"
"6392"	"SDHD"	"0.499"	"0.793"	"C0024586"	"Malignant Carcinoid Syndrome"	"disease"	"C04"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6392"	"SDHD"	"0.499"	"0.793"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"6392"	"SDHD"	"0.499"	"0.793"	"C0030421"	"Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9834711"	"1996"	"2018"	"5"	"5"	"CGI;CTD_human;UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C0030422"	"Extra-Adrenal Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2016"	"4"	"5"	"UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9880952"	"2000"	"2018"	"3"	"19"	"CGI;CTD_human;UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"2013"	"9"	"0"	"CLINGEN"
"6392"	"SDHD"	"0.499"	"0.793"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"2013"	"9"	"0"	"CLINGEN"
"6392"	"SDHD"	"0.499"	"0.793"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6392"	"SDHD"	"0.499"	"0.793"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"2013"	"9"	"0"	"CLINGEN"
"6392"	"SDHD"	"0.499"	"0.793"	"C0349535"	"Carcinoid tumor of intestine"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6392"	"SDHD"	"0.499"	"0.793"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1997"	"2013"	"9"	"0"	"CLINGEN"
"6392"	"SDHD"	"0.499"	"0.793"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6392"	"SDHD"	"0.499"	"0.793"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2005"	"2008"	"0"	"0"	"CTD_human"
"6392"	"SDHD"	"0.499"	"0.793"	"C1847319"	"PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.64"	"1"	"2000"	"2017"	"0"	"11"	"CTD_human;ORPHANET"
"6392"	"SDHD"	"0.499"	"0.793"	"C1855008"	"Mitochondrial Complex II Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2014"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C1868633"	"Paragangliomas with Sensorineural Hearing Loss"	"disease"	"C04;C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2000"	"2017"	"4"	"30"	"UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6392"	"SDHD"	"0.499"	"0.793"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2001"	"2004"	"3"	"2"	"UNIPROT"
"6392"	"SDHD"	"0.499"	"0.793"	"C3494181"	"Glomus Tumors, Familial, 1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2004"	"4"	"5"	"UNIPROT"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"				"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2009"	"0"	"0"	"CTD_human"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.69"	"1"	"2000"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.80"	"1"	"1999"	"2015"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"6399"	"TRAPPC2"	"0.752"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"6401"	"SELE"	"0.479"	"0.793"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6401"	"SELE"	"0.479"	"0.793"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6402"	"SELL"	"0.538"	"0.655"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"1999"	"2006"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2005"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6403"	"SELP"	"0.519"	"0.724"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6403"	"SELP"	"0.519"	"0.724"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6404"	"SELPLG"	"0.621"	"0.517"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6404"	"SELPLG"	"0.621"	"0.517"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6405"	"SEMA3F"	"0.667"	"0.448"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6405"	"SEMA3F"	"0.667"	"0.448"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0006635"	"Cadmium poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6414"	"SELENOP"	"0.602"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6415"	"SELENOW"	"0.815"	"0.207"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6415"	"SELENOW"	"0.815"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6415"	"SELENOW"	"0.815"	"0.207"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6415"	"SELENOW"	"0.815"	"0.207"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6415"	"SELENOW"	"0.815"	"0.207"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2014"	"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2014"	"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2007"	"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.50"		"2007"	"2007"	"1"	"1"	"CGI;UNIPROT"
"6416"	"MAP2K4"	"0.582"	"0.586"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"UNIPROT"
"6418"	"SET"	"0.582"	"0.621"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6418"	"SET"	"0.582"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6418"	"SET"	"0.582"	"0.621"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2014"	"0"	"0"	"ORPHANET"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6421"	"SFPQ"	"0.656"	"0.414"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"2002"	"2015"	"2"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2009"	"2"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"6422"	"SFRP1"	"0.5"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2004"	"2009"	"2"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"6423"	"SFRP2"	"0.579"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0265294"	"Pyle metaphyseal dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2016"	"2018"	"0"	"3"	"CTD_human;ORPHANET"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6424"	"SFRP4"	"0.569"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2009"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6425"	"SFRP5"	"0.6"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6426"	"SRSF1"	"0.609"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"0"	"0"	"UNIPROT"
"6426"	"SRSF1"	"0.609"	"0.552"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6426"	"SRSF1"	"0.609"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"6426"	"SRSF1"	"0.609"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"6426"	"SRSF1"	"0.609"	"0.552"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6427"	"SRSF2"	"0.584"	"0.621"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.40"	"0.9473684"	"2012"	"2016"	"0"	"0"	"CGI"
"6428"	"SRSF3"	"0.676"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6430"	"SRSF5"	"0.672"	"0.552"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6430"	"SRSF5"	"0.672"	"0.552"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6430"	"SRSF5"	"0.672"	"0.552"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6430"	"SRSF5"	"0.672"	"0.552"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6430"	"SRSF5"	"0.672"	"0.552"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6431"	"SRSF6"	"0.785"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6433"	"SFSWAP"	"0.857"	"0.138"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6434"	"TRA2B"	"0.773"	"0.31"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2000"	"2006"	"2"	"0"	"CTD_human"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0020192"	"Hyaline Membrane Disease"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2001"	"0"	"0"	"ORPHANET"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.60"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0035220"	"Respiratory Distress Syndrome, Newborn"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.40"	"0.9130435"	"1995"	"2016"	"0"	"0"	"ORPHANET"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6439"	"SFTPB"	"0.596"	"0.586"	"C0852283"	"Respiratory Distress Syndrome"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"1995"	"2006"	"0"	"0"	"ORPHANET"
"6439"	"SFTPB"	"0.596"	"0.586"	"C1968602"	"Surfactant Metabolism Dysfunction, Pulmonary, 1"	"disease"	"C08"	"Disease or Syndrome"	"0.70"		"1994"	"2006"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0020192"	"Hyaline Membrane Disease"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2001"	"0"	"0"	"ORPHANET"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0035220"	"Respiratory Distress Syndrome, Newborn"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2018"	"0"	"0"	"ORPHANET"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2002"	"2011"	"0"	"0"	"ORPHANET"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"6440"	"SFTPC"	"0.588"	"0.483"	"C0852283"	"Respiratory Distress Syndrome"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2000"	"2006"	"0"	"0"	"ORPHANET"
"6440"	"SFTPC"	"0.588"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6440"	"SFTPC"	"0.588"	"0.483"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"0.8181818"	"2002"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"6440"	"SFTPC"	"0.588"	"0.483"	"C1970470"	"SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2 (disorder)"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"1959"	"2009"	"5"	"6"	"CTD_human;UNIPROT"
"6441"	"SFTPD"	"0.569"	"0.69"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.70"	"0.9"	"2002"	"2018"	"1"	"3"	"CTD_human"
"6441"	"SFTPD"	"0.569"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2002"	"2008"	"2"	"0"	"CTD_human"
"6441"	"SFTPD"	"0.569"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"6441"	"SFTPD"	"0.569"	"0.69"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6442"	"SGCA"	"0.663"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6442"	"SGCA"	"0.663"	"0.31"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1996"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6442"	"SGCA"	"0.663"	"0.31"	"C2936331"	"Sarcoglycanopathies"	"disease"	"C05;C08;C10;C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2018"	"0"	"0"	"CTD_human"
"6442"	"SGCA"	"0.663"	"0.31"	"C2936332"	"Alpha-Sarcoglycanopathies"	"disease"	"C05;C08;C10;C14;C16"	"Disease or Syndrome"	"1.00"	"1"	"1994"	"2017"	"6"	"40"	"CTD_human;ORPHANET;UNIPROT"
"6442"	"SGCA"	"0.663"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6443"	"SGCB"	"0.656"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6443"	"SGCB"	"0.656"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6443"	"SGCB"	"0.656"	"0.31"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6443"	"SGCB"	"0.656"	"0.31"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6443"	"SGCB"	"0.656"	"0.31"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.57"	"1"	"1995"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6443"	"SGCB"	"0.656"	"0.31"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"6443"	"SGCB"	"0.656"	"0.31"	"C1858593"	"Limb-girdle muscular dystrophy, type 2E"	"disease"	"C05;C08;C10;C14;C16"	"Disease or Syndrome"	"0.94"	"1"	"1995"	"2017"	"4"	"20"	"CTD_human;ORPHANET;UNIPROT"
"6443"	"SGCB"	"0.656"	"0.31"	"C2930900"	"Beta-sarcoglycanopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"1997"	"2015"	"0"	"1"	"ORPHANET"
"6444"	"SGCD"	"0.633"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6444"	"SGCD"	"0.633"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1999"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6444"	"SGCD"	"0.633"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6444"	"SGCD"	"0.633"	"0.414"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"6444"	"SGCD"	"0.633"	"0.414"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"6444"	"SGCD"	"0.633"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6444"	"SGCD"	"0.633"	"0.414"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"6444"	"SGCD"	"0.633"	"0.414"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"0.9285714"	"1997"	"2018"	"0"	"2"	"GENOMICS_ENGLAND"
"6444"	"SGCD"	"0.633"	"0.414"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"1997"	"2016"	"2"	"0"	"CTD_human"
"6444"	"SGCD"	"0.633"	"0.414"	"C1832525"	"Limb-girdle muscular dystrophy type 2F"	"disease"	"C05;C08;C10;C14;C16"	"Disease or Syndrome"	"0.94"	"1"	"1999"	"2011"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"6444"	"SGCD"	"0.633"	"0.414"	"C1847667"	"CARDIOMYOPATHY, DILATED, 1L"	"disease"	"C14"	"Disease or Syndrome"	"0.70"		"1999"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"6445"	"SGCG"	"0.559"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6445"	"SGCG"	"0.559"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6445"	"SGCG"	"0.559"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6445"	"SGCG"	"0.559"	"0.69"	"C0410173"	"Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)"	"disease"	"C05;C08;C10;C14;C16"	"Disease or Syndrome"	"1.00"	"1"	"1995"	"2017"	"2"	"14"	"CTD_human;ORPHANET;UNIPROT"
"6445"	"SGCG"	"0.559"	"0.69"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"1996"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6446"	"SGK1"	"0.53"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6446"	"SGK1"	"0.53"	"0.621"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"6446"	"SGK1"	"0.53"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6446"	"SGK1"	"0.53"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"PSYGENET"
"6446"	"SGK1"	"0.53"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6447"	"SCG5"	"0.676"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6448"	"SGSH"	"0.707"	"0.414"	"C0026706"	"Mucopolysaccharidosis III"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.67"	"1"	"1986"	"2017"	"0"	"6"	"CTD_human"
"6448"	"SGSH"	"0.707"	"0.414"	"C0086647"	"Mucopolysaccharidosis Type IIIA"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.9459459"	"1991"	"2018"	"16"	"42"	"CTD_human;ORPHANET;UNIPROT"
"6448"	"SGSH"	"0.707"	"0.414"	"C0086648"	"MPS III B"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"0"	"0"	"CTD_human"
"6448"	"SGSH"	"0.707"	"0.414"	"C0086649"	"MPS III C"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6448"	"SGSH"	"0.707"	"0.414"	"C0086650"	"MPS III D"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"6448"	"SGSH"	"0.707"	"0.414"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6448"	"SGSH"	"0.707"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6452"	"SH3BP2"	"0.713"	"0.517"	"C0008029"	"Cherubism"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"1.00"	"0.962963"	"2001"	"2015"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6453"	"ITSN1"	"0.762"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6453"	"ITSN1"	"0.762"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1994"	"1996"	"2"	"0"	"CTD_human;PSYGENET"
"6462"	"SHBG"	"0.512"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2014"	"2"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"6462"	"SHBG"	"0.512"	"0.621"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"6464"	"SHC1"	"0.659"	"0.414"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6464"	"SHC1"	"0.659"	"0.414"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6464"	"SHC1"	"0.659"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6464"	"SHC1"	"0.659"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6468"	"FBXW4"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2016"	"4"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.70"	"0.9833333"	"1994"	"2017"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.34"	"1"	"1998"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C0265581"	"Longitudinal deficiency of radius"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0265596"	"Talipomanus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0265598"	"Manus vara"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0266484"	"Schizencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.41"	"1"	"2010"	"2015"	"0"	"1"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2004"	"2016"	"4"	"0"	"CTD_human;ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2004"	"2016"	"4"	"0"	"CTD_human;ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2004"	"2016"	"4"	"0"	"CTD_human;ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C1840235"	"SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.74"	"1"	"2001"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6469"	"SHH"	"0.434"	"0.724"	"C1840529"	"HOLOPROSENCEPHALY 3"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2015"	"12"	"31"	"CTD_human;UNIPROT"
"6469"	"SHH"	"0.434"	"0.724"	"C1856892"	"Facial Dysmorphism with Multiple Malformations"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C1861355"	"Syndactyly, Type IV"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C1868114"	"POLYDACTYLY, PREAXIAL II (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C1968843"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6469"	"SHH"	"0.434"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6469"	"SHH"	"0.434"	"0.724"	"C2931870"	"Familial schizencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6469"	"SHH"	"0.434"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"6470"	"SHMT1"	"0.607"	"0.517"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6472"	"SHMT2"	"0.727"	"0.276"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6473"	"SHOX"	"0.596"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6473"	"SHOX"	"0.596"	"0.586"	"C0152441"	"Madelung Deformity"	"disease"	"C05;C16;C23"	"Congenital Abnormality"	"0.50"	"0.9411765"	"2000"	"2013"	"2"	"3"	"UNIPROT"
"6473"	"SHOX"	"0.596"	"0.586"	"C0265309"	"Leri-Weill dyschondrosteosis"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.70"	"0.942029"	"1998"	"2017"	"2"	"10"	"ORPHANET;UNIPROT"
"6473"	"SHOX"	"0.596"	"0.586"	"C0432230"	"Langer Mesomelic Dysplasia Syndrome"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9473684"	"2001"	"2016"	"1"	"3"	"ORPHANET;UNIPROT"
"6473"	"SHOX"	"0.596"	"0.586"	"C1845118"	"SHORT STATURE, IDIOPATHIC, X-LINKED"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.40"		"1997"	"2017"	"0"	"9"	"ORPHANET"
"6473"	"SHOX"	"0.596"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1990"	"2014"	"5"	"0"	"GENOMICS_ENGLAND"
"6473"	"SHOX"	"0.596"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6474"	"SHOX2"	"0.681"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"6474"	"SHOX2"	"0.681"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6474"	"SHOX2"	"0.681"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"6474"	"SHOX2"	"0.681"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"6474"	"SHOX2"	"0.681"	"0.448"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"6476"	"SI"	"0.645"	"0.483"	"C1283620"	"Sucrase-isomaltase deficiency, congenital"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.67"	"1"	"1996"	"2012"	"5"	"10"	"CTD_human;UNIPROT"
"6478"	"SIAH2"	"0.672"	"0.345"	"C0023308"	"Lens Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6480"	"ST6GAL1"	"0.636"	"0.517"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"6480"	"ST6GAL1"	"0.636"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2011"	"2013"	"1"	"1"	"CTD_human"
"6480"	"ST6GAL1"	"0.636"	"0.517"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6480"	"ST6GAL1"	"0.636"	"0.517"	"C0337677"	"Moderate drinker"	"phenotype"		"Finding"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"6482"	"ST3GAL1"	"0.701"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6482"	"ST3GAL1"	"0.701"	"0.414"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6482"	"ST3GAL1"	"0.701"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6482"	"ST3GAL1"	"0.701"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6482"	"ST3GAL1"	"0.701"	"0.414"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6484"	"ST3GAL4"	"0.667"	"0.379"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6484"	"ST3GAL4"	"0.667"	"0.379"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6484"	"ST3GAL4"	"0.667"	"0.379"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6484"	"ST3GAL4"	"0.667"	"0.379"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6484"	"ST3GAL4"	"0.667"	"0.379"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C1970200"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2007"	"2011"	"1"	"1"	"UNIPROT"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C3554316"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"UNIPROT"
"6487"	"ST3GAL3"	"0.701"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"6489"	"ST8SIA1"	"0.72"	"0.448"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6489"	"ST8SIA1"	"0.72"	"0.448"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6489"	"ST8SIA1"	"0.72"	"0.448"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6489"	"ST8SIA1"	"0.72"	"0.448"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6489"	"ST8SIA1"	"0.72"	"0.448"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6490"	"PMEL"	"0.6"	"0.517"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9770115"	"1994"	"2017"	"1"	"0"	"CTD_human"
"6491"	"STIL"	"0.616"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.35"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6491"	"STIL"	"0.616"	"0.483"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.35"	"1"	"2009"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6491"	"STIL"	"0.616"	"0.483"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2014"	"0"	"0"	"ORPHANET"
"6491"	"STIL"	"0.616"	"0.483"	"C2675187"	"MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 7 (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2015"	"2"	"6"	"CTD_human;UNIPROT"
"6491"	"STIL"	"0.616"	"0.483"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"0"	"0"	"ORPHANET"
"6491"	"STIL"	"0.616"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"		"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"6492"	"SIM1"	"0.701"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.70"	"1"	"1998"	"2016"	"0"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6492"	"SIM1"	"0.701"	"0.345"	"C3809877"	"SCHAAF-YANG SYNDROME"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"6493"	"SIM2"	"0.648"	"0.517"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6493"	"SIM2"	"0.648"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6493"	"SIM2"	"0.648"	"0.517"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6494"	"SIPA1"	"0.672"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6495"	"SIX1"	"0.537"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0265234"	"Branchio-Oto-Renal Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.90"	"1"	"1993"	"2014"	"0"	"4"	"CTD_human;ORPHANET"
"6495"	"SIX1"	"0.537"	"0.621"	"C0376524"	"Branchio-Oculo-Facial Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C1842124"	"BRANCHIOOTIC SYNDROME 3 (disorder)"	"disease"	"C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2013"	"6"	"9"	"CTD_human;UNIPROT"
"6495"	"SIX1"	"0.537"	"0.621"	"C1854594"	"DEAFNESS, AUTOSOMAL DOMINANT 23"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2011"	"0"	"3"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C1865143"	"BRANCHIOOTIC SYNDROME 1"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"6495"	"SIX1"	"0.537"	"0.621"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6495"	"SIX1"	"0.537"	"0.621"	"C1970479"	"Branchiootorenal Syndrome 2"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6495"	"SIX1"	"0.537"	"0.621"	"C3551443"	"ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6495"	"SIX1"	"0.537"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6496"	"SIX3"	"0.607"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"6496"	"SIX3"	"0.607"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.70"	"1"	"1996"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6496"	"SIX3"	"0.607"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6496"	"SIX3"	"0.607"	"0.552"	"C0266484"	"Schizencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.61"	"1"	"2010"	"2010"	"1"	"2"	"ORPHANET;UNIPROT"
"6496"	"SIX3"	"0.607"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"6496"	"SIX3"	"0.607"	"0.552"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"6496"	"SIX3"	"0.607"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6496"	"SIX3"	"0.607"	"0.552"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"6496"	"SIX3"	"0.607"	"0.552"	"C1834877"	"HOLOPROSENCEPHALY 2 (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.82"	"1"	"1993"	"2010"	"6"	"9"	"CTD_human;UNIPROT"
"6496"	"SIX3"	"0.607"	"0.552"	"C2931870"	"Familial schizencephaly"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6496"	"SIX3"	"0.607"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0003486"	"Aortic Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2013"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"6497"	"SKI"	"0.545"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6497"	"SKI"	"0.545"	"0.69"	"C1321551"	"Shprintzen-Goldberg syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.74"	"1"	"2013"	"2017"	"4"	"11"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"6497"	"SKI"	"0.545"	"0.69"	"C1842870"	"Chromosome 1p36 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"6497"	"SKI"	"0.545"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6498"	"SKIL"	"0.701"	"0.31"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6498"	"SKIL"	"0.701"	"0.31"	"C2931434"	"Paraquat lung"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6499"	"SKIV2L"	"0.69"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6499"	"SKIV2L"	"0.69"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6499"	"SKIV2L"	"0.69"	"0.483"	"C1857276"	"Trichohepatoenteric Syndrome"	"disease"	"C13;C16;C17;C23"	"Disease or Syndrome"	"0.56"	"1"	"2012"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"6499"	"SKIV2L"	"0.69"	"0.483"	"C3281289"	"TRICHOHEPATOENTERIC SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"6499"	"SKIV2L"	"0.69"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6502"	"SKP2"	"0.526"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6502"	"SKP2"	"0.526"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9411765"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6503"	"SLA"	"0.815"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6503"	"SLA"	"0.815"	"0.241"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6504"	"SLAMF1"	"0.672"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8181818"	"2001"	"2014"	"0"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0152136"	"Low Tension Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0393729"	"Immersion Related Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C1857253"	"Dicarboxylicaminoaciduria"	"disease"	"C10;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.81"	"1"	"1997"	"2011"	"1"	"2"	"ORPHANET;UNIPROT"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6505"	"SLC1A1"	"0.582"	"0.448"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2012"	"3"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"	"0.8076923"	"1996"	"2016"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2016"	"4"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2012"	"3"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2012"	"3"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.43"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1999"	"2016"	"4"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"1997"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6506"	"SLC1A2"	"0.572"	"0.517"	"C4310717"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"0"	"1995"	"2010"	"1"	"0"	"CTD_human"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2002"	"2016"	"4"	"0"	"PSYGENET"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0338488"	"Alternating hemiplegia of childhood"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2009"	"0"	"0"	"ORPHANET"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6507"	"SLC1A3"	"0.619"	"0.552"	"C2675211"	"EPISODIC ATAXIA, TYPE 6 (disorder)"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6508"	"SLC4A3"	"0.886"	"0.034"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6509"	"SLC1A4"	"0.72"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"6509"	"SLC1A4"	"0.72"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6509"	"SLC1A4"	"0.72"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"1"	"2001"	"2008"	"3"	"0"	"PSYGENET"
"6509"	"SLC1A4"	"0.72"	"0.276"	"C4225254"	"SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"3"	"3"	"ORPHANET;UNIPROT"
"6510"	"SLC1A5"	"0.633"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"1997"	"2008"	"1"	"0"	"PSYGENET"
"6511"	"SLC1A6"	"0.785"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6511"	"SLC1A6"	"0.785"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"PSYGENET"
"6511"	"SLC1A6"	"0.785"	"0.103"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6511"	"SLC1A6"	"0.785"	"0.103"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"6512"	"SLC1A7"	"0.785"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.95"	"2000"	"2018"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0007124"	"Noninfiltrating Intraductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"0.6666667"	"1994"	"2017"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.8148148"	"1990"	"2014"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.57"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"1"	"1998"	"2016"	"3"	"1"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2007"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9047619"	"2000"	"2018"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2015"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1176475"	"Ductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1332347"	"Atypical Ductal Breast Hyperplasia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1832855"	"CHOREOATHETOSIS/SPASTICITY, EPISODIC"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.61"	"1"	"1996"	"2011"	"1"	"2"	"ORPHANET;UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1837206"	"Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly"	"disease"	"C06;C10;C11;C18;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2004"	"2012"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1842534"	"DYSTONIA 18 (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.64"	"1"	"2004"	"2015"	"9"	"10"	"ORPHANET;UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1847501"	"Glut1 Deficiency Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.9393939"	"1998"	"2018"	"13"	"15"	"CTD_human;ORPHANET;UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2017"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C3149117"	"GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"1997"	"2017"	"11"	"22"	"UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C3553859"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12"	"phenotype"		"Finding"	"0.40"		"2009"	"2015"	"3"	"12"	"UNIPROT"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.64"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6513"	"SLC2A1"	"0.441"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.8333333"	"1991"	"2017"	"1"	"2"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0015624"	"Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0341703"	"Adult Fanconi syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C1857395"	"De Toni-Debre-Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2006"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C3495427"	"Fanconi-Bickel Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1949"	"2017"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"6514"	"SLC2A2"	"0.596"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6515"	"SLC2A3"	"0.594"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2012"	"4"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2012"	"4"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.80"	"0.9583333"	"1990"	"2016"	"6"	"1"	"CTD_human;UNIPROT"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2012"	"4"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1991"	"1992"	"3"	"1"	"UNIPROT"
"6517"	"SLC2A4"	"0.564"	"0.586"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"1991"	"1992"	"3"	"1"	"UNIPROT"
"6518"	"SLC2A5"	"0.727"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"2005"	"2018"	"1"	"0"	"CTD_human"
"6518"	"SLC2A5"	"0.727"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"2005"	"2018"	"1"	"0"	"CTD_human"
"6518"	"SLC2A5"	"0.727"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6518"	"SLC2A5"	"0.727"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C0010691"	"Cystinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9591837"	"1994"	"2018"	"12"	"40"	"CTD_human;UNIPROT"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C1848030"	"Hypotonia-Cystinuria Syndrome"	"disease"	"C05;C10;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.55"	"0.8"	"2007"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C1857388"	"Cystinuria, Type A"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"1994"	"2010"	"12"	"34"	"ORPHANET;UNIPROT"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C1857389"	"Cystinuria, Type B"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"12"	"34"	"UNIPROT"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C1857390"	"Cystinuria, Type A-B"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"12"	"34"	"UNIPROT"
"6519"	"SLC3A1"	"0.627"	"0.552"	"C4304537"	"2p21 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6520"	"SLC3A2"	"0.462"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6520"	"SLC3A2"	"0.462"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.69"	"1"	"1996"	"2013"	"2"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.45"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0013902"	"Elliptocytosis, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.42"	"1"	"1992"	"2005"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2016"	"0"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0221409"	"Anemia, hereditary spherocytic hemolytic"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0268435"	"Renal Tubular Acidosis, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1997"	"2013"	"2"	"0"	"CTD_human"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C0272051"	"Xerocytosis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1704380"	"Distal Renal Tubular Acidosis"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.80"	"0.975"	"1997"	"2015"	"6"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1861453"	"Pseudohyperkalemia Cardiff"	"disease"	"C18"	"Disease or Syndrome"	"0.72"	"1"	"1995"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1862322"	"Ovalocytosis, Malaysian-Melanesian-Filipino Type"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1862323"	"Southeast Asian ovalocytosis"	"disease"		"Disease or Syndrome"	"0.40"	"0.9285714"	"1999"	"2012"	"0"	"0"	"ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1862324"	"Elliptocytosis 4"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1969038"	"RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)"	"disease"	"C12;C13;C15;C16;C18"	"Disease or Syndrome"	"0.70"		"1997"	"2004"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C1969039"	"Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"		"1999"	"2004"	"3"	"3"	"UNIPROT"
"6521"	"SLC4A1"	"0.575"	"0.552"	"C2675212"	"Spherocytosis, Type 4"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"		"1992"	"2015"	"15"	"16"	"CTD_human;UNIPROT"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0008340"	"Choledochal Cyst"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0009439"	"Choledochal Cyst, Type I"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C1257796"	"Choledochal Cyst, Type II"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C1257797"	"Choledochal Cyst, Type III"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C1257798"	"Choledochal Cyst, Type IV"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6522"	"SLC4A2"	"0.69"	"0.276"	"C1257799"	"Choledochal Cyst, Type V"	"disease"	"C04;C06;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6523"	"SLC5A1"	"0.681"	"0.517"	"C0268186"	"Congenital glucose-galactose malabsorption"	"disease"	"C06;C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.80"	"1"	"1991"	"2013"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6524"	"SLC5A2"	"0.72"	"0.345"	"C0017980"	"Glycosuria, Renal"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.78"	"1"	"2003"	"2017"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"6524"	"SLC5A2"	"0.72"	"0.345"	"C3245525"	"Familial renal glucosuria"	"disease"		"Disease or Syndrome"	"0.38"	"0.75"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"6524"	"SLC5A2"	"0.72"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6525"	"SMTN"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6526"	"SLC5A3"	"0.735"	"0.276"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.37"	"1"	"1997"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.9375"	"1999"	"2014"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2007"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.9830508"	"1998"	"2018"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1997"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"0.8"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.70"		"1985"	"1999"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"2"	"0"	"CTD_human"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6528"	"SLC5A5"	"0.524"	"0.759"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"PSYGENET"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2001"	"2015"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4085238"	"MYOCLONIC-ATONIC EPILEPSY"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2015"	"2018"	"1"	"8"	"CTD_human;UNIPROT"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6529"	"SLC6A1"	"0.607"	"0.31"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"2000"	"2012"	"5"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"1995"	"2007"	"3"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"2008"	"2018"	"5"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2008"	"2018"	"5"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2004"	"2018"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0026267"	"Mitral Valve Prolapse Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"1"	"1"	"ORPHANET;UNIPROT"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0027821"	"Neurocirculatory Asthenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2000"	"2000"	"1"	"1"	"ORPHANET;UNIPROT"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2002"	"2018"	"2"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2008"	"2014"	"2"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2012"	"3"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"1999"	"2016"	"5"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C1535893"	"Orthostatic intolerance"	"phenotype"	"C10;C23"	"Finding"	"0.71"		"2000"	"2003"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C2930833"	"Irritable heart"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"1"	"1"	"ORPHANET;UNIPROT"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6530"	"SLC6A2"	"0.534"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1995"	"2016"	"5"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1997"	"2016"	"5"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0008701"	"Chronic Motor or Vocal Tic Disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2000"	"2013"	"6"	"0"	"CTD_human;PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"1997"	"2010"	"5"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2008"	"2016"	"5"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2008"	"2016"	"5"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2003"	"2008"	"2"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.85"	"1994"	"2017"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9459459"	"1993"	"2018"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0040188"	"Tic disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0040702"	"Transient Tic Disorder"	"phenotype"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"1995"	"2015"	"4"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2009"	"4"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"1995"	"1"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0338468"	"Tic Disorders, Vocal"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9583333"	"1999"	"2018"	"2"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1997"	"2016"	"4"	"0"	"PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.56"	"0.8"	"2001"	"2011"	"9"	"0"	"CTD_human;PSYGENET"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751553"	"Childhood Tic Disorders"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751554"	"Motor Tic Disorders"	"group"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0751555"	"Post-Traumatic Tic Disorder"	"disease"	"C10;F03"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9464286"	"1995"	"2018"	"4"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2012"	"4"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1995"	"1997"	"1"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C2751067"	"Parkinsonism-Dystonia, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.75"	"1"	"2009"	"2017"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6531"	"SLC6A3"	"0.484"	"0.69"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1998"	"2017"	"7"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.9333333"	"1996"	"2016"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0003944"	"As If Personality"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8863636"	"1997"	"2015"	"5"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0004444"	"Avoidant Personality Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1995"	"2016"	"7"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2000"	"2006"	"4"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2001"	"2006"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1997"	"2018"	"5"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2012"	"4"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"1997"	"2018"	"9"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9285714"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0013415"	"Dysthymic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.53"		"2001"	"2009"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0021124"	"Impulse-Ridden Personality"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0021139"	"Inadequate Personality"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2014"	"1"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"1998"	"2012"	"9"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0027402"	"Narcissistic Personality Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9142857"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0031212"	"Personality Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.6666667"	"1998"	"2014"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.60"	"0.9166667"	"2001"	"2014"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1995"	"2017"	"9"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2015"	"5"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2002"	"2007"	"4"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2012"	"4"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.31"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2013"	"3"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0233477"	"Dysphoric mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2007"	"2012"	"3"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236792"	"Asperger Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2012"	"4"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2006"	"2007"	"2"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2001"	"2012"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2015"	"2015"	"5"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1997"	"2017"	"6"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0581391"	"Chronic depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.33"	"0.75"	"2011"	"2014"	"4"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0588008"	"Severe depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.53"	"0.75"	"2001"	"2015"	"5"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"1998"	"2017"	"6"	"0"	"CTD_human;PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2015"	"3"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"6532"	"SLC6A4"	"0.446"	"0.724"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6533"	"SLC6A6"	"0.785"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C1845862"	"Creatine deficiency, X-linked"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"9"	"13"	"CTD_human;ORPHANET;UNIPROT"
"6535"	"SLC6A8"	"0.567"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2006"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2006"	"2016"	"4"	"0"	"PSYGENET"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"6536"	"SLC6A9"	"0.701"	"0.276"	"C4310943"	"GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"6538"	"SLC6A11"	"0.815"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6538"	"SLC6A11"	"0.815"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6539"	"SLC6A12"	"0.815"	"0.207"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6539"	"SLC6A12"	"0.815"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"6540"	"SLC6A13"	"0.857"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6540"	"SLC6A13"	"0.857"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6540"	"SLC6A13"	"0.857"	"0.034"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6540"	"SLC6A13"	"0.857"	"0.034"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6541"	"SLC7A1"	"0.701"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6541"	"SLC7A1"	"0.701"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6541"	"SLC7A1"	"0.701"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2003"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0025160"	"Megacolon"	"phenotype"	"C06"	"Pathologic Function"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6546"	"SLC8A1"	"0.609"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6547"	"SLC8A3"	"0.672"	"0.207"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6548"	"SLC9A1"	"0.6"	"0.448"	"C4225383"	"LICHTENSTEIN-KNORR SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6549"	"SLC9A2"	"0.928"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6549"	"SLC9A2"	"0.928"	"0.172"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6549"	"SLC9A2"	"0.928"	"0.172"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0021843"	"Intestinal Obstruction"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C0267663"	"Congenital secretory diarrhea, sodium type (disorder)"	"disease"	"C16;C18;C23"	"Congenital Abnormality"	"0.61"	"1"	"2016"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C1859047"	"CYSTIC FIBROSIS MODIFIER 1"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6550"	"SLC9A3"	"0.672"	"0.379"	"C3276246"	"MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6554"	"SLC10A1"	"0.735"	"0.207"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.9230769"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6554"	"SLC10A1"	"0.735"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6554"	"SLC10A1"	"0.735"	"0.207"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C2750087"	"Bile Acid Malabsorption, Primary"	"disease"	"C06;C18;C23"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"1997"	"1"	"3"	"CTD_human;UNIPROT"
"6555"	"SLC10A2"	"0.656"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2009"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.7"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0016470"	"Food Allergy"	"group"	"C20"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.40"	"0.8461538"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0025294"	"Meningococcal meningitis"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0041296"	"Tuberculosis"	"disease"	"C01"	"Disease or Syndrome"	"0.60"	"0.984127"	"1995"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0085568"	"Buruli Ulcer"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2016"	"0"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1135745"	"Meningitis, Meningococcal, Serogroup A"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1135746"	"Meningitis, Meningococcal, Serogroup B"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1135747"	"Meningitis, Meningococcal, Serogroup C"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1136209"	"Meningitis, Meningococcal, Serogroup Y"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1136210"	"Meningitis, Meningococcal, Serogroup W-135"	"disease"	"C01;C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6556"	"SLC11A1"	"0.537"	"0.793"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6557"	"SLC12A1"	"0.645"	"0.552"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"6557"	"SLC12A1"	"0.645"	"0.552"	"C0004775"	"Bartter Disease"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"6557"	"SLC12A1"	"0.645"	"0.552"	"C1866495"	"Bartter syndrome, antenatal type 1"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.91"	"1"	"1996"	"2017"	"1"	"13"	"CTD_human;ORPHANET;UNIPROT"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.75"	"2011"	"2014"	"4"	"0"	"PSYGENET"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6558"	"SLC12A2"	"0.6"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6559"	"SLC12A3"	"0.564"	"0.69"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6559"	"SLC12A3"	"0.564"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6559"	"SLC12A3"	"0.564"	"0.69"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6559"	"SLC12A3"	"0.564"	"0.69"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6559"	"SLC12A3"	"0.564"	"0.69"	"C0268450"	"Gitelman Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1996"	"2018"	"17"	"91"	"CTD_human;ORPHANET;UNIPROT"
"6563"	"SLC14A1"	"0.743"	"0.379"	"C0002880"	"Autoimmune hemolytic anemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"6563"	"SLC14A1"	"0.743"	"0.379"	"C0002883"	"Anemia, Hemolytic, Idiopathic Acquired"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"6563"	"SLC14A1"	"0.743"	"0.379"	"C0175816"	"Cold Hemagglutinin Disease"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"6563"	"SLC14A1"	"0.743"	"0.379"	"C0543663"	"Idiopathic Autoimmune Hemolytic Anemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"1984"	"1984"	"1"	"0"	"CTD_human"
"6565"	"SLC15A2"	"0.857"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6565"	"SLC15A2"	"0.857"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2002"	"2007"	"1"	"0"	"CTD_human"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C1855577"	"Erythrocyte Lactate Transporter Defect"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"		"1986"	"2000"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C1864902"	"Hyperinsulinemic hypoglycemia, familial, 7"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2001"	"2007"	"0"	"2"	"CTD_human;ORPHANET"
"6566"	"SLC16A1"	"0.58"	"0.586"	"C4015186"	"MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C0795889"	"Allan-Herndon-Dudley syndrome (AHDS)"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2017"	"8"	"28"	"CTD_human;ORPHANET;UNIPROT"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"6567"	"SLC16A2"	"0.619"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6568"	"SLC17A1"	"0.762"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0015624"	"Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.42"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0020438"	"Hypercalciuria"	"phenotype"	"C23"	"Disease or Syndrome"	"0.44"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0085682"	"Hypophosphatemia"	"disease"	"C18"	"Disease or Syndrome"	"0.65"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0268080"	"Hypercalcemia, Idiopathic, of Infancy"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0341703"	"Adult Fanconi syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C0475732"	"Hypercalcemia, Infantile"	"phenotype"	"C18"	"Finding"	"0.30"				"0"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C1857395"	"De Toni-Debre-Fanconi Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C2676786"	"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2002"	"2002"	"1"	"2"	"CTD_human;UNIPROT"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C3495427"	"Fanconi-Bickel Syndrome"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C4310232"	"Hypercalcemia, Infantile, 1"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6569"	"SLC34A1"	"0.636"	"0.345"	"C4310473"	"Hypercalcemia, infantile, 2"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2011"	"2016"	"1"	"8"	"CTD_human;UNIPROT"
"6570"	"SLC18A1"	"0.69"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2010"	"4"	"0"	"PSYGENET"
"6570"	"SLC18A1"	"0.69"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6570"	"SLC18A1"	"0.69"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6570"	"SLC18A1"	"0.69"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2007"	"2010"	"1"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2014"	"3"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2008"	"3"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1996"	"2014"	"3"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0236701"	"Cocaine-induced mood disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1996"	"1996"	"1"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6571"	"SLC18A2"	"0.575"	"0.621"	"C4303546"	"Brain dopamine-serotonin vesicular transport disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6572"	"SLC18A3"	"0.713"	"0.379"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6572"	"SLC18A3"	"0.713"	"0.379"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6572"	"SLC18A3"	"0.713"	"0.379"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6572"	"SLC18A3"	"0.713"	"0.379"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6572"	"SLC18A3"	"0.713"	"0.379"	"C4310654"	"MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.7777778"	"2004"	"2014"	"2"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6573"	"SLC19A1"	"0.552"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6574"	"SLC20A1"	"0.656"	"0.345"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0393590"	"Fahr's syndrome (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.97"	"1"	"1993"	"2016"	"8"	"12"	"CTD_human;ORPHANET;UNIPROT"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6575"	"SLC20A2"	"0.69"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6576"	"SLC25A1"	"0.667"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"1996"	"2003"	"1"	"0"	"PSYGENET"
"6576"	"SLC25A1"	"0.667"	"0.483"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6576"	"SLC25A1"	"0.667"	"0.483"	"C2746066"	"Combined D-2- and L-2-hydroxyglutaric aciduria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2013"	"2016"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C0029411"	"Osteoarthropathy, Primary Hypertrophic"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.59"	"1"	"2012"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C0345408"	"Hereditary clubbing"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C2674695"	"Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C2678439"	"CRANIOOSTEOARTHROPATHY"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6578"	"SLCO2A1"	"0.656"	"0.345"	"C3280800"	"HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2015"	"4"	"9"	"UNIPROT"
"6579"	"SLCO1A2"	"0.72"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6580"	"SLC22A1"	"0.582"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6580"	"SLC22A1"	"0.582"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6580"	"SLC22A1"	"0.582"	"0.655"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6580"	"SLC22A1"	"0.582"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6581"	"SLC22A3"	"0.5"	"0.69"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6582"	"SLC22A2"	"0.633"	"0.552"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6582"	"SLC22A2"	"0.633"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6582"	"SLC22A2"	"0.633"	"0.552"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6583"	"SLC22A4"	"0.676"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.8888889"	"2004"	"2016"	"0"	"0"	"CTD_human"
"6583"	"SLC22A4"	"0.676"	"0.483"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6583"	"SLC22A4"	"0.676"	"0.483"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6583"	"SLC22A4"	"0.676"	"0.483"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6583"	"SLC22A4"	"0.676"	"0.483"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0342788"	"Renal carnitine transport defect"	"disease"	"C05;C10;C14;C23"	"Disease or Syndrome"	"1.00"	"0.9375"	"1988"	"2018"	"18"	"103"	"CTD_human;ORPHANET;UNIPROT"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6584"	"SLC22A5"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1985"	"2010"	"11"	"0"	"GENOMICS_ENGLAND"
"6586"	"SLIT3"	"0.685"	"0.345"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"2003"	"2014"	"1"	"0"	"CTD_human"
"6586"	"SLIT3"	"0.685"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6586"	"SLIT3"	"0.685"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6586"	"SLIT3"	"0.685"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6590"	"SLPI"	"0.521"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6590"	"SLPI"	"0.521"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8461538"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0080024"	"Piebaldism"	"disease"	"C16;C17;C18"	"Congenital Abnormality"	"0.63"	"1"	"2004"	"2006"	"0"	"0"	"CTD_human;ORPHANET"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8461538"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.75"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C1837203"	"WAARDENBURG SYNDROME, TYPE IID"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"1998"	"2003"	"0"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C2700265"	"Waardenburg Syndrome Type 2"	"disease"	"C16"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2006"	"0"	"0"	"ORPHANET"
"6591"	"SNAI2"	"0.558"	"0.552"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6591"	"SNAI2"	"0.558"	"0.552"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6594"	"SMARCA1"	"0.567"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6594"	"SMARCA1"	"0.567"	"0.724"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2016"	"2"	"0"	"CLINGEN"
"6594"	"SMARCA1"	"0.567"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6594"	"SMARCA1"	"0.567"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2012"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C1303073"	"Nicolaides Baraitser syndrome"	"disease"	"C05;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.74"	"0.75"	"2009"	"2017"	"4"	"33"	"CTD_human;ORPHANET;UNIPROT"
"6595"	"SMARCA2"	"0.559"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6596"	"HLTF"	"0.663"	"0.276"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"6596"	"HLTF"	"0.663"	"0.276"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2017"	"0"	"0"	"CGI"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CLINGEN"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0039981"	"Thoracic Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0206743"	"Rhabdoid Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"1"	"2008"	"2015"	"0"	"0"	"CGI;ORPHANET"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2014"	"2018"	"4"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.54"	"0.75"	"2012"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.51"	"1"	"2014"	"2015"	"4"	"0"	"CGI;CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2016"	"2"	"0"	"CLINGEN"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.50"		"2014"	"2015"	"4"	"0"	"CGI;CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CLINGEN"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C2212006"	"Ovarian Small Cell Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"CGI"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C2750074"	"Rhabdoid Tumor Predisposition Syndrome 2"	"disease"	"C04"	"Disease or Syndrome"	"0.60"		"1994"	"2017"	"7"	"16"	"CLINGEN;CTD_human"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C3553249"	"COFFIN-SIRIS SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2015"	"1"	"10"	"UNIPROT"
"6597"	"SMARCA4"	"0.503"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.35"	"0.8"	"2010"	"2013"	"0"	"0"	"ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C0206743"	"Rhabdoid Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9666667"	"1999"	"2018"	"2"	"0"	"CGI;CTD_human;ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.54"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C0917817"	"Neurofibromatosis 3"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C1266184"	"Atypical Teratoid Rhabdoid Tumor"	"disease"		"Neoplastic Process"	"0.60"	"0.969697"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C1335929"	"Schwannomatosis"	"disease"	"C04;C10;C16;C17"	"Neoplastic Process"	"0.70"	"0.9142857"	"2007"	"2018"	"1"	"2"	"CTD_human;ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C1836327"	"RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder)"	"disease"	"C04;C10;C12;C13"	"Neoplastic Process"	"0.41"	"1"	"1999"	"2017"	"0"	"6"	"CTD_human"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C2750405"	"Malignant Rhabdoid Tumor, Somatic"	"disease"	"C04;C10;C12;C13"	"Disease or Syndrome"	"0.40"		"1998"	"1998"	"0"	"1"	"CTD_human"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C2931480"	"Neurofibromatosis, Type 3, mixed central and peripheral"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C3553248"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 15"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2015"	"3"	"6"	"UNIPROT"
"6598"	"SMARCB1"	"0.5"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6599"	"SMARCC1"	"0.72"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6601"	"SMARCC2"	"0.928"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6602"	"SMARCD1"	"0.735"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6602"	"SMARCD1"	"0.735"	"0.241"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6602"	"SMARCD1"	"0.735"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6602"	"SMARCD1"	"0.735"	"0.241"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6602"	"SMARCD1"	"0.735"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C0398593"	"Specific granule deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"3"	"CTD_human;ORPHANET"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"6603"	"SMARCD2"	"0.815"	"0.138"	"C4479548"	"SPECIFIC GRANULE DEFICIENCY 2"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"ORPHANET"
"6604"	"SMARCD3"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.40"		"2013"	"2017"	"1"	"8"	"CTD_human"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6605"	"SMARCE1"	"0.616"	"0.621"	"C4310788"	"COFFIN-SIRIS SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2014"	"2"	"1"	"UNIPROT"
"6606"	"SMN1"	"0.503"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6606"	"SMN1"	"0.503"	"0.724"	"C0026847"	"Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9725086"	"1993"	"2018"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0043116"	"HMN (Hereditary Motor Neuropathy) Proximal Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9655172"	"1990"	"2016"	"7"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6606"	"SMN1"	"0.503"	"0.724"	"C0152109"	"Juvenile Spinal Muscular Atrophy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.98"	"1"	"1997"	"2016"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"6606"	"SMN1"	"0.503"	"0.724"	"C0270765"	"Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0393538"	"Muscular Atrophy, Spinal, Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.74"	"1"	"1997"	"2013"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"6606"	"SMN1"	"0.503"	"0.724"	"C0393541"	"Distal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0393546"	"Oculopharyngeal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0393547"	"Bulbospinal Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0700595"	"Spinal Muscular Atrophies of Childhood"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"		"2003"	"2011"	"1"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0751334"	"Progressive Proximal Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0751335"	"Scapuloperoneal Form of Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C0917981"	"Progressive Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2017"	"5"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C1838230"	"SPINAL MUSCULAR ATROPHY, TYPE IV"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6606"	"SMN1"	"0.503"	"0.724"	"C2931358"	"Muscular atrophy, spinal, infantile chronic form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2008"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6606"	"SMN1"	"0.503"	"0.724"	"C2931844"	"Spinal muscular atrophy 4"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6606"	"SMN1"	"0.503"	"0.724"	"C3661519"	"Hereditary Motor Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2017"	"5"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0026847"	"Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9671458"	"1993"	"2018"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0043116"	"HMN (Hereditary Motor Neuropathy) Proximal Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9565217"	"1990"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"6607"	"SMN2"	"0.51"	"0.724"	"C0152109"	"Juvenile Spinal Muscular Atrophy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.89"	"1"	"1993"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"6607"	"SMN2"	"0.51"	"0.724"	"C0270765"	"Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0393538"	"Muscular Atrophy, Spinal, Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2006"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"6607"	"SMN2"	"0.51"	"0.724"	"C0393541"	"Distal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0393546"	"Oculopharyngeal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0393547"	"Bulbospinal Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0700595"	"Spinal Muscular Atrophies of Childhood"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"		"2004"	"2011"	"0"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0751334"	"Progressive Proximal Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0751335"	"Scapuloperoneal Form of Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C0917981"	"Progressive Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"6607"	"SMN2"	"0.51"	"0.724"	"C1838230"	"SPINAL MUSCULAR ATROPHY, TYPE IV"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6607"	"SMN2"	"0.51"	"0.724"	"C2931358"	"Muscular atrophy, spinal, infantile chronic form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6607"	"SMN2"	"0.51"	"0.724"	"C3661519"	"Hereditary Motor Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0002448"	"Ameloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.72"		"1998"	"2016"	"2"	"3"	"CGI;CTD_human;UNIPROT"
"6608"	"SMO"	"0.52"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6608"	"SMO"	"0.52"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6608"	"SMO"	"0.52"	"0.69"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0022360"	"Jaw Abnormalities"	"group"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0024954"	"Maxillary Neoplasms"	"group"	"C04;C05;C07"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.64"	"1"	"2001"	"2015"	"0"	"1"	"CGI"
"6608"	"SMO"	"0.52"	"0.69"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6608"	"SMO"	"0.52"	"0.69"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C0795915"	"Winter Shortland Temple syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.70"		"1988"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6608"	"SMO"	"0.52"	"0.69"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2016"	"2"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6608"	"SMO"	"0.52"	"0.69"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6608"	"SMO"	"0.52"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0028064"	"Niemann-Pick Diseases"	"group"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1991"	"2016"	"1"	"11"	"CTD_human"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0268242"	"Niemann-Pick Disease, Type A"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1991"	"2017"	"18"	"60"	"CTD_human;ORPHANET;UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0268243"	"Niemann-Pick Disease, Type B"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1991"	"2018"	"24"	"26"	"CTD_human;ORPHANET;UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C0268248"	"Niemann-Pick Disease, Type E"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.50"		"1991"	"2016"	"24"	"0"	"CTD_human;UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6609"	"SMPD1"	"0.555"	"0.759"	"C1843418"	"Niemann-Pick Disease, Type F"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"2016"	"24"	"0"	"UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C2675644"	"Niemann-Pick Disease, Intermediate, With Visceral Involvement And Rapid Progression"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.30"		"1991"	"2016"	"24"	"0"	"UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C2675646"	"NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.40"		"1991"	"2016"	"18"	"2"	"UNIPROT"
"6609"	"SMPD1"	"0.555"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6611"	"SMS"	"0.621"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"6611"	"SMS"	"0.621"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6611"	"SMS"	"0.621"	"0.69"	"C0236788"	"Bipolar II disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6611"	"SMS"	"0.621"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6611"	"SMS"	"0.621"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6611"	"SMS"	"0.621"	"0.69"	"C0796160"	"MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1969"	"2016"	"6"	"8"	"CTD_human;ORPHANET;UNIPROT"
"6611"	"SMS"	"0.621"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2008"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6614"	"SIGLEC1"	"0.743"	"0.276"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2013"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6615"	"SNAI1"	"0.537"	"0.552"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2005"	"2014"	"4"	"0"	"CTD_human;PSYGENET"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2005"	"2009"	"2"	"0"	"CTD_human;PSYGENET"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0278076"	"Behavioral tic"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751898"	"Tic, Gestural"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751899"	"Tic, Transient"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751900"	"Tic, Motor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0751901"	"Tic, Vocal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0752251"	"Muscle Disease Manifestations"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C0752252"	"Neuromuscular Manifestations"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6616"	"SNAP25"	"0.536"	"0.655"	"C4225364"	"MYASTHENIC SYNDROME, CONGENITAL, 18"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"6620"	"SNCB"	"0.707"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6620"	"SNCB"	"0.707"	"0.241"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.47"	"1"	"2005"	"2012"	"0"	"2"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2005"	"2015"	"6"	"0"	"CTD_human;PSYGENET"
"6622"	"SNCA"	"0.513"	"0.793"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0017205"	"Gaucher Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0022976"	"Lameness, Animal"	"phenotype"	"C22"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2017"	"3"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.90"	"0.9733333"	"1997"	"2018"	"28"	"22"	"CTD_human;GENOMICS_ENGLAND"
"6622"	"SNCA"	"0.513"	"0.793"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.98"	"1998"	"2018"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0268250"	"Gaucher Disease, Type 2 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0268251"	"Gaucher Disease, Type 3 (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2015"	"4"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"4"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2015"	"4"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9411765"	"1999"	"2018"	"3"	"3"	"CTD_human;UNIPROT"
"6622"	"SNCA"	"0.513"	"0.793"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C1850100"	"PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6622"	"SNCA"	"0.513"	"0.793"	"C1851957"	"Diffuse Lewy Body Disease with Gaze Palsy"	"disease"	"C10;C11;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"6622"	"SNCA"	"0.513"	"0.793"	"C1851958"	"Lewy Body Variant of Alzheimer Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2004"	"1"	"1"	"UNIPROT"
"6622"	"SNCA"	"0.513"	"0.793"	"C1854182"	"PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C1868595"	"PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)"	"disease"		"Disease or Syndrome"	"0.80"		"1997"	"2017"	"7"	"5"	"CTD_human;UNIPROT"
"6622"	"SNCA"	"0.513"	"0.793"	"C1868596"	"Atypical Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"1997"	"2015"	"7"	"4"	"CTD_human;UNIPROT"
"6622"	"SNCA"	"0.513"	"0.793"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C1961835"	"Gaucher Disease, Type 1"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"6622"	"SNCA"	"0.513"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6622"	"SNCA"	"0.513"	"0.793"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6622"	"SNCA"	"0.513"	"0.793"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.40"	"0.9285714"	"1998"	"2018"	"0"	"0"	"ORPHANET"
"6623"	"SNCG"	"0.59"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9545455"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9583333"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6623"	"SNCG"	"0.59"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"6625"	"SNRNP70"	"0.636"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"6628"	"SNRPB"	"0.648"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6628"	"SNRPB"	"0.648"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6628"	"SNRPB"	"0.648"	"0.552"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6628"	"SNRPB"	"0.648"	"0.552"	"C0265342"	"Cerebrocostomandibular Syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.74"	"1"	"2015"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6628"	"SNRPB"	"0.648"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6628"	"SNRPB"	"0.648"	"0.552"	"C3501912"	"Cerebrocostomandibular-Like Syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6628"	"SNRPB"	"0.648"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6629"	"SNRPB2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6634"	"SNRPD3"	"0.857"	"0.138"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6635"	"SNRPE"	"0.815"	"0.207"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"6635"	"SNRPE"	"0.815"	"0.207"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"6635"	"SNRPE"	"0.815"	"0.207"	"C3554409"	"HYPOTRICHOSIS 11"	"disease"		"Disease or Syndrome"	"0.40"		"1998"	"2013"	"1"	"2"	"UNIPROT"
"6637"	"SNRPG"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6638"	"SNRPN"	"0.562"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"6638"	"SNRPN"	"0.562"	"0.655"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9275362"	"1993"	"2018"	"0"	"0"	"CTD_human"
"6638"	"SNRPN"	"0.562"	"0.655"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6640"	"SNTA1"	"0.707"	"0.241"	"C2751830"	"Long Qt Syndrome 12"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.60"		"2008"	"2009"	"2"	"2"	"CTD_human;UNIPROT"
"6646"	"SOAT1"	"0.484"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.9636824"	"1993"	"2018"	"24"	"0"	"CTD_human;ORPHANET"
"6647"	"SOD1"	"0.406"	"0.931"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.34"	"0.75"	"1997"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"0.6666667"	"1997"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2012"	"2018"	"1"	"0"	"PSYGENET"
"6647"	"SOD1"	"0.406"	"0.931"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1985"	"2012"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"0.5"	"2002"	"2007"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011156"	"Deficiency Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.50"		"2003"	"2004"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2000"	"2012"	"2"	"0"	"PSYGENET"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2000"	"2012"	"3"	"0"	"CTD_human;PSYGENET"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.9545455"	"1980"	"2016"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0015696"	"Fatty Liver, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"0.8"	"1994"	"2015"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2010"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.33"		"2005"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2000"	"2007"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0025312"	"Meningomyelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2009"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.43"		"2004"	"2014"	"3"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"0.75"	"1995"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8666667"	"1994"	"2016"	"3"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0033626"	"Protein Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"1991"	"1991"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.31"		"2005"	"2013"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0036330"	"Schistosomiasis mansoni"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2004"	"2012"	"1"	"0"	"PSYGENET"
"6647"	"SOD1"	"0.406"	"0.931"	"C0036457"	"Scrapie"	"disease"	"C10;C22"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0041408"	"Turner Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0085084"	"Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"0.92"	"1995"	"2017"	"1"	"5"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0086664"	"Myelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0154681"	"Anterior Horn Cell Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0154682"	"Lateral Sclerosis"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0162316"	"Iron deficiency anemia"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231686"	"Gait, Unsteady"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231687"	"Spastic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231688"	"Gait, Shuffling"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231689"	"Gait, Athetotic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231693"	"Charcot Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231694"	"Gait, Festinating"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231695"	"Cerebellar ataxic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231696"	"Gait, Hemiplegic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231698"	"Gait, Scissors"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0231712"	"Waddling gait"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0234996"	"Gait, Rigid"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0235000"	"Gait, Broadened"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0242497"	"Intestinal schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0242526"	"Gonadal Dysgenesis, 45,X"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0270763"	"Familial Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0270764"	"Motor Neuron Disease, Lower"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.40"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0337210"	"Gait, Stumbling"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"1995"	"2015"	"24"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0427128"	"Rapid Fatigue of Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0427149"	"Gait, Drop Foot"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0427169"	"Marche a Petit Pas"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0427177"	"Gait, Hysterical"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0521659"	"Motor Neuron Disease, Upper"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0543858"	"Motor Neuron Disease, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.32"	"0.5"	"1995"	"2015"	"24"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751316"	"Acquired Meningomyelocele"	"phenotype"	"C10;C16"	"Acquired Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751829"	"Gait Disorder, Sensorimotor"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751830"	"Gait Disorders, Neurologic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751831"	"Gait, Frontal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751832"	"Gait, Widebased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.34"	"1"	"1992"	"2004"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1456865"	"Ureteral Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1527168"	"Bonnevie-Ullrich Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.90"	"0.9583333"	"1951"	"2018"	"65"	"33"	"CTD_human;UNIPROT"
"6647"	"SOD1"	"0.406"	"0.931"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.80"	"0.9677419"	"1993"	"2018"	"65"	"31"	"CTD_human;UNIPROT"
"6647"	"SOD1"	"0.406"	"0.931"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C2718067"	"Alcoholic Steatohepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C3542025"	"AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2016"	"46"	"32"	"UNIPROT"
"6647"	"SOD1"	"0.406"	"0.931"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6647"	"SOD1"	"0.406"	"0.931"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2013"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002390"	"Extrinsic allergic alveolitis"	"group"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.35"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1997"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2011"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0003493"	"Aortic Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"0.3333333"	"2000"	"2014"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0004045"	"Asphyxia Neonatorum"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2012"	"2"	"0"	"PSYGENET"
"6648"	"SOD2"	"0.396"	"0.897"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2014"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2014"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"		"2008"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9428571"	"1995"	"2016"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2009"	"6"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2015"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2007"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"		"2002"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"0.8"	"1997"	"2008"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2011"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"1997"	"2015"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007682"	"CNS disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2013"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"PSYGENET"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2013"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.34"	"0.6666667"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0014866"	"Esophageal Stenosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0014868"	"Esophagitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0018200"	"Granuloma, Respiratory Tract"	"phenotype"	"C08;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2006"	"2014"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2014"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2017"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2008"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0022672"	"Acute Kidney Tubular Necrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2002"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2000"	"2011"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2014"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0025312"	"Meningomyelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0"	"1998"	"2007"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2005"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"1998"	"2009"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2000"	"2012"	"6"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.37"	"0.8"	"1996"	"2016"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2018"	"6"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2013"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2009"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"		"2004"	"2008"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"1997"	"2015"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"8"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0034530"	"Radiation injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2010"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0034535"	"Radiation Syndrome"	"disease"	"C26"	"Disease or Syndrome"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"1993"	"2013"	"6"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.25"	"2004"	"2015"	"4"	"0"	"PSYGENET"
"6648"	"SOD2"	"0.396"	"0.897"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0036980"	"Shock, Cardiogenic"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2001"	"2015"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2000"	"2014"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2005"	"2013"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0041408"	"Turner Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0042164"	"Uveitis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"0.5"	"2005"	"2008"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0086664"	"Myelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2009"	"6"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2012"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0162671"	"MELAS Syndrome"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0162674"	"Chronic progressive external ophthalmoplegia"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2004"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0206061"	"Pneumonia, Interstitial"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0206062"	"Lung Diseases, Interstitial"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0206160"	"Reticulocytosis"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2000"	"2012"	"7"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0238461"	"Anaplastic thyroid carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0242526"	"Gonadal Dysgenesis, 45,X"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0242992"	"Multiple Chemical Sensitivity"	"phenotype"	"C20;C21"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0268255"	"Farber Lipogranulomatosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2012"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9444444"	"2003"	"2016"	"8"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0376618"	"Endotoxemia"	"phenotype"	"C01;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2013"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2005"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9444444"	"1995"	"2016"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751316"	"Acquired Meningomyelocele"	"phenotype"	"C10;C16"	"Acquired Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2000"	"2005"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2009"	"3"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2008"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2011"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1510432"	"Radiation Sickness"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1527168"	"Bonnevie-Ullrich Syndrome"	"disease"	"C12;C13;C14;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2011"	"2"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.34"	"0.75"	"2003"	"2017"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2014"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1859317"	"Cataract and cardiomyopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2011"	"5"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"4"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2675128"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2000"	"2008"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6648"	"SOD2"	"0.396"	"0.897"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6648"	"SOD2"	"0.396"	"0.897"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"0"	"2003"	"2010"	"2"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2010"	"2"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6649"	"SOD3"	"0.58"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6650"	"CAPN15"	"1"	"0.034"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6651"	"SON"	"0.652"	"0.552"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6651"	"SON"	"0.652"	"0.552"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6651"	"SON"	"0.652"	"0.552"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6651"	"SON"	"0.652"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6651"	"SON"	"0.652"	"0.552"	"C4310696"	"ZTTK SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2017"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6652"	"SORD"	"0.707"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6652"	"SORD"	"0.707"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9855072"	"2004"	"2018"	"3"	"4"	"CTD_human;UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2006"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"6653"	"SORL1"	"0.619"	"0.483"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2018"	"0"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"0"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C1541844"	"PRESENILE AND SENILE DEMENTIA"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C1863052"	"ALZHEIMER DISEASE, FAMILIAL, 1"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C1863053"	"Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C3549448"	"ALZHEIMER DISEASE, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"6653"	"SORL1"	"0.619"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6653"	"SORL1"	"0.619"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6654"	"SOS1"	"0.536"	"0.655"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6654"	"SOS1"	"0.536"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6654"	"SOS1"	"0.536"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"4"	"0"	"GENOMICS_ENGLAND"
"6654"	"SOS1"	"0.536"	"0.655"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.70"	"0.9333333"	"1991"	"2018"	"2"	"22"	"CTD_human;ORPHANET"
"6654"	"SOS1"	"0.536"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6654"	"SOS1"	"0.536"	"0.655"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.40"	"0.9047619"	"2007"	"2018"	"2"	"0"	"CTD_human"
"6654"	"SOS1"	"0.536"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"6654"	"SOS1"	"0.536"	"0.655"	"C0399440"	"Hereditary gingival fibromatosis"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.67"	"0.8571429"	"2002"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"6654"	"SOS1"	"0.536"	"0.655"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"6654"	"SOS1"	"0.536"	"0.655"	"C1853120"	"Noonan Syndrome 4"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.90"		"2007"	"2016"	"13"	"27"	"CLINGEN;CTD_human;UNIPROT"
"6654"	"SOS1"	"0.536"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6655"	"SOS2"	"0.681"	"0.517"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"6655"	"SOS2"	"0.681"	"0.517"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"6655"	"SOS2"	"0.681"	"0.517"	"C4225282"	"NOONAN SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"6657"	"SOX2"	"0.459"	"0.759"	"C0003119"	"Anophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.50"	"0.9"	"2003"	"2016"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"0.875"	"2010"	"2017"	"0"	"0"	"CGI"
"6657"	"SOX2"	"0.459"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9565217"	"2009"	"2016"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.45"	"0.6"	"2003"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6657"	"SOX2"	"0.459"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"6657"	"SOX2"	"0.459"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6657"	"SOX2"	"0.459"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0039981"	"Thoracic Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6657"	"SOX2"	"0.459"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6657"	"SOX2"	"0.459"	"0.759"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2011"	"0"	"0"	"ORPHANET"
"6657"	"SOX2"	"0.459"	"0.759"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2003"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"6657"	"SOX2"	"0.459"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6657"	"SOX2"	"0.459"	"0.759"	"C1859773"	"Microphthalmia, Syndromic 3"	"disease"	"C06;C10;C11;C16"	"Disease or Syndrome"	"0.74"	"1"	"2003"	"2017"	"2"	"17"	"CTD_human;ORPHANET;UNIPROT"
"6657"	"SOX2"	"0.459"	"0.759"	"C1859774"	"Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2003"	"2015"	"2"	"2"	"UNIPROT"
"6657"	"SOX2"	"0.459"	"0.759"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6657"	"SOX2"	"0.459"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6658"	"SOX3"	"0.559"	"0.655"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6658"	"SOX3"	"0.559"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6658"	"SOX3"	"0.559"	"0.655"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C0242343"	"Panhypopituitarism"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.44"	"1"	"2005"	"2015"	"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C0342376"	"Panhypopituitarism - X-linked"	"disease"	"C10;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6658"	"SOX3"	"0.559"	"0.655"	"C0432475"	"XX males"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2003"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6658"	"SOX3"	"0.559"	"0.655"	"C1848068"	"Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C1855900"	"HYPERTRICHOSIS, CONGENITAL GENERALIZED"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C2678223"	"Mental Retardation, X-Linked, With Panhypopituitarism"	"disease"	"C10;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6658"	"SOX3"	"0.559"	"0.655"	"C2936419"	"46, XX Testicular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6658"	"SOX3"	"0.559"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2003"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6659"	"SOX4"	"0.555"	"0.517"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6659"	"SOX4"	"0.555"	"0.517"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6660"	"SOX5"	"0.616"	"0.621"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6660"	"SOX5"	"0.616"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6660"	"SOX5"	"0.616"	"0.621"	"C4225202"	"LAMB-SHAFFER SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2015"	"2018"	"0"	"2"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"0"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6662"	"SOX9"	"0.459"	"0.724"	"C0031900"	"Pierre Robin Syndrome"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.60"	"0.8181818"	"2007"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.35"	"0.8"	"2011"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6662"	"SOX9"	"0.459"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6662"	"SOX9"	"0.459"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0265998"	"ANONYCHIA"	"disease"	"C23"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0266361"	"True Hermaphroditism (disorder)"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C0432475"	"XX males"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2009"	"2012"	"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6662"	"SOX9"	"0.459"	"0.724"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C1842462"	"CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.40"		"1992"	"2014"	"12"	"8"	"UNIPROT"
"6662"	"SOX9"	"0.459"	"0.724"	"C1861922"	"CAMPOMELIC DYSPLASIA"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"0.9615385"	"1992"	"2017"	"12"	"11"	"CTD_human;ORPHANET;UNIPROT"
"6662"	"SOX9"	"0.459"	"0.724"	"C1861923"	"Acampomelic Campomelic Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.82"	"1"	"1995"	"2017"	"12"	"6"	"CTD_human;UNIPROT"
"6662"	"SOX9"	"0.459"	"0.724"	"C2748895"	"Ovotesticular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.33"	"0.6666667"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C2936419"	"46, XX Testicular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.37"	"0.8571429"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"0"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"6662"	"SOX9"	"0.459"	"0.724"	"C3549544"	"ACAMPOMELIC CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2014"	"12"	"6"	"UNIPROT"
"6662"	"SOX9"	"0.459"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"6662"	"SOX9"	"0.459"	"0.724"	"C4225331"	"46,XY SEX REVERSAL 10"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6662"	"SOX9"	"0.459"	"0.724"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6663"	"SOX10"	"0.537"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"6663"	"SOX10"	"0.537"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"6663"	"SOX10"	"0.537"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"6663"	"SOX10"	"0.537"	"0.621"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"1990"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"6663"	"SOX10"	"0.537"	"0.621"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.54"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"6663"	"SOX10"	"0.537"	"0.621"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6663"	"SOX10"	"0.537"	"0.621"	"C1656427"	"Early onset schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"6663"	"SOX10"	"0.537"	"0.621"	"C1836727"	"Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.92"	"1"	"1992"	"2016"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6663"	"SOX10"	"0.537"	"0.621"	"C1848519"	"WAARDENBURG SYNDROME, TYPE 4A"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.40"	"1"	"1998"	"2016"	"0"	"0"	"ORPHANET"
"6663"	"SOX10"	"0.537"	"0.621"	"C2700265"	"Waardenburg Syndrome Type 2"	"disease"	"C16"	"Disease or Syndrome"	"0.57"	"1"	"2012"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"6663"	"SOX10"	"0.537"	"0.621"	"C2700405"	"WAARDENBURG SYNDROME, TYPE IIE"	"disease"	"C16"	"Disease or Syndrome"	"0.60"		"2000"	"2012"	"3"	"3"	"CTD_human;UNIPROT"
"6663"	"SOX10"	"0.537"	"0.621"	"C2750452"	"Waardenburg Syndrome, Type 4c"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.90"		"1998"	"2017"	"10"	"8"	"CLINGEN;CTD_human;UNIPROT"
"6663"	"SOX10"	"0.537"	"0.621"	"C3266898"	"Waardenburg Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2017"	"0"	"1"	"ORPHANET"
"6663"	"SOX10"	"0.537"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6664"	"SOX11"	"0.559"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6664"	"SOX11"	"0.559"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6664"	"SOX11"	"0.559"	"0.69"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6664"	"SOX11"	"0.559"	"0.69"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6664"	"SOX11"	"0.559"	"0.69"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"6664"	"SOX11"	"0.559"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6664"	"SOX11"	"0.559"	"0.69"	"C4014528"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 27"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"6665"	"SOX15"	"0.773"	"0.207"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6665"	"SOX15"	"0.773"	"0.207"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.37"	"0.8571429"	"2003"	"2016"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6667"	"SP1"	"0.508"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2014"	"3"	"0"	"PSYGENET"
"6667"	"SP1"	"0.508"	"0.724"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6667"	"SP1"	"0.508"	"0.724"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6667"	"SP1"	"0.508"	"0.724"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6667"	"SP1"	"0.508"	"0.724"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6670"	"SP3"	"0.762"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6670"	"SP3"	"0.762"	"0.345"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6671"	"SP4"	"0.707"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.53"	"1"	"2009"	"2016"	"2"	"0"	"CTD_human;PSYGENET"
"6671"	"SP4"	"0.707"	"0.276"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6671"	"SP4"	"0.707"	"0.276"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6671"	"SP4"	"0.707"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2009"	"2016"	"1"	"2"	"CTD_human"
"6671"	"SP4"	"0.707"	"0.276"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6674"	"SPAG1"	"0.701"	"0.31"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2014"	"0"	"2"	"ORPHANET"
"6674"	"SPAG1"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6674"	"SPAG1"	"0.701"	"0.31"	"C3809706"	"CILIARY DYSKINESIA, PRIMARY, 28"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"0"	"6"	"CTD_human"
"6674"	"SPAG1"	"0.701"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6674"	"SPAG1"	"0.701"	"0.31"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6678"	"SPARC"	"0.466"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0023931"	"Lobstein Disease"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0024031"	"Low Back Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.51"	"1"	"1992"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6678"	"SPARC"	"0.466"	"0.793"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0158266"	"Intervertebral Disc Degeneration"	"disease"	"C05"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6678"	"SPARC"	"0.466"	"0.793"	"C0423682"	"Low Back Pain, Mechanical"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0423689"	"Low Back Pain, Posterior Compartment"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0577660"	"Low Back Pain, Postural"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0751648"	"Recurrent Low Back Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.38"	"1"	"1999"	"2013"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C2717759"	"Degenerative Intervertebral Discs"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6678"	"SPARC"	"0.466"	"0.793"	"C4225301"	"OSTEOGENESIS IMPERFECTA, TYPE XVII"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"6683"	"SPAST"	"0.604"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6683"	"SPAST"	"0.604"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6683"	"SPAST"	"0.604"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6683"	"SPAST"	"0.604"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.9814815"	"2000"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6683"	"SPAST"	"0.604"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6683"	"SPAST"	"0.604"	"0.517"	"C1866855"	"Spastic paraplegia 4, autosomal dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.99"	"0.8888889"	"1997"	"2017"	"43"	"46"	"CTD_human;ORPHANET;UNIPROT"
"6683"	"SPAST"	"0.604"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C0030486"	"Paraplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0037772"	"Spastic Paraplegia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.45"	"1"	"1998"	"2015"	"1"	"2"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1999"	"2018"	"0"	"5"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C0154682"	"Lateral Sclerosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6687"	"SPG7"	"0.542"	"0.655"	"C0242036"	"Paraplegia, Ataxic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0278114"	"Paraplegia, Cerebral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0278115"	"Paraplegia, Spinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0452143"	"Paraplegia, Flaccid"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6687"	"SPG7"	"0.542"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"1999"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"6687"	"SPG7"	"0.542"	"0.655"	"C1846564"	"SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.92"	"1"	"1998"	"2017"	"5"	"28"	"CTD_human;ORPHANET;UNIPROT"
"6687"	"SPG7"	"0.542"	"0.655"	"C1968845"	"Primary Lateral Sclerosis, Adult, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6687"	"SPG7"	"0.542"	"0.655"	"C3711370"	"Spastic Paraplegia Type 7"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2013"	"0"	"0"	"ORPHANET"
"6687"	"SPG7"	"0.542"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6688"	"SPI1"	"0.676"	"0.483"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6688"	"SPI1"	"0.676"	"0.483"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"6688"	"SPI1"	"0.676"	"0.483"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"6688"	"SPI1"	"0.676"	"0.483"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6688"	"SPI1"	"0.676"	"0.483"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6688"	"SPI1"	"0.676"	"0.483"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"6689"	"SPIB"	"0.685"	"0.345"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.62"	"1"	"2010"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"6689"	"SPIB"	"0.685"	"0.345"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2010"	"2011"	"1"	"2"	"CTD_human"
"6689"	"SPIB"	"0.685"	"0.345"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.41"		"2003"	"2010"	"1"	"0"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.70"	"0.8979592"	"1996"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9761905"	"2000"	"2018"	"1"	"1"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"5"	"9"	"CTD_human;ORPHANET;UNIPROT"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.50"	"0.8181818"	"2003"	"2017"	"1"	"0"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"6690"	"SPINK1"	"0.536"	"0.621"	"C1832108"	"PANCREATITIS, CHRONIC, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2000"	"2010"	"5"	"3"	"UNIPROT"
"6690"	"SPINK1"	"0.536"	"0.621"	"C1842402"	"TROPICAL CALCIFIC PANCREATITIS"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.70"	"0.8"	"2002"	"2013"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6690"	"SPINK1"	"0.536"	"0.621"	"C1868653"	"Pancreatitis, Calcific"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2010"	"5"	"3"	"UNIPROT"
"6690"	"SPINK1"	"0.536"	"0.621"	"C1969419"	"PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2000"	"2010"	"5"	"3"	"UNIPROT"
"6690"	"SPINK1"	"0.536"	"0.621"	"C4080064"	"Autosomal Dominant Hereditary Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2007"	"0"	"0"	"CTD_human"
"6693"	"SPN"	"0.624"	"0.483"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6693"	"SPN"	"0.624"	"0.483"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6693"	"SPN"	"0.624"	"0.483"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6693"	"SPN"	"0.624"	"0.483"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6695"	"SPOCK1"	"0.701"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6695"	"SPOCK1"	"0.701"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.34"	"1"	"1995"	"2008"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.98"	"1998"	"2017"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.50"		"2008"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2016"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.37"	"1"	"1993"	"2012"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0023896"	"Alcoholic Liver Diseases"	"group"	"C06;C25"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"1997"	"2013"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.38"	"0.875"	"1999"	"2014"	"0"	"0"	"ORPHANET"
"6696"	"SPP1"	"0.391"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2010"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9928571"	"1996"	"2018"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.31"	"1"	"1997"	"2012"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0030286"	"Pancreatic Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0032229"	"Pleural Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9811321"	"1998"	"2017"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2002"	"2017"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2001"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6696"	"SPP1"	"0.391"	"0.862"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6697"	"SPR"	"0.667"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6697"	"SPR"	"0.667"	"0.379"	"C0268468"	"Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency"	"disease"	"C10;C16;C18;C23;F01"	"Disease or Syndrome"	"0.71"	"0"	"1993"	"2015"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6697"	"SPR"	"0.667"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6698"	"SPRR1A"	"0.743"	"0.207"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6698"	"SPRR1A"	"0.743"	"0.207"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6698"	"SPRR1A"	"0.743"	"0.207"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6698"	"SPRR1A"	"0.743"	"0.207"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"6700"	"SPRR2A"	"0.696"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6700"	"SPRR2A"	"0.696"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6700"	"SPRR2A"	"0.696"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6701"	"SPRR2B"	"0.928"	"0.103"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1987"	"2006"	"9"	"0"	"GENOMICS_ENGLAND"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0013902"	"Elliptocytosis, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.44"	"1"	"1999"	"2014"	"0"	"0"	"ORPHANET"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2003"	"0"	"0"	"ORPHANET"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1987"	"2006"	"9"	"0"	"GENOMICS_ENGLAND"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0221409"	"Anemia, hereditary spherocytic hemolytic"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6708"	"SPTA1"	"0.696"	"0.31"	"C0520739"	"Hereditary pyropoikilocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.61"	"1"	"1975"	"2006"	"1"	"6"	"CTD_human;UNIPROT"
"6708"	"SPTA1"	"0.696"	"0.31"	"C1851741"	"ELLIPTOCYTOSIS 2 (disorder)"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1975"	"2015"	"12"	"16"	"CTD_human;UNIPROT"
"6708"	"SPTA1"	"0.696"	"0.31"	"C2678338"	"SPHEROCYTOSIS, TYPE 3 (disorder)"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1962"	"2016"	"0"	"2"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2017"	"0"	"0"	"ORPHANET"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C3150731"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2013"	"0"	"3"	"CTD_human"
"6709"	"SPTAN1"	"0.611"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"6710"	"SPTB"	"0.752"	"0.172"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6710"	"SPTB"	"0.752"	"0.172"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6710"	"SPTB"	"0.752"	"0.172"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6710"	"SPTB"	"0.752"	"0.172"	"C0002891"	"Anemia, Neonatal"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6710"	"SPTB"	"0.752"	"0.172"	"C0013902"	"Elliptocytosis, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.54"	"1"	"1990"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"6710"	"SPTB"	"0.752"	"0.172"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.53"	"1"	"1990"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"6710"	"SPTB"	"0.752"	"0.172"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6710"	"SPTB"	"0.752"	"0.172"	"C0221409"	"Anemia, hereditary spherocytic hemolytic"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6710"	"SPTB"	"0.752"	"0.172"	"C0520739"	"Hereditary pyropoikilocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C1866810"	"ELLIPTOCYTOSIS 3"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1987"	"1997"	"4"	"8"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C2674219"	"SPHEROCYTOSIS, HEREDITARY, 2"	"disease"		"Disease or Syndrome"	"0.60"		"1982"	"2015"	"2"	"7"	"CTD_human;UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C3889607"	"SPECTRIN SAINT CHAMOND PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C3889608"	"SPECTRIN TLEMCEN PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C3889609"	"SPECTRIN PROVIDENCE PHENOTYPE"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C3890218"	"SPHEROCYTOSIS, TYPE 2, AUTOSOMAL DOMINANT"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C4016380"	"ANEMIA, NEONATAL HEMOLYTIC, FATAL AND NEAR-FATAL"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6710"	"SPTB"	"0.752"	"0.172"	"C4016381"	"ELLIPTOCYTOSIS 3 DUE TO SPECTRIN COSENZA"	"phenotype"		"Finding"	"0.30"		"1990"	"1995"	"4"	"5"	"UNIPROT"
"6711"	"SPTBN1"	"0.667"	"0.483"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6711"	"SPTBN1"	"0.667"	"0.483"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6711"	"SPTBN1"	"0.667"	"0.483"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"2006"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"6712"	"SPTBN2"	"0.648"	"0.483"	"C3809327"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"2"	"ORPHANET"
"6713"	"SQLE"	"0.743"	"0.31"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6713"	"SQLE"	"0.743"	"0.31"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6713"	"SQLE"	"0.743"	"0.31"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6713"	"SQLE"	"0.743"	"0.31"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"2"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"0.6666667"	"1999"	"2015"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2003"	"2009"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"0.8888889"	"1995"	"2017"	"0"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"0"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6714"	"SRC"	"0.502"	"0.69"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.38"	"0.625"	"1999"	"2015"	"0"	"0"	"CGI"
"6714"	"SRC"	"0.502"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1995"	"2017"	"0"	"0"	"CTD_human"
"6714"	"SRC"	"0.502"	"0.69"	"C4310789"	"THROMBOCYTOPENIA 6"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"		"2004"	"2010"	"2"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"6715"	"SRD5A1"	"0.636"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.34"	"0.5"	"2003"	"2013"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0005001"	"Benign prostatic hypertrophy"	"phenotype"	"C12"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2002"	"2013"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2015"	"5"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.42"	"1"	"2003"	"2017"	"1"	"1"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0266435"	"Congenital hypoplasia of penis"	"disease"		"Congenital Abnormality"	"0.43"	"0.6666667"	"1992"	"2010"	"16"	"3"	"UNIPROT"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0268297"	"Pseudovaginal Perineoscrotal Hypospadias"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.77"	"1"	"1979"	"2017"	"16"	"26"	"CTD_human;ORPHANET;UNIPROT"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.8823529"	"1995"	"2017"	"5"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C0520477"	"Prostatic Adenoma"	"disease"	"C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C1704272"	"Benign Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.40"	"0.9"	"2001"	"2018"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C1739363"	"Prostatic Hypertrophy"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C2937421"	"Prostatic Hyperplasia"	"disease"	"C12"	"Disease or Syndrome"	"0.33"		"2002"	"2010"	"1"	"0"	"CTD_human"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C3669122"	"5-Alpha Reductase Deficiency"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.53"	"1"	"1992"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"6716"	"SRD5A2"	"0.58"	"0.483"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"6717"	"SRI"	"0.667"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C1856127"	"Bile acid synthesis defect, congenital, 2"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.70"		"2003"	"2015"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6718"	"AKR1D1"	"0.727"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2000"	"2013"	"2"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2000"	"2013"	"2"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"PSYGENET"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2000"	"2013"	"2"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"0.8888889"	"2008"	"2017"	"2"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9583333"	"2007"	"2017"	"1"	"0"	"CTD_human"
"6720"	"SREBF1"	"0.57"	"0.517"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2018"	"2"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2003"	"2016"	"0"	"0"	"UNIPROT"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6721"	"SREBF2"	"0.611"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6722"	"SRF"	"0.598"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6722"	"SRF"	"0.598"	"0.69"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"6722"	"SRF"	"0.598"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6722"	"SRF"	"0.598"	"0.69"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6722"	"SRF"	"0.598"	"0.69"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6722"	"SRF"	"0.598"	"0.69"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"6722"	"SRF"	"0.598"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6723"	"SRM"	"0.773"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6725"	"SRMS"	"0.928"	"0.103"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6725"	"SRMS"	"0.928"	"0.103"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6729"	"SRP54"	"0.727"	"0.345"	"C0272170"	"Shwachman syndrome"	"disease"	"C06;C15;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6730"	"SRP68"	"0.834"	"0.069"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6730"	"SRP68"	"0.834"	"0.069"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6731"	"SRP72"	"0.72"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6731"	"SRP72"	"0.72"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C2931245"	"Bone Marrow failure syndromes"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C3808553"	"Bone marrow failure syndrome 1"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6731"	"SRP72"	"0.72"	"0.276"	"C3810350"	"Bone marrow failure syndrome 2"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6731"	"SRP72"	"0.72"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6733"	"SRPK2"	"0.701"	"0.276"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6736"	"SRY"	"0.5"	"0.655"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"0.95"	"1992"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C0018055"	"Gonadal Dysgenesis, Mixed"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.45"	"1"	"1997"	"2015"	"0"	"0"	"ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.36"	"1"	"1992"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"6736"	"SRY"	"0.5"	"0.655"	"C0266361"	"True Hermaphroditism (disorder)"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.50"	"0.8947368"	"1995"	"2012"	"0"	"0"	"ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C0432475"	"XX males"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1988"	"2015"	"0"	"0"	"ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C2748895"	"Ovotesticular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.60"	"1"	"2002"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C2748896"	"46,Xy Gonadal Dysgenesis, Complete, Sry-Related"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"1990"	"2017"	"24"	"22"	"CTD_human;UNIPROT"
"6736"	"SRY"	"0.5"	"0.655"	"C2748897"	"46,Xy True Hermaphroditism, Sry-Related"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"1991"	"2017"	"24"	"13"	"CTD_human;UNIPROT"
"6736"	"SRY"	"0.5"	"0.655"	"C2748898"	"TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY"	"phenotype"		"Finding"	"0.50"		"1991"	"2017"	"24"	"13"	"CTD_human;UNIPROT"
"6736"	"SRY"	"0.5"	"0.655"	"C2748899"	"SEX-REVERSING LOCUS ON X, FORMERLY"	"phenotype"		"Finding"	"0.50"		"1991"	"2017"	"24"	"13"	"CTD_human;UNIPROT"
"6736"	"SRY"	"0.5"	"0.655"	"C2936419"	"46, XX Testicular Disorders of Sex Development"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.40"	"1"	"2001"	"2016"	"0"	"0"	"ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"1"	"1992"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"6736"	"SRY"	"0.5"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6736"	"SRY"	"0.5"	"0.655"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6742"	"SSBP1"	"0.72"	"0.31"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6746"	"SSR2"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6746"	"SSR2"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6748"	"SSR4"	"0.727"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6748"	"SSR4"	"0.727"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"6748"	"SSR4"	"0.727"	"0.414"	"C4012395"	"Congenital disorder of glycosylation type 1y"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"6750"	"SST"	"0.457"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"PSYGENET"
"6750"	"SST"	"0.457"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0011993"	"Vipoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0014849"	"Esophageal and Gastric Varices"	"phenotype"	"C06"	"Acquired Abnormality"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0014867"	"Esophageal Varices"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"2002"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0017145"	"Gastric Varix"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0020621"	"Hypokalemia"	"phenotype"	"C18"	"Finding"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"1986"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"PSYGENET"
"6750"	"SST"	"0.457"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2008"	"2016"	"5"	"0"	"PSYGENET"
"6750"	"SST"	"0.457"	"0.724"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1994"	"2012"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2015"	"2"	"0"	"PSYGENET"
"6750"	"SST"	"0.457"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0086768"	"Pancreatic Cholera"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"1986"	"1993"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"1986"	"2011"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1988"	"2016"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2015"	"2"	"0"	"PSYGENET"
"6750"	"SST"	"0.457"	"0.724"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6750"	"SST"	"0.457"	"0.724"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"3"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6751"	"SSTR1"	"0.633"	"0.414"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2010"	"3"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2010"	"3"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6752"	"SSTR2"	"0.551"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6753"	"SSTR3"	"0.681"	"0.31"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6754"	"SSTR4"	"0.558"	"0.69"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2011"	"2"	"0"	"PSYGENET"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6755"	"SSTR5"	"0.604"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6756"	"SSX1"	"0.735"	"0.241"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9183673"	"1995"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"6757"	"SSX2"	"0.642"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6757"	"SSX2"	"0.642"	"0.345"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9784173"	"1994"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"6757"	"SSX2"	"0.642"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6760"	"SS18"	"0.727"	"0.207"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9419355"	"1994"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"6768"	"ST14"	"0.55"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6768"	"ST14"	"0.55"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"		"2006"	"2009"	"1"	"0"	"CTD_human"
"6768"	"ST14"	"0.55"	"0.724"	"C0265962"	"Ichthyosis linearis circumflexa"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6768"	"ST14"	"0.55"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6768"	"ST14"	"0.55"	"0.724"	"C1835851"	"Ichthyosis with hypotrichosis, autosomal recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.64"	"1"	"2007"	"2014"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6769"	"STAC"	"1"	"0.069"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6770"	"STAR"	"0.584"	"0.483"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2009"	"2013"	"1"	"0"	"CTD_human"
"6770"	"STAR"	"0.584"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.55"	"0.6"	"1999"	"2011"	"1"	"0"	"CTD_human"
"6770"	"STAR"	"0.584"	"0.483"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6770"	"STAR"	"0.584"	"0.483"	"C0342474"	"Lipoid congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.70"	"1"	"1995"	"2017"	"5"	"12"	"CTD_human;UNIPROT"
"6770"	"STAR"	"0.584"	"0.483"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"6770"	"STAR"	"0.584"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2017"	"1"	"0"	"CTD_human"
"6770"	"STAR"	"0.584"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6770"	"STAR"	"0.584"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6770"	"STAR"	"0.584"	"0.483"	"C4049650"	"Familial Glucocorticoid Deficiency Type 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6772"	"STAT1"	"0.434"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9"	"1996"	"2016"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"0.9444444"	"2000"	"2018"	"0"	"0"	"UNIPROT"
"6772"	"STAT1"	"0.434"	"0.793"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.50"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0010823"	"Cytomegalovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0026918"	"Mycobacterium Infections"	"group"	"C01"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9166667"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6772"	"STAT1"	"0.434"	"0.793"	"C3151088"	"IMMUNODEFICIENCY 31B"	"disease"		"Disease or Syndrome"	"0.70"		"2003"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6772"	"STAT1"	"0.434"	"0.793"	"C3279990"	"CANDIDIASIS, FAMILIAL, 7"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2016"	"5"	"16"	"CTD_human;ORPHANET;UNIPROT"
"6772"	"STAT1"	"0.434"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6772"	"STAT1"	"0.434"	"0.793"	"C4013950"	"IMMUNODEFICIENCY 31A"	"disease"		"Disease or Syndrome"	"0.70"		"2001"	"2012"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6773"	"STAT2"	"0.616"	"0.414"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6773"	"STAT2"	"0.616"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6773"	"STAT2"	"0.616"	"0.414"	"C4225252"	"IMMUNODEFICIENCY 45"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6773"	"STAT2"	"0.616"	"0.414"	"C4225260"	"IMMUNODEFICIENCY 44"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"6774"	"STAT3"	"0.358"	"0.862"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.50"	"0.9411765"	"2010"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.990566"	"1997"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9642857"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.875"	"2008"	"2017"	"2"	"1"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"6774"	"STAT3"	"0.358"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"6774"	"STAT3"	"0.358"	"0.862"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2003"	"2014"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2000"	"2014"	"3"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2014"	"3"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023492"	"Leukemia, T-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9906542"	"2001"	"2018"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2014"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"3"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.69"	"0.8888889"	"2005"	"2017"	"1"	"1"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2014"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0206180"	"Ki-1+ Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9"	"2004"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.984375"	"2000"	"2018"	"3"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6774"	"STAT3"	"0.358"	"0.862"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.990566"	"1997"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"		"2000"	"2014"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2004"	"2012"	"2"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.969697"	"2000"	"2017"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2000"	"2014"	"3"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9473684"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6774"	"STAT3"	"0.358"	"0.862"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C1955861"	"T-Cell Large Granular Lymphocyte Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2016"	"0"	"0"	"CGI"
"6774"	"STAT3"	"0.358"	"0.862"	"C1968689"	"Hyper-Immunoglobulin E Syndrome, Autosomal Recessive"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C2936739"	"Hyper-Immunoglobulin E Syndrome, Autosomal Dominant"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.90"	"1"	"2007"	"2016"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"6774"	"STAT3"	"0.358"	"0.862"	"C3489795"	"Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.70"		"1966"	"2018"	"4"	"13"	"CTD_human;ORPHANET;UNIPROT"
"6774"	"STAT3"	"0.358"	"0.862"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C3887645"	"Job Syndrome"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.80"	"1"	"2004"	"2016"	"5"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6774"	"STAT3"	"0.358"	"0.862"	"C4014795"	"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2017"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"6774"	"STAT3"	"0.358"	"0.862"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"6774"	"STAT3"	"0.358"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6775"	"STAT4"	"0.515"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.8913043"	"2000"	"2016"	"2"	"5"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.66"	"1"	"2011"	"2018"	"1"	"3"	"CTD_human;ORPHANET"
"6775"	"STAT4"	"0.515"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"UNIPROT"
"6775"	"STAT4"	"0.515"	"0.69"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.44"	"1"	"2011"	"2017"	"1"	"3"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2013"	"1"	"1"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.70"	"0.9607843"	"2002"	"2017"	"2"	"12"	"CTD_human;ORPHANET"
"6775"	"STAT4"	"0.515"	"0.69"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.43"	"1"	"2008"	"2018"	"1"	"2"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.9166667"	"2009"	"2018"	"1"	"5"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.45"	"1"	"2008"	"2017"	"2"	"4"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"1"	"2013"	"2016"	"1"	"5"	"CTD_human"
"6775"	"STAT4"	"0.515"	"0.69"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9411765"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0007124"	"Noninfiltrating Intraductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"5"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2007"	"3"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9428571"	"1998"	"2018"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C1176475"	"Ductal Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2010"	"5"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C1332347"	"Atypical Ductal Breast Hyperplasia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6776"	"STAT5A"	"0.489"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.57"	"0.8571429"	"2000"	"2012"	"0"	"0"	"CGI;ORPHANET"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.75"	"2003"	"2016"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C1522378"	"Leukemia, Large Granular Lymphocytic"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C1855548"	"Laron syndrome type 2"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.70"		"2003"	"2012"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6777"	"STAT5B"	"0.49"	"0.69"	"C1955860"	"Leukemia, Natural Killer Cell Large Granular Lymphocytic"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C1955861"	"T-Cell Large Granular Lymphocyte Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.52"	"1"	"2013"	"2016"	"1"	"0"	"CGI;CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C2931322"	"T-Lymphocytopenia"	"disease"	"C15;C20"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6777"	"STAT5B"	"0.49"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6778"	"STAT6"	"0.533"	"0.724"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0018922"	"hemangiopericytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"6778"	"STAT6"	"0.533"	"0.724"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CGI"
"6778"	"STAT6"	"0.533"	"0.724"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6778"	"STAT6"	"0.533"	"0.724"	"C1266119"	"Solitary fibrous tumor"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.8695652"	"2013"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"6779"	"STATH"	"0.713"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0019187"	"Hepatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2009"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0524610"	"Chronic Alcoholic Hepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6783"	"SULT1E1"	"0.538"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C0271093"	"Stargardt's disease"	"phenotype"	"C11"	"Disease or Syndrome"	"0.50"		"2006"	"2007"	"0"	"0"	"ORPHANET"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C1838644"	"Stargardt disease 3"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"0.9"	"1998"	"2013"	"0"	"3"	"CTD_human"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C1851481"	"Erythrokeratodermia with ataxia"	"disease"	"C10;C16;C17;C23"	"Disease or Syndrome"	"0.61"	"1"	"1972"	"2015"	"1"	"2"	"ORPHANET;UNIPROT"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C1855465"	"STARGARDT DISEASE 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2007"	"0"	"0"	"ORPHANET"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C3280856"	"ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"2"	"ORPHANET"
"6785"	"ELOVL4"	"0.633"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6786"	"STIM1"	"0.554"	"0.655"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"6786"	"STIM1"	"0.554"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6786"	"STIM1"	"0.554"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6786"	"STIM1"	"0.554"	"0.655"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.80"	"1"	"2013"	"2018"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6786"	"STIM1"	"0.554"	"0.655"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C1861451"	"Stormorken Syndrome"	"disease"	"C10;C11;C15;C16;C17;C23;F03"	"Disease or Syndrome"	"0.64"	"1"	"1986"	"2017"	"3"	"2"	"ORPHANET;UNIPROT"
"6786"	"STIM1"	"0.554"	"0.655"	"C2748557"	"Immune dysfunction with T-cell inactivation due to calcium entry defect 2"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.72"	"1"	"2009"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6786"	"STIM1"	"0.554"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6786"	"STIM1"	"0.554"	"0.655"	"C4011726"	"MYOPATHY, TUBULAR AGGREGATE, 1"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2016"	"4"	"6"	"UNIPROT"
"6787"	"NEK4"	"0.785"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2015"	"2"	"5"	"PSYGENET"
"6787"	"NEK4"	"0.785"	"0.138"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6788"	"STK3"	"0.707"	"0.345"	"C3544205"	"Ovarian clear cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6789"	"STK4"	"0.727"	"0.345"	"C3553943"	"T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2012"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"6790"	"AURKA"	"0.508"	"0.621"	"C0002938"	"Aneuploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.972973"	"1997"	"2017"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"6790"	"AURKA"	"0.508"	"0.621"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6790"	"AURKA"	"0.508"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2006"	"2014"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6790"	"AURKA"	"0.508"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9736842"	"1997"	"2017"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6790"	"AURKA"	"0.508"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"6790"	"AURKA"	"0.508"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2006"	"2014"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0035372"	"Rett Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.9692308"	"2005"	"2017"	"1"	"2"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"1"	"2005"	"2017"	"1"	"1"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9642857"	"2003"	"2018"	"0"	"1"	"ORPHANET"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0162635"	"Angelman Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2009"	"1"	"1"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.50"	"0.9583333"	"2007"	"2018"	"0"	"4"	"GENOMICS_ENGLAND"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"6792"	"CDKL5"	"0.551"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6792"	"CDKL5"	"0.551"	"0.448"	"C1839333"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"2003"	"2017"	"18"	"98"	"CTD_human;UNIPROT"
"6792"	"CDKL5"	"0.551"	"0.448"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.9"	"2008"	"2017"	"0"	"42"	"ORPHANET"
"6792"	"CDKL5"	"0.551"	"0.448"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2003"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6792"	"CDKL5"	"0.551"	"0.448"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6792"	"CDKL5"	"0.551"	"0.448"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6793"	"STK10"	"0.773"	"0.172"	"C0014145"	"Yolk Sac Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6793"	"STK10"	"0.773"	"0.172"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C0238451"	"Teratoma of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C0334517"	"Spermatocytic seminoma"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C1266158"	"Nongerminomatous Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6793"	"STK10"	"0.773"	"0.172"	"C3463918"	"EMBRYONAL CELL CARCINOMA"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9677419"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.50"	"0.9"	"2006"	"2018"	"0"	"1"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.875"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0014145"	"Yolk Sac Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"6794"	"STK11"	"0.467"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"1999"	"2017"	"2"	"3"	"CGI;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.56"	"1"	"1999"	"2016"	"1"	"1"	"CGI;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.61"	"1"	"2004"	"2015"	"1"	"1"	"CGI;CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0031269"	"Peutz-Jeghers Syndrome"	"disease"	"C04;C06;C16;C17"	"Disease or Syndrome"	"1.00"	"0.9690722"	"1949"	"2018"	"17"	"47"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0036631"	"Seminoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2000"	"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"1"	"2002"	"2017"	"1"	"2"	"CGI;CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.42"	"0.5"	"1998"	"1999"	"0"	"1"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0154007"	"Benign neoplasm of testis"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.45"	"1"	"1999"	"2010"	"0"	"3"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0238451"	"Teratoma of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.60"	"1"	"2003"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0265323"	"Peutz-Jeghers polyps of small bowel"	"disease"		"Neoplastic Process"	"0.50"		"1997"	"2016"	"10"	"0"	"CLINGEN"
"6794"	"STK11"	"0.467"	"0.655"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0282207"	"Cronkhite-Canada Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0302592"	"Cervix carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2000"	"2017"	"0"	"0"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0334517"	"Spermatocytic seminoma"	"disease"		"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"6794"	"STK11"	"0.467"	"0.655"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.68"	"1"	"1999"	"2015"	"1"	"0"	"CGI;CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0456487"	"Peutz Jehgers polyp"	"disease"		"Neoplastic Process"	"0.50"		"1997"	"2016"	"10"	"0"	"CLINGEN"
"6794"	"STK11"	"0.467"	"0.655"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0496924"	"Neoplasm of uncertain or unknown behavior of testis"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2016"	"1"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"1998"	"2005"	"1"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"0.6666667"	"1999"	"2015"	"0"	"0"	"CGI"
"6794"	"STK11"	"0.467"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.55"	"1"	"1999"	"2016"	"0"	"0"	"CGI;CLINGEN"
"6794"	"STK11"	"0.467"	"0.655"	"C1257915"	"Intestinal Polyposis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2008"	"2015"	"1"	"1"	"CTD_human"
"6794"	"STK11"	"0.467"	"0.655"	"C1266158"	"Nongerminomatous Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C1333088"	"Colonic hamartomatous polyps"	"disease"		"Disease or Syndrome"	"0.50"		"1997"	"2016"	"10"	"0"	"CLINGEN"
"6794"	"STK11"	"0.467"	"0.655"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.50"		"1998"	"1999"	"2"	"1"	"CTD_human;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.55"	"1"	"1998"	"2015"	"1"	"3"	"GENOMICS_ENGLAND;UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C3463918"	"EMBRYONAL CELL CARCINOMA"	"disease"		"Neoplastic Process"	"0.30"		"1998"	"1999"	"2"	"1"	"UNIPROT"
"6794"	"STK11"	"0.467"	"0.655"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2017"	"1"	"1"	"UNIPROT"
"6795"	"AURKC"	"0.72"	"0.276"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6795"	"AURKC"	"0.72"	"0.276"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6795"	"AURKC"	"0.72"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6795"	"AURKC"	"0.72"	"0.276"	"C0403812"	"Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa"	"disease"	"C12"	"Disease or Syndrome"	"0.60"		"2008"	"2012"	"0"	"3"	"CTD_human;ORPHANET"
"6795"	"AURKC"	"0.72"	"0.276"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6795"	"AURKC"	"0.72"	"0.276"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6799"	"SULT1A2"	"0.928"	"0.069"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6799"	"SULT1A2"	"0.928"	"0.069"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6804"	"STX1A"	"0.652"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"6804"	"STX1A"	"0.652"	"0.621"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6804"	"STX1A"	"0.652"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2004"	"2008"	"2"	"0"	"PSYGENET"
"6809"	"STX3"	"0.815"	"0.31"	"C0341306"	"Microvillus inclusion disease"	"disease"	"C05;C06;C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"6809"	"STX3"	"0.815"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6811"	"STX5"	"0.886"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.48"	"1"	"2010"	"2014"	"0"	"0"	"ORPHANET"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.50"	"0.8571429"	"2010"	"2017"	"0"	"13"	"ORPHANET"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.50"	"1"	"2010"	"2017"	"0"	"6"	"GENOMICS_ENGLAND"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.52"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"6812"	"STXBP1"	"0.596"	"0.483"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"6812"	"STXBP1"	"0.596"	"0.483"	"C2677326"	"Epileptic Encephalopathy, Early Infantile, 4"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"11"	"25"	"CTD_human;UNIPROT"
"6812"	"STXBP1"	"0.596"	"0.483"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6812"	"STXBP1"	"0.596"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6813"	"STXBP2"	"0.743"	"0.345"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6813"	"STXBP2"	"0.743"	"0.345"	"C0272199"	"Familial Hemophagocytic Lymphocytosis"	"phenotype"	"C15"	"Disease or Syndrome"	"0.40"		"2009"	"2014"	"0"	"1"	"ORPHANET"
"6813"	"STXBP2"	"0.743"	"0.345"	"C2751293"	"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2009"	"2017"	"2"	"6"	"CTD_human;UNIPROT"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2009"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"0.6666667"	"2001"	"2010"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6817"	"SULT1A1"	"0.564"	"0.517"	"C0919532"	"Genomic Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"ORPHANET"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6820"	"SULT2B1"	"0.663"	"0.31"	"C4539754"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14"	"disease"		"Congenital Abnormality"	"0.40"		"2007"	"2017"	"1"	"4"	"UNIPROT"
"6821"	"SUOX"	"0.667"	"0.448"	"C0268624"	"Sulfite oxidase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1998"	"2015"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"6821"	"SUOX"	"0.667"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"6821"	"SUOX"	"0.667"	"0.448"	"C2931746"	"Sulfocysteinuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1998"	"2002"	"5"	"7"	"CTD_human;ORPHANET;UNIPROT"
"6821"	"SUOX"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"6822"	"SULT2A1"	"0.611"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6822"	"SULT2A1"	"0.611"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6822"	"SULT2A1"	"0.611"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0020757"	"Ichthyoses"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0043345"	"Xeroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C0872084"	"Sarcopenia"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"6832"	"SUPV3L1"	"0.815"	"0.103"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9056604"	"1996"	"2018"	"2"	"3"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0027773"	"Nesidioblastosis"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.50"		"1996"	"2016"	"21"	"38"	"UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0271714"	"Hypoglycemia, leucine-induced"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"6833"	"ABCC8"	"0.508"	"0.69"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1832386"	"Diabetes Mellitus, Transient Neonatal, 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.55"	"1"	"2000"	"2015"	"0"	"0"	"ORPHANET"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1833102"	"DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES"	"disease"	"C10;C18;C19;C23"	"Disease or Syndrome"	"0.40"		"2006"	"2007"	"4"	"15"	"UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1833104"	"DIABETES MELLITUS, PERMANENT NEONATAL"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2015"	"4"	"19"	"CTD_human;ORPHANET;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1835887"	"DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.80"		"2000"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C1853564"	"Developmental Delay, Epilepsy, and Neonatal Diabetes"	"disease"	"C10;C16;C18;C19;C23;F01"	"Disease or Syndrome"	"0.56"	"1"	"2006"	"2013"	"4"	"15"	"ORPHANET;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C2931832"	"Hyperinsulinemic hypoglycemia, familial, 1"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.60"		"1976"	"2017"	"21"	"90"	"CTD_human;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C2931833"	"Hyperinsulinemic hypoglycemia, familial, 2"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6833"	"ABCC8"	"0.508"	"0.69"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6833"	"ABCC8"	"0.508"	"0.69"	"C3888018"	"Congenital Hyperinsulinism"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.70"	"0.972973"	"1995"	"2017"	"21"	"44"	"CTD_human;UNIPROT"
"6833"	"ABCC8"	"0.508"	"0.69"	"C4274080"	"Autosomal dominant hyperinsulinism due to SUR1 deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6834"	"SURF1"	"0.596"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9824561"	"1998"	"2018"	"7"	"16"	"CTD_human;UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"GENOMICS_ENGLAND"
"6834"	"SURF1"	"0.596"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6834"	"SURF1"	"0.596"	"0.483"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"6834"	"SURF1"	"0.596"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2013"	"6"	"5"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2013"	"6"	"5"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2013"	"6"	"5"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"		"1998"	"2013"	"6"	"7"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2013"	"6"	"5"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C1857355"	"Leigh syndrome , French Canadian type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6834"	"SURF1"	"0.596"	"0.483"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2013"	"6"	"5"	"UNIPROT"
"6834"	"SURF1"	"0.596"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6834"	"SURF1"	"0.596"	"0.483"	"C4225246"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6836"	"SURF4"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6836"	"SURF4"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6840"	"SVIL"	"0.857"	"0.103"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6840"	"SVIL"	"0.857"	"0.103"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6840"	"SVIL"	"0.857"	"0.103"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6843"	"VAMP1"	"0.735"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6843"	"VAMP1"	"0.735"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"6843"	"VAMP1"	"0.735"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"6843"	"VAMP1"	"0.735"	"0.276"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6843"	"VAMP1"	"0.735"	"0.276"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6843"	"VAMP1"	"0.735"	"0.276"	"C1970107"	"ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.60"		"2002"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"6843"	"VAMP1"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6844"	"VAMP2"	"0.762"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"6844"	"VAMP2"	"0.762"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6844"	"VAMP2"	"0.762"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6845"	"VAMP7"	"0.663"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"6845"	"VAMP7"	"0.663"	"0.379"	"C0343641"	"Human papilloma virus infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6845"	"VAMP7"	"0.663"	"0.379"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6845"	"VAMP7"	"0.663"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"6845"	"VAMP7"	"0.663"	"0.379"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6847"	"SYCP1"	"0.696"	"0.345"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6850"	"SYK"	"0.564"	"0.69"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2018"	"0"	"0"	"CGI"
"6850"	"SYK"	"0.564"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"6850"	"SYK"	"0.564"	"0.69"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6850"	"SYK"	"0.564"	"0.69"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"6853"	"SYN1"	"0.659"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"1995"	"2013"	"4"	"0"	"PSYGENET"
"6853"	"SYN1"	"0.659"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"1995"	"2013"	"4"	"0"	"PSYGENET"
"6853"	"SYN1"	"0.659"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"6853"	"SYN1"	"0.659"	"0.345"	"C1845343"	"Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders"	"disease"	"C10;C16;C23;F03"	"Disease or Syndrome"	"0.60"		"2004"	"2013"	"0"	"4"	"CTD_human;ORPHANET"
"6853"	"SYN1"	"0.659"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6854"	"SYN2"	"0.681"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2014"	"2"	"0"	"PSYGENET"
"6854"	"SYN2"	"0.681"	"0.276"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8571429"	"1991"	"2014"	"0"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6854"	"SYN2"	"0.681"	"0.276"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6855"	"SYP"	"0.55"	"0.69"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6855"	"SYP"	"0.55"	"0.69"	"C3275408"	"MENTAL RETARDATION, X-LINKED 96"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2017"	"4"	"2"	"CLINGEN;CTD_human;UNIPROT"
"6855"	"SYP"	"0.55"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6860"	"SYT4"	"0.857"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0008487"	"Chordoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"		"2008"	"2013"	"2"	"0"	"CTD_human;ORPHANET"
"6862"	"TBXT"	"0.735"	"0.103"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.31"		"2002"	"2002"	"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"6862"	"TBXT"	"0.735"	"0.103"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"6862"	"TBXT"	"0.735"	"0.103"	"C3810343"	"SACRAL AGENESIS WITH VERTEBRAL ANOMALIES"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"ORPHANET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"3"	"0"	"PSYGENET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0010034"	"Corneal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2015"	"5"	"0"	"PSYGENET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2015"	"5"	"0"	"PSYGENET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0013132"	"Drooling"	"phenotype"	"C07"	"Finding"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"1997"	"1998"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"1997"	"1998"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0017168"	"Gastroesophageal reflux disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1994"	"1999"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1987"	"2010"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"1997"	"2011"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"1"	"1993"	"2018"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0037036"	"Sialorrhea"	"disease"	"C07"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1999"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1999"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1994"	"1999"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"1992"	"1992"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1987"	"1997"	"2"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"1988"	"2013"	"5"	"0"	"PSYGENET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0556385"	"Craving for alcohol"	"phenotype"		"Finding"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6863"	"TAC1"	"0.473"	"0.793"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"1997"	"2012"	"5"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"2010"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"1997"	"2014"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1993"	"2009"	"3"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6863"	"TAC1"	"0.473"	"0.793"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1997"	"2009"	"9"	"0"	"CTD_human"
"6865"	"TACR2"	"0.762"	"0.345"	"C0006261"	"Bronchial Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6866"	"TAC3"	"0.648"	"0.483"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6866"	"TAC3"	"0.648"	"0.483"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.44"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"6866"	"TAC3"	"0.648"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.44"	"1"	"2009"	"2015"	"2"	"1"	"GENOMICS_ENGLAND"
"6866"	"TAC3"	"0.648"	"0.483"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6866"	"TAC3"	"0.648"	"0.483"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"6866"	"TAC3"	"0.648"	"0.483"	"C3553843"	"HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"6867"	"TACC1"	"0.799"	"0.103"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6867"	"TACC1"	"0.799"	"0.103"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6868"	"ADAM17"	"0.507"	"0.724"	"C0005758"	"Bulla"	"phenotype"	"C17;C23"	"Anatomical Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6868"	"ADAM17"	"0.507"	"0.724"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"6868"	"ADAM17"	"0.507"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6868"	"ADAM17"	"0.507"	"0.724"	"C3280501"	"INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"0"	"1"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"2008"	"2015"	"5"	"0"	"CTD_human;PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2009"	"2015"	"3"	"0"	"CTD_human;PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0006261"	"Bronchial Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.8"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.8"	"2003"	"2015"	"5"	"0"	"PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0"	"2006"	"2007"	"1"	"0"	"PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"1998"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2015"	"5"	"0"	"PSYGENET"
"6869"	"TACR1"	"0.559"	"0.724"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2012"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6869"	"TACR1"	"0.559"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human;PSYGENET"
"6870"	"TACR3"	"0.582"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"6870"	"TACR3"	"0.582"	"0.552"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.50"		"2007"	"2012"	"0"	"0"	"ORPHANET"
"6870"	"TACR3"	"0.582"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.63"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.44"	"1"	"2009"	"2015"	"2"	"1"	"GENOMICS_ENGLAND"
"6870"	"TACR3"	"0.582"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"6870"	"TACR3"	"0.582"	"0.552"	"C3553844"	"HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.80"		"2007"	"2015"	"3"	"7"	"CTD_human;UNIPROT"
"6872"	"TAF1"	"0.672"	"0.414"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"6872"	"TAF1"	"0.672"	"0.414"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6872"	"TAF1"	"0.672"	"0.414"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6872"	"TAF1"	"0.672"	"0.414"	"C1839130"	"Dystonia 3, Torsion, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.8823529"	"1992"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"6872"	"TAF1"	"0.672"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"6872"	"TAF1"	"0.672"	"0.414"	"C4225418"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC 33"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6873"	"TAF2"	"0.735"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6873"	"TAF2"	"0.735"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6873"	"TAF2"	"0.735"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6873"	"TAF2"	"0.735"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6873"	"TAF2"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2012"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6873"	"TAF2"	"0.735"	"0.276"	"C3810080"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6875"	"TAF4B"	"0.815"	"0.172"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"6875"	"TAF4B"	"0.815"	"0.172"	"C4014449"	"SPERMATOGENIC FAILURE 13"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6876"	"TAGLN"	"0.611"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6878"	"TAF6"	"0.762"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"6878"	"TAF6"	"0.762"	"0.345"	"C4310702"	"ALAZAMI-YUAN SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"6880"	"TAF9"	"0.886"	"0.172"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6880"	"TAF9"	"0.886"	"0.172"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6884"	"TAF13"	"0.752"	"0.276"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6884"	"TAF13"	"0.752"	"0.276"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6884"	"TAF13"	"0.752"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6884"	"TAF13"	"0.752"	"0.276"	"C4479476"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2017"	"2017"	"0"	"2"	"CTD_human;UNIPROT"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C0265293"	"Frontometaphyseal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C2931461"	"Forney Robinson Pascoe syndrome"	"disease"	"C05;C09;C10;C14;C16;C23"	"Disease or Syndrome"	"0.70"		"2010"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"6885"	"MAP3K7"	"0.541"	"0.724"	"C4310697"	"FRONTOMETAPHYSEAL DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2017"	"1"	"4"	"UNIPROT"
"6886"	"TAL1"	"0.572"	"0.483"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"6886"	"TAL1"	"0.572"	"0.483"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6886"	"TAL1"	"0.572"	"0.483"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.9891304"	"1990"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"6886"	"TAL1"	"0.572"	"0.483"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"1996"	"2012"	"0"	"0"	"CTD_human"
"6887"	"TAL2"	"0.815"	"0.103"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6887"	"TAL2"	"0.815"	"0.103"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6887"	"TAL2"	"0.815"	"0.103"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6888"	"TALDO1"	"0.614"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.41"		"2007"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"6888"	"TALDO1"	"0.614"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6888"	"TALDO1"	"0.614"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C1291329"	"Transaldolase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.64"	"1"	"2001"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"6888"	"TALDO1"	"0.614"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6888"	"TALDO1"	"0.614"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6890"	"TAP1"	"0.545"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6890"	"TAP1"	"0.545"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6890"	"TAP1"	"0.545"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6890"	"TAP1"	"0.545"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"6890"	"TAP1"	"0.545"	"0.759"	"C1858266"	"Bare Lymphocyte Syndrome, Type I"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6891"	"TAP2"	"0.555"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"6891"	"TAP2"	"0.555"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6891"	"TAP2"	"0.555"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2005"	"2014"	"2"	"0"	"PSYGENET"
"6891"	"TAP2"	"0.555"	"0.759"	"C1858266"	"Bare Lymphocyte Syndrome, Type I"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.51"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human;ORPHANET"
"6892"	"TAPBP"	"0.627"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6892"	"TAPBP"	"0.627"	"0.69"	"C1858266"	"Bare Lymphocyte Syndrome, Type I"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human;ORPHANET"
"6895"	"TARBP2"	"0.752"	"0.345"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6895"	"TARBP2"	"0.752"	"0.345"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6897"	"TARS"	"0.762"	"0.31"	"C0027121"	"Myositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6897"	"TARS"	"0.762"	"0.31"	"C0158353"	"Myositis, Infectious"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6897"	"TARS"	"0.762"	"0.31"	"C0544796"	"Myositis, Proliferative"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6897"	"TARS"	"0.762"	"0.31"	"C0751356"	"Idiopathic Inflammatory Myopathies"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6897"	"TARS"	"0.762"	"0.31"	"C0751357"	"Myositis, Focal"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6898"	"TAT"	"0.527"	"0.759"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6898"	"TAT"	"0.527"	"0.759"	"C0268483"	"Tyrosinemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1984"	"2012"	"0"	"0"	"CTD_human"
"6898"	"TAT"	"0.527"	"0.759"	"C0268487"	"Tyrosine Transaminase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1987"	"2013"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6898"	"TAT"	"0.527"	"0.759"	"C0268490"	"Tyrosinemia, Type I"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6898"	"TAT"	"0.527"	"0.759"	"C0268623"	"Tyrosinemia, Type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6898"	"TAT"	"0.527"	"0.759"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6898"	"TAT"	"0.527"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"1982"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"6899"	"TBX1"	"0.479"	"0.724"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2017"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.62"	"1"	"2006"	"2016"	"0"	"1"	"CTD_human;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.40"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"6899"	"TBX1"	"0.479"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6899"	"TBX1"	"0.479"	"0.724"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"2"	"0"	"PSYGENET"
"6899"	"TBX1"	"0.479"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1997"	"2016"	"5"	"1"	"PSYGENET"
"6899"	"TBX1"	"0.479"	"0.724"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.46"	"0.6666667"	"1995"	"2016"	"1"	"0"	"CTD_human"
"6899"	"TBX1"	"0.479"	"0.724"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.50"				"0"	"1"	"CTD_human;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.60"				"0"	"1"	"CTD_human;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"1.00"	"0.9767442"	"1996"	"2017"	"5"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"2"	"0"	"PSYGENET"
"6899"	"TBX1"	"0.479"	"0.724"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"6899"	"TBX1"	"0.479"	"0.724"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6899"	"TBX1"	"0.479"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2007"	"2"	"0"	"PSYGENET"
"6899"	"TBX1"	"0.479"	"0.724"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.61"	"1"	"2004"	"2006"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6899"	"TBX1"	"0.479"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"0"	"0"	"UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"1995"	"1995"	"0"	"1"	"CTD_human;UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C1861129"	"Takao VCF Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"6899"	"TBX1"	"0.479"	"0.724"	"C2675369"	"Chromosome 22q11.2 Microduplication Syndrome"	"disease"	"C05;C14;C15;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6899"	"TBX1"	"0.479"	"0.724"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.39"	"0.8888889"	"1997"	"2013"	"0"	"0"	"ORPHANET"
"6899"	"TBX1"	"0.479"	"0.724"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"6900"	"CNTN2"	"0.611"	"0.552"	"C1832841"	"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6900"	"CNTN2"	"0.611"	"0.552"	"C3809374"	"EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"2"	"CTD_human"
"6901"	"TAZ"	"0.543"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.46"	"1"	"2002"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6901"	"TAZ"	"0.543"	"0.655"	"C0574083"	"3-Methylglutaconic aciduria type 2"	"disease"	"C14;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9574468"	"1973"	"2017"	"5"	"18"	"CTD_human;ORPHANET;UNIPROT"
"6901"	"TAZ"	"0.543"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"6901"	"TAZ"	"0.543"	"0.655"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"6902"	"TBCA"	"0.735"	"0.483"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"6904"	"TBCD"	"0.681"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6904"	"TBCD"	"0.681"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6904"	"TBCD"	"0.681"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"6904"	"TBCD"	"0.681"	"0.345"	"C4310671"	"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2017"	"4"	"14"	"CTD_human;ORPHANET;UNIPROT"
"6905"	"TBCE"	"0.596"	"0.586"	"C0004623"	"Bacterial Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6905"	"TBCE"	"0.596"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6905"	"TBCE"	"0.596"	"0.586"	"C0029464"	"Osteosclerosis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"6905"	"TBCE"	"0.596"	"0.586"	"C0265291"	"Kenny-Caffey syndrome"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"6905"	"TBCE"	"0.596"	"0.586"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6905"	"TBCE"	"0.596"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6905"	"TBCE"	"0.596"	"0.586"	"C1855648"	"KENNY-CAFFEY SYNDROME, TYPE 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2002"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"6905"	"TBCE"	"0.596"	"0.586"	"C1855840"	"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME"	"disease"	"C05;C10;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.63"	"1"	"2002"	"2016"	"1"	"3"	"CTD_human;ORPHANET"
"6905"	"TBCE"	"0.596"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"6905"	"TBCE"	"0.596"	"0.586"	"C4310667"	"ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"6905"	"TBCE"	"0.596"	"0.586"	"C4316787"	"Kenny-Caffey syndrome, type 2"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6906"	"SERPINA7"	"0.672"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6906"	"SERPINA7"	"0.672"	"0.379"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"6907"	"TBL1X"	"0.701"	"0.414"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6907"	"TBL1X"	"0.701"	"0.414"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"6907"	"TBL1X"	"0.701"	"0.414"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6908"	"TBP"	"0.564"	"0.793"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"6908"	"TBP"	"0.564"	"0.793"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"0.8"	"2004"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"6908"	"TBP"	"0.564"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"6908"	"TBP"	"0.564"	"0.793"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9"	"2003"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"6908"	"TBP"	"0.564"	"0.793"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6908"	"TBP"	"0.564"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"6910"	"TBX5"	"0.592"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6910"	"TBX5"	"0.592"	"0.586"	"C0265239"	"Wildervanck's syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6910"	"TBX5"	"0.592"	"0.586"	"C0265264"	"Holt-Oram syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"1.00"	"0.9583333"	"1997"	"2017"	"7"	"8"	"CTD_human;ORPHANET;UNIPROT"
"6910"	"TBX5"	"0.592"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6910"	"TBX5"	"0.592"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"1996"	"1996"	"1"	"0"	"GENOMICS_ENGLAND"
"6911"	"TBX6"	"0.713"	"0.31"	"C4083048"	"SPONDYLOCOSTAL DYSOSTOSIS 5"	"disease"		"Disease or Syndrome"	"0.70"		"1985"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"6911"	"TBX6"	"0.713"	"0.31"	"C4274761"	"Autosomal dominant spondylocostal dysostosis"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"6913"	"TBX15"	"0.633"	"0.483"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6913"	"TBX15"	"0.633"	"0.483"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"6913"	"TBX15"	"0.633"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6913"	"TBX15"	"0.633"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6913"	"TBX15"	"0.633"	"0.483"	"C1850040"	"Pelviscapular dysplasia"	"disease"	"C05"	"Disease or Syndrome"	"0.52"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"6913"	"TBX15"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0005818"	"Blood Platelet Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"2010"	"2"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0019087"	"Hemorrhagic Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.32"	"0.5"	"2006"	"2010"	"2"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C3279614"	"BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"1987"	"2012"	"2"	"3"	"ORPHANET;UNIPROT"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C3501679"	"Bleeding Disorder due to Defective Thromboxane A2 Receptor"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6915"	"TBXA2R"	"0.627"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C0398635"	"Thromboxane synthetase deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C1856465"	"Ghosal Hematodiaphyseal Dysplasia"	"disease"	"C05;C15;C16"	"Congenital Abnormality"	"0.70"		"2008"	"2008"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"6916"	"TBXAS1"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6919"	"TCEA2"	"0.799"	"0.138"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6919"	"TCEA2"	"0.799"	"0.138"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6919"	"TCEA2"	"0.799"	"0.138"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.42"	"1"	"2013"	"2017"	"1"	"2"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6921"	"ELOC"	"0.707"	"0.241"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.45"	"0.6"	"1999"	"2014"	"5"	"1"	"PSYGENET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0016781"	"Fuchs Endothelial Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"2010"	"2017"	"0"	"1"	"ORPHANET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6925"	"TCF4"	"0.494"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1999"	"2018"	"4"	"6"	"PSYGENET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6925"	"TCF4"	"0.494"	"0.655"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"6925"	"TCF4"	"0.494"	"0.655"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C1970431"	"PITT-HOPKINS SYNDROME"	"disease"	"C08;C10;C23;F01;F03"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"8"	"32"	"CTD_human;ORPHANET;UNIPROT"
"6925"	"TCF4"	"0.494"	"0.655"	"C2750451"	"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2007"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"6925"	"TCF4"	"0.494"	"0.655"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6925"	"TCF4"	"0.494"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.55"	"1"	"2004"	"2016"	"1"	"0"	"CGI;CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6926"	"TBX3"	"0.588"	"0.655"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6926"	"TBX3"	"0.588"	"0.655"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.55"	"1"	"2004"	"2016"	"1"	"0"	"CGI;CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"6926"	"TBX3"	"0.588"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6926"	"TBX3"	"0.588"	"0.655"	"C1866994"	"Ulnar-mammary syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1997"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"6926"	"TBX3"	"0.588"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"6926"	"TBX3"	"0.588"	"0.655"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.42"	"1"	"1994"	"1999"	"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"1"	"1998"	"2017"	"1"	"1"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"1"	"1998"	"2016"	"0"	"2"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9381443"	"1995"	"2018"	"1"	"3"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9166667"	"2003"	"2016"	"0"	"0"	"CGI"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"				"0"	"1"	"CGI;CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9913793"	"1995"	"2018"	"0"	"0"	"ORPHANET"
"6927"	"HNF1A"	"0.515"	"0.621"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1838100"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.90"	"0.96875"	"1997"	"2018"	"17"	"35"	"CTD_human;UNIPROT"
"6927"	"HNF1A"	"0.515"	"0.621"	"C1840646"	"Hepatic Adenomas, Familial"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.962963"	"1990"	"2016"	"0"	"0"	"CGI;UNIPROT"
"6927"	"HNF1A"	"0.515"	"0.621"	"C2675866"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.60"		"1997"	"1999"	"3"	"3"	"CTD_human;UNIPROT"
"6927"	"HNF1A"	"0.515"	"0.621"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6927"	"HNF1A"	"0.515"	"0.621"	"C4303475"	"Hyperinsulinism due to HNF1A deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6927"	"HNF1A"	"0.515"	"0.621"	"C4518333"	"Clear cell papillary renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.37"	"0.8571429"	"1999"	"2017"	"0"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9615385"	"1999"	"2017"	"2"	"7"	"CTD_human;UNIPROT"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2004"	"2008"	"2"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.7272727"	"2007"	"2013"	"2"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C0431693"	"Renal cysts and diabetes syndrome"	"disease"	"C10;C12;C13;C18;C19"	"Disease or Syndrome"	"0.80"	"1"	"1983"	"2018"	"10"	"26"	"CTD_human;ORPHANET;UNIPROT"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"1997"	"2015"	"11"	"0"	"GENOMICS_ENGLAND"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"		"2005"	"2005"	"0"	"1"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1567426"	"Unilateral Multicystic Dysplastic Kidney"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1567427"	"Bilateral Multicystic Dysplastic Kidneys"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1835171"	"Hypomagnesemia 2, renal"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1840451"	"MULTICYSTIC RENAL DYSPLASIA, BILATERAL"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"6928"	"HNF1B"	"0.526"	"0.621"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"6928"	"HNF1B"	"0.526"	"0.621"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C3281138"	"CHROMOSOME 17q12 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6928"	"HNF1B"	"0.526"	"0.621"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"6928"	"HNF1B"	"0.526"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6929"	"TCF3"	"0.58"	"0.621"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.55"	"1"	"1990"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"6929"	"TCF3"	"0.58"	"0.621"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"0.7142857"	"1990"	"2016"	"1"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"1990"	"2007"	"2"	"0"	"CTD_human"
"6929"	"TCF3"	"0.58"	"0.621"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.32"	"0.5"	"1991"	"1999"	"0"	"0"	"ORPHANET"
"6929"	"TCF3"	"0.58"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"6929"	"TCF3"	"0.58"	"0.621"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6929"	"TCF3"	"0.58"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6932"	"TCF7"	"0.59"	"0.448"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2016"	"1"	"2"	"PSYGENET"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2006"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.88"	"2002"	"2016"	"2"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"0.75"	"2008"	"2017"	"1"	"2"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9611307"	"2006"	"2018"	"3"	"11"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2018"	"4"	"0"	"PSYGENET"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.9166667"	"1999"	"2018"	"2"	"1"	"CTD_human;UNIPROT"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2015"	"2017"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6934"	"TCF7L2"	"0.538"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.969697"	"2005"	"2017"	"2"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0016781"	"Fuchs Endothelial Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.38"	"0.75"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0339284"	"Polymorphous corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"2006"	"2017"	"0"	"1"	"ORPHANET"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.96875"	"2005"	"2017"	"2"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C1836724"	"CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2003"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"6935"	"ZEB1"	"0.501"	"0.621"	"C2750448"	"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2010"	"2016"	"3"	"7"	"CTD_human;UNIPROT"
"6935"	"ZEB1"	"0.501"	"0.621"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6935"	"ZEB1"	"0.501"	"0.621"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"2013"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"6938"	"TCF12"	"0.633"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"6938"	"TCF12"	"0.633"	"0.414"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"6938"	"TCF12"	"0.633"	"0.414"	"C0265529"	"Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"6938"	"TCF12"	"0.633"	"0.414"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C1275278"	"Extraskeletal Myxoid Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2003"	"0"	"0"	"ORPHANET"
"6938"	"TCF12"	"0.633"	"0.414"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"6938"	"TCF12"	"0.633"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"6938"	"TCF12"	"0.633"	"0.414"	"C3715051"	"CRANIOSYNOSTOSIS 3"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2016"	"2"	"13"	"UNIPROT"
"6939"	"TCF15"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6939"	"TCF15"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"6941"	"TCF19"	"0.707"	"0.517"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6941"	"TCF19"	"0.707"	"0.517"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"6942"	"TCF20"	"0.815"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"6942"	"TCF20"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"6943"	"TCF21"	"0.633"	"0.448"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"2"	"0"	"CTD_human"
"6943"	"TCF21"	"0.633"	"0.448"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"2"	"2"	"CTD_human"
"6944"	"VPS72"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6945"	"MLX"	"0.727"	"0.276"	"C0039263"	"Takayasu Arteritis"	"disease"	"C14;C17"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"ORPHANET"
"6947"	"TCN1"	"0.713"	"0.414"	"C0002888"	"Anemia, Megaloblastic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1972"	"1972"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0002888"	"Anemia, Megaloblastic"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"1972"	"2004"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0270612"	"Leukoencephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C0342701"	"Transcobalamin II deficiency"	"disease"		"Disease or Syndrome"	"0.63"	"0.6666667"	"1984"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"6948"	"TCN2"	"0.592"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"6948"	"TCN2"	"0.592"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1994"	"2014"	"5"	"0"	"GENOMICS_ENGLAND"
"6949"	"TCOF1"	"0.621"	"0.448"	"C0242387"	"Mandibulofacial Dysostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.90"	"0.952381"	"1997"	"2016"	"2"	"0"	"CTD_human;ORPHANET;UNIPROT"
"6949"	"TCOF1"	"0.621"	"0.448"	"C0265241"	"Franceschetti-Klein syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"6949"	"TCOF1"	"0.621"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.35"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"6949"	"TCOF1"	"0.621"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"6949"	"TCOF1"	"0.621"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"6950"	"TCP1"	"0.701"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"6950"	"TCP1"	"0.701"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6950"	"TCP1"	"0.701"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"6950"	"TCP1"	"0.701"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"6955"	"TRA"	"0.645"	"0.517"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"6955"	"TRA"	"0.645"	"0.517"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"0"	"2010"	"2013"	"1"	"0"	"CTD_human"
"6955"	"TRA"	"0.645"	"0.517"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2007"	"0"	"0"	"ORPHANET"
"6957"	"TRB"	"0.667"	"0.517"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"ORPHANET"
"6964"	"TRD"	"0.762"	"0.345"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2008"	"0"	"0"	"ORPHANET"
"6965"	"TRG"	"0.676"	"0.379"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"1987"	"2014"	"0"	"0"	"ORPHANET"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0175707"	"Asplenia Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0265357"	"Polysplenia Syndrome"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2002"	"2002"	"1"	"0"	"CTD_human;ORPHANET"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2002"	"2002"	"1"	"0"	"CTD_human;ORPHANET"
"6997"	"TDGF1"	"0.6"	"0.552"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2002"	"2002"	"1"	"0"	"CTD_human;ORPHANET"
"6997"	"TDGF1"	"0.6"	"0.552"	"C3178805"	"Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C3178806"	"Right Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6997"	"TDGF1"	"0.6"	"0.552"	"C3178807"	"Left Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"6999"	"TDO2"	"0.713"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"6999"	"TDO2"	"0.713"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C0038187"	"Starvation"	"phenotype"	"C18"	"Finding"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"6999"	"TDO2"	"0.713"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.8"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C0220702"	"SCHIZOPHRENIA 1 (disorder)"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.8"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"6999"	"TDO2"	"0.713"	"0.276"	"C2931837"	"Familial hypertryptophanemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2017"	"2017"	"1"	"1"	"ORPHANET;UNIPROT"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2003"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7001"	"PRDX2"	"0.535"	"0.759"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7003"	"TEAD1"	"0.59"	"0.552"	"C1862382"	"SVEINSSON CHORIORETINAL ATROPHY"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.72"	"1"	"2004"	"2015"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7006"	"TEC"	"0.928"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7007"	"TECTA"	"0.727"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"7007"	"TECTA"	"0.727"	"0.31"	"C1832187"	"Deafness, Autosomal Dominant 12"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"1998"	"2014"	"2"	"20"	"CTD_human;UNIPROT"
"7007"	"TECTA"	"0.727"	"0.31"	"C1863655"	"Deafness, Autosomal Recessive 21"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"				"0"	"3"	"CTD_human"
"7008"	"TEF"	"0.773"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7008"	"TEF"	"0.773"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2017"	"1"	"0"	"PSYGENET"
"7010"	"TEK"	"0.511"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2017"	"0"	"0"	"UNIPROT"
"7010"	"TEK"	"0.511"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7010"	"TEK"	"0.511"	"0.655"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2004"	"2008"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0020302"	"Hydrophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7010"	"TEK"	"0.511"	"0.655"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2002"	"2007"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7010"	"TEK"	"0.511"	"0.655"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7010"	"TEK"	"0.511"	"0.655"	"C0346072"	"Blue rubber bleb nevus syndrome"	"disease"	"C04;C06;C17"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"7010"	"TEK"	"0.511"	"0.655"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7010"	"TEK"	"0.511"	"0.655"	"C1832977"	"GLAUCOMA 3, PRIMARY INFANTILE, B"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7010"	"TEK"	"0.511"	"0.655"	"C1838437"	"VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.73"	"1"	"1993"	"2016"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7010"	"TEK"	"0.511"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7010"	"TEK"	"0.511"	"0.655"	"C4310639"	"GLAUCOMA 3, PRIMARY CONGENITAL, E"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"7011"	"TEP1"	"0.652"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"7011"	"TEP1"	"0.652"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2006"	"2011"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7012"	"TERC"	"0.514"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"7012"	"TERC"	"0.514"	"0.655"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7012"	"TERC"	"0.514"	"0.655"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"	"0.9375"	"2003"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"7012"	"TERC"	"0.514"	"0.655"	"C0348890"	"Aplastic anemia, idiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7012"	"TERC"	"0.514"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7012"	"TERC"	"0.514"	"0.655"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2015"	"3"	"1"	"CTD_human;ORPHANET"
"7012"	"TERC"	"0.514"	"0.655"	"C1851970"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2014"	"0"	"16"	"CTD_human"
"7012"	"TERC"	"0.514"	"0.655"	"C3553622"	"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"5"	"CTD_human"
"7014"	"TERF2"	"0.59"	"0.552"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"0.5"	"2006"	"2008"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.69"	"1"	"1993"	"2013"	"5"	"11"	"CTD_human;UNIPROT"
"7015"	"TERT"	"0.393"	"0.828"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9090909"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.92"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.96"	"2002"	"2017"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.96"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"		"2007"	"2009"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0010314"	"Cri-du-Chat Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9803922"	"2004"	"2018"	"2"	"1"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.36"	"0.8333333"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2009"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2017"	"1"	"1"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"0.75"	"2015"	"2018"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.9"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"7015"	"TERT"	"0.393"	"0.828"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9756098"	"2001"	"2016"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"2005"	"2016"	"3"	"2"	"CTD_human;ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2005"	"2008"	"2"	"0"	"GENOMICS_ENGLAND"
"7015"	"TERT"	"0.393"	"0.828"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0346037"	"Acral Lentiginous Malignant Melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7015"	"TERT"	"0.393"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0348890"	"Aplastic anemia, idiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"0"	"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7015"	"TERT"	"0.393"	"0.828"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.50"	"1"	"2003"	"2017"	"1"	"1"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.962963"	"2002"	"2018"	"1"	"7"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2008"	"2013"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"3"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"7015"	"TERT"	"0.393"	"0.828"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2009"	"2017"	"0"	"2"	"CGI"
"7015"	"TERT"	"0.393"	"0.828"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.69"	"1"	"1993"	"2015"	"4"	"12"	"CTD_human;ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.52"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C1851970"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.44"	"1"	"1993"	"2007"	"0"	"4"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9827586"	"1998"	"2018"	"4"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7015"	"TERT"	"0.393"	"0.828"	"C2684859"	"APLASTIC ANEMIA, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2005"	"2010"	"4"	"6"	"UNIPROT"
"7015"	"TERT"	"0.393"	"0.828"	"C3151443"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2017"	"5"	"9"	"CTD_human;UNIPROT"
"7015"	"TERT"	"0.393"	"0.828"	"C3151444"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2008"	"5"	"7"	"CTD_human;UNIPROT"
"7015"	"TERT"	"0.393"	"0.828"	"C3553617"	"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2015"	"5"	"16"	"CTD_human;UNIPROT"
"7015"	"TERT"	"0.393"	"0.828"	"C3554574"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7015"	"TERT"	"0.393"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7015"	"TERT"	"0.393"	"0.828"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"7016"	"TESK1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7018"	"TF"	"0.548"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2012"	"2"	"1"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0013502"	"Echinococcosis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2005"	"2011"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0035258"	"Restless Legs Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7018"	"TF"	"0.548"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.3333333"	"2007"	"2012"	"3"	"0"	"PSYGENET"
"7018"	"TF"	"0.548"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2012"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0271901"	"Microcytic hypochromic anemia (disorder)"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0282193"	"Iron Overload"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0521802"	"Congenital atransferrinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.91"	"1"	"1988"	"2008"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7018"	"TF"	"0.548"	"0.724"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1999"	"2006"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C3277918"	"TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.50"		"1988"	"2004"	"2"	"2"	"UNIPROT"
"7018"	"TF"	"0.548"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7018"	"TF"	"0.548"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.35"	"0.8"	"2005"	"2014"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0006079"	"Bowen's Disease"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7019"	"TFAM"	"0.565"	"0.655"	"C4310690"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8947368"	"1998"	"2013"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0265234"	"Branchio-Oto-Renal Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0376524"	"Branchio-Oculo-Facial Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2016"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2011"	"2"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.952381"	"1998"	"2013"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C1970479"	"Branchiootorenal Syndrome 2"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7020"	"TFAP2A"	"0.502"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.66"	"0.8333333"	"2000"	"2014"	"2"	"0"	"CTD_human;ORPHANET"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C1868570"	"CHAR SYNDROME"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.96"	"0.8333333"	"1993"	"2018"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2009"	"2"	"0"	"CTD_human"
"7021"	"TFAP2B"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7022"	"TFAP2C"	"0.752"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7022"	"TFAP2C"	"0.752"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7022"	"TFAP2C"	"0.752"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7022"	"TFAP2C"	"0.752"	"0.276"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7024"	"TFCP2"	"0.785"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"7024"	"TFCP2"	"0.785"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"7025"	"NR2F1"	"0.696"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7025"	"NR2F1"	"0.696"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2014"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7025"	"NR2F1"	"0.696"	"0.517"	"C3810363"	"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0344735"	"Partial atrioventricular canal"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7026"	"NR2F2"	"0.6"	"0.483"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7026"	"NR2F2"	"0.6"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7026"	"NR2F2"	"0.6"	"0.483"	"C4014310"	"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"7027"	"TFDP1"	"0.69"	"0.379"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7027"	"TFDP1"	"0.69"	"0.379"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7027"	"TFDP1"	"0.69"	"0.379"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7029"	"TFDP2"	"0.72"	"0.345"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"1"	"1997"	"2018"	"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C0206657"	"Alveolar Soft Part Sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"7030"	"TFE3"	"0.616"	"0.448"	"C0206732"	"Epithelioid hemangioendothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2013"	"2017"	"0"	"0"	"ORPHANET"
"7030"	"TFE3"	"0.616"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2017"	"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7030"	"TFE3"	"0.616"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"1993"	"2002"	"0"	"0"	"CTD_human"
"7030"	"TFE3"	"0.616"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7030"	"TFE3"	"0.616"	"0.448"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7031"	"TFF1"	"0.542"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7031"	"TFF1"	"0.542"	"0.655"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7031"	"TFF1"	"0.542"	"0.655"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"0"	"0"	"UNIPROT"
"7032"	"TFF2"	"0.636"	"0.448"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C0019188"	"Hepatitis, Animal"	"disease"	"C06;C22"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7033"	"TFF3"	"0.554"	"0.793"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0001883"	"Airway Obstruction"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0008301"	"Choking"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0034155"	"Purpura, Thrombotic Thrombocytopenic"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2001"	"2008"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0600433"	"Activated Protein C Resistance"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"		"2001"	"2008"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C1268935"	"Congenital Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C1956258"	"Familial Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7035"	"TFPI"	"0.507"	"0.759"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7036"	"TFR2"	"0.594"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7036"	"TFR2"	"0.594"	"0.517"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"4"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7036"	"TFR2"	"0.594"	"0.517"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7036"	"TFR2"	"0.594"	"0.517"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2017"	"4"	"1"	"CTD_human"
"7036"	"TFR2"	"0.594"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7036"	"TFR2"	"0.594"	"0.517"	"C1858664"	"HEMOCHROMATOSIS, TYPE 3"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.99"	"1"	"1993"	"2014"	"2"	"15"	"CTD_human;ORPHANET;UNIPROT"
"7037"	"TFRC"	"0.471"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0003756"	"Arenaviridae Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"1990"	"2008"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2000"	"2016"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0012715"	"Iron Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0162316"	"Iron deficiency anemia"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.34"	"1"	"1990"	"2016"	"3"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0205671"	"Infections, Arenavirus"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2000"	"2016"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7037"	"TFRC"	"0.471"	"0.759"	"C4225219"	"IMMUNODEFICIENCY 46"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7038"	"TG"	"0.537"	"0.724"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"0.9"	"1994"	"2016"	"1"	"0"	"CTD_human"
"7038"	"TG"	"0.537"	"0.724"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"7038"	"TG"	"0.537"	"0.724"	"C0018021"	"Goiter"	"phenotype"	"C19"	"Pathologic Function"	"0.42"		"1993"	"2014"	"2"	"0"	"CTD_human"
"7038"	"TG"	"0.537"	"0.724"	"C0342194"	"Thyroid Dyshormonogenesis 3"	"disease"	"C19"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"6"	"13"	"CTD_human;UNIPROT"
"7038"	"TG"	"0.537"	"0.724"	"C0920350"	"Autoimmune thyroiditis"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.40"	"0.75"	"1995"	"2018"	"1"	"0"	"CTD_human"
"7038"	"TG"	"0.537"	"0.724"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7039"	"TGFA"	"0.447"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"0.7777778"	"1993"	"2015"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.31"		"2003"	"2008"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7039"	"TGFA"	"0.447"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2001"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1991"	"1999"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.39"	"1"	"1990"	"2015"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2005"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0162770"	"Right Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2002"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2010"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0333355"	"Inflammatory disease of mucous membrane"	"group"	"C06;C07"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2011"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"2"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C3711374"	"Nonsyndromic Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7039"	"TGFA"	"0.447"	"0.724"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"	"0.974359"	"1994"	"2018"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.31"		"2005"	"2007"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0007140"	"Carcinosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9642857"	"1994"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.58"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.972973"	"1996"	"2017"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.50"		"2007"	"2008"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0011989"	"Camurati-Engelmann Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0013238"	"Dry Eye Syndromes"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2012"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"1999"	"2015"	"6"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.34"	"0.75"	"1997"	"2010"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"1991"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"2000"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2004"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0021290"	"Neonatal disorder"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.38"		"2002"	"2010"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.59"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1991"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2003"	"2016"	"5"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.56"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"0.8333333"	"1994"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2012"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.67"	"1"	"1996"	"2017"	"1"	"1"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2016"	"5"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9846154"	"1995"	"2018"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2003"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0030354"	"Papilloma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1994"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0030848"	"Peyronie Disease"	"disease"	"C12;C17"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.50"		"2004"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.70"	"1"	"1991"	"2018"	"7"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"0"	"2005"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2008"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.38"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.39"	"0.8888889"	"1991"	"2018"	"7"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2010"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0158266"	"Intervertebral Disc Degeneration"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205874"	"Papilloma, Squamous Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0205875"	"Papillomatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.952381"	"1992"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2018"	"3"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"0"	"2005"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0265287"	"Acromicric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.952381"	"1996"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.96875"	"1996"	"2018"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0455503"	"H/O: depression"	"phenotype"		"Finding"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0521607"	"Peritoneal Fibrosis"	"disease"	"C06;C23"	"Disease or Syndrome"	"0.34"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0600519"	"Ventricular Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0600520"	"Left Ventricle Remodeling"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0878576"	"Posterior Leukoencephalopathy Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C0917713"	"Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9642857"	"1994"	"2018"	"1"	"1"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2015"	"6"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9622642"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2717759"	"Degenerative Intervertebral Discs"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2717859"	"Peritoneal Sclerosis"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C2717860"	"Encapsulating Peritoneal Sclerosis"	"disease"	"C06;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3160858"	"Posterior reversible encephalopathy syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3489726"	"Geleophysic dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3542021"	"Duchenne and Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7040"	"TGFB1"	"0.336"	"0.931"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2001"	"2016"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0010520"	"Cyanosis"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.38"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2015"	"3"	"0"	"CLINGEN"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0035238"	"Congenital abnormality of respiratory system"	"group"	"C08;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0041956"	"Ureteral obstruction"	"phenotype"	"C12;C13"	"Anatomical Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0042063"	"Urogenital Abnormalities"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C1836635"	"Loeys-Dietz Aortic Aneurysm Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C2697932"	"Loeys-Dietz Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.65"	"1"	"2012"	"2016"	"1"	"3"	"CTD_human"
"7042"	"TGFB2"	"0.48"	"0.793"	"C3553762"	"LOEYS-DIETZ SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"2"	"7"	"UNIPROT"
"7042"	"TGFB2"	"0.48"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.37"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2015"	"3"	"0"	"CLINGEN"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0035238"	"Congenital abnormality of respiratory system"	"group"	"C08;C16"	"Congenital Abnormality"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2003"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C1836635"	"Loeys-Dietz Aortic Aneurysm Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.35"	"1"	"1996"	"2016"	"2"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C1862511"	"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"1"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C2697932"	"Loeys-Dietz Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C3711374"	"Nonsyndromic Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7043"	"TGFB3"	"0.535"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7043"	"TGFB3"	"0.535"	"0.724"	"C3810012"	"RIENHOFF SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"1"	"6"	"UNIPROT"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C0175707"	"Asplenia Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C0265357"	"Polysplenia Syndrome"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.50"		"1999"	"1999"	"1"	"0"	"CTD_human;ORPHANET"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C1866091"	"Left-Right Axis Malformations"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"1"	"UNIPROT"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C3178805"	"Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C3178806"	"Right Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7044"	"LEFTY2"	"0.752"	"0.172"	"C3178807"	"Left Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0339278"	"Reis-Bucklers' corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"0.9333333"	"1998"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C0521723"	"Corneal dystrophy, epithelial basement membrane"	"disease"	"C10;C11;C14"	"Disease or Syndrome"	"0.70"		"2006"	"2006"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1275685"	"Avellino corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"1"	"1997"	"2016"	"6"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1562894"	"Thiel-Behnke corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.75"	"1"	"1997"	"2016"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1641846"	"Groenouw corneal dystrophy type I (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.73"	"1"	"1997"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1690006"	"Lattice corneal dystrophy Type I"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"0.9512195"	"1997"	"2016"	"9"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1837974"	"Corneal Dystrophy, Lattice Type IIIA"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.63"	"1"	"1991"	"2011"	"2"	"2"	"CTD_human;UNIPROT"
"7045"	"TGFBI"	"0.51"	"0.724"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"1998"	"2006"	"5"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0002949"	"Aneurysm, Dissecting"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2018"	"8"	"0"	"CLINGEN"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2011"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0340643"	"Dissection of aorta"	"disease"	"C14"	"Pathologic Function"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0546476"	"Multiple self-healing squamous epithelioma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.74"	"1"	"1971"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9047619"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C1836635"	"Loeys-Dietz Aortic Aneurysm Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.83"	"1"	"2005"	"2014"	"8"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C2674127"	"LOEYS-DIETZ SYNDROME, TYPE 2A (disorder)"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2012"	"6"	"6"	"UNIPROT"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C2697932"	"Loeys-Dietz Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.90"	"1"	"2006"	"2016"	"2"	"6"	"CTD_human;ORPHANET"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C2931764"	"Furlong syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2012"	"6"	"6"	"UNIPROT"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C4083047"	"MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2011"	"2011"	"1"	"3"	"UNIPROT"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C4277533"	"Dissection, Blood Vessel"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7046"	"TGFBR1"	"0.495"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0002949"	"Aneurysm, Dissecting"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2012"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0003486"	"Aortic Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9444444"	"1995"	"2018"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"1995"	"2008"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.32"		"1998"	"2004"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"		"2000"	"2000"	"1"	"0"	"CGI;CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0015672"	"Fatigue"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0019294"	"Hernia, Inguinal"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0019295"	"Inguinal Hernia, Direct"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0019296"	"Inguinal Hernia, Indirect"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.60"	"0.9333333"	"1995"	"2018"	"14"	"0"	"CLINGEN;CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.53"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0086525"	"Lassitude"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.42"	"0"	"2006"	"2014"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.61"	"1"	"2000"	"2000"	"1"	"1"	"CGI;UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0340630"	"Aortic Aneurysm, Thoracoabdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0340643"	"Dissection of aorta"	"disease"	"C14"	"Pathologic Function"	"0.42"	"1"	"2006"	"2011"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.34"	"1"	"2006"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.58"	"1"	"1999"	"2015"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"		"2000"	"2000"	"1"	"1"	"CGI;CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1995"	"2018"	"0"	"0"	"CGI"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1995"	"2016"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.59"	"1"	"1995"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2010"	"2"	"1"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9615385"	"1995"	"2017"	"0"	"0"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1995"	"2016"	"2"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1836635"	"Loeys-Dietz Aortic Aneurysm Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.73"	"1"	"2004"	"2014"	"5"	"0"	"CTD_human;ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C1860896"	"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.60"		"1995"	"2005"	"1"	"3"	"CTD_human;UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C2674574"	"Aortic aneurysm, familial thoracic 3"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.50"		"2004"	"2012"	"10"	"15"	"CTD_human;UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C2697932"	"Loeys-Dietz Syndrome"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.90"	"1"	"2004"	"2017"	"5"	"13"	"CTD_human;ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C2751126"	"AERODIGESTIVE TRACT CANCER, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C2931058"	"Marfan Syndrome type 2"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2011"	"0"	"0"	"ORPHANET"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C3149254"	"ESCC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C3149255"	"GASTRIC CARDIA ADENOCARCINOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"7048"	"TGFBR2"	"0.437"	"0.793"	"C4277533"	"Dissection, Blood Vessel"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"7049"	"TGFBR3"	"0.594"	"0.655"	"C1862932"	"ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.60"	"1"	"1995"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human;ORPHANET"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"7050"	"TGIF1"	"0.663"	"0.448"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.60"		"2006"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"7050"	"TGIF1"	"0.663"	"0.448"	"C1840528"	"HOLOPROSENCEPHALY 4 (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2000"	"2004"	"2"	"6"	"CTD_human;UNIPROT"
"7050"	"TGIF1"	"0.663"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7051"	"TGM1"	"0.596"	"0.69"	"C0013238"	"Dry Eye Syndromes"	"group"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2017"	"7"	"43"	"CTD_human;ORPHANET;UNIPROT"
"7051"	"TGM1"	"0.596"	"0.69"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0042842"	"Vitamin A Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"1994"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"7051"	"TGM1"	"0.596"	"0.69"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human;ORPHANET"
"7051"	"TGM1"	"0.596"	"0.69"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"7051"	"TGM1"	"0.596"	"0.69"	"C1855789"	"Self-Healing Collodion Baby"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.72"	"1"	"1995"	"2016"	"7"	"43"	"ORPHANET;UNIPROT"
"7051"	"TGM1"	"0.596"	"0.69"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.90"		"1995"	"2016"	"7"	"51"	"CTD_human;ORPHANET;UNIPROT"
"7051"	"TGM1"	"0.596"	"0.69"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"1995"	"2016"	"7"	"43"	"CTD_human;ORPHANET;UNIPROT"
"7051"	"TGM1"	"0.596"	"0.69"	"C4305324"	"Acral self-healing collodion baby"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7051"	"TGM1"	"0.596"	"0.69"	"C4511230"	"Bathing suit ichthyosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7052"	"TGM2"	"0.499"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"7052"	"TGM2"	"0.499"	"0.69"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9333333"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"0.9529412"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"7052"	"TGM2"	"0.499"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.75"	"2001"	"2009"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2018"	"0"	"0"	"UNIPROT"
"7052"	"TGM2"	"0.499"	"0.69"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7052"	"TGM2"	"0.499"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2007"	"2"	"0"	"CTD_human"
"7053"	"TGM3"	"0.696"	"0.276"	"C0432347"	"Uncombable hair syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"7054"	"TH"	"0.498"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.6"	"1994"	"2005"	"5"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"1987"	"2003"	"5"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0011206"	"Delirium"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"2005"	"2"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.50"	"0.8"	"2002"	"2014"	"5"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2000"	"2014"	"5"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.50"	"0.9166667"	"1989"	"2017"	"1"	"1"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9661017"	"1989"	"2015"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1985"	"2016"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1991"	"2013"	"4"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"1995"	"2014"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1991"	"1991"	"1"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"1994"	"2012"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.33"	"1"	"1989"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6"	"1990"	"2014"	"5"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1991"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1991"	"2013"	"4"	"0"	"PSYGENET"
"7054"	"TH"	"0.498"	"0.759"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"1999"	"2000"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1997"	"2001"	"2"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7054"	"TH"	"0.498"	"0.759"	"C2673535"	"DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.62"	"1"	"1995"	"2015"	"23"	"17"	"CTD_human;ORPHANET;UNIPROT"
"7054"	"TH"	"0.498"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0002902"	"Anencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1985"	"1990"	"2"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0019326"	"Ventral Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0039978"	"Thoracic Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0302356"	"incomplete anencephaly, hemicrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0431349"	"Aprosencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C0559483"	"Pentalogy of Cantrell"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7055"	"THAS"	"0.656"	"0.379"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0012739"	"Disseminated Intravascular Coagulation"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1994"	"2006"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"1998"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0034155"	"Purpura, Thrombotic Thrombocytopenic"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.53"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2001"	"2003"	"2"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"2"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.66"	"0.6666667"	"1991"	"2010"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C1268935"	"Congenital Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C1850383"	"Neuropathy, Painful"	"disease"	"C10;C23;F02"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C1956258"	"Familial Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.30"		"1995"	"1995"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C2752036"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6"	"phenotype"		"Finding"	"0.60"		"2009"	"2010"	"2"	"6"	"ORPHANET;UNIPROT"
"7056"	"THBD"	"0.505"	"0.759"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.56"	"1"	"2009"	"2015"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7056"	"THBD"	"0.505"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7056"	"THBD"	"0.505"	"0.759"	"C3280976"	"Thrombophilia due to Thrombomodulin Defect"	"disease"	"C15"	"Disease or Syndrome"	"0.70"		"1995"	"2002"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7057"	"THBS1"	"0.448"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0027707"	"Nephritis, Interstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0041349"	"Nephritis, Tubulointerstitial"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7057"	"THBS1"	"0.448"	"0.759"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7058"	"THBS2"	"0.582"	"0.586"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7058"	"THBS2"	"0.582"	"0.586"	"C0011875"	"Diabetic Angiopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7058"	"THBS2"	"0.582"	"0.586"	"C0025945"	"Microangiopathy, Diabetic"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7058"	"THBS2"	"0.582"	"0.586"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CTD_human"
"7058"	"THBS2"	"0.582"	"0.586"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7059"	"THBS3"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7062"	"TCHH"	"0.886"	"0.069"	"C0432347"	"Uncombable hair syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.8421053"	"1996"	"2016"	"0"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C0836924"	"Thrombocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.50"	"0.8275862"	"1995"	"2016"	"1"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7066"	"THPO"	"0.542"	"0.552"	"C4303761"	"Familial thrombocytosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7067"	"THRA"	"0.594"	"0.621"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.40"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"7067"	"THRA"	"0.594"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7067"	"THRA"	"0.594"	"0.621"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7067"	"THRA"	"0.594"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7067"	"THRA"	"0.594"	"0.621"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"7067"	"THRA"	"0.594"	"0.621"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.49"	"0.8888889"	"1989"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"7067"	"THRA"	"0.594"	"0.621"	"C3280817"	"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"4"	"5"	"CTD_human;UNIPROT"
"7067"	"THRA"	"0.594"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1993"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"7068"	"THRB"	"0.584"	"0.69"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7068"	"THRB"	"0.584"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7068"	"THRB"	"0.584"	"0.69"	"C0206682"	"Follicular thyroid carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.53"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7068"	"THRB"	"0.584"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7068"	"THRB"	"0.584"	"0.69"	"C1840364"	"THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY"	"disease"	"C19"	"Disease or Syndrome"	"0.70"		"1975"	"2006"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"7068"	"THRB"	"0.584"	"0.69"	"C2937288"	"THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT"	"disease"	"C19"	"Disease or Syndrome"	"0.70"	"1"	"1975"	"2015"	"19"	"26"	"CTD_human;UNIPROT"
"7068"	"THRB"	"0.584"	"0.69"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"1.00"	"0.9885057"	"1989"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"7068"	"THRB"	"0.584"	"0.69"	"C3489796"	"Thyroid Hormone Resistance, Generalized, Autosomal Recessive"	"disease"	"C19"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"1996"	"0"	"2"	"CTD_human;ORPHANET"
"7068"	"THRB"	"0.584"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"7069"	"THRSP"	"0.773"	"0.241"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7069"	"THRSP"	"0.773"	"0.241"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7070"	"THY1"	"0.534"	"0.724"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7070"	"THY1"	"0.534"	"0.724"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.50"		"2008"	"2013"	"1"	"0"	"CTD_human"
"7071"	"KLF10"	"0.69"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"1995"	"2017"	"6"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"7071"	"KLF10"	"0.69"	"0.414"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1995"	"2017"	"6"	"0"	"CLINGEN"
"7072"	"TIA1"	"0.633"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7072"	"TIA1"	"0.633"	"0.517"	"C0221054"	"Welander Distal Myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"2013"	"2014"	"2"	"1"	"ORPHANET;UNIPROT"
"7072"	"TIA1"	"0.633"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7072"	"TIA1"	"0.633"	"0.517"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7072"	"TIA1"	"0.633"	"0.517"	"C2931290"	"Welander distal myopathy, Swedish type"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"7073"	"TIAL1"	"0.752"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7074"	"TIAM1"	"0.636"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"7074"	"TIAM1"	"0.636"	"0.586"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7074"	"TIAM1"	"0.636"	"0.586"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7074"	"TIAM1"	"0.636"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"0"	"0"	"UNIPROT"
"7074"	"TIAM1"	"0.636"	"0.586"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7074"	"TIAM1"	"0.636"	"0.586"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0008311"	"Cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2008"	"2014"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2015"	"5"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.31"		"1992"	"2002"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0042345"	"Varicosity"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7076"	"TIMP1"	"0.418"	"0.759"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7077"	"TIMP2"	"0.467"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0005686"	"Urinary Bladder Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0036323"	"Schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.6923077"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7078"	"TIMP3"	"0.473"	"0.793"	"C1850938"	"FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY"	"disease"	"C11"	"Disease or Syndrome"	"1.00"	"0.9411765"	"1983"	"2016"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7079"	"TIMP4"	"0.607"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"7079"	"TIMP4"	"0.607"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7079"	"TIMP4"	"0.607"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2017"	"0"	"0"	"CGI"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0008489"	"Chorea"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.44"	"0.6666667"	"2005"	"2008"	"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"	"0.9166667"	"1995"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.50"		"2000"	"2007"	"2"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0152113"	"Rheumatic Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0238056"	"Chorea, Senile"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.70"	"1"	"2008"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0393584"	"Benign Hereditary Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.80"	"1"	"2003"	"2016"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0699728"	"Chronic progressive chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0699731"	"Hereditary Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.60"		"2002"	"2015"	"2"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C0752210"	"Dyskinesias, Paroxysmal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C1859098"	"Chorea, Benign Familial"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C1970269"	"Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress"	"disease"	"C05;C08;C10;C16;C19;C23"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2018"	"5"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C1970270"	"Choreoathetosis And Congenital Hypothyroidism"	"disease"	"C05;C08;C10;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.51"	"1"	"2009"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.50"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"7080"	"NKX2-1"	"0.528"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7083"	"TK1"	"0.663"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2005"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7083"	"TK1"	"0.663"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7084"	"TK2"	"0.627"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7084"	"TK2"	"0.627"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7084"	"TK2"	"0.627"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7084"	"TK2"	"0.627"	"0.448"	"C1850303"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"7084"	"TK2"	"0.627"	"0.448"	"C3149750"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)"	"disease"		"Disease or Syndrome"	"0.80"		"1992"	"2015"	"4"	"29"	"CTD_human;UNIPROT"
"7084"	"TK2"	"0.627"	"0.448"	"C3501891"	"Mitochondrial DNA Depletion Syndrome, Myopathic Form"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7084"	"TK2"	"0.627"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7084"	"TK2"	"0.627"	"0.448"	"C4310734"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"2"	"CTD_human;UNIPROT"
"7086"	"TKT"	"0.624"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1987"	"2015"	"2"	"0"	"PSYGENET"
"7086"	"TKT"	"0.624"	"0.655"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0043121"	"Wernicke Encephalopathy"	"disease"	"C10;C18;C25;F03"	"Disease or Syndrome"	"0.32"	"1"	"1986"	"1993"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7086"	"TKT"	"0.624"	"0.655"	"C4310751"	"SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"3"	"ORPHANET;UNIPROT"
"7087"	"ICAM5"	"0.762"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.52"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human;UNIPROT"
"7087"	"ICAM5"	"0.762"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"7087"	"ICAM5"	"0.762"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"7087"	"ICAM5"	"0.762"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"7087"	"ICAM5"	"0.762"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7087"	"ICAM5"	"0.762"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"7087"	"ICAM5"	"0.762"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"7088"	"TLE1"	"0.685"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"7088"	"TLE1"	"0.685"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"7090"	"TLE3"	"0.773"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7090"	"TLE3"	"0.773"	"0.31"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7091"	"TLE4"	"0.735"	"0.345"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7092"	"TLL1"	"0.743"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7092"	"TLL1"	"0.743"	"0.345"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7092"	"TLL1"	"0.743"	"0.345"	"C2751315"	"Atrial Septal Defect 6"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"3"	"CTD_human;UNIPROT"
"7093"	"TLL2"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7094"	"TLN1"	"0.707"	"0.414"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7094"	"TLN1"	"0.707"	"0.414"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7094"	"TLN1"	"0.707"	"0.414"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7094"	"TLN1"	"0.707"	"0.414"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7094"	"TLN1"	"0.707"	"0.414"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2017"	"0"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7096"	"TLR1"	"0.529"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9545455"	"2003"	"2017"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2014"	"2017"	"1"	"0"	"PSYGENET"
"7097"	"TLR2"	"0.407"	"0.897"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"2"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"0.5"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0015404"	"Eye Infections, Bacterial"	"group"	"C01;C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.36"		"2005"	"2012"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0022568"	"Keratitis"	"disease"	"C11"	"Disease or Syndrome"	"0.53"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.38"	"0.875"	"2003"	"2014"	"0"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2013"	"2015"	"2"	"0"	"PSYGENET"
"7097"	"TLR2"	"0.407"	"0.897"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0038160"	"Staphylococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7097"	"TLR2"	"0.407"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C1318973"	"Staphylococcus aureus infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"2004"	"2012"	"0"	"1"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7097"	"TLR2"	"0.407"	"0.897"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7098"	"TLR3"	"0.475"	"0.862"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7098"	"TLR3"	"0.475"	"0.862"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"0"	"0"	"CTD_human"
"7098"	"TLR3"	"0.475"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7098"	"TLR3"	"0.475"	"0.862"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"7098"	"TLR3"	"0.475"	"0.862"	"C2751803"	"HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.40"		"2007"	"2015"	"1"	"3"	"UNIPROT"
"7098"	"TLR3"	"0.475"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7098"	"TLR3"	"0.475"	"0.862"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9298246"	"2002"	"2018"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2015"	"0"	"0"	"ORPHANET"
"7099"	"TLR4"	"0.359"	"0.931"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2014"	"2017"	"1"	"0"	"PSYGENET"
"7099"	"TLR4"	"0.359"	"0.931"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.7857143"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2006"	"2012"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.8333333"	"2004"	"2018"	"1"	"1"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0011882"	"Diabetic Neuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2008"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.35"		"2005"	"2012"	"4"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7099"	"TLR4"	"0.359"	"0.931"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2013"	"2013"	"2"	"0"	"PSYGENET"
"7099"	"TLR4"	"0.359"	"0.931"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.36"	"0.6666667"	"2005"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"0.975"	"2002"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271673"	"Symmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271674"	"Asymmetric Diabetic Proximal Motor Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271678"	"Diabetic Mononeuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271680"	"Diabetic Polyneuropathies"	"group"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271685"	"Diabetic Amyotrophy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0271686"	"Diabetic Autonomic Neuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0340288"	"Stable angina"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0393835"	"Diabetic Asymmetric Polyneuropathy"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"0.8888889"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0751074"	"Diabetic Neuralgia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.7272727"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.34"	"0.75"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8571429"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C1969108"	"Macular Degeneration, Age-Related, 10"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7099"	"TLR4"	"0.359"	"0.931"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7100"	"TLR5"	"0.573"	"0.69"	"C0023241"	"Legionnaires' Disease"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2005"	"0"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"0.9"	"2001"	"2017"	"0"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0025229"	"Melioidosis"	"disease"	"C01"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2017"	"0"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0343528"	"Pontiac Fever"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7100"	"TLR5"	"0.573"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7101"	"NR2E1"	"0.727"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"7101"	"NR2E1"	"0.727"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"7101"	"NR2E1"	"0.727"	"0.345"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7102"	"TSPAN7"	"0.72"	"0.414"	"C1846174"	"Mental Retardation, X-Linked 58"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2000"	"2012"	"3"	"2"	"CLINGEN;CTD_human;UNIPROT"
"7102"	"TSPAN7"	"0.72"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7102"	"TSPAN7"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2000"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2008"	"2018"	"1"	"1"	"PSYGENET"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7103"	"TSPAN8"	"0.652"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7104"	"TM4SF4"	"0.857"	"0.172"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7104"	"TM4SF4"	"0.857"	"0.172"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7106"	"TSPAN4"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7109"	"TRAPPC10"	"0.735"	"0.379"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7110"	"TMF1"	"0.857"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7110"	"TMF1"	"0.857"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"7110"	"TMF1"	"0.857"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7110"	"TMF1"	"0.857"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7111"	"TMOD1"	"0.713"	"0.379"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7111"	"TMOD1"	"0.713"	"0.379"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7111"	"TMOD1"	"0.713"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7111"	"TMOD1"	"0.713"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7112"	"TMPO"	"0.752"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7112"	"TMPO"	"0.752"	"0.241"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.61"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7112"	"TMPO"	"0.752"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7112"	"TMPO"	"0.752"	"0.241"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7112"	"TMPO"	"0.752"	"0.241"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CLINGEN;ORPHANET"
"7112"	"TMPO"	"0.752"	"0.241"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"7113"	"TMPRSS2"	"0.639"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9230769"	"2001"	"2018"	"4"	"0"	"CTD_human"
"7113"	"TMPRSS2"	"0.639"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9740933"	"2001"	"2018"	"4"	"0"	"CTD_human"
"7114"	"TMSB4X"	"0.598"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7114"	"TMSB4X"	"0.598"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7114"	"TMSB4X"	"0.598"	"0.552"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7114"	"TMSB4X"	"0.598"	"0.552"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7122"	"CLDN5"	"0.656"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2006"	"2"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2014"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.8955224"	"1999"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9411765"	"1999"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0002893"	"Refractory anemias"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.8823529"	"1999"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"2000"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.37"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"2012"	"9"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003869"	"Arthritis, Infectious"	"group"	"C01;C05"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.70"	"0.9507874"	"1989"	"2018"	"4"	"2"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003875"	"Arthritis, Viral"	"disease"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9809524"	"1990"	"2016"	"5"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9692308"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.31"		"1993"	"2007"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0005398"	"Cholestasis, Extrahepatic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2017"	"5"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9545455"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9368421"	"1990"	"2018"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0006267"	"Bronchiectasis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0006434"	"Burn injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.962963"	"1989"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1988"	"2013"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0008149"	"Chlamydia Infections"	"group"	"C01;C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2014"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9439252"	"1996"	"2018"	"2"	"1"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8888889"	"1993"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"5"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"5"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0011633"	"Dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.40"	"0.8333333"	"1999"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011644"	"Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.35"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2014"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"	"0.9571429"	"1989"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9555556"	"1995"	"2018"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2001"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.40"	"0.8"	"1994"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.34"		"2002"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9833333"	"1993"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2016"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018790"	"Cardiac Arrest"	"disease"	"C14"	"Disease or Syndrome"	"0.56"	"0.8333333"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9047619"	"1996"	"2013"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9310345"	"1996"	"2018"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018843"	"Heat Stroke"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2006"	"2014"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"1992"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019061"	"Hemolytic-Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019147"	"Hepatic Coma"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019151"	"Hepatic Encephalopathy"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019187"	"Hepatitis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.39"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"1995"	"2012"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.31"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020433"	"Hyperbilirubinemia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1989"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020615"	"Hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.40"		"2001"	"2014"	"15"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.60"	"0.962963"	"1992"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2016"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023283"	"Leishmaniasis, Cutaneous"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.38"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023290"	"Leishmaniasis, Visceral"	"disease"	"C03"	"Disease or Syndrome"	"0.35"	"1"	"1991"	"2016"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023860"	"Listeriosis"	"disease"	"C01"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.35"	"1"	"1991"	"2013"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"	"0.9130435"	"1992"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9574468"	"1989"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.57"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.8918919"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.40"	"0.9047619"	"1997"	"2016"	"0"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9655172"	"1992"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9692308"	"1989"	"2017"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"1998"	"2004"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9473684"	"2001"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027059"	"Myocarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2014"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2000"	"2014"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2015"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9710145"	"1991"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"1988"	"2003"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1998"	"2013"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.35"	"0.8"	"2009"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9352941"	"1995"	"2018"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.9333333"	"2007"	"2016"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1995"	"2007"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"1991"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9375"	"1999"	"2013"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032045"	"Placenta Disorders"	"group"	"C13"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032227"	"Pleural effusion disorder"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"1990"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032231"	"Pleurisy"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1998"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0032963"	"Pregnancy Complications, Cardiovascular"	"disease"	"C13;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.9789474"	"1991"	"2018"	"2"	"1"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0034067"	"Pulmonary Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2000"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"1993"	"2015"	"5"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0034189"	"Pyemia"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"1996"	"2005"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0034531"	"Radiation Injuries, Experimental"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2000"	"2013"	"9"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0035242"	"Respiratory Tract Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.37"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9375"	"1997"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036420"	"Localized scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036690"	"Septicemia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2018"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036981"	"Endotoxic shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036982"	"Shock, Hemorrhagic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0036983"	"Septic Shock"	"phenotype"	"C01;C23"	"Pathologic Function"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0037579"	"Soft Tissue Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0037926"	"Compression of spinal cord"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1992"	"2014"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"0.8"	"2002"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2014"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2003"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0040997"	"Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2014"	"5"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2012"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0043250"	"Injury wounds"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0043251"	"Wounds and Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0079218"	"Fibromatosis, Aggressive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0085655"	"Polymyositis"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1994"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.35"	"1"	"1993"	"2015"	"5"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0086540"	"Leishmaniasis, New World"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0086541"	"Urban cutaneous leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2002"	"2017"	"0"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0151526"	"Premature Birth"	"phenotype"	"C13"	"Pathologic Function"	"0.33"		"2004"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2000"	"2012"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0178324"	"Vascular System Injuries"	"group"	"C14;C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1992"	"2009"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"1996"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2007"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2007"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0206145"	"Stunned Myocardium"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0206146"	"Myocardial Stunning"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0206617"	"Cardiovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0221056"	"Adult type dermatomyositis"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.40"	"0.8181818"	"1999"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0221227"	"Centriacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2008"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9666667"	"1994"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0242973"	"Ventricular Dysfunction"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0243026"	"Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2018"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0263409"	"Linear Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.38"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0263984"	"Polymyositis Ossificans"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0264393"	"Panacinar Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0271708"	"Fasting Hypoglycemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0271710"	"Reactive hypoglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"1990"	"2016"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0340288"	"Stable angina"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0343755"	"HIV Wasting Syndrome"	"disease"	"C02;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"1995"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.8965517"	"1995"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0376416"	"Hibernation, Myocardial"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1992"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0393786"	"Trigeminal Neuralgia, Idiopathic"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0393787"	"Secondary Trigeminal Neuralgia"	"disease"	"C07;C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0524610"	"Chronic Alcoholic Hepatitis"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2001"	"2016"	"4"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.39"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0554591"	"Polymyositis, Idiopathic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0600228"	"Cardiopulmonary Arrest"	"phenotype"	"C14"	"Pathologic Function"	"0.50"		"1998"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0600327"	"Toxic Shock Syndrome"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.54"	"1"	"1990"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9464286"	"1987"	"2018"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0742803"	"Conus Medullaris Syndrome"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751197"	"Fulminant Hepatic Failure with Cerebral Edema"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751198"	"Hepatic Stupor"	"disease"	"C06;C10;C18"	"Disease or Syndrome"	"0.30"		"1998"	"2006"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0853897"	"Diabetic Cardiomyopathies"	"disease"	"C14;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"0.5"	"1995"	"2012"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0869523"	"Carditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2014"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.59"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2010"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0948480"	"Coronary Restenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"2012"	"9"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1995"	"2012"	"9"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2009"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1985"	"2015"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"1995"	"2012"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2004"	"2014"	"5"	"0"	"PSYGENET"
"7124"	"TNF"	"0.263"	"0.966"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2008"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2016"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1989"	"2017"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2005"	"2011"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1527383"	"Morphea"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"0.8"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1692886"	"Arthritis, Bacterial"	"group"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1998"	"2000"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1992"	"2005"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1719672"	"Severe Sepsis"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.36"	"1"	"1996"	"2013"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1861172"	"Venous Thromboembolism"	"phenotype"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2008"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.968"	"1989"	"2018"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"1990"	"2016"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2007"	"4"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2350878"	"Focal Emphysema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2007"	"2011"	"3"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9545455"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1995"	"2016"	"11"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3263723"	"Traumatic injury"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.40"		"2002"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.37"	"1"	"1998"	"2018"	"2"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3887485"	"MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C3891815"	"Arthritis, Suppurative"	"disease"	"C01;C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C4046002"	"Research-Related Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"6"	"0"	"CTD_human"
"7124"	"TNF"	"0.263"	"0.966"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"1995"	"2012"	"6"	"0"	"CTD_human"
"7125"	"TNNC2"	"0.928"	"0.069"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"7125"	"TNNC2"	"0.928"	"0.069"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CLINGEN"
"7126"	"TNFAIP1"	"0.752"	"0.448"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7126"	"TNFAIP1"	"0.752"	"0.448"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7127"	"TNFAIP2"	"0.727"	"0.276"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2017"	"4"	"3"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2017"	"0"	"0"	"CGI"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.96"	"2009"	"2018"	"4"	"5"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2015"	"1"	"2"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2018"	"2"	"3"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2011"	"0"	"0"	"CGI"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"4"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C0751422"	"Hereditary Autoinflammatory Diseases"	"group"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2014"	"2"	"1"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C4225218"	"AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7128"	"TNFAIP3"	"0.538"	"0.621"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7130"	"TNFAIP6"	"0.639"	"0.448"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2004"	"2017"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"2001"	"2009"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2005"	"2006"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2017"	"1"	"2"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"		"2001"	"2007"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"1"	"5"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"1"	"1999"	"2018"	"2"	"2"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0149910"	"Intermittent joint effusion"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0242706"	"Hyperoxia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"2"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C1275126"	"TNF receptor-associated periodic fever syndrome (TRAPS)"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"1.00"	"1"	"1983"	"2018"	"5"	"15"	"CTD_human;ORPHANET;UNIPROT"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"1999"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"7132"	"TNFRSF1A"	"0.443"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"2006"	"2014"	"4"	"0"	"PSYGENET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"2006"	"2014"	"4"	"0"	"PSYGENET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0026948"	"Mycosis Fungoides"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.51"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.37"	"0.7142857"	"1999"	"2008"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2001"	"2011"	"2"	"0"	"PSYGENET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0239981"	"Hypoalbuminemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7133"	"TNFRSF1B"	"0.467"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7134"	"TNNC1"	"0.701"	"0.276"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.875"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7134"	"TNNC1"	"0.701"	"0.276"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9166667"	"1997"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"7134"	"TNNC1"	"0.701"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7134"	"TNNC1"	"0.701"	"0.276"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7134"	"TNNC1"	"0.701"	"0.276"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7134"	"TNNC1"	"0.701"	"0.276"	"C2678475"	"Cardiomyopathy, Dilated, 1z"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"7134"	"TNNC1"	"0.701"	"0.276"	"C2750472"	"Cardiomyopathy, Familial Hypertrophic, 13"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"2001"	"2017"	"13"	"6"	"CLINGEN;CTD_human;UNIPROT"
"7136"	"TNNI2"	"0.707"	"0.172"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2005"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"7136"	"TNNI2"	"0.707"	"0.172"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"7136"	"TNNI2"	"0.707"	"0.172"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"7136"	"TNNI2"	"0.707"	"0.172"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"7136"	"TNNI2"	"0.707"	"0.172"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.74"	"1"	"2003"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"7136"	"TNNI2"	"0.707"	"0.172"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.66"	"1"	"2004"	"2018"	"1"	"3"	"CTD_human;GENOMICS_ENGLAND"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9166667"	"1997"	"2017"	"0"	"12"	"GENOMICS_ENGLAND"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0007196"	"Restrictive cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.90"	"1"	"2003"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0348616"	"Other restrictive cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2002"	"3"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2002"	"3"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.46"	"1"	"2003"	"2016"	"1"	"2"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.32"		"2005"	"2008"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"	"1"	"1988"	"2018"	"3"	"15"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"0.8"	"2004"	"2014"	"1"	"0"	"CTD_human"
"7137"	"TNNI3"	"0.6"	"0.586"	"C1860752"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7"	"disease"		"Disease or Syndrome"	"0.90"		"1997"	"2017"	"18"	"12"	"CLINGEN;CTD_human;UNIPROT"
"7137"	"TNNI3"	"0.6"	"0.586"	"C1861861"	"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.66"	"1"	"1999"	"2015"	"1"	"8"	"CTD_human;UNIPROT"
"7137"	"TNNI3"	"0.6"	"0.586"	"C2678474"	"CARDIOMYOPATHY, DILATED, 2A (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2003"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"7137"	"TNNI3"	"0.6"	"0.586"	"C2750091"	"Cardiomyopathy, Dilated, 1FF"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2003"	"2015"	"2"	"4"	"CTD_human;UNIPROT"
"7137"	"TNNI3"	"0.6"	"0.586"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7138"	"TNNT1"	"0.713"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"7138"	"TNNT1"	"0.713"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"7138"	"TNNT1"	"0.713"	"0.276"	"C1854380"	"NEMALINE MYOPATHY 5"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007172"	"Heart Rupture, Traumatic"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.90"	"1"	"2000"	"2018"	"2"	"11"	"CTD_human;GENOMICS_ENGLAND"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"0.9130435"	"1997"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007196"	"Restrictive cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"ORPHANET"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0017921"	"Glycogen storage disease type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0018805"	"Heart Injuries"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0035220"	"Respiratory Distress Syndrome, Newborn"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0042514"	"Tachycardia, Ventricular"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2005"	"0"	"0"	"ORPHANET"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0342751"	"Generalized glycogen storage disease of infants"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0348616"	"Other restrictive cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1997"	"2003"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0751172"	"Adult Glycogen Storage Disease Type II"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0751173"	"Glycogen Storage Disease Type II, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0751174"	"Glycogen Storage Disease Type II, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.49"	"0.875"	"2001"	"2017"	"2"	"2"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"0"	"2005"	"2016"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"	"1"	"1994"	"2017"	"2"	"17"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"0.8888889"	"2002"	"2016"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1720824"	"Sudden Cardiac Arrest"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1832243"	"CARDIOMYOPATHY, DILATED, 1D (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.80"		"1994"	"2017"	"5"	"15"	"CTD_human;UNIPROT"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1861864"	"Cardiomyopathy, Familial Hypertrophic, 2"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.90"		"1991"	"2017"	"23"	"25"	"CLINGEN;CTD_human;UNIPROT"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"7139"	"TNNT2"	"0.611"	"0.241"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2007"	"2"	"0"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C2676271"	"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"1994"	"2017"	"0"	"9"	"CTD_human"
"7139"	"TNNT2"	"0.611"	"0.241"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"7140"	"TNNT3"	"0.707"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"1999"	"2014"	"6"	"0"	"GENOMICS_ENGLAND"
"7140"	"TNNT3"	"0.707"	"0.207"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"1997"	"2013"	"0"	"0"	"ORPHANET"
"7140"	"TNNT3"	"0.707"	"0.207"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7140"	"TNNT3"	"0.707"	"0.207"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1999"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7140"	"TNNT3"	"0.707"	"0.207"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7143"	"TNR"	"0.773"	"0.138"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7143"	"TNR"	"0.773"	"0.138"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7143"	"TNR"	"0.773"	"0.138"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7143"	"TNR"	"0.773"	"0.138"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7145"	"TNS1"	"0.621"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"0.75"	"2001"	"2012"	"0"	"0"	"UNIPROT"
"7148"	"TNXB"	"0.598"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"1997"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"7148"	"TNXB"	"0.598"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7148"	"TNXB"	"0.598"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"0.6666667"	"2004"	"2018"	"3"	"1"	"PSYGENET"
"7148"	"TNXB"	"0.598"	"0.621"	"C0042580"	"Vesico-Ureteral Reflux"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"7148"	"TNXB"	"0.598"	"0.621"	"C0268337"	"Ehlers-Danlos syndrome, type 3 (disorder)"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2015"	"0"	"1"	"ORPHANET"
"7148"	"TNXB"	"0.598"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7148"	"TNXB"	"0.598"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7148"	"TNXB"	"0.598"	"0.621"	"C1848029"	"Ehlers-Danlos syndrome caused by tenascin-X deficiency"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"1997"	"2014"	"3"	"0"	"CTD_human;ORPHANET;UNIPROT"
"7148"	"TNXB"	"0.598"	"0.621"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7148"	"TNXB"	"0.598"	"0.621"	"C4014831"	"VESICOURETERAL REFLUX 8"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"7150"	"TOP1"	"0.58"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2016"	"0"	"0"	"UNIPROT"
"7150"	"TOP1"	"0.58"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7150"	"TOP1"	"0.58"	"0.655"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7150"	"TOP1"	"0.58"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7150"	"TOP1"	"0.58"	"0.655"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7150"	"TOP1"	"0.58"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9642857"	"2000"	"2017"	"4"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9607843"	"2000"	"2017"	"4"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2012"	"4"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2000"	"2016"	"4"	"0"	"CTD_human"
"7153"	"TOP2A"	"0.542"	"0.621"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7155"	"TOP2B"	"0.639"	"0.621"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7155"	"TOP2B"	"0.639"	"0.621"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7155"	"TOP2B"	"0.639"	"0.621"	"C0282612"	"Prostatic Intraepithelial Neoplasias"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.70"	"0.9465409"	"1986"	"2018"	"3"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.84"	"1986"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0001618"	"Tumors of Adrenal Cortex"	"group"	"C04;C19"	"Neoplastic Process"	"0.47"	"1"	"2006"	"2012"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2009"	"2"	"0"	"PSYGENET"
"7157"	"TP53"	"0.251"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1999"	"2018"	"2"	"0"	"PSYGENET"
"7157"	"TP53"	"0.251"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.50"		"2011"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2000"	"2015"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0004698"	"Balkan Nephropathy"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.9806452"	"1991"	"2018"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.9877551"	"1991"	"2018"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.70"	"0.9770115"	"1991"	"2017"	"0"	"69"	"UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.9658635"	"1983"	"2018"	"5"	"0"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9585062"	"1991"	"2018"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9120879"	"1991"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"		"2001"	"2016"	"3"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9663866"	"1990"	"2018"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"0.8529412"	"1991"	"2017"	"4"	"25"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9426386"	"1991"	"2018"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.972973"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.50"		"2005"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0007847"	"Malignant tumor of cervix"	"disease"		"Neoplastic Process"	"0.40"	"0.8527132"	"1991"	"2017"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2013"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9473684"	"1986"	"2017"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.945679"	"1989"	"2018"	"8"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9361702"	"1991"	"2016"	"8"	"65"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9230769"	"1996"	"2016"	"1"	"3"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.50"		"2011"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9166667"	"1991"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.90"	"0.9359431"	"1991"	"2017"	"3"	"1"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2002"	"2015"	"0"	"1"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.8571429"	"1994"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.50"		"2000"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.50"		"2000"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.50"		"2004"	"2008"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0022593"	"Keratosis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"1992"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0022594"	"Keratosis Blennorrhagica"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0022783"	"Vulvar Lichen Sclerosus"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.80"	"0.9593496"	"1991"	"2018"	"1"	"23"	"CGI;CTD_human;ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9550562"	"1986"	"2018"	"0"	"25"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.939759"	"1991"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.50"		"2000"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.80"	"0.9607843"	"1990"	"2017"	"5"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9192547"	"1991"	"2018"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7157"	"TP53"	"0.251"	"0.897"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9398148"	"1991"	"2018"	"3"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.56"	"0.5"	"1995"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"0"	"4"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.60"	"0.8979592"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.50"	"0.9189189"	"1993"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"1.00"	"0.9102564"	"1987"	"2017"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9496644"	"1991"	"2018"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.90"	"1"	"1993"	"2016"	"0"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0030849"	"Penile Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0032578"	"Polyploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.92"	"1994"	"2018"	"7"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"1996"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.8611111"	"1993"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9230769"	"1991"	"2016"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.50"		"2011"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2002"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0040100"	"Thymoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.36"	"0.8333333"	"1995"	"2015"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.972973"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0042065"	"Genitourinary Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"		"2006"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9574468"	"1992"	"2017"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9090909"	"1994"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.39"	"0.6666667"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0085136"	"Central Nervous System Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.8181818"	"1991"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0085390"	"Li-Fraumeni Syndrome"	"disease"	"C04;C16;C18"	"Neoplastic Process"	"1.00"	"0.9194631"	"1989"	"2018"	"9"	"73"	"CLINGEN;CTD_human;ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.50"		"2000"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0086501"	"Keratoma"	"phenotype"	"C17"	"Acquired Abnormality"	"0.30"		"2007"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.70"	"0.9846154"	"1991"	"2017"	"2"	"31"	"CTD_human;ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"1993"	"2017"	"0"	"37"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.60"	"0.9607843"	"1993"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"1997"	"2016"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0153601"	"Malignant neoplasm of penis"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"1996"	"1998"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.54"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"1994"	"2012"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"1994"	"2012"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"1994"	"2012"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"1994"	"2012"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"1994"	"2013"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"1994"	"2012"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1994"	"2007"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1998"	"2007"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205770"	"Choroid Plexus Papilloma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.64"	"0.6666667"	"2002"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2009"	"2010"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.53"	"1"	"1997"	"2015"	"1"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0206681"	"Adenocarcinoma, Clear Cell"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"0.6666667"	"1994"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.80"	"0.95"	"1992"	"2018"	"3"	"18"	"CGI;CTD_human;ORPHANET;UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9411765"	"1994"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1995"	"2018"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.50"	"0.9823009"	"1992"	"2018"	"0"	"2"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.80"	"0.9668246"	"1989"	"2018"	"5"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2007"	"2014"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.984375"	"1992"	"2018"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"0.9705882"	"1991"	"2018"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9117647"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.38"	"1"	"1999"	"2017"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0302592"	"Cervix carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.8913043"	"1991"	"2017"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2010"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.88"	"1993"	"2017"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1995"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9230769"	"1992"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0346402"	"Malignant neoplasm of adrenal cortex"	"disease"	"C04;C19"	"Neoplastic Process"	"0.37"	"0.8571429"	"1994"	"2013"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.90"	"0.953125"	"1992"	"2018"	"0"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.50"	"0.9573643"	"1991"	"2018"	"7"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"	"0.9259259"	"1993"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0431109"	"Choroid Plexus Carcinoma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.50"	"1"	"2001"	"2017"	"0"	"1"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.70"	"0.9466667"	"1991"	"2017"	"2"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.95"	"1991"	"2018"	"1"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9215686"	"1992"	"2015"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.40"	"0.9"	"1994"	"2014"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.9541985"	"1991"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.90"	"0.9672447"	"1983"	"2018"	"5"	"0"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.40"	"0.96"	"1989"	"2018"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.38"	"1"	"1993"	"2016"	"0"	"0"	"UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0751569"	"Genitourinary Cancer"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0751620"	"Central Nervous System Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0851140"	"Carcinoma in situ of uterine cervix"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2000"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.45"	"1"	"1991"	"2007"	"0"	"1"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"1999"	"2009"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.50"	"0.9433962"	"1992"	"2016"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.70"	"0.940678"	"1991"	"2018"	"4"	"0"	"CGI;CLINGEN"
"7157"	"TP53"	"0.251"	"0.897"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9548023"	"1991"	"2018"	"1"	"73"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"		"2002"	"2016"	"5"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"1.00"	"0.95"	"1987"	"2018"	"1"	"1"	"CGI;CTD_human;GENOMICS_ENGLAND"
"7157"	"TP53"	"0.251"	"0.897"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"4"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.40"	"0.9411765"	"1990"	"2009"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2016"	"3"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9714286"	"1983"	"2016"	"5"	"82"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9364641"	"1990"	"2018"	"8"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1835398"	"LI-FRAUMENI SYNDROME 1"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"1991"	"2018"	"9"	"61"	"UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C1859972"	"ADRENOCORTICAL CARCINOMA, HEREDITARY"	"disease"	"C04;C19"	"Neoplastic Process"	"0.41"	"1"	"1994"	"2015"	"0"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.31"	"1"	"1995"	"1995"	"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.90"	"0.9446494"	"1990"	"2018"	"6"	"62"	"CGI;CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2675080"	"Li-Fraumeni-Like Syndrome"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.50"	"0.8823529"	"1991"	"2016"	"9"	"55"	"UNIPROT"
"7157"	"TP53"	"0.251"	"0.897"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7157"	"TP53"	"0.251"	"0.897"	"C2931713"	"Chromosome 17 deletion"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.50"	"0.9452055"	"1992"	"2017"	"1"	"1"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.50"	"0.9342105"	"1992"	"2018"	"1"	"2"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C3683846"	"Chromosome 17p Deletion Syndrome"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C3714644"	"Thymus Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.51"	"1"	"1999"	"2000"	"0"	"0"	"CGI"
"7157"	"TP53"	"0.251"	"0.897"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7157"	"TP53"	"0.251"	"0.897"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"1998"	"2018"	"0"	"0"	"CGI"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C0206692"	"Carcinoma, Lobular"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7159"	"TP53BP2"	"0.69"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"		"2004"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7161"	"TP73"	"0.472"	"0.724"	"C0206655"	"Alveolar rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7161"	"TP73"	"0.472"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"7162"	"TPBG"	"0.799"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7162"	"TPBG"	"0.799"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7163"	"TPD52"	"0.656"	"0.448"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7163"	"TPD52"	"0.656"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2007"	"2017"	"2"	"0"	"CTD_human"
"7163"	"TPD52"	"0.656"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"7164"	"TPD52L1"	"0.857"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7164"	"TPD52L1"	"0.857"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7166"	"TPH1"	"0.611"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1998"	"2012"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"1998"	"2012"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.59"	"1"	"2004"	"2014"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2004"	"2014"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7166"	"TPH1"	"0.611"	"0.586"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7166"	"TPH1"	"0.611"	"0.586"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2011"	"3"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.75"	"2000"	"2012"	"1"	"0"	"CTD_human"
"7166"	"TPH1"	"0.611"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"1999"	"2012"	"5"	"0"	"PSYGENET"
"7166"	"TPH1"	"0.611"	"0.586"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7166"	"TPH1"	"0.611"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2002"	"2015"	"5"	"0"	"PSYGENET"
"7167"	"TPI1"	"0.564"	"0.655"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002735"	"Oppenheim's Disease"	"disease"	"C10"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.45"	"1"	"1986"	"2016"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002882"	"Anemia, Hemolytic, Congenital Nonspherocytic"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1995"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"7167"	"TPI1"	"0.564"	"0.655"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1986"	"1993"	"2"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0027868"	"Neuromuscular Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7167"	"TPI1"	"0.564"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1995"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"7167"	"TPI1"	"0.564"	"0.655"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0398562"	"Triose phosphate isomerase deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"7167"	"TPI1"	"0.564"	"0.655"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0751381"	"Foley-Denny-Brown Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0752251"	"Muscle Disease Manifestations"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1986"	"1993"	"2"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0752252"	"Neuromuscular Manifestations"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1986"	"1993"	"2"	"0"	"CTD_human"
"7167"	"TPI1"	"0.564"	"0.655"	"C0857501"	"Acute schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7167"	"TPI1"	"0.564"	"0.655"	"C1860808"	"Triosephosphate Isomerase Deficiency"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"		"1986"	"2010"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"7168"	"TPM1"	"0.592"	"0.448"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2018"	"0"	"9"	"GENOMICS_ENGLAND"
"7168"	"TPM1"	"0.592"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2017"	"18"	"1"	"CLINGEN;GENOMICS_ENGLAND"
"7168"	"TPM1"	"0.592"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7168"	"TPM1"	"0.592"	"0.448"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7168"	"TPM1"	"0.592"	"0.448"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2018"	"0"	"0"	"ORPHANET"
"7168"	"TPM1"	"0.592"	"0.448"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0597124"	"Obstructive asymmetric septal hypertrophy"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2017"	"19"	"6"	"CLINGEN;CTD_human"
"7168"	"TPM1"	"0.592"	"0.448"	"C1861863"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1994"	"2012"	"6"	"4"	"CTD_human;UNIPROT"
"7168"	"TPM1"	"0.592"	"0.448"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"7168"	"TPM1"	"0.592"	"0.448"	"C2678476"	"Cardiomyopathy, Dilated, 1y"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2001"	"2015"	"2"	"6"	"CTD_human;UNIPROT"
"7168"	"TPM1"	"0.592"	"0.448"	"C3808145"	"LEFT VENTRICULAR NONCOMPACTION 9"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2012"	"2"	"4"	"UNIPROT"
"7168"	"TPM1"	"0.592"	"0.448"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"7169"	"TPM2"	"0.58"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.44"	"1"	"2005"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7169"	"TPM2"	"0.58"	"0.517"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2017"	"0"	"0"	"ORPHANET"
"7169"	"TPM2"	"0.58"	"0.517"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.72"	"1"	"1994"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7169"	"TPM2"	"0.58"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.40"	"1"	"2007"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"7169"	"TPM2"	"0.58"	"0.517"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7169"	"TPM2"	"0.58"	"0.517"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"7169"	"TPM2"	"0.58"	"0.517"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"2007"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7169"	"TPM2"	"0.58"	"0.517"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C1836447"	"Nemaline myopathy 4"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"1993"	"2016"	"6"	"8"	"CTD_human;UNIPROT"
"7169"	"TPM2"	"0.58"	"0.517"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7169"	"TPM2"	"0.58"	"0.517"	"C2750413"	"Cap Myopathy, Tpm2-Related"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7169"	"TPM2"	"0.58"	"0.517"	"C3710589"	"Cap Myopathy"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.39"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"7169"	"TPM2"	"0.58"	"0.517"	"C3807907"	"CAP MYOPATHY 2"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2015"	"6"	"6"	"UNIPROT"
"7170"	"TPM3"	"0.551"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"7170"	"TPM3"	"0.551"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2014"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.9473684"	"2000"	"2014"	"0"	"0"	"ORPHANET"
"7170"	"TPM3"	"0.551"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.34"	"1"	"2010"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"7170"	"TPM3"	"0.551"	"0.655"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2015"	"0"	"0"	"ORPHANET"
"7170"	"TPM3"	"0.551"	"0.655"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7170"	"TPM3"	"0.551"	"0.655"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.74"	"1"	"1975"	"2017"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"7170"	"TPM3"	"0.551"	"0.655"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"1993"	"2014"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C1836448"	"Nemaline myopathy 1"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"1975"	"2017"	"8"	"10"	"CTD_human;UNIPROT"
"7170"	"TPM3"	"0.551"	"0.655"	"C2750414"	"CAP MYOPATHY, TPM3-RELATED (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7170"	"TPM3"	"0.551"	"0.655"	"C3710589"	"Cap Myopathy"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.35"	"1"	"2009"	"2014"	"0"	"0"	"ORPHANET"
"7170"	"TPM3"	"0.551"	"0.655"	"C3714994"	"CAP MYOPATHY 1"	"disease"		"Disease or Syndrome"	"0.40"		"1975"	"2015"	"8"	"4"	"UNIPROT"
"7171"	"TPM4"	"0.713"	"0.414"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7171"	"TPM4"	"0.713"	"0.414"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0334121"	"Inflammatory Myofibroblastic Tumor"	"disease"	"C23"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2012"	"0"	"0"	"ORPHANET"
"7171"	"TPM4"	"0.713"	"0.414"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7171"	"TPM4"	"0.713"	"0.414"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7172"	"TPMT"	"0.636"	"0.483"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7172"	"TPMT"	"0.636"	"0.483"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9333333"	"1987"	"2017"	"3"	"0"	"CTD_human"
"7172"	"TPMT"	"0.636"	"0.483"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"7172"	"TPMT"	"0.636"	"0.483"	"C0342801"	"Thiopurine S methyltranferase deficiency"	"disease"	"C16;C18;C20;C25"	"Disease or Syndrome"	"0.60"	"0.9166667"	"2000"	"2014"	"0"	"0"	"CTD_human"
"7172"	"TPMT"	"0.636"	"0.483"	"C2750088"	"HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7172"	"TPMT"	"0.636"	"0.483"	"C2931223"	"6 alpha mercaptopurine sensitivity"	"disease"	"C16;C18;C20;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7173"	"TPO"	"0.514"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.37"	"0.8571429"	"1991"	"2016"	"1"	"0"	"CTD_human"
"7173"	"TPO"	"0.514"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"7173"	"TPO"	"0.514"	"0.793"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.90"	"1"	"1991"	"2018"	"10"	"2"	"CTD_human;GENOMICS_ENGLAND"
"7173"	"TPO"	"0.514"	"0.793"	"C0018021"	"Goiter"	"phenotype"	"C19"	"Pathologic Function"	"0.41"		"2003"	"2008"	"3"	"0"	"CTD_human"
"7173"	"TPO"	"0.514"	"0.793"	"C0342200"	"Endemic Cretinism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"		"2003"	"2007"	"4"	"0"	"CTD_human"
"7173"	"TPO"	"0.514"	"0.793"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1994"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"7173"	"TPO"	"0.514"	"0.793"	"C1291299"	"Deficiency of iodide peroxidase (disorder)"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.60"		"1995"	"2017"	"17"	"18"	"CTD_human;UNIPROT"
"7173"	"TPO"	"0.514"	"0.793"	"C1578691"	"Myxedema, Congenital"	"disease"	"C05;C16;C19"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2003"	"2007"	"4"	"0"	"CTD_human"
"7173"	"TPO"	"0.514"	"0.793"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"7175"	"TPR"	"0.72"	"0.379"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7175"	"TPR"	"0.72"	"0.379"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7175"	"TPR"	"0.72"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"7175"	"TPR"	"0.72"	"0.379"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0009782"	"Connective Tissue Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0013363"	"Dysautonomia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0022104"	"Irritable Bowel Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7177"	"TPSAB1"	"0.762"	"0.345"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7178"	"TPT1"	"0.6"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7178"	"TPT1"	"0.6"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7178"	"TPT1"	"0.6"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"7178"	"TPT1"	"0.6"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"7178"	"TPT1"	"0.6"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7179"	"TPTE"	"0.857"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"7181"	"NR2C1"	"0.834"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7181"	"NR2C1"	"0.834"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7182"	"NR2C2"	"0.616"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7182"	"NR2C2"	"0.616"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7184"	"HSP90B1"	"0.567"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2009"	"3"	"0"	"PSYGENET"
"7184"	"HSP90B1"	"0.567"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"7184"	"HSP90B1"	"0.567"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.9032258"	"2007"	"2016"	"2"	"2"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7185"	"TRAF1"	"0.58"	"0.69"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7187"	"TRAF3"	"0.639"	"0.621"	"C0001338"	"Herpetic Acute Necrotizing Encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7187"	"TRAF3"	"0.639"	"0.621"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"7187"	"TRAF3"	"0.639"	"0.621"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.53"	"1"	"2010"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"7187"	"TRAF3"	"0.639"	"0.621"	"C3553868"	"HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 3"	"disease"		"Finding"	"0.30"		"2010"	"2010"	"1"	"1"	"UNIPROT"
"7188"	"TRAF5"	"0.713"	"0.379"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7189"	"TRAF6"	"0.528"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.46"	"1"	"2009"	"2015"	"2"	"1"	"CTD_human"
"7189"	"TRAF6"	"0.528"	"0.724"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7189"	"TRAF6"	"0.528"	"0.724"	"C0265331"	"Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7189"	"TRAF6"	"0.528"	"0.724"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1985"	"1996"	"4"	"0"	"PSYGENET"
"7200"	"TRH"	"0.547"	"0.621"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0005899"	"Body Rocking"	"phenotype"	"F03"	"Individual Behavior"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1983"	"2015"	"5"	"0"	"PSYGENET"
"7200"	"TRH"	"0.547"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1983"	"2015"	"5"	"0"	"PSYGENET"
"7200"	"TRH"	"0.547"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0018672"	"Head Banging"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.53"	"1"	"1983"	"2007"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"1996"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0038273"	"Stereotypic Movement Disorder"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0040822"	"Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0040827"	"Saturnine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0041657"	"Unconscious State"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1982"	"1982"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"1982"	"1995"	"3"	"0"	"PSYGENET"
"7200"	"TRH"	"0.547"	"0.621"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0085628"	"Stupor"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1978"	"1996"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0149840"	"Senile Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0220998"	"Hypothalamic hypothyroidism"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"7200"	"TRH"	"0.547"	"0.621"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234370"	"Persistent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234371"	"Continuous Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234372"	"Intermittent Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234373"	"Fine Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234374"	"Coarse Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234375"	"Massive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234376"	"Action Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234377"	"Passive Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234378"	"Static Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234379"	"Resting Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234381"	"Darkness Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234447"	"Narcosis"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"1978"	"1996"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235078"	"Tremor, Perioral"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235081"	"Tremor, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235082"	"Tremor, Muscle"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235083"	"Nerve Tremors"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0235843"	"Tremor, Neonatal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0394016"	"Coma, Post-Head Injury"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"1982"	"1983"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1995"	"3"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751564"	"Pill Rolling Tremor"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751565"	"Tremor, Semirhythmic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C0751812"	"Coma, Post-Traumatic, Prolonged"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"1991"	"1993"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C1527384"	"Involuntary Quiver"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1978"	"1979"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C3887992"	"THYROTROPIN-RELEASING HORMONE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"7200"	"TRH"	"0.547"	"0.621"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7200"	"TRH"	"0.547"	"0.621"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"1999"	"2005"	"2"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.51"	"1"	"1997"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"7201"	"TRHR"	"0.713"	"0.241"	"C0020676"	"Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C0271801"	"Central hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1997"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"7201"	"TRHR"	"0.713"	"0.241"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C3665349"	"Secondary hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7201"	"TRHR"	"0.713"	"0.241"	"C4316995"	"Primary Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7201"	"TRHR"	"0.713"	"0.241"	"C4511136"	"Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7203"	"CCT3"	"0.735"	"0.448"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7203"	"CCT3"	"0.735"	"0.448"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7204"	"TRIO"	"0.636"	"0.517"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7204"	"TRIO"	"0.636"	"0.517"	"C4310740"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 44"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2016"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"7220"	"TRPC1"	"0.616"	"0.586"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7220"	"TRPC1"	"0.616"	"0.586"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7222"	"TRPC3"	"0.633"	"0.379"	"C4225158"	"SPINOCEREBELLAR ATAXIA 41"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"ORPHANET;UNIPROT"
"7223"	"TRPC4"	"0.743"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7224"	"TRPC5"	"0.834"	"0.276"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.70"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7225"	"TRPC6"	"0.567"	"0.552"	"C1858915"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.80"		"1999"	"2017"	"11"	"10"	"CTD_human;UNIPROT"
"7225"	"TRPC6"	"0.567"	"0.552"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7226"	"TRPM2"	"0.648"	"0.379"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7226"	"TRPM2"	"0.648"	"0.379"	"C2939186"	"Disturbance in mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0023003"	"Langer-Giedion Syndrome"	"disease"	"C05"	"Disease or Syndrome"	"0.59"	"0.7777778"	"1996"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2001"	"2009"	"2"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C0432233"	"Trichorhinophalangeal dysplasia type I"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.84"	"1"	"1993"	"2017"	"1"	"14"	"CTD_human;UNIPROT"
"7227"	"TRPS1"	"0.594"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7227"	"TRPS1"	"0.594"	"0.552"	"C1860823"	"Trichorhinophalangeal Syndrome, Type III"	"disease"	"C05;C16;C17;C23"	"Disease or Syndrome"	"0.60"		"2001"	"2017"	"2"	"6"	"CTD_human;UNIPROT"
"7227"	"TRPS1"	"0.594"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2016"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"7234"	"TRU-TCA1-1"	"1"	"0.034"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"0.9285714"	"1993"	"2016"	"0"	"5"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.9375"	"1993"	"2016"	"1"	"2"	"CGI;UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"1"	"1988"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2016"	"2"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.48"	"0.875"	"1999"	"2017"	"1"	"2"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0041341"	"Tuberous Sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"1.00"	"0.987013"	"1990"	"2018"	"16"	"90"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.32"	"1"	"1996"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0265319"	"Fibrous skin tumor of tuberous sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.40"		"2008"	"2015"	"3"	"1"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7248"	"TSC1"	"0.403"	"0.759"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.58"	"1"	"1995"	"2017"	"1"	"0"	"CGI;CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.40"	"0.9354839"	"1993"	"2016"	"0"	"0"	"CGI"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"2"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751674"	"Lymphangioleiomyomatosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"1971"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C1846385"	"FOCAL CORTICAL DYSPLASIA OF TAYLOR"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2017"	"2"	"4"	"CTD_human;UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C1846386"	"Focal Cortical Dysplasia of Taylor, Type IIa"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2017"	"2"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C1846388"	"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C1846389"	"Focal Cortical Dysplasia of Taylor, Type IIb"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2002"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C1854465"	"TUBEROUS SCLEROSIS 1 (disorder)"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.79"	"1"	"1996"	"2017"	"13"	"78"	"CLINGEN;CTD_human;UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2002"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"0.8571429"	"1997"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7248"	"TSC1"	"0.403"	"0.759"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7248"	"TSC1"	"0.403"	"0.759"	"C4478700"	"FOCAL CORTICAL DYSPLASIA, TYPE IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C4478701"	"FOCAL CORTICAL DYSPLASIA, TYPE IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C4479708"	"FCD IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C4479709"	"FCD IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7248"	"TSC1"	"0.403"	"0.759"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.66"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"7249"	"TSC2"	"0.463"	"0.69"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7249"	"TSC2"	"0.463"	"0.69"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.38"	"1"	"2001"	"2013"	"3"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.46"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.37"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0041341"	"Tuberous Sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"1.00"	"0.9851852"	"1994"	"2018"	"10"	"151"	"CLINGEN;CTD_human;ORPHANET"
"7249"	"TSC2"	"0.463"	"0.69"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.53"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0265319"	"Fibrous skin tumor of tuberous sclerosis"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.40"		"2000"	"2011"	"4"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7249"	"TSC2"	"0.463"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"0.5"	"2001"	"2017"	"0"	"0"	"CGI"
"7249"	"TSC2"	"0.463"	"0.69"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7249"	"TSC2"	"0.463"	"0.69"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"7249"	"TSC2"	"0.463"	"0.69"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2001"	"2011"	"3"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C0751674"	"Lymphangioleiomyomatosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.80"	"0.9183673"	"1996"	"2017"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7249"	"TSC2"	"0.463"	"0.69"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7249"	"TSC2"	"0.463"	"0.69"	"C1838327"	"Polycystic kidneys, severe infantile with tuberous sclerosis"	"disease"	"C04;C10;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7249"	"TSC2"	"0.463"	"0.69"	"C1846385"	"FOCAL CORTICAL DYSPLASIA OF TAYLOR"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C1846386"	"Focal Cortical Dysplasia of Taylor, Type IIa"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C1846388"	"CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C1846389"	"Focal Cortical Dysplasia of Taylor, Type IIb"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C1854465"	"TUBEROUS SCLEROSIS 1 (disorder)"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2017"	"6"	"0"	"CLINGEN"
"7249"	"TSC2"	"0.463"	"0.69"	"C1860707"	"TUBEROUS SCLEROSIS 2 (disorder)"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1971"	"2018"	"16"	"153"	"CTD_human;UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2008"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7249"	"TSC2"	"0.463"	"0.69"	"C2750460"	"Tsc2 Angiomyolipomas, Renal, Modifier Of"	"disease"	"C04;C10;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2005"	"16"	"50"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"1999"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"7249"	"TSC2"	"0.463"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7249"	"TSC2"	"0.463"	"0.69"	"C4478700"	"FOCAL CORTICAL DYSPLASIA, TYPE IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C4478701"	"FOCAL CORTICAL DYSPLASIA, TYPE IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C4479708"	"FCD IIA"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C4479709"	"FCD IIB"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7249"	"TSC2"	"0.463"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7251"	"TSG101"	"0.619"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8947368"	"1997"	"2017"	"0"	"0"	"CTD_human"
"7251"	"TSG101"	"0.619"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.8888889"	"1997"	"2017"	"0"	"0"	"CTD_human"
"7251"	"TSG101"	"0.619"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"7251"	"TSG101"	"0.619"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0009421"	"Comatose"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.40"		"1989"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7252"	"TSHB"	"0.672"	"0.483"	"C0020672"	"Hypothermia, natural"	"phenotype"	"C23"	"Finding"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0020676"	"Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.42"	"1"	"1996"	"2014"	"2"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0271789"	"Hypothyroidism, Congenital, Nongoitrous, 4"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.60"		"1989"	"2015"	"0"	"4"	"CTD_human;ORPHANET"
"7252"	"TSHB"	"0.672"	"0.483"	"C0271801"	"Central hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2017"	"2"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0274285"	"Hypothermia, Accidental"	"disease"	"C23"	"Injury or Poisoning"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1981"	"1981"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1989"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7252"	"TSHB"	"0.672"	"0.483"	"C0860634"	"Psychogenic coma"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7252"	"TSHB"	"0.672"	"0.483"	"C3665349"	"Secondary hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2008"	"2014"	"2"	"0"	"CTD_human;ORPHANET"
"7252"	"TSHB"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"1989"	"1"	"0"	"GENOMICS_ENGLAND"
"7252"	"TSHB"	"0.672"	"0.483"	"C4082174"	"Thyrotropin deficiency, isolated"	"disease"	"C19"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"7252"	"TSHB"	"0.672"	"0.483"	"C4316995"	"Primary Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2008"	"2014"	"2"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.8529412"	"1993"	"2015"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0001624"	"Adrenal Gland Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.90"	"0.9347826"	"1992"	"2018"	"7"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7253"	"TSHR"	"0.51"	"0.69"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.50"	"0.95"	"1983"	"2017"	"2"	"14"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"	"0.9255319"	"1991"	"2016"	"3"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.7916667"	"1992"	"2015"	"2"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0040156"	"Thyrotoxicosis"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.8888889"	"1992"	"2009"	"2"	"0"	"CGI;CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0151516"	"Thyroid Hypoplasia"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2016"	"0"	"0"	"ORPHANET"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1993"	"2009"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"1992"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1992"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0342200"	"Endemic Cretinism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"0.9354839"	"1992"	"2015"	"2"	"0"	"CTD_human;UNIPROT"
"7253"	"TSHR"	"0.51"	"0.69"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.64"	"1"	"1995"	"2018"	"6"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"7253"	"TSHR"	"0.51"	"0.69"	"C0750887"	"Adrenal Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C0920350"	"Autoimmune thyroiditis"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.33"	"1"	"1993"	"2008"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C1578691"	"Myxedema, Congenital"	"disease"	"C05;C16;C19"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C1836706"	"Hyperthyroidism, Nonautoimmune"	"disease"	"C19"	"Disease or Syndrome"	"0.80"	"1"	"1982"	"2015"	"16"	"9"	"CTD_human;ORPHANET;UNIPROT"
"7253"	"TSHR"	"0.51"	"0.69"	"C1863959"	"Hyperthyroidism, Familial Gestational"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.70"		"1998"	"1998"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7253"	"TSHR"	"0.51"	"0.69"	"C3493776"	"HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.80"	"1"	"1995"	"2018"	"12"	"16"	"CTD_human;ORPHANET;UNIPROT"
"7253"	"TSHR"	"0.51"	"0.69"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"1993"	"2010"	"3"	"0"	"CTD_human"
"7253"	"TSHR"	"0.51"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"7257"	"TSNAX"	"0.785"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2012"	"3"	"0"	"PSYGENET"
"7257"	"TSNAX"	"0.785"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.07"	"1"	"2001"	"2012"	"1"	"0"	"PSYGENET"
"7257"	"TSNAX"	"0.785"	"0.138"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7258"	"TSPY1"	"0.656"	"0.414"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"7258"	"TSPY1"	"0.656"	"0.414"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7259"	"TSPYL1"	"0.72"	"0.379"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2004"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"7259"	"TSPYL1"	"0.72"	"0.379"	"C1837371"	"Sudden Infant Death with Dysgenesis of the Testes Syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.53"	"1"	"2004"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7260"	"EIPR1"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7262"	"PHLDA2"	"0.752"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7262"	"PHLDA2"	"0.752"	"0.345"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7262"	"PHLDA2"	"0.752"	"0.345"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"7263"	"TST"	"0.663"	"0.276"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7263"	"TST"	"0.663"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7263"	"TST"	"0.663"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7263"	"TST"	"0.663"	"0.276"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7266"	"DNAJC7"	"1"	"0.069"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7266"	"DNAJC7"	"1"	"0.069"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7267"	"TTC3"	"0.857"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7270"	"TTF1"	"0.616"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7272"	"TTK"	"0.624"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7272"	"TTK"	"0.624"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7273"	"TTN"	"0.534"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.90"	"1"	"1995"	"2017"	"3"	"201"	"CTD_human;GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.65"	"1"	"1996"	"2017"	"10"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.50"	"0.9090909"	"2002"	"2018"	"1"	"3"	"CTD_human"
"7273"	"TTN"	"0.534"	"0.655"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7273"	"TTN"	"0.534"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0221054"	"Welander Distal Myopathy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7273"	"TTN"	"0.534"	"0.655"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.32"	"1"	"2007"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"7"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"6"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.61"	"1"	"2002"	"2015"	"1"	"4"	"CTD_human;ORPHANET"
"7273"	"TTN"	"0.534"	"0.655"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0410204"	"Myopathy, Centronuclear, Autosomal Recessive"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2012"	"2013"	"0"	"2"	"ORPHANET"
"7273"	"TTN"	"0.534"	"0.655"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"2002"	"2018"	"2"	"1"	"GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.77"	"1"	"2002"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7273"	"TTN"	"0.534"	"0.655"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1996"	"2017"	"9"	"0"	"CLINGEN"
"7273"	"TTN"	"0.534"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.8571429"	"2002"	"2017"	"3"	"0"	"CTD_human"
"7273"	"TTN"	"0.534"	"0.655"	"C1450052"	"Tibial Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.67"	"1"	"2002"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1837342"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"2002"	"2018"	"0"	"67"	"CTD_human;ORPHANET"
"7273"	"TTN"	"0.534"	"0.655"	"C1838244"	"TIBIAL MUSCULAR DYSTROPHY, TARDIVE"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.98"	"1"	"1993"	"2016"	"2"	"44"	"CTD_human;ORPHANET;UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1858763"	"Cardiomyopathy, Dilated, 1g"	"disease"	"C14"	"Disease or Syndrome"	"0.80"		"1999"	"2018"	"3"	"134"	"CTD_human;UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1861065"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2015"	"2"	"34"	"CTD_human;UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C1863599"	"Hereditary Myopathy with Early Respiratory Failure"	"disease"	"C05;C08;C10;C16"	"Disease or Syndrome"	"0.80"	"0.9166667"	"1993"	"2017"	"1"	"39"	"CTD_human;ORPHANET;UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C2673677"	"Myopathy, Early-Onset, with Fatal Cardiomyopathy"	"disease"	"C05;C10;C14"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2014"	"0"	"35"	"CTD_human;ORPHANET"
"7273"	"TTN"	"0.534"	"0.655"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"7273"	"TTN"	"0.534"	"0.655"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7273"	"TTN"	"0.534"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7274"	"TTPA"	"0.642"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7274"	"TTPA"	"0.642"	"0.379"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7274"	"TTPA"	"0.642"	"0.379"	"C0009090"	"Cluttering"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0034933"	"Reflex, Abnormal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0037822"	"Speech Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0042035"	"Urination Disorders"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0042875"	"Vitamin E Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0151572"	"Reflex, Corneal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0151888"	"Hyporeflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0151889"	"Hyperreflexia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0155536"	"Paracousis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0233726"	"Aprosodia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0234146"	"Absent reflex"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0234784"	"Reflex, Gag, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0241772"	"Reflex, Deep Tendon, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0260662"	"Hearing problem"	"group"	"C09;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0277839"	"Hoffman's Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0277850"	"Reflex, Pendular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0278211"	"Reflex, Corneal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0522345"	"Reflex, Acoustic, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0558845"	"Reflex, Ankle, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0558846"	"Reflex, Triceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0558847"	"Reflex, Biceps, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0576612"	"Reflex, Anal, Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0743002"	"Abnormal Deep Tendon Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751468"	"Bulbocavernosus Reflex, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751469"	"Bulbocavernousus Reflex Absent"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751470"	"Palmo-Mental Reflex"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751471"	"Reflex, Anal, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751472"	"Reflex, Ankle, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751473"	"Reflex, Ankle, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751474"	"Reflex, Biceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751475"	"Reflex, Biceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751476"	"Reflex, Gag, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751477"	"Reflex, Knee, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751478"	"Reflex, Knee, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751479"	"Reflex, Moro, Asymmetric"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751480"	"Reflex, Triceps, Abnormal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751481"	"Reflex, Triceps, Decreased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751512"	"Dysglossia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751513"	"Rhinolalia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0751514"	"Verbal Fluency Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752255"	"Impairment, Light Touch Sensation"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752256"	"Pain Sensation Diminished"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752257"	"Pinprick Sensation Diminished"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752258"	"Position Sense Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752260"	"Proprioceptive Disorders"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752261"	"Thermal Sensation Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0752262"	"Somatosensory Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C0877848"	"Distorted hearing"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C1510450"	"Dysacusis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C1848533"	"Ataxia with vitamin E deficiency"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"1.00"	"1"	"1985"	"2015"	"10"	"23"	"CTD_human;ORPHANET;UNIPROT"
"7274"	"TTPA"	"0.642"	"0.379"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C3495145"	"Dyslalia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7274"	"TTPA"	"0.642"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7275"	"TUB"	"0.667"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"7275"	"TUB"	"0.667"	"0.345"	"C4015424"	"RETINAL DYSTROPHY AND OBESITY"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"1"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9609544"	"1981"	"2018"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0007286"	"Carpal Tunnel Syndrome"	"disease"	"C10;C26"	"Disease or Syndrome"	"0.70"	"1"	"1991"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"7276"	"TTR"	"0.471"	"0.897"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1985"	"2010"	"5"	"0"	"PSYGENET"
"7276"	"TTR"	"0.471"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1985"	"2010"	"5"	"0"	"PSYGENET"
"7276"	"TTR"	"0.471"	"0.897"	"C0011609"	"Drug Eruptions"	"group"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1952"	"1952"	"1"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2007"	"2009"	"2"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2007"	"2010"	"2"	"0"	"PSYGENET"
"7276"	"TTR"	"0.471"	"0.897"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0155127"	"Familial Amyloid Polyneuropathy, Type V"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0206245"	"Amyloid Neuropathies, Familial"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1983"	"2018"	"4"	"0"	"CTD_human;ORPHANET"
"7276"	"TTR"	"0.471"	"0.897"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0268383"	"Familial amyloid polyneuropathy, type VI"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0268384"	"Familial Amyloid Neuropathy, Portuguese Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.38"	"1"	"1991"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0268385"	"Familial Amyloid Polyneuropathy, Jewish Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0268386"	"Amyloid Polyneuropathy, Swiss Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0342608"	"Amyloid Polyneuropathy, British Type (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1986"	"2018"	"9"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C0406537"	"Morbilliform Drug Reaction"	"disease"	"C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0740340"	"Amyloidosis, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9736842"	"1981"	"2018"	"2"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C0936273"	"Familial Amyloid Polyneuropathy, Type IV"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C1527337"	"Familial Amyloid Polyneuropathy, Appalachian Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1999"	"2010"	"4"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C2750824"	"Dystransthyretinemic Euthyroidal Hyperthyroxinemia"	"disease"	"C19"	"Disease or Syndrome"	"0.60"		"1991"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"7276"	"TTR"	"0.471"	"0.897"	"C2751492"	"AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.9647887"	"1956"	"2018"	"72"	"45"	"CTD_human;UNIPROT"
"7276"	"TTR"	"0.471"	"0.897"	"C3151470"	"AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED"	"disease"		"Disease or Syndrome"	"0.40"		"1980"	"2013"	"72"	"42"	"UNIPROT"
"7276"	"TTR"	"0.471"	"0.897"	"C3151471"	"AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED"	"disease"		"Disease or Syndrome"	"0.40"		"1984"	"2013"	"72"	"42"	"UNIPROT"
"7276"	"TTR"	"0.471"	"0.897"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"7276"	"TTR"	"0.471"	"0.897"	"C4275067"	"Transthyretin related familial amyloid cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7276"	"TTR"	"0.471"	"0.897"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7276"	"TTR"	"0.471"	"0.897"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7277"	"TUBA4A"	"0.834"	"0.207"	"C4015512"	"AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7280"	"TUBB2A"	"0.707"	"0.31"	"C3810407"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"7283"	"TUBG1"	"0.735"	"0.241"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7283"	"TUBG1"	"0.735"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7283"	"TUBG1"	"0.735"	"0.241"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7283"	"TUBG1"	"0.735"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7283"	"TUBG1"	"0.735"	"0.241"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"1993"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7283"	"TUBG1"	"0.735"	"0.241"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"7283"	"TUBG1"	"0.735"	"0.241"	"C3809420"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"7283"	"TUBG1"	"0.735"	"0.241"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7284"	"TUFM"	"0.696"	"0.448"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7284"	"TUFM"	"0.696"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7284"	"TUFM"	"0.696"	"0.448"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7284"	"TUFM"	"0.696"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7284"	"TUFM"	"0.696"	"0.448"	"C1857682"	"Combined Oxidative Phosphorylation Deficiency 4"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2007"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"7284"	"TUFM"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"7286"	"TUFT1"	"0.857"	"0.138"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"1994"	"1994"	"1"	"0"	"GENOMICS_ENGLAND"
"7287"	"TULP1"	"0.636"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2016"	"0"	"2"	"ORPHANET"
"7287"	"TULP1"	"0.636"	"0.345"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.36"	"1"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"7287"	"TULP1"	"0.636"	"0.345"	"C1838603"	"Retinitis Pigmentosa 14"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.81"	"1"	"1997"	"2015"	"6"	"14"	"CTD_human;UNIPROT"
"7287"	"TULP1"	"0.636"	"0.345"	"C3151206"	"LEBER CONGENITAL AMAUROSIS 15"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"7289"	"TULP3"	"0.799"	"0.172"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7289"	"TULP3"	"0.799"	"0.172"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7290"	"HIRA"	"0.633"	"0.517"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2007"	"0"	"0"	"ORPHANET"
"7290"	"HIRA"	"0.633"	"0.517"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"1998"	"2007"	"0"	"0"	"ORPHANET"
"7290"	"HIRA"	"0.633"	"0.517"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7290"	"HIRA"	"0.633"	"0.517"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7290"	"HIRA"	"0.633"	"0.517"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2017"	"0"	"0"	"ORPHANET"
"7290"	"HIRA"	"0.633"	"0.517"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0001193"	"Apert syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2013"	"2"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"0.9333333"	"1992"	"2015"	"4"	"2"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"2004"	"2017"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9620253"	"2004"	"2018"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0175699"	"Saethre-Chotzen Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"1.00"	"0.9387755"	"1995"	"2016"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0206180"	"Ki-1+ Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0220658"	"Pfeiffer Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"		"2003"	"2003"	"1"	"0"	"CTD_human;ORPHANET"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0265529"	"Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.61"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"7291"	"TWIST1"	"0.464"	"0.759"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1510455"	"Acrocephalosyndactylia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.32"		"2002"	"2013"	"2"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1863370"	"Saethre-Chotzen Syndrome with Eyelid Anomalies"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1997"	"2002"	"4"	"4"	"CTD_human;UNIPROT"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1863371"	"BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2002"	"3"	"3"	"UNIPROT"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1863389"	"Apert-Crouzon Disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C1867146"	"Robinow Sorauf syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1975"	"2003"	"0"	"1"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"7291"	"TWIST1"	"0.464"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"7292"	"TNFSF4"	"0.582"	"0.69"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2016"	"2"	"12"	"CTD_human"
"7292"	"TNFSF4"	"0.582"	"0.69"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2005"	"2014"	"0"	"0"	"CTD_human"
"7292"	"TNFSF4"	"0.582"	"0.69"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"ORPHANET"
"7292"	"TNFSF4"	"0.582"	"0.69"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"7292"	"TNFSF4"	"0.582"	"0.69"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7293"	"TNFRSF4"	"0.645"	"0.414"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7293"	"TNFRSF4"	"0.645"	"0.414"	"C3810053"	"IMMUNODEFICIENCY 16"	"disease"		"Disease or Syndrome"	"0.71"	"0"	"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7295"	"TXN"	"0.503"	"0.793"	"C0006287"	"Bronchopulmonary Dysplasia"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7295"	"TXN"	"0.503"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0243038"	"Carcinoma, Lewis Lung"	"disease"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7296"	"TXNRD1"	"0.528"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.44"	"0.75"	"2007"	"2016"	"1"	"1"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2012"	"2016"	"1"	"2"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"2"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.49"	"1"	"2009"	"2014"	"1"	"1"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.45"	"1"	"2010"	"2017"	"1"	"4"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7297"	"TYK2"	"0.546"	"0.69"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0206182"	"Lymphomatoid Papulosis"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7297"	"TYK2"	"0.546"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7297"	"TYK2"	"0.546"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7297"	"TYK2"	"0.546"	"0.69"	"C1301362"	"Primary Cutaneous Anaplastic Large Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7297"	"TYK2"	"0.546"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7297"	"TYK2"	"0.546"	"0.69"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"7297"	"TYK2"	"0.546"	"0.69"	"C1969086"	"Tyrosine Kinase 2 Deficiency"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.61"	"1"	"2006"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"7298"	"TYMS"	"0.457"	"0.759"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9090909"	"2002"	"2013"	"3"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.974359"	"1993"	"2016"	"6"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0007113"	"Rectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9166667"	"2002"	"2015"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1988"	"2009"	"6"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9186047"	"1997"	"2018"	"11"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"1999"	"2016"	"11"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0012243"	"Digestive System Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"		"2003"	"2009"	"2"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"0.5"	"2006"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"0.8571429"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1993"	"2016"	"4"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2004"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0034885"	"Rectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"1995"	"2009"	"4"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0274576"	"Poisoning by fluorouracil"	"disease"		"Injury or Poisoning"	"0.30"				"0"	"0"	"ORPHANET"
"7298"	"TYMS"	"0.457"	"0.759"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"1999"	"2012"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2002"	"2013"	"3"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0751075"	"Cancer of Digestive System"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"		"2002"	"2011"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2011"	"3"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"1994"	"2011"	"3"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9176471"	"1991"	"2018"	"11"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"4"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2018"	"2"	"0"	"CTD_human"
"7298"	"TYMS"	"0.457"	"0.759"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"		"2008"	"2016"	"1"	"1"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9649123"	"1985"	"2018"	"4"	"3"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1990"	"2001"	"1"	"0"	"PSYGENET"
"7299"	"TYR"	"0.505"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"1990"	"2001"	"1"	"0"	"PSYGENET"
"7299"	"TYR"	"0.505"	"0.724"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0078918"	"Albinism, Oculocutaneous"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.50"	"0.9791667"	"1982"	"2017"	"2"	"5"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0078921"	"Albinism, Tyrosinase-Negative"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.31"	"1"	"1989"	"1997"	"2"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0078922"	"Albinism, Tyrosinase-Positive"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"1989"	"1997"	"2"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0078923"	"Albinism, Yellow-Mutant"	"phenotype"	"C11;C16;C17;C18"	"Finding"	"0.30"		"1989"	"1997"	"2"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C0268494"	"Oculocutaneous albinism type 1"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.96875"	"1981"	"2017"	"20"	"87"	"CTD_human;ORPHANET;UNIPROT"
"7299"	"TYR"	"0.505"	"0.724"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"7299"	"TYR"	"0.505"	"0.724"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C1845069"	"ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)"	"disease"	"C09;C10;C11;C16;C17;C18;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7299"	"TYR"	"0.505"	"0.724"	"C1847024"	"ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.91"	"1"	"1970"	"2015"	"4"	"18"	"CTD_human;ORPHANET;UNIPROT"
"7299"	"TYR"	"0.505"	"0.724"	"C1847132"	"ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.80"		"1981"	"2011"	"4"	"9"	"ORPHANET;UNIPROT"
"7299"	"TYR"	"0.505"	"0.724"	"C1863198"	"ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"ORPHANET"
"7301"	"TYRO3"	"0.63"	"0.69"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7301"	"TYRO3"	"0.63"	"0.69"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"7305"	"TYROBP"	"0.624"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7305"	"TYROBP"	"0.624"	"0.621"	"C1857316"	"POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY"	"disease"	"C02;C05;C10;C16;C17;C18"	"Disease or Syndrome"	"0.90"	"0.9230769"	"1993"	"2018"	"0"	"5"	"CTD_human;ORPHANET"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9722222"	"1990"	"2017"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.42"	"1"	"1999"	"2015"	"0"	"2"	"GENOMICS_ENGLAND"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7306"	"TYRP1"	"0.543"	"0.621"	"C0342683"	"ALBINISM, OCULOCUTANEOUS, TYPE III"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.54"	"1"	"1997"	"2014"	"1"	"2"	"ORPHANET;UNIPROT"
"7306"	"TYRP1"	"0.543"	"0.621"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7306"	"TYRP1"	"0.543"	"0.621"	"C2931599"	"Oculocutaneous albinism type 3"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.54"	"1"	"2004"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"7306"	"TYRP1"	"0.543"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2012"	"2016"	"0"	"2"	"CGI"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7307"	"U2AF1"	"0.624"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.80"	"1"	"2012"	"2017"	"2"	"2"	"CGI;CTD_human;UNIPROT"
"7307"	"U2AF1"	"0.624"	"0.552"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7314"	"UBB"	"0.633"	"0.552"	"C0266122"	"Cleft uvula"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7314"	"UBB"	"0.633"	"0.552"	"C0432090"	"Cleft of hard palate"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7314"	"UBB"	"0.633"	"0.552"	"C0432098"	"Cleft Soft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7314"	"UBB"	"0.633"	"0.552"	"C0432103"	"Submucous cleft of hard palate"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7314"	"UBB"	"0.633"	"0.552"	"C1970095"	"Cleft Palate, Isolated, And Mental Retardation"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7317"	"UBA1"	"0.69"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2008"	"2"	"0"	"GENOMICS_ENGLAND"
"7317"	"UBA1"	"0.69"	"0.379"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7317"	"UBA1"	"0.69"	"0.379"	"C1844934"	"Arthrogryposis multiplex congenita, distal, X-linked"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7318"	"UBA7"	"0.743"	"0.31"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7319"	"UBE2A"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7319"	"UBE2A"	"0.727"	"0.31"	"C3275464"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE"	"disease"		"Disease or Syndrome"	"0.70"		"2006"	"2010"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7319"	"UBE2A"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.46"	"0.8333333"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7324"	"UBE2E1"	"0.785"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7325"	"UBE2E2"	"0.743"	"0.276"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2017"	"1"	"49"	"CTD_human"
"7325"	"UBE2E2"	"0.743"	"0.276"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7325"	"UBE2E2"	"0.743"	"0.276"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7328"	"UBE2H"	"0.886"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"7328"	"UBE2H"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7328"	"UBE2H"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7329"	"UBE2I"	"0.642"	"0.552"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7332"	"UBE2L3"	"0.701"	"0.31"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7334"	"UBE2N"	"0.645"	"0.448"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7334"	"UBE2N"	"0.645"	"0.448"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7334"	"UBE2N"	"0.645"	"0.448"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1999"	"2017"	"3"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.45"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0162635"	"Angelman Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9734513"	"1997"	"2017"	"11"	"120"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"1990"	"2011"	"8"	"0"	"GENOMICS_ENGLAND"
"7337"	"UBE3A"	"0.59"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7337"	"UBE3A"	"0.59"	"0.483"	"C2675336"	"Duplication 15q11-q13 Syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7337"	"UBE3A"	"0.59"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7341"	"SUMO1"	"0.579"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"7341"	"SUMO1"	"0.579"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"7341"	"SUMO1"	"0.579"	"0.621"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7341"	"SUMO1"	"0.579"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7341"	"SUMO1"	"0.579"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7341"	"SUMO1"	"0.579"	"0.621"	"C1866070"	"OROFACIAL CLEFT 10"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7341"	"SUMO1"	"0.579"	"0.621"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7343"	"UBTF"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"7343"	"UBTF"	"0.815"	"0.241"	"C4540086"	"NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"ORPHANET;UNIPROT"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"0.5"	"2007"	"2012"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9811321"	"2000"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"7345"	"UCHL1"	"0.527"	"0.759"	"C3150899"	"PARKINSON DISEASE 5, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2006"	"3"	"1"	"CTD_human;UNIPROT"
"7345"	"UCHL1"	"0.527"	"0.759"	"C3809665"	"SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"1972"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7345"	"UCHL1"	"0.527"	"0.759"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7347"	"UCHL3"	"0.857"	"0.241"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7348"	"UPK1B"	"0.799"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7348"	"UPK1B"	"0.799"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7348"	"UPK1B"	"0.799"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7348"	"UPK1B"	"0.799"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2008"	"2"	"0"	"PSYGENET"
"7349"	"UCN"	"0.557"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2008"	"2"	"0"	"PSYGENET"
"7349"	"UCN"	"0.557"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"1999"	"2003"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7349"	"UCN"	"0.557"	"0.655"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9324324"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7350"	"UCP1"	"0.616"	"0.552"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"7351"	"UCP2"	"0.53"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9090909"	"1998"	"2016"	"2"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.8947368"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2012"	"2"	"0"	"PSYGENET"
"7351"	"UCP2"	"0.53"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.35"	"0.8"	"2003"	"2018"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0678306"	"alcohol sensitivity"	"phenotype"		"Finding"	"0.30"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"7351"	"UCP2"	"0.53"	"0.69"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C1843898"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2012"	"1"	"0"	"CTD_human"
"7351"	"UCP2"	"0.53"	"0.69"	"C4303082"	"Hyperinsulinism due to uncoupling protein 2 deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7352"	"UCP3"	"0.652"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.9393939"	"1998"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"7352"	"UCP3"	"0.652"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7352"	"UCP3"	"0.652"	"0.414"	"C0039870"	"Thinness"	"phenotype"	"C23"	"Finding"	"0.30"		"1998"	"1998"	"1"	"1"	"UNIPROT"
"7352"	"UCP3"	"0.652"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7353"	"UFD1"	"0.63"	"0.552"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1997"	"2001"	"0"	"0"	"ORPHANET"
"7353"	"UFD1"	"0.63"	"0.552"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7353"	"UFD1"	"0.63"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2014"	"2"	"0"	"PSYGENET"
"7353"	"UFD1"	"0.63"	"0.552"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.32"	"0.5"	"1998"	"2001"	"0"	"0"	"ORPHANET"
"7353"	"UFD1"	"0.63"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7353"	"UFD1"	"0.63"	"0.552"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7353"	"UFD1"	"0.63"	"0.552"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7353"	"UFD1"	"0.63"	"0.552"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2002"	"0"	"0"	"ORPHANET"
"7353"	"UFD1"	"0.63"	"0.552"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7355"	"SLC35A2"	"0.636"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"0"	"0"	"UNIPROT"
"7355"	"SLC35A2"	"0.636"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"7355"	"SLC35A2"	"0.636"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2014"	"2017"	"2"	"1"	"GENOMICS_ENGLAND"
"7355"	"SLC35A2"	"0.636"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7355"	"SLC35A2"	"0.636"	"0.448"	"C3806688"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2016"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"7356"	"SCGB1A1"	"0.592"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7356"	"SCGB1A1"	"0.592"	"0.552"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"7356"	"SCGB1A1"	"0.592"	"0.552"	"C0035204"	"Respiration Disorders"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7356"	"SCGB1A1"	"0.592"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2001"	"2006"	"1"	"0"	"PSYGENET"
"7357"	"UGCG"	"0.645"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7357"	"UGCG"	"0.645"	"0.517"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7358"	"UGDH"	"0.743"	"0.379"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7358"	"UGDH"	"0.743"	"0.379"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7361"	"UGT1A"	"0.588"	"0.552"	"C0017551"	"Gilbert Disease (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.95"	"1997"	"2012"	"1"	"0"	"CTD_human"
"7364"	"UGT2B7"	"0.645"	"0.448"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"7364"	"UGT2B7"	"0.645"	"0.448"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"7365"	"UGT2B10"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7366"	"UGT2B15"	"0.743"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"7366"	"UGT2B15"	"0.743"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0018133"	"Graft-vs-Host Disease"	"disease"	"C20"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2005"	"2012"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9375"	"1998"	"2016"	"1"	"0"	"CTD_human"
"7367"	"UGT2B17"	"0.663"	"0.379"	"C2675513"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 12"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7369"	"UMOD"	"0.6"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"1"	"2006"	"2018"	"1"	"2"	"CTD_human"
"7369"	"UMOD"	"0.6"	"0.517"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2017"	"2"	"0"	"CTD_human"
"7369"	"UMOD"	"0.6"	"0.517"	"C0268113"	"Familial juvenile gout"	"disease"	"C05;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"1.00"	"1"	"2002"	"2017"	"14"	"12"	"CTD_human;ORPHANET;UNIPROT"
"7369"	"UMOD"	"0.6"	"0.517"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"		"2002"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7369"	"UMOD"	"0.6"	"0.517"	"C1835934"	"Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2007"	"2"	"2"	"CTD_human;UNIPROT"
"7369"	"UMOD"	"0.6"	"0.517"	"C1859040"	"Medullary Cystic Kidney Disease Type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.78"	"1"	"1993"	"2017"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7369"	"UMOD"	"0.6"	"0.517"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7369"	"UMOD"	"0.6"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7371"	"UCK2"	"0.762"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7371"	"UCK2"	"0.762"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7371"	"UCK2"	"0.762"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2013"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0023440"	"Acute Erythroblastic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"3"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0037889"	"Hereditary spherocytosis"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2005"	"2008"	"3"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0220987"	"Hereditary orotic aciduria"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"7372"	"UMPS"	"0.598"	"0.483"	"C0268130"	"Hereditary orotic aciduria, type 1"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1989"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7372"	"UMPS"	"0.598"	"0.483"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C0949116"	"Congenital hypoplastic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"1979"	"1979"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2008"	"3"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"7372"	"UMPS"	"0.598"	"0.483"	"C3278622"	"OROTIC ACIDURIA WITHOUT MEGALOBLASTIC ANEMIA"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"3"	"UNIPROT"
"7372"	"UMPS"	"0.598"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"GENOMICS_ENGLAND"
"7373"	"COL14A1"	"0.69"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7373"	"COL14A1"	"0.69"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7373"	"COL14A1"	"0.69"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7373"	"COL14A1"	"0.69"	"0.414"	"C1835662"	"Keratosis palmoplantaris papulosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7373"	"COL14A1"	"0.69"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7373"	"COL14A1"	"0.69"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7373"	"COL14A1"	"0.69"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C0005859"	"Bloom Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1986"	"1992"	"1"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2006"	"1"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C0272236"	"Hyperimmunoglobulin M syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2010"	"0"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C1720956"	"Hyper-IgM Immunodeficiency Syndrome, Type 2"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C1720957"	"Hyper-IgM Immunodeficiency Syndrome, Type 3"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7374"	"UNG"	"0.656"	"0.552"	"C1720958"	"Hyper-IgM Immunodeficiency Syndrome, Type 5"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.70"		"2003"	"2005"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7376"	"NR1H2"	"0.552"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7376"	"NR1H2"	"0.552"	"0.552"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7376"	"NR1H2"	"0.552"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"7378"	"UPP1"	"0.752"	"0.276"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7378"	"UPP1"	"0.752"	"0.276"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7379"	"UPK2"	"0.762"	"0.172"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7380"	"UPK3A"	"0.762"	"0.207"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7380"	"UPK3A"	"0.762"	"0.207"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7381"	"UQCRB"	"0.773"	"0.138"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.32"	"0.5"	"2003"	"2008"	"0"	"0"	"ORPHANET"
"7381"	"UQCRB"	"0.773"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"7381"	"UQCRB"	"0.773"	"0.138"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7381"	"UQCRB"	"0.773"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7384"	"UQCRC1"	"0.857"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CTD_human"
"7385"	"UQCRC2"	"0.785"	"0.172"	"C3554608"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2018"	"1"	"1"	"UNIPROT"
"7386"	"UQCRFS1"	"0.639"	"0.345"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7386"	"UQCRFS1"	"0.639"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"GENOMICS_ENGLAND"
"7388"	"UQCRH"	"0.928"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7389"	"UROD"	"0.584"	"0.586"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0162566"	"Porphyria Cutanea Tarda"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"0.9795918"	"1981"	"2016"	"21"	"22"	"CTD_human;ORPHANET;UNIPROT"
"7389"	"UROD"	"0.584"	"0.586"	"C0162569"	"Hepatoerythropoietic Porphyria"	"disease"	"C06;C16;C17;C18"	"Disease or Syndrome"	"0.70"	"0.9583333"	"1981"	"2012"	"19"	"20"	"ORPHANET;UNIPROT"
"7389"	"UROD"	"0.584"	"0.586"	"C0268323"	"Familial porphyria cutanea tarda"	"disease"		"Disease or Syndrome"	"0.70"	"0.88"	"1981"	"2012"	"19"	"22"	"ORPHANET;UNIPROT"
"7389"	"UROD"	"0.584"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0342861"	"Uroporphyrinogen decarboxylase deficiency"	"disease"		"Disease or Syndrome"	"0.50"		"1986"	"2012"	"19"	"20"	"ORPHANET;UNIPROT"
"7389"	"UROD"	"0.584"	"0.586"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7389"	"UROD"	"0.584"	"0.586"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7390"	"UROS"	"0.713"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7390"	"UROS"	"0.713"	"0.379"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"7390"	"UROS"	"0.713"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7390"	"UROS"	"0.713"	"0.379"	"C0162530"	"Porphyria, Erythropoietic"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"1990"	"2017"	"14"	"23"	"CTD_human;ORPHANET;UNIPROT"
"7390"	"UROS"	"0.713"	"0.379"	"C2718078"	"Deficiency of Uroporphyrinogen III Synthase"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.60"		"1990"	"2012"	"14"	"16"	"CTD_human;ORPHANET;UNIPROT"
"7390"	"UROS"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7391"	"USF1"	"0.639"	"0.517"	"C0020474"	"Hyperlipidemia, Familial Combined"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9655172"	"2001"	"2016"	"0"	"0"	"CTD_human"
"7396"	"USH1E"	"0.857"	"0.207"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"ORPHANET"
"7399"	"USH2A"	"0.636"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2018"	"3"	"34"	"CTD_human;ORPHANET"
"7399"	"USH2A"	"0.636"	"0.345"	"C0339534"	"Usher syndrome type 2"	"disease"		"Disease or Syndrome"	"0.38"	"1"	"1994"	"2013"	"0"	"0"	"ORPHANET"
"7399"	"USH2A"	"0.636"	"0.345"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"	"1"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"7399"	"USH2A"	"0.636"	"0.345"	"C1848634"	"USHER SYNDROME, TYPE IIA"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.98"	"1"	"1998"	"2017"	"32"	"171"	"CLINGEN;CTD_human;UNIPROT"
"7399"	"USH2A"	"0.636"	"0.345"	"C3151138"	"RETINITIS PIGMENTOSA 39 (disorder)"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2017"	"10"	"46"	"CTD_human;UNIPROT"
"7401"	"CLRN1"	"0.656"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.85"	"1"	"2002"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"7401"	"CLRN1"	"0.656"	"0.379"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"1.00"	"0.9375"	"1997"	"2017"	"16"	"16"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"7401"	"CLRN1"	"0.656"	"0.379"	"C3280041"	"RETINITIS PIGMENTOSA 61"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"2"	"CTD_human;UNIPROT"
"7402"	"UTRN"	"0.614"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.53"	"1"	"2011"	"2016"	"1"	"0"	"CGI;CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.53"	"1"	"2011"	"2016"	"1"	"0"	"CGI;CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.50"		"2009"	"2009"	"1"	"0"	"CGI;CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2012"	"2012"	"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2014"	"2014"	"1"	"0"	"CGI;CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2011"	"2016"	"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C0796004"	"Kabuki make-up syndrome"	"disease"	"C09;C15;C16"	"Congenital Abnormality"	"0.70"	"1"	"2012"	"2018"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"7403"	"KDM6A"	"0.543"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7403"	"KDM6A"	"0.543"	"0.724"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"7403"	"KDM6A"	"0.543"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"7408"	"VASP"	"0.735"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7409"	"VAV1"	"0.592"	"0.621"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0002895"	"Anemia, Sickle Cell"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.37"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.962963"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.39"	"0.7142857"	"2006"	"2016"	"2"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.34"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0042109"	"Urticaria"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7412"	"VCAM1"	"0.466"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7414"	"VCL"	"0.63"	"0.414"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7414"	"VCL"	"0.63"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.45"	"1"	"2002"	"2015"	"0"	"6"	"GENOMICS_ENGLAND"
"7414"	"VCL"	"0.63"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2006"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"7414"	"VCL"	"0.63"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7414"	"VCL"	"0.63"	"0.414"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7414"	"VCL"	"0.63"	"0.414"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7414"	"VCL"	"0.63"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7414"	"VCL"	"0.63"	"0.414"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7414"	"VCL"	"0.63"	"0.414"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7414"	"VCL"	"0.63"	"0.414"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7414"	"VCL"	"0.63"	"0.414"	"C1969639"	"Cardiomyopathy, Dilated, 1w"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2002"	"2006"	"2"	"1"	"CTD_human;UNIPROT"
"7414"	"VCL"	"0.63"	"0.414"	"C2750459"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"2006"	"2016"	"4"	"2"	"CLINGEN;CTD_human;UNIPROT"
"7415"	"VCP"	"0.502"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.9210526"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"7415"	"VCP"	"0.502"	"0.828"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7415"	"VCP"	"0.502"	"0.828"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"7415"	"VCP"	"0.502"	"0.828"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7415"	"VCP"	"0.502"	"0.828"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7415"	"VCP"	"0.502"	"0.828"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7415"	"VCP"	"0.502"	"0.828"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"7415"	"VCP"	"0.502"	"0.828"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"7415"	"VCP"	"0.502"	"0.828"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"7415"	"VCP"	"0.502"	"0.828"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7415"	"VCP"	"0.502"	"0.828"	"C1833662"	"INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA"	"disease"	"C05;C10;C16;C18;F03"	"Disease or Syndrome"	"1.00"	"1"	"1983"	"2017"	"14"	"7"	"CTD_human;ORPHANET;UNIPROT"
"7415"	"VCP"	"0.502"	"0.828"	"C3151403"	"AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"7415"	"VCP"	"0.502"	"0.828"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7415"	"VCP"	"0.502"	"0.828"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7415"	"VCP"	"0.502"	"0.828"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7415"	"VCP"	"0.502"	"0.828"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7415"	"VCP"	"0.502"	"0.828"	"C4225244"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0033922"	"Psychomotor Disorders"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0679465"	"Psychomotor Impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0751456"	"Developmental Psychomotor Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7416"	"VDAC1"	"0.63"	"0.586"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7417"	"VDAC2"	"0.69"	"0.345"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.50"	"0.92"	"1993"	"2016"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7421"	"VDR"	"0.39"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9680851"	"1995"	"2018"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.35"	"0.8"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0007785"	"Cerebral Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0019247"	"Hereditary Diseases"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.31"		"2003"	"2014"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2000"	"2018"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7421"	"VDR"	"0.39"	"0.793"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.70"	"0.9181818"	"1995"	"2018"	"0"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0035579"	"Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.70"	"0.9756098"	"1989"	"2017"	"3"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"1"	"2005"	"2013"	"1"	"0"	"PSYGENET"
"7421"	"VDR"	"0.39"	"0.793"	"C0037176"	"Single-Gene Defects"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0041948"	"Uremia"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.35"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0042870"	"Vitamin D Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.925"	"1998"	"2018"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"7421"	"VDR"	"0.39"	"0.793"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0342646"	"Vitamin D-Dependent Rickets, Type 2A"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1986"	"2018"	"12"	"15"	"CTD_human;UNIPROT"
"7421"	"VDR"	"0.39"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9746835"	"1996"	"2016"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9569892"	"1995"	"2018"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751010"	"Cerebral Infarction, Left Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751011"	"Cerebral Infarction, Right Hemisphere"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751012"	"Anterior Choroidal Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751014"	"Subcortical Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0887799"	"Posterior Choroidal Artery Infarction"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C0950123"	"Genetic Diseases, Inborn"	"group"	"C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.7"	"1998"	"2015"	"2"	"0"	"CTD_human"
"7421"	"VDR"	"0.39"	"0.793"	"C3536983"	"Familial Hypophosphatemic Rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"1989"	"2017"	"12"	"10"	"ORPHANET;UNIPROT"
"7421"	"VDR"	"0.39"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7421"	"VDR"	"0.39"	"0.793"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"1993"	"2012"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.925"	"1998"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.95"	"2005"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1998"	"2016"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9565217"	"2001"	"2014"	"3"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.962963"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"2"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.40"	"0.8333333"	"1995"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9354839"	"1995"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9907407"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9756098"	"1998"	"2017"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"		"2007"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0008677"	"Bronchitis, Chronic"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8888889"	"1998"	"2015"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.925"	"1996"	"2018"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0010398"	"Cruveilhier-Baumgarten Syndrome"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2009"	"2016"	"5"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2009"	"2016"	"5"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.40"	"0.9487179"	"1997"	"2018"	"3"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9901961"	"1992"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2016"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1996"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0020541"	"Hypertension, Portal"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.33"		"2004"	"2009"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2013"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0024440"	"Macular Edema, Cystoid"	"disease"	"C11"	"Disease or Syndrome"	"0.35"	"0.8"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9510086"	"1994"	"2018"	"3"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2002"	"2007"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1999"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2013"	"4"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.60"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0035328"	"Retinal Vein Occlusion"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.52"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2010"	"2015"	"1"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"0.8333333"	"1997"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"1999"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0085109"	"Corneal Neovascularization"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.9473684"	"1997"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0085605"	"Liver Failure"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2018"	"5"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0178540"	"Cerebral Hypoxia-Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2002"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.32"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.970297"	"2000"	"2018"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0271051"	"Macular retinal edema"	"disease"	"C11"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0271178"	"Irvine-Gass Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0342257"	"Complications of Diabetes Mellitus"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9886364"	"1997"	"2017"	"4"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.9615385"	"1993"	"2017"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"2"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0600518"	"Choroidal Neovascularization"	"phenotype"	"C11;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0678807"	"prenatal alcohol exposure"	"phenotype"		"Finding"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0752304"	"Hypoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0752305"	"Anoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0752306"	"Anoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0752307"	"Anoxia-Ischemia, Cerebral"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0752308"	"Hypoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1998"	"2016"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"1998"	"2016"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2007"	"2018"	"5"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2011"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1527411"	"Thrombosis of retinal vein"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9545455"	"1993"	"2015"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.86"	"1998"	"2018"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2005"	"2005"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2063866"	"Depressive Disorder, Treatment-Resistant"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676832"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676833"	"MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676835"	"NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676836"	"END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676837"	"PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676838"	"NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2676839"	"NEUROPATHY, DIABETIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2717961"	"Thrombotic Microangiopathies"	"group"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2931852"	"Clear-cell metastatic renal cell carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C2937358"	"Cerebral Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C4017829"	"MICROVASCULAR COMPLICATIONS OF DIABETES, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7422"	"VEGFA"	"0.298"	"0.897"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7423"	"VEGFB"	"0.642"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9545455"	"2001"	"2018"	"2"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"7424"	"VEGFC"	"0.501"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.39"	"0.875"	"2001"	"2014"	"1"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"2"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.6666667"	"2003"	"2017"	"2"	"0"	"CTD_human"
"7424"	"VEGFC"	"0.501"	"0.69"	"C1704423"	"Milroy Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2015"	"0"	"0"	"ORPHANET"
"7424"	"VEGFC"	"0.501"	"0.69"	"C4014628"	"LYMPHEDEMA, HEREDITARY, ID"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"2"	"CTD_human"
"7425"	"VGF"	"0.676"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"7425"	"VGF"	"0.676"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"2008"	"2013"	"4"	"0"	"PSYGENET"
"7425"	"VGF"	"0.676"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.75"	"2008"	"2013"	"4"	"0"	"PSYGENET"
"7425"	"VGF"	"0.676"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"7425"	"VGF"	"0.676"	"0.414"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7425"	"VGF"	"0.676"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7428"	"VHL"	"0.464"	"0.586"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"0.8"	"1996"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"7428"	"VHL"	"0.464"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"0.9633028"	"1989"	"2018"	"9"	"5"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0019562"	"Von Hippel-Lindau Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"1.00"	"0.9234973"	"1962"	"2018"	"18"	"122"	"CTD_human;ORPHANET;UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"0.9473684"	"1995"	"2016"	"1"	"0"	"CGI;CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.50"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9589041"	"1994"	"2017"	"4"	"18"	"CGI;CTD_human;UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"7428"	"VHL"	"0.464"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1991"	"2012"	"12"	"0"	"CLINGEN"
"7428"	"VHL"	"0.464"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1991"	"2012"	"12"	"0"	"CLINGEN"
"7428"	"VHL"	"0.464"	"0.586"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2004"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7428"	"VHL"	"0.464"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.52"	"1"	"1994"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"0.9464286"	"1995"	"2018"	"10"	"1"	"CGI;CTD_human;UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1991"	"2012"	"12"	"0"	"CLINGEN"
"7428"	"VHL"	"0.464"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1991"	"2012"	"12"	"0"	"CLINGEN"
"7428"	"VHL"	"0.464"	"0.586"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"0.9444444"	"1995"	"2018"	"1"	"0"	"CGI;CTD_human;GENOMICS_ENGLAND"
"7428"	"VHL"	"0.464"	"0.586"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"1997"	"2006"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1997"	"2014"	"9"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1997"	"2014"	"9"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"1997"	"2014"	"9"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.36"	"0.6666667"	"1996"	"2016"	"9"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C1378703"	"Renal carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"0.9791667"	"1994"	"2018"	"0"	"0"	"CGI"
"7428"	"VHL"	"0.464"	"0.586"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7428"	"VHL"	"0.464"	"0.586"	"C1837915"	"ERYTHROCYTOSIS, FAMILIAL, 2"	"disease"	"C15"	"Disease or Syndrome"	"0.90"		"1995"	"2017"	"2"	"21"	"CTD_human;ORPHANET;UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C2674004"	"VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2006"	"17"	"47"	"UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C2750825"	"NONPAPILLARY RENAL CARCINOMA 1 LOCUS"	"phenotype"		"Finding"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7428"	"VHL"	"0.464"	"0.586"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"1998"	"2003"	"3"	"14"	"UNIPROT"
"7428"	"VHL"	"0.464"	"0.586"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7429"	"VIL1"	"0.72"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9423077"	"1999"	"2018"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2015"	"3"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"3"	"0"	"CTD_human"
"7430"	"EZR"	"0.533"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.95"	"1989"	"2017"	"4"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0007140"	"Carcinosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9649123"	"1997"	"2018"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2015"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0085084"	"Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0154681"	"Anterior Horn Cell Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0154682"	"Lateral Sclerosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0270763"	"Familial Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0270764"	"Motor Neuron Disease, Lower"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0521659"	"Motor Neuron Disease, Upper"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0543858"	"Motor Neuron Disease, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9761905"	"1989"	"2017"	"4"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8888889"	"1990"	"2017"	"4"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"7431"	"VIM"	"0.432"	"0.793"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7431"	"VIM"	"0.432"	"0.793"	"C1861827"	"Cataract, Nuclear Diffuse Nonprogressive"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C3805411"	"CATARACT 30"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2017"	"3"	"3"	"UNIPROT"
"7431"	"VIM"	"0.432"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7431"	"VIM"	"0.432"	"0.793"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2007"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2014"	"2"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C0005686"	"Urinary Bladder Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2009"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2004"	"2009"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0035455"	"Rhinitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"1988"	"1988"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"2"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C1542327"	"Fetus or newborn affected by alcohol transmitted via placenta or breast milk"	"disease"		"Finding"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"7432"	"VIP"	"0.526"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7432"	"VIP"	"0.526"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7433"	"VIPR1"	"0.624"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7434"	"VIPR2"	"0.667"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7434"	"VIPR2"	"0.667"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8571429"	"2011"	"2014"	"1"	"0"	"CTD_human"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2002"	"2008"	"3"	"0"	"PSYGENET"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"2006"	"2008"	"2"	"0"	"GENOMICS_ENGLAND"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0394006"	"Dysequilibrium syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.56"	"1"	"2006"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"7436"	"VLDLR"	"0.572"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7436"	"VLDLR"	"0.572"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7439"	"BEST1"	"0.521"	"0.586"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"0.6666667"	"2009"	"2016"	"0"	"1"	"ORPHANET"
"7439"	"BEST1"	"0.521"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7439"	"BEST1"	"0.521"	"0.586"	"C0339510"	"Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"1.00"	"0.9736842"	"1964"	"2018"	"17"	"85"	"CTD_human;ORPHANET;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C1842914"	"Adult-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.75"	"0.8"	"2000"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"7439"	"BEST1"	"0.521"	"0.586"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7439"	"BEST1"	"0.521"	"0.586"	"C1860406"	"VITREORETINOCHOROIDOPATHY (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.68"	"1"	"1958"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C2674009"	"Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.71"	"0"	"2003"	"2006"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C2675055"	"BEST VITELLIFORM MACULAR DYSTROPHY, MULTIFOCAL (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"1998"	"2011"	"17"	"78"	"UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C2745945"	"Juvenile-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.82"	"0.5"	"1998"	"2011"	"17"	"78"	"CTD_human;ORPHANET;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C2750789"	"RETINITIS PIGMENTOSA, CONCENTRIC (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1998"	"2009"	"1"	"4"	"CTD_human;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C3888099"	"Autosomal dominant vitreoretinochoroidopathy"	"disease"		"Disease or Syndrome"	"0.54"	"1"	"2004"	"2014"	"1"	"3"	"ORPHANET;UNIPROT"
"7439"	"BEST1"	"0.521"	"0.586"	"C3888198"	"BESTROPHINOPATHY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"1.00"	"1"	"2000"	"2017"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"7441"	"VPREB1"	"0.727"	"0.31"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7441"	"VPREB1"	"0.727"	"0.31"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7441"	"VPREB1"	"0.727"	"0.31"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0010200"	"Coughing"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.34"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0014852"	"Esophageal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0014868"	"Esophagitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0018834"	"Heartburn"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"1"	"2002"	"2016"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.32"		"2007"	"2011"	"2"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.40"	"0.96"	"2004"	"2018"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0037383"	"Sneezing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2002"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.39"	"1"	"2002"	"2016"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2013"	"4"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7442"	"TRPV1"	"0.532"	"0.724"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2013"	"4"	"0"	"CTD_human"
"7443"	"VRK1"	"0.663"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7443"	"VRK1"	"0.663"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7443"	"VRK1"	"0.663"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7443"	"VRK1"	"0.663"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"7443"	"VRK1"	"0.663"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"2009"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"7443"	"VRK1"	"0.663"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7443"	"VRK1"	"0.663"	"0.414"	"C1843504"	"Pontocerebellar Hypoplasia Type 1"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.62"	"1"	"2009"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"7443"	"VRK1"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7444"	"VRK2"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2018"	"2"	"5"	"PSYGENET"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.45"	"1"	"2002"	"2016"	"1"	"3"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2013"	"2"	"0"	"PSYGENET"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7447"	"VSNL1"	"0.652"	"0.345"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7448"	"VTN"	"0.534"	"0.724"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7450"	"VWF"	"0.462"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7450"	"VWF"	"0.462"	"0.724"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C0007222"	"Cardiovascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2006"	"2016"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.35"	"0.8"	"1997"	"2012"	"3"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.34"		"1985"	"2012"	"2"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0079102"	"Cerebral Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"1985"	"2012"	"2"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0752143"	"Intracranial Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0752144"	"Brain Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0936261"	"Brain Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C0936263"	"Cerebral Thrombus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C1264039"	"von Willebrand Disease, Type 1"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.980198"	"1985"	"2018"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1264040"	"von Willebrand Disease, Type 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"	"1"	"1987"	"2016"	"29"	"36"	"CTD_human;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1264041"	"von Willebrand Disease, Type 3"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.9038462"	"1989"	"2016"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1282968"	"von Willebrand Disease, Type 2A"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.8965517"	"1987"	"2014"	"29"	"34"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1282971"	"von Willebrand Disease, Type 2B"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.9574468"	"1980"	"2017"	"29"	"34"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1282974"	"von Willebrand disease type 2M"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"0.9285714"	"1984"	"2016"	"29"	"35"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1282975"	"von Willebrand Disease, Type 2N"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1989"	"2014"	"29"	"37"	"CTD_human;ORPHANET;UNIPROT"
"7450"	"VWF"	"0.462"	"0.724"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7450"	"VWF"	"0.462"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7453"	"WARS"	"0.701"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"7453"	"WARS"	"0.701"	"0.414"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7453"	"WARS"	"0.701"	"0.414"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7453"	"WARS"	"0.701"	"0.414"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7453"	"WARS"	"0.701"	"0.414"	"C4540265"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7454"	"WAS"	"0.586"	"0.69"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7454"	"WAS"	"0.586"	"0.69"	"C0043194"	"Wiskott-Aldrich Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"1.00"	"0.9776119"	"1980"	"2018"	"12"	"14"	"CTD_human;ORPHANET;UNIPROT"
"7454"	"WAS"	"0.586"	"0.69"	"C1839163"	"THROMBOCYTOPENIA 1 (disorder)"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"5"	"9"	"CTD_human;ORPHANET;UNIPROT"
"7454"	"WAS"	"0.586"	"0.69"	"C1839164"	"Thrombocytopenia, X-Linked, Intermittent"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"1995"	"2002"	"5"	"5"	"ORPHANET;UNIPROT"
"7454"	"WAS"	"0.586"	"0.69"	"C1845987"	"Neutropenia, Severe Congenital, X-Linked"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"		"1988"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7456"	"WIPF1"	"0.659"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1998"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"7456"	"WIPF1"	"0.659"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7456"	"WIPF1"	"0.659"	"0.448"	"C0043194"	"Wiskott-Aldrich Syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.60"	"1"	"1999"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"7456"	"WIPF1"	"0.659"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1998"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"7461"	"CLIP2"	"0.573"	"0.724"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.57"	"1"	"1998"	"2012"	"0"	"0"	"ORPHANET"
"7465"	"WEE1"	"0.621"	"0.483"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"7466"	"WFS1"	"0.545"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7466"	"WFS1"	"0.545"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2000"	"2012"	"5"	"0"	"PSYGENET"
"7466"	"WFS1"	"0.545"	"0.655"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"7466"	"WFS1"	"0.545"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2000"	"2005"	"3"	"0"	"PSYGENET"
"7466"	"WFS1"	"0.545"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"0.6666667"	"2000"	"2005"	"3"	"0"	"PSYGENET"
"7466"	"WFS1"	"0.545"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9545455"	"2002"	"2016"	"1"	"5"	"CTD_human"
"7466"	"WFS1"	"0.545"	"0.655"	"C0043207"	"Wolfram Syndrome"	"disease"	"C09;C10;C11;C12;C13;C16;C18;C19"	"Disease or Syndrome"	"1.00"	"0.9880952"	"1992"	"2018"	"8"	"26"	"CTD_human;ORPHANET;UNIPROT"
"7466"	"WFS1"	"0.545"	"0.655"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"7466"	"WFS1"	"0.545"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2000"	"2015"	"5"	"0"	"PSYGENET"
"7466"	"WFS1"	"0.545"	"0.655"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7466"	"WFS1"	"0.545"	"0.655"	"C1833021"	"DEAFNESS, AUTOSOMAL DOMINANT 6"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2016"	"9"	"14"	"CTD_human;UNIPROT"
"7466"	"WFS1"	"0.545"	"0.655"	"C3280358"	"Wolfram-Like Syndrome, Autosomal Dominant"	"disease"	"C09;C10;C11;C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.70"		"2001"	"2011"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7466"	"WFS1"	"0.545"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7466"	"WFS1"	"0.545"	"0.655"	"C3805412"	"CATARACT 41"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"7466"	"WFS1"	"0.545"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7467"	"WHCR"	"0.928"	"0.034"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7467"	"WHCR"	"0.928"	"0.034"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"2009"	"2015"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7468"	"NSD2"	"0.558"	"0.69"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.80"	"0.9375"	"1999"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"7468"	"NSD2"	"0.558"	"0.69"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7469"	"NELFA"	"0.648"	"0.517"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2009"	"2012"	"0"	"0"	"ORPHANET"
"7471"	"WNT1"	"0.555"	"0.655"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"7471"	"WNT1"	"0.555"	"0.655"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.65"	"1"	"2013"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C0029458"	"Osteoporosis, Postmenopausal"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"2"	"UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"2"	"2"	"CTD_human;UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C0264080"	"Juvenile osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7471"	"WNT1"	"0.555"	"0.655"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.32"	"0.5"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"7471"	"WNT1"	"0.555"	"0.655"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"7471"	"WNT1"	"0.555"	"0.655"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7471"	"WNT1"	"0.555"	"0.655"	"C2674640"	"FRACTURE, HIP, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"2"	"2"	"UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C3554428"	"OSTEOGENESIS IMPERFECTA, TYPE XIV"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C3808844"	"OSTEOGENESIS IMPERFECTA, TYPE XV"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"4"	"7"	"CTD_human;UNIPROT"
"7471"	"WNT1"	"0.555"	"0.655"	"C3888192"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"2"	"2"	"UNIPROT"
"7472"	"WNT2"	"0.607"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.7142857"	"2001"	"2012"	"2"	"0"	"CTD_human"
"7472"	"WNT2"	"0.607"	"0.552"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"		"2005"	"2014"	"1"	"0"	"CTD_human"
"7472"	"WNT2"	"0.607"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7472"	"WNT2"	"0.607"	"0.552"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7473"	"WNT3"	"0.567"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"7473"	"WNT3"	"0.567"	"0.655"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"7473"	"WNT3"	"0.567"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7473"	"WNT3"	"0.567"	"0.655"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7473"	"WNT3"	"0.567"	"0.655"	"C2931216"	"Tetra-amelia autosomal recessive"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"7473"	"WNT3"	"0.567"	"0.655"	"C2931218"	"Tetraamelia multiple malformations"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7473"	"WNT3"	"0.567"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C0265205"	"Robinow Syndrome"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.96"	"1"	"1969"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"7474"	"WNT5A"	"0.5"	"0.759"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"7474"	"WNT5A"	"0.5"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7474"	"WNT5A"	"0.5"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C0042065"	"Genitourinary Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7476"	"WNT7A"	"0.588"	"0.517"	"C0751569"	"Genitourinary Cancer"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1848651"	"Al Awadi syndrome"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.77"	"1"	"2006"	"2018"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1856728"	"Fuhrmann syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.93"	"1"	"1997"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7476"	"WNT7A"	"0.588"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7476"	"WNT7A"	"0.588"	"0.517"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7478"	"WNT8A"	"0.886"	"0.103"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.41"	"0"	"2012"	"2015"	"1"	"1"	"CTD_human"
"7478"	"WNT8A"	"0.886"	"0.103"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7478"	"WNT8A"	"0.886"	"0.103"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7478"	"WNT8A"	"0.886"	"0.103"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7479"	"WNT8B"	"0.834"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"UNIPROT"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2003"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2003"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"7480"	"WNT10B"	"0.645"	"0.448"	"C2749665"	"SPLIT-HAND/FOOT MALFORMATION 6 (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2008"	"1"	"2"	"CTD_human;UNIPROT"
"7480"	"WNT10B"	"0.645"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7480"	"WNT10B"	"0.645"	"0.448"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7480"	"WNT10B"	"0.645"	"0.448"	"C4310730"	"TOOTH AGENESIS, SELECTIVE, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"7481"	"WNT11"	"0.648"	"0.379"	"C0000771"	"Abnormalities, Drug-Induced"	"phenotype"	"C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7481"	"WNT11"	"0.648"	"0.379"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7481"	"WNT11"	"0.648"	"0.379"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7481"	"WNT11"	"0.648"	"0.379"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7482"	"WNT2B"	"0.69"	"0.448"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7482"	"WNT2B"	"0.69"	"0.448"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7485"	"WRB"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7486"	"WRN"	"0.545"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7486"	"WRN"	"0.545"	"0.586"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"7486"	"WRN"	"0.545"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7486"	"WRN"	"0.545"	"0.586"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.42"	"1"	"2006"	"2012"	"0"	"0"	"CGI"
"7486"	"WRN"	"0.545"	"0.586"	"C0043119"	"Werner Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.9152542"	"1993"	"2017"	"3"	"29"	"CTD_human;ORPHANET;UNIPROT"
"7486"	"WRN"	"0.545"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2013"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"7486"	"WRN"	"0.545"	"0.586"	"C0231341"	"Premature aging syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"0.9545455"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7486"	"WRN"	"0.545"	"0.586"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"1993"	"1996"	"2"	"0"	"GENOMICS_ENGLAND"
"7486"	"WRN"	"0.545"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2008"	"2015"	"0"	"0"	"UNIPROT"
"7486"	"WRN"	"0.545"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7490"	"WT1"	"0.444"	"0.69"	"C0003076"	"Aniridia"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.44"	"1"	"1989"	"2006"	"0"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1996"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"7490"	"WT1"	"0.444"	"0.69"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2002"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7490"	"WT1"	"0.444"	"0.69"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.51"	"1"	"1995"	"2007"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9672131"	"1994"	"2018"	"2"	"1"	"CGI;CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1994"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.80"	"0.9666667"	"1989"	"2018"	"6"	"1"	"CGI;CTD_human;ORPHANET;UNIPROT"
"7490"	"WT1"	"0.444"	"0.69"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7490"	"WT1"	"0.444"	"0.69"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1996"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"7490"	"WT1"	"0.444"	"0.69"	"C0206115"	"WAGR Syndrome"	"disease"	"C04;C10;C11;C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"	"1"	"1989"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"7490"	"WT1"	"0.444"	"0.69"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.43"	"1"	"1995"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2004"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0281508"	"Desmoplastic Small Round Cell Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.972973"	"1994"	"2014"	"0"	"0"	"CGI;ORPHANET"
"7490"	"WT1"	"0.444"	"0.69"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.42"	"1"	"1995"	"2013"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0751374"	"Schwannomatosis, Plexiform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C0950121"	"Denys-Drash Syndrome"	"disease"	"C04;C12;C13;C16;C19"	"Disease or Syndrome"	"1.00"	"0.96"	"1983"	"2017"	"17"	"13"	"CTD_human;ORPHANET;UNIPROT"
"7490"	"WT1"	"0.444"	"0.69"	"C0950122"	"Frasier Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2018"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"7490"	"WT1"	"0.444"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"1997"	"2008"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C1837026"	"MEACHAM SYNDROME (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"		"1983"	"2008"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"7490"	"WT1"	"0.444"	"0.69"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C2931803"	"Deletion 11p13"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7490"	"WT1"	"0.444"	"0.69"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7490"	"WT1"	"0.444"	"0.69"	"C3151568"	"NEPHROTIC SYNDROME, TYPE 4"	"disease"		"Disease or Syndrome"	"0.50"		"1998"	"2011"	"5"	"0"	"CTD_human;UNIPROT"
"7490"	"WT1"	"0.444"	"0.69"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1989"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"7490"	"WT1"	"0.444"	"0.69"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7490"	"WT1"	"0.444"	"0.69"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7494"	"XBP1"	"0.54"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2015"	"2"	"0"	"PSYGENET"
"7494"	"XBP1"	"0.54"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"0"	"0"	"UNIPROT"
"7494"	"XBP1"	"0.54"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.3333333"	"2004"	"2008"	"3"	"0"	"PSYGENET"
"7494"	"XBP1"	"0.54"	"0.69"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"7494"	"XBP1"	"0.54"	"0.69"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C2700438"	"MAJOR AFFECTIVE DISORDER 7"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"7494"	"XBP1"	"0.54"	"0.69"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"7498"	"XDH"	"0.567"	"0.655"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0026766"	"Multiple Organ Failure"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0268118"	"Xanthinuria, Type I"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.76"	"1"	"1997"	"2015"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7498"	"XDH"	"0.567"	"0.655"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"1989"	"1989"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7498"	"XDH"	"0.567"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7503"	"XIST"	"0.611"	"0.586"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7503"	"XIST"	"0.611"	"0.586"	"C1848138"	"X INACTIVATION, FAMILIAL SKEWED, 1 (disorder)"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7503"	"XIST"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"7504"	"XK"	"0.639"	"0.517"	"C0002735"	"Oppenheim's Disease"	"disease"	"C10"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7504"	"XK"	"0.639"	"0.517"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0027868"	"Neuromuscular Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7504"	"XK"	"0.639"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0393576"	"Chorea Acanthocytosis Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2007"	"2"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0398568"	"Blood group deletion syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2001"	"2003"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7504"	"XK"	"0.639"	"0.517"	"C0751381"	"Foley-Denny-Brown Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1994"	"1996"	"2"	"0"	"CTD_human"
"7504"	"XK"	"0.639"	"0.517"	"C0878670"	"McLeod phenotype"	"phenotype"		"Finding"	"0.30"		"2002"	"2003"	"2"	"1"	"UNIPROT"
"7504"	"XK"	"0.639"	"0.517"	"C3151853"	"MCLEOD SYNDROME WITH CHRONIC GRANULOMATOUS DISEASE"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2003"	"2"	"1"	"UNIPROT"
"7504"	"XK"	"0.639"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"7504"	"XK"	"0.639"	"0.517"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"1994"	"2017"	"2"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.52"		"2006"	"2007"	"1"	"0"	"CGI;CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2011"	"0"	"0"	"CGI"
"7507"	"XPA"	"0.551"	"0.655"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"CGI"
"7507"	"XPA"	"0.551"	"0.655"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1995"	"2007"	"2"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.60"	"1"	"1991"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"7507"	"XPA"	"0.551"	"0.655"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"7507"	"XPA"	"0.551"	"0.655"	"C0268135"	"Xeroderma pigmentosum, group A"	"disease"		"Disease or Syndrome"	"0.50"	"0.8983051"	"1985"	"2018"	"4"	"10"	"UNIPROT"
"7507"	"XPA"	"0.551"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7507"	"XPA"	"0.551"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"7508"	"XPC"	"0.523"	"0.655"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9090909"	"1997"	"2016"	"0"	"0"	"CGI"
"7508"	"XPC"	"0.523"	"0.655"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"7508"	"XPC"	"0.523"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.54"	"0.6666667"	"2005"	"2016"	"1"	"0"	"CGI;CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1983"	"2013"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2013"	"2"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2005"	"2017"	"0"	"0"	"CGI"
"7508"	"XPC"	"0.523"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CGI"
"7508"	"XPC"	"0.523"	"0.655"	"C0043346"	"Xeroderma Pigmentosum"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality"	"0.90"	"0.9565217"	"1994"	"2017"	"1"	"4"	"CTD_human;ORPHANET"
"7508"	"XPC"	"0.523"	"0.655"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.45"	"1"	"2005"	"2017"	"0"	"0"	"CGI"
"7508"	"XPC"	"0.523"	"0.655"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2016"	"2"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2014"	"2"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"7508"	"XPC"	"0.523"	"0.655"	"C2752147"	"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C"	"disease"	"C04;C16;C17;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.90"	"0.974359"	"1989"	"2016"	"5"	"13"	"CTD_human;UNIPROT"
"7508"	"XPC"	"0.523"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C0002994"	"Angioedema"	"phenotype"	"C14;C17;C20"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C0085215"	"Ovarian Failure, Premature"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C0086367"	"Gonadotropin-Resistant Ovary Syndrome"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C3494522"	"Hypergonadotropic Ovarian Failure, X-Linked"	"disease"	"C10;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7512"	"XPNPEP2"	"0.785"	"0.207"	"C3806711"	"ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"7514"	"XPO1"	"0.586"	"0.655"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.42"	"1"	"2012"	"2016"	"0"	"2"	"CGI"
"7514"	"XPO1"	"0.586"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7514"	"XPO1"	"0.586"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"7514"	"XPO1"	"0.586"	"0.655"	"C1292754"	"Mediastinal (Thymic) Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.952381"	"2008"	"2018"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.95"	"2000"	"2018"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2003"	"2007"	"3"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"PSYGENET"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2003"	"2012"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0038362"	"Stomatitis"	"disease"	"C07"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0041834"	"Erythema"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.95"	"2003"	"2016"	"3"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"2000"	"2015"	"0"	"0"	"UNIPROT"
"7515"	"XRCC1"	"0.449"	"0.828"	"C1568868"	"Oral Mucositis"	"disease"	"C07"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7515"	"XRCC1"	"0.449"	"0.828"	"C4539948"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8421053"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.62"	"1"	"1999"	"2013"	"4"	"0"	"CLINGEN;GENOMICS_ENGLAND;ORPHANET"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7516"	"XRCC2"	"0.609"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.8"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7516"	"XRCC2"	"0.609"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2016"	"0"	"0"	"CLINGEN"
"7516"	"XRCC2"	"0.609"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7516"	"XRCC2"	"0.609"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2002"	"2009"	"1"	"0"	"CTD_human"
"7516"	"XRCC2"	"0.609"	"0.586"	"C4310651"	"FANCONI ANEMIA, COMPLEMENTATION GROUP U"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9230769"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2000"	"2015"	"2"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2002"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"0.6"	"2000"	"2016"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2000"	"2006"	"2"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9230769"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"		"2002"	"2007"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7517"	"XRCC3"	"0.534"	"0.655"	"C3151417"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6"	"phenotype"		"Finding"	"0.60"		"1998"	"2000"	"2"	"1"	"CTD_human;UNIPROT"
"7518"	"XRCC4"	"0.55"	"0.724"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7518"	"XRCC4"	"0.55"	"0.724"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7518"	"XRCC4"	"0.55"	"0.724"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"7518"	"XRCC4"	"0.55"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7518"	"XRCC4"	"0.55"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"7518"	"XRCC4"	"0.55"	"0.724"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"7518"	"XRCC4"	"0.55"	"0.724"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"7518"	"XRCC4"	"0.55"	"0.724"	"C1847827"	"LIG4 Syndrome"	"disease"	"C05;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7518"	"XRCC4"	"0.55"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"7518"	"XRCC4"	"0.55"	"0.724"	"C4225288"	"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2016"	"4"	"9"	"UNIPROT"
"7520"	"XRCC5"	"0.575"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"7520"	"XRCC5"	"0.575"	"0.724"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"7520"	"XRCC5"	"0.575"	"0.724"	"C0678306"	"alcohol sensitivity"	"phenotype"		"Finding"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"7525"	"YES1"	"0.69"	"0.276"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C0158570"	"Vascular anomaly"	"phenotype"	"C14;C16"	"Anatomical Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C1956410"	"Double Outlet Right Ventricle, Noncommitted VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C1956411"	"Double Outlet Right Ventricle, Subaortic VSD"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C1956412"	"Double Outlet Right Ventricle, Subpulmonary VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7525"	"YES1"	"0.69"	"0.276"	"C1956413"	"Taussig-Bing Anomaly"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"1993"	"2004"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2010"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7528"	"YY1"	"0.519"	"0.724"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7528"	"YY1"	"0.519"	"0.724"	"C4479652"	"GABRIELE-DE VRIES SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2017"	"2"	"5"	"ORPHANET;UNIPROT"
"7528"	"YY1"	"0.519"	"0.724"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2011"	"2013"	"2"	"0"	"PSYGENET"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.45"	"0.5"	"2008"	"2017"	"4"	"1"	"PSYGENET"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0206630"	"Endometrial Stromal Sarcoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0265219"	"Miller Dieker syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"7531"	"YWHAE"	"0.534"	"0.655"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.36"	"0.8333333"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"7531"	"YWHAE"	"0.534"	"0.655"	"C2750748"	"Chromosome 17p13.3 Duplication Syndrome"	"disease"	"C10;C16;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7532"	"YWHAG"	"0.727"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7532"	"YWHAG"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7532"	"YWHAG"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"7532"	"YWHAG"	"0.727"	"0.31"	"C4540034"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.04"	"1"	"1999"	"2009"	"1"	"0"	"PSYGENET"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7533"	"YWHAH"	"0.743"	"0.207"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.8"	"1997"	"2012"	"5"	"0"	"PSYGENET"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7534"	"YWHAZ"	"0.52"	"0.759"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2008"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C0085110"	"Severe Combined Immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.40"	"0.8333333"	"1994"	"2017"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C0242583"	"Bare Lymphocyte Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"1994"	"2012"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C2931299"	"ZAP70 deficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.62"	"1"	"1994"	"2013"	"5"	"3"	"CTD_human;ORPHANET;UNIPROT"
"7535"	"ZAP70"	"0.572"	"0.69"	"C2931320"	"T cell immunodeficiency primary"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1994"	"1994"	"1"	"0"	"CTD_human"
"7535"	"ZAP70"	"0.572"	"0.69"	"C4310768"	"AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"7536"	"SF1"	"0.752"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0003864"	"Arthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.34"	"1"	"2001"	"2013"	"2"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0162323"	"Polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7538"	"ZFP36"	"0.559"	"0.586"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7539"	"ZFP37"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7543"	"ZFX"	"0.681"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0265529"	"Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7545"	"ZIC1"	"0.557"	"0.552"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7545"	"ZIC1"	"0.557"	"0.552"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7545"	"ZIC1"	"0.557"	"0.552"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7545"	"ZIC1"	"0.557"	"0.552"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7545"	"ZIC1"	"0.557"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7545"	"ZIC1"	"0.557"	"0.552"	"C4225269"	"CRANIOSYNOSTOSIS 6"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"4"	"UNIPROT"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.34"	"0.75"	"2002"	"2013"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"	"0.9310345"	"1998"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7546"	"ZIC2"	"0.607"	"0.586"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7546"	"ZIC2"	"0.607"	"0.586"	"C1864827"	"HOLOPROSENCEPHALY 5"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2017"	"5"	"8"	"CTD_human;UNIPROT"
"7546"	"ZIC2"	"0.607"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0011813"	"Dextrocardia"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2010"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.40"	"1"	"1997"	"2014"	"0"	"0"	"ORPHANET"
"7547"	"ZIC3"	"0.6"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7547"	"ZIC3"	"0.6"	"0.448"	"C1306710"	"Facial asymmetry"	"phenotype"	"C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C1844020"	"HETEROTAXY, VISCERAL, 1, X-LINKED"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.81"	"1"	"1952"	"2015"	"6"	"10"	"CTD_human;UNIPROT"
"7547"	"ZIC3"	"0.6"	"0.448"	"C1848599"	"VACTERL Association With Hydrocephalus"	"disease"	"C05;C06;C10;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C2931228"	"VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"UNIPROT"
"7547"	"ZIC3"	"0.6"	"0.448"	"C3151867"	"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED"	"disease"		"Disease or Syndrome"	"0.60"		"1952"	"2014"	"6"	"7"	"UNIPROT"
"7547"	"ZIC3"	"0.6"	"0.448"	"C3495537"	"Heterotaxy, Visceral, 5, Autosomal"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"7547"	"ZIC3"	"0.6"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"7547"	"ZIC3"	"0.6"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7552"	"ZNF711"	"0.815"	"0.172"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"7552"	"ZNF711"	"0.815"	"0.172"	"C2749020"	"Mental Retardation, X-Linked, Znf711-Related"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2000"	"2017"	"2"	"6"	"UNIPROT"
"7552"	"ZNF711"	"0.815"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7552"	"ZNF711"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"7555"	"CNBP"	"0.616"	"0.586"	"C0027126"	"Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"0.95"	"2000"	"2013"	"0"	"0"	"CTD_human"
"7555"	"CNBP"	"0.616"	"0.586"	"C0410226"	"Congenital Myotonic Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7555"	"CNBP"	"0.616"	"0.586"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7555"	"CNBP"	"0.616"	"0.586"	"C2931689"	"Dystrophia myotonica 2"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"0.9534884"	"2002"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"7570"	"ZNF22"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7571"	"ZNF23"	"0.815"	"0.172"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"7592"	"ZNF41"	"0.834"	"0.172"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"7592"	"ZNF41"	"0.834"	"0.172"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"7592"	"ZNF41"	"0.834"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"7592"	"ZNF41"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"7594"	"ZNF43"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"7625"	"ZNF74"	"0.857"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2003"	"1"	"0"	"PSYGENET"
"7627"	"ZNF75A"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7681"	"MKRN3"	"0.645"	"0.448"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1993"	"2016"	"0"	"0"	"CTD_human"
"7681"	"MKRN3"	"0.645"	"0.448"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7681"	"MKRN3"	"0.645"	"0.448"	"C0342543"	"Central Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"7681"	"MKRN3"	"0.645"	"0.448"	"C0342544"	"Idiopathic central precocious puberty"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2016"	"2018"	"0"	"0"	"ORPHANET"
"7681"	"MKRN3"	"0.645"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"7681"	"MKRN3"	"0.645"	"0.448"	"C3809199"	"PRECOCIOUS PUBERTY, CENTRAL, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2016"	"5"	"5"	"UNIPROT"
"7700"	"ZNF141"	"0.815"	"0.138"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7700"	"ZNF141"	"0.815"	"0.138"	"C3808889"	"POLYDACTYLY, POSTAXIAL, TYPE A6"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"7700"	"ZNF141"	"0.815"	"0.138"	"C3887487"	"Postaxial polydactyly type A"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"7703"	"PCGF2"	"0.735"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9864865"	"1993"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2015"	"1"	"0"	"CTD_human"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C2676231"	"Skeletal Defects, Genital Hypoplasia, And Mental Retardation"	"disease"	"C05;C10;C12;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2002"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"7704"	"ZBTB16"	"0.598"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"7707"	"ZNF148"	"0.642"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7707"	"ZNF148"	"0.642"	"0.655"	"C4310644"	"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"CTD_human"
"7711"	"ZNF155"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7730"	"ZNF177"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7730"	"ZNF177"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7730"	"ZNF177"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7737"	"RNF113A"	"0.713"	"0.483"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"7737"	"RNF113A"	"0.713"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"7737"	"RNF113A"	"0.713"	"0.483"	"C4225420"	"TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"7750"	"ZMYM2"	"0.656"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7750"	"ZMYM2"	"0.656"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7750"	"ZMYM2"	"0.656"	"0.517"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2014"	"1"	"0"	"CTD_human"
"7750"	"ZMYM2"	"0.656"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7750"	"ZMYM2"	"0.656"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7755"	"ZNF205"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7755"	"ZNF205"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7763"	"ZFAND5"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7763"	"ZFAND5"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7764"	"ZNF217"	"0.663"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2016"	"1"	"1"	"UNIPROT"
"7775"	"ZNF232"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7779"	"SLC30A1"	"0.645"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7780"	"SLC30A2"	"0.834"	"0.138"	"C1842485"	"ZINC IN BREAST MILK, REDUCED"	"phenotype"		"Finding"	"0.30"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"7780"	"SLC30A2"	"0.834"	"0.138"	"C1842486"	"Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc"	"disease"	"C23"	"Disease or Syndrome"	"0.62"	"1"	"2007"	"2018"	"2"	"2"	"CTD_human;UNIPROT"
"7781"	"SLC30A3"	"0.762"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0036344"	"Schizophrenia, Catatonic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7782"	"SLC30A4"	"0.72"	"0.31"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7783"	"ZP2"	"0.928"		"C4014291"	"OOCYTE MATURATION DEFECT 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7783"	"ZP2"	"0.928"		"C4540205"	"OOCYTE MATURATION DEFECT 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7784"	"ZP3"	"0.886"	"0.034"	"C4014291"	"OOCYTE MATURATION DEFECT 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7784"	"ZP3"	"0.886"	"0.034"	"C4540205"	"OOCYTE MATURATION DEFECT 3"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"ORPHANET;UNIPROT"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7799"	"PRDM2"	"0.579"	"0.69"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"7802"	"DNALI1"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7803"	"PTP4A1"	"0.713"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"7804"	"LRP8"	"0.707"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"7804"	"LRP8"	"0.707"	"0.207"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2015"	"0"	"0"	"CTD_human"
"7804"	"LRP8"	"0.707"	"0.207"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7804"	"LRP8"	"0.707"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"7804"	"LRP8"	"0.707"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7804"	"LRP8"	"0.707"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"7805"	"LAPTM5"	"0.857"	"0.379"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7805"	"LAPTM5"	"0.857"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7809"	"BSND"	"0.663"	"0.586"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"7809"	"BSND"	"0.663"	"0.586"	"C1865270"	"BARTTER SYNDROME, TYPE 4A"	"disease"	"C09;C10;C12;C13;C19;C23"	"Disease or Syndrome"	"0.81"	"1"	"1998"	"2011"	"3"	"6"	"CTD_human;UNIPROT"
"7809"	"BSND"	"0.663"	"0.586"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7809"	"BSND"	"0.663"	"0.586"	"C2748440"	"Sensorineural Deafness With Mild Renal Dysfunction"	"disease"	"C09;C10;C12;C13;C19;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2011"	"3"	"6"	"UNIPROT"
"7809"	"BSND"	"0.663"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"7818"	"DAP3"	"0.743"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7818"	"DAP3"	"0.743"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2011"	"2018"	"1"	"1"	"CTD_human"
"7818"	"DAP3"	"0.743"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7818"	"DAP3"	"0.743"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"0.9090909"	"2002"	"2016"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"1996"	"2009"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.70"	"0.9047619"	"1996"	"2017"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7827"	"NPHS2"	"0.609"	"0.483"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7827"	"NPHS2"	"0.609"	"0.483"	"C1868672"	"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2015"	"15"	"20"	"CTD_human;UNIPROT"
"7827"	"NPHS2"	"0.609"	"0.483"	"C3496337"	"Idiopathic Nephrotic Syndrome"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.46"	"0.8333333"	"1996"	"2015"	"13"	"20"	"UNIPROT"
"7827"	"NPHS2"	"0.609"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7832"	"BTG2"	"0.642"	"0.517"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7832"	"BTG2"	"0.642"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7837"	"PXDN"	"0.707"	"0.31"	"C1862839"	"Anterior segment mesenchymal dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7837"	"PXDN"	"0.707"	"0.31"	"C3151617"	"ANTERIOR SEGMENT DYSGENESIS 7"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"4"	"ORPHANET;UNIPROT"
"7840"	"ALMS1"	"0.59"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7840"	"ALMS1"	"0.59"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7840"	"ALMS1"	"0.59"	"0.621"	"C0268425"	"Alstrom Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"1.00"	"0.9677419"	"2002"	"2017"	"6"	"30"	"CLINGEN;CTD_human;ORPHANET"
"7840"	"ALMS1"	"0.59"	"0.621"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7840"	"ALMS1"	"0.59"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2012"	"6"	"0"	"GENOMICS_ENGLAND"
"7840"	"ALMS1"	"0.59"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7841"	"MOGS"	"0.642"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1973"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"7841"	"MOGS"	"0.642"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7841"	"MOGS"	"0.642"	"0.483"	"C1853736"	"Congenital Disorder Of Glycosylation, Type IIB"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2001"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"7841"	"MOGS"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"7844"	"RNF103"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7844"	"RNF103"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7844"	"RNF103"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C1969029"	"Lissencephaly 3"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"2"	"31"	"CTD_human;ORPHANET;UNIPROT"
"7846"	"TUBA1A"	"0.663"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"7849"	"PAX8"	"0.558"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7849"	"PAX8"	"0.558"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"7849"	"PAX8"	"0.558"	"0.621"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.70"	"1"	"1998"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"7849"	"PAX8"	"0.558"	"0.621"	"C0151516"	"Thyroid Hypoplasia"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.70"	"0.9090909"	"1998"	"2015"	"3"	"4"	"ORPHANET;UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"0"	"0"	"ORPHANET"
"7849"	"PAX8"	"0.558"	"0.621"	"C0266283"	"Ectopic thyroid tissue (disorder)"	"phenotype"	"C16;C19"	"Finding"	"0.60"		"1998"	"2001"	"3"	"4"	"ORPHANET;UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.71"	"1"	"1998"	"2018"	"4"	"4"	"GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7849"	"PAX8"	"0.558"	"0.621"	"C1563716"	"Thyroid Dysgenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.50"	"1"	"1998"	"2018"	"3"	"7"	"UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C1869118"	"HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.50"		"1998"	"2001"	"3"	"4"	"CTD_human;UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7849"	"PAX8"	"0.558"	"0.621"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1998"	"2001"	"3"	"4"	"UNIPROT"
"7849"	"PAX8"	"0.558"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7850"	"IL1R2"	"0.645"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9550562"	"2003"	"2018"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9868421"	"2001"	"2018"	"2"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0472817"	"WHIM syndrome"	"disease"	"C02;C17;C20"	"Disease or Syndrome"	"0.90"	"0.9714286"	"2000"	"2017"	"1"	"4"	"CTD_human;ORPHANET"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9615385"	"2003"	"2018"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2003"	"2016"	"1"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"2"	"0"	"CTD_human"
"7852"	"CXCR4"	"0.391"	"0.897"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"7855"	"FZD5"	"0.619"	"0.586"	"C0155299"	"Coloboma of optic disc"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7855"	"FZD5"	"0.619"	"0.586"	"C0266551"	"Congenital coloboma of iris"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7855"	"FZD5"	"0.619"	"0.586"	"C0344516"	"Coloboma of lens"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7855"	"FZD5"	"0.619"	"0.586"	"C0521573"	"Coloboma of eyelid"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7855"	"FZD5"	"0.619"	"0.586"	"C1852767"	"Hereditary macular coloboma"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"7862"	"BRPF1"	"0.707"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7862"	"BRPF1"	"0.707"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7862"	"BRPF1"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"7862"	"BRPF1"	"0.707"	"0.345"	"C4310617"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"10"	"CTD_human;UNIPROT"
"7867"	"MAPKAPK3"	"0.785"	"0.207"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7867"	"MAPKAPK3"	"0.785"	"0.207"	"C1837029"	"Macular Dystrophy, Butterfly-Shaped Pigmentary, 2"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7867"	"MAPKAPK3"	"0.785"	"0.207"	"C1868569"	"Patterned dystrophy of retinal pigment epithelium"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7867"	"MAPKAPK3"	"0.785"	"0.207"	"C4310713"	"MACULAR DYSTROPHY, PATTERNED, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"7869"	"SEMA3B"	"0.672"	"0.414"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7869"	"SEMA3B"	"0.672"	"0.414"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"7869"	"SEMA3B"	"0.672"	"0.414"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"7871"	"SLMAP"	"0.785"	"0.31"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"7874"	"USP7"	"0.602"	"0.69"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7874"	"USP7"	"0.602"	"0.69"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"7874"	"USP7"	"0.602"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7874"	"USP7"	"0.602"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"7874"	"USP7"	"0.602"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"7874"	"USP7"	"0.602"	"0.69"	"C4225667"	"CHROMOSOME 16p13.2 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"7879"	"RAB7A"	"0.648"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.39"	"1"	"2003"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"7879"	"RAB7A"	"0.648"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"7879"	"RAB7A"	"0.648"	"0.586"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"7879"	"RAB7A"	"0.648"	"0.586"	"C1833219"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"2000"	"2014"	"5"	"4"	"CTD_human;ORPHANET;UNIPROT"
"7903"	"ST8SIA4"	"0.584"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2006"	"2013"	"1"	"0"	"PSYGENET"
"7903"	"ST8SIA4"	"0.584"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"7905"	"REEP5"	"0.645"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7905"	"REEP5"	"0.645"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"7905"	"REEP5"	"0.645"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7905"	"REEP5"	"0.645"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7913"	"DEK"	"0.598"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0006112"	"Brain Diseases, Metabolic"	"group"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0027854"	"Neurologic Manifestations"	"group"	"C10;C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0235031"	"Neurologic Symptoms"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0268631"	"succinic semialdehyde dehydrogenase deficiency"	"disease"	"C16;C18;F03"	"Disease or Syndrome"	"0.79"	"1"	"2000"	"2018"	"7"	"12"	"CTD_human;ORPHANET;UNIPROT"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0422837"	"Neurological observations"	"group"	"C10;C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0521654"	"Neurologic Deficits"	"group"	"C10;C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0746857"	"Focal Neurologic Deficits"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0750968"	"Central Nervous System Metabolic Disorders"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0751377"	"Neurologic Dysfunction"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0751378"	"Neurologic Signs"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0751743"	"Metabolic Disorder, Central Nervous System, Acquired"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0751744"	"Brain Diseases, Metabolic, Acquired"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C1135773"	"Acquired Metabolic Diseases, Nervous System"	"phenotype"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"7915"	"ALDH5A1"	"0.609"	"0.345"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7916"	"PRRC2A"	"0.681"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"7923"	"HSD17B8"	"0.886"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.33"	"1"	"1999"	"2003"	"1"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.8928571"	"1997"	"2017"	"1"	"1"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"1996"	"1996"	"1"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"1998"	"2002"	"1"	"0"	"PSYGENET"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.36"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7941"	"PLA2G7"	"0.584"	"0.552"	"C3280315"	"Platelet-Activating Factor Acetylhydrolase Deficiency"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.60"		"1996"	"1998"	"5"	"2"	"CTD_human;UNIPROT"
"7942"	"TFEB"	"0.645"	"0.448"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"1999"	"2017"	"1"	"1"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751783"	"Lafora Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.9672131"	"1993"	"2017"	"14"	"10"	"CTD_human;ORPHANET;UNIPROT"
"7957"	"EPM2A"	"0.652"	"0.345"	"C0751784"	"Lafora Body Disease, Late Onset"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"7957"	"EPM2A"	"0.652"	"0.345"	"C1850764"	"EPILEPSY, PROGRESSIVE MYOCLONIC 2B"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1998"	"2015"	"14"	"7"	"UNIPROT"
"7957"	"EPM2A"	"0.652"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"7971"	"GHS"	"0.713"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"7976"	"FZD3"	"0.743"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"7976"	"FZD3"	"0.743"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.4"	"2004"	"2012"	"5"	"0"	"PSYGENET"
"7976"	"FZD3"	"0.743"	"0.31"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"7976"	"FZD3"	"0.743"	"0.31"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"7976"	"FZD3"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"7979"	"SEM1"	"0.676"	"0.345"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"7979"	"SEM1"	"0.676"	"0.345"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.35"	"1"	"1995"	"2004"	"0"	"0"	"ORPHANET"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2007"	"2"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2006"	"2012"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9545455"	"2001"	"2015"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2005"	"2006"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2001"	"2008"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"7980"	"TFPI2"	"0.545"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"7984"	"ARHGEF5"	"0.627"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7984"	"ARHGEF5"	"0.627"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"7991"	"TUSC3"	"0.659"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"7991"	"TUSC3"	"0.659"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"2008"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"7991"	"TUSC3"	"0.659"	"0.414"	"C1970197"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"0"	"1"	"CTD_human"
"7991"	"TUSC3"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2008"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"7994"	"KAT6A"	"0.602"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"7994"	"KAT6A"	"0.602"	"0.517"	"C4225396"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 32"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2015"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"7994"	"KAT6A"	"0.602"	"0.517"	"C4511003"	"Acute myeloid leukemia with t(8;16)(p11;p13) translocation"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8000"	"PSCA"	"0.604"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0010474"	"Curling Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0013295"	"Duodenal Ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.44"	"0.75"	"2012"	"2015"	"1"	"4"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0023743"	"Linitis Plastica"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0079487"	"Helicobacter Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"8000"	"PSCA"	"0.604"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C1275278"	"Extraskeletal Myxoid Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"1"	"1998"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"8013"	"NR4A3"	"0.545"	"0.759"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8013"	"NR4A3"	"0.545"	"0.759"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8019"	"BRD3"	"0.735"	"0.379"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8019"	"BRD3"	"0.735"	"0.379"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8019"	"BRD3"	"0.735"	"0.379"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8021"	"NUP214"	"0.609"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"8021"	"NUP214"	"0.609"	"0.552"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8021"	"NUP214"	"0.609"	"0.552"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8021"	"NUP214"	"0.609"	"0.552"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2014"	"0"	"0"	"ORPHANET"
"8021"	"NUP214"	"0.609"	"0.552"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8022"	"LHX3"	"0.667"	"0.414"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2000"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"8022"	"LHX3"	"0.667"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8022"	"LHX3"	"0.667"	"0.414"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"8022"	"LHX3"	"0.667"	"0.414"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2000"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"8022"	"LHX3"	"0.667"	"0.414"	"C3489787"	"Pituitary Hormone Deficiency, Combined, 3"	"disease"	"C05;C09;C10;C19;C23"	"Disease or Syndrome"	"0.70"		"2000"	"2018"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"8022"	"LHX3"	"0.667"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8027"	"STAM"	"0.815"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.42"	"1"	"2011"	"2015"	"1"	"1"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8028"	"MLLT10"	"0.569"	"0.379"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2013"	"0"	"0"	"ORPHANET"
"8028"	"MLLT10"	"0.569"	"0.379"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8029"	"CUBN"	"0.63"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"8029"	"CUBN"	"0.63"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"8029"	"CUBN"	"0.63"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8029"	"CUBN"	"0.63"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"8029"	"CUBN"	"0.63"	"0.586"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8029"	"CUBN"	"0.63"	"0.586"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8029"	"CUBN"	"0.63"	"0.586"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8029"	"CUBN"	"0.63"	"0.586"	"C1306856"	"Megaloblastic anemia due to inborn errors of metabolism"	"disease"	"C06;C12;C13;C15;C18;C23"	"Disease or Syndrome"	"0.80"	"0.9"	"1998"	"2015"	"2"	"30"	"CTD_human;ORPHANET;UNIPROT"
"8029"	"CUBN"	"0.63"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2006"	"2016"	"1"	"2"	"UNIPROT"
"8030"	"CCDC6"	"0.584"	"0.586"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.60"	"1"	"1990"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"8030"	"CCDC6"	"0.584"	"0.586"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8030"	"CCDC6"	"0.584"	"0.586"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8031"	"NCOA4"	"0.663"	"0.379"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.34"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"8031"	"NCOA4"	"0.663"	"0.379"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8031"	"NCOA4"	"0.663"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"0.952381"	"1994"	"2016"	"0"	"0"	"ORPHANET"
"8031"	"NCOA4"	"0.663"	"0.379"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2015"	"1"	"0"	"CTD_human"
"8036"	"SHOC2"	"0.681"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"8036"	"SHOC2"	"0.681"	"0.448"	"C0018500"	"Hair Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8036"	"SHOC2"	"0.681"	"0.448"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"8036"	"SHOC2"	"0.681"	"0.448"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.50"	"0.9166667"	"2009"	"2016"	"1"	"1"	"CTD_human"
"8036"	"SHOC2"	"0.681"	"0.448"	"C0041409"	"Turner Syndrome, Male"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"8036"	"SHOC2"	"0.681"	"0.448"	"C1527404"	"Female Pseudo-Turner Syndrome"	"disease"	"C05;C14;C16;C17"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8036"	"SHOC2"	"0.681"	"0.448"	"C1843181"	"Noonan syndrome-like disorder with loose anagen hair"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"8036"	"SHOC2"	"0.681"	"0.448"	"C3501846"	"Noonan-Like Syndrome With Loose Anagen Hair"	"disease"	"C05;C14;C16;C17;C23"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"8036"	"SHOC2"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8036"	"SHOC2"	"0.681"	"0.448"	"C4478716"	"NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1"	"disease"		"Disease or Syndrome"	"0.50"		"2009"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"8038"	"ADAM12"	"0.619"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"0"	"0"	"UNIPROT"
"8038"	"ADAM12"	"0.619"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8038"	"ADAM12"	"0.619"	"0.621"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.70"	"0.9166667"	"1997"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8048"	"CSRP3"	"0.633"	"0.517"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8048"	"CSRP3"	"0.633"	"0.517"	"C1843808"	"CARDIOMYOPATHY, DILATED, 1M"	"disease"	"C14"	"Disease or Syndrome"	"0.70"		"1997"	"2010"	"3"	"2"	"CTD_human;UNIPROT"
"8048"	"CSRP3"	"0.633"	"0.517"	"C2677491"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12"	"disease"		"Disease or Syndrome"	"0.90"		"2003"	"2016"	"12"	"4"	"CLINGEN;CTD_human;UNIPROT"
"8048"	"CSRP3"	"0.633"	"0.517"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8050"	"PDHX"	"0.594"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8050"	"PDHX"	"0.594"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8050"	"PDHX"	"0.594"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8050"	"PDHX"	"0.594"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8050"	"PDHX"	"0.594"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8050"	"PDHX"	"0.594"	"0.552"	"C1855553"	"Pyruvate Dehydrogenase E3-Binding Protein Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1998"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"8050"	"PDHX"	"0.594"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8065"	"CUL5"	"0.743"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2004"	"2011"	"1"	"0"	"CTD_human"
"8065"	"CUL5"	"0.743"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2004"	"2011"	"1"	"0"	"CTD_human"
"8065"	"CUL5"	"0.743"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8065"	"CUL5"	"0.743"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"8074"	"FGF23"	"0.545"	"0.586"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.32"		"2005"	"2007"	"1"	"0"	"CTD_human"
"8074"	"FGF23"	"0.545"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8074"	"FGF23"	"0.545"	"0.586"	"C0085681"	"Hyperphosphatemia (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9473684"	"2005"	"2015"	"1"	"0"	"CTD_human"
"8074"	"FGF23"	"0.545"	"0.586"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"8074"	"FGF23"	"0.545"	"0.586"	"C0342642"	"Autosomal dominant hypophosphatemic rickets"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.94"	"1"	"1971"	"2014"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8074"	"FGF23"	"0.545"	"0.586"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8074"	"FGF23"	"0.545"	"0.586"	"C1704375"	"Hypophosphatemic Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2017"	"0"	"0"	"ORPHANET"
"8074"	"FGF23"	"0.545"	"0.586"	"C1876187"	"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.69"	"1"	"2005"	"2015"	"4"	"5"	"ORPHANET;UNIPROT"
"8076"	"MFAP5"	"0.69"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"UNIPROT"
"8076"	"MFAP5"	"0.69"	"0.483"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"1996"	"2015"	"7"	"0"	"CLINGEN"
"8076"	"MFAP5"	"0.69"	"0.483"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"8076"	"MFAP5"	"0.69"	"0.483"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8076"	"MFAP5"	"0.69"	"0.483"	"C4015368"	"AORTIC ANEURYSM, FAMILIAL THORACIC 9"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"8079"	"MLF2"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0010701"	"Phyllodes Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.75"	"2011"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0600066"	"Malignant Cystosarcoma Phyllodes"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0796004"	"Kabuki make-up syndrome"	"disease"	"C09;C15;C16"	"Congenital Abnormality"	"1.00"	"1"	"2003"	"2018"	"11"	"18"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8085"	"KMT2D"	"0.52"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2006"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"8086"	"AAAS"	"0.567"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8086"	"AAAS"	"0.567"	"0.586"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"8086"	"AAAS"	"0.567"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8086"	"AAAS"	"0.567"	"0.586"	"C0271742"	"Glucocorticoid deficiency with achalasia"	"disease"	"C06;C19"	"Disease or Syndrome"	"0.80"	"0.8918919"	"2000"	"2016"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"8086"	"AAAS"	"0.567"	"0.586"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8086"	"AAAS"	"0.567"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8086"	"AAAS"	"0.567"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"8087"	"FXR1"	"0.727"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8089"	"YEATS4"	"0.696"	"0.172"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2008"	"2010"	"1"	"0"	"CTD_human"
"8089"	"YEATS4"	"0.696"	"0.172"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8089"	"YEATS4"	"0.696"	"0.172"	"C0205825"	"Liposarcoma, Pleomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2013"	"2017"	"1"	"2"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.50"	"0.9411765"	"1996"	"2016"	"0"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0205824"	"Liposarcoma, Dedifferentiated"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"8091"	"HMGA2"	"0.474"	"0.655"	"C0745730"	"Multiple lipomata"	"disease"		"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8091"	"HMGA2"	"0.474"	"0.655"	"C1370889"	"Liposarcoma, well differentiated"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"8091"	"HMGA2"	"0.474"	"0.655"	"C1519176"	"Salivary Gland Pleomorphic Adenoma"	"disease"	"C04;C07"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2009"	"0"	"0"	"ORPHANET"
"8091"	"HMGA2"	"0.474"	"0.655"	"C4305140"	"12q14 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8092"	"ALX1"	"0.696"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"8092"	"ALX1"	"0.696"	"0.483"	"C1876203"	"Frontonasal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"2010"	"2017"	"0"	"0"	"CTD_human"
"8092"	"ALX1"	"0.696"	"0.483"	"C3150706"	"FRONTONASAL DYSPLASIA 3"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"1"	"ORPHANET"
"8092"	"ALX1"	"0.696"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"8100"	"IFT88"	"0.727"	"0.345"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1997"	"2013"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.53"	"1"	"1994"	"2009"	"2"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"8100"	"IFT88"	"0.727"	"0.345"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8106"	"PABPN1"	"0.707"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8106"	"PABPN1"	"0.707"	"0.379"	"C0270952"	"Muscular Dystrophy, Oculopharyngeal"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.90"	"0.9571429"	"1998"	"2017"	"3"	"1"	"CTD_human;ORPHANET"
"8106"	"PABPN1"	"0.707"	"0.379"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8110"	"DPF3"	"0.886"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8111"	"GPR68"	"0.785"	"0.172"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"		"2017"	"2017"	"1"	"2"	"GENOMICS_ENGLAND"
"8111"	"GPR68"	"0.785"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8111"	"GPR68"	"0.785"	"0.172"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8111"	"GPR68"	"0.785"	"0.172"	"C4310665"	"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"8115"	"TCL1A"	"0.607"	"0.414"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"8120"	"AP3B2"	"0.799"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8120"	"AP3B2"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8120"	"AP3B2"	"0.799"	"0.207"	"C4310637"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"5"	"CTD_human"
"8125"	"ANP32A"	"0.696"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"8125"	"ANP32A"	"0.696"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8125"	"ANP32A"	"0.696"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8125"	"ANP32A"	"0.696"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"8128"	"ST8SIA2"	"0.72"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"8128"	"ST8SIA2"	"0.72"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2016"	"2"	"0"	"PSYGENET"
"8128"	"ST8SIA2"	"0.72"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"2006"	"2016"	"5"	"0"	"PSYGENET"
"8131"	"NPRL3"	"0.752"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8131"	"NPRL3"	"0.752"	"0.172"	"C1858477"	"Epilepsy, Partial, with Variable Foci"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8131"	"NPRL3"	"0.752"	"0.172"	"C4310708"	"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"3"	"8"	"UNIPROT"
"8139"	"GAN"	"0.72"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8139"	"GAN"	"0.72"	"0.31"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8139"	"GAN"	"0.72"	"0.31"	"C1850386"	"GIANT AXONAL NEUROPATHY 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.95"	"1990"	"2016"	"6"	"15"	"CTD_human;ORPHANET;UNIPROT"
"8139"	"GAN"	"0.72"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8140"	"SLC7A5"	"0.611"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"8140"	"SLC7A5"	"0.611"	"0.517"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8140"	"SLC7A5"	"0.611"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8148"	"TAF15"	"0.667"	"0.345"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2011"	"2013"	"0"	"0"	"ORPHANET"
"8148"	"TAF15"	"0.667"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8148"	"TAF15"	"0.667"	"0.345"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8148"	"TAF15"	"0.667"	"0.345"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8148"	"TAF15"	"0.667"	"0.345"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8148"	"TAF15"	"0.667"	"0.345"	"C1275278"	"Extraskeletal Myxoid Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.56"	"1"	"1999"	"2004"	"0"	"0"	"CTD_human;ORPHANET"
"8148"	"TAF15"	"0.667"	"0.345"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8163"	"CDR3"	"0.499"	"0.724"	"C1865782"	"CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"8165"	"AKAP1"	"0.857"	"0.207"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8174"	"MADCAM1"	"0.696"	"0.345"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"CTD_human"
"8174"	"MADCAM1"	"0.696"	"0.345"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8174"	"MADCAM1"	"0.696"	"0.345"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8189"	"SYMPK"	"0.834"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8189"	"SYMPK"	"0.834"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8189"	"SYMPK"	"0.834"	"0.103"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8189"	"SYMPK"	"0.834"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8190"	"MIA"	"0.596"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"8190"	"MIA"	"0.596"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8190"	"MIA"	"0.596"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8192"	"CLPP"	"0.762"	"0.241"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.53"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"8192"	"CLPP"	"0.762"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8192"	"CLPP"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8192"	"CLPP"	"0.762"	"0.241"	"C3808414"	"PERRAULT SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"8193"	"DPF1"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8195"	"MKKS"	"0.579"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.43"	"1"	"2002"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8195"	"MKKS"	"0.579"	"0.69"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9411765"	"1993"	"2016"	"0"	"2"	"ORPHANET"
"8195"	"MKKS"	"0.579"	"0.69"	"C0948368"	"Kaufman-McKusick syndrome"	"disease"	"C05;C13;C14;C16"	"Disease or Syndrome"	"0.78"	"1"	"2000"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8195"	"MKKS"	"0.579"	"0.69"	"C1858054"	"BARDET-BIEDL SYNDROME 6"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"2000"	"2018"	"17"	"16"	"CTD_human;UNIPROT"
"8195"	"MKKS"	"0.579"	"0.69"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8195"	"MKKS"	"0.579"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"8195"	"MKKS"	"0.579"	"0.69"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2007"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"8200"	"GDF5"	"0.557"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"8200"	"GDF5"	"0.557"	"0.517"	"C0019555"	"Hip Dislocation, Congenital"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.44"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"8200"	"GDF5"	"0.557"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"0.9722222"	"2007"	"2017"	"1"	"0"	"CTD_human"
"8200"	"GDF5"	"0.557"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8200"	"GDF5"	"0.557"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8200"	"GDF5"	"0.557"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8200"	"GDF5"	"0.557"	"0.517"	"C0175700"	"Multiple synostosis syndrome"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C0265260"	"Chondrodysplasia, Grebe type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.95"	"1"	"1997"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C0342282"	"Multiple synostoses syndrome 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C1300268"	"Brachydactyly syndrome type C"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C1306065"	"DEVELOPMENTAL DYSPLASIA OF THE HIP 1"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8200"	"GDF5"	"0.557"	"0.517"	"C1739384"	"Angel shaped phalangoepiphyseal dysplasia"	"disease"	"C05"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C1832702"	"BRACHYDACTYLY, TYPE A2"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.95"	"1"	"2003"	"2012"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C1832708"	"MULTIPLE SYNOSTOSES SYNDROME 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.81"	"1"	"2005"	"2014"	"4"	"3"	"CTD_human;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C1856738"	"Fibular hypoplasia and complex brachydactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.92"	"1"	"2003"	"2008"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C1861385"	"SYMPHALANGISM, PROXIMAL"	"disease"	"C05"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2008"	"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C1862103"	"Brachydactyly type C"	"disease"	"C05;C16"	"Congenital Abnormality"	"1.00"	"1"	"1997"	"2016"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C1862151"	"BRACHYDACTYLY, TYPE A1 (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C2930970"	"Acromesomelic dysplasia Hunter-Thompson type"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.71"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"8200"	"GDF5"	"0.557"	"0.517"	"C3554446"	"BRACHYDACTYLY, TYPE A1, C"	"disease"		"Disease or Syndrome"	"0.80"		"2011"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"8200"	"GDF5"	"0.557"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8200"	"GDF5"	"0.557"	"0.517"	"C3809104"	"SYMPHALANGISM, PROXIMAL, 1B"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2008"	"3"	"3"	"CTD_human;UNIPROT"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.943662"	"1996"	"2018"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"2"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2002"	"2008"	"2"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.942029"	"1996"	"2018"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"8202"	"NCOA3"	"0.548"	"0.448"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.43"	"1"	"2000"	"2018"	"1"	"1"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2005"	"2012"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8204"	"NRIP1"	"0.659"	"0.414"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8208"	"CHAF1B"	"0.785"	"0.241"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8214"	"DGCR6"	"0.69"	"0.448"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2005"	"0"	"0"	"CTD_human"
"8214"	"DGCR6"	"0.69"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2002"	"2005"	"1"	"0"	"PSYGENET"
"8214"	"DGCR6"	"0.69"	"0.448"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"8214"	"DGCR6"	"0.69"	"0.448"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C0917817"	"Neurofibromatosis 3"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C1335929"	"Schwannomatosis"	"disease"	"C04;C10;C16;C17"	"Neoplastic Process"	"0.56"	"0.8333333"	"2014"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8216"	"LZTR1"	"0.63"	"0.517"	"C2931480"	"Neurofibromatosis, Type 3, mixed central and peripheral"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8216"	"LZTR1"	"0.63"	"0.517"	"C3810283"	"SCHWANNOMATOSIS 2"	"disease"		"Disease or Syndrome"	"0.41"	"0"	"2014"	"2018"	"1"	"7"	"UNIPROT"
"8216"	"LZTR1"	"0.63"	"0.517"	"C4225280"	"NOONAN SYNDROME 10"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"8218"	"CLTCL1"	"0.834"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8218"	"CLTCL1"	"0.834"	"0.207"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8220"	"ESS2"	"0.707"	"0.448"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8220"	"ESS2"	"0.707"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2007"	"2"	"0"	"PSYGENET"
"8220"	"ESS2"	"0.707"	"0.448"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8220"	"ESS2"	"0.707"	"0.448"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8224"	"SYN3"	"0.701"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"8224"	"SYN3"	"0.701"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.5"	"2000"	"2010"	"4"	"0"	"PSYGENET"
"8224"	"SYN3"	"0.701"	"0.379"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8226"	"PUDP"	"0.928"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8227"	"AKAP17A"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8228"	"PNPLA4"	"0.928"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8233"	"ZRSR2"	"0.815"	"0.138"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.53"	"1"	"2012"	"2017"	"1"	"0"	"CGI;CTD_human"
"8239"	"USP9X"	"0.584"	"0.69"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8239"	"USP9X"	"0.584"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8239"	"USP9X"	"0.584"	"0.69"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8239"	"USP9X"	"0.584"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8239"	"USP9X"	"0.584"	"0.69"	"C3806746"	"MENTAL RETARDATION, X-LINKED 99"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"8239"	"USP9X"	"0.584"	"0.69"	"C4225416"	"MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2016"	"2016"	"0"	"5"	"CTD_human;ORPHANET"
"8241"	"RBM10"	"0.659"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8241"	"RBM10"	"0.659"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8241"	"RBM10"	"0.659"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8241"	"RBM10"	"0.659"	"0.517"	"C1839463"	"TARP syndrome"	"disease"	"C05;C07;C14;C16"	"Disease or Syndrome"	"0.63"	"1"	"1970"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"8241"	"RBM10"	"0.659"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.58"	"1"	"2012"	"2016"	"1"	"0"	"CGI;CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8242"	"KDM5C"	"0.619"	"0.483"	"C1845243"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1992"	"2018"	"7"	"22"	"CTD_human;ORPHANET;UNIPROT"
"8242"	"KDM5C"	"0.619"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"0.96"	"2006"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C1802395"	"Congenital muscular hypertrophy-cerebral syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.63"	"1"	"2006"	"2017"	"8"	"31"	"CTD_human;UNIPROT"
"8243"	"SMC1A"	"0.565"	"0.724"	"C1853099"	"Cornelia de Lange Syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8243"	"SMC1A"	"0.565"	"0.724"	"C1854630"	"Growth Deficiency and Mental Retardation with Facial Dysmorphism"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"2"	"ORPHANET"
"8243"	"SMC1A"	"0.565"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2007"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"8243"	"SMC1A"	"0.565"	"0.724"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"8260"	"NAA10"	"0.577"	"0.586"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"8260"	"NAA10"	"0.577"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8260"	"NAA10"	"0.577"	"0.586"	"C0796016"	"Microphthalmia, syndromic 1"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"1993"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"8260"	"NAA10"	"0.577"	"0.586"	"C3275447"	"OGDEN SYNDROME"	"disease"		"Disease or Syndrome"	"0.73"	"1"	"2011"	"2018"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"8260"	"NAA10"	"0.577"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8270"	"LAGE3"	"0.762"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8270"	"LAGE3"	"0.762"	"0.241"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"8270"	"LAGE3"	"0.762"	"0.241"	"C4538784"	"GALLOWAY-MOWAT SYNDROME 2, X-LINKED"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"8277"	"TKTL1"	"0.636"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8284"	"KDM5D"	"0.735"	"0.345"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8287"	"USP9Y"	"0.743"	"0.241"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"8287"	"USP9Y"	"0.743"	"0.241"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8287"	"USP9Y"	"0.743"	"0.241"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8288"	"EPX"	"0.727"	"0.345"	"C1850000"	"Presentey Anomaly"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"1995"	"2001"	"1"	"3"	"CTD_human;UNIPROT"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1992"	"2013"	"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2012"	"2018"	"3"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2014"	"3"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.38"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1988"	"2015"	"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2014"	"3"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2018"	"3"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8289"	"ARID1A"	"0.505"	"0.724"	"C3544205"	"Ovarian clear cell carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"8289"	"ARID1A"	"0.505"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"8289"	"ARID1A"	"0.505"	"0.724"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8290"	"HIST3H3"	"0.785"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8291"	"DYSF"	"0.611"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8291"	"DYSF"	"0.611"	"0.483"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8291"	"DYSF"	"0.611"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"0.9411765"	"1996"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.50"		"1999"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"1993"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8291"	"DYSF"	"0.611"	"0.483"	"C1847532"	"MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"2009"	"0"	"7"	"CTD_human;ORPHANET"
"8291"	"DYSF"	"0.611"	"0.483"	"C1850808"	"Miyoshi myopathy"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.80"	"0.9861111"	"1996"	"2016"	"17"	"105"	"CTD_human;ORPHANET;UNIPROT"
"8291"	"DYSF"	"0.611"	"0.483"	"C1850889"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"0.9787234"	"1993"	"2018"	"14"	"158"	"CTD_human;ORPHANET;UNIPROT"
"8291"	"DYSF"	"0.611"	"0.483"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8291"	"DYSF"	"0.611"	"0.483"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8291"	"DYSF"	"0.611"	"0.483"	"C4511057"	"Congenital muscular dystrophy Paradas type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8292"	"COLQ"	"0.773"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1998"	"2002"	"2"	"0"	"GENOMICS_ENGLAND"
"8292"	"COLQ"	"0.773"	"0.241"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.37"	"1"	"1998"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"8292"	"COLQ"	"0.773"	"0.241"	"C1864233"	"ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.64"	"1"	"1977"	"2018"	"4"	"13"	"CTD_human;UNIPROT"
"8295"	"TRRAP"	"0.713"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2011"	"2011"	"1"	"0"	"CGI;CTD_human"
"8295"	"TRRAP"	"0.713"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"8295"	"TRRAP"	"0.713"	"0.345"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8295"	"TRRAP"	"0.713"	"0.345"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"8295"	"TRRAP"	"0.713"	"0.345"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"8295"	"TRRAP"	"0.713"	"0.345"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"8295"	"TRRAP"	"0.713"	"0.345"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8295"	"TRRAP"	"0.713"	"0.345"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8301"	"PICALM"	"0.639"	"0.31"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.9574468"	"2009"	"2018"	"2"	"12"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8947368"	"2009"	"2016"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"8301"	"PICALM"	"0.639"	"0.31"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2005"	"0"	"0"	"ORPHANET"
"8302"	"KLRC4"	"0.752"	"0.414"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2013"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"8302"	"KLRC4"	"0.752"	"0.414"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8309"	"ACOX2"	"0.762"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8309"	"ACOX2"	"0.762"	"0.414"	"C4310624"	"BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"0.75"	"2001"	"2007"	"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.51"	"1"	"2002"	"2002"	"1"	"3"	"CGI;UNIPROT"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0279607"	"Adult Hepatocellular Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2013"	"1"	"3"	"UNIPROT"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8312"	"AXIN1"	"0.6"	"0.483"	"C1842884"	"Caudal Duplication Anomaly"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8312"	"AXIN1"	"0.6"	"0.483"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.80"	"1"	"2000"	"2017"	"2"	"4"	"CGI;CTD_human;UNIPROT"
"8312"	"AXIN1"	"0.6"	"0.483"	"C2676033"	"Hepatoblastoma Caused By Somatic Mutation"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"3"	"UNIPROT"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0004991"	"Benign neoplasm of colon"	"disease"		"Neoplastic Process"	"0.30"		"2004"	"2017"	"7"	"0"	"CLINGEN"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2016"	"0"	"0"	"CTD_human"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"		"2004"	"2007"	"0"	"0"	"CTD_human"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"	"1"	"2004"	"2016"	"0"	"0"	"ORPHANET"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2009"	"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2016"	"0"	"0"	"CTD_human"
"8313"	"AXIN2"	"0.57"	"0.552"	"C1837750"	"Oligodontia-Colorectal Cancer Syndrome"	"disease"	"C04;C06;C07;C16"	"Neoplastic Process"	"0.61"	"1"	"2004"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"8313"	"AXIN2"	"0.57"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CGI"
"8313"	"AXIN2"	"0.57"	"0.552"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.50"	"1"	"2004"	"2016"	"0"	"0"	"ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0005967"	"Bone neoplasms"	"group"	"C04;C05"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.56"	"1"	"1998"	"2018"	"2"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"8314"	"BAP1"	"0.488"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8314"	"BAP1"	"0.488"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9166667"	"2012"	"2016"	"4"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"		"2016"	"2016"	"1"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0023798"	"Lipoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.9130435"	"2010"	"2017"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"8314"	"BAP1"	"0.488"	"0.586"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.45"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.9259259"	"2011"	"2018"	"4"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0030421"	"Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0040100"	"Thymoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0085136"	"Central Nervous System Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9"	"2012"	"2017"	"2"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CLINGEN"
"8314"	"BAP1"	"0.488"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CLINGEN"
"8314"	"BAP1"	"0.488"	"0.586"	"C0205822"	"Hibernoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0205823"	"Pleomorphic Lipoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206694"	"Mucoepidermoid Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206739"	"Epithelioid and spindle cell nevus"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206754"	"Neuroendocrine Tumors"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0206769"	"Nevi and Melanomas"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.80"	"0.9428571"	"2010"	"2018"	"3"	"0"	"CGI;CTD_human;ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.51"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"8314"	"BAP1"	"0.488"	"0.586"	"C0259785"	"Malignant Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0279530"	"Malignant Bone Neoplasm"	"disease"	"C04;C05"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"2012"	"2018"	"4"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0281784"	"Benign Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334605"	"Meningothelial meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334606"	"Fibrous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334607"	"Psammomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334608"	"Angiomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334609"	"Hemangioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334610"	"Hemangiopericytic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0334611"	"Transitional Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CLINGEN"
"8314"	"BAP1"	"0.488"	"0.586"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"5"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0346373"	"Malignant melanoma of iris"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C0346388"	"Malignant melanoma of choroid"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0347515"	"Spinal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0349604"	"Intracranial Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0431121"	"Clear Cell Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CLINGEN"
"8314"	"BAP1"	"0.488"	"0.586"	"C0457190"	"Xanthomatous Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8314"	"BAP1"	"0.488"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.57"	"1"	"1998"	"2018"	"2"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.52"	"0.5"	"2014"	"2016"	"1"	"0"	"CGI;CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0751303"	"Cerebral Convexity Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0751304"	"Parasagittal Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0751620"	"Central Nervous System Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8314"	"BAP1"	"0.488"	"0.586"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"4"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"4"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"4"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"4"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1334261"	"Intraorbital Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1334271"	"Intraventricular Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1335107"	"Olfactory Groove Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1378703"	"Renal carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2016"	"0"	"0"	"CGI"
"8314"	"BAP1"	"0.488"	"0.586"	"C1384406"	"Secretory meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1384408"	"Microcystic meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1527197"	"Angioblastic Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1565950"	"Posterior Fossa Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1565951"	"Sphenoid Wing Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C3163622"	"Papillary Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C3280492"	"TUMOR PREDISPOSITION SYNDROME"	"disease"		"Disease or Syndrome"	"0.67"	"1"	"2008"	"2017"	"0"	"21"	"CTD_human;ORPHANET"
"8314"	"BAP1"	"0.488"	"0.586"	"C3489413"	"Lipomatosis, Multiple"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8314"	"BAP1"	"0.488"	"0.586"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"2"	"0"	"CTD_human"
"8315"	"BRAP"	"0.685"	"0.517"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"0.8"	"2009"	"2015"	"1"	"1"	"CTD_human"
"8315"	"BRAP"	"0.685"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"8318"	"CDC45"	"0.602"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8318"	"CDC45"	"0.602"	"0.621"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"8318"	"CDC45"	"0.602"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8320"	"EOMES"	"0.667"	"0.517"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8320"	"EOMES"	"0.667"	"0.517"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"8320"	"EOMES"	"0.667"	"0.517"	"C0751871"	"Autoimmune Diseases of the Nervous System"	"group"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C0751872"	"Immune Disorders, Nervous System"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8320"	"EOMES"	"0.667"	"0.517"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"8320"	"EOMES"	"0.667"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8322"	"FZD4"	"0.598"	"0.552"	"C0003706"	"Arachnodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"8322"	"FZD4"	"0.598"	"0.552"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C0035344"	"Retinopathy of Prematurity"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.64"	"1"	"2002"	"2015"	"13"	"16"	"ORPHANET;UNIPROT"
"8322"	"FZD4"	"0.598"	"0.552"	"C0039075"	"Syndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8322"	"FZD4"	"0.598"	"0.552"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C0266568"	"Persistent Hyperplastic Primary Vitreous"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.32"	"1"	"2009"	"2010"	"0"	"0"	"ORPHANET"
"8322"	"FZD4"	"0.598"	"0.552"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.50"	"0.9722222"	"2000"	"2018"	"0"	"2"	"ORPHANET"
"8322"	"FZD4"	"0.598"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8322"	"FZD4"	"0.598"	"0.552"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8322"	"FZD4"	"0.598"	"0.552"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"8322"	"FZD4"	"0.598"	"0.552"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.74"	"0.75"	"2002"	"2010"	"13"	"18"	"CTD_human;ORPHANET;UNIPROT"
"8322"	"FZD4"	"0.598"	"0.552"	"C1857299"	"RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL"	"disease"	"C11"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8323"	"FZD6"	"0.72"	"0.414"	"C3279974"	"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8323"	"FZD6"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8325"	"FZD8"	"0.707"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8328"	"GFI1B"	"0.701"	"0.207"	"C0032197"	"Platelet Storage Pool Deficiency"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"8328"	"GFI1B"	"0.701"	"0.207"	"C0272302"	"Gray Platelet Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"8328"	"GFI1B"	"0.701"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"8328"	"GFI1B"	"0.701"	"0.207"	"C1861194"	"Thrombasthenia-Thrombocytopenia, Hereditary"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"		"1968"	"2017"	"0"	"3"	"CTD_human"
"8328"	"GFI1B"	"0.701"	"0.207"	"C2717750"	"Platelet alpha-Granule Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8332"	"HIST1H2AL"	"1"	"0.034"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8339"	"HIST1H2BG"	"0.857"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8339"	"HIST1H2BG"	"0.857"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8339"	"HIST1H2BG"	"0.857"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8339"	"HIST1H2BG"	"0.857"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8339"	"HIST1H2BG"	"0.857"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8342"	"HIST1H2BM"	"0.857"	"0.103"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8342"	"HIST1H2BM"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8347"	"HIST1H2BC"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8347"	"HIST1H2BC"	"0.886"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8347"	"HIST1H2BC"	"0.886"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8347"	"HIST1H2BC"	"0.886"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8347"	"HIST1H2BC"	"0.886"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C0206725"	"Subependymal Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C1842010"	"Glioma of Brain, Familial"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8350"	"HIST1H3A"	"0.785"	"0.069"	"C2750850"	"GLIOMA SUSCEPTIBILITY 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"UNIPROT"
"8351"	"HIST1H3D"	"0.834"	"0.103"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8352"	"HIST1H3C"	"0.928"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8353"	"HIST1H3E"	"0.886"	"0.103"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8354"	"HIST1H3I"	"0.857"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8355"	"HIST1H3G"	"0.928"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8356"	"HIST1H3J"	"0.886"	"0.172"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8357"	"HIST1H3H"	"0.928"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.52"	"1"	"2012"	"2016"	"1"	"0"	"CGI;CTD_human"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8358"	"HIST1H3B"	"0.785"	"0.069"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8359"	"HIST1H4A"	"0.676"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"UNIPROT"
"8360"	"HIST1H4D"	"0.667"	"0.552"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8360"	"HIST1H4D"	"0.667"	"0.552"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8360"	"HIST1H4D"	"0.667"	"0.552"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8364"	"HIST1H4C"	"0.656"	"0.621"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8365"	"HIST1H4H"	"0.676"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8365"	"HIST1H4H"	"0.676"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8366"	"HIST1H4B"	"0.667"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8366"	"HIST1H4B"	"0.667"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8366"	"HIST1H4B"	"0.667"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8366"	"HIST1H4B"	"0.667"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"CGI"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2018"	"1"	"8"	"PSYGENET"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"				"0"	"0"	"CTD_human"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2017"	"1"	"1"	"CTD_human"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8379"	"MAD1L1"	"0.609"	"0.483"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8388"	"OR1E2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0027960"	"Nevus"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2009"	"2016"	"1"	"2"	"CTD_human"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"1"	"2012"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2003"	"2016"	"1"	"0"	"PSYGENET"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0270724"	"Infantile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"1.00"	"1"	"2004"	"2018"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C1857747"	"NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.62"	"1"	"2006"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C2750220"	"Karak Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.43"	"1"	"2006"	"2015"	"1"	"2"	"UNIPROT"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C2751842"	"PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE"	"disease"	"C10"	"Disease or Syndrome"	"0.74"	"1"	"2009"	"2017"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"8398"	"PLA2G6"	"0.494"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8402"	"SLC25A11"	"1"	"0.034"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8404"	"SPARCL1"	"0.659"	"0.276"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8405"	"SPOP"	"0.656"	"0.207"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"8405"	"SPOP"	"0.656"	"0.207"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.42"	"1"	"2015"	"2017"	"0"	"9"	"CGI"
"8405"	"SPOP"	"0.656"	"0.207"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8405"	"SPOP"	"0.656"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human"
"8405"	"SPOP"	"0.656"	"0.207"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8405"	"SPOP"	"0.656"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9444444"	"2012"	"2018"	"2"	"0"	"CTD_human"
"8405"	"SPOP"	"0.656"	"0.207"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.52"	"1"	"2013"	"2015"	"1"	"0"	"CGI;CTD_human"
"8405"	"SPOP"	"0.656"	"0.207"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8407"	"TAGLN2"	"0.659"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8408"	"ULK1"	"0.676"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"8408"	"ULK1"	"0.676"	"0.414"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"8409"	"UXT"	"0.799"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2009"	"1"	"0"	"CTD_human"
"8409"	"UXT"	"0.799"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"1998"	"2015"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"1998"	"2015"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8412"	"BCAR3"	"0.743"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8419"	"BFSP2"	"0.72"	"0.241"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.35"	"1"	"2000"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"8419"	"BFSP2"	"0.72"	"0.241"	"C1833118"	"Cataract, Pulverulent"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"8419"	"BFSP2"	"0.72"	"0.241"	"C1852438"	"CATARACT, COPPOCK-LIKE"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8419"	"BFSP2"	"0.72"	"0.241"	"C1854021"	"Cataract, Central Saccular, With Sutural Opacities"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8419"	"BFSP2"	"0.72"	"0.241"	"C1969032"	"Cataract, Autosomal Dominant, Multiple Types 1"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8419"	"BFSP2"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8419"	"BFSP2"	"0.72"	"0.241"	"C3808115"	"CATARACT 12, MULTIPLE TYPES"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2005"	"3"	"2"	"UNIPROT"
"8424"	"BBOX1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8425"	"LTBP4"	"0.627"	"0.552"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"8425"	"LTBP4"	"0.627"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"8425"	"LTBP4"	"0.627"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8425"	"LTBP4"	"0.627"	"0.552"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8425"	"LTBP4"	"0.627"	"0.552"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8425"	"LTBP4"	"0.627"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8425"	"LTBP4"	"0.627"	"0.552"	"C2750804"	"Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities"	"disease"	"C05;C06;C08;C12;C13;C16;C17"	"Disease or Syndrome"	"0.70"		"1993"	"2013"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"8431"	"NR0B2"	"0.516"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8431"	"NR0B2"	"0.516"	"0.69"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"8431"	"NR0B2"	"0.516"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8431"	"NR0B2"	"0.516"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.49"	"1"	"2001"	"2015"	"0"	"0"	"CTD_human"
"8431"	"NR0B2"	"0.516"	"0.69"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"8431"	"NR0B2"	"0.516"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"8434"	"RECK"	"0.575"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8434"	"RECK"	"0.575"	"0.586"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"8436"	"CAVIN2"	"0.707"	"0.345"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"8436"	"CAVIN2"	"0.707"	"0.345"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8436"	"CAVIN2"	"0.707"	"0.345"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8436"	"CAVIN2"	"0.707"	"0.345"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8437"	"RASAL1"	"0.69"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"1999"	"1999"	"1"	"1"	"CTD_human;UNIPROT"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"		"1999"	"1999"	"1"	"1"	"CGI;CTD_human;UNIPROT"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0338106"	"Adenocarcinoma of colon"	"disease"		"Neoplastic Process"	"0.60"		"1999"	"1999"	"1"	"1"	"CGI;UNIPROT"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"				"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"8438"	"RAD54L"	"0.676"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1997"	"1997"	"0"	"0"	"CTD_human"
"8438"	"RAD54L"	"0.676"	"0.276"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8440"	"NCK2"	"0.815"	"0.103"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8440"	"NCK2"	"0.815"	"0.103"	"C0027726"	"Nephrotic Syndrome"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8440"	"NCK2"	"0.815"	"0.103"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8443"	"GNPAT"	"0.713"	"0.414"	"C0008445"	"Chondrodysplasia Punctata"	"disease"	"C05"	"Congenital Abnormality"	"0.52"	"1"	"2004"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"8443"	"GNPAT"	"0.713"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"8443"	"GNPAT"	"0.713"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8443"	"GNPAT"	"0.713"	"0.414"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8443"	"GNPAT"	"0.713"	"0.414"	"C1857242"	"Rhizomelic chondrodysplasia punctata, type 2"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.91"	"1"	"1994"	"2012"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8443"	"GNPAT"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8445"	"DYRK2"	"0.743"	"0.241"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8445"	"DYRK2"	"0.743"	"0.241"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8445"	"DYRK2"	"0.743"	"0.241"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8450"	"CUL4B"	"0.636"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8450"	"CUL4B"	"0.636"	"0.552"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8450"	"CUL4B"	"0.636"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2007"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"8450"	"CUL4B"	"0.636"	"0.552"	"C1845861"	"MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"1994"	"2015"	"5"	"8"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"8450"	"CUL4B"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2010"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"8451"	"CUL4A"	"0.633"	"0.552"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8451"	"CUL4A"	"0.633"	"0.552"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8451"	"CUL4A"	"0.633"	"0.552"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8451"	"CUL4A"	"0.633"	"0.552"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8451"	"CUL4A"	"0.633"	"0.552"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8452"	"CUL3"	"0.639"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8452"	"CUL3"	"0.639"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8452"	"CUL3"	"0.639"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8452"	"CUL3"	"0.639"	"0.483"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8452"	"CUL3"	"0.639"	"0.483"	"C3469606"	"PSEUDOHYPOALDOSTERONISM, TYPE IIE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2012"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8452"	"CUL3"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8453"	"CUL2"	"0.743"	"0.31"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8454"	"CUL1"	"0.667"	"0.483"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8454"	"CUL1"	"0.667"	"0.483"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8454"	"CUL1"	"0.667"	"0.483"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8454"	"CUL1"	"0.667"	"0.483"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8454"	"CUL1"	"0.667"	"0.483"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8455"	"ATRN"	"0.752"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8455"	"ATRN"	"0.752"	"0.345"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8456"	"FOXN1"	"0.672"	"0.483"	"C1866426"	"T-cell immunodeficiency, congenital alopecia and nail dystrophy"	"disease"	"C16;C17;C18;C20;C23"	"Disease or Syndrome"	"0.80"		"1966"	"2011"	"0"	"2"	"CTD_human;ORPHANET"
"8456"	"FOXN1"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8462"	"KLF11"	"0.707"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8462"	"KLF11"	"0.707"	"0.276"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8462"	"KLF11"	"0.707"	"0.276"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"8462"	"KLF11"	"0.707"	"0.276"	"C1864839"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"2"	"CTD_human;UNIPROT"
"8463"	"TEAD2"	"0.799"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8463"	"TEAD2"	"0.799"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8467"	"SMARCA5"	"0.743"	"0.207"	"C0279980"	"Extraosseous Ewings sarcoma-primitive neuroepithelial tumor"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"8468"	"FKBP6"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"8470"	"SORBS2"	"0.799"	"0.138"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8471"	"IRS4"	"0.743"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8473"	"OGT"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8473"	"OGT"	"0.672"	"0.448"	"C4478379"	"MENTAL RETARDATION, X-LINKED 106"	"disease"		"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2017"	"3"	"3"	"UNIPROT"
"8481"	"OFD1"	"0.547"	"0.724"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C0008780"	"Ciliary Motility Disorders"	"group"	"C08;C09;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"4"	"0"	"CLINGEN"
"8481"	"OFD1"	"0.547"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8481"	"OFD1"	"0.547"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"8481"	"OFD1"	"0.547"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C0265251"	"Oto-Palato-digital syndrome type 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8481"	"OFD1"	"0.547"	"0.724"	"C1419610"	"RP23 gene"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2013"	"0"	"1"	"CTD_human"
"8481"	"OFD1"	"0.547"	"0.724"	"C1510460"	"Orofaciodigital Syndrome I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.66"	"1"	"1993"	"2017"	"5"	"101"	"ORPHANET;UNIPROT"
"8481"	"OFD1"	"0.547"	"0.724"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C1846175"	"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)"	"disease"	"C16"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2013"	"0"	"1"	"CTD_human"
"8481"	"OFD1"	"0.547"	"0.724"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8481"	"OFD1"	"0.547"	"0.724"	"C2749019"	"JOUBERT SYNDROME 10 (disorder)"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"2008"	"2016"	"2"	"7"	"CTD_human;UNIPROT"
"8481"	"OFD1"	"0.547"	"0.724"	"C2931426"	"Orofaciodigital syndrome type1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.56"	"1"	"2005"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"8481"	"OFD1"	"0.547"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"8481"	"OFD1"	"0.547"	"0.724"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8482"	"SEMA7A"	"0.743"	"0.31"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"8483"	"CILP"	"0.785"	"0.207"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8483"	"CILP"	"0.785"	"0.207"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.32"	"0.5"	"2005"	"2007"	"0"	"0"	"CTD_human"
"8484"	"GALR3"	"0.762"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"8484"	"GALR3"	"0.762"	"0.138"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8484"	"GALR3"	"0.762"	"0.138"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"8484"	"GALR3"	"0.762"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8484"	"GALR3"	"0.762"	"0.138"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8484"	"GALR3"	"0.762"	"0.138"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8490"	"RGS5"	"0.707"	"0.31"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2012"	"1"	"0"	"CTD_human"
"8490"	"RGS5"	"0.707"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8490"	"RGS5"	"0.707"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"8490"	"RGS5"	"0.707"	"0.31"	"C0085580"	"Essential Hypertension"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"8491"	"MAP4K3"	"0.743"	"0.379"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8492"	"PRSS12"	"0.815"	"0.207"	"C1855304"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"0"	"1"	"CTD_human"
"8492"	"PRSS12"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2002"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.95"	"2002"	"2016"	"0"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"				"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0677866"	"Brain Stem Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.95"	"2002"	"2016"	"0"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0751886"	"Brain Stem Neoplasms, Primary"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0751887"	"Medullary Neoplasms"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0751888"	"Mesencephalic Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C0751889"	"Pontine Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"0"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8493"	"PPM1D"	"0.573"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"8493"	"PPM1D"	"0.573"	"0.724"	"C4479517"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"5"	"CTD_human"
"8495"	"PPFIBP2"	"0.886"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"8495"	"PPFIBP2"	"0.886"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"8496"	"PPFIBP1"	"0.886"	"0.138"	"C0085269"	"Plasma Cell Granuloma, Pulmonary"	"disease"	"C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8497"	"PPFIA4"	"0.834"	"0.241"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2018"	"1"	"2"	"CTD_human"
"8497"	"PPFIA4"	"0.834"	"0.241"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8497"	"PPFIA4"	"0.834"	"0.241"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8497"	"PPFIA4"	"0.834"	"0.241"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8504"	"PEX3"	"0.588"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.56"	"0.8333333"	"2000"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"8504"	"PEX3"	"0.588"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8504"	"PEX3"	"0.588"	"0.552"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"8504"	"PEX3"	"0.588"	"0.552"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"8504"	"PEX3"	"0.588"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2000"	"2000"	"1"	"0"	"CTD_human"
"8504"	"PEX3"	"0.588"	"0.552"	"C1864171"	"Peroxisome Biogenesis Disorder, Complementation Group 12"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"2"	"0"	"CTD_human;UNIPROT"
"8504"	"PEX3"	"0.588"	"0.552"	"C1864172"	"Peroxisome Biogenesis Disorder, Complementation Group G"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"2"	"0"	"CTD_human;UNIPROT"
"8504"	"PEX3"	"0.588"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C3553999"	"PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.50"		"2000"	"2000"	"2"	"0"	"CTD_human;UNIPROT"
"8504"	"PEX3"	"0.588"	"0.552"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2018"	"1"	"0"	"CTD_human"
"8504"	"PEX3"	"0.588"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"8504"	"PEX3"	"0.588"	"0.552"	"C4479254"	"PEROXISOME BIOGENESIS DISORDER 10B"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"8505"	"PARG"	"0.727"	"0.276"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"8505"	"PARG"	"0.727"	"0.276"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8505"	"PARG"	"0.727"	"0.276"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8505"	"PARG"	"0.727"	"0.276"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8506"	"CNTNAP1"	"0.627"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8506"	"CNTNAP1"	"0.627"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8506"	"CNTNAP1"	"0.627"	"0.448"	"C4225386"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"4"	"6"	"CTD_human;UNIPROT"
"8507"	"ENC1"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8509"	"NDST2"	"0.886"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8509"	"NDST2"	"0.886"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8514"	"KCNAB2"	"0.676"	"0.448"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"8514"	"KCNAB2"	"0.676"	"0.448"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8514"	"KCNAB2"	"0.676"	"0.448"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8514"	"KCNAB2"	"0.676"	"0.448"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8514"	"KCNAB2"	"0.676"	"0.448"	"C1842870"	"Chromosome 1p36 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2011"	"0"	"0"	"ORPHANET"
"8515"	"ITGA10"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8515"	"ITGA10"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8516"	"ITGA8"	"0.672"	"0.414"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8516"	"ITGA8"	"0.672"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8516"	"ITGA8"	"0.672"	"0.414"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8516"	"ITGA8"	"0.672"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8516"	"ITGA8"	"0.672"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"8516"	"ITGA8"	"0.672"	"0.414"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"8516"	"ITGA8"	"0.672"	"0.414"	"C1619700"	"RENAL ADYSPLASIA"	"disease"	"C12;C13;C16"	"Congenital Abnormality"	"0.40"		"2014"	"2015"	"1"	"5"	"UNIPROT"
"8516"	"ITGA8"	"0.672"	"0.414"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8516"	"ITGA8"	"0.672"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0021171"	"Bloch Sulzberger syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"0.9791667"	"1982"	"2018"	"7"	"6"	"CTD_human;ORPHANET;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8517"	"IKBKG"	"0.533"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1845073"	"INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 (disorder)"	"disease"	"C01;C20"	"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1845117"	"Immunodeficiency without anhidrotic ectodermal dysplasia"	"disease"	"C20"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"2"	"1"	"CTD_human;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1845919"	"Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema"	"disease"	"C05;C15;C16;C17;C20"	"Disease or Syndrome"	"0.60"		"2000"	"2001"	"0"	"1"	"CTD_human;ORPHANET"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1846006"	"Ectodermal dysplasia, hypohidrotic, with immune deficiency"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.80"	"1"	"2001"	"2018"	"9"	"13"	"CTD_human;ORPHANET;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1846008"	"HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC"	"disease"	"C15;C16;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2001"	"2011"	"9"	"8"	"UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C1970879"	"ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder)"	"disease"	"C01;C16"	"Disease or Syndrome"	"0.70"		"2006"	"2009"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C2930820"	"Incontinentia pigmenti, familial male-lethal type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2000"	"2014"	"7"	"4"	"ORPHANET;UNIPROT"
"8517"	"IKBKG"	"0.533"	"0.759"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8517"	"IKBKG"	"0.533"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8518"	"ELP1"	"0.633"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8518"	"ELP1"	"0.633"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8518"	"ELP1"	"0.633"	"0.69"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"6"	"9"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"8518"	"ELP1"	"0.633"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8518"	"ELP1"	"0.633"	"0.69"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1993"	"2008"	"4"	"0"	"GENOMICS_ENGLAND"
"8518"	"ELP1"	"0.633"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8518"	"ELP1"	"0.633"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8518"	"ELP1"	"0.633"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8519"	"IFITM1"	"0.743"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8520"	"HAT1"	"0.834"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8522"	"GAS7"	"0.735"	"0.276"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"8525"	"DGKZ"	"0.773"	"0.207"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8526"	"DGKE"	"0.727"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8526"	"DGKE"	"0.727"	"0.379"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8526"	"DGKE"	"0.727"	"0.379"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8526"	"DGKE"	"0.727"	"0.379"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.65"	"1"	"2013"	"2016"	"2"	"8"	"CTD_human;GENOMICS_ENGLAND"
"8526"	"DGKE"	"0.727"	"0.379"	"C3554330"	"NEPHROTIC SYNDROME, TYPE 7"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"9"	"CTD_human;UNIPROT"
"8526"	"DGKE"	"0.727"	"0.379"	"C3808620"	"HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7"	"phenotype"		"Finding"	"0.50"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"8528"	"DDO"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8528"	"DDO"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8530"	"CST7"	"0.815"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8530"	"CST7"	"0.815"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8530"	"CST7"	"0.815"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8533"	"COPS3"	"0.886"	"0.034"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8536"	"CAMK1"	"0.785"	"0.207"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"8537"	"BCAS1"	"0.886"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8537"	"BCAS1"	"0.886"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8540"	"AGPS"	"0.735"	"0.276"	"C0008445"	"Chondrodysplasia Punctata"	"disease"	"C05"	"Congenital Abnormality"	"0.52"	"1"	"2005"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"8540"	"AGPS"	"0.735"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8540"	"AGPS"	"0.735"	"0.276"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"8540"	"AGPS"	"0.735"	"0.276"	"C1838612"	"Rhizomelic chondrodysplasia punctata, type 3"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.90"		"1994"	"2012"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8540"	"AGPS"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1994"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"8542"	"APOL1"	"0.59"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8542"	"APOL1"	"0.59"	"0.621"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"0.9545455"	"2010"	"2018"	"0"	"1"	"CTD_human"
"8542"	"APOL1"	"0.59"	"0.621"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8542"	"APOL1"	"0.59"	"0.621"	"C2675525"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2010"	"2013"	"2"	"3"	"UNIPROT"
"8544"	"PIR"	"0.815"	"0.103"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8544"	"PIR"	"0.815"	"0.103"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8546"	"AP3B1"	"0.621"	"0.69"	"C1842362"	"HERMANSKY-PUDLAK SYNDROME 2"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.94"	"1"	"1981"	"2015"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"8546"	"AP3B1"	"0.621"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"8547"	"FCN3"	"0.735"	"0.345"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8547"	"FCN3"	"0.735"	"0.345"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8547"	"FCN3"	"0.735"	"0.345"	"C3151226"	"FICOLIN 3 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"8549"	"LGR5"	"0.598"	"0.448"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"8549"	"LGR5"	"0.598"	"0.448"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"8549"	"LGR5"	"0.598"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"8549"	"LGR5"	"0.598"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"8549"	"LGR5"	"0.598"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2008"	"2014"	"3"	"0"	"CTD_human;PSYGENET"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0393770"	"Delayed Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0494410"	"Nonorganic Sleep Wake Cycle Disorders"	"group"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0751758"	"Advanced Sleep Phase Syndrome"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0751759"	"Non-24 Hour Sleep-Wake Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0751760"	"Shift-Work Sleep Disorder"	"disease"	"C10;C24;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C0877792"	"Sleep Disorders, Circadian Rhythm"	"group"	"C10;C24;F03"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8553"	"BHLHE40"	"0.633"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8554"	"PIAS1"	"0.69"	"0.379"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8556"	"CDC14A"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8556"	"CDC14A"	"0.857"	"0.103"	"C4310777"	"DEAFNESS, AUTOSOMAL RECESSIVE 105"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"CTD_human"
"8557"	"TCAP"	"0.685"	"0.138"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2000"	"2004"	"0"	"1"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"1997"	"2006"	"4"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8557"	"TCAP"	"0.685"	"0.138"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2002"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.50"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"8557"	"TCAP"	"0.685"	"0.138"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"1997"	"2006"	"4"	"0"	"CLINGEN"
"8557"	"TCAP"	"0.685"	"0.138"	"C1843791"	"CARDIOMYOPATHY, DILATED, 1N"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"0"	"2"	"CTD_human"
"8557"	"TCAP"	"0.685"	"0.138"	"C1866008"	"Muscular Dystrophy, Limb-Girdle, Type 2G"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"2000"	"2014"	"0"	"6"	"CTD_human;ORPHANET"
"8557"	"TCAP"	"0.685"	"0.138"	"C4225408"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"4"	"UNIPROT"
"8558"	"CDK10"	"0.735"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8560"	"DEGS1"	"0.799"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8560"	"DEGS1"	"0.799"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8563"	"THOC5"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8564"	"KMO"	"0.752"	"0.276"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"8564"	"KMO"	"0.752"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8564"	"KMO"	"0.752"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"0.8"	"2006"	"2016"	"5"	"0"	"PSYGENET"
"8564"	"KMO"	"0.752"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"8564"	"KMO"	"0.752"	"0.276"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8564"	"KMO"	"0.752"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"8565"	"YARS"	"0.762"	"0.345"	"C1842237"	"Charcot-Marie-Tooth Disease, Dominant Intermediate C"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2004"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8566"	"PDXK"	"0.743"	"0.241"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8566"	"PDXK"	"0.743"	"0.241"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8567"	"MADD"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8569"	"MKNK1"	"0.72"	"0.31"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8570"	"KHSRP"	"0.602"	"0.552"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8572"	"PDLIM4"	"0.663"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.58"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0220769"	"FG syndrome"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2012"	"0"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.45"	"1"	"2010"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8573"	"CASK"	"0.584"	"0.517"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"8573"	"CASK"	"0.584"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1845546"	"FG SYNDROME 4 (disorder)"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"8573"	"CASK"	"0.584"	"0.517"	"C1845567"	"FG SYNDROME 3"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1845902"	"FG SYNDROME 2"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8573"	"CASK"	"0.584"	"0.517"	"C2677903"	"Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2008"	"2015"	"2"	"28"	"CTD_human;ORPHANET;UNIPROT"
"8573"	"CASK"	"0.584"	"0.517"	"C3275356"	"MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"1"	"UNIPROT"
"8573"	"CASK"	"0.584"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.48"	"1"	"2008"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"8573"	"CASK"	"0.584"	"0.517"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.39"	"1"	"2008"	"2015"	"0"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2016"	"8"	"0"	"GENOMICS_ENGLAND"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.45"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"				"0"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8575"	"PRKRA"	"0.6"	"0.448"	"C2677567"	"DYSTONIA 16 (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.61"	"1"	"2008"	"2015"	"2"	"2"	"ORPHANET;UNIPROT"
"8575"	"PRKRA"	"0.6"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8575"	"PRKRA"	"0.6"	"0.448"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0002382"	"Alveolar Bone Loss"	"disease"	"C05;C07"	"Disease or Syndrome"	"0.32"		"2004"	"2009"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0029454"	"Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.46"	"0.75"	"2002"	"2014"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2018"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0266929"	"Chronic Periodontitis"	"disease"	"C07"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C1318518"	"Infantile malignant osteopetrosis"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C1850126"	"Osteopetrosis, mild autosomal recessive form"	"disease"	"C05"	"Disease or Syndrome"	"0.80"		"2000"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C3179239"	"Osteopetrosis Autosomal Dominant Type 2"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8600"	"TNFSF11"	"0.51"	"0.69"	"C3645711"	"Congenital Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8601"	"RGS20"	"1"	"0.069"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8461538"	"2004"	"2012"	"2"	"0"	"CTD_human"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C2751855"	"Hypomyelination, Global Cerebral"	"disease"	"C10;C16;C18;C23;F01"	"Disease or Syndrome"	"0.70"		"2009"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8604"	"SLC25A12"	"0.762"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"8605"	"PLA2G4C"	"0.743"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2018"	"1"	"0"	"PSYGENET"
"8611"	"PLPP1"	"0.773"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8611"	"PLPP1"	"0.773"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8611"	"PLPP1"	"0.773"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8611"	"PLPP1"	"0.773"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8612"	"PLPP2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8613"	"PLPP3"	"0.752"	"0.138"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"8613"	"PLPP3"	"0.752"	"0.138"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.44"	"1"	"2011"	"2018"	"1"	"7"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2009"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"8614"	"STC2"	"0.642"	"0.552"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8615"	"USO1"	"0.58"	"0.759"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8621"	"CDK13"	"0.696"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8621"	"CDK13"	"0.696"	"0.448"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8621"	"CDK13"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8621"	"CDK13"	"0.696"	"0.448"	"C4479246"	"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2018"	"2"	"4"	"CTD_human;UNIPROT"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0001627"	"Congenital adrenal hyperplasia"	"disease"	"C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0013362"	"Dysarthria"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0026837"	"Muscle Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0151564"	"Cogwheel Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0231519"	"Gegenhalten"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0233608"	"Catatonic Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0239325"	"Extensor Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0240952"	"Dysarthria, Scanning"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0277821"	"Extrapyramidal Rigidity"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0454596"	"Dysarthria, Spastic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0454597"	"Dysarthria, Flaccid"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0454598"	"Dysarthria, Mixed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C1320474"	"Nuchal Rigidity"	"phenotype"	"C05;C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C1563666"	"Dysarthria, Guttural"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8622"	"PDE8B"	"0.672"	"0.379"	"C1836694"	"Striatal Degeneration, Autosomal Dominant"	"disease"	"C23"	"Disease or Syndrome"	"0.52"	"1"	"2010"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"8622"	"PDE8B"	"0.672"	"0.379"	"C3280094"	"PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"8622"	"PDE8B"	"0.672"	"0.379"	"C4304832"	"Primary pigmented nodular adrenocortical disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8623"	"ASMTL"	"0.857"	"0.103"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8623"	"ASMTL"	"0.857"	"0.103"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8623"	"ASMTL"	"0.857"	"0.103"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8623"	"ASMTL"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8624"	"PSMG1"	"0.667"	"0.483"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"8625"	"RFXANK"	"0.681"	"0.483"	"C1859534"	"Bare Lymphocyte Syndrome, Type II, Complementation Group A"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"4"	"1"	"UNIPROT"
"8625"	"RFXANK"	"0.681"	"0.483"	"C1859535"	"Bare Lymphocyte Syndrome, Type II, Complementation Group B"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.40"		"1998"	"2012"	"4"	"2"	"UNIPROT"
"8625"	"RFXANK"	"0.681"	"0.483"	"C1859536"	"Bare Lymphocyte Syndrome, Type II, Complementation Group C"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"4"	"1"	"UNIPROT"
"8625"	"RFXANK"	"0.681"	"0.483"	"C1859537"	"Bare Lymphocyte Syndrome, Type II, Complementation Group D"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"4"	"1"	"UNIPROT"
"8625"	"RFXANK"	"0.681"	"0.483"	"C1859538"	"Bare Lymphocyte Syndrome, Type II, Complementation Group E"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.30"		"1998"	"2012"	"4"	"1"	"UNIPROT"
"8625"	"RFXANK"	"0.681"	"0.483"	"C2931418"	"Bare lymphocyte syndrome 2"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.64"	"0.75"	"1998"	"2016"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8626"	"TP63"	"0.419"	"0.759"	"C0005689"	"Bladder Exstrophy"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.62"	"1"	"1999"	"2014"	"0"	"0"	"ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C0006145"	"Breast Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9761905"	"2001"	"2016"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.62"	"1"	"2006"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.32"	"1"	"2001"	"2012"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2006"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0016508"	"Congenital Foot Deformity"	"group"	"C05;C16"	"Congenital Abnormality"	"0.32"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2001"	"2005"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9230769"	"2001"	"2016"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0038987"	"Sweat Gland Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.46"	"0.8333333"	"2010"	"2017"	"1"	"4"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.47"	"1"	"2003"	"2013"	"0"	"0"	"ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0206720"	"Squamous Cell Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.38"	"1"	"2000"	"2015"	"2"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"1999"	"2002"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0406704"	"Rudiger syndrome 1"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.80"	"0.9333333"	"1999"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C0406709"	"Hay-Wells syndrome"	"disease"	"C05;C07;C11;C16;C17"	"Congenital Abnormality"	"0.70"	"1"	"1998"	"2017"	"3"	"3"	"CTD_human;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.49"	"1"	"2000"	"2016"	"0"	"2"	"UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C0751688"	"Malignant Squamous Cell Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.53"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1298692"	"Cleft lip and alveolus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C1449718"	"Endocrine Breast Diseases"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C1785148"	"RAPP-HODGKIN SYNDROME"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.99"	"1"	"2000"	"2013"	"7"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8626"	"TP63"	"0.419"	"0.759"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8626"	"TP63"	"0.419"	"0.759"	"C1851841"	"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C1851878"	"OROFACIAL CLEFT 8"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.40"		"2003"	"2006"	"4"	"4"	"UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1851879"	"Cleft Lip with or without Cleft Palate, Nonsyndromic, 8"	"disease"	"C07;C16;C17"	"Disease or Syndrome"	"0.30"		"2003"	"2006"	"4"	"4"	"UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1854442"	"SPLIT-HAND/FOOT MALFORMATION 4"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.64"	"1"	"1988"	"2016"	"2"	"4"	"CTD_human;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1858562"	"ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.60"		"1996"	"2016"	"4"	"12"	"CTD_human;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1863204"	"ADULT SYNDROME"	"disease"	"C05;C07;C11;C16;C17;C23"	"Disease or Syndrome"	"0.78"	"1"	"1993"	"2012"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"8626"	"TP63"	"0.419"	"0.759"	"C1863753"	"LIMB-MAMMARY SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2001"	"2010"	"1"	"1"	"CTD_human;ORPHANET"
"8626"	"TP63"	"0.419"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8626"	"TP63"	"0.419"	"0.759"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8629"	"JRK"	"0.701"	"0.034"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0014548"	"Epilepsy, Generalized"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0017332"	"Generalized Nonconvulsive Seizure Disorder"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0086236"	"Epilepsy, Atonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0086241"	"Epilepsy, Tonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human;ORPHANET"
"8629"	"JRK"	"0.701"	"0.034"	"C0270854"	"Symptomatic Generalized Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0311334"	"Generalized convulsive epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0347869"	"Epilepsy, Akinetic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0393676"	"Panayiotopoulos Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8629"	"JRK"	"0.701"	"0.034"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8629"	"JRK"	"0.701"	"0.034"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"8630"	"HSD17B6"	"0.551"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8631"	"SKAP1"	"0.773"	"0.172"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8631"	"SKAP1"	"0.773"	"0.172"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8633"	"UNC5C"	"0.656"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8633"	"UNC5C"	"0.656"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8635"	"RNASET2"	"0.727"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8635"	"RNASET2"	"0.727"	"0.448"	"C2751843"	"Leukoencephalopathy, Cystic, Without Megalencephaly"	"disease"	"C04;C10;C23"	"Disease or Syndrome"	"0.70"		"2009"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8635"	"RNASET2"	"0.727"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8636"	"SSNA1"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8638"	"OASL"	"0.799"	"0.276"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0030524"	"Paratuberculosis"	"disease"	"C01;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8639"	"AOC3"	"0.609"	"0.69"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8642"	"DCHS1"	"0.63"	"0.586"	"C0340364"	"Familial mitral valve prolapse"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8642"	"DCHS1"	"0.63"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"8642"	"DCHS1"	"0.63"	"0.586"	"C1832390"	"Van Maldergem Wetzburger Verloes syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2013"	"2014"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8642"	"DCHS1"	"0.63"	"0.586"	"C1842563"	"Heterotopia, Periventricular, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8642"	"DCHS1"	"0.63"	"0.586"	"C1843003"	"MITRAL VALVE PROLAPSE, MYXOMATOUS 2"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2003"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"8642"	"DCHS1"	"0.63"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0004779"	"Basal Cell Nevus Syndrome"	"disease"	"C04;C05;C07;C16"	"Neoplastic Process"	"0.64"	"1"	"1999"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1985"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0024433"	"Macrostomia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"1999"	"1999"	"0"	"1"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C0812437"	"Oculo-dento-digital syndrome"	"disease"	"C05;C07;C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"8643"	"PTCH2"	"0.59"	"0.517"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8643"	"PTCH2"	"0.59"	"0.517"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"2"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0019269"	"Hermaphroditism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0027661"	"Neoplasms, Hormone-Dependent"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.54"	"0.75"	"1993"	"2015"	"3"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0033804"	"Pseudohermaphroditism"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0266362"	"Ambiguous Genitalia"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2006"	"2012"	"3"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C2930618"	"Intersex Conditions"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C2930619"	"Sex Differentiation Disorders"	"group"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C3658266"	"Prostatic Cancer, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8644"	"AKR1C3"	"0.561"	"0.621"	"C3658267"	"Prostatic Neoplasms, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8645"	"KCNK5"	"0.72"	"0.345"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0001733"	"Afibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.80"	"0.9411765"	"2001"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2002"	"2016"	"1"	"1"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.44"	"0.75"	"2008"	"2015"	"1"	"1"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0268312"	"Progressive intrahepatic cholestasis (disorder)"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9787234"	"1997"	"2017"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2014"	"0"	"0"	"ORPHANET"
"8647"	"ABCB11"	"0.6"	"0.414"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8647"	"ABCB11"	"0.6"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C2584774"	"Congenital hypofibrinogenemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8647"	"ABCB11"	"0.6"	"0.414"	"C2608083"	"Cholestasis, benign recurrent intrahepatic 2"	"disease"	"C06"	"Disease or Syndrome"	"0.72"	"1"	"2004"	"2014"	"2"	"23"	"CTD_human;ORPHANET;UNIPROT"
"8647"	"ABCB11"	"0.6"	"0.414"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8647"	"ABCB11"	"0.6"	"0.414"	"C3489789"	"Cholestasis, Progressive Familial Intrahepatic, 2"	"disease"	"C06"	"Disease or Syndrome"	"0.79"	"1"	"1998"	"2016"	"4"	"27"	"CTD_human;ORPHANET;UNIPROT"
"8647"	"ABCB11"	"0.6"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8647"	"ABCB11"	"0.6"	"0.414"	"C4316812"	"Fibrinogen Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"2004"	"2017"	"1"	"1"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8648"	"NCOA1"	"0.642"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2009"	"0"	"0"	"CGI"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.6666667"	"2003"	"2013"	"0"	"0"	"CGI"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2009"	"0"	"0"	"CGI"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8651"	"SOCS1"	"0.483"	"0.759"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8653"	"DDX3Y"	"0.752"	"0.241"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"8653"	"DDX3Y"	"0.752"	"0.241"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8653"	"DDX3Y"	"0.752"	"0.241"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8654"	"PDE5A"	"0.611"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"8655"	"DYNLL1"	"0.63"	"0.586"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"8655"	"DYNLL1"	"0.63"	"0.586"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"8659"	"ALDH4A1"	"0.785"	"0.276"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8659"	"ALDH4A1"	"0.785"	"0.276"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8659"	"ALDH4A1"	"0.785"	"0.276"	"C2931835"	"Hyperprolinemia type 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"1990"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8659"	"ALDH4A1"	"0.785"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8660"	"IRS2"	"0.559"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.96"	"1998"	"2016"	"0"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"0.5"	"2005"	"2016"	"2"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2010"	"2016"	"2"	"0"	"CTD_human"
"8660"	"IRS2"	"0.559"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"8661"	"EIF3A"	"0.619"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8661"	"EIF3A"	"0.619"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8662"	"EIF3B"	"0.799"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8662"	"EIF3B"	"0.799"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8666"	"EIF3G"	"0.886"	"0.069"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8667"	"EIF3H"	"0.735"	"0.241"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"8667"	"EIF3H"	"0.735"	"0.241"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8667"	"EIF3H"	"0.735"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8667"	"EIF3H"	"0.735"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"2000"	"2008"	"1"	"0"	"CTD_human"
"8667"	"EIF3H"	"0.735"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"8667"	"EIF3H"	"0.735"	"0.241"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"8668"	"EIF3I"	"0.857"	"0.172"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8668"	"EIF3I"	"0.857"	"0.172"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2002"	"2014"	"2"	"0"	"CTD_human"
"8668"	"EIF3I"	"0.857"	"0.172"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1999"	"2011"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0010038"	"Corneal Opacity"	"phenotype"	"C11"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.44"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0268435"	"Renal Tubular Acidosis, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C1704380"	"Distal Renal Tubular Acidosis"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C1970309"	"Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation"	"disease"	"C10;C11;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1999"	"2008"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8671"	"SLC4A4"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2001"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8673"	"VAMP8"	"0.72"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C1864100"	"PSEUDOHYPOPARATHYROIDISM, TYPE IB"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"8675"	"STX16"	"0.713"	"0.276"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8675"	"STX16"	"0.713"	"0.276"	"C2932715"	"Pseudohypoparathyroidism Type 1B"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"8676"	"STX11"	"0.752"	"0.345"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8676"	"STX11"	"0.752"	"0.345"	"C0272199"	"Familial Hemophagocytic Lymphocytosis"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8676"	"STX11"	"0.752"	"0.345"	"C1863728"	"Hemophagocytic lymphohistiocytosis, familial, 4"	"disease"	"C15"	"Disease or Syndrome"	"0.63"	"1"	"2005"	"2016"	"0"	"4"	"CTD_human"
"8676"	"STX11"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8678"	"BECN1"	"0.497"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2010"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8678"	"BECN1"	"0.497"	"0.759"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2015"	"2"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8678"	"BECN1"	"0.497"	"0.759"	"C0752347"	"Lewy Body Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8682"	"PEA15"	"0.621"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8682"	"PEA15"	"0.621"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8683"	"SRSF9"	"0.799"	"0.276"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8683"	"SRSF9"	"0.799"	"0.276"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8694"	"DGAT1"	"0.701"	"0.379"	"C0011991"	"Diarrhea"	"phenotype"	"C23"	"Sign or Symptom"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"8694"	"DGAT1"	"0.701"	"0.379"	"C4014516"	"DIARRHEA 7"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"0"	"2"	"ORPHANET"
"8698"	"S1PR4"	"0.815"	"0.172"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8698"	"S1PR4"	"0.815"	"0.172"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8698"	"S1PR4"	"0.815"	"0.172"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8701"	"DNAH11"	"0.69"	"0.345"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2009"	"2011"	"1"	"1"	"CTD_human"
"8701"	"DNAH11"	"0.69"	"0.345"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.57"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"8701"	"DNAH11"	"0.69"	"0.345"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8701"	"DNAH11"	"0.69"	"0.345"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8701"	"DNAH11"	"0.69"	"0.345"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8701"	"DNAH11"	"0.69"	"0.345"	"C2678473"	"CILIARY DYSKINESIA, PRIMARY, 7 (disorder)"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.80"		"1993"	"2015"	"2"	"15"	"CTD_human;UNIPROT"
"8701"	"DNAH11"	"0.69"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8701"	"DNAH11"	"0.69"	"0.345"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8702"	"B4GALT4"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8702"	"B4GALT4"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8708"	"B3GALT1"	"0.928"	"0.138"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"8710"	"SERPINB7"	"0.799"	"0.172"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2017"	"10"	"0"	"GENOMICS_ENGLAND"
"8710"	"SERPINB7"	"0.799"	"0.172"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2017"	"10"	"0"	"GENOMICS_ENGLAND"
"8710"	"SERPINB7"	"0.799"	"0.172"	"C3810072"	"Palmoplantar keratoderma Nagashima type"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"0"	"4"	"CTD_human;ORPHANET"
"8711"	"TNK1"	"0.815"	"0.207"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8714"	"ABCC3"	"0.542"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"8714"	"ABCC3"	"0.542"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.52"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"8714"	"ABCC3"	"0.542"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1997"	"2017"	"1"	"0"	"CTD_human"
"8714"	"ABCC3"	"0.542"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8714"	"ABCC3"	"0.542"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8714"	"ABCC3"	"0.542"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human"
"8720"	"MBTPS1"	"0.619"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8720"	"MBTPS1"	"0.619"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"8720"	"MBTPS1"	"0.619"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8720"	"MBTPS1"	"0.619"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"8722"	"CTSF"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8722"	"CTSF"	"0.735"	"0.31"	"C3715049"	"CEROID LIPOFUSCINOSIS, NEURONAL, 13"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"8724"	"SNX3"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"8725"	"URI1"	"0.701"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8725"	"URI1"	"0.701"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2016"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"8726"	"EED"	"0.676"	"0.448"	"C0206727"	"Nerve Sheath Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0265210"	"Weaver syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8726"	"EED"	"0.676"	"0.448"	"C0751374"	"Schwannomatosis, Plexiform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0751689"	"Peripheral Nerve Sheath Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C0751691"	"Perineurioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8726"	"EED"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"8726"	"EED"	"0.676"	"0.448"	"C4479654"	"COHEN-GIBSON SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2018"	"5"	"4"	"UNIPROT"
"8728"	"ADAM19"	"0.713"	"0.31"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8728"	"ADAM19"	"0.713"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"8733"	"GPAA1"	"0.707"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8733"	"GPAA1"	"0.707"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8733"	"GPAA1"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8735"	"MYH13"	"0.928"	"0.034"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8735"	"MYH13"	"0.928"	"0.034"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8736"	"MYOM1"	"0.928"	"0.207"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8737"	"RIPK1"	"0.572"	"0.621"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"3"	"UNIPROT"
"8738"	"CRADD"	"0.701"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8738"	"CRADD"	"0.701"	"0.414"	"C3281044"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"8738"	"CRADD"	"0.701"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8740"	"TNFSF14"	"0.58"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"8740"	"TNFSF14"	"0.58"	"0.586"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2014"	"1"	"1"	"CTD_human"
"8740"	"TNFSF14"	"0.58"	"0.586"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.46"	"1"	"2011"	"2018"	"1"	"1"	"CTD_human"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8741"	"TNFSF13"	"0.561"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8742"	"TNFSF12"	"0.598"	"0.655"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8742"	"TNFSF12"	"0.598"	"0.655"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8742"	"TNFSF12"	"0.598"	"0.655"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8742"	"TNFSF12"	"0.598"	"0.655"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8742"	"TNFSF12"	"0.598"	"0.655"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.975"	"2002"	"2017"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9459459"	"2000"	"2016"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.31"		"2008"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9090909"	"2007"	"2017"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.962963"	"1999"	"2014"	"2"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"1998"	"2015"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.95"	"2003"	"2015"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.31"	"1"	"2008"	"2014"	"2"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0027686"	"Pathologic Neovascularization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9333333"	"1999"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2011"	"4"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2009"	"2"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"4"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9534884"	"2002"	"2017"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2018"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"8743"	"TNFSF10"	"0.44"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9464286"	"2003"	"2018"	"1"	"0"	"CTD_human"
"8744"	"TNFSF9"	"0.642"	"0.483"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8744"	"TNFSF9"	"0.642"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8744"	"TNFSF9"	"0.642"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8744"	"TNFSF9"	"0.642"	"0.483"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8744"	"TNFSF9"	"0.642"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8749"	"ADAM18"	"1"		"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"8754"	"ADAM9"	"0.586"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"8754"	"ADAM9"	"0.586"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"8754"	"ADAM9"	"0.586"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"8754"	"ADAM9"	"0.586"	"0.517"	"C1423873"	"CONE-ROD DYSTROPHY 9"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2001"	"2015"	"0"	"5"	"CTD_human"
"8756"	"ADAM7"	"0.886"	"0.103"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"7"	"UNIPROT"
"8761"	"PABPC4"	"0.785"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8763"	"CD164"	"0.735"	"0.276"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8763"	"CD164"	"0.735"	"0.276"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8763"	"CD164"	"0.735"	"0.276"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8763"	"CD164"	"0.735"	"0.276"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"8763"	"CD164"	"0.735"	"0.276"	"C4283893"	"DEAFNESS, AUTOSOMAL DOMINANT 66"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CLINGEN;CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2015"	"0"	"0"	"CGI"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8764"	"TNFRSF14"	"0.63"	"0.517"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8766"	"RAB11A"	"0.672"	"0.448"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8767"	"RIPK2"	"0.676"	"0.517"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C0038368"	"Stomatognathic Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C1704330"	"Dental Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8772"	"FADD"	"0.573"	"0.759"	"C2750325"	"Oculootodental Syndrome"	"disease"	"C07;C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8772"	"FADD"	"0.573"	"0.759"	"C3151062"	"INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8773"	"SNAP23"	"0.834"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8773"	"SNAP23"	"0.834"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8774"	"NAPG"	"0.857"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2009"	"3"	"0"	"PSYGENET"
"8776"	"MTMR1"	"0.857"	"0.103"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8776"	"MTMR1"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2006"	"2016"	"4"	"0"	"PSYGENET"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2013"	"2017"	"2"	"1"	"GENOMICS_ENGLAND"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0149821"	"ACUTE ALCOHOL WITHDRAWAL"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0586323"	"Alcohol Withdrawal Seizures"	"disease"	"C10;C23;C25"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C3554691"	"HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 2"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"0"	"4"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8777"	"MPDZ"	"0.645"	"0.31"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8777"	"MPDZ"	"0.645"	"0.31"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8778"	"SIGLEC5"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8784"	"TNFRSF18"	"0.701"	"0.379"	"C0023281"	"Leishmaniasis"	"disease"	"C03;C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8785"	"MATN4"	"0.886"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8785"	"MATN4"	"0.886"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"2"	"0"	"CTD_human"
"8787"	"RGS9"	"0.743"	"0.172"	"C1842073"	"Prolonged Electroretinal Response Suppression"	"phenotype"	"C11;C16"	"Finding"	"0.70"		"2004"	"2004"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8788"	"DLK1"	"0.57"	"0.552"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8788"	"DLK1"	"0.57"	"0.552"	"C0342544"	"Idiopathic central precocious puberty"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8788"	"DLK1"	"0.57"	"0.552"	"C1842466"	"Uniparental disomy, paternal, chromosome 14"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"8788"	"DLK1"	"0.57"	"0.552"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8788"	"DLK1"	"0.57"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2013"	"1"	"0"	"CTD_human"
"8789"	"FBP2"	"0.886"	"0.138"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8789"	"FBP2"	"0.886"	"0.138"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8789"	"FBP2"	"0.886"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8790"	"FPGT"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8790"	"FPGT"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8790"	"FPGT"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8790"	"FPGT"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8790"	"FPGT"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8790"	"FPGT"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2013"	"1"	"0"	"CTD_human"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C0268414"	"Hyperphosphatasemia with bone disease"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2015"	"0"	"0"	"ORPHANET"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C0432292"	"Familial expansile osteolysis"	"disease"	"C05"	"Congenital Abnormality"	"0.70"	"1"	"1994"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2001"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"8792"	"TNFRSF11A"	"0.526"	"0.724"	"C2676766"	"Osteopetrosis, Autosomal Recessive 7"	"disease"	"C05;C15;C20"	"Disease or Syndrome"	"0.70"		"2008"	"2010"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"8794"	"TNFRSF10C"	"0.639"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8794"	"TNFRSF10C"	"0.639"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8794"	"TNFRSF10C"	"0.639"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0280302"	"Squamous cell carcinoma of lip"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0280313"	"Squamous cell carcinoma of oropharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0280321"	"Squamous cell carcinoma of the hypopharynx"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0280324"	"Laryngeal Squamous Cell Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C0585362"	"Squamous cell carcinoma of mouth"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8795"	"TNFRSF10B"	"0.54"	"0.621"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"1998"	"2010"	"0"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0015672"	"Fatigue"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0027497"	"Nausea"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0086525"	"Lassitude"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2011"	"2014"	"1"	"1"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"0.8333333"	"2003"	"2015"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8797"	"TNFRSF10A"	"0.536"	"0.655"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"0"	"2002"	"2012"	"0"	"0"	"ORPHANET"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8799"	"PEX11B"	"0.592"	"0.586"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8799"	"PEX11B"	"0.592"	"0.586"	"C3554055"	"PEROXISOME BIOGENESIS DISORDER 14B"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2015"	"0"	"3"	"CTD_human"
"8799"	"PEX11B"	"0.592"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8800"	"PEX11A"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8800"	"PEX11A"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8800"	"PEX11A"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8800"	"PEX11A"	"0.815"	"0.069"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"8800"	"PEX11A"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8800"	"PEX11A"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8800"	"PEX11A"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8801"	"SUCLG2"	"0.785"	"0.31"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C3151476"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)"	"disease"		"Disease or Syndrome"	"0.70"		"2007"	"2015"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"8802"	"SUCLG1"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8803"	"SUCLA2"	"0.607"	"0.517"	"C2749864"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)"	"disease"		"Disease or Syndrome"	"0.90"		"1993"	"2015"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8804"	"CREG1"	"0.707"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8804"	"CREG1"	"0.707"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8805"	"TRIM24"	"0.614"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8805"	"TRIM24"	"0.614"	"0.448"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8805"	"TRIM24"	"0.614"	"0.448"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"8805"	"TRIM24"	"0.614"	"0.448"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8805"	"TRIM24"	"0.614"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"8805"	"TRIM24"	"0.614"	"0.448"	"C3658266"	"Prostatic Cancer, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8805"	"TRIM24"	"0.614"	"0.448"	"C3658267"	"Prostatic Neoplasms, Castration-Resistant"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8807"	"IL18RAP"	"0.72"	"0.517"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"8807"	"IL18RAP"	"0.72"	"0.517"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2016"	"1"	"1"	"CTD_human"
"8809"	"IL18R1"	"0.529"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"8809"	"IL18R1"	"0.529"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8809"	"IL18R1"	"0.529"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8809"	"IL18R1"	"0.529"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8809"	"IL18R1"	"0.529"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8811"	"GALR2"	"0.701"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"8811"	"GALR2"	"0.701"	"0.276"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8811"	"GALR2"	"0.701"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"2"	"0"	"PSYGENET"
"8811"	"GALR2"	"0.701"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8811"	"GALR2"	"0.701"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human;PSYGENET"
"8811"	"GALR2"	"0.701"	"0.276"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8811"	"GALR2"	"0.701"	"0.276"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8813"	"DPM1"	"0.676"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8813"	"DPM1"	"0.676"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"8813"	"DPM1"	"0.676"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8813"	"DPM1"	"0.676"	"0.448"	"C1837396"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"2000"	"2017"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"8813"	"DPM1"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8815"	"BANF1"	"0.663"	"0.552"	"C3151446"	"NESTOR-GUILLERMO PROGERIA SYNDROME"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2011"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8817"	"FGF18"	"0.701"	"0.345"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8817"	"FGF18"	"0.701"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8817"	"FGF18"	"0.701"	"0.345"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8817"	"FGF18"	"0.701"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8818"	"DPM2"	"0.743"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8818"	"DPM2"	"0.743"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8818"	"DPM2"	"0.743"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8818"	"DPM2"	"0.743"	"0.207"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"8818"	"DPM2"	"0.743"	"0.207"	"C3554385"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8818"	"DPM2"	"0.743"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"1998"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2013"	"0"	"0"	"ORPHANET"
"8820"	"HESX1"	"0.598"	"0.517"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1996"	"2017"	"5"	"11"	"ORPHANET;UNIPROT"
"8820"	"HESX1"	"0.598"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"1998"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C2750027"	"Growth Hormone Deficiency With Pituitary Anomalies"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1998"	"2017"	"5"	"7"	"UNIPROT"
"8820"	"HESX1"	"0.598"	"0.517"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.40"				"0"	"3"	"ORPHANET"
"8820"	"HESX1"	"0.598"	"0.517"	"C2930844"	"Hypopituitarism and septooptic 'dysplasia'"	"disease"	"C10;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"8820"	"HESX1"	"0.598"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"8820"	"HESX1"	"0.598"	"0.517"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"8821"	"INPP4B"	"0.642"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"0"	"0"	"CGI"
"8821"	"INPP4B"	"0.642"	"0.483"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8821"	"INPP4B"	"0.642"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2011"	"2017"	"0"	"0"	"CGI"
"8821"	"INPP4B"	"0.642"	"0.483"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8822"	"FGF17"	"0.627"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8822"	"FGF17"	"0.627"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8822"	"FGF17"	"0.627"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8822"	"FGF17"	"0.627"	"0.483"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8822"	"FGF17"	"0.627"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8822"	"FGF17"	"0.627"	"0.483"	"C3808983"	"HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"1983"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"8823"	"FGF16"	"0.799"	"0.172"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8823"	"FGF16"	"0.799"	"0.172"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8823"	"FGF16"	"0.799"	"0.172"	"C1839728"	"METACARPAL 4-5 FUSION"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"2014"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8824"	"CES2"	"0.648"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8824"	"CES2"	"0.648"	"0.448"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8824"	"CES2"	"0.648"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8824"	"CES2"	"0.648"	"0.448"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8824"	"CES2"	"0.648"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8824"	"CES2"	"0.648"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8825"	"LIN7A"	"0.762"	"0.276"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8826"	"IQGAP1"	"0.6"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8828"	"NRP2"	"0.559"	"0.483"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"		"2004"	"2008"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"8829"	"NRP1"	"0.521"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.38"	"0.875"	"2000"	"2015"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.36"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2018"	"1"	"1"	"PSYGENET"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C2675473"	"Mental Retardation, Autosomal Dominant 5"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2008"	"2018"	"5"	"27"	"CTD_human;UNIPROT"
"8831"	"SYNGAP1"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.68"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8832"	"CD84"	"0.815"	"0.207"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8832"	"CD84"	"0.815"	"0.207"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8835"	"SOCS2"	"0.602"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8835"	"SOCS2"	"0.602"	"0.552"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8835"	"SOCS2"	"0.602"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8835"	"SOCS2"	"0.602"	"0.552"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8835"	"SOCS2"	"0.602"	"0.552"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8836"	"GGH"	"0.636"	"0.379"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2010"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2004"	"2010"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8836"	"GGH"	"0.636"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"0.8"	"2003"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"		"2003"	"2007"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C0392788"	"Nasal Type Extranodal NK/T-Cell Lymphoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C1955906"	"Lymphoma, Extranodal NK-T-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8837"	"CFLAR"	"0.526"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"8838"	"WISP3"	"0.627"	"0.448"	"C0432215"	"Progressive pseudorheumatoid dysplasia"	"disease"	"C05"	"Congenital Abnormality"	"1.00"	"1"	"1999"	"2018"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"8841"	"HDAC3"	"0.569"	"0.586"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8841"	"HDAC3"	"0.569"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"8842"	"PROM1"	"0.45"	"0.793"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.5"	"2007"	"2013"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.90625"	"2008"	"2017"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.974026"	"2006"	"2018"	"3"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.49"	"1"	"2008"	"2017"	"0"	"2"	"ORPHANET"
"8842"	"PROM1"	"0.45"	"0.793"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2015"	"1"	"1"	"PSYGENET"
"8842"	"PROM1"	"0.45"	"0.793"	"C0042138"	"Uterine Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8842"	"PROM1"	"0.45"	"0.793"	"C0153567"	"Uterine Cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0206627"	"Mixed Tumor, Mullerian"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0271093"	"Stargardt's disease"	"phenotype"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8842"	"PROM1"	"0.45"	"0.793"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2010"	"3"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C0339512"	"Bull's eye macular dystrophy"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"		"1999"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8842"	"PROM1"	"0.45"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8842"	"PROM1"	"0.45"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"2008"	"2017"	"1"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"3"	"0"	"CTD_human"
"8842"	"PROM1"	"0.45"	"0.793"	"C1855465"	"STARGARDT DISEASE 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8842"	"PROM1"	"0.45"	"0.793"	"C1863534"	"Stargardt disease 4"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1999"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"8842"	"PROM1"	"0.45"	"0.793"	"C2675210"	"CONE-ROD DYSTROPHY 12 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"8842"	"PROM1"	"0.45"	"0.793"	"C2677516"	"RETINITIS PIGMENTOSA 41 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"0"	"6"	"CTD_human"
"8843"	"HCAR3"	"0.659"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"8843"	"HCAR3"	"0.659"	"0.552"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8843"	"HCAR3"	"0.659"	"0.552"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8843"	"HCAR3"	"0.659"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"8843"	"HCAR3"	"0.659"	"0.552"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8847"	"DLEU2"	"0.773"	"0.172"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"8847"	"DLEU2"	"0.773"	"0.172"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8847"	"DLEU2"	"0.773"	"0.172"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2005"	"2007"	"2"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8848"	"TSC22D1"	"0.659"	"0.414"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8850"	"KAT2B"	"0.609"	"0.483"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8851"	"CDK5R1"	"0.639"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8852"	"AKAP4"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0025312"	"Meningomyelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2018"	"1"	"1"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0086664"	"Myelocele"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0751316"	"Acquired Meningomyelocele"	"phenotype"	"C10;C16"	"Acquired Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8854"	"ALDH1A2"	"0.621"	"0.552"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2018"	"2"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0022353"	"Neonatal Jaundice"	"phenotype"	"C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0085682"	"Hypophosphatemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2018"	"2"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2018"	"2"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C1565887"	"Newborn physiological jaundice"	"phenotype"	"C16;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C1566050"	"Icterus Gravis Neonatorum"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2018"	"2"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2018"	"2"	"0"	"CTD_human"
"8856"	"NR1I2"	"0.455"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2018"	"2"	"0"	"CTD_human"
"8857"	"FCGBP"	"0.785"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8857"	"FCGBP"	"0.785"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8857"	"FCGBP"	"0.785"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8859"	"STK19"	"0.713"	"0.345"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8859"	"STK19"	"0.713"	"0.345"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"8859"	"STK19"	"0.713"	"0.345"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8861"	"LDB1"	"0.785"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"8863"	"PER3"	"0.607"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2016"	"5"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"8863"	"PER3"	"0.607"	"0.517"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8863"	"PER3"	"0.607"	"0.517"	"C1858496"	"Advanced Sleep-Phase Syndrome, Familial"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"8864"	"PER2"	"0.548"	"0.793"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"8864"	"PER2"	"0.548"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2016"	"4"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2013"	"0"	"0"	"UNIPROT"
"8864"	"PER2"	"0.548"	"0.793"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"8864"	"PER2"	"0.548"	"0.793"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"8864"	"PER2"	"0.548"	"0.793"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"8864"	"PER2"	"0.548"	"0.793"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"8864"	"PER2"	"0.548"	"0.793"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"8864"	"PER2"	"0.548"	"0.793"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2013"	"2"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C0858355"	"Addicted to cocaine"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8864"	"PER2"	"0.548"	"0.793"	"C1858496"	"Advanced Sleep-Phase Syndrome, Familial"	"disease"	"C10;C24;F03"	"Disease or Syndrome"	"0.59"	"1"	"2001"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"8864"	"PER2"	"0.548"	"0.793"	"C3807327"	"ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"1"	"UNIPROT"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"0.5"	"2016"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C3809824"	"PARKINSON DISEASE 20, EARLY-ONSET"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2014"	"2017"	"3"	"2"	"CTD_human;UNIPROT"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C4479313"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"8867"	"SYNJ1"	"0.627"	"0.345"	"C4510873"	"Atypical juvenile parkinsonism"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8869"	"ST3GAL5"	"0.676"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2004"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"8869"	"ST3GAL5"	"0.676"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8869"	"ST3GAL5"	"0.676"	"0.448"	"C1836824"	"Amish Infantile Epilepsy Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2004"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"8869"	"ST3GAL5"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"8870"	"IER3"	"0.621"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8870"	"IER3"	"0.621"	"0.517"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8871"	"SYNJ2"	"0.785"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"8871"	"SYNJ2"	"0.785"	"0.241"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8871"	"SYNJ2"	"0.785"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"8871"	"SYNJ2"	"0.785"	"0.241"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8871"	"SYNJ2"	"0.785"	"0.241"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"8875"	"VNN2"	"0.834"	"0.172"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8875"	"VNN2"	"0.834"	"0.172"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8875"	"VNN2"	"0.834"	"0.172"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"8875"	"VNN2"	"0.834"	"0.172"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8876"	"VNN1"	"0.727"	"0.31"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8877"	"SPHK1"	"0.524"	"0.621"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.60"	"0.9259259"	"2002"	"2017"	"0"	"0"	"CTD_human"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"1997"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C1833373"	"Inclusion Body Myopathy, Autosomal Recessive"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C1853926"	"NONAKA MYOPATHY"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C4085252"	"PAGET DISEASE OF BONE 3"	"disease"		"Disease or Syndrome"	"0.40"		"2002"	"2010"	"8"	"8"	"UNIPROT"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C4225326"	"FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2015"	"4"	"21"	"CTD_human;UNIPROT"
"8878"	"SQSTM1"	"0.49"	"0.828"	"C4310693"	"NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"CTD_human"
"8879"	"SGPL1"	"0.743"	"0.379"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"8879"	"SGPL1"	"0.743"	"0.379"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"8879"	"SGPL1"	"0.743"	"0.379"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"8879"	"SGPL1"	"0.743"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"8879"	"SGPL1"	"0.743"	"0.379"	"C4539778"	"NEPHROTIC SYNDROME 14"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2018"	"3"	"9"	"ORPHANET;UNIPROT"
"8880"	"FUBP1"	"0.72"	"0.207"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2013"	"2016"	"0"	"0"	"CGI"
"8886"	"DDX18"	"0.886"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"8887"	"TAX1BP1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8888"	"MCM3AP"	"0.696"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.39"	"0.8888889"	"2004"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.73"	"1"	"2002"	"2008"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"8890"	"EIF2B4"	"0.701"	"0.414"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"0.9411765"	"2001"	"2016"	"3"	"8"	"ORPHANET;UNIPROT"
"8891"	"EIF2B3"	"0.727"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8891"	"EIF2B3"	"0.727"	"0.31"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8891"	"EIF2B3"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8891"	"EIF2B3"	"0.727"	"0.31"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.60"		"2002"	"2011"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"8891"	"EIF2B3"	"0.727"	"0.31"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2002"	"2011"	"3"	"4"	"ORPHANET;UNIPROT"
"8892"	"EIF2B2"	"0.701"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8892"	"EIF2B2"	"0.701"	"0.345"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"	"0.9"	"2003"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"8892"	"EIF2B2"	"0.701"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8892"	"EIF2B2"	"0.701"	"0.345"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.73"	"1"	"2001"	"2014"	"6"	"10"	"CTD_human;ORPHANET;UNIPROT"
"8892"	"EIF2B2"	"0.701"	"0.345"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"1"	"2001"	"2017"	"6"	"9"	"ORPHANET;UNIPROT"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.90"		"2001"	"2016"	"6"	"24"	"CTD_human;ORPHANET;UNIPROT"
"8893"	"EIF2B5"	"0.707"	"0.448"	"C1858991"	"Childhood Ataxia with Central Nervous System Hypomyelinization"	"disease"	"C10"	"Disease or Syndrome"	"0.87"	"1"	"2001"	"2016"	"6"	"29"	"ORPHANET;UNIPROT"
"8894"	"EIF2S2"	"0.681"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8894"	"EIF2S2"	"0.681"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8894"	"EIF2S2"	"0.681"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8894"	"EIF2S2"	"0.681"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"8895"	"CPNE3"	"0.834"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8895"	"CPNE3"	"0.834"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8897"	"MTMR3"	"0.762"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"8898"	"MTMR2"	"0.685"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"1997"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"8898"	"MTMR2"	"0.685"	"0.345"	"C1832399"	"Charcot-Marie-Tooth disease, Type 4B1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.97"	"1"	"1993"	"2013"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8898"	"MTMR2"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8899"	"PRPF4B"	"0.743"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8900"	"CCNA1"	"0.598"	"0.621"	"C0343641"	"Human papilloma virus infection"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"8900"	"CCNA1"	"0.598"	"0.621"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"8900"	"CCNA1"	"0.598"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"8905"	"AP1S2"	"0.676"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8905"	"AP1S2"	"0.676"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8905"	"AP1S2"	"0.676"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"8905"	"AP1S2"	"0.676"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8905"	"AP1S2"	"0.676"	"0.414"	"C0796254"	"DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.81"	"1"	"1972"	"2015"	"3"	"7"	"CTD_human;ORPHANET"
"8905"	"AP1S2"	"0.676"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1991"	"2016"	"12"	"0"	"CLINGEN"
"8905"	"AP1S2"	"0.676"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"8905"	"AP1S2"	"0.676"	"0.414"	"C4305134"	"Fried syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8907"	"AP1M1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"8908"	"GYG2"	"1"	"0.103"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"8910"	"SGCE"	"0.633"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2013"	"2"	"0"	"PSYGENET"
"8910"	"SGCE"	"0.633"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8910"	"SGCE"	"0.633"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8910"	"SGCE"	"0.633"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2002"	"2"	"0"	"GENOMICS_ENGLAND"
"8910"	"SGCE"	"0.633"	"0.517"	"C1834570"	"Myoclonic dystonia"	"disease"	"C10"	"Disease or Syndrome"	"1.00"	"0.961039"	"1999"	"2018"	"9"	"10"	"CTD_human;ORPHANET;UNIPROT"
"8910"	"SGCE"	"0.633"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2017"	"0"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C1838604"	"EPILEPSY, CHILDHOOD ABSENCE, 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C2677793"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6"	"phenotype"		"Finding"	"0.30"		"2004"	"2004"	"2"	"12"	"UNIPROT"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C2749872"	"EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6"	"phenotype"		"Finding"	"0.40"		"2004"	"2004"	"2"	"12"	"UNIPROT"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C4310756"	"HYPERALDOSTERONISM, FAMILIAL, TYPE IV"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"8912"	"CACNA1H"	"0.735"	"0.103"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2018"	"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2007"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2018"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"8913"	"CACNA1G"	"0.627"	"0.379"	"C4225205"	"SPINOCEREBELLAR ATAXIA 42"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"2"	"1"	"ORPHANET;UNIPROT"
"8914"	"TIMELESS"	"0.614"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2007"	"2015"	"5"	"0"	"PSYGENET"
"8914"	"TIMELESS"	"0.614"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2018"	"1"	"1"	"UNIPROT"
"8914"	"TIMELESS"	"0.614"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"8914"	"TIMELESS"	"0.614"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"8914"	"TIMELESS"	"0.614"	"0.69"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"8915"	"BCL10"	"0.505"	"0.655"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.61"	"0"	"1999"	"2004"	"0"	"6"	"CGI;CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0039538"	"Teratoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C0242647"	"Mucosa-Associated Lymphoid Tissue Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.80"	"0.9444444"	"1999"	"2014"	"0"	"3"	"CGI;CTD_human;ORPHANET"
"8915"	"BCL10"	"0.505"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"		"1999"	"1999"	"0"	"1"	"CGI"
"8915"	"BCL10"	"0.505"	"0.655"	"C3496549"	"Male Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8915"	"BCL10"	"0.505"	"0.655"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"8915"	"BCL10"	"0.505"	"0.655"	"C4015195"	"IMMUNODEFICIENCY 37"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"8916"	"HERC3"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8916"	"HERC3"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8924"	"HERC2"	"0.6"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8924"	"HERC2"	"0.6"	"0.552"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"8924"	"HERC2"	"0.6"	"0.552"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8924"	"HERC2"	"0.6"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"8924"	"HERC2"	"0.6"	"0.552"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8924"	"HERC2"	"0.6"	"0.552"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"8924"	"HERC2"	"0.6"	"0.552"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8924"	"HERC2"	"0.6"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8924"	"HERC2"	"0.6"	"0.552"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8924"	"HERC2"	"0.6"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"8924"	"HERC2"	"0.6"	"0.552"	"C3809753"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8925"	"HERC1"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8925"	"HERC1"	"0.707"	"0.276"	"C4310766"	"MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"8927"	"BSN"	"0.799"	"0.172"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8928"	"FOXH1"	"0.69"	"0.379"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8928"	"FOXH1"	"0.69"	"0.379"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"8928"	"FOXH1"	"0.69"	"0.379"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8928"	"FOXH1"	"0.69"	"0.379"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8928"	"FOXH1"	"0.69"	"0.379"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8928"	"FOXH1"	"0.69"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"1998"	"1998"	"1"	"2"	"UNIPROT"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2008"	"2011"	"1"	"0"	"CTD_human"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.70"	"0.9534884"	"2004"	"2017"	"1"	"0"	"CGI;CTD_human;ORPHANET"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2004"	"2011"	"3"	"0"	"PSYGENET"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"1.00"	"0.9761905"	"2003"	"2017"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C1859049"	"CCHS WITH HIRSCHSPRUNG DISEASE"	"disease"	"C08;C10;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.80"		"2003"	"2008"	"4"	"0"	"CTD_human;ORPHANET;UNIPROT"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C2751683"	"Hirschsprung disease ganglioneuroblastoma"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"0"	"1"	"ORPHANET"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"8929"	"PHOX2B"	"0.611"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"8930"	"MBD4"	"0.672"	"0.448"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8932"	"MBD2"	"0.524"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"8932"	"MBD2"	"0.524"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1997"	"2015"	"1"	"0"	"PSYGENET"
"8932"	"MBD2"	"0.524"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"8935"	"SKAP2"	"0.713"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8936"	"WASF1"	"0.639"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"8936"	"WASF1"	"0.639"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"8940"	"TOP3B"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"8942"	"KYNU"	"0.707"	"0.448"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8942"	"KYNU"	"0.707"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8942"	"KYNU"	"0.707"	"0.448"	"C0268474"	"Hydroxykynureninuria"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2007"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8942"	"KYNU"	"0.707"	"0.448"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8942"	"KYNU"	"0.707"	"0.448"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8942"	"KYNU"	"0.707"	"0.448"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8942"	"KYNU"	"0.707"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8942"	"KYNU"	"0.707"	"0.448"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"8943"	"AP3D1"	"0.69"	"0.276"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"8943"	"AP3D1"	"0.69"	"0.276"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2016"	"0"	"0"	"CTD_human"
"8945"	"BTRC"	"0.642"	"0.552"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"8968"	"HIST1H3F"	"0.928"	"0.069"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"8970"	"HIST1H2BJ"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"8971"	"H1FX"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2012"	"2"	"0"	"PSYGENET"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8973"	"CHRNA6"	"0.743"	"0.241"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8974"	"P4HA2"	"0.743"	"0.379"	"C4310655"	"MYOPIA 25, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"8975"	"USP13"	"0.752"	"0.241"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8975"	"USP13"	"0.752"	"0.241"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8975"	"USP13"	"0.752"	"0.241"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8975"	"USP13"	"0.752"	"0.241"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8975"	"USP13"	"0.752"	"0.241"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8975"	"USP13"	"0.752"	"0.241"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8976"	"WASL"	"0.701"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8985"	"PLOD3"	"0.685"	"0.517"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"8985"	"PLOD3"	"0.685"	"0.517"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"8985"	"PLOD3"	"0.685"	"0.517"	"C2676285"	"Bone Fragility with Contractures, Arterial Rupture, and Deafness"	"disease"	"C05;C17;C23"	"Disease or Syndrome"	"0.70"		"2008"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"8985"	"PLOD3"	"0.685"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"8986"	"RPS6KA4"	"0.886"	"0.172"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"8988"	"HSPB3"	"0.489"	"0.724"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"8988"	"HSPB3"	"0.489"	"0.724"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"8988"	"HSPB3"	"0.489"	"0.724"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"8988"	"HSPB3"	"0.489"	"0.724"	"C3150619"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC"	"disease"		"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"8988"	"HSPB3"	"0.489"	"0.724"	"C3711384"	"Distal Hereditary Motor Neuropathy, Type II"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0010200"	"Coughing"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.50"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0037383"	"Sneezing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0268849"	"Overactive Detrusor"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2018"	"8"	"0"	"GENOMICS_ENGLAND"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"0"	"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2013"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C0878773"	"Overactive Bladder"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2008"	"2015"	"3"	"0"	"CTD_human"
"8989"	"TRPA1"	"0.639"	"0.621"	"C3808667"	"EPISODIC PAIN SYNDROME, FAMILIAL, 1"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2010"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2010"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0018520"	"Halitosis"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2010"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2005"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8991"	"SELENBP1"	"0.596"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8993"	"PGLYRP1"	"0.815"	"0.241"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8993"	"PGLYRP1"	"0.815"	"0.241"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8993"	"PGLYRP1"	"0.815"	"0.241"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8993"	"PGLYRP1"	"0.815"	"0.241"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"8996"	"NOL3"	"0.667"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8996"	"NOL3"	"0.667"	"0.552"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8996"	"NOL3"	"0.667"	"0.552"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8996"	"NOL3"	"0.667"	"0.552"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"8996"	"NOL3"	"0.667"	"0.552"	"C3539916"	"MYOCLONUS, FAMILIAL CORTICAL"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2012"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"8997"	"KALRN"	"0.72"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8997"	"KALRN"	"0.72"	"0.207"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"0"	"0"	"CTD_human"
"8997"	"KALRN"	"0.72"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8997"	"KALRN"	"0.72"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"8997"	"KALRN"	"0.72"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"8999"	"CDKL2"	"0.815"	"0.172"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8999"	"CDKL2"	"0.815"	"0.172"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8999"	"CDKL2"	"0.815"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8999"	"CDKL2"	"0.815"	"0.172"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"8999"	"CDKL2"	"0.815"	"0.172"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"9002"	"F2RL3"	"0.573"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C0030781"	"Peliosis Hepatis"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9002"	"F2RL3"	"0.573"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9013"	"TAF1C"	"1"	"0.069"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2013"	"1"	"1"	"CTD_human"
"9015"	"TAF1A"	"1"	"0.034"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9019"	"MPZL1"	"0.785"	"0.276"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9020"	"MAP3K14"	"0.648"	"0.552"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9021"	"SOCS3"	"0.487"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"9025"	"RNF8"	"0.815"	"0.241"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9026"	"HIP1R"	"0.735"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"2"	"0"	"PSYGENET"
"9027"	"NAT8"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9030"	"ERDA1"	"0.773"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.4"	"1999"	"2005"	"5"	"0"	"PSYGENET"
"9030"	"ERDA1"	"0.773"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"0.6666667"	"1999"	"2003"	"1"	"0"	"PSYGENET"
"9030"	"ERDA1"	"0.773"	"0.069"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1998"	"1998"	"1"	"0"	"PSYGENET"
"9031"	"BAZ1B"	"0.609"	"0.552"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.78"	"1"	"1999"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2006"	"1"	"0"	"CTD_human"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9034"	"CCRL2"	"0.696"	"0.414"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9037"	"SEMA5A"	"0.685"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9037"	"SEMA5A"	"0.685"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"9037"	"SEMA5A"	"0.685"	"0.345"	"C0010314"	"Cri-du-Chat Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"9037"	"SEMA5A"	"0.685"	"0.345"	"C2931860"	"Monosomy 5p"	"disease"	"C10;C16"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"9045"	"RPL14"	"0.72"	"0.276"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9045"	"RPL14"	"0.72"	"0.276"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9046"	"DOK2"	"0.72"	"0.241"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9046"	"DOK2"	"0.72"	"0.241"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9048"	"ARTN"	"0.592"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9048"	"ARTN"	"0.592"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2013"	"5"	"0"	"PSYGENET"
"9048"	"ARTN"	"0.592"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2013"	"5"	"0"	"PSYGENET"
"9048"	"ARTN"	"0.592"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"9048"	"ARTN"	"0.592"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"9048"	"ARTN"	"0.592"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9048"	"ARTN"	"0.592"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2015"	"4"	"0"	"PSYGENET"
"9048"	"ARTN"	"0.592"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0001206"	"Acromegaly"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"9049"	"AIP"	"0.545"	"0.621"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.65"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"9049"	"AIP"	"0.545"	"0.621"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0338078"	"Non-Functioning Pituitary Gland Neoplasm"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9049"	"AIP"	"0.545"	"0.621"	"C0344452"	"Microprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0344453"	"Macroprolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0346302"	"Growth Hormone-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.46"	"1"	"1965"	"2017"	"0"	"46"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9049"	"AIP"	"0.545"	"0.621"	"C1306214"	"ACTH-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"0"	"0"	"CTD_human"
"9049"	"AIP"	"0.545"	"0.621"	"C1863340"	"PITUITARY ADENOMA PREDISPOSITION (disorder)"	"phenotype"	"C04;C10;C19"	"Finding"	"0.70"	"1"	"2006"	"2015"	"6"	"2"	"ORPHANET;UNIPROT"
"9049"	"AIP"	"0.545"	"0.621"	"C2676191"	"PITUITARY ADENOMA, FAMILIAL ISOLATED (disorder)"	"disease"		"Neoplastic Process"	"0.50"	"0.9"	"2006"	"2017"	"6"	"1"	"UNIPROT"
"9049"	"AIP"	"0.545"	"0.621"	"C3489630"	"Somatotrophinoma, Familial"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.54"	"1"	"2006"	"2010"	"6"	"0"	"CTD_human;UNIPROT"
"9049"	"AIP"	"0.545"	"0.621"	"C4521132"	"ACROMEGALY DUE TO PITUITARY ADENOMA 1"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2009"	"6"	"0"	"UNIPROT"
"9049"	"AIP"	"0.545"	"0.621"	"C4538355"	"PITUITARY ADENOMA 1, MULTIPLE TYPES"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2009"	"6"	"0"	"UNIPROT"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C1858361"	"Pyogenic Arthritis, Pyoderma Gangrenosum and Acne"	"disease"	"C01;C05;C17"	"Disease or Syndrome"	"0.80"	"0.9166667"	"2003"	"2016"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C1860229"	"Hyperzincemia and Hypercalprotectinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9051"	"PSTPIP1"	"0.681"	"0.483"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"1975"	"1993"	"2"	"0"	"GENOMICS_ENGLAND"
"9052"	"GPRC5A"	"0.609"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9054"	"NFS1"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9055"	"PRC1"	"0.72"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"9055"	"PRC1"	"0.72"	"0.345"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9055"	"PRC1"	"0.72"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.44"	"1"	"2007"	"2018"	"1"	"4"	"CTD_human"
"9055"	"PRC1"	"0.72"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9055"	"PRC1"	"0.72"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2015"	"1"	"0"	"CTD_human"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C0268647"	"Lysinuric Protein Intolerance"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1981"	"2018"	"7"	"44"	"CTD_human;ORPHANET;UNIPROT"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9056"	"SLC7A7"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9060"	"PAPSS2"	"0.72"	"0.345"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9060"	"PAPSS2"	"0.72"	"0.345"	"C0432228"	"Brachyolmia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2014"	"0"	"1"	"ORPHANET"
"9060"	"PAPSS2"	"0.72"	"0.345"	"C2748515"	"Spondyloepimetaphyseal Dysplasia, Pakistani Type"	"disease"	"C05;C16;C23"	"Congenital Abnormality"	"0.92"	"1"	"1968"	"2016"	"5"	"11"	"CTD_human;ORPHANET;UNIPROT"
"9060"	"PAPSS2"	"0.72"	"0.345"	"C2748516"	"Spondylodysplasia And Premature Pubarche"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"		"1968"	"2016"	"5"	"2"	"UNIPROT"
"9060"	"PAPSS2"	"0.72"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"9064"	"MAP3K6"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9064"	"MAP3K6"	"0.815"	"0.241"	"C0346163"	"Endometrioid carcinoma ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9064"	"MAP3K6"	"0.815"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9071"	"CLDN10"	"0.857"	"0.172"	"C4522164"	"HELIX SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2018"	"2"	"2"	"UNIPROT"
"9075"	"CLDN2"	"0.642"	"0.276"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2013"	"1"	"3"	"CTD_human;GENOMICS_ENGLAND"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2000"	"2017"	"2"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2000"	"2017"	"2"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2000"	"2013"	"2"	"0"	"CTD_human"
"9076"	"CLDN1"	"0.541"	"0.69"	"C1843355"	"ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS"	"disease"	"C06;C15;C16;C17;C23"	"Disease or Syndrome"	"0.64"	"1"	"2002"	"2012"	"0"	"2"	"CTD_human;ORPHANET"
"9080"	"CLDN9"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9080"	"CLDN9"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9081"	"PRY"	"0.857"	"0.103"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9082"	"XKRY"	"0.928"	"0.069"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9083"	"BPY2"	"0.773"	"0.172"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9084"	"VCY"	"0.886"	"0.207"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9085"	"CDY1"	"0.857"	"0.207"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9088"	"PKMYT1"	"0.773"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9091"	"PIGQ"	"0.834"	"0.172"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"9091"	"PIGQ"	"0.834"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9091"	"PIGQ"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"9094"	"UNC119"	"0.727"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.53"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"9094"	"UNC119"	"0.727"	"0.31"	"C0206744"	"T-Lymphocytopenia, Idiopathic CD4-Positive"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9094"	"UNC119"	"0.727"	"0.31"	"C3809768"	"IMMUNODEFICIENCY 13"	"disease"		"Disease or Syndrome"	"0.52"	"1"	"2012"	"2013"	"1"	"1"	"ORPHANET;UNIPROT"
"9095"	"TBX19"	"0.72"	"0.345"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9095"	"TBX19"	"0.72"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9095"	"TBX19"	"0.72"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9095"	"TBX19"	"0.72"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9095"	"TBX19"	"0.72"	"0.345"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9095"	"TBX19"	"0.72"	"0.345"	"C0271583"	"ACTH Deficiency, Isolated"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.81"	"1"	"2001"	"2012"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9095"	"TBX19"	"0.72"	"0.345"	"C0342388"	"Adrenocorticotropic hormone (ACTH) deficiency (disorder)"	"disease"	"C19"	"Disease or Syndrome"	"0.82"	"0"	"1988"	"2012"	"1"	"5"	"ORPHANET;UNIPROT"
"9095"	"TBX19"	"0.72"	"0.345"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"9096"	"TBX18"	"0.696"	"0.241"	"C0266316"	"Congenital hydronephrosis"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9096"	"TBX18"	"0.696"	"0.241"	"C0521619"	"Obstruction of pelviureteric junction"	"phenotype"	"C12;C13;C16"	"Pathologic Function"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"9096"	"TBX18"	"0.696"	"0.241"	"C1840451"	"MULTICYSTIC RENAL DYSPLASIA, BILATERAL"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"9096"	"TBX18"	"0.696"	"0.241"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9096"	"TBX18"	"0.696"	"0.241"	"C4048262"	"Hydronephrosis Due To Pujo"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"9098"	"USP6"	"0.72"	"0.31"	"C0410005"	"Nodular fasciitis"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2011"	"2018"	"0"	"0"	"ORPHANET"
"9099"	"USP2"	"0.773"	"0.207"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9101"	"USP8"	"0.652"	"0.552"	"C0010481"	"Cushing Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9101"	"USP8"	"0.652"	"0.552"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9101"	"USP8"	"0.652"	"0.552"	"C0221406"	"Pituitary-dependent Cushing's disease"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.80"	"1"	"2015"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9101"	"USP8"	"0.652"	"0.552"	"C0751220"	"Inappropriate ACTH Secretion Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9101"	"USP8"	"0.652"	"0.552"	"C1306214"	"ACTH-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.36"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"9103"	"FCGR2C"	"0.602"	"0.655"	"C0398650"	"Immune thrombocytopenic purpura"	"disease"	"C15;C20;C23"	"Disease or Syndrome"	"0.52"	"1"	"2008"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"9104"	"RGN"	"0.642"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9104"	"RGN"	"0.642"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9104"	"RGN"	"0.642"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9108"	"MTMR7"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9110"	"MTMR4"	"1"	"0.069"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9111"	"NMI"	"0.752"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9112"	"MTA1"	"0.579"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9112"	"MTA1"	"0.579"	"0.655"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"9112"	"MTA1"	"0.579"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0027660"	"Neoplasms, Glandular and Epithelial"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9113"	"LATS1"	"0.602"	"0.379"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0205854"	"Glandular Neoplasms"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9113"	"LATS1"	"0.602"	"0.379"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C1368683"	"Epithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9113"	"LATS1"	"0.602"	"0.379"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9118"	"INA"	"0.681"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9118"	"INA"	"0.681"	"0.414"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9118"	"INA"	"0.681"	"0.414"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9118"	"INA"	"0.681"	"0.414"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9118"	"INA"	"0.681"	"0.414"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9118"	"INA"	"0.681"	"0.414"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9119"	"KRT75"	"0.886"	"0.103"	"C0406468"	"Loose Anagen Hair Syndrome"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"1"	"UNIPROT"
"9119"	"KRT75"	"0.886"	"0.103"	"C0549150"	"Pseudofolliculitis barbae (disorder)"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"9120"	"SLC16A6"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9120"	"SLC16A6"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9126"	"SMC3"	"0.572"	"0.759"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9126"	"SMC3"	"0.572"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9126"	"SMC3"	"0.572"	"0.759"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"9126"	"SMC3"	"0.572"	"0.759"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"9126"	"SMC3"	"0.572"	"0.759"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C1802395"	"Congenital muscular hypertrophy-cerebral syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C1853099"	"Cornelia de Lange Syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2017"	"0"	"16"	"CTD_human"
"9126"	"SMC3"	"0.572"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"9126"	"SMC3"	"0.572"	"0.759"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9128"	"PRPF4"	"0.663"	"0.448"	"C4014681"	"RETINITIS PIGMENTOSA 70"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"9128"	"PRPF4"	"0.663"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9129"	"PRPF3"	"0.69"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2010"	"0"	"0"	"ORPHANET"
"9129"	"PRPF3"	"0.69"	"0.379"	"C1832378"	"Retinitis Pigmentosa 18"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.83"	"1"	"2002"	"2014"	"3"	"3"	"CTD_human;UNIPROT"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"GENOMICS_ENGLAND"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2001"	"2008"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0795910"	"COWCHOCK SYNDROME"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"1985"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9131"	"AIFM1"	"0.558"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C1845095"	"DEAFNESS, X-LINKED 5 (disorder)"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.70"		"2006"	"2016"	"1"	"16"	"CTD_human;ORPHANET;UNIPROT"
"9131"	"AIFM1"	"0.558"	"0.655"	"C1846148"	"Sketetal dysplasia coarse facies mental retardation"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9131"	"AIFM1"	"0.558"	"0.655"	"C3151753"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2017"	"2"	"2"	"ORPHANET;UNIPROT"
"9131"	"AIFM1"	"0.558"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9131"	"AIFM1"	"0.558"	"0.655"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9131"	"AIFM1"	"0.558"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9132"	"KCNQ4"	"0.701"	"0.31"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9132"	"KCNQ4"	"0.701"	"0.31"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9132"	"KCNQ4"	"0.701"	"0.31"	"C2677637"	"Deafness, Autosomal Dominant 2A"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"4"	"21"	"CTD_human;UNIPROT"
"9132"	"KCNQ4"	"0.701"	"0.31"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9133"	"CCNB2"	"0.72"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9134"	"CCNE2"	"0.659"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9134"	"CCNE2"	"0.659"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9134"	"CCNE2"	"0.659"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9134"	"CCNE2"	"0.659"	"0.345"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9134"	"CCNE2"	"0.659"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9136"	"RRP9"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9136"	"RRP9"	"0.886"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9136"	"RRP9"	"0.886"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9136"	"RRP9"	"0.886"	"0.103"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9136"	"RRP9"	"0.886"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9138"	"ARHGEF1"	"0.696"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2004"	"2010"	"5"	"0"	"PSYGENET"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9145"	"SYNGR1"	"0.743"	"0.241"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9147"	"NEMF"	"0.799"	"0.138"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9148"	"NEURL1"	"0.579"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"9148"	"NEURL1"	"0.579"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9148"	"NEURL1"	"0.579"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"9149"	"DYRK1B"	"0.667"	"0.31"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9149"	"DYRK1B"	"0.667"	"0.31"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9149"	"DYRK1B"	"0.667"	"0.31"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"9149"	"DYRK1B"	"0.667"	"0.31"	"C4014361"	"ABDOMINAL OBESITY-METABOLIC SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"9150"	"CTDP1"	"0.627"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9150"	"CTDP1"	"0.627"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"9150"	"CTDP1"	"0.627"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"		"2003"	"2003"	"0"	"0"	"GENOMICS_ENGLAND"
"9150"	"CTDP1"	"0.627"	"0.517"	"C1858726"	"Congenital Cataracts, Facial Dysmorphism, And Neuropathy"	"disease"	"C05;C10;C11;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"1993"	"2004"	"0"	"1"	"CTD_human;ORPHANET"
"9150"	"CTDP1"	"0.627"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0003578"	"Apnea"	"phenotype"	"C08;C23"	"Sign or Symptom"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C1835614"	"Hereditary Hyperexplexia"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C3553288"	"HYPEREKPLEXIA 3"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2006"	"1"	"10"	"UNIPROT"
"9152"	"SLC6A5"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9154"	"SLC28A1"	"0.707"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"9154"	"SLC28A1"	"0.707"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"9154"	"SLC28A1"	"0.707"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9154"	"SLC28A1"	"0.707"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"0"	"2004"	"2008"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.31"		"2000"	"2014"	"6"	"0"	"CLINGEN"
"9156"	"EXO1"	"0.672"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2018"	"1"	"1"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2000"	"2014"	"6"	"0"	"CLINGEN"
"9156"	"EXO1"	"0.672"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2017"	"6"	"0"	"CLINGEN"
"9156"	"EXO1"	"0.672"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"9156"	"EXO1"	"0.672"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"9158"	"FIBP"	"0.685"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9158"	"FIBP"	"0.685"	"0.414"	"C4310715"	"THAUVIN-ROBINET-FAIVRE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"9168"	"TMSB10"	"0.681"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9168"	"TMSB10"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9168"	"TMSB10"	"0.681"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9168"	"TMSB10"	"0.681"	"0.483"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9173"	"IL1RL1"	"0.616"	"0.586"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9173"	"IL1RL1"	"0.616"	"0.586"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.50"	"0.95"	"2008"	"2018"	"5"	"10"	"CTD_human"
"9173"	"IL1RL1"	"0.616"	"0.586"	"C0242488"	"Acute Lung Injury"	"disease"	"C08"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9173"	"IL1RL1"	"0.616"	"0.586"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9173"	"IL1RL1"	"0.616"	"0.586"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9175"	"MAP3K13"	"0.743"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9175"	"MAP3K13"	"0.743"	"0.172"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9175"	"MAP3K13"	"0.743"	"0.172"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9175"	"MAP3K13"	"0.743"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9175"	"MAP3K13"	"0.743"	"0.172"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2013"	"4"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"2"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2011"	"1"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2008"	"2"	"0"	"PSYGENET"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9177"	"HTR3B"	"0.696"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2008"	"2"	"0"	"PSYGENET"
"9179"	"AP4M1"	"0.663"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9179"	"AP4M1"	"0.663"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9179"	"AP4M1"	"0.663"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9179"	"AP4M1"	"0.663"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9179"	"AP4M1"	"0.663"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9179"	"AP4M1"	"0.663"	"0.31"	"C2752008"	"Spastic Paraplegia-50, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2015"	"0"	"6"	"CTD_human"
"9179"	"AP4M1"	"0.663"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9180"	"OSMR"	"0.648"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9180"	"OSMR"	"0.648"	"0.448"	"C0268398"	"Familial lichen amyloidosis"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.71"	"1"	"2008"	"2010"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"9180"	"OSMR"	"0.648"	"0.448"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9180"	"OSMR"	"0.648"	"0.448"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"9181"	"ARHGEF2"	"0.59"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2016"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9183"	"ZW10"	"1"	"0.034"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9184"	"BUB3"	"0.676"	"0.414"	"C1850343"	"MOSAIC VARIEGATED ANEUPLOIDY SYNDROME"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9184"	"BUB3"	"0.676"	"0.414"	"C2931286"	"Warburton Anyane Yeboa syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9185"	"REPS2"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"9185"	"REPS2"	"0.815"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"9185"	"REPS2"	"0.815"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9185"	"REPS2"	"0.815"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9187"	"SLC24A1"	"0.713"	"0.172"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9189"	"ZBED1"	"0.735"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"9189"	"ZBED1"	"0.735"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"9194"	"SLC16A7"	"0.735"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C2675528"	"Spastic Paraplegia 42, Autosomal Dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2009"	"2015"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C3280965"	"CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION"	"disease"		"Disease or Syndrome"	"0.70"		"2005"	"2012"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9197"	"SLC33A1"	"0.551"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"9200"	"HACD1"	"0.648"	"0.655"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9200"	"HACD1"	"0.648"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9200"	"HACD1"	"0.648"	"0.655"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9200"	"HACD1"	"0.648"	"0.655"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9201"	"DCLK1"	"0.607"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9201"	"DCLK1"	"0.607"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"9201"	"DCLK1"	"0.607"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9201"	"DCLK1"	"0.607"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9201"	"DCLK1"	"0.607"	"0.379"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9201"	"DCLK1"	"0.607"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"9202"	"ZMYM4"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9203"	"ZMYM3"	"0.815"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2018"	"3"	"0"	"CTD_human"
"9203"	"ZMYM3"	"0.815"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2018"	"3"	"0"	"CTD_human"
"9203"	"ZMYM3"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1997"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"9204"	"ZMYM6"	"1"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9205"	"ZMYM5"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9205"	"ZMYM5"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9208"	"LRRFIP1"	"0.743"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9208"	"LRRFIP1"	"0.743"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9210"	"BMP15"	"0.645"	"0.345"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9"	"2000"	"2018"	"1"	"0"	"CTD_human"
"9210"	"BMP15"	"0.645"	"0.345"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9210"	"BMP15"	"0.645"	"0.345"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2008"	"0"	"0"	"ORPHANET"
"9210"	"BMP15"	"0.645"	"0.345"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9210"	"BMP15"	"0.645"	"0.345"	"C1845294"	"Ovarian Dysgenesis 2"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"2004"	"2010"	"6"	"11"	"CTD_human;UNIPROT"
"9210"	"BMP15"	"0.645"	"0.345"	"C1845295"	"Premature Ovarian Failure 4"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"2004"	"2010"	"6"	"12"	"CTD_human;UNIPROT"
"9210"	"BMP15"	"0.645"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9211"	"LGI1"	"0.633"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9211"	"LGI1"	"0.633"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9211"	"LGI1"	"0.633"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9211"	"LGI1"	"0.633"	"0.379"	"C1838062"	"EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"1.00"	"0.9090909"	"1993"	"2018"	"10"	"13"	"CTD_human;ORPHANET;UNIPROT"
"9211"	"LGI1"	"0.633"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9212"	"AURKB"	"0.557"	"0.552"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9212"	"AURKB"	"0.557"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"9212"	"AURKB"	"0.557"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9212"	"AURKB"	"0.557"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0393590"	"Fahr's syndrome (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9213"	"XPR1"	"0.551"	"0.69"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9213"	"XPR1"	"0.551"	"0.69"	"C4225335"	"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6"	"disease"		"Disease or Syndrome"	"0.60"		"1977"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"9214"	"FCMR"	"0.773"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9214"	"FCMR"	"0.773"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9214"	"FCMR"	"0.773"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9214"	"FCMR"	"0.773"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9214"	"FCMR"	"0.773"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9214"	"FCMR"	"0.773"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2004"	"2009"	"3"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"2004"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C1837229"	"Muscular Dystrophy, Congenital, Type 1D"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.80"		"2004"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"9215"	"LARGE1"	"0.53"	"0.621"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9215"	"LARGE1"	"0.53"	"0.621"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9215"	"LARGE1"	"0.53"	"0.621"	"C3150414"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2015"	"3"	"3"	"UNIPROT"
"9215"	"LARGE1"	"0.53"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2004"	"2011"	"5"	"0"	"GENOMICS_ENGLAND"
"9217"	"VAPB"	"0.672"	"0.414"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.9583333"	"2005"	"2017"	"0"	"0"	"ORPHANET"
"9217"	"VAPB"	"0.672"	"0.414"	"C1837728"	"AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.62"	"0.5"	"2005"	"2015"	"4"	"2"	"CTD_human;UNIPROT"
"9217"	"VAPB"	"0.672"	"0.414"	"C1854058"	"SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2005"	"2012"	"1"	"1"	"ORPHANET;UNIPROT"
"9217"	"VAPB"	"0.672"	"0.414"	"C1866777"	"Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant"	"disease"	"C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"9218"	"VAPA"	"0.799"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"9219"	"MTA2"	"0.659"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9219"	"MTA2"	"0.659"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9223"	"MAGI1"	"0.69"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"9223"	"MAGI1"	"0.69"	"0.448"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9223"	"MAGI1"	"0.69"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9223"	"MAGI1"	"0.69"	"0.448"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9227"	"LRAT"	"0.602"	"0.621"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"				"0"	"1"	"CTD_human;ORPHANET"
"9227"	"LRAT"	"0.602"	"0.621"	"C0042842"	"Vitamin A Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.55"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"9227"	"LRAT"	"0.602"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C0917796"	"Optic Atrophy, Hereditary, Leber"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2008"	"0"	"0"	"ORPHANET"
"9227"	"LRAT"	"0.602"	"0.621"	"C2750063"	"Leber Congenital Amaurosis 14"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"2001"	"2011"	"3"	"1"	"CTD_human;UNIPROT"
"9227"	"LRAT"	"0.602"	"0.621"	"C2750064"	"Retinal Dystrophy, Early-Onset Severe, Lrat-Related"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"		"2001"	"2011"	"3"	"1"	"CTD_human;UNIPROT"
"9227"	"LRAT"	"0.602"	"0.621"	"C2750065"	"RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"		"2001"	"2011"	"3"	"1"	"CTD_human;UNIPROT"
"9227"	"LRAT"	"0.602"	"0.621"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9227"	"LRAT"	"0.602"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9227"	"LRAT"	"0.602"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9228"	"DLGAP2"	"0.857"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9228"	"DLGAP2"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9228"	"DLGAP2"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9229"	"DLGAP1"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.3333333"	"2003"	"2013"	"3"	"0"	"PSYGENET"
"9229"	"DLGAP1"	"0.815"	"0.172"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9230"	"RAB11B"	"0.834"	"0.276"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9230"	"RAB11B"	"0.834"	"0.276"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9230"	"RAB11B"	"0.834"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9230"	"RAB11B"	"0.834"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9230"	"RAB11B"	"0.834"	"0.276"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9232"	"PTTG1"	"0.562"	"0.552"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9232"	"PTTG1"	"0.562"	"0.552"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"9232"	"PTTG1"	"0.562"	"0.552"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9232"	"PTTG1"	"0.562"	"0.552"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9235"	"IL32"	"0.537"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9241"	"NOG"	"0.558"	"0.621"	"C0175700"	"Multiple synostosis syndrome"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"9241"	"NOG"	"0.558"	"0.621"	"C0342282"	"Multiple synostoses syndrome 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.75"	"1"	"1987"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9241"	"NOG"	"0.558"	"0.621"	"C1861305"	"TARSAL-CARPAL COALITION SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.77"	"1"	"1985"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9241"	"NOG"	"0.558"	"0.621"	"C1861306"	"Synostosis of Talus and Calcaneus with Short Stature"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"3"	"UNIPROT"
"9241"	"NOG"	"0.558"	"0.621"	"C1861385"	"SYMPHALANGISM, PROXIMAL"	"disease"	"C05"	"Disease or Syndrome"	"0.70"	"1"	"1916"	"2016"	"0"	"8"	"CTD_human;ORPHANET"
"9241"	"NOG"	"0.558"	"0.621"	"C1866656"	"STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"1998"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"9241"	"NOG"	"0.558"	"0.621"	"C1969652"	"BRACHYDACTYLY, TYPE B2 (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.72"	"1"	"1998"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9241"	"NOG"	"0.558"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9241"	"NOG"	"0.558"	"0.621"	"C3714899"	"SYMPHALANGISM, PROXIMAL, 1A"	"disease"		"Disease or Syndrome"	"0.39"	"1"	"2001"	"2016"	"3"	"8"	"UNIPROT"
"9244"	"CRLF1"	"0.652"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"9244"	"CRLF1"	"0.652"	"0.414"	"C0014848"	"Esophageal Achalasia"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"9244"	"CRLF1"	"0.652"	"0.414"	"C0859976"	"Idiopathic achalasia of esophagus"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9244"	"CRLF1"	"0.652"	"0.414"	"C1832409"	"Crisponi syndrome"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.70"	"1"	"2003"	"2015"	"7"	"9"	"CTD_human;ORPHANET;UNIPROT"
"9244"	"CRLF1"	"0.652"	"0.414"	"C1848947"	"COLD-INDUCED SWEATING SYNDROME 1"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2015"	"7"	"19"	"CTD_human;ORPHANET;UNIPROT"
"9244"	"CRLF1"	"0.652"	"0.414"	"C1853198"	"COLD-INDUCED SWEATING SYNDROME 2"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9246"	"UBE2L6"	"0.773"	"0.276"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9247"	"GCM2"	"0.645"	"0.379"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9247"	"GCM2"	"0.645"	"0.379"	"C0342344"	"Hypoparathyroidism - X-linked"	"disease"	"C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9247"	"GCM2"	"0.645"	"0.379"	"C0342345"	"Hypoparathyroidism - autosomal dominant"	"disease"	"C18;C19;C23"	"Disease or Syndrome"	"0.34"	"0.5"	"2005"	"2015"	"5"	"4"	"UNIPROT"
"9247"	"GCM2"	"0.645"	"0.379"	"C1321907"	"Congenital absence of parathyroid gland"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"9247"	"GCM2"	"0.645"	"0.379"	"C1832648"	"Hypoparathyroidism familial isolated"	"disease"	"C19"	"Disease or Syndrome"	"0.61"	"0"	"2005"	"2017"	"5"	"5"	"CTD_human;UNIPROT"
"9247"	"GCM2"	"0.645"	"0.379"	"C1840334"	"Hypoparathyroidism, Autosomal Recessive"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2017"	"5"	"4"	"UNIPROT"
"9247"	"GCM2"	"0.645"	"0.379"	"C1840402"	"HYPERPARATHYROIDISM 1"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"9247"	"GCM2"	"0.645"	"0.379"	"C4479229"	"HYPERPARATHYROIDISM 4"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"9248"	"GPR50"	"0.799"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2010"	"5"	"0"	"PSYGENET"
"9248"	"GPR50"	"0.799"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"9248"	"GPR50"	"0.799"	"0.103"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9248"	"GPR50"	"0.799"	"0.103"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2012"	"4"	"0"	"PSYGENET"
"9248"	"GPR50"	"0.799"	"0.103"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9249"	"DHRS3"	"0.785"	"0.379"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9249"	"DHRS3"	"0.785"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9252"	"RPS6KA5"	"0.743"	"0.345"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9252"	"RPS6KA5"	"0.743"	"0.345"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9252"	"RPS6KA5"	"0.743"	"0.345"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9253"	"NUMBL"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0008489"	"Chorea"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0152113"	"Rheumatic Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0238056"	"Chorea, Senile"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0393584"	"Benign Hereditary Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0699728"	"Chronic progressive chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0699731"	"Hereditary Chorea"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0752210"	"Dyskinesias, Paroxysmal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9254"	"CACNA2D2"	"0.645"	"0.414"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9255"	"AIMP1"	"0.611"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9255"	"AIMP1"	"0.611"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9255"	"AIMP1"	"0.611"	"0.552"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"9255"	"AIMP1"	"0.611"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9255"	"AIMP1"	"0.611"	"0.552"	"C1850053"	"Pelizaeus-Merzbacher-like disease, autosomal recessive, 2"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.60"		"2011"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"9255"	"AIMP1"	"0.611"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9260"	"PDLIM7"	"0.521"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2015"	"0"	"0"	"UNIPROT"
"9270"	"ITGB1BP1"	"0.928"	"0.138"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9270"	"ITGB1BP1"	"0.928"	"0.138"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9271"	"PIWIL1"	"0.624"	"0.345"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9274"	"BCL7C"	"0.815"	"0.103"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9274"	"BCL7C"	"0.815"	"0.103"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9274"	"BCL7C"	"0.815"	"0.103"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9274"	"BCL7C"	"0.815"	"0.103"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9274"	"BCL7C"	"0.815"	"0.103"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9276"	"COPB2"	"0.815"	"0.31"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9277"	"WDR46"	"0.886"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9277"	"WDR46"	"0.886"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9277"	"WDR46"	"0.886"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9277"	"WDR46"	"0.886"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9282"	"MED14"	"0.834"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"UNIPROT"
"9282"	"MED14"	"0.834"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9282"	"MED14"	"0.834"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"2004"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C1845668"	"Perisylvian syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C1847352"	"POLYMICROGYRIA, BILATERAL FRONTOPARIETAL"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"0.9545455"	"2004"	"2017"	"6"	"23"	"CTD_human;ORPHANET;UNIPROT"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"9289"	"ADGRG1"	"0.667"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9290"	"GPR55"	"0.713"	"0.379"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9290"	"GPR55"	"0.713"	"0.379"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9290"	"GPR55"	"0.713"	"0.379"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9293"	"GPR52"	"0.928"	"0.103"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9293"	"GPR52"	"0.928"	"0.103"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9294"	"S1PR2"	"0.672"	"0.552"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9294"	"S1PR2"	"0.672"	"0.552"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9294"	"S1PR2"	"0.672"	"0.552"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9294"	"S1PR2"	"0.672"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9294"	"S1PR2"	"0.672"	"0.552"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9294"	"S1PR2"	"0.672"	"0.552"	"C1835854"	"DEAFNESS, AUTOSOMAL RECESSIVE 68"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"2006"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"9294"	"S1PR2"	"0.672"	"0.552"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"6"	"0"	"CLINGEN"
"9304"	"SNORD22"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"0.5"	"2003"	"2018"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"1992"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9308"	"CD83"	"0.584"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9311"	"ASIC3"	"0.799"	"0.207"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9312"	"KCNB2"	"0.857"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9313"	"MMP20"	"0.713"	"0.276"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.70"	"1"	"2002"	"2017"	"10"	"0"	"GENOMICS_ENGLAND"
"9313"	"MMP20"	"0.713"	"0.276"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9313"	"MMP20"	"0.713"	"0.276"	"C2675858"	"Amelogenesis Imperfecta, Hypomaturation Type, Iia2"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2013"	"0"	"4"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"9314"	"KLF4"	"0.498"	"0.655"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9314"	"KLF4"	"0.498"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9315"	"NREP"	"0.707"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9317"	"PTER"	"0.773"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9317"	"PTER"	"0.773"	"0.241"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9317"	"PTER"	"0.773"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9317"	"PTER"	"0.773"	"0.241"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9318"	"COPS2"	"0.799"	"0.207"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9318"	"COPS2"	"0.799"	"0.207"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0002938"	"Aneuploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.61"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C1850343"	"MOSAIC VARIEGATED ANEUPLOIDY SYNDROME"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"9319"	"TRIP13"	"0.639"	"0.552"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C2931286"	"Warburton Anyane Yeboa syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9319"	"TRIP13"	"0.639"	"0.552"	"C2931383"	"Chromosomal mosaicism due to mitotic instability"	"disease"	"C16"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9319"	"TRIP13"	"0.639"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9320"	"TRIP12"	"0.928"	"0.069"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9320"	"TRIP12"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"9321"	"TRIP11"	"0.72"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9321"	"TRIP11"	"0.72"	"0.414"	"C0265273"	"Achondrogenesis type 1A"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.80"		"2010"	"2015"	"0"	"4"	"CTD_human;ORPHANET"
"9321"	"TRIP11"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9325"	"TRIP4"	"0.701"	"0.345"	"C4225177"	"SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"9325"	"TRIP4"	"0.701"	"0.345"	"C4310736"	"MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"9326"	"ZNHIT3"	"0.676"	"0.345"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9326"	"ZNHIT3"	"0.676"	"0.345"	"C0796122"	"Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9326"	"ZNHIT3"	"0.676"	"0.345"	"C1850055"	"PEHO syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.71"	"1"	"2017"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9326"	"ZNHIT3"	"0.676"	"0.345"	"C1850056"	"PEHO-Like Syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9330"	"GTF3C3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9332"	"CD163"	"0.52"	"0.793"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9332"	"CD163"	"0.52"	"0.793"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9332"	"CD163"	"0.52"	"0.793"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9333"	"TGM5"	"0.727"	"0.276"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2006"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"9333"	"TGM5"	"0.727"	"0.276"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2006"	"2016"	"0"	"1"	"GENOMICS_ENGLAND"
"9333"	"TGM5"	"0.727"	"0.276"	"C1853354"	"Peeling skin syndrome, acral type"	"disease"	"C17"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"9334"	"B4GALT5"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9334"	"B4GALT5"	"0.815"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9334"	"B4GALT5"	"0.815"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9334"	"B4GALT5"	"0.815"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9342"	"SNAP29"	"0.663"	"0.517"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"9342"	"SNAP29"	"0.663"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9342"	"SNAP29"	"0.663"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"9342"	"SNAP29"	"0.663"	"0.517"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"9342"	"SNAP29"	"0.663"	"0.517"	"C1836033"	"Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome"	"disease"	"C10;C16;C17"	"Disease or Syndrome"	"0.81"	"1"	"2011"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"9342"	"SNAP29"	"0.663"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9343"	"EFTUD2"	"0.672"	"0.379"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.41"	"1"	"2012"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"9343"	"EFTUD2"	"0.672"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9343"	"EFTUD2"	"0.672"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"9343"	"EFTUD2"	"0.672"	"0.379"	"C1864652"	"Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.77"	"1"	"2006"	"2018"	"1"	"13"	"CTD_human;ORPHANET;UNIPROT"
"9343"	"EFTUD2"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9348"	"NDST3"	"0.857"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"9348"	"NDST3"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2014"	"2016"	"2"	"0"	"PSYGENET"
"9348"	"NDST3"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9349"	"RPL23"	"0.857"	"0.138"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9351"	"SLC9A3R2"	"0.63"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2005"	"2012"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9353"	"SLIT2"	"0.55"	"0.621"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"9353"	"SLIT2"	"0.55"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"9355"	"LHX2"	"0.752"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9356"	"SLC22A6"	"0.834"	"0.276"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9356"	"SLC22A6"	"0.834"	"0.276"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9356"	"SLC22A6"	"0.834"	"0.276"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9361"	"LONP1"	"0.557"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9361"	"LONP1"	"0.557"	"0.655"	"C1838180"	"CODAS syndrome"	"disease"	"C05;C07;C11;C16;C23"	"Disease or Syndrome"	"0.74"	"1"	"1991"	"2018"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"9361"	"LONP1"	"0.557"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1991"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"9364"	"RAB28"	"0.815"	"0.069"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"9364"	"RAB28"	"0.815"	"0.069"	"C3809299"	"CONE-ROD DYSTROPHY 18"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"4"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0003850"	"Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9230769"	"1997"	"2013"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.53"	"0.3333333"	"1998"	"2017"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0020437"	"Hypercalcemia"	"disease"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0021359"	"Infertility"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"0.75"	"2010"	"2016"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0026141"	"Milk-Alkali Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.34"	"1"	"1997"	"2007"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0085681"	"Hyperphosphatemia (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0231341"	"Premature aging syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"0.9411765"	"1997"	"2017"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2018"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0268080"	"Hypercalcemia, Idiopathic, of Infancy"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0729353"	"Subfertility"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"9365"	"KL"	"0.495"	"0.621"	"C1876187"	"TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2007"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"9365"	"KL"	"0.495"	"0.621"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9"	"2003"	"2017"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C2931105"	"Hypercalciuria, childhood idiopathic"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9365"	"KL"	"0.495"	"0.621"	"C4074771"	"Sterility, Reproductive"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"1997"	"1997"	"1"	"0"	"CTD_human"
"9368"	"SLC9A3R1"	"0.594"	"0.448"	"C0021367"	"Mammary Ductal Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9368"	"SLC9A3R1"	"0.594"	"0.448"	"C1134719"	"Invasive Ductal Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9368"	"SLC9A3R1"	"0.594"	"0.448"	"C2676782"	"Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"2008"	"2012"	"2"	"4"	"CTD_human;UNIPROT"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"1"	"PSYGENET"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"PSYGENET"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9369"	"NRXN3"	"0.696"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9369"	"NRXN3"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9369"	"NRXN3"	"0.696"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.35"	"0.5"	"2004"	"2012"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2002"	"2017"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9285714"	"1999"	"2018"	"3"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2004"	"2015"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0020452"	"Hyperemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2004"	"2005"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.8461538"	"2002"	"2016"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.36"		"2004"	"2008"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.58"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"0.96"	"1998"	"2018"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0034063"	"Pulmonary Edema"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0042484"	"Venous Engorgement"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.57"		"2004"	"2013"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0178824"	"Reactive Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0333233"	"Active Hyperemia"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.39"	"0.8888889"	"2009"	"2017"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9787234"	"2001"	"2017"	"4"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0948480"	"Coronary Restenosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1847529"	"ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1847530"	"ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2016"	"2"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C2675517"	"ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C2675518"	"Adiponectin Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2000"	"2000"	"1"	"1"	"CTD_human;UNIPROT"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C2675519"	"Hypoadiponectinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.66"	"1"	"2000"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9370"	"ADIPOQ"	"0.485"	"0.724"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9373"	"PLAA"	"0.752"	"0.241"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9373"	"PLAA"	"0.752"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2010"	"2012"	"1"	"1"	"PSYGENET"
"9373"	"PLAA"	"0.752"	"0.241"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9373"	"PLAA"	"0.752"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"9373"	"PLAA"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9373"	"PLAA"	"0.752"	"0.241"	"C4479631"	"NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"2"	"3"	"UNIPROT"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9376"	"SLC22A8"	"0.701"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9377"	"COX5A"	"0.58"	"0.655"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.34"	"1"	"1998"	"2011"	"0"	"0"	"ORPHANET"
"9377"	"COX5A"	"0.58"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.9411765"	"2007"	"2016"	"4"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"2"	"0"	"PSYGENET"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2017"	"2"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2017"	"2"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9459459"	"2008"	"2016"	"3"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2017"	"2"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C1970431"	"PITT-HOPKINS SYNDROME"	"disease"	"C08;C10;C23;F01;F03"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C3280479"	"PITT-HOPKINS-LIKE SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"2"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C3280524"	"SCHIZOPHRENIA 17"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9378"	"NRXN1"	"0.614"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9378"	"NRXN1"	"0.614"	"0.483"	"C3808494"	"CHROMOSOME 2p16.3 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9379"	"NRXN2"	"0.815"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9379"	"NRXN2"	"0.815"	"0.276"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"9379"	"NRXN2"	"0.815"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9380"	"GRHPR"	"0.743"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9380"	"GRHPR"	"0.743"	"0.241"	"C0268165"	"Primary hyperoxaluria type 2"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.68"	"1"	"1993"	"2017"	"0"	"37"	"CTD_human;ORPHANET"
"9380"	"GRHPR"	"0.743"	"0.241"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9380"	"GRHPR"	"0.743"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9381"	"OTOF"	"0.707"	"0.276"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C1832828"	"Deafness, Autosomal Recessive 9"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.84"	"1"	"1993"	"2016"	"7"	"71"	"CTD_human;UNIPROT"
"9381"	"OTOF"	"0.707"	"0.276"	"C1832830"	"Auditory Neuropathy, Nonsyndromic Recessive"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"		"1999"	"2016"	"7"	"12"	"UNIPROT"
"9381"	"OTOF"	"0.707"	"0.276"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.42"	"1"	"1999"	"2016"	"6"	"1"	"CLINGEN"
"9381"	"OTOF"	"0.707"	"0.276"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9381"	"OTOF"	"0.707"	"0.276"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9382"	"COG1"	"0.735"	"0.414"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9382"	"COG1"	"0.735"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9382"	"COG1"	"0.735"	"0.414"	"C2931011"	"Congenital disorder of glycosylation, type 2G"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"9382"	"COG1"	"0.735"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9394"	"HS6ST1"	"0.659"	"0.483"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9394"	"HS6ST1"	"0.659"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"9394"	"HS6ST1"	"0.659"	"0.483"	"C3553977"	"HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"9397"	"NMT2"	"0.886"	"0.103"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9397"	"NMT2"	"0.886"	"0.103"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9401"	"RECQL4"	"0.524"	"0.759"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9401"	"RECQL4"	"0.524"	"0.759"	"C0032339"	"Rothmund-Thomson syndrome"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.70"	"0.9818182"	"1998"	"2018"	"1"	"15"	"CTD_human"
"9401"	"RECQL4"	"0.524"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9401"	"RECQL4"	"0.524"	"0.759"	"C0265308"	"Baller-Gerold syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"1999"	"2017"	"1"	"24"	"CTD_human;ORPHANET;UNIPROT"
"9401"	"RECQL4"	"0.524"	"0.759"	"C0280100"	"Solid Neoplasm"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9401"	"RECQL4"	"0.524"	"0.759"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"9401"	"RECQL4"	"0.524"	"0.759"	"C1849453"	"Rapadilino syndrome"	"disease"	"C05;C14;C16;C17;C18;C19"	"Disease or Syndrome"	"0.65"	"1"	"2000"	"2015"	"0"	"13"	"CTD_human;ORPHANET"
"9401"	"RECQL4"	"0.524"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9401"	"RECQL4"	"0.524"	"0.759"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9404"	"LPXN"	"0.696"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"9409"	"PEX16"	"0.586"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9409"	"PEX16"	"0.586"	"0.586"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9409"	"PEX16"	"0.586"	"0.586"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2003"	"2"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C1863998"	"Peroxisome Biogenesis Disorder, Complementation Group 9"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C1863999"	"Peroxisome Biogenesis Disorder, Complementation Group D"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9409"	"PEX16"	"0.586"	"0.586"	"C3553959"	"PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.40"		"1999"	"1999"	"0"	"1"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C3553960"	"PEROXISOME BIOGENESIS DISORDER 8B"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"9409"	"PEX16"	"0.586"	"0.586"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9409"	"PEX16"	"0.586"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9411"	"ARHGAP29"	"0.857"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9411"	"ARHGAP29"	"0.857"	"0.241"	"C0158646"	"Cleft palate with cleft lip"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9411"	"ARHGAP29"	"0.857"	"0.241"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9411"	"ARHGAP29"	"0.857"	"0.241"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9414"	"TJP2"	"0.696"	"0.379"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9414"	"TJP2"	"0.696"	"0.379"	"C0008372"	"Intrahepatic Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9414"	"TJP2"	"0.696"	"0.379"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9414"	"TJP2"	"0.696"	"0.379"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9414"	"TJP2"	"0.696"	"0.379"	"C1843139"	"Hypercholanemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2003"	"2003"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9414"	"TJP2"	"0.696"	"0.379"	"C2931067"	"Cholestasis, progressive familial intrahepatic 4"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.60"		"2014"	"2015"	"0"	"12"	"CTD_human;ORPHANET"
"9415"	"FADS2"	"0.627"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2018"	"1"	"2"	"PSYGENET"
"9415"	"FADS2"	"0.627"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9415"	"FADS2"	"0.627"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2014"	"2018"	"1"	"1"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9415"	"FADS2"	"0.627"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9419"	"CRIPT"	"0.762"	"0.207"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9419"	"CRIPT"	"0.762"	"0.207"	"C4014339"	"SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"2"	"3"	"UNIPROT"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"1998"	"1998"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.67"	"1"	"2008"	"2018"	"1"	"1"	"CTD_human;GENOMICS_ENGLAND"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"1998"	"1998"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0751602"	"Hereditary Autosomal Dominant Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0751603"	"Autosomal Recessive Hereditary Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0751604"	"Hereditary X-Linked Recessive Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C0751605"	"X-Linked, Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.31"	"0"	"1998"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C1849115"	"SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1995"	"2017"	"6"	"14"	"ORPHANET;UNIPROT"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C2931356"	"Spastic paraplegia type 5A, recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C3151147"	"Bile Acid Synthesis Defect, Congenital, 3"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.60"				"0"	"1"	"CTD_human;ORPHANET"
"9420"	"CYP7B1"	"0.604"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9421"	"HAND1"	"0.696"	"0.207"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9421"	"HAND1"	"0.696"	"0.207"	"C0678807"	"prenatal alcohol exposure"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9425"	"CDYL"	"0.857"	"0.138"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9426"	"CDY2A"	"0.857"	"0.069"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9427"	"ECEL1"	"0.762"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9427"	"ECEL1"	"0.762"	"0.241"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9427"	"ECEL1"	"0.762"	"0.241"	"C3554415"	"ARTHROGRYPOSIS, DISTAL, TYPE 5D"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2016"	"4"	"14"	"CTD_human;ORPHANET;UNIPROT"
"9427"	"ECEL1"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.962963"	"1999"	"2018"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9"	"2004"	"2018"	"2"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2017"	"1"	"7"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9661017"	"1999"	"2018"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C0740394"	"Hyperuricemia"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"0.875"	"2004"	"2018"	"2"	"0"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1841837"	"URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.40"		"2006"	"2012"	"0"	"2"	"CTD_human"
"9429"	"ABCG2"	"0.449"	"0.793"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9437"	"NCR1"	"0.659"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9439"	"MED23"	"0.69"	"0.379"	"C3280265"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"3"	"CTD_human;UNIPROT"
"9439"	"MED23"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"9440"	"MED17"	"0.735"	"0.31"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9440"	"MED17"	"0.735"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9440"	"MED17"	"0.735"	"0.31"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9440"	"MED17"	"0.735"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9440"	"MED17"	"0.735"	"0.31"	"C3150921"	"MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY"	"disease"		"Disease or Syndrome"	"0.70"		"2008"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9440"	"MED17"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9444"	"QKI"	"0.696"	"0.379"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"9444"	"QKI"	"0.696"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.8"	"2006"	"2014"	"5"	"0"	"PSYGENET"
"9444"	"QKI"	"0.696"	"0.379"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9444"	"QKI"	"0.696"	"0.379"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9444"	"QKI"	"0.696"	"0.379"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9444"	"QKI"	"0.696"	"0.379"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9444"	"QKI"	"0.696"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9444"	"QKI"	"0.696"	"0.379"	"C2363903"	"Angiocentric glioma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"9444"	"QKI"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"9445"	"ITM2B"	"0.667"	"0.448"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9445"	"ITM2B"	"0.667"	"0.448"	"C1861735"	"Dementia, familial Danish"	"disease"	"C09;C10;C11;C23;F03"	"Disease or Syndrome"	"0.70"	"0.9375"	"1970"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"9445"	"ITM2B"	"0.667"	"0.448"	"C1867773"	"Dementia, familial British"	"disease"	"C10;C14;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1933"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"9445"	"ITM2B"	"0.667"	"0.448"	"C4015146"	"RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.31"	"0"	"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"9446"	"GSTO1"	"0.627"	"0.552"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9448"	"MAP4K4"	"0.667"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9448"	"MAP4K4"	"0.667"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9450"	"LY86"	"0.886"	"0.138"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2015"	"1"	"1"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0432217"	"Wolcott-Rallison syndrome"	"disease"	"C05;C16;C18;C19;C20"	"Disease or Syndrome"	"1.00"	"0.9473684"	"1995"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9451"	"EIF2AK3"	"0.559"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9454"	"HOMER3"	"0.928"	"0.069"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9454"	"HOMER3"	"0.928"	"0.069"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9454"	"HOMER3"	"0.928"	"0.069"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9455"	"HOMER2"	"0.773"	"0.276"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9455"	"HOMER2"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9455"	"HOMER2"	"0.773"	"0.276"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9455"	"HOMER2"	"0.773"	"0.276"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9455"	"HOMER2"	"0.773"	"0.276"	"C4225240"	"DEAFNESS, AUTOSOMAL DOMINANT 68"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"3"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"3"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0013386"	"Dyskinesia, Drug-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0018524"	"Hallucinations"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0029226"	"Hallucinations, Organic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2004"	"2016"	"4"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233759"	"Hallucinations, Elementary"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233762"	"Hallucinations, Auditory"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233763"	"Hallucinations, Visual"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233765"	"Hallucinations, Olfactory"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233766"	"Hallucinations, Gustatory"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233767"	"Hallucinations, Tactile"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233773"	"Hallucinations, Hypnagogic"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233774"	"Hallucinations, Somatic"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233775"	"Hallucinations, Mood Congruent"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0233776"	"Hallucinations, Mood Incongruent"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0235153"	"Hallucinations, Sensory"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0237123"	"Alcohol or Other Drugs use"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0424068"	"Verbal auditory hallucinations"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0424071"	"Hallucinations, Visual, Unformed"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0424072"	"Hallucinations, Visual, Formed"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0424082"	"Hallucinations, Hypnapompic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0424083"	"Hallucinations, Dissociative"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0544668"	"Hallucinations, Kinesthetic"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0563608"	"Hallucinations, Formed, of People"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0563661"	"Hallucinations, Reflex"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0751088"	"Dyskinesia, Medication-Induced"	"disease"	"C10;C23;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0751175"	"Hallucination of Body Sensation"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C0751176"	"Hallucinations, Internal Body Sensation"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9456"	"HOMER1"	"0.69"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"PSYGENET"
"9457"	"FHL5"	"0.696"	"0.345"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"0"	"2013"	"2017"	"1"	"3"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9457"	"FHL5"	"0.696"	"0.345"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9459"	"ARHGEF6"	"0.785"	"0.241"	"C1845526"	"Mental Retardation, X-Linked 46"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9459"	"ARHGEF6"	"0.785"	"0.241"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9459"	"ARHGEF6"	"0.785"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2000"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"9462"	"RASAL2"	"0.752"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2013"	"2015"	"0"	"0"	"UNIPROT"
"9462"	"RASAL2"	"0.752"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9463"	"PICK1"	"0.713"	"0.345"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9463"	"PICK1"	"0.713"	"0.345"	"C0033941"	"Psychoses, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9463"	"PICK1"	"0.713"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9463"	"PICK1"	"0.713"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.75"	"2004"	"2007"	"4"	"0"	"PSYGENET"
"9463"	"PICK1"	"0.713"	"0.345"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9463"	"PICK1"	"0.713"	"0.345"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9463"	"PICK1"	"0.713"	"0.345"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9463"	"PICK1"	"0.713"	"0.345"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9464"	"HAND2"	"0.72"	"0.31"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9464"	"HAND2"	"0.72"	"0.31"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"9464"	"HAND2"	"0.72"	"0.31"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"9464"	"HAND2"	"0.72"	"0.31"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9464"	"HAND2"	"0.72"	"0.31"	"C0678807"	"prenatal alcohol exposure"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9464"	"HAND2"	"0.72"	"0.31"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9464"	"HAND2"	"0.72"	"0.31"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9465"	"AKAP7"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9466"	"IL27RA"	"0.701"	"0.448"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9466"	"IL27RA"	"0.701"	"0.448"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9468"	"PCYT1B"	"0.773"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9468"	"PCYT1B"	"0.773"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9468"	"PCYT1B"	"0.773"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9469"	"CHST3"	"0.534"	"0.69"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9469"	"CHST3"	"0.534"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9469"	"CHST3"	"0.534"	"0.69"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"9469"	"CHST3"	"0.534"	"0.69"	"C1837657"	"Spondyloepiphyseal dysplasia, Omani type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.54"	"1"	"2008"	"2012"	"1"	"5"	"CTD_human;UNIPROT"
"9469"	"CHST3"	"0.534"	"0.69"	"C2931649"	"Larsen syndrome, recessive type"	"disease"	"C05;C16;C26"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"9469"	"CHST3"	"0.534"	"0.69"	"C3278404"	"MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9469"	"CHST3"	"0.534"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9472"	"AKAP6"	"0.762"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9472"	"AKAP6"	"0.762"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9472"	"AKAP6"	"0.762"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9473"	"THEMIS2"	"0.799"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"9473"	"THEMIS2"	"0.799"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"9473"	"THEMIS2"	"0.799"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9473"	"THEMIS2"	"0.799"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0023380"	"Lethargy"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"9474"	"ATG5"	"0.546"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9474"	"ATG5"	"0.546"	"0.793"	"C4539808"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2016"	"1"	"1"	"UNIPROT"
"9475"	"ROCK2"	"0.648"	"0.552"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9475"	"ROCK2"	"0.648"	"0.552"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9479"	"MAPK8IP1"	"0.799"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.61"	"1"	"2000"	"2000"	"1"	"1"	"CTD_human;UNIPROT"
"9479"	"MAPK8IP1"	"0.799"	"0.207"	"C1852091"	"INSULIN RESISTANCE, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"9479"	"MAPK8IP1"	"0.799"	"0.207"	"C4017238"	"DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"9481"	"SLC25A27"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"2"	"0"	"PSYGENET"
"9487"	"PIGL"	"0.636"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9487"	"PIGL"	"0.636"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9487"	"PIGL"	"0.636"	"0.621"	"C1848392"	"Zunich neuroectodermal syndrome"	"disease"	"C09;C10;C11;C14;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9487"	"PIGL"	"0.636"	"0.621"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9487"	"PIGL"	"0.636"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9493"	"KIF23"	"0.727"	"0.207"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1981"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"9493"	"KIF23"	"0.727"	"0.207"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1981"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"9493"	"KIF23"	"0.727"	"0.207"	"C0271934"	"Congenital dyserythropoietic anemia, type III"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9495"	"AKAP5"	"0.799"	"0.172"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"9496"	"TBX4"	"0.676"	"0.448"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9496"	"TBX4"	"0.676"	"0.448"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9496"	"TBX4"	"0.676"	"0.448"	"C1840061"	"SMALL PATELLA SYNDROME"	"disease"	"C05"	"Disease or Syndrome"	"0.72"	"1"	"2001"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9496"	"TBX4"	"0.676"	"0.448"	"C1868581"	"Patella aplasia, coxa vara, tarsal synostosis"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"2"	"ORPHANET;UNIPROT"
"9496"	"TBX4"	"0.676"	"0.448"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"9496"	"TBX4"	"0.676"	"0.448"	"C3150607"	"CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9496"	"TBX4"	"0.676"	"0.448"	"C3150880"	"CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9496"	"TBX4"	"0.676"	"0.448"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"9496"	"TBX4"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9497"	"SLC4A7"	"0.743"	"0.345"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9499"	"MYOT"	"0.701"	"0.241"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"9499"	"MYOT"	"0.701"	"0.241"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1996"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9499"	"MYOT"	"0.701"	"0.241"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"9499"	"MYOT"	"0.701"	"0.241"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.41"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9499"	"MYOT"	"0.701"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9499"	"MYOT"	"0.701"	"0.241"	"C1834659"	"Muscular dystrophy, limb-girdle, type 1A"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9499"	"MYOT"	"0.701"	"0.241"	"C1836607"	"MYOTILINOPATHY"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.75"	"0.8"	"1988"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9499"	"MYOT"	"0.701"	"0.241"	"C1866785"	"Spheroid body myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.72"	"1"	"1978"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9499"	"MYOT"	"0.701"	"0.241"	"C3714934"	"MYOPATHY, MYOFIBRILLAR, 3"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"0"	"ORPHANET;UNIPROT"
"9500"	"MAGED1"	"0.69"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"9501"	"RPH3AL"	"0.857"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9506"	"PAGE4"	"0.799"	"0.103"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9508"	"ADAMTS3"	"0.645"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9508"	"ADAMTS3"	"0.645"	"0.621"	"C0340834"	"Hennekam lymphangiectasia lymphedema syndrome"	"disease"	"C05;C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"9509"	"ADAMTS2"	"0.63"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.35"	"1"	"1992"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"9509"	"ADAMTS2"	"0.63"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9509"	"ADAMTS2"	"0.63"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9509"	"ADAMTS2"	"0.63"	"0.621"	"C2700425"	"EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.65"	"0.8"	"1992"	"2013"	"0"	"3"	"CTD_human;ORPHANET"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"9510"	"ADAMTS1"	"0.596"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2002"	"2016"	"1"	"0"	"CTD_human"
"9516"	"LITAF"	"0.648"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"9516"	"LITAF"	"0.648"	"0.552"	"C0270913"	"Charcot-Marie-Tooth disease, Type 1C"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.78"	"1"	"1990"	"2017"	"7"	"10"	"CTD_human;ORPHANET;UNIPROT"
"9516"	"LITAF"	"0.648"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.36"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C3150896"	"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2018"	"2"	"5"	"CTD_human;UNIPROT"
"9517"	"SPTLC2"	"0.727"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9518"	"GDF15"	"0.496"	"0.621"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2014"	"2"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0149721"	"Left Ventricular Hypertrophy"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9444444"	"2003"	"2014"	"2"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C0685938"	"Malignant neoplasm of gastrointestinal tract"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9518"	"GDF15"	"0.496"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"9524"	"TECR"	"0.857"	"0.207"	"C3151462"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"9524"	"TECR"	"0.857"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9525"	"VPS4B"	"0.834"	"0.276"	"C0399379"	"Dentin dysplasia, type 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9526"	"MPDU1"	"0.713"	"0.379"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"9526"	"MPDU1"	"0.713"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9526"	"MPDU1"	"0.713"	"0.379"	"C1836669"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.73"	"1"	"2002"	"2006"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9526"	"MPDU1"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9529"	"BAG5"	"0.799"	"0.241"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9531"	"BAG3"	"0.558"	"0.69"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9531"	"BAG3"	"0.558"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9531"	"BAG3"	"0.558"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.68"	"1"	"2011"	"2017"	"0"	"10"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9531"	"BAG3"	"0.558"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2016"	"0"	"2"	"ORPHANET"
"9531"	"BAG3"	"0.558"	"0.69"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"9531"	"BAG3"	"0.558"	"0.69"	"C2678065"	"Myofibrillar Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2016"	"0"	"0"	"CTD_human"
"9531"	"BAG3"	"0.558"	"0.69"	"C2751831"	"Myopathy, Myofibrillar, Bag3-Related"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"11"	"3"	"CLINGEN;ORPHANET;UNIPROT"
"9531"	"BAG3"	"0.558"	"0.69"	"C3151293"	"CARDIOMYOPATHY, DILATED, 1HH"	"disease"		"Disease or Syndrome"	"0.80"		"2009"	"2017"	"3"	"14"	"CTD_human;UNIPROT"
"9531"	"BAG3"	"0.558"	"0.69"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9533"	"POLR1C"	"0.681"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9533"	"POLR1C"	"0.681"	"0.448"	"C0242387"	"Mandibulofacial Dysostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.65"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"9533"	"POLR1C"	"0.681"	"0.448"	"C0265241"	"Franceschetti-Klein syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9533"	"POLR1C"	"0.681"	"0.448"	"C1855433"	"Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2000"	"2018"	"2"	"4"	"CTD_human;UNIPROT"
"9533"	"POLR1C"	"0.681"	"0.448"	"C2676243"	"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism"	"disease"	"C07;C10;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9533"	"POLR1C"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9533"	"POLR1C"	"0.681"	"0.448"	"C4225305"	"LEUKODYSTROPHY, HYPOMYELINATING, 11"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"12"	"CTD_human;UNIPROT"
"9535"	"GMFG"	"0.799"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9536"	"PTGES"	"0.562"	"0.69"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9536"	"PTGES"	"0.562"	"0.69"	"C0020295"	"Hydronephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"9536"	"PTGES"	"0.562"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2003"	"2015"	"1"	"0"	"CTD_human"
"9536"	"PTGES"	"0.562"	"0.69"	"C0032617"	"Polyuria"	"phenotype"	"C12;C13;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9538"	"EI24"	"0.727"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9538"	"EI24"	"0.727"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9538"	"EI24"	"0.727"	"0.241"	"C4016951"	"BREAST CANCER, EARLY-ONSET"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"UNIPROT"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"1"	"UNIPROT"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9540"	"TP53I3"	"0.727"	"0.207"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9547"	"CXCL14"	"0.611"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9557"	"CHD1L"	"0.707"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2015"	"2"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"9557"	"CHD1L"	"0.707"	"0.414"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9559"	"VPS26A"	"0.886"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"9562"	"MINPP1"	"0.727"	"0.241"	"C4225426"	"THYROID CANCER, NONMEDULLARY, 2"	"disease"		"Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"2"	"UNIPROT"
"9563"	"H6PD"	"0.663"	"0.552"	"C1291245"	"Cortisone reductase deficiency"	"disease"	"C12;C13;C16;C17;C18;C19;C23"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"9563"	"H6PD"	"0.663"	"0.552"	"C3551716"	"CORTISONE REDUCTASE DEFICIENCY 1"	"disease"		"Disease or Syndrome"	"0.40"		"1999"	"2013"	"2"	"6"	"UNIPROT"
"9564"	"BCAR1"	"0.584"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9655172"	"1993"	"2017"	"0"	"0"	"UNIPROT"
"9564"	"BCAR1"	"0.584"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9564"	"BCAR1"	"0.584"	"0.655"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9564"	"BCAR1"	"0.584"	"0.655"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9568"	"GABBR2"	"0.701"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"9568"	"GABBR2"	"0.701"	"0.379"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9568"	"GABBR2"	"0.701"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9568"	"GABBR2"	"0.701"	"0.379"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9568"	"GABBR2"	"0.701"	"0.379"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"9568"	"GABBR2"	"0.701"	"0.379"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9568"	"GABBR2"	"0.701"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9569"	"GTF2IRD1"	"0.596"	"0.69"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.80"	"0.95"	"1999"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"9569"	"GTF2IRD1"	"0.596"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2018"	"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9570"	"GOSR2"	"0.676"	"0.379"	"C3279627"	"EPILEPSY, PROGRESSIVE MYOCLONIC, 6"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"3"	"ORPHANET;UNIPROT"
"9570"	"GOSR2"	"0.676"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9572"	"NR1D1"	"0.648"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"5"	"0"	"PSYGENET"
"9572"	"NR1D1"	"0.648"	"0.483"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"9572"	"NR1D1"	"0.648"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9572"	"NR1D1"	"0.648"	"0.483"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"9572"	"NR1D1"	"0.648"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9573"	"GDF3"	"0.645"	"0.379"	"C0022738"	"Klippel-Feil Syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"9573"	"GDF3"	"0.645"	"0.379"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9573"	"GDF3"	"0.645"	"0.379"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9573"	"GDF3"	"0.645"	"0.379"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9573"	"GDF3"	"0.645"	"0.379"	"C3150967"	"KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"9573"	"GDF3"	"0.645"	"0.379"	"C3150968"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"2"	"CTD_human;UNIPROT"
"9573"	"GDF3"	"0.645"	"0.379"	"C3150969"	"MICROPHTHALMIA, ISOLATED 7"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"2"	"CTD_human;UNIPROT"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0001957"	"Alcohol Withdrawal Delirium"	"disease"	"C10;C25;F03"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2011"	"1"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2000"	"2018"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2000"	"2017"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2000"	"2017"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2001"	"2015"	"1"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2000"	"2016"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2012"	"3"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2003"	"2016"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2000"	"2016"	"5"	"0"	"PSYGENET"
"9575"	"CLOCK"	"0.505"	"0.897"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"9576"	"SPAG6"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"9578"	"CDC42BPB"	"0.773"	"0.31"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9578"	"CDC42BPB"	"0.773"	"0.31"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9578"	"CDC42BPB"	"0.773"	"0.31"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9578"	"CDC42BPB"	"0.773"	"0.31"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9581"	"PREPL"	"0.659"	"0.448"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9581"	"PREPL"	"0.659"	"0.448"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9581"	"PREPL"	"0.659"	"0.448"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9581"	"PREPL"	"0.659"	"0.448"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9581"	"PREPL"	"0.659"	"0.448"	"C1848030"	"Hypotonia-Cystinuria Syndrome"	"disease"	"C05;C10;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.57"	"0.8571429"	"2006"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"9581"	"PREPL"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"9581"	"PREPL"	"0.659"	"0.448"	"C4304537"	"2p21 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2016"	"4"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2016"	"4"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2016"	"4"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"4"	"0"	"CTD_human"
"9582"	"APOBEC3B"	"0.611"	"0.552"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9583"	"ENTPD4"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0013080"	"Down Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2002"	"2003"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"0.75"	"2010"	"2016"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0432416"	"Down Syndrome, Partial Trisomy 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0432417"	"Trisomy 21, Meiotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C0751081"	"Trisomy 21, Mitotic Nondisjunction"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9588"	"PRDX6"	"0.596"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9590"	"AKAP12"	"0.616"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9590"	"AKAP12"	"0.616"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9590"	"AKAP12"	"0.616"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9590"	"AKAP12"	"0.616"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9590"	"AKAP12"	"0.616"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"9592"	"IER2"	"0.928"	"0.138"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9592"	"IER2"	"0.928"	"0.138"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9600"	"PITPNM1"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2003"	"2014"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"1999"	"2011"	"3"	"0"	"CTD_human;PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2014"	"4"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2014"	"4"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0020550"	"Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.9230769"	"1999"	"2016"	"0"	"1"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2004"	"2010"	"1"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0236664"	"Alcohol-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9607"	"CARTPT"	"0.633"	"0.448"	"C3714618"	"Primary Hyperthyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9610"	"RIN1"	"0.701"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.53"	"1"	"2006"	"2010"	"1"	"0"	"CGI;CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.54"	"1"	"2006"	"2010"	"1"	"0"	"CGI;CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0857007"	"Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"9611"	"NCOR1"	"0.611"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2005"	"2010"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C1565885"	"Direct Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C1565886"	"Indirect Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9611"	"NCOR1"	"0.611"	"0.517"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9612"	"NCOR2"	"0.63"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"9612"	"NCOR2"	"0.63"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9615"	"GDA"	"0.857"	"0.138"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9618"	"TRAF4"	"0.713"	"0.345"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9618"	"TRAF4"	"0.713"	"0.345"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9618"	"TRAF4"	"0.713"	"0.345"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9618"	"TRAF4"	"0.713"	"0.345"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9619"	"ABCG1"	"0.598"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"9619"	"ABCG1"	"0.598"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"9620"	"CELSR1"	"0.762"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"9620"	"CELSR1"	"0.762"	"0.345"	"C0036344"	"Schizophrenia, Catatonic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"9620"	"CELSR1"	"0.762"	"0.345"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2014"	"1"	"4"	"UNIPROT"
"9620"	"CELSR1"	"0.762"	"0.345"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2012"	"2012"	"1"	"4"	"UNIPROT"
"9622"	"KLK4"	"0.588"	"0.586"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.47"	"1"	"2004"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"9622"	"KLK4"	"0.588"	"0.586"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"9622"	"KLK4"	"0.588"	"0.586"	"C1290537"	"Amelogenesis imperfecta pigmented hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"9623"	"TCL1B"	"0.604"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"9623"	"TCL1B"	"0.604"	"0.448"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9623"	"TCL1B"	"0.604"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"9623"	"TCL1B"	"0.604"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9623"	"TCL1B"	"0.604"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9625"	"AATK"	"0.834"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9625"	"AATK"	"0.834"	"0.103"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9627"	"SNCAIP"	"0.69"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9627"	"SNCAIP"	"0.69"	"0.379"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9628"	"RGS6"	"0.63"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9630"	"GNA14"	"0.773"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9630"	"GNA14"	"0.773"	"0.207"	"C0346073"	"Tufted angioma of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9630"	"GNA14"	"0.773"	"0.207"	"C1367420"	"Kaposiform Hemangioendothelioma"	"disease"	"C02;C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9631"	"NUP155"	"0.857"	"0.172"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9631"	"NUP155"	"0.857"	"0.172"	"C4014269"	"ATRIAL FIBRILLATION, FAMILIAL, 15"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9632"	"SEC24C"	"0.63"	"0.517"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9635"	"CLCA2"	"0.752"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"1999"	"2013"	"0"	"0"	"UNIPROT"
"9635"	"CLCA2"	"0.752"	"0.31"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9635"	"CLCA2"	"0.752"	"0.31"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9636"	"ISG15"	"0.592"	"0.724"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.34"	"1"	"1992"	"2013"	"1"	"0"	"CTD_human"
"9636"	"ISG15"	"0.592"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"9636"	"ISG15"	"0.592"	"0.724"	"C4015293"	"IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2015"	"0"	"3"	"CTD_human;ORPHANET"
"9637"	"FEZ2"	"1"	"0.034"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9637"	"FEZ2"	"1"	"0.034"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9638"	"FEZ1"	"0.707"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"9638"	"FEZ1"	"0.707"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"PSYGENET"
"9638"	"FEZ1"	"0.707"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"0.6666667"	"2005"	"2014"	"3"	"1"	"PSYGENET"
"9639"	"ARHGEF10"	"0.799"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9639"	"ARHGEF10"	"0.799"	"0.172"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"9639"	"ARHGEF10"	"0.799"	"0.172"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9639"	"ARHGEF10"	"0.799"	"0.172"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9639"	"ARHGEF10"	"0.799"	"0.172"	"C1842357"	"Slowed Nerve Conduction Velocity, Autosomal Dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1998"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9640"	"ZNF592"	"0.642"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9640"	"ZNF592"	"0.642"	"0.379"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"9640"	"ZNF592"	"0.642"	"0.379"	"C1847114"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"9640"	"ZNF592"	"0.642"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9641"	"IKBKE"	"0.642"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"9641"	"IKBKE"	"0.642"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2018"	"1"	"2"	"CTD_human"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0206729"	"Neurofibrosarcoma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9644"	"SH3PXD2A"	"0.735"	"0.276"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9647"	"PPM1F"	"0.834"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9647"	"PPM1F"	"0.834"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9649"	"RALGPS1"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9649"	"RALGPS1"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9652"	"TTC37"	"0.69"	"0.448"	"C1857276"	"Trichohepatoenteric Syndrome"	"disease"	"C13;C16;C17;C23"	"Disease or Syndrome"	"0.69"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9652"	"TTC37"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9657"	"IQCB1"	"0.667"	"0.414"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.42"	"1"	"2005"	"2017"	"0"	"3"	"ORPHANET"
"9657"	"IQCB1"	"0.667"	"0.414"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.36"	"1"	"2005"	"2014"	"0"	"0"	"ORPHANET"
"9657"	"IQCB1"	"0.667"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9657"	"IQCB1"	"0.667"	"0.414"	"C1836517"	"Senior-Loken Syndrome 5"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2005"	"2015"	"0"	"13"	"CTD_human"
"9657"	"IQCB1"	"0.667"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"9662"	"CEP135"	"0.752"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9662"	"CEP135"	"0.752"	"0.345"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"9662"	"CEP135"	"0.752"	"0.345"	"C3553414"	"MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"0"	"3"	"CTD_human"
"9662"	"CEP135"	"0.752"	"0.345"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"9662"	"CEP135"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9663"	"LPIN2"	"0.663"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1989"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"9663"	"LPIN2"	"0.663"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1989"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"9663"	"LPIN2"	"0.663"	"0.517"	"C1864997"	"Majeed syndrome"	"disease"	"C01;C05;C15;C16"	"Disease or Syndrome"	"0.74"	"1"	"1989"	"2013"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9663"	"LPIN2"	"0.663"	"0.517"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"9668"	"ZNF432"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2006"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"9668"	"ZNF432"	"0.815"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9668"	"ZNF432"	"0.815"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9668"	"ZNF432"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9668"	"ZNF432"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9668"	"ZNF432"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9668"	"ZNF432"	"0.815"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9672"	"SDC3"	"0.785"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2010"	"0"	"0"	"CTD_human"
"9674"	"KIAA0040"	"0.928"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"3"	"1"	"PSYGENET"
"9679"	"FAM53B"	"0.928"	"0.138"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"1"	"PSYGENET"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C1838062"	"EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C1858477"	"Epilepsy, Partial, with Variable Foci"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2018"	"7"	"66"	"CTD_human;UNIPROT"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.46"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"9681"	"DEPDC5"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2013"	"6"	"0"	"GENOMICS_ENGLAND"
"9687"	"GREB1"	"0.713"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.44"	"1"	"2013"	"2017"	"1"	"2"	"CTD_human"
"9687"	"GREB1"	"0.713"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9687"	"GREB1"	"0.713"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9687"	"GREB1"	"0.713"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"9688"	"NUP93"	"0.815"	"0.103"	"C1868672"	"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9688"	"NUP93"	"0.815"	"0.103"	"C4225166"	"NEPHROTIC SYNDROME, TYPE 12"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"9689"	"BZW1"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9690"	"UBE3C"	"0.773"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9690"	"UBE3C"	"0.773"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9690"	"UBE3C"	"0.773"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9693"	"RAPGEF2"	"0.752"	"0.069"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9695"	"EDEM1"	"0.743"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9695"	"EDEM1"	"0.743"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9695"	"EDEM1"	"0.743"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9699"	"RIMS2"	"0.489"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2009"	"1"	"0"	"PSYGENET"
"9699"	"RIMS2"	"0.489"	"0.759"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9700"	"ESPL1"	"0.672"	"0.414"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9702"	"CEP57"	"0.667"	"0.414"	"C1850343"	"MOSAIC VARIEGATED ANEUPLOIDY SYNDROME"	"disease"	"C16"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"9702"	"CEP57"	"0.667"	"0.414"	"C2931286"	"Warburton Anyane Yeboa syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9702"	"CEP57"	"0.667"	"0.414"	"C2931383"	"Chromosomal mosaicism due to mitotic instability"	"disease"	"C16"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"9702"	"CEP57"	"0.667"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2002"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"9705"	"ST18"	"0.727"	"0.448"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9705"	"ST18"	"0.727"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9706"	"ULK2"	"0.857"	"0.069"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9706"	"ULK2"	"0.857"	"0.069"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9709"	"HERPUD1"	"0.69"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"9709"	"HERPUD1"	"0.69"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9709"	"HERPUD1"	"0.69"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9711"	"RUBCN"	"0.735"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"9711"	"RUBCN"	"0.735"	"0.207"	"C3810326"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2014"	"0"	"1"	"ORPHANET"
"9712"	"USP6NL"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0009917"	"Contracture"	"group"	"C05"	"Anatomical Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0018566"	"Congenital Hand Deformities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0265287"	"Acromicric Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C3278147"	"GELEOPHYSIC DYSPLASIA 1"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2011"	"2"	"11"	"UNIPROT"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C3489726"	"Geleophysic dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.59"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"9719"	"ADAMTSL2"	"0.676"	"0.276"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9721"	"GPRIN2"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9722"	"NOS1AP"	"0.652"	"0.345"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"9722"	"NOS1AP"	"0.652"	"0.345"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9722"	"NOS1AP"	"0.652"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2005"	"2016"	"2"	"1"	"PSYGENET"
"9723"	"SEMA3E"	"0.588"	"0.69"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9723"	"SEMA3E"	"0.588"	"0.69"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"9723"	"SEMA3E"	"0.588"	"0.69"	"C0265354"	"CHARGE Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.60"		"2004"	"2004"	"0"	"1"	"CTD_human;ORPHANET"
"9723"	"SEMA3E"	"0.588"	"0.69"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9723"	"SEMA3E"	"0.588"	"0.69"	"C2936502"	"Familial CHARGE Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9725"	"TMEM63A"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9725"	"TMEM63A"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9725"	"TMEM63A"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9725"	"TMEM63A"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9726"	"ZNF646"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9728"	"SECISBP2L"	"0.886"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9728"	"SECISBP2L"	"0.886"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"9731"	"CEP104"	"0.785"	"0.31"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"9731"	"CEP104"	"0.785"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9731"	"CEP104"	"0.785"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9732"	"DOCK4"	"0.762"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2004"	"2014"	"1"	"0"	"CTD_human"
"9732"	"DOCK4"	"0.762"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2013"	"2"	"1"	"PSYGENET"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.50"	"1"	"2012"	"2017"	"1"	"2"	"CTD_human"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9734"	"HDAC9"	"0.501"	"0.759"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9737"	"GPRASP1"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9739"	"SETD1A"	"0.681"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2016"	"1"	"5"	"PSYGENET"
"9739"	"SETD1A"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9742"	"IFT140"	"0.607"	"0.552"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9742"	"IFT140"	"0.607"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9742"	"IFT140"	"0.607"	"0.552"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"0"	"2"	"ORPHANET"
"9742"	"IFT140"	"0.607"	"0.552"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9742"	"IFT140"	"0.607"	"0.552"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9742"	"IFT140"	"0.607"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9742"	"IFT140"	"0.607"	"0.552"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.62"	"1"	"2012"	"2018"	"0"	"5"	"ORPHANET"
"9742"	"IFT140"	"0.607"	"0.552"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9742"	"IFT140"	"0.607"	"0.552"	"C1849437"	"Mainzer-Saldino Disease"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.82"	"1"	"2012"	"2018"	"3"	"14"	"ORPHANET;UNIPROT"
"9742"	"IFT140"	"0.607"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9742"	"IFT140"	"0.607"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"9743"	"ARHGAP32"	"0.834"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9744"	"ACAP1"	"0.886"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9744"	"ACAP1"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9745"	"ZNF536"	"0.762"	"0.241"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9745"	"ZNF536"	"0.762"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9745"	"ZNF536"	"0.762"	"0.241"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9745"	"ZNF536"	"0.762"	"0.241"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9745"	"ZNF536"	"0.762"	"0.241"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9745"	"ZNF536"	"0.762"	"0.241"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9746"	"CLSTN3"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9748"	"SLK"	"0.752"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9748"	"SLK"	"0.752"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"9748"	"SLK"	"0.752"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9748"	"SLK"	"0.752"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9750"	"RIPOR2"	"0.834"	"0.207"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"CLINGEN"
"9750"	"RIPOR2"	"0.834"	"0.207"	"C4225298"	"DEAFNESS, AUTOSOMAL RECESSIVE 104"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"9752"	"PCDHA9"	"0.928"	"0.103"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9752"	"PCDHA9"	"0.928"	"0.103"	"C0152101"	"Hypoplastic Left Heart Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2006"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"9754"	"STARD8"	"0.815"	"0.138"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"9754"	"STARD8"	"0.815"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9755"	"TBKBP1"	"1"	"0.034"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"9757"	"KMT2B"	"0.596"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2018"	"6"	"0"	"GENOMICS_ENGLAND"
"9757"	"KMT2B"	"0.596"	"0.655"	"C4310633"	"DYSTONIA 28, CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"2"	"9"	"UNIPROT"
"9757"	"KMT2B"	"0.596"	"0.655"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9758"	"FRMPD4"	"0.834"	"0.172"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"9758"	"FRMPD4"	"0.834"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9758"	"FRMPD4"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"9758"	"FRMPD4"	"0.834"	"0.172"	"C4310817"	"MENTAL RETARDATION, X-LINKED 104"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2016"	"0"	"0"	"UNIPROT"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0221357"	"Brachydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.44"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C1862102"	"BRACHYDACTYLY, TYPE E1"	"phenotype"	"C05;C16"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C2931817"	"Chromosome 2q37 deletion syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.57"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"9759"	"HDAC4"	"0.558"	"0.655"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9759"	"HDAC4"	"0.558"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"0.5"	"2010"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9759"	"HDAC4"	"0.558"	"0.655"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9765"	"ZFYVE16"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9770"	"RASSF2"	"0.619"	"0.379"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9770"	"RASSF2"	"0.619"	"0.379"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9770"	"RASSF2"	"0.619"	"0.379"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9770"	"RASSF2"	"0.619"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2013"	"1"	"1"	"UNIPROT"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9771"	"RAPGEF5"	"0.614"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9774"	"BCLAF1"	"0.785"	"0.345"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9775"	"EIF4A3"	"0.696"	"0.414"	"C1849348"	"Richieri Costa Pereira syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.73"	"1"	"2014"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9775"	"EIF4A3"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2006"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C0272051"	"Xerocytosis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.70"	"1"	"1971"	"2017"	"6"	"12"	"ORPHANET;UNIPROT"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C1863769"	"Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema"	"disease"	"C13;C15;C16;C18;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9780"	"PIEZO1"	"0.639"	"0.655"	"C4225184"	"LYMPHEDEMA, HEREDITARY, III"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"9"	"CTD_human;UNIPROT"
"9782"	"MATR3"	"0.648"	"0.448"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.47"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"9782"	"MATR3"	"0.648"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9782"	"MATR3"	"0.648"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9782"	"MATR3"	"0.648"	"0.448"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"9782"	"MATR3"	"0.648"	"0.448"	"C1853723"	"MYOPATHY, DISTAL 2"	"disease"	"C05;C07;C08;C09;C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"1999"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"9782"	"MATR3"	"0.648"	"0.448"	"C3807521"	"AMYOTROPHIC LATERAL SCLEROSIS 21"	"disease"		"Disease or Syndrome"	"0.40"		"1999"	"2017"	"4"	"4"	"UNIPROT"
"9783"	"RIMS3"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"CTD_human"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.51"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.44"	"1"	"2013"	"2016"	"0"	"1"	"ORPHANET"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C4084822"	"JOUBERT SYNDROME 23"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2015"	"2017"	"5"	"15"	"UNIPROT"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9786"	"KIAA0586"	"0.659"	"0.517"	"C4518774"	"Joubert syndrome with Jeune asphyxiating thoracic dystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9788"	"MTSS1"	"0.627"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"9788"	"MTSS1"	"0.627"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9788"	"MTSS1"	"0.627"	"0.448"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9788"	"MTSS1"	"0.627"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9788"	"MTSS1"	"0.627"	"0.448"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9788"	"MTSS1"	"0.627"	"0.448"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9790"	"BMS1"	"0.567"	"0.724"	"C0013575"	"Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9790"	"BMS1"	"0.567"	"0.724"	"C0162361"	"Hidrotic Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9790"	"BMS1"	"0.567"	"0.724"	"C0282160"	"Aplasia Cutis Congenita"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.75"	"1"	"1995"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9790"	"BMS1"	"0.567"	"0.724"	"C1706004"	"Anhydrotic Ectodermal Dysplasias"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"9790"	"BMS1"	"0.567"	"0.724"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"9791"	"PTDSS1"	"0.624"	"0.724"	"C0432269"	"Lenz Majewski hyperostotic dwarfism"	"disease"	"C05;C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.72"	"1"	"1989"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"9791"	"PTDSS1"	"0.624"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9793"	"CKAP5"			"C0002938"	"Aneuploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9793"	"CKAP5"			"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9801"	"MRPL19"	"0.857"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9801"	"MRPL19"	"0.857"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9801"	"MRPL19"	"0.857"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9801"	"MRPL19"	"0.857"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"9805"	"SCRN1"	"0.762"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"9805"	"SCRN1"	"0.762"	"0.276"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9805"	"SCRN1"	"0.762"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9805"	"SCRN1"	"0.762"	"0.276"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9805"	"SCRN1"	"0.762"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9811"	"CTIF"	"0.857"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2016"	"0"	"0"	"UNIPROT"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9285714"	"2007"	"2016"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0022593"	"Keratosis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0022594"	"Keratosis Blennorrhagica"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0086501"	"Keratoma"	"phenotype"	"C17"	"Acquired Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0302859"	"Euthyroid Goiter"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2018"	"2"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9817"	"KEAP1"	"0.541"	"0.621"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9820"	"CUL7"	"0.645"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9820"	"CUL7"	"0.645"	"0.448"	"C1848862"	"Miller-McKusick-Malvaux-Syndrome (3M Syndrome)"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.80"	"0.9230769"	"2005"	"2016"	"3"	"16"	"CTD_human;ORPHANET;UNIPROT"
"9820"	"CUL7"	"0.645"	"0.448"	"C1851996"	"Dwarfism tall vertebrae"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9820"	"CUL7"	"0.645"	"0.448"	"C2678312"	"Three M Syndrome 1"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.70"		"2005"	"2013"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9820"	"CUL7"	"0.645"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2009"	"3"	"0"	"GENOMICS_ENGLAND"
"9821"	"RB1CC1"	"0.727"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.57"	"1"	"2002"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"9821"	"RB1CC1"	"0.727"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"9821"	"RB1CC1"	"0.727"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.46"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"9821"	"RB1CC1"	"0.727"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9821"	"RB1CC1"	"0.727"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"9824"	"ARHGAP11A"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"9826"	"ARHGEF11"	"0.799"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2015"	"2"	"0"	"PSYGENET"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2012"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C3809811"	"PARKINSON DISEASE 19A, JUVENILE-ONSET"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C4310802"	"PARKINSON DISEASE 19B, EARLY-ONSET"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"9829"	"DNAJC6"	"0.681"	"0.276"	"C4510873"	"Atypical juvenile parkinsonism"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9832"	"JAKMIP2"	"0.857"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9832"	"JAKMIP2"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"9833"	"MELK"	"0.672"	"0.172"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9839"	"ZEB2"	"0.513"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2014"	"0"	"0"	"UNIPROT"
"9839"	"ZEB2"	"0.513"	"0.655"	"C1856113"	"Mowat-Wilson syndrome"	"disease"	"C05;C06;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.90"	"1"	"1991"	"2018"	"7"	"83"	"CTD_human;UNIPROT"
"9839"	"ZEB2"	"0.513"	"0.655"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9839"	"ZEB2"	"0.513"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2002"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"9841"	"ZBTB24"	"0.696"	"0.448"	"C3279748"	"IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2011"	"2011"	"1"	"3"	"CTD_human;UNIPROT"
"9841"	"ZBTB24"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"9842"	"PLEKHM1"	"0.785"	"0.138"	"C0432261"	"Osteopetrosis - intermediate type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9842"	"PLEKHM1"	"0.785"	"0.138"	"C1969093"	"Osteopetrosis, Autosomal Recessive 6"	"disease"	"C05"	"Disease or Syndrome"	"0.80"		"2007"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"9843"	"HEPH"	"0.735"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9843"	"HEPH"	"0.735"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9843"	"HEPH"	"0.735"	"0.31"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9844"	"ELMO1"	"0.663"	"0.517"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9846"	"GAB2"	"0.627"	"0.586"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"9846"	"GAB2"	"0.627"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9846"	"GAB2"	"0.627"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"9851"	"KIAA0753"	"0.762"	"0.31"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9851"	"KIAA0753"	"0.762"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9851"	"KIAA0753"	"0.762"	"0.31"	"C4310701"	"OROFACIODIGITAL SYNDROME XV"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9853"	"RUSC2"	"0.928"	"0.103"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9853"	"RUSC2"	"0.928"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9855"	"FARP2"	"0.735"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"9855"	"FARP2"	"0.735"	"0.483"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2010"	"2013"	"1"	"2"	"CTD_human"
"9855"	"FARP2"	"0.735"	"0.483"	"C2931817"	"Chromosome 2q37 deletion syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9856"	"KIAA0319"	"0.727"	"0.345"	"C0002018"	"Alexia"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"9856"	"KIAA0319"	"0.727"	"0.345"	"C0476254"	"Dyslexia"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9705882"	"1999"	"2017"	"0"	"0"	"CTD_human"
"9856"	"KIAA0319"	"0.727"	"0.345"	"C0920296"	"Developmental reading disorder"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2018"	"0"	"0"	"CTD_human"
"9860"	"LRIG2"	"0.701"	"0.241"	"C0403555"	"Ochoa syndrome"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.53"	"1"	"2013"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"9860"	"LRIG2"	"0.701"	"0.241"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9861"	"PSMD6"	"0.815"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2016"	"1"	"1"	"CTD_human"
"9861"	"PSMD6"	"0.815"	"0.207"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9861"	"PSMD6"	"0.815"	"0.207"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.64"	"1"	"2008"	"2017"	"3"	"1"	"CTD_human;PSYGENET"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9863"	"MAGI2"	"0.624"	"0.586"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"9863"	"MAGI2"	"0.624"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9869"	"SETDB1"	"0.672"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"9871"	"SEC24D"	"0.72"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"9871"	"SEC24D"	"0.72"	"0.379"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2015"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"9871"	"SEC24D"	"0.72"	"0.379"	"C1862178"	"Cole Carpenter syndrome"	"disease"	"C05;C10;C11;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"9871"	"SEC24D"	"0.72"	"0.379"	"C4225382"	"COLE-CARPENTER SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"3"	"UNIPROT"
"9873"	"FCHSD2"	"0.799"	"0.241"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9873"	"FCHSD2"	"0.799"	"0.241"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9873"	"FCHSD2"	"0.799"	"0.241"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9874"	"TLK1"	"0.713"	"0.414"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9874"	"TLK1"	"0.713"	"0.414"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9877"	"ZC3H11A"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"9877"	"ZC3H11A"	"0.886"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2018"	"1"	"2"	"CTD_human"
"9877"	"ZC3H11A"	"0.886"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9877"	"ZC3H11A"	"0.886"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9882"	"TBC1D4"	"0.785"	"0.31"	"C4015183"	"DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"9885"	"OSBPL2"	"0.886"	"0.103"	"C4084712"	"DEAFNESS, AUTOSOMAL DOMINANT 67"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2016"	"0"	"2"	"CTD_human"
"9886"	"RHOBTB1"	"0.785"	"0.241"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9886"	"RHOBTB1"	"0.785"	"0.241"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9886"	"RHOBTB1"	"0.785"	"0.241"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9891"	"NUAK1"	"0.676"	"0.414"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"9891"	"NUAK1"	"0.676"	"0.414"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"9894"	"TELO2"	"0.743"	"0.483"	"C4310778"	"YOU-HOOVER-FONG SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0037771"	"Paraparesis, Spastic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0270724"	"Infantile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0338473"	"Neuroaxonal Dystrophies"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751602"	"Hereditary Autosomal Dominant Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751603"	"Autosomal Recessive Hereditary Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751604"	"Hereditary X-Linked Recessive Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751605"	"X-Linked, Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751716"	"Adult Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751717"	"Juvenile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C0751718"	"Late Infantile Neuroaxonal Dystrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9895"	"TECPR2"	"0.676"	"0.345"	"C3542549"	"SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"9895"	"TECPR2"	"0.676"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"9896"	"FIG4"	"0.561"	"0.655"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"9896"	"FIG4"	"0.561"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9896"	"FIG4"	"0.561"	"0.655"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2007"	"2012"	"1"	"0"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9896"	"FIG4"	"0.561"	"0.655"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C1857663"	"Yunis Varon syndrome"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.95"	"1"	"1990"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"9896"	"FIG4"	"0.561"	"0.655"	"C1970011"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.99"	"1"	"1993"	"2016"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"9896"	"FIG4"	"0.561"	"0.655"	"C2675191"	"Polymicrogyria, Bilateral Occipital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2014"	"0"	"1"	"CTD_human"
"9896"	"FIG4"	"0.561"	"0.655"	"C2675491"	"AMYOTROPHIC LATERAL SCLEROSIS 11"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.60"		"2009"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"9896"	"FIG4"	"0.561"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"9896"	"FIG4"	"0.561"	"0.655"	"C4013648"	"POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"9896"	"FIG4"	"0.561"	"0.655"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"9897"	"WASHC5"	"0.602"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9897"	"WASHC5"	"0.602"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9897"	"WASHC5"	"0.602"	"0.621"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9897"	"WASHC5"	"0.602"	"0.621"	"C0796137"	"3C syndrome"	"disease"	"C05;C10;C14;C16"	"Disease or Syndrome"	"0.61"	"1"	"1995"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"9897"	"WASHC5"	"0.602"	"0.621"	"C1863704"	"Spastic paraplegia 8, autosomal dominant"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2018"	"6"	"5"	"CTD_human;ORPHANET;UNIPROT"
"9897"	"WASHC5"	"0.602"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9899"	"SV2B"	"0.886"	"0.103"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"9900"	"SV2A"	"0.815"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C2931337"	"Chromosome 3, monosomy 3p25"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9901"	"SRGAP3"	"0.713"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"2002"	"2016"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9902"	"MRC2"	"0.707"	"0.276"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9902"	"MRC2"	"0.707"	"0.276"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9903"	"KLHL21"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"9907"	"AP5Z1"	"0.672"	"0.345"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"0.5"	"2010"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9907"	"AP5Z1"	"0.672"	"0.345"	"C3150901"	"SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"9907"	"AP5Z1"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"9908"	"G3BP2"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"9910"	"RABGAP1L"	"0.834"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9915"	"ARNT2"	"0.633"	"0.552"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9915"	"ARNT2"	"0.633"	"0.552"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"9915"	"ARNT2"	"0.633"	"0.552"	"C4014708"	"WEBB-DATTANI SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9918"	"NCAPD2"	"0.928"	"0.138"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9922"	"IQSEC1"	"0.743"	"0.241"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9922"	"IQSEC1"	"0.743"	"0.241"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9923"	"ZBTB40"	"0.886"	"0.138"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9923"	"ZBTB40"	"0.886"	"0.138"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9923"	"ZBTB40"	"0.886"	"0.138"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9923"	"ZBTB40"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9924"	"PAN2"	"0.773"	"0.103"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"UNIPROT"
"9924"	"PAN2"	"0.773"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9924"	"PAN2"	"0.773"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9926"	"LPGAT1"	"1"	"0.069"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9927"	"MFN2"	"0.541"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9927"	"MFN2"	"0.541"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"1997"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"9927"	"MFN2"	"0.541"	"0.759"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9927"	"MFN2"	"0.541"	"0.759"	"C0023804"	"Lipomatosis, Multiple Symmetrical"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"9927"	"MFN2"	"0.541"	"0.759"	"C0024445"	"Lipomatosis, Familial Benign Cervical"	"disease"	"C17;C18"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"9927"	"MFN2"	"0.541"	"0.759"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"9927"	"MFN2"	"0.541"	"0.759"	"C0393807"	"Hereditary motor and sensory neuropathy with optic atrophy (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.75"	"1"	"2004"	"2016"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"9927"	"MFN2"	"0.541"	"0.759"	"C0751602"	"Hereditary Autosomal Dominant Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9927"	"MFN2"	"0.541"	"0.759"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"9927"	"MFN2"	"0.541"	"0.759"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9927"	"MFN2"	"0.541"	"0.759"	"C1836485"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"5"	"28"	"CTD_human;ORPHANET;UNIPROT"
"9927"	"MFN2"	"0.541"	"0.759"	"C2931642"	"Benign symmetrical lipomatosis"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9927"	"MFN2"	"0.541"	"0.759"	"C4310725"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2017"	"5"	"5"	"CTD_human;UNIPROT"
"9928"	"KIF14"	"0.611"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"9928"	"KIF14"	"0.611"	"0.483"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9928"	"KIF14"	"0.611"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"9928"	"KIF14"	"0.611"	"0.483"	"C4015701"	"MECKEL SYNDROME 12"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"ORPHANET"
"9934"	"P2RY14"	"0.886"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9935"	"MAFB"	"0.636"	"0.621"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"9935"	"MAFB"	"0.636"	"0.621"	"C0013261"	"Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"9935"	"MAFB"	"0.636"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9935"	"MAFB"	"0.636"	"0.621"	"C0751083"	"Duane Retraction Syndrome, Type 2"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"CTD_human"
"9935"	"MAFB"	"0.636"	"0.621"	"C0751084"	"Duane Retraction Syndrome, Type 3"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9935"	"MAFB"	"0.636"	"0.621"	"C0994516"	"Type 1 Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"CTD_human"
"9935"	"MAFB"	"0.636"	"0.621"	"C1623209"	"Okihiro Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9935"	"MAFB"	"0.636"	"0.621"	"C2674705"	"Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy"	"disease"	"C05"	"Disease or Syndrome"	"0.73"	"1"	"2012"	"2015"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"9935"	"MAFB"	"0.636"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"9939"	"RBM8A"	"0.639"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9939"	"RBM8A"	"0.639"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9939"	"RBM8A"	"0.639"	"0.621"	"C0175703"	"Thrombocytopenia-Absent Radius Syndrome"	"disease"	"C05;C15;C16"	"Congenital Abnormality"	"0.64"	"1"	"1993"	"2015"	"1"	"4"	"CTD_human;ORPHANET"
"9939"	"RBM8A"	"0.639"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"9939"	"RBM8A"	"0.639"	"0.621"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2005"	"0"	"0"	"UNIPROT"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9940"	"DLEC1"	"0.609"	"0.517"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"9943"	"OXSR1"	"0.928"	"0.069"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"9943"	"OXSR1"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"9943"	"OXSR1"	"0.928"	"0.069"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9947"	"MAGEC1"	"0.735"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"9947"	"MAGEC1"	"0.735"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9947"	"MAGEC1"	"0.735"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9948"	"WDR1"	"0.713"	"0.483"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9948"	"WDR1"	"0.713"	"0.483"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9948"	"WDR1"	"0.713"	"0.483"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9948"	"WDR1"	"0.713"	"0.483"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9948"	"WDR1"	"0.713"	"0.483"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9948"	"WDR1"	"0.713"	"0.483"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9949"	"AMMECR1"	"0.743"	"0.414"	"C1846242"	"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis"	"disease"	"C05;C10;C12;C13;C15;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"9949"	"AMMECR1"	"0.743"	"0.414"	"C4310810"	"MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2018"	"2"	"3"	"CTD_human;UNIPROT"
"9950"	"GOLGA5"	"0.857"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"9951"	"HS3ST4"	"0.886"	"0.103"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9951"	"HS3ST4"	"0.886"	"0.103"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9951"	"HS3ST4"	"0.886"	"0.103"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9953"	"HS3ST3B1"	"0.815"	"0.172"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9953"	"HS3ST3B1"	"0.815"	"0.172"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9961"	"MVP"	"0.569"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9961"	"MVP"	"0.569"	"0.69"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9961"	"MVP"	"0.569"	"0.69"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"9962"	"SLC23A2"	"0.69"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0151699"	"Intracranial Hemorrhages"	"group"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0553692"	"Brain hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C0751893"	"Posterior Fossa Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9963"	"SLC23A1"	"0.735"	"0.31"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"9965"	"FGF19"	"0.63"	"0.379"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9230769"	"2002"	"2018"	"1"	"0"	"CTD_human"
"9966"	"TNFSF15"	"0.584"	"0.621"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.44"	"1"	"2013"	"2017"	"0"	"1"	"ORPHANET"
"9966"	"TNFSF15"	"0.584"	"0.621"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9411765"	"2004"	"2016"	"1"	"2"	"CTD_human"
"9966"	"TNFSF15"	"0.584"	"0.621"	"C0014335"	"Enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9966"	"TNFSF15"	"0.584"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2004"	"2011"	"1"	"0"	"CTD_human"
"9966"	"TNFSF15"	"0.584"	"0.621"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2017"	"1"	"3"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9968"	"MED12"	"0.528"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0010701"	"Phyllodes Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2002"	"2"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2000"	"2002"	"2"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9968"	"MED12"	"0.528"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2004"	"2008"	"1"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2000"	"2010"	"5"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9968"	"MED12"	"0.528"	"0.655"	"C0206650"	"Fibroadenoma"	"disease"	"C04"	"Neoplastic Process"	"0.38"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0220769"	"FG syndrome"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"9968"	"MED12"	"0.528"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2008"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"9968"	"MED12"	"0.528"	"0.655"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2008"	"1"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9968"	"MED12"	"0.528"	"0.655"	"C0600066"	"Malignant Cystosarcoma Phyllodes"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C0796022"	"Lujan Fryns syndrome"	"disease"	"C05;C10;C14;C16;C17"	"Congenital Abnormality"	"0.73"	"1"	"1984"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"9968"	"MED12"	"0.528"	"0.655"	"C0796094"	"Blepharophimosis syndrome Ohdo type"	"disease"	"C10;C11;C14;C16;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2016"	"2"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"9968"	"MED12"	"0.528"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.42"	"1"	"2015"	"2016"	"2"	"1"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C1845546"	"FG SYNDROME 4 (disorder)"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C1845567"	"FG SYNDROME 3"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C1845902"	"FG SYNDROME 2"	"disease"	"C06;C10;C16;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9968"	"MED12"	"0.528"	"0.655"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9968"	"MED12"	"0.528"	"0.655"	"C3698541"	"Ohdo syndrome, Maat-Kievit-Brunner type"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"1993"	"2017"	"1"	"4"	"ORPHANET;UNIPROT"
"9968"	"MED12"	"0.528"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9166667"	"1984"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2015"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2015"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2013"	"2015"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"4"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2015"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2010"	"1"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2007"	"2015"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2015"	"2"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2014"	"4"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"9970"	"NR1I3"	"0.555"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9970"	"NR1I3"	"0.555"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2018"	"3"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"0.7272727"	"2003"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0021841"	"Intestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2003"	"2017"	"4"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0268318"	"Cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.36"	"1"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2017"	"4"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0346627"	"Intestinal Cancer"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"9971"	"NR1H4"	"0.522"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9333333"	"2003"	"2016"	"2"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C3489728"	"Familial intrahepatic cholestasis of pregnancy"	"disease"	"C06;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9971"	"NR1H4"	"0.522"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9971"	"NR1H4"	"0.522"	"0.655"	"C4310747"	"CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"9973"	"CCS"	"0.743"	"0.172"	"C0011156"	"Deficiency Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"9973"	"CCS"	"0.743"	"0.172"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9973"	"CCS"	"0.743"	"0.172"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9973"	"CCS"	"0.743"	"0.172"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9973"	"CCS"	"0.743"	"0.172"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"9975"	"NR1D2"	"0.785"	"0.172"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9975"	"NR1D2"	"0.785"	"0.172"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"9978"	"RBX1"	"0.656"	"0.414"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9978"	"RBX1"	"0.656"	"0.414"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9978"	"RBX1"	"0.656"	"0.414"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9978"	"RBX1"	"0.656"	"0.414"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9978"	"RBX1"	"0.656"	"0.414"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"9985"	"REC8"	"0.785"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9985"	"REC8"	"0.785"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9985"	"REC8"	"0.785"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"9986"	"RCE1"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"9987"	"HNRNPDL"	"0.656"	"0.483"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"9987"	"HNRNPDL"	"0.656"	"0.483"	"C1836765"	"LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"		"2005"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"9990"	"SLC12A6"	"0.63"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2009"	"3"	"0"	"PSYGENET"
"9990"	"SLC12A6"	"0.63"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9990"	"SLC12A6"	"0.63"	"0.345"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.44"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"9990"	"SLC12A6"	"0.63"	"0.345"	"C0795950"	"Corpus callosum agenesis neuronopathy"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.87"	"1"	"1993"	"2015"	"0"	"29"	"CTD_human;ORPHANET"
"9990"	"SLC12A6"	"0.63"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"9992"	"KCNE2"	"0.659"	"0.31"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.43"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"9992"	"KCNE2"	"0.659"	"0.31"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.60"	"1"	"1998"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9992"	"KCNE2"	"0.659"	"0.31"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2009"	"0"	"0"	"ORPHANET"
"9992"	"KCNE2"	"0.659"	"0.31"	"C0042510"	"Ventricular Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.41"	"1"	"1999"	"1999"	"1"	"0"	"CTD_human"
"9992"	"KCNE2"	"0.659"	"0.31"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9992"	"KCNE2"	"0.659"	"0.31"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"9992"	"KCNE2"	"0.659"	"0.31"	"C1862394"	"Atrial Fibrillation, Familial, 4"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"9992"	"KCNE2"	"0.659"	"0.31"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9992"	"KCNE2"	"0.659"	"0.31"	"C3150953"	"Long Qt Syndrome 6"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2010"	"3"	"10"	"CTD_human;UNIPROT"
"9992"	"KCNE2"	"0.659"	"0.31"	"C3150954"	"LONG QT SYNDROME 6, ACQUIRED, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2003"	"2010"	"3"	"10"	"UNIPROT"
"9992"	"KCNE2"	"0.659"	"0.31"	"C3276241"	"LONG QT SYNDROME 3/6, DIGENIC Disorder"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2010"	"3"	"10"	"UNIPROT"
"9992"	"KCNE2"	"0.659"	"0.31"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"9993"	"DGCR2"	"0.645"	"0.655"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.32"	"0.5"	"2000"	"2009"	"0"	"0"	"CTD_human"
"9993"	"DGCR2"	"0.645"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2007"	"2011"	"1"	"0"	"CTD_human"
"9993"	"DGCR2"	"0.645"	"0.655"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human"
"9993"	"DGCR2"	"0.645"	"0.655"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.69"	"0.8888889"	"2000"	"2008"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"9997"	"SCO2"	"0.648"	"0.414"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"0.5"	"2000"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"GENOMICS_ENGLAND"
"9997"	"SCO2"	"0.648"	"0.414"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"9997"	"SCO2"	"0.648"	"0.414"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"2"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.60"	"1"	"1999"	"2016"	"2"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"9997"	"SCO2"	"0.648"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"9997"	"SCO2"	"0.648"	"0.414"	"C0752107"	"Brain Diseases, Metabolic, Inherited"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0752109"	"Brain Diseases, Metabolic, Inborn"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0752110"	"Central Nervous System Inborn Metabolic Diseases"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.38"	"0.875"	"2001"	"2016"	"1"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C1837148"	"MYOPIA 6 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1999"	"2016"	"3"	"6"	"CTD_human;UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C1858424"	"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.70"		"1999"	"2016"	"10"	"8"	"CTD_human;ORPHANET;UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C2931111"	"Myopia, susceptibility to"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"9997"	"SCO2"	"0.648"	"0.414"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"9997"	"SCO2"	"0.648"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"0"	"1"	"UNIPROT"
"10000"	"AKT3"	"0.558"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10000"	"AKT3"	"0.558"	"0.621"	"C0431391"	"Hemimegalencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.45"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"10000"	"AKT3"	"0.558"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"UNIPROT"
"10000"	"AKT3"	"0.558"	"0.621"	"C1863924"	"Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"10000"	"AKT3"	"0.558"	"0.621"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2012"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10000"	"AKT3"	"0.558"	"0.621"	"C4014738"	"MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2015"	"4"	"4"	"UNIPROT"
"10002"	"NR2E3"	"0.616"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.48"	"1"	"2007"	"2014"	"0"	"1"	"ORPHANET"
"10002"	"NR2E3"	"0.616"	"0.517"	"C0339541"	"Goldmann-Favre syndrome (disorder)"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.95"	"1"	"2000"	"2014"	"8"	"8"	"CTD_human;ORPHANET;UNIPROT"
"10002"	"NR2E3"	"0.616"	"0.517"	"C1849394"	"Enhanced S-Cone Syndrome"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"1.00"	"0.9545455"	"2000"	"2016"	"8"	"8"	"CTD_human;ORPHANET;UNIPROT"
"10002"	"NR2E3"	"0.616"	"0.517"	"C1970163"	"RETINITIS PIGMENTOSA 37 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"10007"	"GNPDA1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10008"	"KCNE3"	"0.696"	"0.31"	"C0238357"	"Hyperkalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"1992"	"2007"	"0"	"0"	"ORPHANET"
"10008"	"KCNE3"	"0.696"	"0.31"	"C0238358"	"Hypokalemic periodic paralysis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"ORPHANET"
"10008"	"KCNE3"	"0.696"	"0.31"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"10008"	"KCNE3"	"0.696"	"0.31"	"C2751089"	"Brugada Syndrome 6"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10008"	"KCNE3"	"0.696"	"0.31"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10010"	"TANK"	"0.752"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10010"	"TANK"	"0.752"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10010"	"TANK"	"0.752"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10010"	"TANK"	"0.752"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10011"	"SRA1"	"0.621"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2010"	"2012"	"2"	"0"	"PSYGENET"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2005"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"10013"	"HDAC6"	"0.562"	"0.69"	"C3275476"	"CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"1"	"CTD_human;ORPHANET"
"10013"	"HDAC6"	"0.562"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0001546"	"Adjustment Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.50"	"0.5"	"2006"	"2014"	"2"	"0"	"PSYGENET"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0011579"	"Reactive depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2006"	"2014"	"2"	"0"	"PSYGENET"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"10014"	"HDAC5"	"0.636"	"0.552"	"C1522512"	"Transient Situational Disturbance"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C1969342"	"PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C1969343"	"Pulmonary Hypertension, Primary, Fenfluramine-Associated"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10014"	"HDAC5"	"0.636"	"0.552"	"C3714844"	"Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10015"	"PDCD6IP"	"0.752"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10015"	"PDCD6IP"	"0.752"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10016"	"PDCD6"	"0.69"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10016"	"PDCD6"	"0.69"	"0.31"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10018"	"BCL2L11"	"0.55"	"0.621"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10018"	"BCL2L11"	"0.55"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10018"	"BCL2L11"	"0.55"	"0.621"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"0.40"		"2010"	"2010"	"0"	"1"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CGI"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2010"	"0"	"1"	"CTD_human;ORPHANET"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.50"		"2013"	"2017"	"2"	"0"	"CGI;GENOMICS_ENGLAND"
"10019"	"SH2B3"	"0.575"	"0.552"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2018"	"1"	"1"	"CTD_human"
"10019"	"SH2B3"	"0.575"	"0.552"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"10019"	"SH2B3"	"0.575"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10019"	"SH2B3"	"0.575"	"0.552"	"C3489628"	"Thrombocytosis, Autosomal Dominant"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10020"	"GNE"	"0.624"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10020"	"GNE"	"0.624"	"0.517"	"C0238190"	"Inclusion Body Myositis (disorder)"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2015"	"1"	"0"	"CTD_human"
"10020"	"GNE"	"0.624"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10020"	"GNE"	"0.624"	"0.517"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10020"	"GNE"	"0.624"	"0.517"	"C0342853"	"Sialuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1987"	"2017"	"3"	"19"	"CTD_human;ORPHANET;UNIPROT"
"10020"	"GNE"	"0.624"	"0.517"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10020"	"GNE"	"0.624"	"0.517"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"10020"	"GNE"	"0.624"	"0.517"	"C0751713"	"Inclusion Body Myopathy, Sporadic"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"10020"	"GNE"	"0.624"	"0.517"	"C1096902"	"Infantile Sialic Acid Storage Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10020"	"GNE"	"0.624"	"0.517"	"C1096903"	"Sialic Acid Storage Disease, Finnish Type (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2010"	"0"	"0"	"CTD_human"
"10020"	"GNE"	"0.624"	"0.517"	"C1833373"	"Inclusion Body Myopathy, Autosomal Recessive"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2017"	"1"	"38"	"CTD_human;ORPHANET"
"10020"	"GNE"	"0.624"	"0.517"	"C1853926"	"NONAKA MYOPATHY"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"	"0.9677419"	"1993"	"2017"	"12"	"31"	"CTD_human;ORPHANET;UNIPROT"
"10020"	"GNE"	"0.624"	"0.517"	"C2931471"	"Sialuria, French type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"		"1989"	"2001"	"3"	"3"	"ORPHANET;UNIPROT"
"10021"	"HCN4"	"0.69"	"0.172"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2012"	"2018"	"1"	"1"	"CTD_human"
"10021"	"HCN4"	"0.69"	"0.172"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CLINGEN"
"10021"	"HCN4"	"0.69"	"0.172"	"C0037052"	"Sick Sinus Syndrome"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"10021"	"HCN4"	"0.69"	"0.172"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10021"	"HCN4"	"0.69"	"0.172"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10021"	"HCN4"	"0.69"	"0.172"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"10021"	"HCN4"	"0.69"	"0.172"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"10021"	"HCN4"	"0.69"	"0.172"	"C1834144"	"Sick Sinus Syndrome 2, Autosomal Dominant"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.60"		"2003"	"2016"	"4"	"8"	"CTD_human;UNIPROT"
"10021"	"HCN4"	"0.69"	"0.172"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10021"	"HCN4"	"0.69"	"0.172"	"C2751083"	"Brugada Syndrome 8"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.40"		"2014"	"2017"	"0"	"1"	"CTD_human"
"10021"	"HCN4"	"0.69"	"0.172"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10025"	"MED16"	"0.886"	"0.172"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10025"	"MED16"	"0.886"	"0.172"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10036"	"CHAF1A"	"0.652"	"0.483"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10038"	"PARP2"	"0.762"	"0.207"	"C0023787"	"Lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10040"	"TOM1L1"	"0.928"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10040"	"TOM1L1"	"0.928"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10042"	"HMGXB4"	"0.886"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"10042"	"HMGXB4"	"0.886"	"0.103"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"10043"	"TOM1"	"0.785"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"10043"	"TOM1"	"0.785"	"0.276"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"10045"	"SH2D3A"	"0.857"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10046"	"MAMLD1"	"0.752"	"0.276"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2007"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"10046"	"MAMLD1"	"0.752"	"0.276"	"C0848558"	"Hypospadias"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.50"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"10046"	"MAMLD1"	"0.752"	"0.276"	"C1846169"	"Myotubular Myopathy with Abnormal Genital Development"	"disease"	"C05;C10;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10046"	"MAMLD1"	"0.752"	"0.276"	"C2677879"	"Hypospadias 2, X-Linked"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2015"	"0"	"4"	"CTD_human"
"10046"	"MAMLD1"	"0.752"	"0.276"	"C2678098"	"Hypospadias 1, X-Linked"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10047"	"CST8"	"0.928"	"0.069"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10047"	"CST8"	"0.928"	"0.069"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10047"	"CST8"	"0.928"	"0.069"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10048"	"RANBP9"	"0.785"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C3148763"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1999"	"2017"	"2"	"8"	"CTD_human;UNIPROT"
"10049"	"DNAJB6"	"0.685"	"0.448"	"C3501858"	"Muscular Dystrophy, Limb-Girdle, Type 1D"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10052"	"GJC1"	"0.799"	"0.241"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10057"	"ABCC5"	"0.636"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"10057"	"ABCC5"	"0.636"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"10057"	"ABCC5"	"0.636"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10057"	"ABCC5"	"0.636"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10057"	"ABCC5"	"0.636"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2001"	"2018"	"0"	"0"	"UNIPROT"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2012"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0155299"	"Coloboma of optic disc"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0266551"	"Congenital coloboma of iris"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0344516"	"Coloboma of lens"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C0521573"	"Coloboma of eyelid"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1306229"	"Dyschromatosis universalis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1836705"	"Pseudohyperkalemia, Familial, 2, due to Red Cell Leak"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1982"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1852767"	"Hereditary macular coloboma"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C1861453"	"Pseudohyperkalemia Cardiff"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"3"	"UNIPROT"
"10058"	"ABCB6"	"0.487"	"0.828"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10058"	"ABCB6"	"0.487"	"0.828"	"C3281027"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2012"	"1"	"2"	"CTD_human;UNIPROT"
"10058"	"ABCB6"	"0.487"	"0.828"	"C3809394"	"DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"4"	"4"	"CTD_human;UNIPROT"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0001125"	"Acidosis, Lactic"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0029124"	"Optic Atrophy"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0338508"	"Optic Atrophy, Autosomal Dominant"	"disease"	"C10;C11;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10059"	"DNM1L"	"0.57"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"10059"	"DNM1L"	"0.57"	"0.655"	"C1853139"	"OPTIC ATROPHY 5 (disorder)"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10059"	"DNM1L"	"0.57"	"0.655"	"C3280660"	"ENCEPHALOPATHY, LETHAL, DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION"	"disease"		"Disease or Syndrome"	"0.70"		"2007"	"2017"	"4"	"10"	"CTD_human;ORPHANET;UNIPROT"
"10059"	"DNM1L"	"0.57"	"0.655"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2004"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0795905"	"Cantu syndrome"	"disease"	"C05;C14;C16;C17;C23"	"Disease or Syndrome"	"0.78"	"0.75"	"1996"	"2017"	"7"	"9"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"10060"	"ABCC9"	"0.59"	"0.517"	"C0796280"	"Acromegaloid facial appearance syndrome"	"disease"	"C05;C10;C16;C17;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10060"	"ABCC9"	"0.59"	"0.517"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"10060"	"ABCC9"	"0.59"	"0.517"	"C1837839"	"CARDIOMYOPATHY, DILATED, 1O"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2004"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"10060"	"ABCC9"	"0.59"	"0.517"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10060"	"ABCC9"	"0.59"	"0.517"	"C3279695"	"ATRIAL FIBRILLATION, FAMILIAL, 12"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"10060"	"ABCC9"	"0.59"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10061"	"ABCF2"	"0.743"	"0.103"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10062"	"NR1H3"	"0.621"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10063"	"COX17"	"0.815"	"0.103"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10068"	"IL18BP"	"0.663"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10075"	"HUWE1"	"0.681"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10075"	"HUWE1"	"0.681"	"0.552"	"C2678046"	"Mental Retardation, X-Linked, Syndromic, Turner Type"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1994"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"10075"	"HUWE1"	"0.681"	"0.552"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2017"	"15"	"0"	"CLINGEN"
"10075"	"HUWE1"	"0.681"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.48"	"1"	"2008"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"10076"	"PTPRU"	"0.609"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"10082"	"GPC6"	"0.648"	"0.517"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10082"	"GPC6"	"0.648"	"0.517"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10082"	"GPC6"	"0.648"	"0.517"	"C1850318"	"Omodysplasia type 1"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"2009"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"10082"	"GPC6"	"0.648"	"0.517"	"C2936816"	"Micromelic dysplasia, congenital, with dislocation of radius"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10083"	"USH1C"	"0.656"	"0.483"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.48"	"1"	"1993"	"2015"	"0"	"4"	"ORPHANET"
"10083"	"USH1C"	"0.656"	"0.483"	"C1848604"	"USHER SYNDROME, TYPE IC"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2016"	"4"	"7"	"CLINGEN"
"10083"	"USH1C"	"0.656"	"0.483"	"C1865870"	"Deafness, Autosomal Recessive 18"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"0"	"6"	"CTD_human"
"10083"	"USH1C"	"0.656"	"0.483"	"C2931206"	"Usher syndrome, type 1B"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10083"	"USH1C"	"0.656"	"0.483"	"C2931207"	"Usher syndrome, type 1C"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2002"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0018817"	"Atrial Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.55"	"1"	"2004"	"2015"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0031192"	"Persistent Ostium Primum"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0751602"	"Hereditary Autosomal Dominant Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0751603"	"Autosomal Recessive Hereditary Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0751604"	"Hereditary X-Linked Recessive Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0751605"	"X-Linked, Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C0796135"	"Renpenning syndrome 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1962"	"2017"	"8"	"7"	"CTD_human;UNIPROT"
"10084"	"PQBP1"	"0.577"	"0.621"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"1994"	"2013"	"2"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10084"	"PQBP1"	"0.577"	"0.621"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"3"	"0"	"CTD_human"
"10084"	"PQBP1"	"0.577"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1998"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10084"	"PQBP1"	"0.577"	"0.621"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2004"	"2006"	"3"	"0"	"CTD_human"
"10085"	"EDIL3"	"0.619"	"0.517"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10085"	"EDIL3"	"0.619"	"0.517"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10087"	"COL4A3BP"	"0.672"	"0.552"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10087"	"COL4A3BP"	"0.672"	"0.552"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10087"	"COL4A3BP"	"0.672"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10087"	"COL4A3BP"	"0.672"	"0.552"	"C4225156"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 34"	"disease"		"Mental or Behavioral Dysfunction"	"0.50"		"2015"	"2015"	"2"	"0"	"CTD_human;UNIPROT"
"10090"	"UST"	"0.886"	"0.069"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10090"	"UST"	"0.886"	"0.069"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10095"	"ARPC1B"	"0.834"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10095"	"ARPC1B"	"0.834"	"0.069"	"C4540232"	"PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"10097"	"ACTR2"	"0.685"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"10100"	"TSPAN2"	"0.834"	"0.138"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10100"	"TSPAN2"	"0.834"	"0.138"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10102"	"TSFM"	"0.696"	"0.345"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10102"	"TSFM"	"0.696"	"0.345"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10102"	"TSFM"	"0.696"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10102"	"TSFM"	"0.696"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"10102"	"TSFM"	"0.696"	"0.345"	"C1864840"	"Combined Oxidative Phosphorylation Deficiency 3"	"disease"	"C05;C10;C18;C23"	"Disease or Syndrome"	"0.70"		"2006"	"2016"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"10102"	"TSFM"	"0.696"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10105"	"PPIF"	"0.676"	"0.517"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10105"	"PPIF"	"0.676"	"0.517"	"C0041582"	"Ulcer"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10107"	"TRIM10"	"0.857"	"0.138"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10108"	"MKRN3-AS1"	"0.707"	"0.276"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"1999"	"0"	"0"	"CTD_human"
"10108"	"MKRN3-AS1"	"0.707"	"0.276"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10109"	"ARPC2"	"0.834"	"0.172"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"10110"	"SGK2"	"0.815"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10110"	"SGK2"	"0.815"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10111"	"RAD50"	"0.6"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.47"	"1"	"2008"	"2017"	"1"	"4"	"CTD_human"
"10111"	"RAD50"	"0.6"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10111"	"RAD50"	"0.6"	"0.69"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.3333333"	"2004"	"2012"	"4"	"0"	"CLINGEN"
"10111"	"RAD50"	"0.6"	"0.69"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"10111"	"RAD50"	"0.6"	"0.69"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"CLINGEN"
"10111"	"RAD50"	"0.6"	"0.69"	"C2751318"	"Nijmegen Breakage Syndrome-Like Disorder"	"disease"	"C05;C10;C16;C18;C23"	"Disease or Syndrome"	"0.60"		"2004"	"2018"	"0"	"10"	"CTD_human;ORPHANET"
"10111"	"RAD50"	"0.6"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1991"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"10112"	"KIF20A"	"0.727"	"0.172"	"C0007196"	"Restrictive cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10112"	"KIF20A"	"0.727"	"0.172"	"C0348616"	"Other restrictive cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10117"	"ENAM"	"0.707"	"0.241"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.90"	"1"	"1997"	"2017"	"18"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10117"	"ENAM"	"0.707"	"0.241"	"C0399367"	"Amelogenesis imperfecta local hypoplastic form"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.32"	"1"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"10117"	"ENAM"	"0.707"	"0.241"	"C0399368"	"Amelogenesis Imperfecta, Type IB"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.81"	"1"	"2001"	"2017"	"3"	"5"	"CTD_human;UNIPROT"
"10117"	"ENAM"	"0.707"	"0.241"	"C2673923"	"Amelogenesis Imperfecta, Type Ic"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2013"	"2014"	"1"	"2"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10125"	"RASGRP1"	"0.667"	"0.448"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10126"	"DNAL4"	"0.928"	"0.034"	"C4015124"	"MIRROR MOVEMENTS 3"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"10128"	"LRPPRC"	"0.554"	"0.724"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10128"	"LRPPRC"	"0.554"	"0.724"	"C1857355"	"Leigh syndrome , French Canadian type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"2003"	"2016"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"10128"	"LRPPRC"	"0.554"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10129"	"FRY"	"0.707"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10129"	"FRY"	"0.707"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10129"	"FRY"	"0.707"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10129"	"FRY"	"0.707"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10129"	"FRY"	"0.707"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10131"	"TRAP1"	"0.676"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10131"	"TRAP1"	"0.676"	"0.448"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10133"	"OPTN"	"0.572"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.974359"	"2010"	"2018"	"2"	"0"	"CTD_human;ORPHANET"
"10133"	"OPTN"	"0.572"	"0.586"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"2002"	"2015"	"2"	"0"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.48"	"0.875"	"2010"	"2018"	"2"	"2"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"0.9555556"	"1998"	"2017"	"13"	"2"	"CTD_human;UNIPROT"
"10133"	"OPTN"	"0.572"	"0.586"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C1842026"	"GLAUCOMA 1, OPEN ANGLE, E"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2002"	"2015"	"11"	"2"	"UNIPROT"
"10133"	"OPTN"	"0.572"	"0.586"	"C1847730"	"GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"10133"	"OPTN"	"0.572"	"0.586"	"C3150692"	"AMYOTROPHIC LATERAL SCLEROSIS 12"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"10133"	"OPTN"	"0.572"	"0.586"	"C3278152"	"GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2015"	"11"	"2"	"UNIPROT"
"10134"	"BCAP31"	"0.642"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10134"	"BCAP31"	"0.642"	"0.586"	"C1845408"	"Contiguous Abcd1-Dxs1375e Deletion Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"4"	"CTD_human;ORPHANET"
"10134"	"BCAP31"	"0.642"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10134"	"BCAP31"	"0.642"	"0.586"	"C3806634"	"DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9047619"	"2006"	"2016"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10135"	"NAMPT"	"0.564"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2014"	"2014"	"1"	"0"	"CTD_human;UNIPROT"
"10137"	"RBM12"	"0.857"	"0.034"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10137"	"RBM12"	"0.857"	"0.034"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"10137"	"RBM12"	"0.857"	"0.034"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10137"	"RBM12"	"0.857"	"0.034"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10139"	"ARFRP1"	"0.762"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10140"	"TOB1"	"0.701"	"0.379"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10140"	"TOB1"	"0.701"	"0.379"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10140"	"TOB1"	"0.701"	"0.379"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10140"	"TOB1"	"0.701"	"0.379"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2012"	"0"	"0"	"UNIPROT"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2016"	"1"	"2"	"GENOMICS_ENGLAND"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10142"	"AKAP9"	"0.681"	"0.379"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10142"	"AKAP9"	"0.681"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"UNIPROT"
"10142"	"AKAP9"	"0.681"	"0.379"	"C2678483"	"Long Qt Syndrome 11"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.70"		"2002"	"2008"	"2"	"1"	"CLINGEN;CTD_human;UNIPROT"
"10144"	"FAM13A"	"0.701"	"0.172"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.50"	"1"	"2010"	"2017"	"2"	"8"	"CTD_human"
"10144"	"FAM13A"	"0.701"	"0.172"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.41"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"10144"	"FAM13A"	"0.701"	"0.172"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"10144"	"FAM13A"	"0.701"	"0.172"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"10144"	"FAM13A"	"0.701"	"0.172"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"10148"	"EBI3"	"0.529"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"10148"	"EBI3"	"0.529"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10148"	"EBI3"	"0.529"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10149"	"ADGRG2"	"0.785"	"0.069"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10149"	"ADGRG2"	"0.785"	"0.069"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10149"	"ADGRG2"	"0.785"	"0.069"	"C0403814"	"Congenital bilateral aplasia of vas deferens"	"disease"	"C12"	"Congenital Abnormality"	"0.60"		"2017"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"10151"	"HNRNPA3P1"	"0.799"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"10154"	"PLXNC1"	"0.815"	"0.103"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10154"	"PLXNC1"	"0.815"	"0.103"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10157"	"AASS"	"0.713"	"0.345"	"C0268553"	"Hyperlysinemias"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1976"	"2014"	"0"	"7"	"CTD_human;ORPHANET"
"10157"	"AASS"	"0.713"	"0.345"	"C0268555"	"Hyperlysinemia, Periodic"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10157"	"AASS"	"0.713"	"0.345"	"C0268556"	"Saccharopinuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10157"	"AASS"	"0.713"	"0.345"	"C0936256"	"Lysine Alpha-Ketoglutarate Reductase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10157"	"AASS"	"0.713"	"0.345"	"C1527317"	"Alpha-Aminoadipic Semialdehyde Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10157"	"AASS"	"0.713"	"0.345"	"C2936921"	"Saccharopine dehydrogenase deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10157"	"AASS"	"0.713"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1976"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"10158"	"PDZK1IP1"	"0.701"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10158"	"PDZK1IP1"	"0.701"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C1845543"	"Mental Retardation, X-Linked, with Epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10159"	"ATP6AP2"	"0.596"	"0.586"	"C3806722"	"PARKINSONISM WITH SPASTICITY, X-LINKED"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2010"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"10160"	"FARP1"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10160"	"FARP1"	"0.799"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10160"	"FARP1"	"0.799"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10161"	"LPAR6"	"0.701"	"0.276"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.50"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human"
"10161"	"LPAR6"	"0.701"	"0.276"	"C0343073"	"Wooly hair"	"phenotype"		"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"10161"	"LPAR6"	"0.701"	"0.276"	"C0345427"	"Woolly hair, congenital"	"disease"	"C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10161"	"LPAR6"	"0.701"	"0.276"	"C1848435"	"WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2016"	"1"	"6"	"UNIPROT"
"10161"	"LPAR6"	"0.701"	"0.276"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"10161"	"LPAR6"	"0.701"	"0.276"	"C3279470"	"HYPOTRICHOSIS 8"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"3"	"UNIPROT"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.42"	"1"	"2006"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C1853942"	"CITRULLINEMIA, TYPE II, NEONATAL-ONSET"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2017"	"1"	"14"	"CTD_human;ORPHANET;UNIPROT"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C1863844"	"Adult-onset citrullinemia type 2"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2018"	"1"	"8"	"CTD_human;ORPHANET"
"10165"	"SLC25A13"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10166"	"SLC25A15"	"0.735"	"0.241"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.43"	"1"	"1999"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"10166"	"SLC25A15"	"0.735"	"0.241"	"C0268540"	"HHH syndrome"	"disease"	"C10;C16;C18;C23"	"Disease or Syndrome"	"0.80"	"1"	"1988"	"2017"	"8"	"17"	"CTD_human;ORPHANET;UNIPROT"
"10166"	"SLC25A15"	"0.735"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10167"	"CFM1"	"1"		"C1859047"	"CYSTIC FIBROSIS MODIFIER 1"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10167"	"CFM1"	"1"		"C3276246"	"MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"10171"	"RCL1"	"0.928"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10178"	"TENM1"	"0.707"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10178"	"TENM1"	"0.707"	"0.414"	"C0393778"	"Congenital anosmia"	"disease"	"C10;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10178"	"TENM1"	"0.707"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2013"	"0"	"0"	"UNIPROT"
"10178"	"TENM1"	"0.707"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10179"	"RBM7"	"1"	"0.069"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10184"	"LHFPL2"	"0.928"	"0.138"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10186"	"LHFPL6"	"0.834"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10188"	"TNK2"	"0.663"	"0.276"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10188"	"TNK2"	"0.663"	"0.276"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10188"	"TNK2"	"0.663"	"0.276"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"UNIPROT"
"10188"	"TNK2"	"0.663"	"0.276"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10188"	"TNK2"	"0.663"	"0.276"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10188"	"TNK2"	"0.663"	"0.276"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10188"	"TNK2"	"0.663"	"0.276"	"C0346163"	"Endometrioid carcinoma ovary"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2010"	"3"	"1"	"UNIPROT"
"10188"	"TNK2"	"0.663"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10188"	"TNK2"	"0.663"	"0.276"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2010"	"2"	"1"	"UNIPROT"
"10189"	"ALYREF"	"0.785"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10189"	"ALYREF"	"0.785"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10193"	"RNF41"	"0.701"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10193"	"RNF41"	"0.701"	"0.414"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10193"	"RNF41"	"0.701"	"0.414"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10194"	"TSHZ1"	"0.621"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"10194"	"TSHZ1"	"0.621"	"0.552"	"C0495499"	"Congenital absence, atresia and stricture of auditory canal (external)"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10194"	"TSHZ1"	"0.621"	"0.552"	"C1842937"	"AURAL ATRESIA, CONGENITAL"	"disease"	"C16"	"Disease or Syndrome"	"0.43"	"1"	"1992"	"2014"	"0"	"2"	"CTD_human"
"10194"	"TSHZ1"	"0.621"	"0.552"	"C2910118"	"Congenital atresia or stricture of osseous meatus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10195"	"ALG3"	"0.676"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"10195"	"ALG3"	"0.676"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10195"	"ALG3"	"0.676"	"0.345"	"C1832736"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.75"	"1"	"1995"	"2014"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"10195"	"ALG3"	"0.676"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10197"	"PSME3"	"0.663"	"0.517"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10197"	"PSME3"	"0.663"	"0.517"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10202"	"DHRS2"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10203"	"CALCRL"	"0.707"	"0.517"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10204"	"NUTF2"	"0.857"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10204"	"NUTF2"	"0.857"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10207"	"PATJ"	"0.799"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10210"	"TOPORS"	"0.667"	"0.483"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"10210"	"TOPORS"	"0.667"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2017"	"0"	"1"	"ORPHANET"
"10210"	"TOPORS"	"0.667"	"0.483"	"C1835923"	"Retinitis Pigmentosa 31"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10211"	"FLOT1"	"0.727"	"0.414"	"C0034362"	"Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10211"	"FLOT1"	"0.727"	"0.414"	"C0519066"	"Acute Q fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10211"	"FLOT1"	"0.727"	"0.414"	"C1443892"	"Chronic Q Fever"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10211"	"FLOT1"	"0.727"	"0.414"	"C2973787"	"Coxiella burnetii Infection"	"disease"	"C01"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10215"	"OLIG2"	"0.621"	"0.379"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10215"	"OLIG2"	"0.621"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.6"	"2006"	"2016"	"5"	"0"	"PSYGENET"
"10215"	"OLIG2"	"0.621"	"0.379"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10216"	"PRG4"	"0.676"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"10216"	"PRG4"	"0.676"	"0.345"	"C0009917"	"Contracture"	"group"	"C05"	"Anatomical Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10216"	"PRG4"	"0.676"	"0.345"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10216"	"PRG4"	"0.676"	"0.345"	"C0031046"	"Pericarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10216"	"PRG4"	"0.676"	"0.345"	"C1167732"	"Pleuropericarditis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10216"	"PRG4"	"0.676"	"0.345"	"C1859690"	"CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9"	"1999"	"2015"	"1"	"1"	"CTD_human;ORPHANET"
"10220"	"GDF11"	"0.773"	"0.241"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10221"	"TRIB1"	"0.659"	"0.379"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"10221"	"TRIB1"	"0.659"	"0.379"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10221"	"TRIB1"	"0.659"	"0.379"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"10225"	"CD96"	"0.616"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10225"	"CD96"	"0.616"	"0.621"	"C0796095"	"Opitz trigonocephaly syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.71"	"1"	"2007"	"2007"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10225"	"CD96"	"0.616"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"10226"	"PLIN3"	"0.815"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10228"	"STX6"	"0.886"	"0.172"	"C0038868"	"Progressive supranuclear palsy"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2013"	"1"	"1"	"CTD_human"
"10228"	"STX6"	"0.886"	"0.172"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10229"	"COQ7"	"0.752"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10229"	"COQ7"	"0.752"	"0.345"	"C4225226"	"COENZYME Q10 DEFICIENCY, PRIMARY, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"10232"	"MSLN"	"0.565"	"0.483"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9642857"	"1997"	"2017"	"3"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0206687"	"Carcinoma, Endometrioid"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"0.8333333"	"2000"	"2016"	"2"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9444444"	"2002"	"2016"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"		"2003"	"2015"	"3"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"1996"	"2016"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C1569637"	"Adenocarcinoma, Endometrioid"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C3714739"	"Mesothelial Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2012"	"2"	"0"	"CTD_human"
"10232"	"MSLN"	"0.565"	"0.483"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10235"	"RASGRP2"	"0.886"	"0.034"	"C4014584"	"BLEEDING DISORDER, PLATELET-TYPE, 18"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2018"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10236"	"HNRNPR"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10236"	"HNRNPR"	"0.886"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10236"	"HNRNPR"	"0.886"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10236"	"HNRNPR"	"0.886"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10238"	"DCAF7"	"0.667"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10238"	"DCAF7"	"0.667"	"0.517"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10239"	"AP3S2"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2017"	"1"	"1"	"CTD_human"
"10241"	"CALCOCO2"	"0.785"	"0.207"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10241"	"CALCOCO2"	"0.785"	"0.207"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10241"	"CALCOCO2"	"0.785"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"10243"	"GPHN"	"0.663"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10243"	"GPHN"	"0.663"	"0.379"	"C1835614"	"Hereditary Hyperexplexia"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10243"	"GPHN"	"0.663"	"0.379"	"C1854990"	"Molybdenum Cofactor Deficiency, Complementation Group C"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2001"	"2016"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10243"	"GPHN"	"0.663"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10246"	"SLC17A2"	"0.857"	"0.069"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10246"	"SLC17A2"	"0.857"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10246"	"SLC17A2"	"0.857"	"0.069"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10249"	"GLYAT"	"0.685"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10251"	"SPRY3"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10252"	"SPRY1"	"0.659"	"0.448"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"0"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10253"	"SPRY2"	"0.604"	"0.517"	"C4225194"	"IgA NEPHROPATHY, SUSCEPTIBILITY TO, 3"	"phenotype"		"Finding"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"10255"	"HCG9"	"0.743"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2016"	"2"	"0"	"PSYGENET"
"10256"	"CNKSR1"	"0.696"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10256"	"CNKSR1"	"0.696"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10256"	"CNKSR1"	"0.696"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10256"	"CNKSR1"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"10257"	"ABCC4"	"0.565"	"0.69"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10261"	"IGSF6"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10261"	"IGSF6"	"0.928"	"0.103"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10262"	"SF3B4"	"0.607"	"0.552"	"C0265245"	"Nager syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.67"	"1"	"2012"	"2016"	"0"	"23"	"CTD_human;ORPHANET"
"10262"	"SF3B4"	"0.607"	"0.552"	"C1860119"	"Acrofacial dysostosis Rodriguez type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10262"	"SF3B4"	"0.607"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10262"	"SF3B4"	"0.607"	"0.552"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10263"	"CDK2AP2"	"0.681"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10263"	"CDK2AP2"	"0.681"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"10265"	"IRX5"	"0.642"	"0.586"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0018784"	"Sensorineural Hearing Loss (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0022904"	"Lacrimal Apparatus Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0152227"	"Excessive tearing"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0271901"	"Microcytic hypochromic anemia (disorder)"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C0399352"	"Developmental absence of tooth"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C1691779"	"Sensory hearing loss"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C1876203"	"Frontonasal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C1970027"	"Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"2007"	"2012"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10265"	"IRX5"	"0.642"	"0.586"	"C3489529"	"Tooth Agenesis, Familial"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10265"	"IRX5"	"0.642"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2006"	"2015"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10266"	"RAMP2"	"0.663"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"10267"	"RAMP1"	"0.707"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0023787"	"Lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0024689"	"Mandibular Diseases"	"group"	"C05;C07"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0033300"	"Progeria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"0.9666667"	"2002"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0406585"	"Lethal tight skin contracture syndrome (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.60"		"1985"	"2015"	"0"	"8"	"CTD_human;ORPHANET"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C0917990"	"Acro-Osteolysis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2010"	"2"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C1136321"	"HIV-Associated Lipodystrophy Syndrome"	"disease"	"C02;C17;C18;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C1837756"	"MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY"	"disease"	"C05;C16;C17;C18"	"Disease or Syndrome"	"0.70"		"1985"	"2012"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"10269"	"ZMPSTE24"	"0.527"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10270"	"AKAP8"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10270"	"AKAP8"	"0.886"	"0.103"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10270"	"AKAP8"	"0.886"	"0.103"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10273"	"STUB1"	"0.619"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10273"	"STUB1"	"0.619"	"0.483"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10273"	"STUB1"	"0.619"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10273"	"STUB1"	"0.619"	"0.483"	"C4014261"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16"	"disease"		"Disease or Syndrome"	"0.81"	"1"	"2003"	"2018"	"5"	"11"	"ORPHANET;UNIPROT"
"10274"	"STAG1"	"0.701"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10274"	"STAG1"	"0.701"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10274"	"STAG1"	"0.701"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10274"	"STAG1"	"0.701"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10274"	"STAG1"	"0.701"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10274"	"STAG1"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2015"	"2018"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10274"	"STAG1"	"0.701"	"0.448"	"C4539951"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 47"	"disease"		"Mental or Behavioral Dysfunction"	"0.50"		"2018"	"2018"	"1"	"1"	"ORPHANET;UNIPROT"
"10276"	"NET1"	"0.713"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2012"	"0"	"0"	"UNIPROT"
"10277"	"UBE4B"	"0.834"	"0.207"	"C0043020"	"Wallerian Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10277"	"UBE4B"	"0.834"	"0.207"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10277"	"UBE4B"	"0.834"	"0.207"	"C0876926"	"Traumatic Brain Injury"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10278"	"EFS"	"0.681"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10279"	"PRSS16"	"0.886"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.49"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0033054"	"Prenatal Exposure Delayed Effects"	"disease"	"C13"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2000"	"2012"	"4"	"0"	"PSYGENET"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2017"	"1"	"0"	"PSYGENET"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2006"	"2"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2010"	"2014"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"2015"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C3280587"	"AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C3468114"	"Juvenile amyotrophic lateral sclerosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10280"	"SIGMAR1"	"0.565"	"0.517"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10283"	"CWC27"	"0.727"	"0.379"	"C1855188"	"Metaphyseal Chondrodysplasia with Retinitis Pigmentosa"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"10283"	"CWC27"	"0.727"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10286"	"BCAS2"	"0.834"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10290"	"SPEG"	"0.707"	"0.276"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2018"	"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10290"	"SPEG"	"0.707"	"0.276"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"10290"	"SPEG"	"0.707"	"0.276"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C0410204"	"Myopathy, Centronuclear, Autosomal Recessive"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10290"	"SPEG"	"0.707"	"0.276"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"10290"	"SPEG"	"0.707"	"0.276"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10290"	"SPEG"	"0.707"	"0.276"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10290"	"SPEG"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10290"	"SPEG"	"0.707"	"0.276"	"C4014814"	"MYOPATHY, CENTRONUCLEAR, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"5"	"UNIPROT"
"10291"	"SF3A1"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"1"	"UNIPROT"
"10293"	"TRAIP"	"0.663"	"0.517"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10293"	"TRAIP"	"0.663"	"0.517"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"10293"	"TRAIP"	"0.663"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10293"	"TRAIP"	"0.663"	"0.517"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10293"	"TRAIP"	"0.663"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10293"	"TRAIP"	"0.663"	"0.517"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10293"	"TRAIP"	"0.663"	"0.517"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10293"	"TRAIP"	"0.663"	"0.517"	"C4225212"	"SECKEL SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"10295"	"BCKDK"	"0.834"	"0.172"	"C3554078"	"BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.90"		"2006"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10295"	"BCKDK"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"10296"	"MAEA"	"0.928"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.42"	"0.5"	"2012"	"2017"	"1"	"7"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human;UNIPROT"
"10297"	"APC2"	"0.633"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C0175695"	"Sotos' syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10297"	"APC2"	"0.633"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10297"	"APC2"	"0.633"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"3"	"0"	"CTD_human"
"10300"	"KATNB1"	"0.701"	"0.379"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10300"	"KATNB1"	"0.701"	"0.379"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10300"	"KATNB1"	"0.701"	"0.379"	"C4015525"	"LISSENCEPHALY 6 WITH MICROCEPHALY"	"disease"		"Congenital Abnormality"	"0.60"		"2015"	"2015"	"2"	"6"	"CTD_human;UNIPROT"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10308"	"ZNF267"	"0.773"	"0.172"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10309"	"CCNO"	"0.743"	"0.31"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2015"	"0"	"7"	"ORPHANET"
"10309"	"CCNO"	"0.743"	"0.31"	"C0600260"	"Lung Diseases, Obstructive"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10309"	"CCNO"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10309"	"CCNO"	"0.743"	"0.31"	"C4014534"	"CILIARY DYSKINESIA, PRIMARY, 29"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2016"	"2"	"8"	"CTD_human;UNIPROT"
"10309"	"CCNO"	"0.743"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10309"	"CCNO"	"0.743"	"0.31"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10312"	"TCIRG1"	"0.63"	"0.586"	"C0432261"	"Osteopetrosis - intermediate type"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10312"	"TCIRG1"	"0.63"	"0.586"	"C1318518"	"Infantile malignant osteopetrosis"	"disease"		"Congenital Abnormality"	"0.37"	"1"	"2000"	"2016"	"0"	"0"	"ORPHANET"
"10312"	"TCIRG1"	"0.63"	"0.586"	"C1850127"	"Osteopetrosis, Autosomal Recessive 1"	"disease"	"C05"	"Disease or Syndrome"	"0.80"		"1985"	"2016"	"2"	"8"	"CTD_human;UNIPROT"
"10312"	"TCIRG1"	"0.63"	"0.586"	"C1859966"	"Neutropenia, Severe Congenital, Autosomal Dominant 1"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"10312"	"TCIRG1"	"0.63"	"0.586"	"C1969093"	"Osteopetrosis, Autosomal Recessive 6"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2014"	"1"	"1"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.9285714"	"2009"	"2018"	"2"	"4"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2009"	"2016"	"2"	"1"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.43"	"1"	"2012"	"2014"	"1"	"2"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"1"	"CTD_human"
"10318"	"TNIP1"	"0.633"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10319"	"LAMC3"	"0.773"	"0.276"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10319"	"LAMC3"	"0.773"	"0.276"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10319"	"LAMC3"	"0.773"	"0.276"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10319"	"LAMC3"	"0.773"	"0.276"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10319"	"LAMC3"	"0.773"	"0.276"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"2"	"CTD_human"
"10319"	"LAMC3"	"0.773"	"0.276"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2017"	"2"	"0"	"CTD_human"
"10319"	"LAMC3"	"0.773"	"0.276"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"10319"	"LAMC3"	"0.773"	"0.276"	"C3279875"	"CORTICAL MALFORMATIONS, OCCIPITAL"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10319"	"LAMC3"	"0.773"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9565217"	"2000"	"2018"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.38"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2008"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2018"	"0"	"0"	"CGI"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10320"	"IKZF1"	"0.575"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.37"	"1"	"2002"	"2017"	"0"	"1"	"ORPHANET"
"10320"	"IKZF1"	"0.575"	"0.621"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"	"1"	"2002"	"2018"	"1"	"6"	"CGI;CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10320"	"IKZF1"	"0.575"	"0.621"	"C4225173"	"IMMUNODEFICIENCY, COMMON VARIABLE, 13"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"2"	"5"	"ORPHANET;UNIPROT"
"10321"	"CRISP3"	"0.773"	"0.379"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10321"	"CRISP3"	"0.773"	"0.379"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10321"	"CRISP3"	"0.773"	"0.379"	"C0032987"	"Ectopic Pregnancy"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10324"	"KLHL41"	"0.857"	"0.103"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10324"	"KLHL41"	"0.857"	"0.103"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.61"	"1"	"2014"	"2015"	"0"	"1"	"ORPHANET"
"10324"	"KLHL41"	"0.857"	"0.103"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10324"	"KLHL41"	"0.857"	"0.103"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10324"	"KLHL41"	"0.857"	"0.103"	"C3810384"	"NEMALINE MYOPATHY 9"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"10326"	"SIRPB1"	"0.928"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2015"	"2"	"0"	"PSYGENET"
"10327"	"AKR1A1"	"0.538"	"0.759"	"C0001969"	"Alcoholic Intoxication"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1980"	"2012"	"5"	"0"	"PSYGENET"
"10327"	"AKR1A1"	"0.538"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1993"	"2016"	"5"	"0"	"PSYGENET"
"10327"	"AKR1A1"	"0.538"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10327"	"AKR1A1"	"0.538"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1992"	"2012"	"5"	"0"	"PSYGENET"
"10327"	"AKR1A1"	"0.538"	"0.759"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10329"	"RXYLT1"	"0.633"	"0.414"	"C3554381"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"4"	"7"	"UNIPROT"
"10330"	"CNPY2"	"0.799"	"0.138"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10330"	"CNPY2"	"0.799"	"0.138"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10330"	"CNPY2"	"0.799"	"0.138"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10330"	"CNPY2"	"0.799"	"0.138"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10333"	"TLR6"	"0.611"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2008"	"1"	"0"	"CTD_human"
"10333"	"TLR6"	"0.611"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"0.8"	"2005"	"2010"	"1"	"0"	"CTD_human"
"10342"	"TFG"	"0.633"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"10342"	"TFG"	"0.633"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"10342"	"TFG"	"0.633"	"0.448"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2010"	"0"	"0"	"ORPHANET"
"10342"	"TFG"	"0.633"	"0.448"	"C1275278"	"Extraskeletal Myxoid Chondrosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"10342"	"TFG"	"0.633"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10342"	"TFG"	"0.633"	"0.448"	"C1858338"	"Neuropathy, hereditary motor and sensory, Okinawa type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2012"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10342"	"TFG"	"0.633"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10342"	"TFG"	"0.633"	"0.448"	"C3714897"	"SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10343"	"PKDREJ"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10345"	"TRDN"	"0.713"	"0.414"	"C0035828"	"Romano-Ward Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10345"	"TRDN"	"0.713"	"0.414"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.72"	"1"	"2012"	"2017"	"0"	"6"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"10345"	"TRDN"	"0.713"	"0.414"	"C3809536"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"10346"	"TRIM22"	"0.815"	"0.241"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"1"	"2011"	"2018"	"2"	"4"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"		"2011"	"2015"	"2"	"0"	"CTD_human;ORPHANET"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9090909"	"2011"	"2018"	"2"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2018"	"2"	"0"	"CTD_human"
"10347"	"ABCA7"	"0.69"	"0.379"	"C1837149"	"Alzheimer Disease 9"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"		"2015"	"2016"	"0"	"2"	"CTD_human"
"10349"	"ABCA10"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10349"	"ABCA10"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10349"	"ABCA10"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10350"	"ABCA9"	"0.857"	"0.138"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10350"	"ABCA9"	"0.857"	"0.138"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10350"	"ABCA9"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10351"	"ABCA8"	"0.785"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10351"	"ABCA8"	"0.785"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10351"	"ABCA8"	"0.785"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10352"	"WARS2"	"0.743"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10352"	"WARS2"	"0.743"	"0.414"	"C4540192"	"NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2018"	"3"	"5"	"UNIPROT"
"10360"	"NPM3"	"0.928"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10363"	"HMG20A"	"0.928"	"0.103"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.45"	"1"	"2011"	"2017"	"1"	"2"	"CTD_human"
"10365"	"KLF2"	"0.602"	"0.586"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10367"	"MICU1"	"0.713"	"0.31"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10367"	"MICU1"	"0.713"	"0.31"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10367"	"MICU1"	"0.713"	"0.31"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10367"	"MICU1"	"0.713"	"0.31"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10367"	"MICU1"	"0.713"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10367"	"MICU1"	"0.713"	"0.31"	"C3810285"	"MYOPATHY WITH EXTRAPYRAMIDAL SIGNS"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2018"	"0"	"4"	"CTD_human;ORPHANET"
"10369"	"CACNG2"	"0.799"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.6666667"	"2008"	"2013"	"3"	"0"	"PSYGENET"
"10369"	"CACNG2"	"0.799"	"0.103"	"C3280284"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 10"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;UNIPROT"
"10369"	"CACNG2"	"0.799"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"10370"	"CITED2"	"0.616"	"0.448"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0018816"	"Heart Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0018818"	"Ventricular Septal Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10370"	"CITED2"	"0.616"	"0.448"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"		"2002"	"2002"	"0"	"0"	"ORPHANET"
"10370"	"CITED2"	"0.616"	"0.448"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10370"	"CITED2"	"0.616"	"0.448"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10370"	"CITED2"	"0.616"	"0.448"	"C0344730"	"Atrial Septal Defect Sinus Venosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10370"	"CITED2"	"0.616"	"0.448"	"C3280790"	"ATRIAL SEPTAL DEFECT 8"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"10371"	"SEMA3A"	"0.604"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10371"	"SEMA3A"	"0.604"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2003"	"2008"	"3"	"0"	"PSYGENET"
"10371"	"SEMA3A"	"0.604"	"0.655"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"10371"	"SEMA3A"	"0.604"	"0.655"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"10371"	"SEMA3A"	"0.604"	"0.655"	"C3554021"	"HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2015"	"3"	"10"	"CTD_human;UNIPROT"
"10376"	"TUBA1B"	"0.642"	"0.586"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10376"	"TUBA1B"	"0.642"	"0.586"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10376"	"TUBA1B"	"0.642"	"0.586"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10376"	"TUBA1B"	"0.642"	"0.586"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"		"2005"	"2008"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C1302995"	"Congenital Fibrosis of the Extraocular Muscles"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.50"	"0.9090909"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"10381"	"TUBB3"	"0.569"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"10381"	"TUBB3"	"0.569"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C2748801"	"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.80"		"1990"	"2017"	"1"	"8"	"CTD_human;UNIPROT"
"10381"	"TUBB3"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10381"	"TUBB3"	"0.569"	"0.655"	"C3808397"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C1851943"	"DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1985"	"2018"	"1"	"2"	"ORPHANET;UNIPROT"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C1860315"	"Whispering dysphonia, hereditary"	"disease"	"C08;C09;C10;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C2676244"	"Leukodystrophy, Hypomyelinating, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"28"	"ORPHANET;UNIPROT"
"10382"	"TUBB4A"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10389"	"SCML2"	"0.815"	"0.034"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10389"	"SCML2"	"0.815"	"0.034"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10389"	"SCML2"	"0.815"	"0.034"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10389"	"SCML2"	"0.815"	"0.034"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10389"	"SCML2"	"0.815"	"0.034"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10389"	"SCML2"	"0.815"	"0.034"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10391"	"CORO2B"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10392"	"NOD1"	"0.598"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2003"	"2016"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.41"		"2003"	"2016"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10395"	"DLC1"	"0.573"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"10395"	"DLC1"	"0.573"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2004"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"		"2003"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"2"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0029295"	"Oropharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2007"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0206658"	"Smooth Muscle Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0206734"	"Hemangioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0751692"	"Multiple Hemangioblastomas"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C1832334"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.86"	"1"	"1993"	"2018"	"0"	"1"	"CTD_human;ORPHANET"
"10397"	"NDRG1"	"0.521"	"0.655"	"C2349952"	"Oropharyngeal Carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10397"	"NDRG1"	"0.521"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10398"	"MYL9"	"0.752"	"0.31"	"C0006114"	"Cerebral Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0472387"	"Vasogenic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0472388"	"Cytotoxic Cerebral Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0750969"	"Vasogenic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C0750970"	"Cytotoxic Brain Edema"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10398"	"MYL9"	"0.752"	"0.31"	"C1527311"	"Brain Edema"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10399"	"RACK1"	"0.611"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"10399"	"RACK1"	"0.611"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"10399"	"RACK1"	"0.611"	"0.552"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"10399"	"RACK1"	"0.611"	"0.552"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10399"	"RACK1"	"0.611"	"0.552"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10400"	"PEMT"	"0.69"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2009"	"2"	"0"	"PSYGENET"
"10401"	"PIAS3"	"0.636"	"0.448"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10401"	"PIAS3"	"0.636"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10401"	"PIAS3"	"0.636"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10401"	"PIAS3"	"0.636"	"0.448"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10404"	"CPQ"	"0.652"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10406"	"WFDC2"	"0.773"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10409"	"BASP1"	"0.785"	"0.241"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10410"	"IFITM3"	"0.727"	"0.379"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.50"	"0.9411765"	"2011"	"2017"	"1"	"1"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0035585"	"Rickettsia Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0162699"	"Tick-Borne Infections"	"disease"	"C01;C02;C03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0162700"	"Tick-Borne Diseases"	"group"	"C01;C02;C03"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10411"	"RAPGEF3"	"0.663"	"0.586"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10412"	"NSA2"	"0.799"	"0.172"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10412"	"NSA2"	"0.799"	"0.172"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10412"	"NSA2"	"0.799"	"0.172"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2014"	"2017"	"3"	"1"	"GENOMICS_ENGLAND"
"10413"	"YAP1"	"0.514"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"0.875"	"2013"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0206732"	"Epithelioid hemangioendothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2013"	"2017"	"0"	"0"	"ORPHANET"
"10413"	"YAP1"	"0.514"	"0.655"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C0795902"	"Coloboma, cleft lip-palate and mental retardation syndrome"	"disease"	"C05;C07;C09;C10;C11;C12;C13;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10413"	"YAP1"	"0.514"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10413"	"YAP1"	"0.514"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10413"	"YAP1"	"0.514"	"0.655"	"C3805432"	"COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10417"	"SPON2"	"0.785"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10417"	"SPON2"	"0.785"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10420"	"TESK2"	"0.928"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10420"	"TESK2"	"0.928"	"0.138"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10426"	"TUBGCP3"	"0.834"	"0.207"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10436"	"EMG1"	"0.743"	"0.517"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10436"	"EMG1"	"0.743"	"0.517"	"C1859405"	"Bowen-Conradi syndrome"	"disease"	"C10;C13;C16;C23;F01"	"Disease or Syndrome"	"0.95"	"1"	"2009"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10436"	"EMG1"	"0.743"	"0.517"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10437"	"IFI30"	"0.72"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10437"	"IFI30"	"0.72"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10437"	"IFI30"	"0.72"	"0.345"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10437"	"IFI30"	"0.72"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10438"	"C1D"	"0.773"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10439"	"OLFM1"	"0.785"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10439"	"OLFM1"	"0.785"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10443"	"N4BP2L2"	"0.773"	"0.207"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10445"	"MCRS1"	"0.735"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"1"	"UNIPROT"
"10449"	"ACAA2"	"0.815"	"0.207"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10449"	"ACAA2"	"0.815"	"0.207"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10449"	"ACAA2"	"0.815"	"0.207"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"1"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0020578"	"Hyperventilation"	"phenotype"	"C08;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2006"	"2007"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10451"	"VAV3"	"0.633"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"10452"	"TOMM40"	"0.636"	"0.483"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10452"	"TOMM40"	"0.636"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"10452"	"TOMM40"	"0.636"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10452"	"TOMM40"	"0.636"	"0.483"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"10452"	"TOMM40"	"0.636"	"0.483"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10452"	"TOMM40"	"0.636"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"10454"	"TAB1"	"0.785"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10454"	"TAB1"	"0.785"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10456"	"HAX1"	"0.667"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"2009"	"4"	"0"	"GENOMICS_ENGLAND"
"10456"	"HAX1"	"0.667"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"2009"	"4"	"0"	"GENOMICS_ENGLAND"
"10456"	"HAX1"	"0.667"	"0.345"	"C0340970"	"Congenital neutropenia"	"disease"	"C15"	"Congenital Abnormality"	"0.40"	"1"	"2007"	"2016"	"0"	"0"	"CTD_human"
"10456"	"HAX1"	"0.667"	"0.345"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10456"	"HAX1"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"10456"	"HAX1"	"0.667"	"0.345"	"C1853118"	"Severe congenital neutropenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.70"	"1"	"2007"	"2016"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10456"	"HAX1"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.59"	"1"	"2006"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1989"	"2016"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10457"	"GPNMB"	"0.55"	"0.586"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10459"	"MAD2L2"	"0.69"	"0.517"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10459"	"MAD2L2"	"0.69"	"0.517"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10459"	"MAD2L2"	"0.69"	"0.517"	"C4310652"	"FANCONI ANEMIA, COMPLEMENTATION GROUP V"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"10460"	"TACC3"	"0.707"	"0.345"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"10460"	"TACC3"	"0.707"	"0.345"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"10460"	"TACC3"	"0.707"	"0.345"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10460"	"TACC3"	"0.707"	"0.345"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"10460"	"TACC3"	"0.707"	"0.345"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"10461"	"MERTK"	"0.557"	"0.69"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"2000"	"2017"	"1"	"4"	"CTD_human;ORPHANET"
"10461"	"MERTK"	"0.557"	"0.69"	"C0040038"	"Thromboembolism"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"10461"	"MERTK"	"0.557"	"0.69"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"10461"	"MERTK"	"0.557"	"0.69"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10461"	"MERTK"	"0.557"	"0.69"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"10461"	"MERTK"	"0.557"	"0.69"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"10461"	"MERTK"	"0.557"	"0.69"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10461"	"MERTK"	"0.557"	"0.69"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10461"	"MERTK"	"0.557"	"0.69"	"C3151228"	"RETINITIS PIGMENTOSA 38 (disorder)"	"disease"		"Disease or Syndrome"	"0.60"		"2000"	"2015"	"1"	"9"	"CTD_human;UNIPROT"
"10462"	"CLEC10A"	"0.685"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"PSYGENET"
"10462"	"CLEC10A"	"0.685"	"0.448"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10463"	"SLC30A9"	"1"		"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10463"	"SLC30A9"	"1"		"C4539828"	"BIRK-LANDAU-PEREZ SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"ORPHANET"
"10464"	"PIBF1"	"0.752"	"0.414"	"C0000821"	"Threatened abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10464"	"PIBF1"	"0.752"	"0.414"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"ORPHANET"
"10466"	"COG5"	"0.752"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"10466"	"COG5"	"0.752"	"0.241"	"C0014378"	"Enterovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10466"	"COG5"	"0.752"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"10466"	"COG5"	"0.752"	"0.241"	"C3150876"	"COG5 congenital disorder of glycosylation"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"10466"	"COG5"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"10467"	"ZNHIT1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10468"	"FST"	"0.551"	"0.655"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1995"	"2002"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0162557"	"Liver Failure, Acute"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10468"	"FST"	"0.551"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"1995"	"2017"	"2"	"0"	"CTD_human"
"10469"	"TIMM44"	"0.785"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10472"	"ZBTB18"	"0.611"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10472"	"ZBTB18"	"0.611"	"0.345"	"C2676727"	"Chromosome 1q43-Q44 Deletion Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2015"	"2017"	"0"	"9"	"CTD_human"
"10472"	"ZBTB18"	"0.611"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"10472"	"ZBTB18"	"0.611"	"0.345"	"C3808184"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 22"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human"
"10472"	"ZBTB18"	"0.611"	"0.345"	"C4273897"	"Distal monosomy 1q"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10476"	"ATP5PD"	"0.857"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10476"	"ATP5PD"	"0.857"	"0.172"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C1846130"	"Mental retardation X-linked, South African type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"0"	"0"	"ORPHANET"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C2678194"	"Mental Retardation, X-Linked, Syndromic, Christianson Type"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.65"	"1"	"1999"	"2015"	"0"	"11"	"CTD_human;ORPHANET"
"10479"	"SLC9A6"	"0.559"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10480"	"EIF3M"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9230769"	"2004"	"2016"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2017"	"4"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"0.9761905"	"2004"	"2018"	"10"	"1"	"CTD_human;UNIPROT"
"10481"	"HOXB13"	"0.656"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9285714"	"2004"	"2016"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"		"2006"	"2014"	"1"	"0"	"CTD_human"
"10481"	"HOXB13"	"0.656"	"0.276"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.69"	"1"	"2012"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0002876"	"Congenital dyserythropoietic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.38"	"1"	"1983"	"2017"	"1"	"0"	"CTD_human"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0271933"	"Congenital dyserythropoietic anemia, type I"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0271934"	"Congenital dyserythropoietic anemia, type III"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10483"	"SEC23B"	"0.596"	"0.517"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"10483"	"SEC23B"	"0.596"	"0.517"	"C1306589"	"Congenital dyserythropoietic anemia, type II"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.80"	"1"	"1986"	"2014"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"10483"	"SEC23B"	"0.596"	"0.517"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10483"	"SEC23B"	"0.596"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10483"	"SEC23B"	"0.596"	"0.517"	"C4225179"	"COWDEN SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"10484"	"SEC23A"	"0.696"	"0.345"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10484"	"SEC23A"	"0.696"	"0.345"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"0"	"2006"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10484"	"SEC23A"	"0.696"	"0.345"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10484"	"SEC23A"	"0.696"	"0.345"	"C1843042"	"Craniolenticulosutural Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"2006"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10487"	"CAP1"	"0.611"	"0.724"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10487"	"CAP1"	"0.611"	"0.724"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10487"	"CAP1"	"0.611"	"0.724"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10487"	"CAP1"	"0.611"	"0.724"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10487"	"CAP1"	"0.611"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0023931"	"Lobstein Disease"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.80"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0268358"	"Osteogenesis imperfecta, dominant perinatal lethal"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10491"	"CRTAP"	"0.652"	"0.552"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10491"	"CRTAP"	"0.652"	"0.552"	"C1853162"	"Osteogenesis Imperfecta Type VII"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2006"	"2017"	"4"	"10"	"UNIPROT"
"10491"	"CRTAP"	"0.652"	"0.552"	"C2931095"	"Osteogenesis imperfecta, type 7"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10492"	"SYNCRIP"	"0.799"	"0.172"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10492"	"SYNCRIP"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"10495"	"ENOX2"	"0.785"	"0.172"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10495"	"ENOX2"	"0.785"	"0.172"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10495"	"ENOX2"	"0.785"	"0.172"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10495"	"ENOX2"	"0.785"	"0.172"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10495"	"ENOX2"	"0.785"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10497"	"UNC13B"	"0.799"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10498"	"CARM1"	"0.659"	"0.448"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10498"	"CARM1"	"0.659"	"0.448"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2003"	"2004"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10499"	"NCOA2"	"0.611"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"10505"	"SEMA4F"	"0.886"	"0.103"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10512"	"SEMA3C"	"0.667"	"0.448"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"10512"	"SEMA3C"	"0.667"	"0.448"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10512"	"SEMA3C"	"0.667"	"0.448"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10514"	"MYBBP1A"	"0.743"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10514"	"MYBBP1A"	"0.743"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0013990"	"Pathological accumulation of air in tissues"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0035243"	"Respiratory Tract Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0041912"	"Upper Respiratory Infections"	"group"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0268350"	"Cutis Laxa, Autosomal Dominant"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0268351"	"Cutis Laxa, Autosomal Recessive, Type I"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.65"	"1"	"2003"	"2010"	"7"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C0432336"	"Cutis laxa, recessive, type I"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"10516"	"FBLN5"	"0.57"	"0.586"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C1837187"	"MACULAR DEGENERATION, AGE-RELATED, 3"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2004"	"2015"	"6"	"11"	"CTD_human;UNIPROT"
"10516"	"FBLN5"	"0.57"	"0.586"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C2931134"	"Cutis laxa, recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"10516"	"FBLN5"	"0.57"	"0.586"	"C3665335"	"Cutis laxa, autosomal recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2003"	"2010"	"7"	"3"	"CTD_human;UNIPROT"
"10516"	"FBLN5"	"0.57"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10516"	"FBLN5"	"0.57"	"0.586"	"C4225406"	"NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2013"	"6"	"11"	"UNIPROT"
"10518"	"CIB2"	"0.567"	"0.724"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1993"	"2016"	"0"	"1"	"ORPHANET"
"10518"	"CIB2"	"0.567"	"0.724"	"C1836199"	"DEAFNESS, AUTOSOMAL RECESSIVE 48"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2016"	"3"	"5"	"CTD_human;UNIPROT"
"10518"	"CIB2"	"0.567"	"0.724"	"C3553944"	"USHER SYNDROME, TYPE IJ"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"10518"	"CIB2"	"0.567"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2016"	"4"	"0"	"PSYGENET"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2016"	"4"	"0"	"PSYGENET"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2012"	"5"	"0"	"PSYGENET"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0795864"	"Smith-Magenis syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10522"	"DEAF1"	"0.6"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10522"	"DEAF1"	"0.6"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2012"	"5"	"0"	"PSYGENET"
"10522"	"DEAF1"	"0.6"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.66"	"0.8333333"	"2010"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10522"	"DEAF1"	"0.6"	"0.552"	"C4014414"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 24"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2018"	"2"	"6"	"CTD_human;UNIPROT"
"10522"	"DEAF1"	"0.6"	"0.552"	"C4310683"	"DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2018"	"0"	"2"	"CTD_human;ORPHANET"
"10524"	"KAT5"	"0.573"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10524"	"KAT5"	"0.573"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10525"	"HYOU1"	"0.701"	"0.379"	"C1846707"	"SPINOCEREBELLAR ATAXIA 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10527"	"IPO7"	"0.799"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"10527"	"IPO7"	"0.799"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10528"	"NOP56"	"0.696"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10528"	"NOP56"	"0.696"	"0.379"	"C3472711"	"Spinocerebellar ataxia 36"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2011"	"2015"	"0"	"1"	"ORPHANET"
"10528"	"NOP56"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10529"	"NEBL"	"0.762"	"0.31"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"10529"	"NEBL"	"0.762"	"0.31"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"10529"	"NEBL"	"0.762"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10529"	"NEBL"	"0.762"	"0.31"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10529"	"NEBL"	"0.762"	"0.31"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10529"	"NEBL"	"0.762"	"0.31"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10529"	"NEBL"	"0.762"	"0.31"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10529"	"NEBL"	"0.762"	"0.31"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10531"	"PITRM1"	"0.815"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10533"	"ATG7"	"0.577"	"0.621"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C0023380"	"Lethargy"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C0024312"	"Lymphopenia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10533"	"ATG7"	"0.577"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2007"	"2014"	"0"	"1"	"ORPHANET"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C1835912"	"AICARDI-GOUTIERES SYNDROME 4"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.60"		"1993"	"2014"	"3"	"12"	"CTD_human;UNIPROT"
"10535"	"RNASEH2A"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10536"	"P3H3"	"0.713"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10536"	"P3H3"	"0.713"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C0019188"	"Hepatitis, Animal"	"disease"	"C06;C22"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10537"	"UBD"	"0.645"	"0.517"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"10539"	"GLRX3"	"0.743"	"0.207"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10539"	"GLRX3"	"0.743"	"0.207"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10542"	"LAMTOR5"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10542"	"LAMTOR5"	"0.857"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10542"	"LAMTOR5"	"0.857"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10542"	"LAMTOR5"	"0.857"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10544"	"PROCR"	"0.598"	"0.552"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10544"	"PROCR"	"0.598"	"0.552"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2005"	"2014"	"1"	"0"	"CTD_human"
"10544"	"PROCR"	"0.598"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10544"	"PROCR"	"0.598"	"0.552"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2017"	"2018"	"1"	"1"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C0020456"	"Hyperglycemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C1855520"	"Hyperglycemia, Postprandial"	"phenotype"	"C18"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10549"	"PRDX4"	"0.707"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C0038587"	"Substance Withdrawal Syndrome"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C0086189"	"Drug Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C0087169"	"Withdrawal Symptoms"	"phenotype"	"C25;F03"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10550"	"ARL6IP5"	"0.727"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2005"	"2015"	"2"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2015"	"2"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10551"	"AGR2"	"0.598"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2010"	"1"	"0"	"CTD_human"
"10553"	"HTATIP2"	"0.663"	"0.31"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.60"	"1"	"2004"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"10554"	"AGPAT1"	"0.752"	"0.31"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10555"	"AGPAT2"	"0.6"	"0.552"	"C0011859"	"Lipoatrophic Diabetes Mellitus"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10555"	"AGPAT2"	"0.6"	"0.552"	"C0221032"	"Familial generalized lipodystrophy"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"10555"	"AGPAT2"	"0.6"	"0.552"	"C1720862"	"Congenital Generalized Lipodystrophy Type 1"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.82"	"1"	"1993"	"2016"	"1"	"24"	"CTD_human;UNIPROT"
"10555"	"AGPAT2"	"0.6"	"0.552"	"C1720863"	"Congenital Generalized Lipodystrophy Type 2"	"disease"	"C16;C17;C18"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2007"	"0"	"0"	"CTD_human"
"10555"	"AGPAT2"	"0.6"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"10557"	"RPP38"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2001"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1964"	"2017"	"6"	"6"	"CTD_human;ORPHANET;UNIPROT"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"10558"	"SPTLC1"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10559"	"SLC35A1"	"0.799"	"0.276"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"10559"	"SLC35A1"	"0.799"	"0.276"	"C1970344"	"Congenital Disorder Of Glycosylation, Type IIF"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2018"	"2018"	"0"	"1"	"CTD_human;ORPHANET"
"10559"	"SLC35A1"	"0.799"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10560"	"SLC19A2"	"0.672"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"10560"	"SLC19A2"	"0.672"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10560"	"SLC19A2"	"0.672"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"10560"	"SLC19A2"	"0.672"	"0.483"	"C0342287"	"Thiamine responsive megaloblastic anemia syndrome"	"disease"	"C09;C10;C15;C18;C19;C23"	"Congenital Abnormality"	"1.00"	"1"	"1998"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"10560"	"SLC19A2"	"0.672"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10561"	"IFI44"	"0.72"	"0.414"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10561"	"IFI44"	"0.72"	"0.414"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10561"	"IFI44"	"0.72"	"0.414"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10562"	"OLFM4"	"0.614"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"10562"	"OLFM4"	"0.614"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10563"	"CXCL13"	"0.552"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10563"	"CXCL13"	"0.552"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.34"	"1"	"2006"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C1842563"	"Heterotopia, Periventricular, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C1868720"	"Periventricular Nodular Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"0.875"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10564"	"ARFGEF2"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10565"	"ARFGEF1"	"0.799"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10566"	"AKAP3"	"0.799"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10568"	"SLC34A2"	"0.72"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2017"	"2"	"0"	"CTD_human"
"10568"	"SLC34A2"	"0.72"	"0.448"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10568"	"SLC34A2"	"0.72"	"0.448"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10568"	"SLC34A2"	"0.72"	"0.448"	"C0155912"	"Pulmonary Alveolar Microlithiasis"	"disease"	"C08;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"2006"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10568"	"SLC34A2"	"0.72"	"0.448"	"C1864873"	"Testicular Microlithiasis"	"disease"	"C12;C19;C23"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"10569"	"SLU7"	"0.696"	"0.448"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10572"	"SIVA1"	"0.815"	"0.138"	"C0010246"	"Coxsackievirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10574"	"CCT7"	"0.799"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10576"	"CCT2"	"0.785"	"0.276"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10576"	"CCT2"	"0.785"	"0.276"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10576"	"CCT2"	"0.785"	"0.276"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10576"	"CCT2"	"0.785"	"0.276"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10577"	"NPC2"	"0.607"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10577"	"NPC2"	"0.607"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10577"	"NPC2"	"0.607"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10577"	"NPC2"	"0.607"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10577"	"NPC2"	"0.607"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2007"	"4"	"0"	"GENOMICS_ENGLAND"
"10577"	"NPC2"	"0.607"	"0.655"	"C1843366"	"NIEMANN-PICK DISEASE, TYPE C2"	"disease"	"C10;C15;C16;C18"	"Disease or Syndrome"	"0.67"	"1"	"1993"	"2017"	"6"	"15"	"CTD_human;UNIPROT"
"10577"	"NPC2"	"0.607"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2001"	"2007"	"4"	"0"	"GENOMICS_ENGLAND"
"10579"	"TACC2"	"0.834"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"0"	"0"	"UNIPROT"
"10580"	"SORBS1"	"0.619"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2015"	"2018"	"0"	"0"	"UNIPROT"
"10584"	"COLEC10"	"0.645"	"0.586"	"C0796032"	"Malpuech facial clefting syndrome"	"disease"	"C05;C14;C16;F03"	"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"10584"	"COLEC10"	"0.645"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10584"	"COLEC10"	"0.645"	"0.586"	"C4303860"	"Craniofacial ulnar renal syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10585"	"POMT1"	"0.559"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2008"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.80"	"0.952381"	"2003"	"2017"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"10585"	"POMT1"	"0.559"	"0.552"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10585"	"POMT1"	"0.559"	"0.552"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human;ORPHANET"
"10585"	"POMT1"	"0.559"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.45"	"1"	"2004"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.71"	"1"	"2003"	"2017"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"10585"	"POMT1"	"0.559"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10585"	"POMT1"	"0.559"	"0.552"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10585"	"POMT1"	"0.559"	"0.552"	"C3150415"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1"	"disease"		"Disease or Syndrome"	"0.60"		"2000"	"2017"	"3"	"13"	"CTD_human;UNIPROT"
"10585"	"POMT1"	"0.559"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2006"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10586"	"MAB21L2"	"0.743"	"0.276"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10586"	"MAB21L2"	"0.743"	"0.276"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"1"	"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"10586"	"MAB21L2"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10586"	"MAB21L2"	"0.743"	"0.276"	"C4014540"	"MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2015"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"1974"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"10587"	"TXNRD2"	"0.609"	"0.517"	"C4049650"	"Familial Glucocorticoid Deficiency Type 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10588"	"MTHFS"	"0.857"	"0.172"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10588"	"MTHFS"	"0.857"	"0.172"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10588"	"MTHFS"	"0.857"	"0.172"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10589"	"DRAP1"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10592"	"SMC2"	"0.762"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10592"	"SMC2"	"0.762"	"0.31"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10592"	"SMC2"	"0.762"	"0.31"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10594"	"PRPF8"	"0.69"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10594"	"PRPF8"	"0.69"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"0.9"	"2001"	"2017"	"0"	"1"	"ORPHANET"
"10594"	"PRPF8"	"0.69"	"0.414"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10594"	"PRPF8"	"0.69"	"0.414"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10594"	"PRPF8"	"0.69"	"0.414"	"C1838702"	"Retinitis Pigmentosa 13"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.82"	"1"	"2001"	"2012"	"4"	"5"	"CTD_human;UNIPROT"
"10594"	"PRPF8"	"0.69"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2005"	"2018"	"5"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0220991"	"Rotor Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.63"	"1"	"2012"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10599"	"SLCO1B1"	"0.59"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10602"	"CDC42EP3"	"0.799"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10610"	"ST6GALNAC2"	"0.815"	"0.241"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2004"	"2015"	"5"	"0"	"PSYGENET"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.75"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"4"	"0"	"PSYGENET"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"10611"	"PDLIM5"	"0.565"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2013"	"4"	"0"	"PSYGENET"
"10613"	"ERLIN1"	"0.857"	"0.034"	"C4284588"	"SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10614"	"HEXIM1"	"0.69"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10615"	"SPAG5"	"0.752"	"0.207"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10615"	"SPAG5"	"0.752"	"0.207"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10616"	"RBCK1"	"0.785"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10616"	"RBCK1"	"0.785"	"0.276"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10616"	"RBCK1"	"0.785"	"0.276"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2013"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"10616"	"RBCK1"	"0.785"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10616"	"RBCK1"	"0.785"	"0.276"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10616"	"RBCK1"	"0.785"	"0.276"	"C4014605"	"POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2014"	"2"	"8"	"UNIPROT"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10617"	"STAMBP"	"0.667"	"0.448"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C1842180"	"CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C2675370"	"Capillary Malformation Without Arteriovenous Malformation"	"disease"	"C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10617"	"STAMBP"	"0.667"	"0.448"	"C3280296"	"Microcephaly-capillary malformation syndrome"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2008"	"2015"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"10617"	"STAMBP"	"0.667"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"10617"	"STAMBP"	"0.667"	"0.448"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10618"	"TGOLN2"	"1"	"0.103"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10618"	"TGOLN2"	"1"	"0.103"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10625"	"IVNS1ABP"	"0.681"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10625"	"IVNS1ABP"	"0.681"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.35"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10628"	"TXNIP"	"0.552"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10630"	"PDPN"	"0.554"	"0.69"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10630"	"PDPN"	"0.554"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10630"	"PDPN"	"0.554"	"0.69"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0006287"	"Bronchopulmonary Dysplasia"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0013264"	"Muscular Dystrophy, Duchenne"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C0917713"	"Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10631"	"POSTN"	"0.598"	"0.724"	"C3542021"	"Duchenne and Becker Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10634"	"GAS2L1"	"0.857"	"0.069"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10634"	"GAS2L1"	"0.857"	"0.069"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10634"	"GAS2L1"	"0.857"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"10634"	"GAS2L1"	"0.857"	"0.069"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10641"	"NPRL2"	"0.701"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10641"	"NPRL2"	"0.701"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10641"	"NPRL2"	"0.701"	"0.276"	"C1858477"	"Epilepsy, Partial, with Variable Foci"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10641"	"NPRL2"	"0.701"	"0.276"	"C4310709"	"EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"2"	"6"	"UNIPROT"
"10643"	"IGF2BP3"	"0.619"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10643"	"IGF2BP3"	"0.619"	"0.379"	"C0031149"	"Peritoneal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10643"	"IGF2BP3"	"0.619"	"0.379"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10643"	"IGF2BP3"	"0.619"	"0.379"	"C4318618"	"Peritoneal Surface Malignancy"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10644"	"IGF2BP2"	"0.645"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9767442"	"2007"	"2018"	"0"	"28"	"CTD_human"
"10644"	"IGF2BP2"	"0.645"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10644"	"IGF2BP2"	"0.645"	"0.414"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2015"	"2016"	"1"	"0"	"PSYGENET"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"10645"	"CAMKK2"	"0.659"	"0.517"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0032045"	"Placenta Disorders"	"group"	"C13"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0267663"	"Congenital secretory diarrhea, sodium type (disorder)"	"disease"	"C16;C18;C23"	"Congenital Abnormality"	"0.63"	"1"	"2009"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10653"	"SPINT2"	"0.577"	"0.621"	"C2678346"	"Diarrhea 3, Secretory Sodium, Congenital, Syndromic"	"disease"	"C16;C18;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2014"	"1"	"6"	"UNIPROT"
"10654"	"PMVK"	"0.815"	"0.207"	"C0949506"	"Porokeratosis of Mibelli"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.70"		"2016"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10659"	"CELF2"	"0.663"	"0.552"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10659"	"CELF2"	"0.663"	"0.552"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10660"	"LBX1"	"0.577"	"0.69"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2003"	"2008"	"1"	"0"	"PSYGENET"
"10660"	"LBX1"	"0.577"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"10660"	"LBX1"	"0.577"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"1994"	"2015"	"1"	"0"	"CTD_human"
"10660"	"LBX1"	"0.577"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10660"	"LBX1"	"0.577"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C0002876"	"Congenital dyserythropoietic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"10661"	"KLF1"	"0.63"	"0.276"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2013"	"0"	"0"	"ORPHANET"
"10661"	"KLF1"	"0.63"	"0.276"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"10661"	"KLF1"	"0.63"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"10661"	"KLF1"	"0.63"	"0.276"	"C0271933"	"Congenital dyserythropoietic anemia, type I"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C0271934"	"Congenital dyserythropoietic anemia, type III"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C1306589"	"Congenital dyserythropoietic anemia, type II"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10661"	"KLF1"	"0.63"	"0.276"	"C3150926"	"Congenital dyserythropoietic anemia type IV"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1991"	"2016"	"2"	"3"	"ORPHANET;UNIPROT"
"10661"	"KLF1"	"0.63"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10664"	"CTCF"	"0.537"	"0.724"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10664"	"CTCF"	"0.537"	"0.724"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.33"	"0.6666667"	"2001"	"2014"	"0"	"0"	"UNIPROT"
"10664"	"CTCF"	"0.537"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"1998"	"1998"	"0"	"0"	"UNIPROT"
"10664"	"CTCF"	"0.537"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"10664"	"CTCF"	"0.537"	"0.724"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10664"	"CTCF"	"0.537"	"0.724"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10664"	"CTCF"	"0.537"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2008"	"0"	"0"	"UNIPROT"
"10664"	"CTCF"	"0.537"	"0.724"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10664"	"CTCF"	"0.537"	"0.724"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10664"	"CTCF"	"0.537"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10664"	"CTCF"	"0.537"	"0.724"	"C3809686"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 21"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10666"	"CD226"	"0.63"	"0.483"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.35"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10666"	"CD226"	"0.63"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10667"	"FARS2"	"0.69"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10667"	"FARS2"	"0.69"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10667"	"FARS2"	"0.69"	"0.276"	"C3554168"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2012"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"10667"	"FARS2"	"0.69"	"0.276"	"C4310750"	"SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10669"	"CGREF1"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10669"	"CGREF1"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10672"	"GNA13"	"0.713"	"0.379"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10672"	"GNA13"	"0.713"	"0.379"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"0"	"0"	"CGI"
"10672"	"GNA13"	"0.713"	"0.379"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10673"	"TNFSF13B"	"0.526"	"0.724"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10675"	"CSPG5"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"10678"	"B3GNT2"	"0.72"	"0.414"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1989"	"2014"	"1"	"0"	"CTD_human"
"10678"	"B3GNT2"	"0.72"	"0.414"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"10678"	"B3GNT2"	"0.72"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"10678"	"B3GNT2"	"0.72"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"10681"	"GNB5"	"0.735"	"0.345"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10681"	"GNB5"	"0.735"	"0.345"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10681"	"GNB5"	"0.735"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10681"	"GNB5"	"0.735"	"0.345"	"C4310678"	"LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"10681"	"GNB5"	"0.735"	"0.345"	"C4310682"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"5"	"CTD_human"
"10682"	"EBP"	"0.512"	"0.793"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C0008445"	"Chondrodysplasia Punctata"	"disease"	"C05"	"Congenital Abnormality"	"0.73"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"1983"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C0263627"	"Calcinosis universalis"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"10682"	"EBP"	"0.512"	"0.793"	"C0282102"	"Chondrodysplasia punctata, X-linked dominant type"	"disease"	"C05"	"Disease or Syndrome"	"1.00"	"1"	"1992"	"2015"	"6"	"34"	"CTD_human;ORPHANET;UNIPROT"
"10682"	"EBP"	"0.512"	"0.793"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1999"	"2003"	"5"	"0"	"GENOMICS_ENGLAND"
"10682"	"EBP"	"0.512"	"0.793"	"C4085243"	"MEND SYNDROME"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2003"	"2015"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"10683"	"DLL3"	"0.609"	"0.414"	"C0000768"	"Congenital Abnormality"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2003"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2002"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0036439"	"Scoliosis, unspecified"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0265343"	"Jarcho-Levin syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.77"	"1"	"2000"	"2011"	"1"	"1"	"ORPHANET;UNIPROT"
"10683"	"DLL3"	"0.609"	"0.414"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C1837549"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"	"disease"	"C05"	"Disease or Syndrome"	"0.52"	"1"	"2002"	"2004"	"0"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C1853296"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05"	"Disease or Syndrome"	"0.50"		"2002"	"2002"	"0"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"10683"	"DLL3"	"0.609"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10686"	"CLDN16"	"0.663"	"0.448"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"10686"	"CLDN16"	"0.663"	"0.448"	"C0268448"	"Primary hypomagnesemia (disorder)"	"disease"	"C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.90"		"1978"	"2016"	"2"	"15"	"CTD_human;ORPHANET;UNIPROT"
"10686"	"CLDN16"	"0.663"	"0.448"	"C3151482"	"HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING"	"disease"		"Disease or Syndrome"	"0.80"		"2000"	"2010"	"2"	"12"	"ORPHANET;UNIPROT"
"10693"	"CCT6B"	"0.928"	"0.138"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10693"	"CCT6B"	"0.928"	"0.138"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10695"	"CNPY3"	"0.928"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10699"	"CORIN"	"0.773"	"0.207"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"10699"	"CORIN"	"0.773"	"0.207"	"C3281288"	"PREECLAMPSIA/ECLAMPSIA 5"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2014"	"1"	"2"	"UNIPROT"
"10712"	"FAM189B"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10714"	"POLD3"	"0.727"	"0.241"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"10714"	"POLD3"	"0.727"	"0.241"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10714"	"POLD3"	"0.727"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.41"	"1"	"2012"	"2016"	"1"	"1"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10715"	"CERS1"	"0.685"	"0.31"	"C4015619"	"EPILEPSY, PROGRESSIVE MYOCLONIC, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2015"	"1"	"1"	"ORPHANET;UNIPROT"
"10716"	"TBR1"	"0.735"	"0.379"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10716"	"TBR1"	"0.735"	"0.379"	"C2931816"	"Chromosome 2, monosomy 2q24"	"disease"	"C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"10716"	"TBR1"	"0.735"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2013"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10717"	"AP4B1"	"0.713"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10717"	"AP4B1"	"0.713"	"0.345"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10717"	"AP4B1"	"0.713"	"0.345"	"C3279738"	"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2017"	"0"	"6"	"CTD_human"
"10717"	"AP4B1"	"0.713"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"10718"	"NRG3"	"0.69"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2009"	"2013"	"2"	"0"	"PSYGENET"
"10718"	"NRG3"	"0.69"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.7777778"	"2009"	"2014"	"1"	"0"	"CTD_human"
"10718"	"NRG3"	"0.69"	"0.517"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10723"	"SLC12A7"	"0.785"	"0.345"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10723"	"SLC12A7"	"0.785"	"0.345"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10730"	"YME1L1"	"0.696"	"0.517"	"C4310628"	"OPTIC ATROPHY 11"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"10733"	"PLK4"	"0.594"	"0.517"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"10733"	"PLK4"	"0.594"	"0.517"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10733"	"PLK4"	"0.594"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10733"	"PLK4"	"0.594"	"0.517"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"10733"	"PLK4"	"0.594"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10733"	"PLK4"	"0.594"	"0.517"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10733"	"PLK4"	"0.594"	"0.517"	"C3502492"	"Microcephaly with Chorioretinopathy, Autosomal Recessive"	"disease"	"C05;C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"10733"	"PLK4"	"0.594"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10733"	"PLK4"	"0.594"	"0.517"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10734"	"STAG3"	"0.815"	"0.276"	"C3810367"	"PREMATURE OVARIAN FAILURE 8"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2018"	"0"	"3"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.54"	"0.75"	"2014"	"2018"	"3"	"0"	"CGI;CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.54"	"0.75"	"2014"	"2018"	"3"	"0"	"CGI;CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"10735"	"STAG2"	"0.672"	"0.31"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0151779"	"Cutaneous Melanoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"10735"	"STAG2"	"0.672"	"0.31"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.34"	"0.75"	"2014"	"2018"	"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"10735"	"STAG2"	"0.672"	"0.31"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10735"	"STAG2"	"0.672"	"0.31"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"10736"	"SIX2"	"0.727"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10736"	"SIX2"	"0.727"	"0.379"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"10736"	"SIX2"	"0.727"	"0.379"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10736"	"SIX2"	"0.727"	"0.379"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10736"	"SIX2"	"0.727"	"0.379"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.44"	"0.5"	"2005"	"2015"	"2"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2004"	"2015"	"1"	"0"	"PSYGENET"
"10743"	"RAI1"	"0.558"	"0.621"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0392156"	"Akathisia"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0700201"	"Dyssomnias"	"group"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0752288"	"Adjustment Sleep Disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0752289"	"Environmental Sleep Disorder"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0752291"	"Limit-Setting Sleep Disorder"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0752292"	"Nocturnal Eating-Drinking Syndrome"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0752293"	"Sleep Disorders, Extrinsic"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C0795864"	"Smith-Magenis syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"0.9117647"	"2001"	"2018"	"12"	"9"	"CTD_human;ORPHANET"
"10743"	"RAI1"	"0.558"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C2931246"	"Potocki-Lupski syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"10743"	"RAI1"	"0.558"	"0.621"	"C3661485"	"17p11.2 Monosomy"	"disease"	"C10;C16"	"Cell or Molecular Dysfunction"	"0.30"		"2005"	"2011"	"12"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10743"	"RAI1"	"0.558"	"0.621"	"C3887612"	"Psychomotor Agitation"	"phenotype"	"C10;C23;F01"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"10743"	"RAI1"	"0.558"	"0.621"	"C4225255"	"YUAN-HAREL-LUPSKI SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10746"	"MAP3K2"	"0.815"	"0.241"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10747"	"MASP2"	"0.642"	"0.655"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10747"	"MASP2"	"0.642"	"0.655"	"C0014742"	"Erythema Multiforme"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10747"	"MASP2"	"0.642"	"0.655"	"C0020951"	"Immune Complex Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10747"	"MASP2"	"0.642"	"0.655"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10747"	"MASP2"	"0.642"	"0.655"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10747"	"MASP2"	"0.642"	"0.655"	"C3151085"	"MASP2 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.60"		"2003"	"2007"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10749"	"KIF1C"	"0.752"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10749"	"KIF1C"	"0.752"	"0.414"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10749"	"KIF1C"	"0.752"	"0.414"	"C1969796"	"ATAXIA, SPASTIC, 2, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.70"		"2014"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"10749"	"KIF1C"	"0.752"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10752"	"CHL1"	"0.573"	"0.759"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"10752"	"CHL1"	"0.573"	"0.759"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10752"	"CHL1"	"0.573"	"0.759"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10752"	"CHL1"	"0.573"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"1997"	"2011"	"2"	"0"	"CTD_human"
"10752"	"CHL1"	"0.573"	"0.759"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10752"	"CHL1"	"0.573"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10752"	"CHL1"	"0.573"	"0.759"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"10752"	"CHL1"	"0.573"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2004"	"2017"	"6"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.47"	"1"	"2010"	"2016"	"2"	"1"	"CTD_human"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"3"	"0"	"CTD_human"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"1"	"2010"	"2017"	"3"	"4"	"CTD_human"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C3279754"	"PSORIASIS 13, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2010"	"2010"	"2"	"1"	"UNIPROT"
"10758"	"TRAF3IP2"	"0.621"	"0.586"	"C3714992"	"CANDIDIASIS, FAMILIAL, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"10763"	"NES"	"0.51"	"0.655"	"C0014549"	"Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10763"	"NES"	"0.51"	"0.655"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10763"	"NES"	"0.51"	"0.655"	"C0751117"	"Cryptogenic Tonic-Clonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10763"	"NES"	"0.51"	"0.655"	"C0751118"	"Epilepsy, Tonic-Clonic, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10763"	"NES"	"0.51"	"0.655"	"C0751119"	"Epilepsy, Tonic-Clonic, Symptomatic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10765"	"KDM5B"	"0.636"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10765"	"KDM5B"	"0.636"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10765"	"KDM5B"	"0.636"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"10766"	"TOB2"	"0.886"	"0.138"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10769"	"PLK2"	"0.621"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C0346163"	"Endometrioid carcinoma ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10769"	"PLK2"	"0.621"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10769"	"PLK2"	"0.621"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10771"	"ZMYND11"	"0.713"	"0.414"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"10771"	"ZMYND11"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"10771"	"ZMYND11"	"0.713"	"0.414"	"C4015167"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 30"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2018"	"0"	"9"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"10772"	"SRSF10"	"0.752"	"0.207"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10772"	"SRSF10"	"0.752"	"0.207"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10775"	"POP4"	"0.928"	"0.103"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10775"	"POP4"	"0.928"	"0.103"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10783"	"NEK6"	"0.762"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10786"	"SLC17A3"	"0.834"	"0.241"	"C2675207"	"URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4"	"phenotype"		"Finding"	"0.40"		"2010"	"2010"	"0"	"2"	"CTD_human"
"10787"	"NCKAP1"	"0.762"	"0.31"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10787"	"NCKAP1"	"0.762"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10788"	"IQGAP2"	"0.713"	"0.207"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10797"	"MTHFD2"	"0.762"	"0.172"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10800"	"CYSLTR1"	"0.648"	"0.517"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10800"	"CYSLTR1"	"0.648"	"0.517"	"C0016659"	"Fractures, Closed"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10800"	"CYSLTR1"	"0.648"	"0.517"	"C0524598"	"Fractures, Occult"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10800"	"CYSLTR1"	"0.648"	"0.517"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2010"	"3"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0007862"	"Cervico-Brachial Neuralgia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0085920"	"Brachial Neuralgia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0221759"	"Brachial Plexus Neuritis"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"10801"	"SEPT9"	"0.588"	"0.655"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"10801"	"SEPT9"	"0.588"	"0.655"	"C1510479"	"Neuralgic Amyotrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"10801"	"SEPT9"	"0.588"	"0.655"	"C1834304"	"AMYOTROPHY, HEREDITARY NEURALGIC"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2015"	"4"	"3"	"CTD_human;UNIPROT"
"10801"	"SEPT9"	"0.588"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10803"	"CCR9"	"0.592"	"0.586"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C0013575"	"Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2002"	"2014"	"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"1996"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"10804"	"GJB6"	"0.559"	"0.655"	"C0162361"	"Hidrotic Ectodermal Dysplasia"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"2000"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10804"	"GJB6"	"0.559"	"0.655"	"C0265336"	"Senter syndrome"	"disease"	"C09;C10;C11;C16;C17;C23"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"10804"	"GJB6"	"0.559"	"0.655"	"C0282160"	"Aplasia Cutis Congenita"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1996"	"2002"	"2"	"0"	"GENOMICS_ENGLAND"
"10804"	"GJB6"	"0.559"	"0.655"	"C1706004"	"Anhydrotic Ectodermal Dysplasias"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C1844678"	"Progressive hearing loss stapes fixation"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C2673759"	"DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2000"	"2017"	"0"	"1"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C2673760"	"DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C2673761"	"DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"		"2003"	"2011"	"0"	"0"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C2675235"	"Deafness, Autosomal Recessive 1b"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2000"	"2017"	"0"	"1"	"CTD_human"
"10804"	"GJB6"	"0.559"	"0.655"	"C2675237"	"Deafness, Autosomal Dominant 3B"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"3"	"CTD_human;UNIPROT"
"10804"	"GJB6"	"0.559"	"0.655"	"C3665333"	"Keratitis-Ichthyosis-Deafness Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"10804"	"GJB6"	"0.559"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2016"	"1"	"6"	"PSYGENET"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2015"	"0"	"1"	"ORPHANET"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2010"	"2010"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C3889474"	"BARDET-BIEDL SYNDROME 16"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2015"	"0"	"4"	"CTD_human"
"10806"	"SDCCAG8"	"0.602"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2010"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"10808"	"HSPH1"	"0.696"	"0.483"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10808"	"HSPH1"	"0.696"	"0.483"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10809"	"STARD10"	"0.886"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10809"	"STARD10"	"0.886"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10810"	"WASF3"	"0.636"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10810"	"WASF3"	"0.636"	"0.483"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10810"	"WASF3"	"0.636"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"10810"	"WASF3"	"0.636"	"0.483"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10810"	"WASF3"	"0.636"	"0.483"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10813"	"UTP14A"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"1998"	"2015"	"2"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10814"	"CPLX2"	"0.713"	"0.172"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0033958"	"Psychosis, Brief Reactive"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0036358"	"Schizophreniform Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10815"	"CPLX1"	"0.6"	"0.517"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10815"	"CPLX1"	"0.6"	"0.517"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10818"	"FRS2"	"0.659"	"0.448"	"C0023827"	"liposarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"CGI"
"10824"	"DIAPH2-AS1"	"1"	"0.034"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10824"	"DIAPH2-AS1"	"1"	"0.034"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10826"	"FAXDC2"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10826"	"FAXDC2"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10826"	"FAXDC2"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0003129"	"Anoxemia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0003130"	"Anoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0242184"	"Hypoxia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C0700292"	"Hypoxemia"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10840"	"ALDH1L1"	"0.72"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"10841"	"FTCD"	"0.752"	"0.414"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10841"	"FTCD"	"0.752"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10841"	"FTCD"	"0.752"	"0.414"	"C0268609"	"Glutamate formiminotransferase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2003"	"2018"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"10841"	"FTCD"	"0.752"	"0.414"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10841"	"FTCD"	"0.752"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"10842"	"PPP1R17"	"0.857"	"0.172"	"C0745103"	"Hyperlipoproteinemia Type IIa"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"10842"	"PPP1R17"	"0.857"	"0.172"	"C3276941"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"10846"	"PDE10A"	"0.652"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10846"	"PDE10A"	"0.652"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2017"	"1"	"1"	"PSYGENET"
"10846"	"PDE10A"	"0.652"	"0.483"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10846"	"PDE10A"	"0.652"	"0.483"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"10846"	"PDE10A"	"0.652"	"0.483"	"C4310791"	"STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10846"	"PDE10A"	"0.652"	"0.483"	"C4310792"	"DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10847"	"SRCAP"	"0.696"	"0.517"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10847"	"SRCAP"	"0.696"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10847"	"SRCAP"	"0.696"	"0.517"	"C0729582"	"Floating-harbor syndrome"	"disease"	"C05;C14;C16;C23"	"Disease or Syndrome"	"0.66"	"1"	"1993"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"10847"	"SRCAP"	"0.696"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"10847"	"SRCAP"	"0.696"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"10848"	"PPP1R13L"	"0.596"	"0.517"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"10850"	"CCL27"	"0.614"	"0.586"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10850"	"CCL27"	"0.614"	"0.586"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10850"	"CCL27"	"0.614"	"0.586"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10855"	"HPSE"	"0.464"	"0.759"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9591837"	"1999"	"2017"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0027720"	"Nephrosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10855"	"HPSE"	"0.464"	"0.759"	"C0349217"	"Depressive episode, unspecified"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10855"	"HPSE"	"0.464"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"10855"	"HPSE"	"0.464"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2002"	"2006"	"1"	"0"	"CTD_human"
"10855"	"HPSE"	"0.464"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1987"	"2015"	"0"	"0"	"UNIPROT"
"10857"	"PGRMC1"	"0.672"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10857"	"PGRMC1"	"0.672"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10857"	"PGRMC1"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.96875"	"2002"	"2016"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10858"	"CYP46A1"	"0.735"	"0.207"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10859"	"LILRB1"	"0.559"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"PSYGENET"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C0020500"	"Hyperoxaluria"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"3"	"UNIPROT"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C0027709"	"Nephrocalcinosis"	"disease"	"C12;C13;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C0451641"	"Urolithiasis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C1298681"	"Oxalosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10861"	"SLC26A1"	"0.707"	"0.414"	"C1833683"	"NEPHROLITHIASIS, CALCIUM OXALATE"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"10863"	"ADAM28"	"0.69"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10863"	"ADAM28"	"0.69"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10863"	"ADAM28"	"0.69"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"10863"	"ADAM28"	"0.69"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"10863"	"ADAM28"	"0.69"	"0.414"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"3"	"UNIPROT"
"10875"	"FGL2"	"0.727"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10875"	"FGL2"	"0.727"	"0.207"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10877"	"CFHR4"	"0.886"	"0.207"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"10878"	"CFHR3"	"0.735"	"0.241"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10878"	"CFHR3"	"0.735"	"0.241"	"C0025303"	"Meningococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2015"	"1"	"1"	"CTD_human"
"10878"	"CFHR3"	"0.735"	"0.241"	"C1864205"	"Macular Degeneration, Age-Related, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"10878"	"CFHR3"	"0.735"	"0.241"	"C2931788"	"Atypical Hemolytic Uremic Syndrome"	"disease"	"C12;C13;C15"	"Disease or Syndrome"	"0.58"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10887"	"PROKR1"	"1"	"0.069"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10887"	"PROKR1"	"1"	"0.069"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.46"	"1"	"2007"	"2015"	"0"	"1"	"ORPHANET"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0006079"	"Bowen's Disease"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"0.9354839"	"2002"	"2018"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2004"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2004"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0026851"	"Muscular Dystrophy, Animal"	"disease"	"C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2013"	"2"	"0"	"CTD_human"
"10891"	"PPARGC1A"	"0.497"	"0.828"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10892"	"MALT1"	"0.596"	"0.552"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"10892"	"MALT1"	"0.596"	"0.552"	"C0242647"	"Mucosa-Associated Lymphoid Tissue Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.9450549"	"1999"	"2018"	"0"	"0"	"ORPHANET"
"10892"	"MALT1"	"0.596"	"0.552"	"C3809583"	"IMMUNODEFICIENCY 12"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"10893"	"MMP24"	"0.762"	"0.276"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10897"	"YIF1A"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10897"	"YIF1A"	"1"	"0.069"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10897"	"YIF1A"	"1"	"0.069"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10897"	"YIF1A"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10902"	"BRD8"	"0.707"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10902"	"BRD8"	"0.707"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10906"	"TRAFD1"	"0.886"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10907"	"TXNL4A"	"0.727"	"0.31"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.41"	"1"	"2015"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"10907"	"TXNL4A"	"0.727"	"0.31"	"C1837822"	"Burn-Mckeown syndrome"	"disease"	"C08;C09;C10;C14;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"1993"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"10907"	"TXNL4A"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0023138"	"Laurence-Moon Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0037050"	"Sick Building Syndrome"	"disease"	"C20;C21"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.56"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0085084"	"Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2011"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0152025"	"Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0154681"	"Anterior Horn Cell Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0154682"	"Lateral Sclerosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0270763"	"Familial Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0270764"	"Motor Neuron Disease, Lower"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0271683"	"Polyneuropathy, Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0393851"	"Polyneuropathy, Critical Illness"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0521659"	"Motor Neuron Disease, Upper"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0543858"	"Motor Neuron Disease, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2010"	"2"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751448"	"Polyneuropathy, Familial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751449"	"Acquired Polyneuropathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751602"	"Hereditary Autosomal Dominant Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751603"	"Autosomal Recessive Hereditary Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751604"	"Hereditary X-Linked Recessive Spastic Paraplegia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C0751605"	"X-Linked, Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C1848745"	"Oliver-McFarlane syndrome"	"disease"	"C05;C10;C11;C16;C17;C19;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"2016"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C1859093"	"Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism"	"disease"	"C10;C11;C16;C19"	"Disease or Syndrome"	"0.75"	"0.8"	"1993"	"2017"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C1859305"	"Cerebellar Ataxia and Hypogonadotropic Hypogonadism"	"disease"	"C10;C19;C23"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C2677586"	"Spastic Paraplegia 39, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2017"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"10908"	"PNPLA6"	"0.55"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"10911"	"UTS2"	"0.609"	"0.586"	"C0003621"	"Appetite Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0013473"	"Eating Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.55"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0043049"	"Water Intoxication"	"disease"	"C18;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C0854145"	"Feeding Disorders"	"disease"	"F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10911"	"UTS2"	"0.609"	"0.586"	"C4042784"	"Feeding and Eating Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10913"	"EDAR"	"0.667"	"0.276"	"C0265331"	"Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10913"	"EDAR"	"0.667"	"0.276"	"C0406702"	"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.67"	"1"	"1999"	"2017"	"0"	"12"	"CTD_human;ORPHANET"
"10913"	"EDAR"	"0.667"	"0.276"	"C1720965"	"Ectodermal Dysplasia 3, Anhidrotic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"		"2012"	"2017"	"0"	"7"	"CTD_human"
"10913"	"EDAR"	"0.667"	"0.276"	"C3887494"	"ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.38"	"0.875"	"2004"	"2016"	"7"	"11"	"UNIPROT"
"10913"	"EDAR"	"0.667"	"0.276"	"C3888065"	"ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.38"	"0.875"	"2004"	"2011"	"1"	"1"	"UNIPROT"
"10916"	"MAGED2"	"0.69"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"0.5"	"2000"	"2015"	"0"	"0"	"UNIPROT"
"10916"	"MAGED2"	"0.69"	"0.414"	"C1866495"	"Bartter syndrome, antenatal type 1"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10916"	"MAGED2"	"0.69"	"0.414"	"C4310820"	"BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT"	"disease"		"Disease or Syndrome"	"0.60"		"1998"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0021359"	"Infertility"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2018"	"2"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0266999"	"Vesicular Stomatitis"	"disease"	"C02;C07;C22"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C0729353"	"Subfertility"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"10919"	"EHMT2"	"0.659"	"0.621"	"C4074771"	"Sterility, Reproductive"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10921"	"RNPS1"	"0.773"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"10922"	"FASTK"	"0.762"	"0.31"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2016"	"1"	"1"	"UNIPROT"
"10924"	"SMPDL3A"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10924"	"SMPDL3A"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10928"	"RALBP1"	"0.573"	"0.552"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10928"	"RALBP1"	"0.573"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10928"	"RALBP1"	"0.573"	"0.552"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10928"	"RALBP1"	"0.573"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"10933"	"MORF4L1"	"0.799"	"0.207"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0085084"	"Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0154681"	"Anterior Horn Cell Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0154682"	"Lateral Sclerosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0270763"	"Familial Motor Neuron Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0270764"	"Motor Neuron Disease, Lower"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0521659"	"Motor Neuron Disease, Upper"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0543858"	"Motor Neuron Disease, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"10935"	"PRDX3"	"0.614"	"0.517"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C1853249"	"SPINOCEREBELLAR ATAXIA 28"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.96"	"0.6666667"	"1993"	"2015"	"5"	"11"	"CTD_human;ORPHANET;UNIPROT"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C3280977"	"SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"10939"	"AFG3L2"	"0.619"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"10940"	"POP1"	"0.815"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"10940"	"POP1"	"0.815"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10940"	"POP1"	"0.815"	"0.207"	"C1846796"	"Anauxetic dysplasia"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"10940"	"POP1"	"0.815"	"0.207"	"C4479357"	"ANAUXETIC DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2018"	"3"	"5"	"UNIPROT"
"10943"	"MSL3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"10945"	"KDELR1"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10945"	"KDELR1"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10946"	"SF3A3"	"1"	"0.069"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10946"	"SF3A3"	"1"	"0.069"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10948"	"STARD3"	"0.773"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"10948"	"STARD3"	"0.773"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"2"	"0"	"CTD_human"
"10948"	"STARD3"	"0.773"	"0.207"	"C3496069"	"cocaine use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"10950"	"BTG3"	"0.602"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"10950"	"BTG3"	"0.602"	"0.586"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10951"	"CBX1"	"0.743"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10951"	"CBX1"	"0.743"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"10955"	"SERINC3"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10955"	"SERINC3"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10959"	"TMED2"	"0.652"	"0.655"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10961"	"ERP29"	"0.799"	"0.207"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"10961"	"ERP29"	"0.799"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10961"	"ERP29"	"0.799"	"0.207"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10961"	"ERP29"	"0.799"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10961"	"ERP29"	"0.799"	"0.207"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10962"	"MLLT11"	"0.69"	"0.31"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"				"0"	"0"	"CTD_human"
"10963"	"STIP1"	"0.672"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"10963"	"STIP1"	"0.672"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10964"	"IFI44L"	"0.886"	"0.207"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"10965"	"ACOT2"	"0.928"	"0.103"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"10966"	"RAB40B"	"0.598"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10971"	"YWHAQ"	"0.72"	"0.379"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10971"	"YWHAQ"	"0.72"	"0.379"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10973"	"ASCC3"	"0.834"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10973"	"ASCC3"	"0.834"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10973"	"ASCC3"	"0.834"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"10973"	"ASCC3"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"10975"	"UQCR11"			"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10975"	"UQCR11"			"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10978"	"CLP1"	"0.735"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10978"	"CLP1"	"0.735"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10978"	"CLP1"	"0.735"	"0.31"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10978"	"CLP1"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"10978"	"CLP1"	"0.735"	"0.31"	"C4014347"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 10"	"disease"		"Disease or Syndrome"	"0.90"		"2013"	"2014"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"10979"	"FERMT2"	"0.676"	"0.414"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10979"	"FERMT2"	"0.676"	"0.414"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"10979"	"FERMT2"	"0.676"	"0.414"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"10980"	"COPS6"	"0.727"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10980"	"COPS6"	"0.727"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10981"	"RAB32"	"0.762"	"0.414"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10981"	"RAB32"	"0.762"	"0.414"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"10981"	"RAB32"	"0.762"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10981"	"RAB32"	"0.762"	"0.414"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"10981"	"RAB32"	"0.762"	"0.414"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"10982"	"MAPRE2"	"0.672"	"0.552"	"C0473586"	"Michelin tire baby syndrome"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"10982"	"MAPRE2"	"0.672"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10982"	"MAPRE2"	"0.672"	"0.552"	"C4225225"	"SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2"	"disease"		"Congenital Abnormality"	"0.40"		"2009"	"2016"	"1"	"4"	"UNIPROT"
"10984"	"KCNQ1OT1"	"0.604"	"0.586"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.40"	"0.9782609"	"1999"	"2016"	"0"	"0"	"CTD_human"
"10984"	"KCNQ1OT1"	"0.604"	"0.586"	"C0332890"	"Congenital hemihypertrophy"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"10984"	"KCNQ1OT1"	"0.604"	"0.586"	"C1856184"	"HEMIHYPERPLASIA, ISOLATED"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"10987"	"COPS5"	"0.624"	"0.552"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10987"	"COPS5"	"0.624"	"0.552"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10987"	"COPS5"	"0.624"	"0.552"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10987"	"COPS5"	"0.624"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"10987"	"COPS5"	"0.624"	"0.552"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10987"	"COPS5"	"0.624"	"0.552"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"10989"	"IMMT"	"0.645"	"0.655"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10989"	"IMMT"	"0.645"	"0.655"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"10993"	"SDS"	"0.54"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"10998"	"SLC27A5"	"0.639"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10998"	"SLC27A5"	"0.639"	"0.483"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10998"	"SLC27A5"	"0.639"	"0.483"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"10998"	"SLC27A5"	"0.639"	"0.483"	"C4274079"	"Bile acid CoA ligase deficiency and defective amidation"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"10999"	"SLC27A4"	"0.676"	"0.448"	"C1837610"	"ICHTHYOSIS PREMATURITY SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.75"	"1"	"2009"	"2014"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"10999"	"SLC27A4"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11001"	"SLC27A2"	"0.752"	"0.31"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"11001"	"SLC27A2"	"0.752"	"0.31"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"11004"	"KIF2C"	"0.685"	"0.276"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11004"	"KIF2C"	"0.685"	"0.276"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11005"	"SPINK5"	"0.636"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11005"	"SPINK5"	"0.636"	"0.517"	"C0265962"	"Ichthyosis linearis circumflexa"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.90"	"0.9777778"	"2000"	"2017"	"1"	"5"	"CTD_human;ORPHANET"
"11005"	"SPINK5"	"0.636"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11005"	"SPINK5"	"0.636"	"0.517"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"11009"	"IL24"	"0.547"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9411765"	"2001"	"2015"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2012"	"2"	"0"	"CTD_human"
"11009"	"IL24"	"0.547"	"0.621"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"11009"	"IL24"	"0.547"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2016"	"2"	"0"	"CTD_human"
"11010"	"GLIPR1"	"0.69"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11010"	"GLIPR1"	"0.69"	"0.276"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11010"	"GLIPR1"	"0.69"	"0.276"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11011"	"TLK2"	"0.773"	"0.241"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11011"	"TLK2"	"0.773"	"0.241"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11011"	"TLK2"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"11018"	"TMED1"	"0.72"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11019"	"LIAS"	"0.707"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11019"	"LIAS"	"0.707"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11019"	"LIAS"	"0.707"	"0.414"	"C3280887"	"HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"11020"	"IFT27"	"0.713"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"11020"	"IFT27"	"0.713"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"11020"	"IFT27"	"0.713"	"0.379"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"11020"	"IFT27"	"0.713"	"0.379"	"C3889475"	"BARDET-BIEDL SYNDROME 19"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"11023"	"VAX1"	"0.743"	"0.379"	"C3553077"	"MICROPHTHALMIA, SYNDROMIC 11"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"11024"	"LILRA1"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"11031"	"RAB31"	"0.752"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11034"	"DSTN"	"0.707"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11035"	"RIPK3"	"0.586"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11040"	"PIM2"	"0.656"	"0.448"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"11040"	"PIM2"	"0.656"	"0.448"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11040"	"PIM2"	"0.656"	"0.448"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11041"	"B4GAT1"	"0.573"	"0.414"	"C3809042"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2014"	"2"	"3"	"UNIPROT"
"11043"	"MID2"	"0.752"	"0.414"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11043"	"MID2"	"0.752"	"0.414"	"C3890168"	"MENTAL RETARDATION, X-LINKED 101"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"11051"	"NUDT21"	"0.886"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11063"	"SOX30"	"0.886"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"11063"	"SOX30"	"0.886"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11065"	"UBE2C"	"0.621"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11067"	"DEPP1"	"0.707"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11073"	"TOPBP1"	"0.69"	"0.483"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11074"	"TRIM31"	"0.685"	"0.379"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11076"	"TPPP"	"0.627"	"0.724"	"C3826462"	"Depression in children"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"11078"	"TRIOBP"	"0.785"	"0.31"	"C1853276"	"Deafness, Autosomal Recessive 28"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.70"		"2006"	"2017"	"8"	"9"	"CLINGEN;CTD_human;UNIPROT"
"11081"	"KERA"	"0.713"	"0.103"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2000"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"11081"	"KERA"	"0.713"	"0.103"	"C1857574"	"CORNEA PLANA 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.85"	"0.8"	"2000"	"2016"	"1"	"8"	"CTD_human;UNIPROT"
"11082"	"ESM1"	"0.672"	"0.345"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11082"	"ESM1"	"0.672"	"0.345"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11086"	"ADAM29"	"0.799"	"0.172"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"9"	"UNIPROT"
"11086"	"ADAM29"	"0.799"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C0034155"	"Purpura, Thrombotic Thrombocytopenic"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.40"	"0.9647887"	"1988"	"2017"	"1"	"0"	"CTD_human"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C0398650"	"Immune thrombocytopenic purpura"	"disease"	"C15;C20;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C1268935"	"Congenital Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.80"	"1"	"1982"	"2017"	"21"	"52"	"CTD_human;ORPHANET;UNIPROT"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C1956258"	"Familial Thrombotic Thrombocytopenic Purpura"	"disease"	"C15;C23"	"Disease or Syndrome"	"0.52"	"0.5"	"1998"	"2012"	"21"	"42"	"CTD_human;UNIPROT"
"11093"	"ADAMTS13"	"0.536"	"0.69"	"C2717961"	"Thrombotic Microangiopathies"	"group"	"C15"	"Disease or Syndrome"	"0.40"	"0.9142857"	"2002"	"2017"	"2"	"0"	"CTD_human"
"11095"	"ADAMTS8"	"0.735"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"11095"	"ADAMTS8"	"0.735"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"11096"	"ADAMTS5"	"0.681"	"0.414"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11098"	"PRSS23"	"0.857"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11099"	"PTPN21"	"0.928"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"11099"	"PTPN21"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11107"	"PRDM5"	"0.652"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"11107"	"PRDM5"	"0.652"	"0.483"	"C0268344"	"Ehlers-Danlos syndrome 6B"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"11107"	"PRDM5"	"0.652"	"0.483"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"11107"	"PRDM5"	"0.652"	"0.483"	"C3280011"	"BRITTLE CORNEA SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"11113"	"CIT"	"0.642"	"0.483"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"ORPHANET"
"11113"	"CIT"	"0.642"	"0.483"	"C4310723"	"MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"4"	"6"	"CTD_human;UNIPROT"
"11117"	"EMILIN1"	"0.815"	"0.138"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11122"	"PTPRT"	"0.735"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11122"	"PTPRT"	"0.735"	"0.345"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11122"	"PTPRT"	"0.735"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11122"	"PTPRT"	"0.735"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"3"	"UNIPROT"
"11127"	"KIF3A"	"0.681"	"0.448"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"11127"	"KIF3A"	"0.681"	"0.448"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11127"	"KIF3A"	"0.681"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11127"	"KIF3A"	"0.681"	"0.448"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11127"	"KIF3A"	"0.681"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11127"	"KIF3A"	"0.681"	"0.448"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11128"	"POLR3A"	"0.676"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"11128"	"POLR3A"	"0.676"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.48"	"0.875"	"2011"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"11128"	"POLR3A"	"0.676"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"11128"	"POLR3A"	"0.676"	"0.448"	"C2676243"	"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism"	"disease"	"C07;C10;C16;C19;C23"	"Disease or Syndrome"	"0.74"	"0.75"	"1993"	"2016"	"4"	"19"	"CTD_human;ORPHANET;UNIPROT"
"11128"	"POLR3A"	"0.676"	"0.448"	"C3502054"	"Leukodystrophy, Dysmyelinating, with Oligodontia"	"disease"	"C07;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11128"	"POLR3A"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11129"	"CLASRP"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11132"	"CAPN10"	"0.63"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9393939"	"2000"	"2016"	"1"	"3"	"CTD_human"
"11132"	"CAPN10"	"0.63"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11132"	"CAPN10"	"0.63"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11132"	"CAPN10"	"0.63"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11132"	"CAPN10"	"0.63"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"11132"	"CAPN10"	"0.63"	"0.483"	"C1832544"	"DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1 (disorder)"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11132"	"CAPN10"	"0.63"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"11133"	"KPTN"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"11133"	"KPTN"	"0.752"	"0.241"	"C3810225"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"11136"	"SLC7A9"	"0.69"	"0.483"	"C0010691"	"Cystinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.90"	"0.9714286"	"1967"	"2016"	"9"	"30"	"CTD_human;UNIPROT"
"11136"	"SLC7A9"	"0.69"	"0.483"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11136"	"SLC7A9"	"0.69"	"0.483"	"C1857388"	"Cystinuria, Type A"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2010"	"9"	"27"	"UNIPROT"
"11136"	"SLC7A9"	"0.69"	"0.483"	"C1857389"	"Cystinuria, Type B"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2010"	"9"	"27"	"ORPHANET;UNIPROT"
"11136"	"SLC7A9"	"0.69"	"0.483"	"C1857390"	"Cystinuria, Type A-B"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2010"	"9"	"27"	"UNIPROT"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2009"	"2014"	"2"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C0796206"	"Atkin syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C0796241"	"MENTAL RETARDATION, X-LINKED 34 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"1992"	"2014"	"1"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2010"	"2016"	"1"	"0"	"CTD_human"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"1999"	"2017"	"6"	"0"	"CLINGEN;ORPHANET"
"11141"	"IL1RAPL1"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9333333"	"2000"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"11146"	"GLMN"	"0.834"	"0.31"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11146"	"GLMN"	"0.834"	"0.31"	"C1841984"	"GLOMUVENOUS MALFORMATIONS"	"disease"	"C04"	"Disease or Syndrome"	"0.69"	"1"	"2001"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"11146"	"GLMN"	"0.834"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11149"	"BVES"	"0.785"	"0.172"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"11149"	"BVES"	"0.785"	"0.172"	"C4225199"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0041296"	"Tuberculosis"	"disease"	"C01"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11151"	"CORO1A"	"0.616"	"0.586"	"C3809383"	"IMMUNODEFICIENCY 8"	"disease"		"Disease or Syndrome"	"0.70"		"2008"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"11152"	"WDR45"	"0.685"	"0.207"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11152"	"WDR45"	"0.685"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"11152"	"WDR45"	"0.685"	"0.207"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11152"	"WDR45"	"0.685"	"0.207"	"C2931845"	"Neurodegeneration with brain iron accumulation (NBIA)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"11152"	"WDR45"	"0.685"	"0.207"	"C3550973"	"NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5"	"disease"		"Disease or Syndrome"	"0.70"	"1"	"2013"	"2018"	"0"	"15"	"CTD_human;ORPHANET"
"11152"	"WDR45"	"0.685"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"11154"	"AP4S1"	"0.762"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11154"	"AP4S1"	"0.762"	"0.241"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11154"	"AP4S1"	"0.762"	"0.241"	"C3279743"	"SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2016"	"0"	"3"	"CTD_human"
"11154"	"AP4S1"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.64"	"1"	"2004"	"2009"	"0"	"1"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11155"	"LDB3"	"0.69"	"0.241"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C1832244"	"CARDIOMYOPATHY, DILATED, 1C (disorder)"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2004"	"2004"	"2"	"5"	"UNIPROT"
"11155"	"LDB3"	"0.69"	"0.241"	"C1836155"	"Myopathy, Myofibrillar, Zasp-Related"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2017"	"0"	"3"	"ORPHANET"
"11155"	"LDB3"	"0.69"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"11155"	"LDB3"	"0.69"	"0.241"	"C2678065"	"Myofibrillar Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2017"	"0"	"2"	"CTD_human"
"11155"	"LDB3"	"0.69"	"0.241"	"C3152137"	"LEFT VENTRICULAR NONCOMPACTION 3"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2004"	"2"	"4"	"UNIPROT"
"11155"	"LDB3"	"0.69"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"11155"	"LDB3"	"0.69"	"0.241"	"C4225414"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2004"	"2"	"4"	"UNIPROT"
"11156"	"PTP4A3"	"0.609"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"11156"	"PTP4A3"	"0.609"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C1853396"	"Primary lateral sclerosis juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C2749936"	"SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2011"	"2013"	"0"	"2"	"CTD_human;ORPHANET"
"11160"	"ERLIN2"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2011"	"2016"	"10"	"0"	"CTD_human;GENOMICS_ENGLAND"
"11167"	"FSTL1"	"0.582"	"0.552"	"C0003504"	"Aortic Valve Insufficiency"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11167"	"FSTL1"	"0.582"	"0.552"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"11167"	"FSTL1"	"0.582"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11167"	"FSTL1"	"0.582"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"11167"	"FSTL1"	"0.582"	"0.552"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11167"	"FSTL1"	"0.582"	"0.552"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11167"	"FSTL1"	"0.582"	"0.552"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11168"	"PSIP1"	"0.555"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"1993"	"2012"	"1"	"0"	"CTD_human"
"11168"	"PSIP1"	"0.555"	"0.655"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11168"	"PSIP1"	"0.555"	"0.655"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11170"	"FAM107A"	"0.762"	"0.276"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11170"	"FAM107A"	"0.762"	"0.276"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11170"	"FAM107A"	"0.762"	"0.276"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11170"	"FAM107A"	"0.762"	"0.276"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11171"	"STRAP"	"0.773"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"11171"	"STRAP"	"0.773"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"11171"	"STRAP"	"0.773"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"11173"	"ADAMTS7"	"0.696"	"0.379"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.37"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"11173"	"ADAMTS7"	"0.696"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11173"	"ADAMTS7"	"0.696"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11173"	"ADAMTS7"	"0.696"	"0.379"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"11176"	"BAZ2A"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11176"	"BAZ2A"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2002"	"1"	"0"	"CTD_human"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"11178"	"LZTS1"	"0.659"	"0.379"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;CTD_human"
"11179"	"ZNF277"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11181"	"TREH"	"0.69"	"0.517"	"C0268187"	"alpha, alpha-Trehalase deficiency"	"disease"	"C16;C18;C23"	"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"11184"	"MAP4K1"	"0.72"	"0.31"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11185"	"INMT"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9583333"	"2001"	"2016"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0005686"	"Urinary Bladder Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9230769"	"2001"	"2013"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9047619"	"2001"	"2017"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"0.8571429"	"2002"	"2012"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.5"	"2001"	"2008"	"2"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0036323"	"Schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.8536585"	"2001"	"2017"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11186"	"RASSF1"	"0.429"	"0.793"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11187"	"PKP3"	"0.762"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11187"	"PKP3"	"0.762"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11188"	"NISCH"	"0.713"	"0.31"	"C0020649"	"Hypotension"	"phenotype"	"C14"	"Finding"	"0.30"		"2001"	"2012"	"2"	"0"	"CTD_human"
"11188"	"NISCH"	"0.713"	"0.31"	"C0428977"	"Bradycardia"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11193"	"WBP4"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11194"	"ABCB8"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11197"	"WIF1"	"0.536"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"11197"	"WIF1"	"0.536"	"0.586"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11199"	"ANXA10"	"0.707"	"0.241"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11199"	"ANXA10"	"0.707"	"0.241"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9421488"	"2001"	"2018"	"7"	"1"	"CGI;CTD_human;UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"0.75"	"2001"	"2008"	"0"	"1"	"UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.85"	"2003"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.37"		"2003"	"2008"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2003"	"2017"	"12"	"0"	"CLINGEN"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"0.5"	"2011"	"2015"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2005"	"2013"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.73"	"1"	"2002"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.38"	"0.875"	"2004"	"2016"	"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2008"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0085390"	"Li-Fraumeni Syndrome"	"disease"	"C04;C16;C18"	"Neoplastic Process"	"0.70"	"0.9444444"	"2000"	"2017"	"2"	"3"	"CTD_human;ORPHANET"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0206720"	"Squamous Cell Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0238033"	"Carcinoma of Male Breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2018"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.39"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0242788"	"Breast Neoplasms, Male"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2002"	"2008"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9473684"	"2000"	"2018"	"11"	"74"	"CLINGEN;UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.70"	"0.9583333"	"2003"	"2018"	"1"	"12"	"CTD_human;UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.42"	"1"	"2011"	"2017"	"0"	"2"	"ORPHANET"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9435484"	"2001"	"2018"	"4"	"1"	"CGI;CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0751688"	"Malignant Squamous Cell Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.44"	"0.6666667"	"2002"	"2007"	"0"	"0"	"CGI"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2003"	"2017"	"12"	"0"	"CLINGEN"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.66"	"0.8333333"	"2000"	"2016"	"6"	"0"	"CGI;CLINGEN"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2002"	"2009"	"4"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2017"	"12"	"0"	"CLINGEN"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.75"	"2002"	"2016"	"4"	"2"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.8571429"	"2003"	"2016"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1836482"	"Li-Fraumeni Syndrome 2"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.60"		"2001"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2016"	"3"	"1"	"UNIPROT"
"11200"	"CHEK2"	"0.494"	"0.621"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.62"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"11200"	"CHEK2"	"0.494"	"0.621"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11202"	"KLK8"	"0.663"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"11202"	"KLK8"	"0.663"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"11212"	"PLPBP"	"0.773"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"11212"	"PLPBP"	"0.773"	"0.207"	"C1291560"	"Deficiency of glutamate decarboxylase"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11212"	"PLPBP"	"0.773"	"0.207"	"C1849508"	"EPILEPSY, PYRIDOXINE-DEPENDENT"	"disease"	"C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"11212"	"PLPBP"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"11212"	"PLPBP"	"0.773"	"0.207"	"C4310632"	"EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"6"	"UNIPROT"
"11213"	"IRAK3"	"0.633"	"0.517"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11213"	"IRAK3"	"0.633"	"0.517"	"C1970224"	"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5"	"phenotype"		"Finding"	"0.40"		"2007"	"2007"	"0"	"1"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11214"	"AKAP13"	"0.681"	"0.379"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11216"	"AKAP10"	"0.762"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"11216"	"AKAP10"	"0.762"	"0.241"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"11216"	"AKAP10"	"0.762"	"0.241"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11216"	"AKAP10"	"0.762"	"0.241"	"C1861884"	"Familial Sudden Death"	"disease"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11217"	"AKAP2"	"0.799"	"0.138"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11219"	"TREX2"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"11221"	"DUSP10"	"0.762"	"0.31"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11222"	"MRPL3"	"0.799"	"0.241"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"11222"	"MRPL3"	"0.799"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11222"	"MRPL3"	"0.799"	"0.241"	"C3281234"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"11224"	"RPL35"	"0.815"	"0.276"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11224"	"RPL35"	"0.815"	"0.276"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11227"	"GALNT5"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11228"	"RASSF8"	"0.752"	"0.241"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11230"	"PRAF2"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11231"	"SEC63"	"0.815"	"0.241"	"C0022680"	"Polycystic Kidney Diseases"	"group"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"11231"	"SEC63"	"0.815"	"0.241"	"C0158683"	"Polycystic liver disease"	"disease"	"C04;C06;C23"	"Disease or Syndrome"	"0.70"	"0.9090909"	"2004"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"11231"	"SEC63"	"0.815"	"0.241"	"C1567435"	"Polycystic Kidney - body part"	"phenotype"	"C12;C13;C16"	"Anatomical Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11231"	"SEC63"	"0.815"	"0.241"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11231"	"SEC63"	"0.815"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11232"	"POLG2"	"0.696"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11232"	"POLG2"	"0.696"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"11232"	"POLG2"	"0.696"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"11232"	"POLG2"	"0.696"	"0.517"	"C1834846"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"	"disease"	"C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11232"	"POLG2"	"0.696"	"0.517"	"C1864668"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.60"		"2006"	"2011"	"1"	"2"	"CTD_human;UNIPROT"
"11234"	"HPS5"	"0.799"	"0.241"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.40"		"2003"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"11234"	"HPS5"	"0.799"	"0.241"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11234"	"HPS5"	"0.799"	"0.241"	"C3888004"	"HERMANSKY-PUDLAK SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1980"	"2018"	"1"	"19"	"UNIPROT"
"11235"	"PDCD10"	"0.713"	"0.379"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"11235"	"PDCD10"	"0.713"	"0.379"	"C1864040"	"Cerebral Cavernous Malformations 3"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.38"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human"
"11235"	"PDCD10"	"0.713"	"0.379"	"C2931263"	"Familial cerebral cavernous malformation"	"disease"	"C04;C10;C14;C15;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"11235"	"PDCD10"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11236"	"RNF139"	"0.707"	"0.207"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.41"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2007"	"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"11236"	"RNF139"	"0.707"	"0.207"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"11240"	"PADI2"	"0.713"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"11249"	"NXPH2"	"0.857"	"0.103"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11249"	"NXPH2"	"0.857"	"0.103"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11250"	"GPR45"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11251"	"PTGDR2"	"0.681"	"0.586"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"11251"	"PTGDR2"	"0.681"	"0.586"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11252"	"PACSIN2"	"0.834"	"0.241"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11252"	"PACSIN2"	"0.834"	"0.241"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11252"	"PACSIN2"	"0.834"	"0.241"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C3280127"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"11253"	"MAN1B1"	"0.713"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"11254"	"SLC6A14"	"0.743"	"0.345"	"C0021843"	"Intestinal Obstruction"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11254"	"SLC6A14"	"0.743"	"0.345"	"C1859047"	"CYSTIC FIBROSIS MODIFIER 1"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11254"	"SLC6A14"	"0.743"	"0.345"	"C2678155"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"11254"	"SLC6A14"	"0.743"	"0.345"	"C3276246"	"MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0002622"	"Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2001"	"2007"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"1997"	"1997"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0233750"	"Hysterical amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0233796"	"Temporary Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0236795"	"Dissociative Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0262497"	"Global Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0750906"	"Tactile Amnesia"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0750907"	"Amnestic State"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11255"	"HRH3"	"0.648"	"0.345"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11257"	"TP53TG1"	"0.886"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11257"	"TP53TG1"	"0.886"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11257"	"TP53TG1"	"0.886"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11262"	"SP140"	"0.707"	"0.414"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.44"	"1"	"2008"	"2017"	"1"	"3"	"CTD_human"
"11262"	"SP140"	"0.707"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"11274"	"USP18"	"0.645"	"0.586"	"C0023269"	"leiomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11274"	"USP18"	"0.645"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"11274"	"USP18"	"0.645"	"0.586"	"C0205815"	"Leiomyosarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0205816"	"Leiomyosarcoma, Myxoid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11274"	"USP18"	"0.645"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11274"	"USP18"	"0.645"	"0.586"	"C4479376"	"PSEUDO-TORCH SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2017"	"0"	"1"	"ORPHANET"
"11276"	"SYNRG"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"11277"	"TREX1"	"0.58"	"0.621"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.60"	"0.9375"	"2007"	"2017"	"3"	"8"	"CTD_human;UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C0024145"	"Chilblain lupus 1"	"disease"	"C17;C26"	"Disease or Syndrome"	"0.68"	"1"	"2007"	"2016"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11277"	"TREX1"	"0.58"	"0.621"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"11277"	"TREX1"	"0.58"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11277"	"TREX1"	"0.58"	"0.621"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.90"	"1"	"1993"	"2017"	"8"	"24"	"CTD_human;UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C1835308"	"EXCESS LYMPHOCYTE LOW MOLECULAR WEIGHT DNA"	"phenotype"		"Finding"	"0.30"		"2007"	"2013"	"3"	"8"	"UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C1835309"	"EXCESS LMW-DNA"	"phenotype"		"Finding"	"0.30"		"2007"	"2013"	"3"	"8"	"UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C1860518"	"Vasculopathy, Retinal, With Cerebral Leukodystrophy"	"disease"	"C10;C11;C14;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"11277"	"TREX1"	"0.58"	"0.621"	"C3150315"	"AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2017"	"8"	"6"	"UNIPROT"
"11277"	"TREX1"	"0.58"	"0.621"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.50"		"2004"	"2017"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11277"	"TREX1"	"0.58"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11278"	"KLF12"	"0.743"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2016"	"1"	"1"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11278"	"KLF12"	"0.743"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11279"	"KLF8"	"0.681"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0014805"	"Primary Erythermalgia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"ORPHANET"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2018"	"9"	"0"	"GENOMICS_ENGLAND"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C1833661"	"PAROXYSMAL EXTREME PAIN DISORDER"	"disease"	"C23;F02"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11280"	"SCN11A"	"0.633"	"0.379"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11280"	"SCN11A"	"0.633"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11280"	"SCN11A"	"0.633"	"0.379"	"C3809882"	"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII"	"disease"		"Disease or Syndrome"	"0.90"		"1993"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"11280"	"SCN11A"	"0.633"	"0.379"	"C3809899"	"EPISODIC PAIN SYNDROME, FAMILIAL, 3"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2016"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"11281"	"POU6F2"	"0.857"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"11281"	"POU6F2"	"0.857"	"0.207"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.42"	"1"	"2005"	"2007"	"0"	"0"	"ORPHANET"
"11281"	"POU6F2"	"0.857"	"0.207"	"C1832099"	"Wilms tumor and radial bilateral aplasia"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.60"		"2001"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"11284"	"PNKP"	"0.616"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11284"	"PNKP"	"0.616"	"0.379"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"11284"	"PNKP"	"0.616"	"0.379"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0268134"	"DNA Repair-Deficiency"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11284"	"PNKP"	"0.616"	"0.379"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.41"	"1"	"2010"	"2015"	"1"	"1"	"GENOMICS_ENGLAND"
"11284"	"PNKP"	"0.616"	"0.379"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C1563696"	"DNA Repair-Deficiency Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C1563697"	"Chromosome Instability Syndromes"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C3150667"	"MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2008"	"2016"	"2"	"7"	"CTD_human;UNIPROT"
"11284"	"PNKP"	"0.616"	"0.379"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11284"	"PNKP"	"0.616"	"0.379"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C4225397"	"ATAXIA-OCULOMOTOR APRAXIA 4"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"11284"	"PNKP"	"0.616"	"0.379"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11284"	"PNKP"	"0.616"	"0.379"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.36"	"1"	"1987"	"2018"	"13"	"0"	"GENOMICS_ENGLAND"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C1869122"	"EHLERS-DANLOS SYNDROME, PROGEROID FORM"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.73"	"1"	"1975"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"11285"	"B4GALT7"	"0.636"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1987"	"1987"	"1"	"0"	"GENOMICS_ENGLAND"
"11309"	"SLCO2B1"	"0.752"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"11311"	"VPS45"	"0.743"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"11311"	"VPS45"	"0.743"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"11311"	"VPS45"	"0.743"	"0.276"	"C0340970"	"Congenital neutropenia"	"disease"	"C15"	"Congenital Abnormality"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"11311"	"VPS45"	"0.743"	"0.276"	"C1853118"	"Severe congenital neutropenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"11311"	"VPS45"	"0.743"	"0.276"	"C2931351"	"Familial myelofibrosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"11311"	"VPS45"	"0.743"	"0.276"	"C3809031"	"NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"11315"	"PARK7"	"0.586"	"0.552"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"0.962963"	"2003"	"2017"	"9"	"0"	"CTD_human;GENOMICS_ENGLAND"
"11315"	"PARK7"	"0.586"	"0.552"	"C0206160"	"Reticulocytosis"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11315"	"PARK7"	"0.586"	"0.552"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2004"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C1853445"	"PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET"	"disease"	"C10"	"Disease or Syndrome"	"0.83"	"1"	"2003"	"2017"	"13"	"5"	"CTD_human;UNIPROT"
"11315"	"PARK7"	"0.586"	"0.552"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2008"	"2016"	"2"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"11315"	"PARK7"	"0.586"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11315"	"PARK7"	"0.586"	"0.552"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2003"	"2018"	"0"	"0"	"ORPHANET"
"11321"	"GPN1"	"0.886"	"0.138"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"11321"	"GPN1"	"0.886"	"0.138"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"11322"	"TMC6"	"0.713"	"0.31"	"C0014522"	"Epidermodysplasia Verruciformis"	"disease"	"C02;C17"	"Neoplastic Process"	"0.70"	"1"	"2003"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"11326"	"VSIG4"	"0.727"	"0.345"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"11326"	"VSIG4"	"0.727"	"0.345"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11326"	"VSIG4"	"0.727"	"0.345"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11326"	"VSIG4"	"0.727"	"0.345"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"11329"	"STK38"	"0.773"	"0.379"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"11330"	"CTRC"	"0.713"	"0.379"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"11330"	"CTRC"	"0.713"	"0.379"	"C0149521"	"Pancreatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"11330"	"CTRC"	"0.713"	"0.379"	"C0238339"	"Hereditary pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.76"	"1"	"1993"	"2017"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"11330"	"CTRC"	"0.713"	"0.379"	"C1832108"	"PANCREATITIS, CHRONIC, PROTECTION AGAINST"	"phenotype"		"Finding"	"0.30"		"2008"	"2013"	"4"	"6"	"UNIPROT"
"11330"	"CTRC"	"0.713"	"0.379"	"C1842402"	"TROPICAL CALCIFIC PANCREATITIS"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"0"	"0"	"ORPHANET"
"11330"	"CTRC"	"0.713"	"0.379"	"C1868653"	"Pancreatitis, Calcific"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2013"	"4"	"6"	"UNIPROT"
"11330"	"CTRC"	"0.713"	"0.379"	"C1969419"	"PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2008"	"2013"	"4"	"7"	"UNIPROT"
"11330"	"CTRC"	"0.713"	"0.379"	"C4080064"	"Autosomal Dominant Hereditary Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"11337"	"GABARAP"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"11340"	"EXOSC8"	"0.743"	"0.345"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"11340"	"EXOSC8"	"0.743"	"0.345"	"C1843504"	"Pontocerebellar Hypoplasia Type 1"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"11340"	"EXOSC8"	"0.743"	"0.345"	"C4015160"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 1C"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"11343"	"MGLL"	"0.672"	"0.448"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11343"	"MGLL"	"0.672"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"11343"	"MGLL"	"0.672"	"0.448"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11343"	"MGLL"	"0.672"	"0.448"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"11343"	"MGLL"	"0.672"	"0.448"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22795"	"NID2"	"0.762"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22795"	"NID2"	"0.762"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22796"	"COG2"	"0.785"	"0.172"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"22796"	"COG2"	"0.785"	"0.172"	"C4479353"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"22797"	"TFEC"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22797"	"TFEC"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"1994"	"1998"	"0"	"0"	"CGI"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"22800"	"RRAS2"	"0.696"	"0.207"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"		"1994"	"1994"	"0"	"1"	"CGI"
"22800"	"RRAS2"	"0.696"	"0.207"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.50"		"1994"	"1994"	"1"	"1"	"CGI;UNIPROT"
"22802"	"CLCA4"	"0.743"	"0.31"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.46"	"1"	"2010"	"2018"	"1"	"7"	"CTD_human"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22806"	"IKZF3"	"0.639"	"0.552"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"22806"	"IKZF3"	"0.639"	"0.552"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"22806"	"IKZF3"	"0.639"	"0.552"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22807"	"IKZF2"	"0.743"	"0.276"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22807"	"IKZF2"	"0.743"	"0.276"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22807"	"IKZF2"	"0.743"	"0.276"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"22807"	"IKZF2"	"0.743"	"0.276"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2002"	"2013"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0007273"	"Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2011"	"2017"	"1"	"2"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0577631"	"Carotid Atherosclerosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0600178"	"External Carotid Artery Diseases"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0750986"	"Internal Carotid Artery Diseases"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C0750987"	"Arterial Diseases, Common Carotid"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22808"	"MRAS"	"0.727"	"0.276"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.44"	"0.75"	"2009"	"2018"	"1"	"4"	"CTD_human"
"22809"	"ATF5"	"0.713"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"22820"	"COPG1"	"1"	"0.069"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"22822"	"PHLDA1"	"0.713"	"0.31"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"22827"	"PUF60"	"0.672"	"0.379"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2009"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"22827"	"PUF60"	"0.672"	"0.379"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22827"	"PUF60"	"0.672"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22827"	"PUF60"	"0.672"	"0.379"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22827"	"PUF60"	"0.672"	"0.379"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22827"	"PUF60"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"22827"	"PUF60"	"0.672"	"0.379"	"C3810023"	"VERHEIJ SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"22827"	"PUF60"	"0.672"	"0.379"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22843"	"PPM1E"	"0.773"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"0"	"0"	"UNIPROT"
"22843"	"PPM1E"	"0.773"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22843"	"PPM1E"	"0.773"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22843"	"PPM1E"	"0.773"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22844"	"FRMPD1"	"0.886"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22845"	"DOLK"	"0.727"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22845"	"DOLK"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"22845"	"DOLK"	"0.727"	"0.31"	"C1835849"	"Congenital Disorder Of Glycosylation, Type Im"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2007"	"2014"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"22845"	"DOLK"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"22850"	"ADNP2"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"PSYGENET"
"22852"	"ANKRD26"	"0.773"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"22852"	"ANKRD26"	"0.773"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"22852"	"ANKRD26"	"0.773"	"0.276"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"22852"	"ANKRD26"	"0.773"	"0.276"	"C1832388"	"Platelet Disorder, Familial, with Associated Myeloid Malignancy"	"disease"	"C04;C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22852"	"ANKRD26"	"0.773"	"0.276"	"C1861185"	"THROMBOCYTOPENIA 2 (disorder)"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"0"	"1"	"CTD_human"
"22853"	"LMTK2"	"0.857"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22853"	"LMTK2"	"0.857"	"0.103"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"22853"	"LMTK2"	"0.857"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"22854"	"NTNG1"	"0.672"	"0.414"	"C2748910"	"Rett Syndrome, Atypical"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"22854"	"NTNG1"	"0.672"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"22856"	"CHSY1"	"0.713"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22856"	"CHSY1"	"0.713"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"22856"	"CHSY1"	"0.713"	"0.414"	"C1854466"	"Temtamy preaxial brachydactyly syndrome"	"disease"	"C05;C07;C09;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"2010"	"2014"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"22856"	"CHSY1"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22858"	"ICK"	"0.602"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"22858"	"ICK"	"0.602"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22858"	"ICK"	"0.602"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22858"	"ICK"	"0.602"	"0.621"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22858"	"ICK"	"0.602"	"0.621"	"C2675227"	"Endocrine-Cerebroosteodysplasia"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.90"		"2009"	"2018"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"22861"	"NLRP1"	"0.555"	"0.69"	"C1847835"	"VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)"	"disease"		"Disease or Syndrome"	"0.70"	"1"	"2002"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"22861"	"NLRP1"	"0.555"	"0.69"	"C3808876"	"PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING"	"disease"		"Neoplastic Process"	"0.70"		"2013"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"22861"	"NLRP1"	"0.555"	"0.69"	"C4479278"	"AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"22864"	"R3HDM2"	"0.799"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22864"	"R3HDM2"	"0.799"	"0.207"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22864"	"R3HDM2"	"0.799"	"0.207"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22864"	"R3HDM2"	"0.799"	"0.207"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22866"	"CNKSR2"	"0.773"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22866"	"CNKSR2"	"0.773"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22866"	"CNKSR2"	"0.773"	"0.241"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22866"	"CNKSR2"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"22868"	"FASTKD2"	"0.667"	"0.517"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2008"	"2008"	"0"	"1"	"CTD_human"
"22868"	"FASTKD2"	"0.667"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22868"	"FASTKD2"	"0.667"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22871"	"NLGN1"	"0.752"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"22871"	"NLGN1"	"0.752"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2018"	"1"	"1"	"PSYGENET"
"22871"	"NLGN1"	"0.752"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2016"	"1"	"1"	"PSYGENET"
"22872"	"SEC31A"	"0.857"	"0.138"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"22874"	"PLEKHA6"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"22878"	"TRAPPC8"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22880"	"MORC2"	"0.762"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2016"	"2018"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"22880"	"MORC2"	"0.762"	"0.207"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22880"	"MORC2"	"0.762"	"0.207"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22880"	"MORC2"	"0.762"	"0.207"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22880"	"MORC2"	"0.762"	"0.207"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"22880"	"MORC2"	"0.762"	"0.207"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22880"	"MORC2"	"0.762"	"0.207"	"C4225243"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z"	"disease"		"Disease or Syndrome"	"0.70"		"1994"	"2017"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"22885"	"ABLIM3"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"		"2011"	"2013"	"1"	"2"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0027404"	"Narcolepsy"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"2010"	"2018"	"1"	"9"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C0751362"	"Narcolepsy-Cataplexy Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"		"2013"	"2015"	"0"	"1"	"ORPHANET"
"22891"	"ZNF365"	"0.685"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C1456240"	"Narcolepsy without cataplexy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22891"	"ZNF365"	"0.685"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22891"	"ZNF365"	"0.685"	"0.448"	"C2700426"	"NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.40"		"2003"	"2003"	"0"	"1"	"CTD_human"
"22897"	"CEP164"	"0.773"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22897"	"CEP164"	"0.773"	"0.345"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22897"	"CEP164"	"0.773"	"0.345"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22897"	"CEP164"	"0.773"	"0.345"	"C3541853"	"NEPHRONOPHTHISIS 15"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"4"	"CTD_human;UNIPROT"
"22897"	"CEP164"	"0.773"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"22900"	"CARD8"	"0.645"	"0.552"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22900"	"CARD8"	"0.645"	"0.552"	"C0028797"	"Occupational Diseases"	"group"	"C24"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"22900"	"CARD8"	"0.645"	"0.552"	"C0032226"	"Pleural Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22902"	"RUFY3"	"0.762"	"0.138"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"22904"	"SBNO2"	"0.743"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"22906"	"TRAK1"	"0.834"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22906"	"TRAK1"	"0.834"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"22906"	"TRAK1"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22907"	"DHX30"	"0.857"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"22907"	"DHX30"	"0.857"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"22907"	"DHX30"	"0.857"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"22909"	"FAN1"	"0.659"	"0.414"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2010"	"2016"	"4"	"0"	"CLINGEN"
"22909"	"FAN1"	"0.659"	"0.414"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.50"		"2010"	"2016"	"4"	"0"	"CLINGEN;ORPHANET"
"22909"	"FAN1"	"0.659"	"0.414"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.50"		"2010"	"2016"	"4"	"0"	"CLINGEN;ORPHANET"
"22909"	"FAN1"	"0.659"	"0.414"	"C2931118"	"Megalocytic interstitial nephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"22909"	"FAN1"	"0.659"	"0.414"	"C3553774"	"INTERSTITIAL NEPHRITIS, KARYOMEGALIC"	"disease"		"Disease or Syndrome"	"0.91"	"1"	"2012"	"2016"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"22913"	"RALY"	"0.685"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22913"	"RALY"	"0.685"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22913"	"RALY"	"0.685"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22914"	"KLRK1"	"0.505"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"22917"	"ZP1"	"0.928"		"C4014291"	"OOCYTE MATURATION DEFECT 1"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"22917"	"ZP1"	"0.928"		"C4540205"	"OOCYTE MATURATION DEFECT 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22918"	"CD93"	"0.735"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22919"	"MAPRE1"	"0.707"	"0.31"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22919"	"MAPRE1"	"0.707"	"0.31"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"22924"	"MAPRE3"	"0.785"	"0.172"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22924"	"MAPRE3"	"0.785"	"0.172"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22924"	"MAPRE3"	"0.785"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22924"	"MAPRE3"	"0.785"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22925"	"PLA2R1"	"0.685"	"0.31"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0009398"	"Color vision defect"	"phenotype"	"C10;C11;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"22926"	"ATF6"	"0.57"	"0.759"	"C0036457"	"Scrapie"	"disease"	"C10;C22"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0085636"	"Photophobia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.72"	"1"	"2015"	"2017"	"2"	"1"	"CLINGEN;CTD_human;ORPHANET"
"22926"	"ATF6"	"0.57"	"0.759"	"C0155015"	"Color Blindness, Red"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0155016"	"Color Blindness, Red-Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0155017"	"Color Blindness, Blue"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0155018"	"Color Blindness, Acquired"	"phenotype"	"C10;C11;C23"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0239777"	"Color Blindness, Green"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0242225"	"Color blindness"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0700501"	"Congenital nystagmus"	"disease"	"C10;C11;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0751042"	"Color Blindness, Inherited"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0751043"	"Monochromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22926"	"ATF6"	"0.57"	"0.759"	"C4225297"	"ACHROMATOPSIA 7"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"2"	"9"	"CTD_human;UNIPROT"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C0796037"	"Martsolf syndrome"	"disease"	"C10;C11;C19;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C1838625"	"Warburg Sjo Fledelius syndrome"	"disease"	"C05;C10;C11;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.69"	"0.8888889"	"1993"	"2017"	"0"	"17"	"CTD_human;ORPHANET"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"22930"	"RAB3GAP1"	"0.57"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"22931"	"RAB18"	"0.586"	"0.552"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22931"	"RAB18"	"0.586"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"22931"	"RAB18"	"0.586"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22931"	"RAB18"	"0.586"	"0.552"	"C1838625"	"Warburg Sjo Fledelius syndrome"	"disease"	"C05;C10;C11;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.55"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"22931"	"RAB18"	"0.586"	"0.552"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"22931"	"RAB18"	"0.586"	"0.552"	"C3280203"	"WARBURG MICRO SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"1"	"4"	"UNIPROT"
"22931"	"RAB18"	"0.586"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22933"	"SIRT2"	"0.594"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"22933"	"SIRT2"	"0.594"	"0.586"	"C2939186"	"Disturbance in mood"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"22934"	"RPIA"	"0.713"	"0.379"	"C1291609"	"Ribose 5-Phosphate Isomerase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"		"1999"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"22937"	"SCAP"	"0.785"	"0.276"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"22941"	"SHANK2"	"0.713"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2010"	"2016"	"2"	"0"	"CTD_human"
"22941"	"SHANK2"	"0.713"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22941"	"SHANK2"	"0.713"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22941"	"SHANK2"	"0.713"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22941"	"SHANK2"	"0.713"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"22943"	"DKK1"	"0.484"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9285714"	"2007"	"2017"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0264080"	"Juvenile osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"22943"	"DKK1"	"0.484"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2007"	"2017"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C0750929"	"Arnold-Chiari Malformation, Type I"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"22943"	"DKK1"	"0.484"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22943"	"DKK1"	"0.484"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"22947"	"DUX4L1"	"1"	"0.103"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.39"	"0.875"	"2007"	"2016"	"0"	"0"	"ORPHANET"
"22948"	"CCT5"	"0.681"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22948"	"CCT5"	"0.681"	"0.379"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22948"	"CCT5"	"0.681"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"22948"	"CCT5"	"0.681"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"22948"	"CCT5"	"0.681"	"0.379"	"C1850395"	"Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2006"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"22948"	"CCT5"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"22948"	"CCT5"	"0.681"	"0.379"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2014"	"4"	"0"	"CLINGEN"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22953"	"P2RX2"	"0.667"	"0.483"	"C1842371"	"DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2002"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"22953"	"P2RX2"	"0.667"	"0.483"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2014"	"4"	"0"	"CLINGEN"
"22953"	"P2RX2"	"0.667"	"0.483"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"22954"	"TRIM32"	"0.609"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22954"	"TRIM32"	"0.609"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"22954"	"TRIM32"	"0.609"	"0.586"	"C0270968"	"Limb-girdle muscular dystrophy type 2H"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"1.00"	"1"	"1973"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"22954"	"TRIM32"	"0.609"	"0.586"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.65"	"1"	"1998"	"2013"	"0"	"1"	"GENOMICS_ENGLAND"
"22954"	"TRIM32"	"0.609"	"0.586"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.49"	"1"	"2006"	"2017"	"0"	"2"	"ORPHANET"
"22954"	"TRIM32"	"0.609"	"0.586"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22954"	"TRIM32"	"0.609"	"0.586"	"C1859569"	"BARDET-BIEDL SYNDROME 11"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"2006"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"22954"	"TRIM32"	"0.609"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"22954"	"TRIM32"	"0.609"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"22974"	"TPX2"	"0.621"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2000"	"2016"	"0"	"0"	"UNIPROT"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2015"	"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"22976"	"PAXIP1"	"0.773"	"0.138"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"22977"	"AKR7A3"			"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22978"	"NT5C2"	"0.572"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"22978"	"NT5C2"	"0.572"	"0.724"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"22978"	"NT5C2"	"0.572"	"0.724"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"22978"	"NT5C2"	"0.572"	"0.724"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"22978"	"NT5C2"	"0.572"	"0.724"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"1983"	"2013"	"1"	"0"	"CTD_human"
"22978"	"NT5C2"	"0.572"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"22978"	"NT5C2"	"0.572"	"0.724"	"C3888209"	"SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2009"	"2018"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"22982"	"DIP2C"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22982"	"DIP2C"	"0.857"	"0.138"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"22982"	"DIP2C"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22983"	"MAST1"	"0.886"	"0.069"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22983"	"MAST1"	"0.886"	"0.069"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"22985"	"ACIN1"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"22985"	"ACIN1"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"22992"	"KDM2A"	"0.735"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22992"	"KDM2A"	"0.735"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22992"	"KDM2A"	"0.735"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"22995"	"CEP152"	"0.667"	"0.379"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"22995"	"CEP152"	"0.667"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"22995"	"CEP152"	"0.667"	"0.379"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"22995"	"CEP152"	"0.667"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"22995"	"CEP152"	"0.667"	"0.379"	"C3151187"	"SECKEL SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"22995"	"CEP152"	"0.667"	"0.379"	"C3553886"	"MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2015"	"1"	"8"	"CTD_human;UNIPROT"
"22995"	"CEP152"	"0.667"	"0.379"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"22995"	"CEP152"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"22996"	"TTC39A"	"0.928"	"0.103"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"22996"	"TTC39A"	"0.928"	"0.103"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22998"	"LIMCH1"	"0.834"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"22999"	"RIMS1"	"0.743"	"0.172"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"22999"	"RIMS1"	"0.743"	"0.172"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2017"	"0"	"0"	"ORPHANET"
"22999"	"RIMS1"	"0.743"	"0.172"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"22999"	"RIMS1"	"0.743"	"0.172"	"C1863634"	"Cone-Rod Dystrophy 7"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.64"	"1"	"1998"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"22999"	"RIMS1"	"0.743"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23001"	"WDFY3"	"0.928"	"0.103"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23001"	"WDFY3"	"0.928"	"0.103"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23001"	"WDFY3"	"0.928"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23001"	"WDFY3"	"0.928"	"0.103"	"C4479608"	"MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"UNIPROT"
"23005"	"MAPKBP1"	"0.815"	"0.103"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23005"	"MAPKBP1"	"0.815"	"0.103"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23005"	"MAPKBP1"	"0.815"	"0.103"	"C4310640"	"NEPHRONOPHTHISIS 20"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"23011"	"RAB21"	"0.857"	"0.172"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23013"	"SPEN"	"0.642"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23013"	"SPEN"	"0.642"	"0.655"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23013"	"SPEN"	"0.642"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23013"	"SPEN"	"0.642"	"0.655"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23013"	"SPEN"	"0.642"	"0.655"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23013"	"SPEN"	"0.642"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23014"	"FBXO21"			"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23020"	"SNRNP200"	"0.69"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.48"	"1"	"2006"	"2017"	"0"	"3"	"ORPHANET"
"23020"	"SNRNP200"	"0.69"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23020"	"SNRNP200"	"0.69"	"0.379"	"C1835895"	"RETINITIS PIGMENTOSA 33 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2014"	"8"	"7"	"CTD_human;UNIPROT"
"23022"	"PALLD"	"0.652"	"0.379"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2016"	"0"	"0"	"CTD_human"
"23022"	"PALLD"	"0.652"	"0.379"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23022"	"PALLD"	"0.652"	"0.379"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.34"	"0.5"	"2007"	"2009"	"0"	"0"	"CTD_human"
"23022"	"PALLD"	"0.652"	"0.379"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2009"	"0"	"0"	"ORPHANET"
"23024"	"PDZRN3"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23025"	"UNC13A"	"0.696"	"0.276"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.66"	"1"	"2009"	"2016"	"1"	"1"	"CTD_human;ORPHANET"
"23025"	"UNC13A"	"0.696"	"0.276"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23025"	"UNC13A"	"0.696"	"0.276"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23025"	"UNC13A"	"0.696"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"23026"	"MYO16"	"0.799"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23028"	"KDM1A"	"0.579"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"23028"	"KDM1A"	"0.579"	"0.655"	"C4225229"	"CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2016"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23030"	"KDM4B"	"0.636"	"0.379"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23030"	"KDM4B"	"0.636"	"0.379"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23030"	"KDM4B"	"0.636"	"0.379"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23030"	"KDM4B"	"0.636"	"0.379"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23030"	"KDM4B"	"0.636"	"0.379"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23030"	"KDM4B"	"0.636"	"0.379"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23033"	"DOPEY1"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23034"	"SAMD4A"	"0.815"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23036"	"ZNF292"	"0.834"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23040"	"MYT1L"	"0.69"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2012"	"2012"	"3"	"0"	"PSYGENET"
"23040"	"MYT1L"	"0.69"	"0.379"	"C0036346"	"Schizophrenia, Childhood"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23040"	"MYT1L"	"0.69"	"0.379"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"PSYGENET"
"23040"	"MYT1L"	"0.69"	"0.379"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"PSYGENET"
"23040"	"MYT1L"	"0.69"	"0.379"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23040"	"MYT1L"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"23040"	"MYT1L"	"0.69"	"0.379"	"C4225296"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 39"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"0"	"3"	"CTD_human"
"23040"	"MYT1L"	"0.69"	"0.379"	"C4225432"	"CHROMOSOME 2p25.3 DUPLICATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23040"	"MYT1L"	"0.69"	"0.379"	"C4225433"	"CHROMOSOME 2p25.3 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23042"	"PDXDC1"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"23043"	"TNIK"	"0.696"	"0.483"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"23043"	"TNIK"	"0.696"	"0.483"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23043"	"TNIK"	"0.696"	"0.483"	"C4310755"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"23046"	"KIF21B"	"0.857"	"0.138"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"23049"	"SMG1"	"0.639"	"0.552"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23054"	"NCOA6"	"0.648"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1996"	"1996"	"0"	"0"	"UNIPROT"
"23054"	"NCOA6"	"0.648"	"0.621"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23054"	"NCOA6"	"0.648"	"0.621"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23061"	"TBC1D9B"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23064"	"SETX"	"0.627"	"0.69"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23064"	"SETX"	"0.627"	"0.69"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"23064"	"SETX"	"0.627"	"0.69"	"C1853761"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"2004"	"2018"	"8"	"19"	"CTD_human;ORPHANET;UNIPROT"
"23064"	"SETX"	"0.627"	"0.69"	"C1865409"	"Amyotrophic Lateral Sclerosis 4, Juvenile"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.76"	"1"	"1998"	"2018"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"23064"	"SETX"	"0.627"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23065"	"EMC1"	"0.713"	"0.31"	"C4225172"	"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"23067"	"SETD1B"	"0.886"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23067"	"SETD1B"	"0.886"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"23071"	"ERP44"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23071"	"ERP44"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23074"	"UHRF1BP1L"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23074"	"UHRF1BP1L"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23074"	"UHRF1BP1L"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23078"	"VWA8"	"0.815"	"0.069"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23080"	"AVL9"	"0.857"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23080"	"AVL9"	"0.857"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23080"	"AVL9"	"0.857"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"23081"	"KDM4C"	"0.676"	"0.345"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23085"	"ERC1"	"0.815"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2002"	"0"	"0"	"ORPHANET"
"23086"	"EXPH5"	"0.886"	"0.069"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.50"		"2013"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23086"	"EXPH5"	"0.886"	"0.069"	"C3554367"	"EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23090"	"ZNF423"	"0.645"	"0.586"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23090"	"ZNF423"	"0.645"	"0.586"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23090"	"ZNF423"	"0.645"	"0.586"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23090"	"ZNF423"	"0.645"	"0.586"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23090"	"ZNF423"	"0.645"	"0.586"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23090"	"ZNF423"	"0.645"	"0.586"	"C3539071"	"NEPHRONOPHTHISIS 14"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"23090"	"ZNF423"	"0.645"	"0.586"	"C3553846"	"JOUBERT SYNDROME 19"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"23090"	"ZNF423"	"0.645"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2011"	"0"	"0"	"CGI"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0027019"	"Myelomonocytic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.60"		"2000"	"2000"	"1"	"1"	"CTD_human;UNIPROT"
"23092"	"ARHGAP26"	"0.713"	"0.276"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.34"	"1"	"2000"	"2011"	"0"	"0"	"CGI"
"23093"	"TTLL5"	"0.752"	"0.276"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23093"	"TTLL5"	"0.752"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23093"	"TTLL5"	"0.752"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23093"	"TTLL5"	"0.752"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23093"	"TTLL5"	"0.752"	"0.276"	"C4014501"	"CONE-ROD DYSTROPHY 19"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"6"	"CTD_human;UNIPROT"
"23094"	"SIPA1L3"	"0.815"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.32"	"1"	"2016"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"23094"	"SIPA1L3"	"0.815"	"0.172"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"23094"	"SIPA1L3"	"0.815"	"0.172"	"C4225182"	"CATARACT 45"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9811321"	"1993"	"2017"	"1"	"1"	"GENOMICS_ENGLAND"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.45"	"0.8"	"2008"	"2012"	"1"	"1"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.48"	"1"	"1997"	"2015"	"0"	"1"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2008"	"2014"	"0"	"1"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2014"	"5"	"0"	"CLINGEN"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2014"	"5"	"0"	"CLINGEN"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2014"	"5"	"0"	"CLINGEN"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2014"	"5"	"0"	"CLINGEN"
"23095"	"KIF1B"	"0.548"	"0.586"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CTD_human"
"23095"	"KIF1B"	"0.548"	"0.586"	"C1861678"	"Charcot-Marie-Tooth Disease, Axonal, Type 2a1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"		"1998"	"2001"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C0795864"	"Smith-Magenis syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C0796224"	"MENTAL RETARDATION, X-LINKED 18"	"disease"		"Disease or Syndrome"	"0.40"		"1994"	"2017"	"2"	"1"	"UNIPROT"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"1992"	"2010"	"1"	"0"	"CTD_human"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C1845181"	"MENTAL RETARDATION, X-LINKED 78"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2010"	"2016"	"2"	"0"	"CTD_human;UNIPROT"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C2749022"	"Chromosome Xp11.23-P11.22 Duplication Syndrome"	"disease"	"C16;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"1992"	"2017"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"23096"	"IQSEC2"	"0.619"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.48"	"1"	"2010"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"23097"	"CDK19"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"23098"	"SARM1"	"0.773"	"0.172"	"C0035235"	"Respiratory Syncytial Virus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"23101"	"MCF2L2"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23101"	"MCF2L2"	"0.815"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"23111"	"SPART"	"0.645"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23111"	"SPART"	"0.645"	"0.586"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23111"	"SPART"	"0.645"	"0.586"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2002"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"23111"	"SPART"	"0.645"	"0.586"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23111"	"SPART"	"0.645"	"0.586"	"C0393559"	"Troyer syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"2002"	"2018"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"23111"	"SPART"	"0.645"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"23112"	"TNRC6B"	"0.815"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23112"	"TNRC6B"	"0.815"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23112"	"TNRC6B"	"0.815"	"0.276"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23112"	"TNRC6B"	"0.815"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23114"	"NFASC"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"23118"	"TAB2"	"0.656"	"0.448"	"C3554279"	"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"2"	"CTD_human;UNIPROT"
"23118"	"TAB2"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23118"	"TAB2"	"0.656"	"0.448"	"C4509918"	"Polyvalvular heart disease syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23126"	"POGZ"	"0.652"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23126"	"POGZ"	"0.652"	"0.414"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"23126"	"POGZ"	"0.652"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23126"	"POGZ"	"0.652"	"0.414"	"C4225351"	"WHITE-SUTTON SYNDROME"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2015"	"2018"	"0"	"15"	"CTD_human;ORPHANET"
"23127"	"COLGALT2"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23129"	"PLXND1"	"0.707"	"0.448"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"23129"	"PLXND1"	"0.707"	"0.448"	"C0221060"	"Mobius Syndrome"	"disease"	"C07;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2016"	"0"	"0"	"ORPHANET"
"23129"	"PLXND1"	"0.707"	"0.448"	"C0853240"	"Mobius II syndrome"	"disease"	"C07;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"23133"	"PHF8"	"0.681"	"0.414"	"C1846055"	"Siderius X-linked mental retardation syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2010"	"9"	"5"	"CTD_human;ORPHANET;UNIPROT"
"23133"	"PHF8"	"0.681"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2006"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"23135"	"KDM6B"	"0.63"	"0.552"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23135"	"KDM6B"	"0.63"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23135"	"KDM6B"	"0.63"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23135"	"KDM6B"	"0.63"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23135"	"KDM6B"	"0.63"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23136"	"EPB41L3"	"0.642"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23136"	"EPB41L3"	"0.642"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23136"	"EPB41L3"	"0.642"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23136"	"EPB41L3"	"0.642"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23137"	"SMC5"	"0.834"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23139"	"MAST2"	"0.834"	"0.103"	"C1334807"	"Mucinous carcinoma of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23139"	"MAST2"	"0.834"	"0.103"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23141"	"ANKLE2"	"0.713"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23141"	"ANKLE2"	"0.713"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"23141"	"ANKLE2"	"0.713"	"0.379"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23141"	"ANKLE2"	"0.713"	"0.379"	"C4225249"	"MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"23143"	"LRCH1"	"0.799"	"0.207"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23143"	"LRCH1"	"0.799"	"0.207"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23149"	"FCHO1"	"1"	"0.034"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"23152"	"CIC"	"0.58"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"1"	"UNIPROT"
"23152"	"CIC"	"0.58"	"0.517"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2013"	"2016"	"0"	"0"	"CGI"
"23152"	"CIC"	"0.58"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"23152"	"CIC"	"0.58"	"0.517"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2017"	"2"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"0"	"0"	"CGI"
"23152"	"CIC"	"0.58"	"0.517"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23152"	"CIC"	"0.58"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2010"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23152"	"CIC"	"0.58"	"0.517"	"C4539848"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 45"	"disease"		"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2017"	"2"	"4"	"UNIPROT"
"23154"	"NCDN"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"23158"	"TBC1D9"	"0.434"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23162"	"MAPK8IP3"	"0.815"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23162"	"MAPK8IP3"	"0.815"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23163"	"GGA3"	"0.834"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"23164"	"MPRIP"	"0.676"	"0.448"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23165"	"NUP205"	"0.752"	"0.207"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"CTD_human"
"23165"	"NUP205"	"0.752"	"0.207"	"C1868672"	"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23165"	"NUP205"	"0.752"	"0.207"	"C4225165"	"NEPHROTIC SYNDROME, TYPE 13"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"23166"	"STAB1"	"0.762"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"23166"	"STAB1"	"0.762"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23166"	"STAB1"	"0.762"	"0.276"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"23166"	"STAB1"	"0.762"	"0.276"	"C0564408"	"Manic mood"	"phenotype"		"Finding"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"23166"	"STAB1"	"0.762"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23166"	"STAB1"	"0.762"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23169"	"SLC35D1"	"0.727"	"0.345"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23169"	"SLC35D1"	"0.727"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"23169"	"SLC35D1"	"0.727"	"0.345"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23169"	"SLC35D1"	"0.727"	"0.345"	"C0432194"	"Schneckenbecken dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.82"	"1"	"2008"	"2009"	"0"	"3"	"CTD_human;ORPHANET"
"23169"	"SLC35D1"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23171"	"GPD1L"	"0.707"	"0.207"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23171"	"GPD1L"	"0.707"	"0.207"	"C0038644"	"Sudden infant death syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2009"	"0"	"3"	"UNIPROT"
"23171"	"GPD1L"	"0.707"	"0.207"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.56"	"1"	"2007"	"2010"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"23171"	"GPD1L"	"0.707"	"0.207"	"C2673193"	"Brugada Syndrome 2"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2007"	"2009"	"3"	"1"	"CTD_human;UNIPROT"
"23171"	"GPD1L"	"0.707"	"0.207"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23174"	"ZCCHC14"	"0.834"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23174"	"ZCCHC14"	"0.834"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23174"	"ZCCHC14"	"0.834"	"0.276"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23174"	"ZCCHC14"	"0.834"	"0.276"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23175"	"LPIN1"	"0.652"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23175"	"LPIN1"	"0.652"	"0.517"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23175"	"LPIN1"	"0.652"	"0.517"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23175"	"LPIN1"	"0.652"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23175"	"LPIN1"	"0.652"	"0.517"	"C1849386"	"Myoglobinuria, Acute Recurrent, Autosomal Recessive"	"disease"	"C05"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"0"	"4"	"CTD_human"
"23175"	"LPIN1"	"0.652"	"0.517"	"C4274324"	"Genetic recurrent myoglobinuria"	"disease"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"23178"	"PASK"	"0.834"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"23178"	"PASK"	"0.834"	"0.138"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23178"	"PASK"	"0.834"	"0.138"	"C2931817"	"Chromosome 2q37 deletion syndrome"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23179"	"RGL1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23181"	"DIP2A"	"0.815"	"0.207"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23186"	"RCOR1"	"0.762"	"0.414"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"23186"	"RCOR1"	"0.762"	"0.414"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23187"	"PHLDB1"	"0.785"	"0.207"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2009"	"2017"	"1"	"1"	"CTD_human"
"23187"	"PHLDB1"	"0.785"	"0.207"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23187"	"PHLDB1"	"0.785"	"0.207"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23189"	"KANK1"	"0.672"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23189"	"KANK1"	"0.672"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23189"	"KANK1"	"0.672"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23189"	"KANK1"	"0.672"	"0.448"	"C2751938"	"Cerebral Palsy, Spastic Quadriplegic, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23189"	"KANK1"	"0.672"	"0.448"	"C2752061"	"Cerebral Palsy, Spastic Quadriplegic, 2"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23189"	"KANK1"	"0.672"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"23191"	"CYFIP1"	"0.735"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"23193"	"GANAB"	"0.762"	"0.31"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"23193"	"GANAB"	"0.762"	"0.31"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23193"	"GANAB"	"0.762"	"0.31"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23193"	"GANAB"	"0.762"	"0.31"	"C3887964"	"POLYCYSTIC KIDNEY DISEASE 3, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"3"	"UNIPROT"
"23197"	"FAF2"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23197"	"FAF2"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23198"	"PSME4"	"1"	"0.069"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"23198"	"PSME4"	"1"	"0.069"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"23199"	"GSE1"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"23201"	"FAM168A"	"0.785"	"0.138"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23201"	"FAM168A"	"0.785"	"0.138"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23201"	"FAM168A"	"0.785"	"0.138"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23201"	"FAM168A"	"0.785"	"0.138"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23203"	"PMPCA"	"0.727"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"23203"	"PMPCA"	"0.727"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"23203"	"PMPCA"	"0.727"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"23203"	"PMPCA"	"0.727"	"0.379"	"C1859298"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1999"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"23204"	"ARL6IP1"	"0.735"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23204"	"ARL6IP1"	"0.735"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23204"	"ARL6IP1"	"0.735"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23204"	"ARL6IP1"	"0.735"	"0.379"	"C3810294"	"SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"23207"	"PLEKHM2"	"0.773"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"23208"	"SYT11"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2005"	"2007"	"2"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23209"	"MLC1"	"0.648"	"0.448"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23209"	"MLC1"	"0.648"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2004"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"23209"	"MLC1"	"0.648"	"0.448"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23209"	"MLC1"	"0.648"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.5"	"2002"	"2016"	"4"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C0036344"	"Schizophrenia, Catatonic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.5"	"2002"	"2005"	"4"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23209"	"MLC1"	"0.648"	"0.448"	"C0221765"	"Chronic schizophrenia"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23209"	"MLC1"	"0.648"	"0.448"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"23209"	"MLC1"	"0.648"	"0.448"	"C1858854"	"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS"	"disease"	"C04;C10;C16;C18;C23"	"Congenital Abnormality"	"0.80"	"0.9666667"	"1993"	"2018"	"5"	"32"	"CTD_human;ORPHANET;UNIPROT"
"23209"	"MLC1"	"0.648"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2011"	"5"	"0"	"GENOMICS_ENGLAND"
"23211"	"ZC3H4"			"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23212"	"RRS1"	"0.773"	"0.345"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23213"	"SULF1"	"0.621"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23213"	"SULF1"	"0.621"	"0.483"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"23213"	"SULF1"	"0.621"	"0.483"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23214"	"XPO6"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23216"	"TBC1D1"	"0.773"	"0.241"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2006"	"2016"	"3"	"0"	"CTD_human"
"23217"	"ZFR2"	"1"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23218"	"NBEAL2"	"0.752"	"0.276"	"C0272302"	"Gray Platelet Syndrome"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.99"	"1"	"2011"	"2017"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"23218"	"NBEAL2"	"0.752"	"0.276"	"C2717750"	"Platelet alpha-Granule Deficiency"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"3"	"0"	"CTD_human;ORPHANET"
"23220"	"DTX4"	"0.928"	"0.103"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23220"	"DTX4"	"0.928"	"0.103"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23221"	"RHOBTB2"	"0.713"	"0.448"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.42"	"0.5"	"2012"	"2017"	"1"	"1"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0410189"	"Muscular Dystrophy, Emery-Dreifuss"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0410190"	"Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23224"	"SYNE2"	"0.676"	"0.414"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C1450051"	"Autosomal Recessive Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23224"	"SYNE2"	"0.676"	"0.414"	"C2751805"	"EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2015"	"1"	"2"	"UNIPROT"
"23224"	"SYNE2"	"0.676"	"0.414"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23228"	"PLCL2"	"0.762"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23229"	"ARHGEF9"	"0.762"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"23229"	"ARHGEF9"	"0.762"	"0.241"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"23229"	"ARHGEF9"	"0.762"	"0.241"	"C1845102"	"Hyperekplexia and Epilepsy"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"2004"	"2018"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23229"	"ARHGEF9"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"23230"	"VPS13A"	"0.633"	"0.448"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"23230"	"VPS13A"	"0.633"	"0.448"	"C0393576"	"Chorea Acanthocytosis Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1988"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23230"	"VPS13A"	"0.633"	"0.448"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"23230"	"VPS13A"	"0.633"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2016"	"1"	"1"	"PSYGENET"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2010"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23236"	"PLCB1"	"0.652"	"0.448"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C3150988"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"23236"	"PLCB1"	"0.652"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23237"	"ARC"	"0.636"	"0.517"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2011"	"3"	"0"	"PSYGENET"
"23237"	"ARC"	"0.636"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"0.5"	"2000"	"2012"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"PSYGENET"
"23237"	"ARC"	"0.636"	"0.517"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23237"	"ARC"	"0.636"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23239"	"PHLPP1"	"0.642"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23244"	"PDS5A"	"0.834"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23244"	"PDS5A"	"0.834"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2016"	"2"	"0"	"PSYGENET"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23245"	"ASTN2"	"0.69"	"0.379"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"1"	"CTD_human"
"23246"	"BOP1"	"0.857"	"0.138"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23246"	"BOP1"	"0.857"	"0.138"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23246"	"BOP1"	"0.857"	"0.138"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23246"	"BOP1"	"0.857"	"0.138"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23247"	"KIAA0556"	"0.72"	"0.448"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"1"	"ORPHANET"
"23248"	"RPRD2"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23248"	"RPRD2"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23250"	"ATP11A"	"0.701"	"0.414"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23250"	"ATP11A"	"0.701"	"0.414"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"23255"	"MTCL1"	"0.886"	"0.069"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"23255"	"MTCL1"	"0.886"	"0.069"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23256"	"SCFD1"	"0.886"	"0.069"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"23256"	"SCFD1"	"0.886"	"0.069"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23256"	"SCFD1"	"0.886"	"0.069"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23258"	"DENND5A"	"0.886"	"0.034"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"23258"	"DENND5A"	"0.886"	"0.034"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23258"	"DENND5A"	"0.886"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"23258"	"DENND5A"	"0.886"	"0.034"	"C4310635"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"6"	"CTD_human;UNIPROT"
"23259"	"DDHD2"	"0.713"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23259"	"DDHD2"	"0.713"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.53"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"23259"	"DDHD2"	"0.713"	"0.448"	"C3539495"	"SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.92"	"1"	"2006"	"2017"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"23259"	"DDHD2"	"0.713"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"23261"	"CAMTA1"	"0.645"	"0.483"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23261"	"CAMTA1"	"0.645"	"0.483"	"C0206732"	"Epithelioid hemangioendothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"0"	"0"	"ORPHANET"
"23261"	"CAMTA1"	"0.645"	"0.483"	"C3553661"	"CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2018"	"0"	"3"	"CTD_human;ORPHANET"
"23261"	"CAMTA1"	"0.645"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23269"	"MGA"	"0.762"	"0.276"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23269"	"MGA"	"0.762"	"0.276"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23269"	"MGA"	"0.762"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23269"	"MGA"	"0.762"	"0.276"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23269"	"MGA"	"0.762"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23270"	"TSPYL4"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23271"	"CAMSAP2"	"0.886"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0001403"	"Addison Disease"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2016"	"1"	"2"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2015"	"2"	"15"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"1"	"12"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2017"	"1"	"3"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2017"	"2"	"7"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0162538"	"Immunoglobulin A deficiency (disorder)"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"		"2010"	"2016"	"2"	"1"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2011"	"2"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"23274"	"CLEC16A"	"0.619"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"23284"	"ADGRL3"	"0.857"	"0.103"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23284"	"ADGRL3"	"0.857"	"0.103"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"23284"	"ADGRL3"	"0.857"	"0.103"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23286"	"WWC1"	"0.663"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"23286"	"WWC1"	"0.663"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"23286"	"WWC1"	"0.663"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"23286"	"WWC1"	"0.663"	"0.552"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23286"	"WWC1"	"0.663"	"0.552"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"23287"	"AGTPBP1"	"0.815"	"0.207"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23287"	"AGTPBP1"	"0.815"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23288"	"IQCE"	"0.886"	"0.069"	"C3887487"	"Postaxial polydactyly type A"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23294"	"ANKS1A"	"0.834"	"0.103"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23294"	"ANKS1A"	"0.834"	"0.103"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23299"	"BICD2"	"0.72"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2017"	"0"	"1"	"GENOMICS_ENGLAND"
"23299"	"BICD2"	"0.72"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23299"	"BICD2"	"0.72"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23299"	"BICD2"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23299"	"BICD2"	"0.72"	"0.414"	"C3809049"	"SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"1994"	"2017"	"3"	"7"	"ORPHANET;UNIPROT"
"23301"	"EHBP1"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23301"	"EHBP1"	"0.857"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23301"	"EHBP1"	"0.857"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"23301"	"EHBP1"	"0.857"	"0.138"	"C2678479"	"Prostate Cancer, Hereditary, 12"	"disease"	"C04;C12;C16"	"Neoplastic Process"	"0.40"		"2008"	"2008"	"0"	"1"	"CTD_human"
"23302"	"WSCD1"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23302"	"WSCD1"	"1"	"0.069"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23302"	"WSCD1"	"1"	"0.069"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23302"	"WSCD1"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.6666667"	"2006"	"2012"	"3"	"0"	"PSYGENET"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23305"	"ACSL6"	"0.785"	"0.276"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23307"	"FKBP15"	"0.815"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23308"	"ICOSLG"	"0.627"	"0.552"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"1"	"CTD_human"
"23308"	"ICOSLG"	"0.627"	"0.552"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"23310"	"NCAPD3"	"0.857"	"0.207"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23312"	"DMXL2"	"0.743"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"23312"	"DMXL2"	"0.743"	"0.31"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2018"	"2"	"0"	"CLINGEN"
"23312"	"DMXL2"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"23312"	"DMXL2"	"0.743"	"0.31"	"C4015261"	"POLYENDOCRINE-POLYNEUROPATHY SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"23312"	"DMXL2"	"0.743"	"0.31"	"C4539881"	"DEAFNESS, AUTOSOMAL DOMINANT 71"	"disease"		"Disease or Syndrome"	"0.40"		"2018"	"2018"	"1"	"1"	"UNIPROT"
"23314"	"SATB2"	"0.588"	"0.517"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23314"	"SATB2"	"0.588"	"0.517"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.55"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"23314"	"SATB2"	"0.588"	"0.517"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23314"	"SATB2"	"0.588"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23314"	"SATB2"	"0.588"	"0.517"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.56"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"23314"	"SATB2"	"0.588"	"0.517"	"C2676739"	"Chromosome 2q32-Q33 Deletion Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2007"	"2018"	"0"	"6"	"CTD_human;ORPHANET"
"23314"	"SATB2"	"0.588"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.46"	"1"	"2014"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"23315"	"SLC9A8"	"0.762"	"0.241"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23315"	"SLC9A8"	"0.762"	"0.241"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23315"	"SLC9A8"	"0.762"	"0.241"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23316"	"CUX2"	"0.743"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2001"	"2007"	"1"	"0"	"PSYGENET"
"23316"	"CUX2"	"0.743"	"0.276"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"23316"	"CUX2"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"23317"	"DNAJC13"	"0.743"	"0.207"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"4"	"UNIPROT"
"23317"	"DNAJC13"	"0.743"	"0.207"	"C4225353"	"PARKINSON DISEASE 21"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23317"	"DNAJC13"	"0.743"	"0.207"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23321"	"TRIM2"	"0.735"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23321"	"TRIM2"	"0.735"	"0.345"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"23321"	"TRIM2"	"0.735"	"0.345"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23321"	"TRIM2"	"0.735"	"0.345"	"C3809655"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0008780"	"Ciliary Motility Disorders"	"group"	"C08;C09;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0015397"	"Disorder of eye"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2007"	"2"	"0"	"CTD_human"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2008"	"2017"	"0"	"1"	"ORPHANET"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1846790"	"JOUBERT SYNDROME 4 (disorder)"	"disease"	"C10;C11;C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1857662"	"COACH syndrome"	"disease"	"C06;C10;C11;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"2010"	"2010"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1969052"	"MECKEL SYNDROME, TYPE 5"	"disease"	"C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.60"		"2007"	"2014"	"2"	"6"	"CTD_human;UNIPROT"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C1969053"	"JOUBERT SYNDROME 7"	"disease"	"C10;C11;C12;C13;C23;F01;F03"	"Disease or Syndrome"	"0.80"		"2007"	"2016"	"4"	"21"	"CTD_human;UNIPROT"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23322"	"RPGRIP1L"	"0.569"	"0.655"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2007"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"23325"	"WASHC4"	"0.815"	"0.241"	"C4014386"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.9375"	"2001"	"2015"	"2"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0039075"	"Syndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0265553"	"Polysyndactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C1848213"	"Periventricular Heterotopia, X-Linked"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C1868720"	"Periventricular Nodular Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"23327"	"NEDD4L"	"0.619"	"0.655"	"C4310669"	"PERIVENTRICULAR NODULAR HETEROTOPIA 7"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"4"	"UNIPROT"
"23328"	"SASH1"	"0.676"	"0.379"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"1"	"1"	"GENOMICS_ENGLAND"
"23328"	"SASH1"	"0.676"	"0.379"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23328"	"SASH1"	"0.676"	"0.379"	"C3492944"	"Lentiginosis Profusa"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23334"	"SZT2"	"0.799"	"0.069"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2013"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"23334"	"SZT2"	"0.799"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"23334"	"SZT2"	"0.799"	"0.069"	"C3809624"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"23338"	"JADE2"	"0.928"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"23338"	"JADE2"	"0.928"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23338"	"JADE2"	"0.928"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23339"	"VPS39"	"0.785"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23339"	"VPS39"	"0.785"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23339"	"VPS39"	"0.785"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23339"	"VPS39"	"0.785"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23339"	"VPS39"	"0.785"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"0.6666667"	"2011"	"2018"	"3"	"3"	"PSYGENET"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0154409"	"Recurrent major depressive episodes"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0410189"	"Muscular Dystrophy, Emery-Dreifuss"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.56"	"1"	"2008"	"2017"	"0"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0410190"	"Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1998"	"2008"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2009"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1450051"	"Autosomal Recessive Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2006"	"2015"	"3"	"3"	"CTD_human;UNIPROT"
"23345"	"SYNE1"	"0.594"	"0.621"	"C1853116"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2007"	"2017"	"0"	"27"	"CTD_human;ORPHANET"
"23345"	"SYNE1"	"0.594"	"0.621"	"C2751807"	"Emery-Dreifuss Muscular Dystrophy 4"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"10"	"UNIPROT"
"23345"	"SYNE1"	"0.594"	"0.621"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23345"	"SYNE1"	"0.594"	"0.621"	"C3683483"	"Autosomal Recessive Cerebellar Ataxia Type 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23345"	"SYNE1"	"0.594"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"23345"	"SYNE1"	"0.594"	"0.621"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"2012"	"2018"	"0"	"0"	"ORPHANET"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C1834671"	"FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.64"	"1"	"2013"	"2017"	"6"	"14"	"CTD_human;UNIPROT"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C1863878"	"Arhinia, choanal atresia, and microphthalmia"	"disease"	"C08;C09;C11;C16"	"Disease or Syndrome"	"0.60"		"1972"	"2017"	"2"	"18"	"CTD_human;UNIPROT"
"23347"	"SMCHD1"	"0.636"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23348"	"DOCK9"	"0.799"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23350"	"U2SURP"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23352"	"UBR4"	"0.762"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"23352"	"UBR4"	"0.762"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"23352"	"UBR4"	"0.762"	"0.276"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23352"	"UBR4"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"23355"	"VPS8"	"1"	"0.069"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"1996"	"2016"	"3"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"23362"	"PSD3"	"0.685"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23362"	"PSD3"	"0.685"	"0.379"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2016"	"1"	"1"	"PSYGENET"
"23362"	"PSD3"	"0.685"	"0.379"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23362"	"PSD3"	"0.685"	"0.379"	"C1867439"	"Pterygium, Antecubital"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CLINGEN"
"23363"	"OBSL1"	"0.727"	"0.207"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23363"	"OBSL1"	"0.727"	"0.207"	"C1848862"	"Miller-McKusick-Malvaux-Syndrome (3M Syndrome)"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2017"	"0"	"0"	"ORPHANET"
"23363"	"OBSL1"	"0.727"	"0.207"	"C1851996"	"Dwarfism tall vertebrae"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23363"	"OBSL1"	"0.727"	"0.207"	"C2678312"	"Three M Syndrome 1"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23363"	"OBSL1"	"0.727"	"0.207"	"C2752041"	"Three M Syndrome 2"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.41"	"0"	"2009"	"2016"	"0"	"5"	"CTD_human"
"23363"	"OBSL1"	"0.727"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"23365"	"ARHGEF12"	"0.727"	"0.276"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23370"	"ARHGEF18"	"0.701"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23370"	"ARHGEF18"	"0.701"	"0.345"	"C4479481"	"RETINITIS PIGMENTOSA 78"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"23373"	"CRTC1"	"0.602"	"0.621"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.41"	"1"	"2014"	"2017"	"1"	"2"	"CTD_human"
"23373"	"CRTC1"	"0.602"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"23382"	"AHCYL2"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23382"	"AHCYL2"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C0024433"	"Macrostomia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C0796179"	"Teebi syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C1801950"	"Opitz-G syndrome, type 2"	"disease"	"C05;C12;C13;C16"	"Disease or Syndrome"	"0.71"	"1"	"1989"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C1838348"	"Oculomaxillofacial dysostosis"	"disease"	"C05;C07;C11;C16"	"Disease or Syndrome"	"0.72"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23384"	"SPECC1L"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1991"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23385"	"NCSTN"	"0.681"	"0.379"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2017"	"9"	"0"	"CTD_human;GENOMICS_ENGLAND;UNIPROT"
"23386"	"NUDCD3"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23386"	"NUDCD3"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23387"	"SIK3"	"0.752"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23389"	"MED13L"	"0.656"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23389"	"MED13L"	"0.656"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23389"	"MED13L"	"0.656"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23389"	"MED13L"	"0.656"	"0.414"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23389"	"MED13L"	"0.656"	"0.414"	"C1837341"	"Transposition of the Great Arteries, Dextro-Looped 1"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"		"2004"	"2004"	"1"	"4"	"CTD_human;UNIPROT"
"23389"	"MED13L"	"0.656"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.58"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23389"	"MED13L"	"0.656"	"0.414"	"C4225208"	"MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2018"	"0"	"12"	"CTD_human;ORPHANET"
"23394"	"ADNP"	"0.663"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"23394"	"ADNP"	"0.663"	"0.517"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"23394"	"ADNP"	"0.663"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"PSYGENET"
"23394"	"ADNP"	"0.663"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23394"	"ADNP"	"0.663"	"0.517"	"C1542327"	"Fetus or newborn affected by alcohol transmitted via placenta or breast milk"	"disease"		"Finding"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"23394"	"ADNP"	"0.663"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2007"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"23394"	"ADNP"	"0.663"	"0.517"	"C4014538"	"HELSMOORTEL-VAN DER AA SYNDROME"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2018"	"0"	"10"	"CTD_human;ORPHANET"
"23395"	"LARS2"	"0.72"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"23395"	"LARS2"	"0.72"	"0.448"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"23395"	"LARS2"	"0.72"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"23395"	"LARS2"	"0.72"	"0.448"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.61"	"1"	"2013"	"2018"	"9"	"1"	"CLINGEN;ORPHANET"
"23395"	"LARS2"	"0.72"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23395"	"LARS2"	"0.72"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23395"	"LARS2"	"0.72"	"0.448"	"C3809105"	"PERRAULT SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2018"	"1"	"7"	"UNIPROT"
"23395"	"LARS2"	"0.72"	"0.448"	"C4310761"	"HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"23396"	"PIP5K1C"	"0.857"	"0.172"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"23396"	"PIP5K1C"	"0.857"	"0.172"	"C1969655"	"LETHAL CONGENITAL CONTRACTURAL SYNDROME 3"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23397"	"NCAPH"	"1"	"0.103"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0022340"	"Late-Infantile Neuronal Ceroid Lipfuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0022797"	"Adult Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2013"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0027877"	"Neuronal Ceroid-Lipofuscinoses"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.9473684"	"2007"	"2018"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0030569"	"Secondary Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0268281"	"Infantile neuronal ceroid lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0751383"	"Juvenile Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0751414"	"Parkinson Disease, Secondary Vascular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0751415"	"Atherosclerotic Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C1834207"	"Ceroid Lipofuscinosis, Neuronal, Parry Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C1847640"	"KUFOR-RAKEB SYNDROME"	"disease"	"C10"	"Disease or Syndrome"	"1.00"	"1"	"1979"	"2018"	"11"	"13"	"CTD_human;ORPHANET;UNIPROT"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23400"	"ATP13A2"	"0.611"	"0.276"	"C4310662"	"SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"23404"	"EXOSC2"	"0.928"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23404"	"EXOSC2"	"0.928"	"0.069"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23404"	"EXOSC2"	"0.928"	"0.069"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23404"	"EXOSC2"	"0.928"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23404"	"EXOSC2"	"0.928"	"0.069"	"C4540367"	"SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0003810"	"Sertoli-Leydig cell tumor of ovary"	"disease"	"C04;C12;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2017"	"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"23405"	"DICER1"	"0.479"	"0.724"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C0018413"	"Gynandroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.55"	"1"	"2011"	"2017"	"1"	"0"	"CGI;CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C0032000"	"Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23405"	"DICER1"	"0.479"	"0.724"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"23405"	"DICER1"	"0.479"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0036769"	"Sertoli Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0206723"	"Sertoli-Leydig Cell Tumor"	"disease"	"C04;C12;C13;C19"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2018"	"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0206724"	"Sex Cord-Stromal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2017"	"0"	"0"	"CGI"
"23405"	"DICER1"	"0.479"	"0.724"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C0302859"	"Euthyroid Goiter"	"disease"	"C19"	"Disease or Syndrome"	"0.61"	"1"	"2004"	"2011"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23405"	"DICER1"	"0.479"	"0.724"	"C0334401"	"Malignant Granulosa Cell Tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"23405"	"DICER1"	"0.479"	"0.724"	"C1266144"	"Pleuropulmonary blastoma"	"disease"	"C04"	"Neoplastic Process"	"0.80"	"0.9677419"	"2006"	"2018"	"4"	"4"	"CGI;CLINGEN;CTD_human;UNIPROT"
"23405"	"DICER1"	"0.479"	"0.724"	"C1567257"	"Granulosa Cell Cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"23405"	"DICER1"	"0.479"	"0.724"	"C1867234"	"Rhabdomyosarcoma, Embryonal, 2"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2012"	"2012"	"0"	"2"	"CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23405"	"DICER1"	"0.479"	"0.724"	"C3496549"	"Male Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23406"	"COTL1"	"0.713"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23406"	"COTL1"	"0.713"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23406"	"COTL1"	"0.713"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23406"	"COTL1"	"0.713"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23406"	"COTL1"	"0.713"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23408"	"SIRT5"	"0.762"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23409"	"SIRT4"	"0.773"	"0.276"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23409"	"SIRT4"	"0.773"	"0.276"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23409"	"SIRT4"	"0.773"	"0.276"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23410"	"SIRT3"	"0.598"	"0.586"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"23410"	"SIRT3"	"0.598"	"0.586"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23410"	"SIRT3"	"0.598"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"23410"	"SIRT3"	"0.598"	"0.586"	"C0085207"	"Gestational Diabetes"	"phenotype"	"C13;C18;C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23410"	"SIRT3"	"0.598"	"0.586"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.60"	"0.9285714"	"2008"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.36"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2011"	"2017"	"2"	"0"	"PSYGENET"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2018"	"3"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011303"	"Demyelinating Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011304"	"Demyelination"	"phenotype"	"C10"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.952381"	"2008"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.60"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0011884"	"Diabetic Retinopathy"	"disease"	"C11;C14;C19"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0014072"	"Experimental Autoimmune Encephalomyelitis"	"disease"	"C10;C20"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.60"	"1"	"2010"	"2018"	"5"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0020564"	"Hypertrophy"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2016"	"5"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.60"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2012"	"2012"	"2"	"0"	"PSYGENET"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0036939"	"Shared Paranoid Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0043020"	"Wallerian Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0155862"	"Streptococcal pneumonia"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0393953"	"Anterior Cerebral Circulation Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.36"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.58"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0751952"	"Anterior Circulation Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0751953"	"Brain Infarction, Posterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0751954"	"Venous Infarction, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0751955"	"Brain Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0919532"	"Genomic Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2016"	"5"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C2350037"	"Clinically Isolated Syndrome, CNS Demyelinating"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2010"	"2018"	"5"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"23411"	"SIRT1"	"0.432"	"0.828"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23413"	"NCS1"	"0.773"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2014"	"2"	"0"	"PSYGENET"
"23413"	"NCS1"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2014"	"2"	"0"	"PSYGENET"
"23413"	"NCS1"	"0.773"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.42"	"1"	"2007"	"2013"	"1"	"5"	"UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.51"	"1"	"2005"	"2007"	"1"	"0"	"CTD_human"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2013"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.98"	"0.875"	"2000"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.46"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C1857781"	"Diaphragmatic Hernia 3"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.40"		"2005"	"2013"	"0"	"3"	"CTD_human"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C4015129"	"46,XY SEX REVERSAL 9"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"23414"	"ZFPM2"	"0.582"	"0.552"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23415"	"KCNH4"	"0.645"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23417"	"MLYCD"	"0.685"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"		"1999"	"2004"	"3"	"0"	"GENOMICS_ENGLAND"
"23417"	"MLYCD"	"0.685"	"0.448"	"C0342793"	"Malonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.67"	"1"	"1984"	"2014"	"0"	"3"	"CTD_human;ORPHANET"
"23417"	"MLYCD"	"0.685"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23418"	"CRB1"	"0.579"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23418"	"CRB1"	"0.579"	"0.552"	"C0035305"	"Retinal Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23418"	"CRB1"	"0.579"	"0.552"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"1999"	"2018"	"3"	"6"	"CTD_human;ORPHANET"
"23418"	"CRB1"	"0.579"	"0.552"	"C0154832"	"Exudative retinopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23418"	"CRB1"	"0.579"	"0.552"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"0.9615385"	"2001"	"2018"	"1"	"2"	"CTD_human;ORPHANET"
"23418"	"CRB1"	"0.579"	"0.552"	"C0339546"	"Retinal Pigment Epithelial Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23418"	"CRB1"	"0.579"	"0.552"	"C1838647"	"RETINITIS PIGMENTOSA 12 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.84"	"1"	"1992"	"2017"	"15"	"34"	"CTD_human;UNIPROT"
"23418"	"CRB1"	"0.579"	"0.552"	"C1868310"	"Pigmented Paravenous Chorioretinal Atrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"2005"	"2005"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23418"	"CRB1"	"0.579"	"0.552"	"C3151202"	"LEBER CONGENITAL AMAUROSIS 8"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2017"	"20"	"34"	"CTD_human;UNIPROT"
"23418"	"CRB1"	"0.579"	"0.552"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23418"	"CRB1"	"0.579"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23421"	"ITGB3BP"	"0.799"	"0.172"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23421"	"ITGB3BP"	"0.799"	"0.172"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0017601"	"Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.61"	"1"	"2011"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23424"	"TDRD7"	"0.799"	"0.138"	"C3151304"	"CATARACT 36"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"23426"	"GRIP1"	"0.565"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"23426"	"GRIP1"	"0.565"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23426"	"GRIP1"	"0.565"	"0.621"	"C0265233"	"Cryptophthalmos syndrome"	"disease"	"C05;C11;C12;C13;C16"	"Disease or Syndrome"	"0.72"	"1"	"2000"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"23426"	"GRIP1"	"0.565"	"0.621"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"23426"	"GRIP1"	"0.565"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23428"	"SLC7A8"	"0.857"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23428"	"SLC7A8"	"0.857"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23431"	"AP4E1"	"0.681"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23431"	"AP4E1"	"0.681"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23431"	"AP4E1"	"0.681"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23431"	"AP4E1"	"0.681"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"23431"	"AP4E1"	"0.681"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23431"	"AP4E1"	"0.681"	"0.276"	"C3151056"	"SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23431"	"AP4E1"	"0.681"	"0.276"	"C3489627"	"Stuttering, Familial Persistent 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"15"	"CTD_human;UNIPROT"
"23431"	"AP4E1"	"0.681"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23432"	"GPR161"	"0.815"	"0.241"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"23433"	"RHOQ"	"0.834"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23435"	"TARDBP"	"0.53"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.9788918"	"2006"	"2018"	"6"	"0"	"CTD_human;ORPHANET"
"23435"	"TARDBP"	"0.53"	"0.586"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"6"	"0"	"CTD_human"
"23435"	"TARDBP"	"0.53"	"0.586"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2015"	"6"	"0"	"CTD_human"
"23435"	"TARDBP"	"0.53"	"0.586"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9668246"	"2006"	"2018"	"2"	"0"	"CTD_human"
"23435"	"TARDBP"	"0.53"	"0.586"	"C2677565"	"AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2018"	"13"	"27"	"UNIPROT"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3148872"	"FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2018"	"13"	"23"	"UNIPROT"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3150169"	"FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2018"	"13"	"23"	"UNIPROT"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3150171"	"FTLD-TDP, TARDBP-RELATED"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2018"	"13"	"23"	"UNIPROT"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3502417"	"Amyotrophic Lateral Sclerosis 10"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23435"	"TARDBP"	"0.53"	"0.586"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23436"	"CELA3B"	"0.857"	"0.138"	"C0267963"	"Exocrine pancreatic insufficiency"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"23438"	"HARS2"	"0.743"	"0.414"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"23438"	"HARS2"	"0.743"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23438"	"HARS2"	"0.743"	"0.414"	"C3554105"	"PERRAULT SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"1979"	"2011"	"1"	"2"	"UNIPROT"
"23438"	"HARS2"	"0.743"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23443"	"SLC35A3"	"0.743"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"23443"	"SLC35A3"	"0.743"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"23443"	"SLC35A3"	"0.743"	"0.241"	"C3809910"	"ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2017"	"2017"	"0"	"0"	"CGI"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.50"	"0.9666667"	"2012"	"2016"	"1"	"4"	"CTD_human"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"0.9607843"	"1990"	"2016"	"0"	"6"	"CGI"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.60"	"1"	"2013"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0346373"	"Malignant melanoma of iris"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0346388"	"Malignant melanoma of choroid"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"23451"	"SF3B1"	"0.526"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23451"	"SF3B1"	"0.526"	"0.552"	"C1264195"	"Refractory anemia with ringed sideroblasts"	"disease"		"Neoplastic Process"	"0.32"	"0.5"	"2014"	"2018"	"0"	"0"	"ORPHANET"
"23451"	"SF3B1"	"0.526"	"0.552"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"23451"	"SF3B1"	"0.526"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.70"	"0.974359"	"1990"	"2017"	"0"	"1"	"CGI;CTD_human"
"23456"	"ABCB10"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23456"	"ABCB10"	"0.886"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23456"	"ABCB10"	"0.886"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23456"	"ABCB10"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23460"	"ABCA6"	"0.857"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23460"	"ABCA6"	"0.857"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23460"	"ABCA6"	"0.857"	"0.172"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23460"	"ABCA6"	"0.857"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23461"	"ABCA5"	"0.773"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23461"	"ABCA5"	"0.773"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23461"	"ABCA5"	"0.773"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23461"	"ABCA5"	"0.773"	"0.276"	"C1851120"	"Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia"	"disease"	"C07;C16;C17;C23"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"ORPHANET"
"23462"	"HEY1"	"0.579"	"0.552"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0206663"	"Neuroectodermal Tumor, Primitive"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334584"	"Spongioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0334596"	"Medulloepithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0700367"	"Ependymoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0751675"	"Cerebral Primitive Neuroectodermal Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"23462"	"HEY1"	"0.579"	"0.552"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23464"	"GCAT"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23468"	"CBX5"	"0.652"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23468"	"CBX5"	"0.652"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23468"	"CBX5"	"0.652"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23469"	"PHF3"	"0.886"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"23474"	"ETHE1"	"0.713"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23474"	"ETHE1"	"0.713"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23474"	"ETHE1"	"0.713"	"0.379"	"C1865349"	"Ethylmalonic encephalopathy"	"disease"	"C10;C15;C16;C18;C23"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2017"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"23474"	"ETHE1"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23476"	"BRD4"	"0.529"	"0.759"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"2"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C1707291"	"NUT midline carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"23476"	"BRD4"	"0.529"	"0.759"	"C1802395"	"Congenital muscular hypertrophy-cerebral syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C1853099"	"Cornelia de Lange Syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23476"	"BRD4"	"0.529"	"0.759"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23479"	"ISCU"	"0.713"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23479"	"ISCU"	"0.713"	"0.276"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"23479"	"ISCU"	"0.713"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"23479"	"ISCU"	"0.713"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"23479"	"ISCU"	"0.713"	"0.276"	"C1850718"	"MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2012"	"0"	"2"	"CTD_human;ORPHANET"
"23483"	"TGDS"	"0.685"	"0.483"	"C1844887"	"Catel Manzke syndrome"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.72"	"1"	"1998"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"23483"	"TGDS"	"0.685"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23491"	"CES3"	"0.815"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23491"	"CES3"	"0.815"	"0.138"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23491"	"CES3"	"0.815"	"0.138"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23492"	"CBX7"	"0.639"	"0.483"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"1"	"6"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2010"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C0887833"	"Carcinoma, Pancreatic Ductal"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23493"	"HEY2"	"0.609"	"0.517"	"C1721096"	"Brugada ECG Pattern"	"phenotype"	"C14;C16"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.60"	"0.902439"	"1986"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.45"	"1"	"2004"	"2016"	"1"	"2"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C1836032"	"Immunoglobulin a deficiency 2"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.60"		"2005"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.40"	"1"	"1999"	"2015"	"0"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23495"	"TNFRSF13B"	"0.572"	"0.724"	"C3150354"	"IMMUNODEFICIENCY, COMMON VARIABLE, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2009"	"1"	"5"	"UNIPROT"
"23498"	"HAAO"	"0.762"	"0.172"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"23499"	"MACF1"	"0.799"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23500"	"DAAM2"	"0.834"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2008"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C1849128"	"Spastic paraplegia 15, autosomal recessive"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.84"	"0.75"	"2001"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"23503"	"ZFYVE26"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2001"	"2009"	"4"	"0"	"GENOMICS_ENGLAND"
"23508"	"TTC9"	"0.928"	"0.069"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23508"	"TTC9"	"0.928"	"0.069"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23508"	"TTC9"	"0.928"	"0.069"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23509"	"POFUT1"	"0.773"	"0.276"	"C0406811"	"Reticulate acropigmentation of Kitamura"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23509"	"POFUT1"	"0.773"	"0.276"	"C3714534"	"dowling-degos disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"2014"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"23511"	"NUP188"	"1"	"0.103"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23511"	"NUP188"	"1"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0027809"	"Neurilemmoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0027830"	"neurofibroma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0027962"	"Melanocytic nevus"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0206630"	"Endometrial Stromal Sarcoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.9375"	"2001"	"2016"	"0"	"0"	"ORPHANET"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0206727"	"Nerve Sheath Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"2"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0265210"	"Weaver syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0751374"	"Schwannomatosis, Plexiform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0751689"	"Peripheral Nerve Sheath Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0751690"	"Malignant Peripheral Nerve Sheath Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C0751691"	"Perineurioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"23512"	"SUZ12"	"0.559"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"23513"	"SCRIB"	"0.727"	"0.276"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"UNIPROT"
"23513"	"SCRIB"	"0.727"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"23513"	"SCRIB"	"0.727"	"0.276"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"UNIPROT"
"23514"	"SPIDR"	"0.713"	"0.448"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"23514"	"SPIDR"	"0.713"	"0.448"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"23516"	"SLC39A14"	"0.735"	"0.414"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23516"	"SLC39A14"	"0.735"	"0.414"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23516"	"SLC39A14"	"0.735"	"0.414"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23516"	"SLC39A14"	"0.735"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23516"	"SLC39A14"	"0.735"	"0.414"	"C4310765"	"HYPERMANGANESEMIA WITH DYSTONIA 2"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2016"	"1"	"6"	"CTD_human;UNIPROT"
"23521"	"RPL13A"	"0.785"	"0.207"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23522"	"KAT6B"	"0.565"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23522"	"KAT6B"	"0.565"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23522"	"KAT6B"	"0.565"	"0.69"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"23522"	"KAT6B"	"0.565"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23522"	"KAT6B"	"0.565"	"0.69"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"23522"	"KAT6B"	"0.565"	"0.69"	"C1853566"	"Genitopatellar Syndrome"	"disease"	"C05;C10;C12;C13;C16;C23;F01;F03"	"Disease or Syndrome"	"0.69"	"1"	"1993"	"2018"	"0"	"7"	"CTD_human;ORPHANET"
"23522"	"KAT6B"	"0.565"	"0.69"	"C1863557"	"Young Simpson syndrome"	"disease"	"C05;C10;C11;C14;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2018"	"0"	"10"	"CTD_human;ORPHANET"
"23522"	"KAT6B"	"0.565"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23522"	"KAT6B"	"0.565"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2013"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"23522"	"KAT6B"	"0.565"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23523"	"CABIN1"	"0.667"	"0.517"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23523"	"CABIN1"	"0.667"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"23523"	"CABIN1"	"0.667"	"0.517"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23526"	"ARHGAP45"	"0.857"	"0.172"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23526"	"ARHGAP45"	"0.857"	"0.172"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23526"	"ARHGAP45"	"0.857"	"0.172"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23526"	"ARHGAP45"	"0.857"	"0.172"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23528"	"ZNF281"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23529"	"CLCF1"	"0.713"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23529"	"CLCF1"	"0.713"	"0.379"	"C1832409"	"Crisponi syndrome"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"23529"	"CLCF1"	"0.713"	"0.379"	"C1848947"	"COLD-INDUCED SWEATING SYNDROME 1"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"23529"	"CLCF1"	"0.713"	"0.379"	"C1853198"	"COLD-INDUCED SWEATING SYNDROME 2"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"1"	"4"	"CTD_human;UNIPROT"
"23530"	"NNT"	"0.72"	"0.241"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"23530"	"NNT"	"0.72"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23530"	"NNT"	"0.72"	"0.241"	"C3553587"	"GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"1"	"13"	"CTD_human;UNIPROT"
"23530"	"NNT"	"0.72"	"0.241"	"C4049650"	"Familial Glucocorticoid Deficiency Type 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23532"	"PRAME"	"0.573"	"0.483"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0018675"	"Head Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.39"	"0.8888889"	"2000"	"2016"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2017"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0027533"	"Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0746787"	"Cancer of Neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0751177"	"Cancer of Head"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C0887900"	"Upper Aerodigestive Tract Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23532"	"PRAME"	"0.573"	"0.483"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23533"	"PIK3R5"	"0.752"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23533"	"PIK3R5"	"0.752"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"23533"	"PIK3R5"	"0.752"	"0.345"	"C1853761"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23533"	"PIK3R5"	"0.752"	"0.345"	"C3554690"	"ATAXIA-OCULOMOTOR APRAXIA 3"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"23534"	"TNPO3"	"0.701"	"0.448"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2015"	"0"	"2"	"ORPHANET"
"23534"	"TNPO3"	"0.701"	"0.448"	"C1842062"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2001"	"2013"	"1"	"2"	"ORPHANET;UNIPROT"
"23539"	"SLC16A8"	"0.785"	"0.138"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2013"	"2016"	"1"	"1"	"CTD_human"
"23543"	"RBFOX2"	"0.645"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23543"	"RBFOX2"	"0.645"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23543"	"RBFOX2"	"0.645"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23544"	"SEZ6L"	"0.799"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"1993"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0268355"	"Cutis Laxa, Autosomal Recessive, Type IIA"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"1993"	"2014"	"0"	"13"	"CTD_human;ORPHANET"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0406587"	"Wrinkly skin syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.63"	"0.6666667"	"2008"	"2014"	"1"	"1"	"CTD_human;ORPHANET"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C4479387"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23545"	"ATP6V0A2"	"0.584"	"0.621"	"C4479409"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23547"	"LILRA4"	"1"	"0.103"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23551"	"RASD2"	"0.785"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"23552"	"CDK20"	"0.72"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23552"	"CDK20"	"0.72"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23552"	"CDK20"	"0.72"	"0.379"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23554"	"TSPAN12"	"0.735"	"0.31"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.40"	"0.9333333"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"23554"	"TSPAN12"	"0.735"	"0.31"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"23554"	"TSPAN12"	"0.735"	"0.31"	"C2750079"	"Exudative Vitreoretinopathy 5"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"3"	"12"	"CTD_human;UNIPROT"
"23556"	"PIGN"	"0.614"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23556"	"PIGN"	"0.614"	"0.621"	"C0220730"	"Fryns syndrome"	"disease"	"C05;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23556"	"PIGN"	"0.614"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"23556"	"PIGN"	"0.614"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23556"	"PIGN"	"0.614"	"0.621"	"C3279775"	"MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2011"	"2017"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"23556"	"PIGN"	"0.614"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"23558"	"WBP2"	"0.886"	"0.069"	"C4539964"	"DEAFNESS, AUTOSOMAL RECESSIVE 107"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.45"	"1"	"2009"	"2018"	"1"	"4"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C3279660"	"DEAFNESS, AUTOSOMAL RECESSIVE 29"	"disease"		"Disease or Syndrome"	"0.80"		"2001"	"2013"	"2"	"6"	"CTD_human;UNIPROT"
"23562"	"CLDN14"	"0.743"	"0.276"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23562"	"CLDN14"	"0.743"	"0.276"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"23564"	"DDAH2"	"0.707"	"0.379"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"23564"	"DDAH2"	"0.707"	"0.379"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23564"	"DDAH2"	"0.707"	"0.379"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"23568"	"ARL2BP"	"0.681"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"23568"	"ARL2BP"	"0.681"	"0.517"	"C3809503"	"RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"23569"	"PADI4"	"0.592"	"0.586"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.50"	"0.8765432"	"2003"	"2018"	"1"	"6"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"23569"	"PADI4"	"0.592"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2011"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23569"	"PADI4"	"0.592"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"23576"	"DDAH1"	"0.663"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23576"	"DDAH1"	"0.663"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23581"	"CASP14"	"0.69"	"0.241"	"C4310621"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"23582"	"CCNDBP1"	"0.752"	"0.276"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23582"	"CCNDBP1"	"0.752"	"0.276"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23582"	"CCNDBP1"	"0.752"	"0.276"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23582"	"CCNDBP1"	"0.752"	"0.276"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2016"	"1"	"1"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23586"	"DDX58"	"0.569"	"0.69"	"C0432254"	"Singleton Merten syndrome"	"disease"	"C05;C07;C10;C14;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23586"	"DDX58"	"0.569"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23586"	"DDX58"	"0.569"	"0.69"	"C4225380"	"SINGLETON-MERTEN SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"23590"	"PDSS1"	"0.727"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"23590"	"PDSS1"	"0.727"	"0.517"	"C3553354"	"COENZYME Q10 DEFICIENCY, PRIMARY, 2"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2013"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"23590"	"PDSS1"	"0.727"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23592"	"LEMD3"	"0.639"	"0.379"	"C0025239"	"Melorheostosis"	"disease"	"C05"	"Disease or Syndrome"	"0.34"	"0.5"	"2004"	"2009"	"0"	"0"	"CTD_human"
"23592"	"LEMD3"	"0.639"	"0.379"	"C0029455"	"Osteopoikilosis (disorder)"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.50"	"0.6666667"	"2004"	"2018"	"0"	"0"	"ORPHANET"
"23592"	"LEMD3"	"0.639"	"0.379"	"C0265514"	"Dermatofibrosis lenticularis disseminata"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.67"	"0.7142857"	"2004"	"2011"	"0"	"1"	"CTD_human;ORPHANET"
"23592"	"LEMD3"	"0.639"	"0.379"	"C1833699"	"Osteopoikilosis, Isolated"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23592"	"LEMD3"	"0.639"	"0.379"	"C2931505"	"Mixed sclerosing bone dystrophy"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"23592"	"LEMD3"	"0.639"	"0.379"	"C3149695"	"Melorheostosis with Osteopoikilosis"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"		"1997"	"2009"	"0"	"1"	"ORPHANET"
"23592"	"LEMD3"	"0.639"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23592"	"LEMD3"	"0.639"	"0.379"	"C4305140"	"12q14 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23593"	"HEBP2"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23593"	"HEBP2"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23594"	"ORC6"	"0.636"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23594"	"ORC6"	"0.636"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"23594"	"ORC6"	"0.636"	"0.517"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.54"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"23594"	"ORC6"	"0.636"	"0.517"	"C3151113"	"MEIER-GORLIN SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"1995"	"2016"	"1"	"7"	"UNIPROT"
"23594"	"ORC6"	"0.636"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1995"	"1995"	"1"	"0"	"GENOMICS_ENGLAND"
"23597"	"ACOT9"	"0.857"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23597"	"ACOT9"	"0.857"	"0.103"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23597"	"ACOT9"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"23600"	"AMACR"	"0.536"	"0.655"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"1998"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23600"	"AMACR"	"0.536"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0019816"	"Hereditary, Type VII, Motor and Sensory Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0027888"	"Hereditary Motor and Sensory Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2015"	"3"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"23600"	"AMACR"	"0.536"	"0.655"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"		"2000"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"23600"	"AMACR"	"0.536"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2018"	"3"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"23600"	"AMACR"	"0.536"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"23600"	"AMACR"	"0.536"	"0.655"	"C1858328"	"Bile acid synthesis defect, congenital, 4"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.70"		"1998"	"2003"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"23600"	"AMACR"	"0.536"	"0.655"	"C3280428"	"Alpha-Methylacyl-CoA Racemase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.91"	"1"	"2000"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23601"	"CLEC5A"	"0.773"	"0.207"	"C0019100"	"Severe Dengue"	"disease"	"C02"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"23601"	"CLEC5A"	"0.773"	"0.207"	"C0376300"	"Dengue Shock Syndrome"	"disease"	"C02"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23603"	"CORO1C"	"0.752"	"0.276"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23603"	"CORO1C"	"0.752"	"0.276"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23604"	"DAPK2"	"0.636"	"0.552"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"1"	"2011"	"2018"	"2"	"2"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.49"	"1"	"2003"	"2014"	"0"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2014"	"2"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"23607"	"CD2AP"	"0.642"	"0.448"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"23616"	"SH3BP1"	"0.886"	"0.172"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"23616"	"SH3BP1"	"0.886"	"0.172"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"23619"	"ZIM2"	"0.928"	"0.069"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23619"	"ZIM2"	"0.928"	"0.069"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23619"	"ZIM2"	"0.928"	"0.069"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"0.9521531"	"1999"	"2018"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2006"	"2016"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2009"	"2011"	"2"	"0"	"PSYGENET"
"23621"	"BACE1"	"0.616"	"0.517"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"23621"	"BACE1"	"0.616"	"0.517"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"23624"	"CBLC"	"0.834"	"0.207"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23624"	"CBLC"	"0.834"	"0.207"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"23624"	"CBLC"	"0.834"	"0.207"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23627"	"PRND"	"0.799"	"0.172"	"C0022107"	"Irritable Mood"	"phenotype"	"F01"	"Finding"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"23630"	"KCNE5"	"0.752"	"0.414"	"C0340493"	"Paroxysmal familial ventricular fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"23630"	"KCNE5"	"0.752"	"0.414"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"23630"	"KCNE5"	"0.752"	"0.414"	"C1846242"	"Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis"	"disease"	"C05;C10;C12;C13;C15;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23635"	"SSBP2"	"0.752"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23635"	"SSBP2"	"0.752"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"23636"	"NUP62"	"0.567"	"0.69"	"C0795996"	"STRIATONIGRAL DEGENERATION, INFANTILE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"23636"	"NUP62"	"0.567"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2002"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"23639"	"LRRC6"	"0.735"	"0.241"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.45"	"1"	"1993"	"2017"	"0"	"1"	"ORPHANET"
"23639"	"LRRC6"	"0.735"	"0.241"	"C3543826"	"CILIARY DYSKINESIA, PRIMARY, 19"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"3"	"8"	"CTD_human;UNIPROT"
"23639"	"LRRC6"	"0.735"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23639"	"LRRC6"	"0.735"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23639"	"LRRC6"	"0.735"	"0.241"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23643"	"LY96"	"0.69"	"0.483"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23643"	"LY96"	"0.69"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23646"	"PLD3"	"0.799"	"0.207"	"C3810349"	"ALZHEIMER DISEASE 19"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23650"	"TRIM29"	"0.713"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2015"	"1"	"1"	"UNIPROT"
"23657"	"SLC7A11"	"0.69"	"0.552"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23657"	"SLC7A11"	"0.69"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"23657"	"SLC7A11"	"0.69"	"0.552"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23658"	"LSM5"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23658"	"LSM5"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23670"	"CEMIP2"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"23671"	"TMEFF2"	"0.645"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23671"	"TMEFF2"	"0.645"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"23671"	"TMEFF2"	"0.645"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"23671"	"TMEFF2"	"0.645"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23673"	"STX12"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23676"	"SMPX"	"0.928"	"0.138"	"C1848204"	"DEAFNESS, X-LINKED 4 (disorder)"	"disease"	"C09;C10;C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"1997"	"2013"	"0"	"6"	"CTD_human"
"23678"	"SGK3"	"0.785"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2015"	"0"	"0"	"UNIPROT"
"23682"	"RAB38"	"0.743"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23683"	"PRKD3"	"0.834"	"0.103"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23683"	"PRKD3"	"0.834"	"0.103"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"23705"	"CADM1"	"0.537"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23705"	"CADM1"	"0.537"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"		"2002"	"2007"	"1"	"0"	"CTD_human"
"23708"	"GSPT2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"23729"	"SHPK"	"0.743"	"0.241"	"C1291373"	"Deficiency of sedoheptulokinase"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"ORPHANET"
"23731"	"TMEM245"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"23732"	"FRRS1L"	"0.743"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"23732"	"FRRS1L"	"0.743"	"0.172"	"C4310770"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2017"	"0"	"5"	"CTD_human"
"23741"	"EID1"	"0.857"	"0.138"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23742"	"NPAP1"	"0.696"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"23742"	"NPAP1"	"0.696"	"0.345"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human"
"23742"	"NPAP1"	"0.696"	"0.345"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23742"	"NPAP1"	"0.696"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"23743"	"BHMT2"	"0.834"	"0.172"	"C0008924"	"Cleft upper lip"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23743"	"BHMT2"	"0.834"	"0.172"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23743"	"BHMT2"	"0.834"	"0.172"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"23746"	"AIPL1"	"0.656"	"0.241"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.67"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"23746"	"AIPL1"	"0.656"	"0.241"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2018"	"0"	"1"	"ORPHANET"
"23746"	"AIPL1"	"0.656"	"0.241"	"C1858386"	"Leber Congenital Amaurosis 4"	"disease"	"C11"	"Disease or Syndrome"	"0.82"	"1"	"1993"	"2017"	"3"	"6"	"CTD_human;UNIPROT"
"23746"	"AIPL1"	"0.656"	"0.241"	"C2751763"	"Retinitis Pigmentosa, Juvenile, Aipl1-Related"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"2000"	"2017"	"3"	"2"	"CTD_human;UNIPROT"
"23746"	"AIPL1"	"0.656"	"0.241"	"C2751764"	"CONE-ROD DYSTROPHY, AIPL1-RELATED (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.80"		"2000"	"2017"	"3"	"2"	"CTD_human;UNIPROT"
"23746"	"AIPL1"	"0.656"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"23753"	"SDF2L1"	"0.857"	"0.207"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23753"	"SDF2L1"	"0.857"	"0.207"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23753"	"SDF2L1"	"0.857"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23753"	"SDF2L1"	"0.857"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"23764"	"MAFF"	"0.834"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23764"	"MAFF"	"0.834"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23764"	"MAFF"	"0.834"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23765"	"IL17RA"	"0.621"	"0.69"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.44"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"23765"	"IL17RA"	"0.621"	"0.69"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23765"	"IL17RA"	"0.621"	"0.69"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"23765"	"IL17RA"	"0.621"	"0.69"	"C4310803"	"IMMUNODEFICIENCY 51"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"23767"	"FLRT3"	"0.72"	"0.379"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23767"	"FLRT3"	"0.72"	"0.379"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"23767"	"FLRT3"	"0.72"	"0.379"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"23767"	"FLRT3"	"0.72"	"0.379"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"23767"	"FLRT3"	"0.72"	"0.379"	"C3808986"	"HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"23774"	"BRD1"	"0.696"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2007"	"2017"	"4"	"0"	"PSYGENET"
"23774"	"BRD1"	"0.696"	"0.345"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"23774"	"BRD1"	"0.696"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.45"	"0.8"	"2007"	"2017"	"5"	"1"	"PSYGENET"
"23780"	"APOL2"	"0.743"	"0.207"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23780"	"APOL2"	"0.743"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"23788"	"MTCH2"	"0.928"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.35"	"0.8"	"2009"	"2016"	"1"	"0"	"CTD_human"
"24137"	"KIF4A"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"24137"	"KIF4A"	"0.762"	"0.276"	"C3890167"	"MENTAL RETARDATION, X-LINKED 100"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"24138"	"IFIT5"	"0.928"	"0.103"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"24139"	"EML2"	"0.799"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"24140"	"FTSJ1"	"0.727"	"0.345"	"C0796215"	"Mental Retardation, X-Linked 9"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"24140"	"FTSJ1"	"0.727"	"0.345"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"1994"	"2016"	"7"	"0"	"CLINGEN;ORPHANET"
"24140"	"FTSJ1"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2005"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"24147"	"FJX1"	"0.735"	"0.31"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24147"	"FJX1"	"0.735"	"0.31"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"24148"	"PRPF6"	"0.616"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2012"	"0"	"1"	"ORPHANET"
"24148"	"PRPF6"	"0.616"	"0.517"	"C3151434"	"RETINITIS PIGMENTOSA 60"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"24149"	"ZNF318"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"25778"	"DSTYK"	"0.743"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"25778"	"DSTYK"	"0.743"	"0.31"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"25778"	"DSTYK"	"0.743"	"0.31"	"C0796019"	"SPASTIC PARAPLEGIA 23 (disorder)"	"disease"	"C10;C16;C17;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"25778"	"DSTYK"	"0.743"	"0.31"	"C1835826"	"Renal Hypodysplasia, Nonsyndromic, 1"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"25778"	"DSTYK"	"0.743"	"0.31"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25778"	"DSTYK"	"0.743"	"0.31"	"C4017279"	"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"25780"	"RASGRP3"	"0.701"	"0.379"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2010"	"1"	"1"	"CTD_human"
"25780"	"RASGRP3"	"0.701"	"0.379"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C0796037"	"Martsolf syndrome"	"disease"	"C10;C11;C19;C23;F01;F03"	"Disease or Syndrome"	"0.73"	"0.6666667"	"1993"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C1838625"	"Warburg Sjo Fledelius syndrome"	"disease"	"C05;C10;C11;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2006"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2006"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"25782"	"RAB3GAP2"	"0.592"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"1999"	"2002"	"1"	"1"	"UNIPROT"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0024302"	"Reticulosarcoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0024304"	"Lymphoma, Mixed-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.70"		"1999"	"1999"	"1"	"1"	"CGI;CTD_human;UNIPROT"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0024306"	"Lymphoma, Undifferentiated"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0079740"	"High Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0079741"	"Lymphoma, Intermediate-Grade"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0079747"	"Low Grade Lymphoma (neoplasm)"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0079757"	"Diffuse Mixed-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0079770"	"Lymphoma, Small Noncleaved-Cell"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25788"	"RAD54B"	"0.701"	"0.345"	"C0699790"	"Colon Carcinoma"	"disease"		"Neoplastic Process"	"0.42"	"1"	"1999"	"2002"	"0"	"1"	"CGI"
"25788"	"RAD54B"	"0.701"	"0.345"	"C3714542"	"Lymphoma, Diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25789"	"TMEM59L"	"0.928"	"0.103"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25789"	"TMEM59L"	"0.928"	"0.103"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25790"	"CFAP45"	"0.928"	"0.138"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0553580"	"Ewings sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C1865818"	"DYSTONIA 7, TORSION (disorder)"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C1865819"	"CERVICAL DYSTONIA, PRIMARY"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"25792"	"CIZ1"	"0.685"	"0.379"	"C3538999"	"DYSTONIA 23"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25793"	"FBXO7"	"0.696"	"0.621"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.39"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"25793"	"FBXO7"	"0.696"	"0.621"	"C1850100"	"PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.76"	"1"	"2008"	"2016"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"25793"	"FBXO7"	"0.696"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"25794"	"FSCN2"	"0.659"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2003"	"2008"	"0"	"0"	"ORPHANET"
"25794"	"FSCN2"	"0.659"	"0.414"	"C1842816"	"RETINITIS PIGMENTOSA 30"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"0"	"0"	"CTD_human"
"25796"	"PGLS"	"0.815"	"0.172"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25796"	"PGLS"	"0.815"	"0.172"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25796"	"PGLS"	"0.815"	"0.172"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25796"	"PGLS"	"0.815"	"0.172"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25797"	"QPCT"	"0.619"	"0.655"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"1"	"1"	"CTD_human"
"25797"	"QPCT"	"0.619"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"1988"	"2007"	"1"	"0"	"CTD_human"
"25797"	"QPCT"	"0.619"	"0.655"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.8571429"	"1997"	"2015"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"0.8333333"	"1997"	"2013"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"25800"	"SLC39A6"	"0.672"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"25802"	"LMOD1"	"0.743"	"0.276"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"25802"	"LMOD1"	"0.743"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25802"	"LMOD1"	"0.743"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25802"	"LMOD1"	"0.743"	"0.276"	"C1608393"	"Megacystis microcolon intestinal hypoperistalsis syndrome"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"25802"	"LMOD1"	"0.743"	"0.276"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2017"	"2018"	"1"	"1"	"CTD_human"
"25803"	"SPDEF"	"0.656"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"25803"	"SPDEF"	"0.656"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25807"	"RHBDD3"	"0.834"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25814"	"ATXN10"	"0.672"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25814"	"ATXN10"	"0.672"	"0.31"	"C1963674"	"Spinocerebellar Ataxia 10"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.66"	"1"	"1993"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"25814"	"ATXN10"	"0.672"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"1997"	"2016"	"1"	"0"	"CTD_human"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25816"	"TNFAIP8"	"0.642"	"0.414"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25818"	"KLK5"	"0.69"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"		"2002"	"2009"	"1"	"0"	"CTD_human"
"25818"	"KLK5"	"0.69"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"25819"	"NOCT"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25820"	"ARIH1"	"0.886"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25821"	"MTO1"	"0.636"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"25821"	"MTO1"	"0.636"	"0.345"	"C3553529"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10"	"disease"		"Disease or Syndrome"	"0.90"		"2012"	"2015"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"25821"	"MTO1"	"0.636"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25824"	"PRDX5"	"0.577"	"0.655"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25824"	"PRDX5"	"0.577"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"UNIPROT"
"25824"	"PRDX5"	"0.577"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25824"	"PRDX5"	"0.577"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25824"	"PRDX5"	"0.577"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25827"	"FBXL2"	"0.815"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25828"	"TXN2"	"0.676"	"0.379"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25828"	"TXN2"	"0.676"	"0.379"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"25828"	"TXN2"	"0.676"	"0.379"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25828"	"TXN2"	"0.676"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25828"	"TXN2"	"0.676"	"0.379"	"C4225200"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"25829"	"TMEM184B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25830"	"SULT4A1"	"0.72"	"0.172"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"PSYGENET"
"25830"	"SULT4A1"	"0.72"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.75"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"25830"	"SULT4A1"	"0.72"	"0.172"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"UNIPROT"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0155536"	"Paracousis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0260662"	"Hearing problem"	"group"	"C09;C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.90"	"1"	"1999"	"2018"	"12"	"11"	"CTD_human;ORPHANET;UNIPROT"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"25836"	"NIPBL"	"0.557"	"0.69"	"C0877848"	"Distorted hearing"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C1510450"	"Dysacusis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C1802395"	"Congenital muscular hypertrophy-cerebral syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"3"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C1853099"	"Cornelia de Lange Syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"3"	"0"	"CTD_human"
"25836"	"NIPBL"	"0.557"	"0.69"	"C2750805"	"Chromosome 5p13 Duplication Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25836"	"NIPBL"	"0.557"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"25836"	"NIPBL"	"0.557"	"0.69"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25839"	"COG4"	"0.72"	"0.276"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"25839"	"COG4"	"0.72"	"0.276"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"25839"	"COG4"	"0.72"	"0.276"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"25839"	"COG4"	"0.72"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25839"	"COG4"	"0.72"	"0.276"	"C3150736"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2013"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"25839"	"COG4"	"0.72"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"25840"	"METTL7A"	"0.834"	"0.103"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25840"	"METTL7A"	"0.834"	"0.103"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25842"	"ASF1A"	"0.799"	"0.276"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25844"	"YIPF3"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25852"	"ARMC8"	"0.762"	"0.241"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25852"	"ARMC8"	"0.762"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25855"	"BRMS1"	"0.633"	"0.448"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"25855"	"BRMS1"	"0.633"	"0.448"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9464286"	"2000"	"2017"	"1"	"0"	"CTD_human"
"25861"	"WHRN"	"0.69"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"25861"	"WHRN"	"0.69"	"0.31"	"C0339534"	"Usher syndrome type 2"	"disease"		"Disease or Syndrome"	"0.54"	"1"	"2003"	"2017"	"9"	"0"	"CLINGEN;ORPHANET"
"25861"	"WHRN"	"0.69"	"0.31"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.94"	"1"	"2003"	"2017"	"9"	"3"	"CLINGEN;CTD_human;ORPHANET"
"25861"	"WHRN"	"0.69"	"0.31"	"C1846839"	"DEAFNESS, AUTOSOMAL RECESSIVE 31"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1963"	"2010"	"0"	"3"	"CTD_human"
"25865"	"PRKD2"	"0.727"	"0.379"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2008"	"1"	"1"	"CTD_human"
"25865"	"PRKD2"	"0.727"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25865"	"PRKD2"	"0.727"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25865"	"PRKD2"	"0.727"	"0.379"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25865"	"PRKD2"	"0.727"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25873"	"RPL36"			"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"25874"	"MPC2"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.13"	"1"	"2012"	"2017"	"1"	"1"	"PSYGENET"
"25878"	"MXRA5"	"0.857"	"0.069"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"25878"	"MXRA5"	"0.857"	"0.069"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.52"	"1"	"2012"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"25878"	"MXRA5"	"0.857"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"25878"	"MXRA5"	"0.857"	"0.069"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"25878"	"MXRA5"	"0.857"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25885"	"POLR1A"	"0.752"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"25885"	"POLR1A"	"0.752"	"0.379"	"C1837822"	"Burn-Mckeown syndrome"	"disease"	"C08;C09;C10;C14;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25885"	"POLR1A"	"0.752"	"0.379"	"C4225317"	"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"25886"	"POC1A"	"0.696"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25886"	"POC1A"	"0.696"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"25886"	"POC1A"	"0.696"	"0.414"	"C3542022"	"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS SYNDROME"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2012"	"2016"	"2"	"2"	"ORPHANET;UNIPROT"
"25886"	"POC1A"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"25890"	"ABI3BP"	"0.727"	"0.276"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25890"	"ABI3BP"	"0.727"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"25890"	"ABI3BP"	"0.727"	"0.276"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"25890"	"ABI3BP"	"0.727"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"25891"	"PAMR1"	"0.785"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25894"	"PLEKHG4"	"0.799"	"0.138"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25898"	"RCHY1"	"0.743"	"0.345"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25898"	"RCHY1"	"0.743"	"0.345"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25898"	"RCHY1"	"0.743"	"0.345"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25902"	"MTHFD1L"	"0.701"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"25903"	"OLFML2B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0004403"	"Autosome Abnormalities"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0008625"	"Chromosome Aberrations"	"group"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0008626"	"Congenital chromosomal disease"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2016"	"0"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.62"	"1"	"2013"	"2014"	"0"	"1"	"CGI;ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.47"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C0969687"	"Autosomal Chromosome Disorders"	"group"	"C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25913"	"POT1"	"0.616"	"0.483"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"25913"	"POT1"	"0.616"	"0.483"	"C4014476"	"MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10"	"phenotype"		"Finding"	"0.60"		"2014"	"2014"	"2"	"8"	"CTD_human;UNIPROT"
"25913"	"POT1"	"0.616"	"0.483"	"C4225278"	"GLIOMA SUSCEPTIBILITY 9"	"phenotype"		"Finding"	"0.40"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"25914"	"RTTN"	"0.752"	"0.241"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25914"	"RTTN"	"0.752"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25914"	"RTTN"	"0.752"	"0.241"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25914"	"RTTN"	"0.752"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25914"	"RTTN"	"0.752"	"0.241"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25914"	"RTTN"	"0.752"	"0.241"	"C3553831"	"MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2016"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"25914"	"RTTN"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"25915"	"NDUFAF3"	"0.656"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25915"	"NDUFAF3"	"0.656"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"25915"	"NDUFAF3"	"0.656"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"3"	"CTD_human;UNIPROT"
"25915"	"NDUFAF3"	"0.656"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"25915"	"NDUFAF3"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25923"	"ATL3"	"0.727"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"25923"	"ATL3"	"0.727"	"0.379"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"25923"	"ATL3"	"0.727"	"0.379"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25923"	"ATL3"	"0.727"	"0.379"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"25923"	"ATL3"	"0.727"	"0.379"	"C3810194"	"NEUROPATHY, HEREDITARY SENSORY, TYPE IF"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"25930"	"PTPN23"	"0.834"	"0.207"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25930"	"PTPN23"	"0.834"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"25930"	"PTPN23"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"25932"	"CLIC4"	"0.696"	"0.241"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25932"	"CLIC4"	"0.696"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"25932"	"CLIC4"	"0.696"	"0.241"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"25932"	"CLIC4"	"0.696"	"0.241"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"25932"	"CLIC4"	"0.696"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"25937"	"WWTR1"	"0.642"	"0.414"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"25937"	"WWTR1"	"0.642"	"0.414"	"C0206732"	"Epithelioid hemangioendothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"25937"	"WWTR1"	"0.642"	"0.414"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0024145"	"Chilblain lupus 1"	"disease"	"C17;C26"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2009"	"2018"	"0"	"0"	"ORPHANET"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.40"	"0.9666667"	"2009"	"2018"	"1"	"0"	"CTD_human"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C2749659"	"AICARDI-GOUTIERES SYNDROME 5 (disorder)"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.60"		"1993"	"2018"	"7"	"21"	"CTD_human;UNIPROT"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C3280721"	"CHILBLAIN LUPUS 2"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C3711385"	"Deoxyguanosine Kinase Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25939"	"SAMHD1"	"0.645"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0175754"	"Agenesis of corpus callosum"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3150674"	"CHROMOSOME 15q24 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2016"	"0"	"6"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3150675"	"CHROMOSOME 15q24 DUPLICATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3179058"	"Corpus Callosum Malformation"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3697269"	"15q24 Microdeletion"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2015"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"25942"	"SIN3A"	"0.558"	"0.621"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"25942"	"SIN3A"	"0.558"	"0.621"	"C4310804"	"WITTEVEEN-KOLK SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"25945"	"NECTIN3"	"0.815"	"0.241"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25953"	"PNKD"	"0.663"	"0.31"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"25953"	"PNKD"	"0.663"	"0.31"	"C1869117"	"Paroxysmal nonkinesigenic dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"1.00"	"0.9166667"	"1996"	"2017"	"6"	"2"	"CTD_human;ORPHANET;UNIPROT"
"25953"	"PNKD"	"0.663"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25959"	"KANK2"	"0.696"	"0.379"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"25959"	"KANK2"	"0.696"	"0.379"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"25959"	"KANK2"	"0.696"	"0.379"	"C4015202"	"PALMOPLANTAR KERATODERMA AND WOOLLY HAIR"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"25970"	"SH2B1"	"0.627"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.8571429"	"2009"	"2017"	"1"	"1"	"CTD_human"
"25970"	"SH2B1"	"0.627"	"0.586"	"C1866432"	"OBESITY, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"25970"	"SH2B1"	"0.627"	"0.586"	"C3150154"	"CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25970"	"SH2B1"	"0.627"	"0.586"	"C3150701"	"CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25970"	"SH2B1"	"0.627"	"0.586"	"C3150702"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 16"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"25970"	"SH2B1"	"0.627"	"0.586"	"C3552491"	"AUTISM, SUSCEPTIBILITY TO, 14A"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"25973"	"PARS2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"25974"	"MMACHC"	"0.663"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"25974"	"MMACHC"	"0.663"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"25974"	"MMACHC"	"0.663"	"0.414"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25974"	"MMACHC"	"0.663"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"25974"	"MMACHC"	"0.663"	"0.414"	"C1848561"	"Methylmalonic acidemia with homocystinuria"	"disease"	"C10;C16;C17;C18"	"Disease or Syndrome"	"0.95"	"1"	"2001"	"2018"	"5"	"27"	"CTD_human;ORPHANET;UNIPROT"
"25974"	"MMACHC"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"25976"	"TIPARP"	"0.565"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"25976"	"TIPARP"	"0.565"	"0.655"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"25976"	"TIPARP"	"0.565"	"0.655"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"25977"	"NECAP1"	"0.886"	"0.034"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"25977"	"NECAP1"	"0.886"	"0.034"	"C4014430"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"0"	"1"	"CTD_human"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.66"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0338451"	"Frontotemporal dementia"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.50"	"0.9642857"	"2005"	"2018"	"1"	"0"	"CTD_human"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2005"	"2005"	"1"	"0"	"CTD_human;ORPHANET"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.7777778"	"2006"	"2013"	"1"	"0"	"CTD_human"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C1833296"	"FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2018"	"1"	"5"	"CTD_human;UNIPROT"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C1836076"	"Amyotrophic Lateral Sclerosis, Chmp2B-Related"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.60"		"2006"	"2011"	"2"	"3"	"CTD_human;UNIPROT"
"25978"	"CHMP2B"	"0.58"	"0.586"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25981"	"DNAH1"	"0.834"	"0.172"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2015"	"0"	"1"	"ORPHANET"
"25981"	"DNAH1"	"0.834"	"0.172"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"25981"	"DNAH1"	"0.834"	"0.172"	"C4539783"	"SPERMATOGENIC FAILURE 18"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"2"	"8"	"UNIPROT"
"25981"	"DNAH1"	"0.834"	"0.172"	"C4539798"	"CILIARY DYSKINESIA, PRIMARY, 37"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"2"	"UNIPROT"
"26005"	"C2CD3"	"0.685"	"0.483"	"C0026363"	"Mohr Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26005"	"C2CD3"	"0.685"	"0.483"	"C0029294"	"Orofaciodigital Syndromes"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"26005"	"C2CD3"	"0.685"	"0.483"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26005"	"C2CD3"	"0.685"	"0.483"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26005"	"C2CD3"	"0.685"	"0.483"	"C1510460"	"Orofaciodigital Syndrome I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"26005"	"C2CD3"	"0.685"	"0.483"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26005"	"C2CD3"	"0.685"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"26005"	"C2CD3"	"0.685"	"0.483"	"C4014780"	"OROFACIODIGITAL SYNDROME XIV"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"26005"	"C2CD3"	"0.685"	"0.483"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26007"	"TKFC"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26009"	"ZZZ3"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26011"	"TENM4"	"0.72"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2011"	"2018"	"1"	"23"	"CTD_human"
"26011"	"TENM4"	"0.72"	"0.31"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26011"	"TENM4"	"0.72"	"0.31"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26011"	"TENM4"	"0.72"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"26011"	"TENM4"	"0.72"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2015"	"1"	"1"	"PSYGENET"
"26011"	"TENM4"	"0.72"	"0.31"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26011"	"TENM4"	"0.72"	"0.31"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"26011"	"TENM4"	"0.72"	"0.31"	"C4225223"	"TREMOR, HEREDITARY ESSENTIAL, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"9"	"CTD_human;UNIPROT"
"26012"	"NSMF"	"0.642"	"0.586"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2014"	"0"	"0"	"ORPHANET"
"26012"	"NSMF"	"0.642"	"0.586"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"26012"	"NSMF"	"0.642"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"26012"	"NSMF"	"0.642"	"0.586"	"C3553842"	"HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2013"	"3"	"3"	"CTD_human;UNIPROT"
"26015"	"RPAP1"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"26022"	"TMEM98"	"0.785"	"0.103"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"26022"	"TMEM98"	"0.785"	"0.103"	"C0266524"	"Dysplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"26022"	"TMEM98"	"0.785"	"0.103"	"C0266527"	"Hypoplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"26022"	"TMEM98"	"0.785"	"0.103"	"C0311249"	"Cryptophthalmos"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"26022"	"TMEM98"	"0.785"	"0.103"	"C4014848"	"NANOPHTHALMOS 4"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"26024"	"PTCD1"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26034"	"IPCEF1"	"0.857"	"0.241"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26034"	"IPCEF1"	"0.857"	"0.241"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26037"	"SIPA1L1"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26037"	"SIPA1L1"	"0.857"	"0.138"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26037"	"SIPA1L1"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26037"	"SIPA1L1"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26037"	"SIPA1L1"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26038"	"CHD5"	"0.636"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"0"	"0"	"UNIPROT"
"26038"	"CHD5"	"0.636"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.6666667"	"2010"	"2014"	"1"	"0"	"CTD_human"
"26038"	"CHD5"	"0.636"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26038"	"CHD5"	"0.636"	"0.379"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"26038"	"CHD5"	"0.636"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"0.6666667"	"2010"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.56"	"1"	"2010"	"2016"	"2"	"1"	"CGI;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.60"		"2013"	"2013"	"1"	"3"	"CGI;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.36"	"0.8333333"	"2013"	"2017"	"1"	"1"	"UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0027019"	"Myelomonocytic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2011"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0265227"	"Schinzel-Giedion syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.76"	"1"	"2008"	"2017"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.53"	"1"	"2013"	"2017"	"2"	"1"	"CTD_human;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"		"2015"	"2018"	"1"	"2"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2014"	"2"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1266177"	"Dysembryoplastic neuroepithelial tumor"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1292772"	"Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative"	"disease"	"C04;C15"	"Neoplastic Process"	"0.65"	"1"	"2013"	"2016"	"1"	"3"	"CGI;CTD_human;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26040"	"SETBP1"	"0.558"	"0.655"	"C3275959"	"LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"2"	"1"	"UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.54"	"1"	"2013"	"2015"	"2"	"2"	"CGI;UNIPROT"
"26040"	"SETBP1"	"0.558"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"26040"	"SETBP1"	"0.558"	"0.655"	"C4015141"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 29"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"0"	"7"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"2008"	"2017"	"4"	"1"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.46"	"1"	"2008"	"2015"	"2"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"3"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2011"	"3"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0038131"	"Stammering"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0038506"	"Stuttering"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2011"	"3"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0454542"	"Stuttering, Acquired"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"3"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"3"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751527"	"Stuttering, Adult"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751528"	"Stuttering, Childhood"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C0751529"	"Stuttering, Developmental"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2008"	"2016"	"4"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C1970431"	"PITT-HOPKINS SYNDROME"	"disease"	"C08;C10;C23;F01;F03"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C2750246"	"Pitt-Hopkins-Like Syndrome 1"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.80"		"2006"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C3489627"	"Stuttering, Familial Persistent 1"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26047"	"CNTNAP2"	"0.582"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"26050"	"SLITRK5"	"0.886"	"0.138"	"C0028768"	"Obsessive-Compulsive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"26052"	"DNM3"	"0.834"	"0.207"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26052"	"DNM3"	"0.834"	"0.207"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2015"	"2"	"0"	"PSYGENET"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26053"	"AUTS2"	"0.59"	"0.483"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26053"	"AUTS2"	"0.59"	"0.483"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"26053"	"AUTS2"	"0.59"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2007"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26053"	"AUTS2"	"0.59"	"0.483"	"C4014435"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 26"	"disease"		"Disease or Syndrome"	"0.80"		"2014"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"26054"	"SENP6"	"0.815"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"26054"	"SENP6"	"0.815"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"26056"	"RAB11FIP5"	"0.928"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26058"	"GIGYF2"	"0.743"	"0.207"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26058"	"GIGYF2"	"0.743"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26058"	"GIGYF2"	"0.743"	"0.207"	"C4083045"	"PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.50"		"2008"	"2016"	"4"	"8"	"CTD_human;UNIPROT"
"26058"	"GIGYF2"	"0.743"	"0.207"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26060"	"APPL1"	"0.656"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"26060"	"APPL1"	"0.656"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26060"	"APPL1"	"0.656"	"0.448"	"C0342276"	"Maturity onset diabetes mellitus in young"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"0"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"26060"	"APPL1"	"0.656"	"0.448"	"C4225299"	"MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"26061"	"HACL1"	"0.799"	"0.069"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26061"	"HACL1"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26086"	"GPSM1"	"0.815"	"0.31"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"26086"	"GPSM1"	"0.815"	"0.31"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"26086"	"GPSM1"	"0.815"	"0.31"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"26088"	"GGA1"	"0.886"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"26090"	"ABHD12"	"0.696"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26090"	"ABHD12"	"0.696"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.33"	"1"	"2013"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"26090"	"ABHD12"	"0.696"	"0.276"	"C2675204"	"Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.94"	"1"	"2010"	"2018"	"6"	"7"	"CLINGEN;CTD_human;ORPHANET"
"26090"	"ABHD12"	"0.696"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26092"	"TOR1AIP1"	"0.815"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"26092"	"TOR1AIP1"	"0.815"	"0.207"	"C4310731"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"26098"	"EDRF1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"26115"	"TANC2"	"0.886"	"0.138"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26115"	"TANC2"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26119"	"LDLRAP1"	"0.656"	"0.31"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"2002"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"26119"	"LDLRAP1"	"0.656"	"0.31"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26119"	"LDLRAP1"	"0.656"	"0.31"	"C1863512"	"HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE"	"disease"	"C18"	"Disease or Syndrome"	"0.90"	"0.9285714"	"1973"	"2018"	"1"	"6"	"CTD_human;UNIPROT"
"26121"	"PRPF31"	"0.609"	"0.552"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"1996"	"2018"	"0"	"3"	"ORPHANET"
"26121"	"PRPF31"	"0.609"	"0.552"	"C1838601"	"Retinitis Pigmentosa 11"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.85"	"1"	"1969"	"2011"	"5"	"7"	"CTD_human;UNIPROT"
"26123"	"TCTN3"	"0.607"	"0.517"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26123"	"TCTN3"	"0.607"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26123"	"TCTN3"	"0.607"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"26123"	"TCTN3"	"0.607"	"0.517"	"C0406727"	"Orofaciodigital syndrome 4"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2012"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"26123"	"TCTN3"	"0.607"	"0.517"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26123"	"TCTN3"	"0.607"	"0.517"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26123"	"TCTN3"	"0.607"	"0.517"	"C3553758"	"JOUBERT SYNDROME 18"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"1"	"2"	"UNIPROT"
"26123"	"TCTN3"	"0.607"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"26123"	"TCTN3"	"0.607"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"26127"	"FGFR1OP2"	"0.886"	"0.138"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C1836123"	"Goldberg-Shprintzen megacolon syndrome"	"disease"	"C05;C06;C16"	"Disease or Syndrome"	"0.84"	"0.75"	"2005"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2005"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"26128"	"KIF1BP"	"0.663"	"0.483"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"26135"	"SERBP1"	"0.762"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26135"	"SERBP1"	"0.762"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26135"	"SERBP1"	"0.762"	"0.276"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26135"	"SERBP1"	"0.762"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26136"	"TES"	"0.672"	"0.379"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"26136"	"TES"	"0.672"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26136"	"TES"	"0.672"	"0.379"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26136"	"TES"	"0.672"	"0.379"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C0796121"	"Primrose syndrome"	"disease"	"C09;C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.71"	"1"	"2011"	"2015"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26137"	"ZBTB20"	"0.596"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"26140"	"TTLL3"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26146"	"TRAF3IP1"	"0.707"	"0.379"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"2"	"ORPHANET"
"26146"	"TRAF3IP1"	"0.707"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26146"	"TRAF3IP1"	"0.707"	"0.379"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26146"	"TRAF3IP1"	"0.707"	"0.379"	"C4225263"	"SENIOR-LOKEN SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"6"	"UNIPROT"
"26146"	"TRAF3IP1"	"0.707"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26149"	"ZNF658"			"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26150"	"RIBC2"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26150"	"RIBC2"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26150"	"RIBC2"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26150"	"RIBC2"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.57"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"2005"	"2018"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"26154"	"ABCA12"	"0.648"	"0.517"	"C0598226"	"Harlequin type ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"		"2006"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"26154"	"ABCA12"	"0.648"	"0.517"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"26154"	"ABCA12"	"0.648"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26154"	"ABCA12"	"0.648"	"0.517"	"C1832550"	"Lamellar ichthyosis, type 2"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.62"	"1"	"1996"	"2012"	"5"	"6"	"CTD_human;UNIPROT"
"26154"	"ABCA12"	"0.648"	"0.517"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"26154"	"ABCA12"	"0.648"	"0.517"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"26160"	"IFT172"	"0.604"	"0.621"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"26160"	"IFT172"	"0.604"	"0.621"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"26160"	"IFT172"	"0.604"	"0.621"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"26160"	"IFT172"	"0.604"	"0.621"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"26160"	"IFT172"	"0.604"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26160"	"IFT172"	"0.604"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26160"	"IFT172"	"0.604"	"0.621"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26160"	"IFT172"	"0.604"	"0.621"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"26160"	"IFT172"	"0.604"	"0.621"	"C1849437"	"Mainzer-Saldino Disease"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"26160"	"IFT172"	"0.604"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26160"	"IFT172"	"0.604"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"26160"	"IFT172"	"0.604"	"0.621"	"C3810175"	"SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2013"	"1"	"6"	"UNIPROT"
"26160"	"IFT172"	"0.604"	"0.621"	"C4225342"	"RETINITIS PIGMENTOSA 71"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"26160"	"IFT172"	"0.604"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"26173"	"INTS1"	"0.815"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.70"	"0.9051724"	"2004"	"2018"	"5"	"4"	"CTD_human;UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.50"	"0.9405405"	"2004"	"2018"	"1"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.90"	"0.9396552"	"2004"	"2018"	"2"	"1"	"CTD_human;UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.50"	"0.9583333"	"2004"	"2018"	"1"	"1"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.36"	"0.6666667"	"2005"	"2014"	"1"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.70"	"0.9534884"	"2004"	"2018"	"3"	"1"	"CTD_human;UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0039483"	"Giant Cell Arteritis"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2015"	"0"	"0"	"ORPHANET"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0042170"	"Uveomeningoencephalitic Syndrome"	"disease"	"C10;C11;C20"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C1833448"	"RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C1835308"	"EXCESS LYMPHOCYTE LOW MOLECULAR WEIGHT DNA"	"phenotype"		"Finding"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C1835309"	"EXCESS LMW-DNA"	"phenotype"		"Finding"	"0.30"		"2004"	"2004"	"1"	"1"	"UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C1956391"	"Temporal Arteritis"	"disease"	"C10;C14;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26191"	"PTPN22"	"0.497"	"0.793"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26191"	"PTPN22"	"0.497"	"0.793"	"C3277701"	"VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6"	"disease"		"Finding"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"26191"	"PTPN22"	"0.497"	"0.793"	"C3495801"	"Granulomatosis with polyangiitis"	"disease"	"C08;C14;C20"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2006"	"2012"	"0"	"0"	"ORPHANET"
"26191"	"PTPN22"	"0.497"	"0.793"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26191"	"PTPN22"	"0.497"	"0.793"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"26223"	"FBXL21"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"26224"	"FBXL3"	"0.815"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0265218"	"Neu-Laxova syndrome"	"disease"	"C05;C10;C13;C16;C17;C23"	"Disease or Syndrome"	"0.63"	"1"	"2005"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"GENOMICS_ENGLAND"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0580190"	"3-Phosphoglycerate dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26227"	"PHGDH"	"0.532"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.47"	"1"	"2011"	"2018"	"1"	"1"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"26227"	"PHGDH"	"0.532"	"0.759"	"C1866174"	"Phosphoglycerate Dehydrogenase Deficiency"	"disease"	"C05;C10;C16;C18;C23;F01"	"Disease or Syndrome"	"0.60"		"2000"	"2015"	"2"	"7"	"CTD_human;UNIPROT"
"26227"	"PHGDH"	"0.532"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"26228"	"STAP1"	"0.886"	"0.103"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2014"	"2016"	"3"	"1"	"GENOMICS_ENGLAND"
"26229"	"B3GAT3"	"0.648"	"0.379"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26229"	"B3GAT3"	"0.648"	"0.379"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26229"	"B3GAT3"	"0.648"	"0.379"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"26229"	"B3GAT3"	"0.648"	"0.379"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"26229"	"B3GAT3"	"0.648"	"0.379"	"C3278404"	"MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2016"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26230"	"TIAM2"	"0.785"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26235"	"FBXL4"	"0.701"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26235"	"FBXL4"	"0.701"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"26235"	"FBXL4"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"26235"	"FBXL4"	"0.701"	"0.31"	"C3809592"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2009"	"2017"	"3"	"27"	"CTD_human;ORPHANET;UNIPROT"
"26239"	"LCE2B"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"26239"	"LCE2B"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.48"	"1"	"2012"	"2017"	"1"	"26"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26249"	"KLHL3"	"0.752"	"0.241"	"C3469605"	"PSEUDOHYPOALDOSTERONISM, TYPE IID"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2012"	"2018"	"11"	"28"	"CTD_human;ORPHANET;UNIPROT"
"26253"	"CLEC4E"	"0.886"	"0.241"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26253"	"CLEC4E"	"0.886"	"0.241"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26253"	"CLEC4E"	"0.886"	"0.241"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26253"	"CLEC4E"	"0.886"	"0.241"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26253"	"CLEC4E"	"0.886"	"0.241"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26256"	"CABYR"	"0.815"	"0.138"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26256"	"CABYR"	"0.815"	"0.138"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26256"	"CABYR"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26258"	"BLOC1S6"	"0.773"	"0.276"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"26258"	"BLOC1S6"	"0.773"	"0.276"	"C3280026"	"HERMANSKY-PUDLAK SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.60"		"1971"	"2017"	"0"	"1"	"ORPHANET"
"26259"	"FBXW8"	"0.799"	"0.241"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26259"	"FBXW8"	"0.799"	"0.241"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26260"	"FBXO25"	"0.834"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26266"	"SLC13A4"	"0.785"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26268"	"FBXO9"	"0.928"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26269"	"FBXO8"	"0.685"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26269"	"FBXO8"	"0.685"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"26270"	"FBXO6"	"0.799"	"0.207"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26270"	"FBXO6"	"0.799"	"0.207"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26270"	"FBXO6"	"0.799"	"0.207"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26270"	"FBXO6"	"0.799"	"0.207"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26270"	"FBXO6"	"0.799"	"0.207"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26272"	"FBXO4"	"0.815"	"0.103"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"26275"	"HIBCH"	"0.735"	"0.276"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26275"	"HIBCH"	"0.735"	"0.276"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26275"	"HIBCH"	"0.735"	"0.276"	"C0342738"	"Beta-Hydroxyisobutyryl CoA Deacylase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1982"	"2016"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"26275"	"HIBCH"	"0.735"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"26275"	"HIBCH"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1982"	"1982"	"1"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.44"	"1"	"2004"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C1859722"	"Arthrogryposis renal dysfunction cholestasis syndrome"	"disease"	"C05;C06;C12;C13;C16"	"Disease or Syndrome"	"1.00"	"1"	"1994"	"2016"	"5"	"11"	"CTD_human;ORPHANET;UNIPROT"
"26276"	"VPS33B"	"0.681"	"0.517"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26276"	"VPS33B"	"0.681"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26277"	"TINF2"	"0.586"	"0.69"	"C0005956"	"Bone Marrow Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26277"	"TINF2"	"0.586"	"0.69"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C0027339"	"Nail Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26277"	"TINF2"	"0.586"	"0.69"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.90"	"0.9444444"	"2008"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"26277"	"TINF2"	"0.586"	"0.69"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2008"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"26277"	"TINF2"	"0.586"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"26277"	"TINF2"	"0.586"	"0.69"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C1327916"	"REVESZ SYNDROME (disorder)"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.71"	"1"	"2008"	"2012"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"26277"	"TINF2"	"0.586"	"0.69"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26277"	"TINF2"	"0.586"	"0.69"	"C1851970"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2009"	"0"	"10"	"CTD_human"
"26277"	"TINF2"	"0.586"	"0.69"	"C3151445"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2015"	"1"	"7"	"CTD_human;UNIPROT"
"26277"	"TINF2"	"0.586"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"26278"	"SACS"	"0.624"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26278"	"SACS"	"0.624"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26278"	"SACS"	"0.624"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26278"	"SACS"	"0.624"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2000"	"2006"	"6"	"0"	"GENOMICS_ENGLAND"
"26278"	"SACS"	"0.624"	"0.517"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26278"	"SACS"	"0.624"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26278"	"SACS"	"0.624"	"0.517"	"C1849140"	"SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"14"	"106"	"CTD_human;ORPHANET;UNIPROT"
"26278"	"SACS"	"0.624"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"26280"	"IL1RAPL2"	"0.785"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26280"	"IL1RAPL2"	"0.785"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"26281"	"FGF20"	"0.727"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"26281"	"FGF20"	"0.727"	"0.345"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"26281"	"FGF20"	"0.727"	"0.345"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"26281"	"FGF20"	"0.727"	"0.345"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26284"	"ERAL1"	"0.762"	"0.448"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"26284"	"ERAL1"	"0.762"	"0.448"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"26284"	"ERAL1"	"0.762"	"0.448"	"C4479656"	"PERRAULT SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"26286"	"ARFGAP3"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26289"	"AK5"	"0.815"	"0.207"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26289"	"AK5"	"0.815"	"0.207"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26289"	"AK5"	"0.815"	"0.207"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.38"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"26291"	"FGF21"	"0.614"	"0.483"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26292"	"MYCBP"	"0.752"	"0.207"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"26298"	"EHF"	"0.735"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"26298"	"EHF"	"0.735"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26330"	"GAPDHS"	"0.799"	"0.069"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26353"	"HSPB8"	"0.639"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.48"	"1"	"1993"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"26353"	"HSPB8"	"0.639"	"0.414"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26353"	"HSPB8"	"0.639"	"0.414"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26353"	"HSPB8"	"0.639"	"0.414"	"C1834692"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1992"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"26353"	"HSPB8"	"0.639"	"0.414"	"C1837552"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2004"	"2013"	"0"	"1"	"CTD_human"
"26353"	"HSPB8"	"0.639"	"0.414"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26353"	"HSPB8"	"0.639"	"0.414"	"C3711384"	"Distal Hereditary Motor Neuropathy, Type II"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"1997"	"2012"	"0"	"0"	"ORPHANET"
"26353"	"HSPB8"	"0.639"	"0.414"	"C3888087"	"Charcot-Marie-Tooth disease, Type 2I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"26468"	"LHX6"	"0.834"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2013"	"2016"	"2"	"0"	"PSYGENET"
"26469"	"PTPN18"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26470"	"SEZ6L2"	"0.743"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"26471"	"NUPR1"	"0.648"	"0.345"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26471"	"NUPR1"	"0.648"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26471"	"NUPR1"	"0.648"	"0.345"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"26472"	"PPP1R14B"	"0.886"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26499"	"PLEK2"	"0.928"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26499"	"PLEK2"	"0.928"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1991"	"1991"	"1"	"0"	"PSYGENET"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.40"		"1995"	"2000"	"2"	"0"	"GENOMICS_ENGLAND"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C0342853"	"Sialuria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9090909"	"1999"	"2018"	"0"	"0"	"CTD_human"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C1096902"	"Infantile Sialic Acid Storage Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.77"	"1"	"1983"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C1096903"	"Sialic Acid Storage Disease, Finnish Type (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9090909"	"1993"	"2018"	"3"	"31"	"CTD_human;ORPHANET;UNIPROT"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C1963905"	"Infantile free sialic acid storage disease"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C2930923"	"N-Acetylneuraminic acid storage disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"26503"	"SLC17A5"	"0.547"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"26504"	"CNNM4"	"0.701"	"0.276"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.44"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"26504"	"CNNM4"	"0.701"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26504"	"CNNM4"	"0.701"	"0.276"	"C1857588"	"Amaurosis hypertrichosis"	"disease"	"C11;C16;C17"	"Disease or Syndrome"	"0.40"		"1989"	"2009"	"0"	"6"	"CTD_human"
"26504"	"CNNM4"	"0.701"	"0.276"	"C2931074"	"Cone rod dystrophy amelogenesis imperfecta"	"disease"	"C07;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26504"	"CNNM4"	"0.701"	"0.276"	"C3495589"	"Jalili syndrome"	"disease"	"C07;C11;C16"	"Disease or Syndrome"	"0.56"	"1"	"2009"	"2017"	"2"	"3"	"ORPHANET;UNIPROT"
"26507"	"CNNM1"	"0.886"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"26508"	"HEYL"	"0.857"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26508"	"HEYL"	"0.857"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26508"	"HEYL"	"0.857"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"26508"	"HEYL"	"0.857"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2010"	"1"	"0"	"CTD_human"
"26519"	"TIMM10"	"0.928"	"0.069"	"C0035412"	"Rhabdomyosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2006"	"2006"	"1"	"0"	"CTD_human"
"26519"	"TIMM10"	"0.928"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26523"	"AGO1"	"0.701"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"26523"	"AGO1"	"0.701"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"26523"	"AGO1"	"0.701"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"26523"	"AGO1"	"0.701"	"0.414"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26523"	"AGO1"	"0.701"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"26524"	"LATS2"	"0.616"	"0.448"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"26524"	"LATS2"	"0.616"	"0.448"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26524"	"LATS2"	"0.616"	"0.448"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"26525"	"IL36RN"	"0.743"	"0.241"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"26525"	"IL36RN"	"0.743"	"0.241"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.45"	"1"	"2011"	"2016"	"0"	"0"	"CTD_human"
"26525"	"IL36RN"	"0.743"	"0.241"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.80"	"1"	"2011"	"2017"	"5"	"7"	"GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"26525"	"IL36RN"	"0.743"	"0.241"	"C0392439"	"Acrodermatitis continua of Hallopeau"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2011"	"2014"	"3"	"4"	"ORPHANET;UNIPROT"
"26525"	"IL36RN"	"0.743"	"0.241"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26528"	"DAZAP1"	"0.799"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"26528"	"DAZAP1"	"0.799"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26528"	"DAZAP1"	"0.799"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"26575"	"RGS17"	"0.727"	"0.31"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"26575"	"RGS17"	"0.727"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26575"	"RGS17"	"0.727"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26575"	"RGS17"	"0.727"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26577"	"PCOLCE2"	"0.857"	"0.103"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26577"	"PCOLCE2"	"0.857"	"0.103"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26577"	"PCOLCE2"	"0.857"	"0.103"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0011859"	"Lipoatrophic Diabetes Mellitus"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0023787"	"Lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0221032"	"Familial generalized lipodystrophy"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.60"	"0.9130435"	"2003"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0403823"	"Asthenozoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"26580"	"BSCL2"	"0.565"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"26580"	"BSCL2"	"0.565"	"0.586"	"C1720862"	"Congenital Generalized Lipodystrophy Type 1"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"26580"	"BSCL2"	"0.565"	"0.586"	"C1720863"	"Congenital Generalized Lipodystrophy Type 2"	"disease"	"C16;C17;C18"	"Congenital Abnormality"	"0.90"	"1"	"1993"	"2017"	"2"	"21"	"CTD_human;UNIPROT"
"26580"	"BSCL2"	"0.565"	"0.586"	"C1833308"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V"	"disease"	"C10"	"Disease or Syndrome"	"0.76"	"1"	"1966"	"2013"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"26580"	"BSCL2"	"0.565"	"0.586"	"C2931276"	"Spastic paraplegia 17"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"	"1"	"1966"	"2016"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"26580"	"BSCL2"	"0.565"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"0.6666667"	"2004"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"26580"	"BSCL2"	"0.565"	"0.586"	"C4014700"	"ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"3"	"CTD_human;ORPHANET"
"26585"	"GREM1"	"0.602"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"2008"	"2017"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0017185"	"Gastrointestinal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26585"	"GREM1"	"0.602"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9090909"	"2008"	"2017"	"1"	"2"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C1832587"	"POLYPOSIS SYNDROME, HEREDITARY MIXED, 1"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2016"	"8"	"0"	"CLINGEN;ORPHANET"
"26585"	"GREM1"	"0.602"	"0.517"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"26585"	"GREM1"	"0.602"	"0.517"	"C2677290"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.50"		"2003"	"2016"	"8"	"0"	"CLINGEN;ORPHANET"
"26585"	"GREM1"	"0.602"	"0.517"	"C2677291"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 15"	"phenotype"		"Finding"	"0.50"		"2003"	"2016"	"8"	"0"	"CLINGEN;ORPHANET"
"26585"	"GREM1"	"0.602"	"0.517"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26585"	"GREM1"	"0.602"	"0.517"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"26608"	"TBL2"	"0.611"	"0.552"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"26610"	"ELP4"	"0.727"	"0.345"	"C0003076"	"Aniridia"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.42"	"0.5"	"1990"	"2002"	"0"	"0"	"CTD_human"
"26610"	"ELP4"	"0.727"	"0.345"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26610"	"ELP4"	"0.727"	"0.345"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26750"	"RPS6KC1"	"0.834"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26750"	"RPS6KC1"	"0.834"	"0.241"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26750"	"RPS6KC1"	"0.834"	"0.241"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2005"	"2017"	"3"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"7"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2017"	"10"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.50"		"2006"	"2009"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2005"	"2017"	"3"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2017"	"10"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2010"	"2017"	"10"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26762"	"HAVCR1"	"0.586"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26799"	"SNORD50A"			"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26799"	"SNORD50A"			"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26799"	"SNORD50A"			"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26799"	"SNORD50A"			"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26873"	"OPLAH"	"0.857"	"0.172"	"C0268525"	"5-oxoprolinase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2012"	"2013"	"0"	"2"	"CTD_human;ORPHANET"
"26958"	"COPG2"	"1"	"0.069"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"26960"	"NBEA"	"0.799"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.54"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"26960"	"NBEA"	"0.799"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"26985"	"AP3M1"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"26986"	"PABPC1"	"0.696"	"0.483"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1992"	"2011"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26986"	"PABPC1"	"0.696"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"26998"	"FETUB"	"0.762"	"0.241"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26998"	"FETUB"	"0.762"	"0.241"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"26999"	"CYFIP2"	"0.773"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"27010"	"TPK1"	"0.928"		"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27010"	"TPK1"	"0.928"		"C3280866"	"THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"27010"	"TPK1"	"0.928"		"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27013"	"CNPPD1"	"0.886"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27013"	"CNPPD1"	"0.886"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27013"	"CNPPD1"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"27013"	"CNPPD1"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27019"	"DNAI1"	"0.633"	"0.552"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"1.00"	"0.9375"	"1993"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"27019"	"DNAI1"	"0.633"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27019"	"DNAI1"	"0.633"	"0.552"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.80"		"2001"	"2014"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"27020"	"NPTN"	"0.773"	"0.276"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"27020"	"NPTN"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"27020"	"NPTN"	"0.773"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27022"	"FOXD3"	"0.636"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"27022"	"FOXD3"	"0.636"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"27022"	"FOXD3"	"0.636"	"0.586"	"C1842979"	"AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.8333333"	"2000"	"2009"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"		"2003"	"2009"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"27030"	"MLH3"	"0.63"	"0.345"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"27030"	"MLH3"	"0.63"	"0.345"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.56"	"0.8333333"	"2001"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"27030"	"MLH3"	"0.63"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"0.8333333"	"2000"	"2009"	"1"	"0"	"CTD_human"
"27030"	"MLH3"	"0.63"	"0.345"	"C1858380"	"COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7 (disorder)"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.70"		"2001"	"2016"	"7"	"11"	"CLINGEN;CTD_human;UNIPROT"
"27031"	"NPHP3"	"0.604"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"27031"	"NPHP3"	"0.604"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"27031"	"NPHP3"	"0.604"	"0.414"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C1858392"	"NEPHRONOPHTHISIS 3"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.84"	"1"	"2000"	"2018"	"1"	"18"	"CTD_human;UNIPROT"
"27031"	"NPHP3"	"0.604"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C2673883"	"RENAL-HEPATIC-PANCREATIC DYSPLASIA"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"1996"	"2017"	"0"	"8"	"ORPHANET"
"27031"	"NPHP3"	"0.604"	"0.414"	"C2673885"	"Renal hepatic pancreatic dysplasia Dandy Walker cyst"	"disease"	"C04;C06;C10;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"0"	"2"	"CTD_human;ORPHANET"
"27031"	"NPHP3"	"0.604"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27031"	"NPHP3"	"0.604"	"0.414"	"C3715199"	"RENAL-HEPATIC-PANCREATIC DYSPLASIA 1"	"disease"		"Disease or Syndrome"	"0.50"		"2008"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"27031"	"NPHP3"	"0.604"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"27032"	"ATP2C1"	"0.72"	"0.345"	"C0085106"	"Familial benign pemphigus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"0.9591837"	"1995"	"2018"	"7"	"5"	"CTD_human;ORPHANET;UNIPROT"
"27034"	"ACAD8"	"0.616"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27034"	"ACAD8"	"0.616"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27034"	"ACAD8"	"0.616"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27034"	"ACAD8"	"0.616"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27034"	"ACAD8"	"0.616"	"0.655"	"C1969809"	"Isobutyryl-CoA dehydrogenase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2003"	"2015"	"3"	"12"	"CTD_human;ORPHANET;UNIPROT"
"27035"	"NOX1"	"0.607"	"0.586"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27035"	"NOX1"	"0.607"	"0.586"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27036"	"SIGLEC7"	"0.602"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27037"	"TRMT2A"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27037"	"TRMT2A"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"27040"	"LAT"	"0.648"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27040"	"LAT"	"0.648"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27040"	"LAT"	"0.648"	"0.483"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"27040"	"LAT"	"0.648"	"0.483"	"C4479588"	"IMMUNODEFICIENCY 52"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"ORPHANET"
"27042"	"UTP25"	"0.834"	"0.103"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27042"	"UTP25"	"0.834"	"0.103"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27042"	"UTP25"	"0.834"	"0.103"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27042"	"UTP25"	"0.834"	"0.103"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27044"	"SND1"	"0.672"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"27044"	"SND1"	"0.672"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27044"	"SND1"	"0.672"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.52"	"1"	"2009"	"2015"	"3"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0036400"	"Scimitar Syndrome"	"disease"	"C08;C14;C16"	"Congenital Abnormality"	"0.32"	"1"	"2008"	"2016"	"1"	"1"	"UNIPROT"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27063"	"ANKRD1"	"0.656"	"0.552"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2015"	"3"	"0"	"CLINGEN"
"27067"	"STAU2"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27068"	"PPA2"	"0.815"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"27068"	"PPA2"	"0.815"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27068"	"PPA2"	"0.815"	"0.103"	"C4310663"	"SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"27068"	"PPA2"	"0.815"	"0.103"	"C4310664"	"SUDDEN CARDIAC FAILURE, INFANTILE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"7"	"CTD_human;UNIPROT"
"27071"	"DAPP1"	"0.928"	"0.034"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27071"	"DAPP1"	"0.928"	"0.034"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27074"	"LAMP3"	"0.63"	"0.655"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"27077"	"B9D1"	"0.633"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27077"	"B9D1"	"0.633"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"27077"	"B9D1"	"0.633"	"0.586"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27077"	"B9D1"	"0.633"	"0.586"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"27077"	"B9D1"	"0.633"	"0.586"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"ORPHANET"
"27077"	"B9D1"	"0.633"	"0.586"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27077"	"B9D1"	"0.633"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"27077"	"B9D1"	"0.633"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"27077"	"B9D1"	"0.633"	"0.586"	"C4310706"	"JOUBERT SYNDROME 27"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"3"	"UNIPROT"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2010"	"2017"	"1"	"2"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0242647"	"Mucosa-Associated Lymphoid Tissue Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2015"	"0"	"0"	"ORPHANET"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C1292769"	"Precursor B-cell lymphoblastic leukemia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"27086"	"FOXP1"	"0.528"	"0.69"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2018"	"1"	"1"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.46"	"1"	"2010"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"27086"	"FOXP1"	"0.528"	"0.69"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27086"	"FOXP1"	"0.528"	"0.69"	"C4013764"	"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"27087"	"B3GAT1"	"0.554"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"PSYGENET"
"27087"	"B3GAT1"	"0.554"	"0.655"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27087"	"B3GAT1"	"0.554"	"0.655"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27089"	"UQCRQ"	"0.762"	"0.276"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"ORPHANET"
"27089"	"UQCRQ"	"0.762"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27089"	"UQCRQ"	"0.762"	"0.276"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"27089"	"UQCRQ"	"0.762"	"0.276"	"C3554607"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"27089"	"UQCRQ"	"0.762"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"27091"	"CACNG5"	"0.928"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"27091"	"CACNG5"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"27098"	"CLUL1"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27098"	"CLUL1"	"0.886"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27098"	"CLUL1"	"0.886"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27098"	"CLUL1"	"0.886"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0002878"	"Anemia, Hemolytic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0002879"	"Anemia, Hemolytic, Acquired"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0002889"	"Anemia, Microangiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0221021"	"Microangiopathic hemolytic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27102"	"EIF2AK1"	"0.676"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27107"	"ZBTB11"	"0.928"	"0.103"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27107"	"ZBTB11"	"0.928"	"0.103"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27111"	"SDCBP2"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"27113"	"BBC3"	"0.557"	"0.759"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27113"	"BBC3"	"0.557"	"0.759"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27115"	"PDE7B"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2017"	"3"	"0"	"PSYGENET"
"27121"	"DKK4"	"0.69"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"27121"	"DKK4"	"0.69"	"0.31"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"27121"	"DKK4"	"0.69"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"27121"	"DKK4"	"0.69"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"27122"	"DKK3"	"0.555"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"27123"	"DKK2"	"0.656"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"PSYGENET"
"27125"	"AFF4"	"0.659"	"0.655"	"C0000772"	"Multiple congenital anomalies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27125"	"AFF4"	"0.659"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"27125"	"AFF4"	"0.659"	"0.655"	"C4085597"	"CHOPS SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2015"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"27127"	"SMC1B"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27127"	"SMC1B"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27130"	"INVS"	"0.633"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27130"	"INVS"	"0.633"	"0.448"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27130"	"INVS"	"0.633"	"0.448"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27130"	"INVS"	"0.633"	"0.448"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"27130"	"INVS"	"0.633"	"0.448"	"C1865872"	"NEPHRONOPHTHISIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.93"	"1"	"1989"	"2009"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"27130"	"INVS"	"0.633"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27131"	"SNX5"	"0.834"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27131"	"SNX5"	"0.834"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27131"	"SNX5"	"0.834"	"0.207"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27131"	"SNX5"	"0.834"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27133"	"KCNH5"	"0.857"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"27134"	"TJP3"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27134"	"TJP3"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27136"	"MORC1"	"0.886"	"0.069"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"27136"	"MORC1"	"0.886"	"0.069"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"27145"	"FILIP1"	"0.886"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"27145"	"FILIP1"	"0.886"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"27145"	"FILIP1"	"0.886"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27146"	"FAM184B"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27148"	"STK36"	"0.815"	"0.276"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"27148"	"STK36"	"0.815"	"0.276"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27148"	"STK36"	"0.815"	"0.276"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27148"	"STK36"	"0.815"	"0.276"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27148"	"STK36"	"0.815"	"0.276"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27151"	"CPAMD8"	"0.762"	"0.207"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27151"	"CPAMD8"	"0.762"	"0.207"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27151"	"CPAMD8"	"0.762"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27151"	"CPAMD8"	"0.762"	"0.207"	"C1862839"	"Anterior segment mesenchymal dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"27151"	"CPAMD8"	"0.762"	"0.207"	"C4310622"	"ANTERIOR SEGMENT DYSGENESIS 8"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"27159"	"CHIA"	"0.773"	"0.241"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27159"	"CHIA"	"0.773"	"0.241"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"27161"	"AGO2"	"0.575"	"0.724"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27161"	"AGO2"	"0.575"	"0.724"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27164"	"SALL3"	"0.785"	"0.207"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27164"	"SALL3"	"0.785"	"0.207"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27164"	"SALL3"	"0.785"	"0.207"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27164"	"SALL3"	"0.785"	"0.207"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27164"	"SALL3"	"0.785"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27164"	"SALL3"	"0.785"	"0.207"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27165"	"GLS2"	"0.713"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27165"	"GLS2"	"0.713"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"27173"	"SLC39A1"	"0.727"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2010"	"2"	"0"	"CTD_human"
"27173"	"SLC39A1"	"0.727"	"0.379"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27173"	"SLC39A1"	"0.727"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"27184"	"DISC2"	"0.834"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2001"	"2011"	"0"	"0"	"CTD_human"
"27184"	"DISC2"	"0.834"	"0.138"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"27184"	"DISC2"	"0.834"	"0.138"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2005"	"2"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2008"	"2012"	"2"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2002"	"2016"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2016"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0030193"	"Pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9698492"	"2001"	"2018"	"2"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2018"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0234230"	"Pain, Burning"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0234238"	"Ache"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0234254"	"Radiating pain"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0236792"	"Asperger Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0458257"	"Pain, Splitting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0458259"	"Pain, Crushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2018"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0751407"	"Pain, Migratory"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0751408"	"Suffering, Physical"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27185"	"DISC1"	"0.592"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2006"	"2018"	"5"	"0"	"PSYGENET"
"27185"	"DISC1"	"0.592"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27189"	"IL17C"	"0.537"	"0.759"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2000"	"2012"	"2"	"0"	"PSYGENET"
"27201"	"GPR78"	"0.743"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"27201"	"GPR78"	"0.743"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"27229"	"TUBGCP4"	"0.713"	"0.345"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"27229"	"TUBGCP4"	"0.713"	"0.345"	"C3502492"	"Microcephaly with Chorioretinopathy, Autosomal Recessive"	"disease"	"C05;C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"27229"	"TUBGCP4"	"0.713"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"27232"	"GNMT"	"0.642"	"0.345"	"C0019158"	"Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0268621"	"Hepatic methionine adenosyltransferase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"1998"	"2011"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C1847720"	"Glycine N-Methyltransferase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.90"		"2002"	"2009"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"27232"	"GNMT"	"0.642"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2017"	"1"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C3151058"	"S-adenosylhomocysteine hydrolase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"2"	"0"	"CTD_human"
"27232"	"GNMT"	"0.642"	"0.345"	"C4048705"	"Hypermethioninemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"2"	"0"	"CTD_human"
"27235"	"COQ2"	"0.639"	"0.552"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"27235"	"COQ2"	"0.639"	"0.552"	"C0020651"	"Hypotension, Orthostatic"	"phenotype"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"UNIPROT"
"27235"	"COQ2"	"0.639"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27235"	"COQ2"	"0.639"	"0.552"	"C0270733"	"Striatonigral Degeneration"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27235"	"COQ2"	"0.639"	"0.552"	"C0393571"	"Multiple System Atrophy"	"phenotype"	"C10"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"27235"	"COQ2"	"0.639"	"0.552"	"C0393911"	"Pure Autonomic Failure"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"UNIPROT"
"27235"	"COQ2"	"0.639"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27235"	"COQ2"	"0.639"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27235"	"COQ2"	"0.639"	"0.552"	"C3551954"	"COENZYME Q10 DEFICIENCY, PRIMARY, 1"	"disease"		"Disease or Syndrome"	"0.50"		"2007"	"2017"	"7"	"0"	"CTD_human;UNIPROT"
"27235"	"COQ2"	"0.639"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"27235"	"COQ2"	"0.639"	"0.552"	"C3714927"	"MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"UNIPROT"
"27241"	"BBS9"	"0.659"	"0.448"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"27241"	"BBS9"	"0.659"	"0.448"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.44"	"1"	"2006"	"2017"	"0"	"8"	"ORPHANET"
"27241"	"BBS9"	"0.659"	"0.448"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27241"	"BBS9"	"0.659"	"0.448"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C1859567"	"BARDET-BIEDL SYNDROME 9"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2016"	"2"	"12"	"CTD_human;UNIPROT"
"27241"	"BBS9"	"0.659"	"0.448"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27241"	"BBS9"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"27241"	"BBS9"	"0.659"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0017639"	"Gliosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27242"	"TNFRSF21"	"0.773"	"0.241"	"C3887640"	"Astrocytosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"27245"	"AHDC1"	"0.727"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"27245"	"AHDC1"	"0.727"	"0.414"	"C4014419"	"XIA-GIBBS SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"0"	"5"	"CTD_human;ORPHANET"
"27246"	"RNF115"	"0.886"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"27246"	"RNF115"	"0.886"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.46"	"1"	"2006"	"2018"	"1"	"1"	"CTD_human"
"27246"	"RNF115"	"0.886"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27246"	"RNF115"	"0.886"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"27247"	"NFU1"	"0.762"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"27247"	"NFU1"	"0.762"	"0.241"	"C3276432"	"MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2011"	"2018"	"5"	"3"	"ORPHANET;UNIPROT"
"27247"	"NFU1"	"0.762"	"0.241"	"C3502075"	"Multiple Mitochondrial Dysfunctions Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"27247"	"NFU1"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27248"	"ERLEC1"	"0.752"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27249"	"MMADHC"	"0.707"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27249"	"MMADHC"	"0.707"	"0.345"	"C1848552"	"Methylmalonic Aciduria and Homocystinuria, CblD Type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1970"	"2016"	"2"	"13"	"CTD_human;ORPHANET;UNIPROT"
"27249"	"MMADHC"	"0.707"	"0.345"	"C1848553"	"Homocystinuria, CblD Type, Variant 1"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2004"	"2016"	"2"	"3"	"CTD_human;UNIPROT"
"27249"	"MMADHC"	"0.707"	"0.345"	"C1848554"	"Methylmalonic Aciduria, CblD Type, Variant 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2004"	"2016"	"2"	"6"	"CTD_human;UNIPROT"
"27249"	"MMADHC"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"27250"	"PDCD4"	"0.532"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"0"	"0"	"UNIPROT"
"27250"	"PDCD4"	"0.532"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"27250"	"PDCD4"	"0.532"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"0.5"	"2003"	"2016"	"1"	"0"	"CTD_human"
"27250"	"PDCD4"	"0.532"	"0.69"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27250"	"PDCD4"	"0.532"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"27253"	"PCDH17"	"0.735"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"27255"	"CNTN6"	"0.743"	"0.241"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"27255"	"CNTN6"	"0.743"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"27255"	"CNTN6"	"0.743"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27255"	"CNTN6"	"0.743"	"0.241"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27283"	"TINAG"	"0.928"	"0.103"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27283"	"TINAG"	"0.928"	"0.103"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27283"	"TINAG"	"0.928"	"0.103"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27286"	"SRPX2"	"0.696"	"0.276"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27286"	"SRPX2"	"0.696"	"0.276"	"C0376532"	"Epilepsy, Rolandic"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"0.5"	"2008"	"2014"	"0"	"0"	"ORPHANET"
"27286"	"SRPX2"	"0.696"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27286"	"SRPX2"	"0.696"	"0.276"	"C1845070"	"Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"2006"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"27286"	"SRPX2"	"0.696"	"0.276"	"C1845668"	"Perisylvian syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.33"	"1"	"2006"	"2011"	"0"	"0"	"ORPHANET"
"27286"	"SRPX2"	"0.696"	"0.276"	"C2363129"	"Benign Rolandic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27286"	"SRPX2"	"0.696"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"27294"	"DHDH"	"0.752"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"27294"	"DHDH"	"0.752"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"27295"	"PDLIM3"	"0.685"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27295"	"PDLIM3"	"0.685"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27295"	"PDLIM3"	"0.685"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27295"	"PDLIM3"	"0.685"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27303"	"RBMS3"	"0.511"	"0.759"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"PSYGENET"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2010"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2003"	"2016"	"4"	"0"	"PSYGENET"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"27306"	"HPGDS"	"0.415"	"0.828"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27306"	"HPGDS"	"0.415"	"0.828"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.42"	"1"	"2009"	"2017"	"1"	"1"	"CTD_human"
"27314"	"RAB30"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27315"	"PGAP2"	"0.834"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"27315"	"PGAP2"	"0.834"	"0.207"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"27315"	"PGAP2"	"0.834"	"0.207"	"C3280153"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2013"	"2"	"6"	"CTD_human;UNIPROT"
"27315"	"PGAP2"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"27316"	"RBMX"	"0.72"	"0.448"	"C1846145"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC 11"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9117647"	"2007"	"2017"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0238033"	"Carcinoma of Male Breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0242788"	"Breast Neoplasms, Male"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"	"0.9090909"	"2007"	"2017"	"1"	"4"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27324"	"TOX3"	"0.696"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2007"	"2016"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27327"	"TNRC6A"	"0.735"	"0.138"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2011"	"1"	"2"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"27328"	"PCDH11X"	"0.72"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27329"	"ANGPTL3"	"0.659"	"0.276"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"27329"	"ANGPTL3"	"0.659"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"27329"	"ANGPTL3"	"0.659"	"0.276"	"C1857970"	"Hypobetalipoproteinemia, Familial, 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1998"	"2012"	"0"	"7"	"CTD_human"
"27330"	"RPS6KA6"	"0.752"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27330"	"RPS6KA6"	"0.752"	"0.241"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27333"	"GOLIM4"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"27339"	"PRPF19"	"0.799"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27339"	"PRPF19"	"0.799"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27339"	"PRPF19"	"0.799"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27339"	"PRPF19"	"0.799"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"27340"	"UTP20"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"27344"	"PCSK1N"	"0.799"	"0.241"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27344"	"PCSK1N"	"0.799"	"0.241"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27344"	"PCSK1N"	"0.799"	"0.241"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"27347"	"STK39"	"0.743"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"27347"	"STK39"	"0.743"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.40"	"0.8666667"	"2009"	"2016"	"1"	"0"	"CTD_human"
"27347"	"STK39"	"0.743"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27348"	"TOR1B"	"0.928"	"0.103"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27349"	"MCAT"	"0.619"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"27350"	"APOBEC3C"	"0.886"	"0.069"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"27350"	"APOBEC3C"	"0.886"	"0.069"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"		"2004"	"2009"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C1853202"	"PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.60"		"2005"	"2012"	"2"	"1"	"CTD_human;UNIPROT"
"27429"	"HTRA2"	"0.582"	"0.448"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"27429"	"HTRA2"	"0.582"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"27429"	"HTRA2"	"0.582"	"0.448"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"27429"	"HTRA2"	"0.582"	"0.448"	"C4310650"	"3-METHYLGLUTACONIC ACIDURIA, TYPE VIII"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"4"	"CTD_human;UNIPROT"
"27436"	"EML4"	"0.614"	"0.448"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.975"	"2007"	"2018"	"6"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"2"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"27436"	"EML4"	"0.614"	"0.448"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27443"	"CECR2"	"0.752"	"0.276"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"27445"	"PCLO"	"0.656"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"27445"	"PCLO"	"0.656"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"27445"	"PCLO"	"0.656"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.37"	"0.6"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"27445"	"PCLO"	"0.656"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.6"	"2010"	"2016"	"5"	"0"	"PSYGENET"
"27445"	"PCLO"	"0.656"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2009"	"2018"	"5"	"5"	"PSYGENET"
"27445"	"PCLO"	"0.656"	"0.448"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"27445"	"PCLO"	"0.656"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"27445"	"PCLO"	"0.656"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2009"	"2018"	"5"	"0"	"PSYGENET"
"27445"	"PCLO"	"0.656"	"0.448"	"C1842687"	"PONTOCEREBELLAR HYPOPLASIA TYPE 3 (disorder)"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2004"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"27445"	"PCLO"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"28232"	"SLCO3A1"	"0.762"	"0.31"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"2"	"0"	"CTD_human"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C0220991"	"Rotor Syndrome"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"2012"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"2"	"0"	"CTD_human"
"28234"	"SLCO1B3"	"0.627"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"1"	"UNIPROT"
"28316"	"CDH20"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"28395"	"IGHV4-34"	"0.762"	"0.172"	"C0349633"	"Hairy cell leukemia variant"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"28444"	"IGHV3-21"	"0.815"	"0.138"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"28444"	"IGHV3-21"	"0.815"	"0.138"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"28444"	"IGHV3-21"	"0.815"	"0.138"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"28514"	"DLL1"	"0.538"	"0.69"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"28514"	"DLL1"	"0.538"	"0.69"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"28514"	"DLL1"	"0.538"	"0.69"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"28514"	"DLL1"	"0.538"	"0.69"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"28514"	"DLL1"	"0.538"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"28514"	"DLL1"	"0.538"	"0.69"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28755"	"TRAC"	"0.735"	"0.448"	"C3809332"	"T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"28952"	"CCDC22"	"0.676"	"0.448"	"C0796137"	"3C syndrome"	"disease"	"C05;C10;C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"28952"	"CCDC22"	"0.676"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"28952"	"CCDC22"	"0.676"	"0.448"	"C4225419"	"RITSCHER-SCHINZEL SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2016"	"2"	"2"	"UNIPROT"
"28956"	"LAMTOR2"	"0.667"	"0.586"	"C1835829"	"Immunodeficiency due to Defect in MAPBP-Interacting Protein"	"disease"	"C20"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"28957"	"MRPS28"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28957"	"MRPS28"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28957"	"MRPS28"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28957"	"MRPS28"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28958"	"COA3"	"0.928"	"0.138"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"2"	"ORPHANET"
"28958"	"COA3"	"0.928"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"28958"	"COA3"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"28960"	"DCPS"	"0.762"	"0.241"	"C4085595"	"AL-RAQAD SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"3"	"CTD_human;UNIPROT"
"28962"	"OSTM1"	"0.799"	"0.138"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"28962"	"OSTM1"	"0.799"	"0.138"	"C1838258"	"Osteopetrosis and infantile neuroaxonal dystrophy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"28962"	"OSTM1"	"0.799"	"0.138"	"C1968603"	"Osteopetrosis, Autosomal Recessive 5"	"disease"	"C05"	"Disease or Syndrome"	"0.60"		"1975"	"2014"	"0"	"2"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"28964"	"GIT1"	"0.663"	"0.483"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28969"	"BZW2"	"0.834"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"28973"	"MRPS18B"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28973"	"MRPS18B"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28973"	"MRPS18B"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28973"	"MRPS18B"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28976"	"ACAD9"	"0.727"	"0.345"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"28976"	"ACAD9"	"0.727"	"0.345"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"28976"	"ACAD9"	"0.727"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"28976"	"ACAD9"	"0.727"	"0.345"	"C1970173"	"Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of"	"disease"	"C05;C10;C14;C16;C18;C23"	"Disease or Syndrome"	"0.71"	"1"	"2007"	"2017"	"8"	"13"	"CTD_human;ORPHANET;UNIPROT"
"28976"	"ACAD9"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"28981"	"IFT81"			"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"28982"	"FLVCR1"	"0.639"	"0.621"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"28982"	"FLVCR1"	"0.639"	"0.621"	"C1836916"	"POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.74"	"1"	"1998"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"28982"	"FLVCR1"	"0.639"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1998"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"28984"	"RGCC"	"0.633"	"0.483"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"28988"	"DBNL"	"0.785"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"28996"	"HIPK2"	"0.621"	"0.517"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"28996"	"HIPK2"	"0.621"	"0.517"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28998"	"MRPL13"	"0.799"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"28999"	"KLF15"	"0.659"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"28999"	"KLF15"	"0.659"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29015"	"SLC43A3"	"0.928"	"0.138"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29058"	"TMEM230"	"0.834"	"0.034"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"29058"	"TMEM230"	"0.834"	"0.034"	"C3160718"	"PARKINSON DISEASE, LATE-ONSET"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2018"	"1"	"2"	"UNIPROT"
"29071"	"C1GALT1C1"	"0.743"	"0.241"	"C0272137"	"Tn Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.60"		"2005"	"2008"	"2"	"5"	"CTD_human;UNIPROT"
"29071"	"C1GALT1C1"	"0.743"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"29072"	"SETD2"	"0.465"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"29072"	"SETD2"	"0.465"	"0.724"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"0.9333333"	"2001"	"2016"	"2"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0010701"	"Phyllodes Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2000"	"2015"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2014"	"2"	"1"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0175695"	"Sotos' syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29072"	"SETD2"	"0.465"	"0.724"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"0.9285714"	"2004"	"2016"	"6"	"0"	"CGI;CTD_human;UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9166667"	"2000"	"2018"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0600066"	"Malignant Cystosarcoma Phyllodes"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29072"	"SETD2"	"0.465"	"0.724"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2750825"	"NONPAPILLARY RENAL CARCINOMA 1 LOCUS"	"phenotype"		"Finding"	"0.30"		"2010"	"2016"	"4"	"0"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2751594"	"LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1"	"disease"		"Neoplastic Process"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2751595"	"LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1"	"disease"		"Neoplastic Process"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2751596"	"LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO"	"disease"		"Neoplastic Process"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2751597"	"LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C2751598"	"LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2014"	"2015"	"2"	"3"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C3275959"	"LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2005"	"2014"	"2"	"1"	"UNIPROT"
"29072"	"SETD2"	"0.465"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"29072"	"SETD2"	"0.465"	"0.724"	"C4085873"	"LUSCAN-LUMISH SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"4"	"4"	"CTD_human;UNIPROT"
"29078"	"NDUFAF4"	"0.656"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29078"	"NDUFAF4"	"0.656"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"29078"	"NDUFAF4"	"0.656"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"29078"	"NDUFAF4"	"0.656"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"29079"	"MED4"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29079"	"MED4"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29083"	"GTPBP8"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"29086"	"BABAM1"	"0.752"	"0.241"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"29086"	"BABAM1"	"0.752"	"0.241"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29087"	"THYN1"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29087"	"THYN1"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29087"	"THYN1"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"29089"	"UBE2T"	"0.681"	"0.448"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29089"	"UBE2T"	"0.681"	"0.448"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"29089"	"UBE2T"	"0.681"	"0.448"	"C4084840"	"FANCONI ANEMIA, COMPLEMENTATION GROUP T"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"29091"	"STXBP6"	"1"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"29094"	"LGALSL"	"0.886"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29098"	"RANGRF"	"0.886"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29098"	"RANGRF"	"0.886"	"0.172"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2012"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"29102"	"DROSHA"	"0.633"	"0.552"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29102"	"DROSHA"	"0.633"	"0.552"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"29102"	"DROSHA"	"0.633"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"29102"	"DROSHA"	"0.633"	"0.552"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29102"	"DROSHA"	"0.633"	"0.552"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29102"	"DROSHA"	"0.633"	"0.552"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29103"	"DNAJC15"	"0.727"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2002"	"2014"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2014"	"2"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0206704"	"Carcinoma, Large Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29108"	"PYCARD"	"0.517"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"29110"	"TBK1"	"0.569"	"0.69"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.9090909"	"2015"	"2017"	"0"	"1"	"ORPHANET"
"29110"	"TBK1"	"0.569"	"0.69"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29110"	"TBK1"	"0.569"	"0.69"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.32"	"0.5"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"29110"	"TBK1"	"0.569"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"29110"	"TBK1"	"0.569"	"0.69"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29110"	"TBK1"	"0.569"	"0.69"	"C4225325"	"FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"12"	"CTD_human;UNIPROT"
"29114"	"TAGLN3"	"0.928"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"29115"	"SAP30BP"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29116"	"MYLIP"	"0.652"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29116"	"MYLIP"	"0.652"	"0.517"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"29116"	"MYLIP"	"0.652"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.42"	"1"	"2013"	"2017"	"0"	"1"	"GENOMICS_ENGLAND"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C3810138"	"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"29119"	"CTNNA3"	"0.656"	"0.517"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C0220687"	"KBG syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2018"	"2"	"19"	"CTD_human;ORPHANET;UNIPROT"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"29123"	"ANKRD11"	"0.621"	"0.517"	"C4304594"	"16q24.3 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29125"	"C11orf21"	"0.857"	"0.138"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"		"2013"	"2017"	"1"	"2"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"29126"	"CD274"	"0.458"	"0.828"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2016"	"0"	"0"	"CGI"
"29126"	"CD274"	"0.458"	"0.828"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.36"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0027666"	"Neoplasms, Radiation-Induced"	"group"	"C04;C26"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2017"	"0"	"0"	"CGI"
"29126"	"CD274"	"0.458"	"0.828"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0751366"	"Radiation-Induced Cancer"	"disease"	"C04;C26"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C0751552"	"Malignant neoplasm of thymus"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C1332201"	"Adult Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"29126"	"CD274"	"0.458"	"0.828"	"C1332967"	"Childhood Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"29126"	"CD274"	"0.458"	"0.828"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C3714644"	"Thymus Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29126"	"CD274"	"0.458"	"0.828"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29127"	"RACGAP1"	"0.696"	"0.31"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29127"	"RACGAP1"	"0.696"	"0.31"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29128"	"UHRF1"	"0.586"	"0.586"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29760"	"BLNK"	"0.584"	"0.724"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2016"	"0"	"0"	"CTD_human"
"29760"	"BLNK"	"0.584"	"0.724"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"29760"	"BLNK"	"0.584"	"0.724"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29777"	"ABT1"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29777"	"ABT1"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29777"	"ABT1"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29777"	"ABT1"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29785"	"CYP2S1"	"0.857"	"0.103"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"29785"	"CYP2S1"	"0.857"	"0.103"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"29789"	"OLA1"	"0.785"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2014"	"2014"	"0"	"0"	"UNIPROT"
"29801"	"ZDHHC8"	"0.799"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"29801"	"ZDHHC8"	"0.799"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.2"	"2005"	"2013"	"5"	"0"	"PSYGENET"
"29851"	"ICOS"	"0.53"	"0.655"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.80"	"1"	"2001"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"29851"	"ICOS"	"0.53"	"0.655"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29851"	"ICOS"	"0.53"	"0.655"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2013"	"0"	"0"	"CTD_human"
"29851"	"ICOS"	"0.53"	"0.655"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29886"	"SNX8"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"29887"	"SNX10"	"0.685"	"0.517"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"29887"	"SNX10"	"0.685"	"0.517"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29887"	"SNX10"	"0.685"	"0.517"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29887"	"SNX10"	"0.685"	"0.517"	"C1318518"	"Infantile malignant osteopetrosis"	"disease"		"Congenital Abnormality"	"0.31"	"0"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"29887"	"SNX10"	"0.685"	"0.517"	"C3554478"	"OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2013"	"3"	"4"	"CTD_human;UNIPROT"
"29893"	"PSMC3IP"	"0.685"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29893"	"PSMC3IP"	"0.685"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"29893"	"PSMC3IP"	"0.685"	"0.31"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"29893"	"PSMC3IP"	"0.685"	"0.31"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"29893"	"PSMC3IP"	"0.685"	"0.31"	"C3280471"	"OVARIAN DYSGENESIS 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29894"	"CPSF1"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29894"	"CPSF1"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29894"	"CPSF1"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29894"	"CPSF1"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29896"	"TRA2A"	"0.815"	"0.138"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29899"	"GPSM2"	"0.681"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"29899"	"GPSM2"	"0.681"	"0.448"	"C1858695"	"Chudley-Mccullough syndrome"	"disease"	"C04;C09;C10;C16;C23"	"Disease or Syndrome"	"0.64"	"1"	"1999"	"2017"	"1"	"9"	"CTD_human;ORPHANET"
"29899"	"GPSM2"	"0.681"	"0.448"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"29899"	"GPSM2"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"29901"	"SAC3D1"	"0.886"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"29904"	"EEF2K"	"0.727"	"0.207"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C0013608"	"Edema, Cardiac"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C0151699"	"Intracranial Hemorrhages"	"group"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C0271287"	"Schnyder crystalline corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.80"	"1"	"1986"	"2018"	"9"	"11"	"CTD_human;ORPHANET;UNIPROT"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C0553692"	"Brain hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C0751893"	"Posterior Fossa Hemorrhage"	"phenotype"	"C10;C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"29914"	"UBIAD1"	"0.701"	"0.414"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"29920"	"PYCR2"	"0.707"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"29920"	"PYCR2"	"0.707"	"0.379"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29920"	"PYCR2"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"29920"	"PYCR2"	"0.707"	"0.379"	"C4225332"	"LEUKODYSTROPHY, HYPOMYELINATING, 10"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2017"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"29922"	"NME7"	"0.752"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"29922"	"NME7"	"0.752"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29922"	"NME7"	"0.752"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29923"	"HILPDA"	"0.676"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29923"	"HILPDA"	"0.676"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29925"	"GMPPB"	"0.645"	"0.345"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29925"	"GMPPB"	"0.645"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"29925"	"GMPPB"	"0.645"	"0.345"	"C3714932"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2018"	"4"	"16"	"CTD_human;ORPHANET;UNIPROT"
"29925"	"GMPPB"	"0.645"	"0.345"	"C3809216"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"1"	"4"	"UNIPROT"
"29925"	"GMPPB"	"0.645"	"0.345"	"C3809221"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"29926"	"GMPPA"	"0.743"	"0.31"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"29926"	"GMPPA"	"0.743"	"0.31"	"C0271742"	"Glucocorticoid deficiency with achalasia"	"disease"	"C06;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29926"	"GMPPA"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"1997"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"29926"	"GMPPA"	"0.743"	"0.31"	"C3809738"	"ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"29927"	"SEC61A1"	"0.773"	"0.276"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29927"	"SEC61A1"	"0.773"	"0.276"	"C4310741"	"HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"29929"	"ALG6"	"0.785"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"29929"	"ALG6"	"0.785"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29929"	"ALG6"	"0.785"	"0.207"	"C2930997"	"Congenital disorder of glycosylation type 1C"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.76"	"0.8333333"	"1999"	"2015"	"6"	"6"	"CTD_human;ORPHANET;UNIPROT"
"29929"	"ALG6"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29940"	"DSE"	"0.762"	"0.241"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"29940"	"DSE"	"0.762"	"0.241"	"C1866294"	"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29940"	"DSE"	"0.762"	"0.241"	"C3809845"	"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"29942"	"PURG"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"29945"	"ANAPC4"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"29947"	"DNMT3L"	"0.713"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"29948"	"OSGIN1"	"0.752"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"29949"	"IL19"	"0.604"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"29949"	"IL19"	"0.604"	"0.655"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"29949"	"IL19"	"0.604"	"0.655"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"29949"	"IL19"	"0.604"	"0.655"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"29950"	"SERTAD1"	"0.773"	"0.172"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"29950"	"SERTAD1"	"0.773"	"0.172"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"29950"	"SERTAD1"	"0.773"	"0.172"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"29951"	"PDZRN4"	"0.886"	"0.172"	"C0037116"	"Silicosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29951"	"PDZRN4"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"29952"	"DPP7"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29952"	"DPP7"	"1"	"0.034"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"29954"	"POMT2"	"0.558"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2006"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.59"	"1"	"2006"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"29954"	"POMT2"	"0.558"	"0.552"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.41"	"1"	"2006"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"CTD_human"
"29954"	"POMT2"	"0.558"	"0.552"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"29954"	"POMT2"	"0.558"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.46"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29954"	"POMT2"	"0.558"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29954"	"POMT2"	"0.558"	"0.552"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"29954"	"POMT2"	"0.558"	"0.552"	"C3150411"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2017"	"5"	"15"	"UNIPROT"
"29954"	"POMT2"	"0.558"	"0.552"	"C3150416"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2017"	"2"	"11"	"CTD_human;UNIPROT"
"29954"	"POMT2"	"0.558"	"0.552"	"C3150418"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2"	"disease"		"Disease or Syndrome"	"0.70"		"2007"	"2017"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"29954"	"POMT2"	"0.558"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"1"	"2006"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"29957"	"SLC25A24"	"0.667"	"0.483"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"29957"	"SLC25A24"	"0.667"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29957"	"SLC25A24"	"0.667"	"0.483"	"C0345382"	"Gorlin Chaudhry Moss syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29957"	"SLC25A24"	"0.667"	"0.483"	"C2931653"	"Petty Laxova Wiedemann syndrome"	"disease"	"C16;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"29957"	"SLC25A24"	"0.667"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29958"	"DMGDH"	"1"	"0.069"	"C1853892"	"Dimethylglycine Dehydrogenase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1999"	"2016"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"29959"	"NRBP1"	"0.799"	"0.138"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0265218"	"Neu-Laxova syndrome"	"disease"	"C05;C10;C13;C16;C17;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"29968"	"PSAT1"	"0.565"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"29968"	"PSAT1"	"0.565"	"0.621"	"C1970253"	"Phosphoserine Aminotransferase Deficiency"	"disease"	"C05;C10;C16;C23;F01"	"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"29968"	"PSAT1"	"0.565"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"29968"	"PSAT1"	"0.565"	"0.621"	"C4015019"	"NEU-LAXOVA SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"3"	"UNIPROT"
"29978"	"UBQLN2"	"0.676"	"0.31"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"	"0.9310345"	"2011"	"2018"	"0"	"1"	"ORPHANET"
"29978"	"UBQLN2"	"0.676"	"0.31"	"C3275459"	"AMYOTROPHIC LATERAL SCLEROSIS 15, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"6"	"7"	"CTD_human;UNIPROT"
"29979"	"UBQLN1"	"0.69"	"0.379"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"29980"	"DONSON"	"0.743"	"0.241"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"29980"	"DONSON"	"0.743"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"29980"	"DONSON"	"0.743"	"0.241"	"C4539873"	"MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"1"	"9"	"UNIPROT"
"29985"	"SLC39A3"	"0.799"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"29985"	"SLC39A3"	"0.799"	"0.172"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"29985"	"SLC39A3"	"0.799"	"0.172"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"29995"	"LMCD1"	"0.886"	"0.138"	"C0026266"	"Mitral Valve Insufficiency"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29995"	"LMCD1"	"0.886"	"0.138"	"C0026267"	"Mitral Valve Prolapse Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"29997"	"NOP53"	"0.696"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"29997"	"NOP53"	"0.696"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"30000"	"TNPO2"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"30000"	"TNPO2"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"30000"	"TNPO2"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2015"	"8"	"0"	"CLINGEN"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0268351"	"Cutis Laxa, Autosomal Recessive, Type I"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.35"	"1"	"2006"	"2015"	"0"	"0"	"ORPHANET"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.31"	"1"	"2006"	"2012"	"4"	"0"	"GENOMICS_ENGLAND"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C0432336"	"Cutis laxa, recessive, type I"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"30008"	"EFEMP2"	"0.594"	"0.655"	"C3280798"	"CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB"	"disease"		"Disease or Syndrome"	"0.60"		"1996"	"2014"	"3"	"9"	"CTD_human;UNIPROT"
"30009"	"TBX21"	"0.582"	"0.759"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.70"	"0.9230769"	"2002"	"2015"	"1"	"0"	"CTD_human"
"30009"	"TBX21"	"0.582"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"30009"	"TBX21"	"0.582"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"30009"	"TBX21"	"0.582"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"30009"	"TBX21"	"0.582"	"0.759"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"30009"	"TBX21"	"0.582"	"0.759"	"C1859648"	"Asthma, Nasal Polyps, And Aspirin Intolerance"	"disease"	"C08;C09;C20;C23;C25"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"30011"	"SH3KBP1"	"0.785"	"0.172"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30011"	"SH3KBP1"	"0.785"	"0.172"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30012"	"TLX3"	"0.707"	"0.276"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"0.95"	"2002"	"2014"	"0"	"0"	"ORPHANET"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2015"	"2"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0019054"	"Hemolysis (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0235574"	"Intravascular hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0282193"	"Iron Overload"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2017"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0312854"	"Extravascular Hemolysis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.875"	"2003"	"2018"	"2"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C0878682"	"Ceruloplasmin deficiency"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C1853733"	"HEMOCHROMATOSIS, TYPE 4"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.98"	"1"	"1993"	"2017"	"12"	"11"	"CTD_human;ORPHANET;UNIPROT"
"30061"	"SLC40A1"	"0.621"	"0.655"	"C2931082"	"Familial apoceruloplasmin deficiency"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"30062"	"RAX"	"0.785"	"0.241"	"C0003119"	"Anophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.46"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"30062"	"RAX"	"0.785"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"30062"	"RAX"	"0.785"	"0.241"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"30062"	"RAX"	"0.785"	"0.241"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"30062"	"RAX"	"0.785"	"0.241"	"C1970237"	"Microphthalmia, Isolated 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"30062"	"RAX"	"0.785"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"30812"	"SOX8"	"0.762"	"0.345"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0004310"	"Auditory Perceptual Disorders"	"group"	"C09;C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0010035"	"Hereditary corneal dystrophy"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0014008"	"Empty Sella Syndrome"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0018179"	"Granular Dystrophy, Corneal"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0018245"	"Groenouw's Dystrophies"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0022578"	"Keratoconus"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.8846154"	"2002"	"2016"	"2"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0024439"	"Macular corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0038457"	"Stromal Dystrophies, Corneal"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0271574"	"Empty Sella Syndrome, Primary"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0339284"	"Polymorphous corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"0.9090909"	"2005"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"30813"	"VSX1"	"0.616"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0750942"	"Auditory Inattention"	"disease"	"C09;C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C0751097"	"Empty Sella Syndrome, Secondary"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30813"	"VSX1"	"0.616"	"0.517"	"C1835677"	"Keratoconus 1"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2002"	"2012"	"6"	"8"	"CTD_human;UNIPROT"
"30813"	"VSX1"	"0.616"	"0.517"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"30813"	"VSX1"	"0.616"	"0.517"	"C3280099"	"CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"30816"	"ERVW-1"	"0.502"	"0.724"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"30816"	"ERVW-1"	"0.502"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2001"	"2016"	"2"	"0"	"PSYGENET"
"30817"	"ADGRE2"	"0.735"	"0.207"	"C0157743"	"Vibratory urticaria"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"30817"	"ADGRE2"	"0.735"	"0.207"	"C0473546"	"Vibratory angioedema"	"disease"	"C14;C17;C20"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"30817"	"ADGRE2"	"0.735"	"0.207"	"C1852145"	"Familial dermographism"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"30817"	"ADGRE2"	"0.735"	"0.207"	"C1852146"	"DERMODISTORTIVE URTICARIA"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.70"		"1981"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"30818"	"KCNIP3"	"0.752"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2013"	"2017"	"0"	"0"	"UNIPROT"
"30833"	"NT5C"	"0.815"	"0.138"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"30833"	"NT5C"	"0.815"	"0.138"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"30833"	"NT5C"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"30834"	"ZNRD1"	"0.743"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human"
"30834"	"ZNRD1"	"0.743"	"0.207"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"30834"	"ZNRD1"	"0.743"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.36"		"2004"	"2008"	"1"	"0"	"CTD_human"
"30834"	"ZNRD1"	"0.743"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C0011311"	"Dengue Fever"	"disease"	"C02"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C0041327"	"Tuberculosis, Pulmonary"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2006"	"2016"	"1"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"30835"	"CD209"	"0.652"	"0.517"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"30845"	"EHD3"	"0.743"	"0.138"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"30845"	"EHD3"	"0.743"	"0.138"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"30845"	"EHD3"	"0.743"	"0.138"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"30845"	"EHD3"	"0.743"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"30845"	"EHD3"	"0.743"	"0.138"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"30849"	"PIK3R4"	"0.735"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"30851"	"TAX1BP3"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"30968"	"STOML2"	"0.676"	"0.379"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"30968"	"STOML2"	"0.676"	"0.379"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"49855"	"SCAPER"	"0.69"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"49855"	"SCAPER"	"0.69"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"49855"	"SCAPER"	"0.69"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"49855"	"SCAPER"	"0.69"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"49855"	"SCAPER"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0001125"	"Acidosis, Lactic"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0022541"	"Kearns-Sayre syndrome"	"disease"	"C05;C10;C11;C14;C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.44"	"1"	"2007"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0872218"	"MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"50484"	"RRM2B"	"0.554"	"0.655"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C1834846"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"	"disease"	"C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"50484"	"RRM2B"	"0.554"	"0.655"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C2749861"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2015"	"3"	"14"	"ORPHANET;UNIPROT"
"50484"	"RRM2B"	"0.554"	"0.655"	"C2749862"	"Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.60"		"2007"	"2009"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"50484"	"RRM2B"	"0.554"	"0.655"	"C2751319"	"Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2011"	"0"	"3"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C3150172"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2009"	"3"	"9"	"ORPHANET;UNIPROT"
"50484"	"RRM2B"	"0.554"	"0.655"	"C3501849"	"Mngie Without Leukoencephalopathy"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C3711125"	"Mitochondrial DNA Depletion Syndrome 8A"	"disease"	"C05;C06;C10;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50484"	"RRM2B"	"0.554"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"50484"	"RRM2B"	"0.554"	"0.655"	"C4511138"	"Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"50485"	"SMARCAL1"	"0.663"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"50485"	"SMARCAL1"	"0.663"	"0.586"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1998"	"1998"	"1"	"0"	"GENOMICS_ENGLAND"
"50485"	"SMARCAL1"	"0.663"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50485"	"SMARCAL1"	"0.663"	"0.586"	"C0877024"	"Schimke immunoosseous dysplasia"	"disease"	"C05;C08;C12;C13;C14;C16;C20"	"Congenital Abnormality"	"1.00"	"1"	"2002"	"2017"	"4"	"11"	"CTD_human;ORPHANET;UNIPROT"
"50485"	"SMARCAL1"	"0.663"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50486"	"G0S2"	"0.701"	"0.379"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50486"	"G0S2"	"0.701"	"0.379"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"50488"	"MINK1"	"0.834"	"0.241"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"50489"	"CD207"	"0.773"	"0.379"	"C3150657"	"BIRBECK GRANULE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"1994"	"2006"	"2"	"1"	"UNIPROT"
"50506"	"DUOX2"	"0.598"	"0.69"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.90"	"1"	"2002"	"2018"	"6"	"2"	"CTD_human;GENOMICS_ENGLAND"
"50506"	"DUOX2"	"0.598"	"0.69"	"C0342200"	"Endemic Cretinism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"2"	"0"	"CTD_human"
"50506"	"DUOX2"	"0.598"	"0.69"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2002"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"50506"	"DUOX2"	"0.598"	"0.69"	"C1578691"	"Myxedema, Congenital"	"disease"	"C05;C16;C19"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2006"	"2006"	"2"	"0"	"CTD_human"
"50506"	"DUOX2"	"0.598"	"0.69"	"C1846632"	"Thyroid Dyshormonogenesis 6"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.60"		"2002"	"2015"	"4"	"10"	"CTD_human;UNIPROT"
"50506"	"DUOX2"	"0.598"	"0.69"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"50507"	"NOX4"	"0.533"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.54"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0035078"	"Kidney Failure"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C1565489"	"Renal Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50507"	"NOX4"	"0.533"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50508"	"NOX3"	"0.857"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50508"	"NOX3"	"0.857"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50509"	"COL5A3"	"0.928"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50509"	"COL5A3"	"0.928"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50511"	"SYCP3"	"0.752"	"0.103"	"C0000809"	"Abortion, Habitual"	"disease"	"C13"	"Disease or Syndrome"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50511"	"SYCP3"	"0.752"	"0.103"	"C0004509"	"Azoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.65"	"0.8"	"2000"	"2013"	"1"	"0"	"CTD_human"
"50511"	"SYCP3"	"0.752"	"0.103"	"C0232981"	"Arrest of spermatogenesis"	"phenotype"	"C12"	"Pathologic Function"	"0.40"		"2009"	"2009"	"0"	"2"	"CTD_human"
"50511"	"SYCP3"	"0.752"	"0.103"	"C3279437"	"PREGNANCY LOSS, RECURRENT, 4"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"50514"	"DEC1"	"0.656"	"0.414"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2008"	"0"	"0"	"CTD_human"
"50514"	"DEC1"	"0.656"	"0.414"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2000"	"2008"	"0"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"50604"	"IL20"	"0.575"	"0.69"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"50604"	"IL20"	"0.575"	"0.69"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"50604"	"IL20"	"0.575"	"0.69"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50615"	"IL21R"	"0.602"	"0.655"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"50615"	"IL21R"	"0.602"	"0.655"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"50615"	"IL21R"	"0.602"	"0.655"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50615"	"IL21R"	"0.602"	"0.655"	"C3554687"	"IL21R IMMUNODEFICIENCY"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"50616"	"IL22"	"0.464"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0241910"	"Hepatitis, Autoimmune"	"disease"	"C06;C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"50616"	"IL22"	"0.464"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50616"	"IL22"	"0.464"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2004"	"2013"	"3"	"0"	"CTD_human"
"50617"	"ATP6V0A4"	"0.743"	"0.345"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"50617"	"ATP6V0A4"	"0.743"	"0.345"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50617"	"ATP6V0A4"	"0.743"	"0.345"	"C1864498"	"RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.76"	"1"	"2000"	"2014"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"50617"	"ATP6V0A4"	"0.743"	"0.345"	"C1864499"	"Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss"	"disease"	"C09;C10;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.40"		"2002"	"2002"	"1"	"5"	"UNIPROT"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"50618"	"ITSN2"	"0.773"	"0.345"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"50619"	"DEF6"	"0.785"	"0.207"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"		"2006"	"2016"	"1"	"0"	"CTD_human"
"50619"	"DEF6"	"0.785"	"0.207"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"50628"	"GEMIN4"	"0.633"	"0.69"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"50628"	"GEMIN4"	"0.633"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"50628"	"GEMIN4"	"0.633"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"50632"	"CALY"	"0.886"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2004"	"2005"	"2"	"0"	"PSYGENET"
"50632"	"CALY"	"0.886"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"50640"	"PNPLA8"	"0.785"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50640"	"PNPLA8"	"0.785"	"0.276"	"C1855033"	"Mitochondrial myopathy with lactic acidosis"	"disease"	"C05;C09;C10;C18;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"0"	"1"	"CTD_human"
"50649"	"ARHGEF4"	"0.886"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"50649"	"ARHGEF4"	"0.886"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"50651"	"SLC45A1"	"0.834"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50651"	"SLC45A1"	"0.834"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"50651"	"SLC45A1"	"0.834"	"0.103"	"C4479636"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"50674"	"NEUROG3"	"0.707"	"0.345"	"C1835888"	"Diarrhea 4, Malabsorptive, Congenital"	"disease"	"C06;C18;C23"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"50717"	"DCAF8"	"0.799"	"0.103"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50717"	"DCAF8"	"0.799"	"0.103"	"C1864695"	"Giant Axonal Neuropathy, Autosomal Dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1985"	"2014"	"0"	"1"	"CTD_human"
"50717"	"DCAF8"	"0.799"	"0.103"	"C4013360"	"GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"50805"	"IRX4"	"0.785"	"0.172"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"50805"	"IRX4"	"0.785"	"0.172"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"50805"	"IRX4"	"0.785"	"0.172"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"50807"	"ASAP1"	"0.645"	"0.586"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"50807"	"ASAP1"	"0.645"	"0.586"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"50807"	"ASAP1"	"0.645"	"0.586"	"C0041327"	"Tuberculosis, Pulmonary"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50809"	"HP1BP3"	"0.857"	"0.103"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"PSYGENET"
"50813"	"COPS7A"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50813"	"COPS7A"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50813"	"COPS7A"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50813"	"COPS7A"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50814"	"NSDHL"	"0.667"	"0.483"	"C0265267"	"Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.76"	"0.8333333"	"1993"	"2015"	"2"	"13"	"CTD_human;ORPHANET;UNIPROT"
"50814"	"NSDHL"	"0.667"	"0.483"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50814"	"NSDHL"	"0.667"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50814"	"NSDHL"	"0.667"	"0.483"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"50814"	"NSDHL"	"0.667"	"0.483"	"C3151781"	"CK SYNDROME"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"1993"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"50814"	"NSDHL"	"0.667"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"50833"	"TAS2R16"	"0.785"	"0.138"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"50833"	"TAS2R16"	"0.785"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2006"	"2007"	"2"	"0"	"CTD_human"
"50833"	"TAS2R16"	"0.785"	"0.138"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"50838"	"TAS2R13"	"0.707"	"0.379"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"50838"	"TAS2R13"	"0.707"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"50846"	"DHH"	"0.611"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50846"	"DHH"	"0.611"	"0.414"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.62"	"1"	"2000"	"2015"	"0"	"0"	"ORPHANET"
"50846"	"DHH"	"0.611"	"0.414"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"50846"	"DHH"	"0.611"	"0.414"	"C1856273"	"46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.60"		"2004"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"50846"	"DHH"	"0.611"	"0.414"	"C2751325"	"46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy"	"disease"	"C10;C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"2000"	"2000"	"0"	"1"	"CTD_human;ORPHANET"
"50846"	"DHH"	"0.611"	"0.414"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"ORPHANET"
"50856"	"CLEC4A"	"0.928"	"0.138"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"50856"	"CLEC4A"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"50856"	"CLEC4A"	"0.928"	"0.138"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"50863"	"NTM"	"0.762"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"50863"	"NTM"	"0.762"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"50863"	"NTM"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"50937"	"CDON"	"0.69"	"0.552"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.44"	"1"	"2003"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"50937"	"CDON"	"0.69"	"0.552"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"50937"	"CDON"	"0.69"	"0.552"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"50937"	"CDON"	"0.69"	"0.552"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"50937"	"CDON"	"0.69"	"0.552"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"50937"	"CDON"	"0.69"	"0.552"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"50937"	"CDON"	"0.69"	"0.552"	"C3280215"	"HOLOPROSENCEPHALY 11"	"disease"		"Disease or Syndrome"	"0.80"		"2003"	"2011"	"1"	"6"	"CTD_human;UNIPROT"
"50937"	"CDON"	"0.69"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50937"	"CDON"	"0.69"	"0.552"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"50939"	"IMPG2"	"0.648"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2017"	"0"	"3"	"ORPHANET"
"50939"	"IMPG2"	"0.648"	"0.345"	"C0339510"	"Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"50939"	"IMPG2"	"0.648"	"0.345"	"C1842914"	"Adult-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"50939"	"IMPG2"	"0.648"	"0.345"	"C2745945"	"Juvenile-Onset Vitelliform Macular Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50939"	"IMPG2"	"0.648"	"0.345"	"C3150819"	"RETINITIS PIGMENTOSA 56"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"5"	"CTD_human"
"50939"	"IMPG2"	"0.648"	"0.345"	"C4015343"	"MACULAR DYSTROPHY, VITELLIFORM, 5"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2015"	"2"	"3"	"UNIPROT"
"50940"	"PDE11A"	"0.627"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"50940"	"PDE11A"	"0.627"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"50940"	"PDE11A"	"0.627"	"0.517"	"C1864851"	"Pigmented Nodular Adrenocortical Disease, Primary, 2"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2006"	"2015"	"0"	"4"	"CTD_human"
"50940"	"PDE11A"	"0.627"	"0.517"	"C4304832"	"Primary pigmented nodular adrenocortical disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2003"	"2016"	"0"	"1"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0342288"	"Insulin-dependent diabetes mellitus secretory diarrhea syndrome"	"disease"	"C16;C18;C19;C20;C23"	"Disease or Syndrome"	"1.00"	"0.9411765"	"1991"	"2016"	"6"	"11"	"CTD_human;ORPHANET;UNIPROT"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C1844663"	"ISLETS OF LANGERHANS, ABSENCE OF"	"phenotype"		"Finding"	"0.50"		"1991"	"2011"	"6"	"6"	"UNIPROT"
"50943"	"FOXP3"	"0.408"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2007"	"5"	"0"	"GENOMICS_ENGLAND"
"50943"	"FOXP3"	"0.408"	"0.759"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50943"	"FOXP3"	"0.408"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"50944"	"SHANK1"	"0.696"	"0.31"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"50944"	"SHANK1"	"0.696"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"50944"	"SHANK1"	"0.696"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"50945"	"TBX22"	"0.659"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50945"	"TBX22"	"0.659"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50945"	"TBX22"	"0.659"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"50945"	"TBX22"	"0.659"	"0.414"	"C1844830"	"CLEFT PALATE, X-LINKED"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.80"	"0.9166667"	"1992"	"2014"	"3"	"4"	"CTD_human;UNIPROT"
"50945"	"TBX22"	"0.659"	"0.414"	"C1844862"	"Abruzzo Erickson syndrome"	"disease"	"C05;C07;C09;C10;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"1977"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"50945"	"TBX22"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50960"	"MYMY1"			"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"50964"	"SOST"	"0.579"	"0.69"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"50964"	"SOST"	"0.579"	"0.69"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"50964"	"SOST"	"0.579"	"0.69"	"C0265301"	"Sclerosteosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.90"	"1"	"1999"	"2017"	"2"	"0"	"CTD_human;ORPHANET;UNIPROT"
"50964"	"SOST"	"0.579"	"0.69"	"C0410539"	"Craniodiaphyseal dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"50964"	"SOST"	"0.579"	"0.69"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"1"	"1986"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"50964"	"SOST"	"0.579"	"0.69"	"C2675746"	"CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"50964"	"SOST"	"0.579"	"0.69"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"51002"	"TPRKB"	"0.762"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51002"	"TPRKB"	"0.762"	"0.241"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"51002"	"TPRKB"	"0.762"	"0.241"	"C4540274"	"GALLOWAY-MOWAT SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"51004"	"COQ6"	"0.762"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51004"	"COQ6"	"0.762"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"51004"	"COQ6"	"0.762"	"0.345"	"C0917817"	"Neurofibromatosis 3"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"51004"	"COQ6"	"0.762"	"0.345"	"C1335929"	"Schwannomatosis"	"disease"	"C04;C10;C16;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"51004"	"COQ6"	"0.762"	"0.345"	"C2931480"	"Neurofibromatosis, Type 3, mixed central and peripheral"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51004"	"COQ6"	"0.762"	"0.345"	"C3553349"	"COENZYME Q10 DEFICIENCY, PRIMARY, 6"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2017"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"51005"	"AMDHD2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51008"	"ASCC1"	"0.54"	"0.724"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"51008"	"ASCC1"	"0.54"	"0.724"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51008"	"ASCC1"	"0.54"	"0.724"	"C4225176"	"SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C1843504"	"Pontocerebellar Hypoplasia Type 1"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.57"	"0.8571429"	"2012"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C3553449"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 1B"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1993"	"2018"	"1"	"9"	"CTD_human;UNIPROT"
"51010"	"EXOSC3"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51014"	"TMED7"	"0.5"	"0.759"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51014"	"TMED7"	"0.5"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51021"	"MRPS16"	"0.815"	"0.207"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51021"	"MRPS16"	"0.815"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51021"	"MRPS16"	"0.815"	"0.207"	"C1864843"	"Combined Oxidative Phosphorylation Deficiency 2"	"disease"	"C05;C10;C16;C18;C23"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"0"	"1"	"CTD_human;ORPHANET"
"51024"	"FIS1"	"0.752"	"0.448"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51025"	"PAM16"	"0.752"	"0.379"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51025"	"PAM16"	"0.752"	"0.379"	"C2750075"	"Chondrodysplasia, Megarbane-Dagher-Melki Type"	"disease"	"C05;C16;C19;C23;F03"	"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"51027"	"BOLA1"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51029"	"DESI2"	"0.785"	"0.172"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51029"	"DESI2"	"0.785"	"0.172"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"51035"	"UBXN1"	"0.886"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51035"	"UBXN1"	"0.886"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51035"	"UBXN1"	"0.886"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51035"	"UBXN1"	"0.886"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51042"	"ZNF593"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51042"	"ZNF593"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51042"	"ZNF593"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51042"	"ZNF593"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51043"	"ZBTB7B"	"1"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"51053"	"GMNN"	"0.604"	"0.655"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"51053"	"GMNN"	"0.604"	"0.655"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"2016"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"51053"	"GMNN"	"0.604"	"0.655"	"C4225188"	"MEIER-GORLIN SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2016"	"1"	"3"	"UNIPROT"
"51057"	"WDPCP"	"0.633"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51057"	"WDPCP"	"0.633"	"0.621"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51057"	"WDPCP"	"0.633"	"0.621"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"51057"	"WDPCP"	"0.633"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51057"	"WDPCP"	"0.633"	"0.621"	"C1857587"	"Orstavik Lindemann Solberg syndrome"	"disease"	"C04;C05;C07;C14;C16"	"Disease or Syndrome"	"0.60"		"2010"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"51057"	"WDPCP"	"0.633"	"0.621"	"C2931046"	"Heart defect, tongue hamartoma and polysyndactyly"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51057"	"WDPCP"	"0.633"	"0.621"	"C3150127"	"BARDET-BIEDL SYNDROME 15"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"1"	"CTD_human"
"51057"	"WDPCP"	"0.633"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51057"	"WDPCP"	"0.633"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51062"	"ATL1"	"0.614"	"0.655"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51062"	"ATL1"	"0.614"	"0.655"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"51062"	"ATL1"	"0.614"	"0.655"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"51062"	"ATL1"	"0.614"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2001"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"51062"	"ATL1"	"0.614"	"0.655"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"51062"	"ATL1"	"0.614"	"0.655"	"C2931355"	"Spastic paraplegia 3, autosomal dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.74"	"1"	"1973"	"2017"	"13"	"16"	"CTD_human;ORPHANET;UNIPROT"
"51062"	"ATL1"	"0.614"	"0.655"	"C3150972"	"NEUROPATHY, HEREDITARY SENSORY, TYPE ID"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"51062"	"ATL1"	"0.614"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"51066"	"SSUH2"	"0.773"	"0.276"	"C0399379"	"Dentin dysplasia, type 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51067"	"YARS2"	"0.69"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51067"	"YARS2"	"0.69"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"51067"	"YARS2"	"0.69"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"51067"	"YARS2"	"0.69"	"0.379"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51067"	"YARS2"	"0.69"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2017"	"0"	"1"	"GENOMICS_ENGLAND"
"51067"	"YARS2"	"0.69"	"0.379"	"C1838103"	"MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.56"	"1"	"2010"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"51067"	"YARS2"	"0.69"	"0.379"	"C3150802"	"MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2003"	"2017"	"2"	"7"	"UNIPROT"
"51076"	"CUTC"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51079"	"NDUFA13"	"0.681"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"51079"	"NDUFA13"	"0.681"	"0.379"	"C0749424"	"Thyroid Hurthle Cell Carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"		"2005"	"2005"	"0"	"1"	"CTD_human"
"51079"	"NDUFA13"	"0.681"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51081"	"MRPS7"	"0.834"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51081"	"MRPS7"	"0.834"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51081"	"MRPS7"	"0.834"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51081"	"MRPS7"	"0.834"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51081"	"MRPS7"	"0.834"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0242387"	"Mandibulofacial Dysostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.56"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0265241"	"Franceschetti-Klein syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51082"	"POLR1D"	"0.707"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51082"	"POLR1D"	"0.707"	"0.379"	"C3150983"	"TREACHER COLLINS SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"51082"	"POLR1D"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51082"	"POLR1D"	"0.707"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2006"	"2015"	"5"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0027796"	"Neuralgia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0038870"	"Neuralgia, Supraorbital"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0039231"	"Tachycardia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0042656"	"Neuralgia, Vidian"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0080203"	"Tachyarrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2015"	"4"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0234247"	"Neuralgia, Atypical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0234249"	"Neuralgia, Stump"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0338715"	"Drug-induced depressive state"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0423711"	"Neuralgia, Perineal"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0423712"	"Neuralgia, Iliohypogastric Nerve"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2014"	"5"	"0"	"PSYGENET"
"51083"	"GAL"	"0.529"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751371"	"Neuralgia, Ilioinguinal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751372"	"Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C0751373"	"Paroxysmal Nerve Pain"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51083"	"GAL"	"0.529"	"0.759"	"C4225318"	"EPILEPSY, FAMILIAL TEMPORAL LOBE, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"51084"	"CRYL1"	"0.727"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51084"	"CRYL1"	"0.727"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51084"	"CRYL1"	"0.727"	"0.448"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51085"	"MLXIPL"	"0.577"	"0.655"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51085"	"MLXIPL"	"0.577"	"0.655"	"C0175702"	"Williams Syndrome"	"disease"	"C10;C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"2000"	"2005"	"0"	"0"	"CTD_human"
"51085"	"MLXIPL"	"0.577"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"51086"	"TNNI3K"	"0.743"	"0.172"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"51086"	"TNNI3K"	"0.743"	"0.172"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51086"	"TNNI3K"	"0.743"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51086"	"TNNI3K"	"0.743"	"0.172"	"C4015285"	"CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"51088"	"KLHL5"	"0.928"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51088"	"KLHL5"	"0.928"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51088"	"KLHL5"	"0.928"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51090"	"PLLP"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"51090"	"PLLP"	"0.928"	"0.103"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2003"	"2015"	"2"	"1"	"GENOMICS_ENGLAND"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C2932714"	"Pontocerebellar Hypoplasia Type 2"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51091"	"SEPSECS"	"0.701"	"0.276"	"C3151140"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 2D"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2003"	"2016"	"2"	"5"	"CTD_human;UNIPROT"
"51092"	"SIDT2"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51092"	"SIDT2"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51094"	"ADIPOR1"	"0.573"	"0.586"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51094"	"ADIPOR1"	"0.573"	"0.586"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2007"	"2015"	"1"	"0"	"CTD_human"
"51094"	"ADIPOR1"	"0.573"	"0.586"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51094"	"ADIPOR1"	"0.573"	"0.586"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51094"	"ADIPOR1"	"0.573"	"0.586"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51095"	"TRNT1"	"0.727"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"51095"	"TRNT1"	"0.727"	"0.207"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51095"	"TRNT1"	"0.727"	"0.207"	"C4015172"	"SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2015"	"2016"	"1"	"8"	"ORPHANET;UNIPROT"
"51095"	"TRNT1"	"0.727"	"0.207"	"C4310776"	"RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"4"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51098"	"IFT52"	"0.676"	"0.379"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C0432235"	"Cranioectodermal Dysplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51098"	"IFT52"	"0.676"	"0.379"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51098"	"IFT52"	"0.676"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51098"	"IFT52"	"0.676"	"0.379"	"C4310718"	"SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"2"	"3"	"UNIPROT"
"51099"	"ABHD5"	"0.667"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51099"	"ABHD5"	"0.667"	"0.621"	"C0268238"	"Triglyceride storage disease with ichthyosis"	"disease"	"C05;C10;C16;C17;C18"	"Disease or Syndrome"	"1.00"	"1"	"2001"	"2016"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"51099"	"ABHD5"	"0.667"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51102"	"MECR"	"0.735"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51102"	"MECR"	"0.735"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51102"	"MECR"	"0.735"	"0.207"	"C4310634"	"DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"51103"	"NDUFAF1"	"0.667"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51103"	"NDUFAF1"	"0.667"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"51103"	"NDUFAF1"	"0.667"	"0.379"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2007"	"2012"	"0"	"3"	"CTD_human"
"51103"	"NDUFAF1"	"0.667"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"51106"	"TFB1M"	"0.815"	"0.207"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51106"	"TFB1M"	"0.815"	"0.207"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51109"	"RDH11"	"0.799"	"0.207"	"C4015242"	"RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"51111"	"KMT5B"	"0.928"	"0.103"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51111"	"KMT5B"	"0.928"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"51112"	"TRAPPC12"	"0.834"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51112"	"TRAPPC12"	"0.834"	"0.241"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51112"	"TRAPPC12"	"0.834"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51112"	"TRAPPC12"	"0.834"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51112"	"TRAPPC12"	"0.834"	"0.241"	"C4540059"	"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"ORPHANET;UNIPROT"
"51114"	"ZDHHC9"	"0.701"	"0.483"	"C0796022"	"Lujan Fryns syndrome"	"disease"	"C05;C10;C14;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"51114"	"ZDHHC9"	"0.701"	"0.483"	"C3275406"	"MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2009"	"2"	"5"	"CTD_human;UNIPROT"
"51114"	"ZDHHC9"	"0.701"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"51117"	"COQ4"	"0.857"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51117"	"COQ4"	"0.857"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"51117"	"COQ4"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"51117"	"COQ4"	"0.857"	"0.138"	"C4225392"	"COENZYME Q10 DEFICIENCY, PRIMARY, 7"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2017"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"51119"	"SBDS"	"0.616"	"0.552"	"C0002874"	"Aplastic Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"0"	"2007"	"2007"	"0"	"0"	"CTD_human"
"51119"	"SBDS"	"0.616"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"51119"	"SBDS"	"0.616"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.41"	"0"	"2006"	"2006"	"0"	"0"	"CGI"
"51119"	"SBDS"	"0.616"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"51119"	"SBDS"	"0.616"	"0.552"	"C0178416"	"Hypoplastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51119"	"SBDS"	"0.616"	"0.552"	"C0272170"	"Shwachman syndrome"	"disease"	"C06;C15;C17;C18"	"Disease or Syndrome"	"0.80"	"0.9361702"	"1993"	"2017"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"51119"	"SBDS"	"0.616"	"0.552"	"C0348890"	"Aplastic anemia, idiopathic"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51119"	"SBDS"	"0.616"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51119"	"SBDS"	"0.616"	"0.552"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.42"	"1"	"2009"	"2012"	"0"	"0"	"CGI"
"51119"	"SBDS"	"0.616"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51119"	"SBDS"	"0.616"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2013"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C3280240"	"MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2006"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51124"	"IER3IP1"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"51128"	"SAR1B"	"0.727"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51128"	"SAR1B"	"0.727"	"0.31"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51128"	"SAR1B"	"0.727"	"0.31"	"C0795956"	"Chylomicron retention disease"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.80"	"0.9230769"	"2003"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.35"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.47"	"0.8571429"	"2008"	"2018"	"1"	"1"	"CTD_human"
"51129"	"ANGPTL4"	"0.567"	"0.621"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"51131"	"PHF11"	"0.785"	"0.207"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.37"	"0.8333333"	"2003"	"2016"	"0"	"0"	"CTD_human"
"51131"	"PHF11"	"0.785"	"0.207"	"C1840253"	"IgE RESPONSIVENESS, ATOPIC"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51132"	"RLIM"	"0.773"	"0.345"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51132"	"RLIM"	"0.773"	"0.345"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51132"	"RLIM"	"0.773"	"0.345"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51132"	"RLIM"	"0.773"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"51132"	"RLIM"	"0.773"	"0.345"	"C4283894"	"MENTAL RETARDATION, X-LINKED 61"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"51133"	"KCTD3"	"0.928"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51133"	"KCTD3"	"0.928"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"51134"	"CEP83"	"0.815"	"0.103"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51134"	"CEP83"	"0.815"	"0.103"	"C1865872"	"NEPHRONOPHTHISIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"51134"	"CEP83"	"0.815"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51134"	"CEP83"	"0.815"	"0.103"	"C3890591"	"NEPHRONOPHTHISIS 18"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"7"	"CTD_human;UNIPROT"
"51134"	"CEP83"	"0.815"	"0.103"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0178540"	"Cerebral Hypoxia-Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"0"	"2006"	"2006"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0752304"	"Hypoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0752305"	"Anoxic-Ischemic Encephalopathy"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0752306"	"Anoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0752307"	"Anoxia-Ischemia, Cerebral"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C0752308"	"Hypoxia-Ischemia, Brain"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C1835828"	"Invasive Pneumococcal Disease, Recurrent Isolated, 1"	"disease"	"C01;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51135"	"IRAK4"	"0.624"	"0.655"	"C1843256"	"IRAK4 Deficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.71"	"1"	"1998"	"2017"	"6"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51141"	"INSIG2"	"0.656"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51141"	"INSIG2"	"0.656"	"0.379"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"51142"	"CHCHD2"	"0.785"	"0.172"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"51142"	"CHCHD2"	"0.785"	"0.172"	"C4225238"	"PARKINSON DISEASE 22, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"51147"	"ING4"	"0.614"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"51147"	"ING4"	"0.614"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51147"	"ING4"	"0.614"	"0.483"	"C0024232"	"Lymphatic Metastasis"	"disease"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51147"	"ING4"	"0.614"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"51150"	"SDF4"	"0.59"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"51150"	"SDF4"	"0.59"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2011"	"1"	"1"	"UNIPROT"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2009"	"2016"	"1"	"1"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2002"	"2017"	"1"	"1"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2002"	"2017"	"2"	"3"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.31"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C1847836"	"Oculocutaneous Albinism, Type IV"	"disease"	"C11;C16;C17;C18"	"Disease or Syndrome"	"0.95"	"1"	"1964"	"2017"	"7"	"21"	"CTD_human;ORPHANET;UNIPROT"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51151"	"SLC45A2"	"0.619"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51156"	"SERPINA10"	"0.857"	"0.138"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"51156"	"SERPINA10"	"0.857"	"0.138"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"51156"	"SERPINA10"	"0.857"	"0.138"	"C0398623"	"Thrombophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"51163"	"DBR1"	"0.834"	"0.241"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"51163"	"DBR1"	"0.834"	"0.241"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51163"	"DBR1"	"0.834"	"0.241"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51164"	"DCTN4"	"0.565"	"0.655"	"C0010674"	"Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"51164"	"DCTN4"	"0.565"	"0.655"	"C0033817"	"Pseudomonas Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51164"	"DCTN4"	"0.565"	"0.655"	"C0392164"	"Pulmonary Cystic Fibrosis"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51164"	"DCTN4"	"0.565"	"0.655"	"C0854135"	"Pseudomonas aeruginosa infection"	"disease"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"51164"	"DCTN4"	"0.565"	"0.655"	"C1527396"	"Fibrocystic Disease of Pancreas"	"disease"	"C06;C08;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51166"	"AADAT"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51167"	"CYB5R4"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51168"	"MYO15A"	"0.727"	"0.207"	"C1838263"	"Deafness, Autosomal Recessive 3"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.81"	"1"	"1995"	"2016"	"3"	"38"	"CTD_human;UNIPROT"
"51176"	"LEF1"	"0.551"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.8571429"	"2004"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1998"	"2015"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2013"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.48"	"1"	"2005"	"2017"	"1"	"3"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0036503"	"Sebaceous Gland Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"0.8333333"	"2006"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"51176"	"LEF1"	"0.551"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2014"	"1"	"1"	"UNIPROT"
"51179"	"HAO2"	"0.735"	"0.276"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51179"	"HAO2"	"0.735"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51181"	"DCXR"	"0.743"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51181"	"DCXR"	"0.743"	"0.276"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51181"	"DCXR"	"0.743"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2007"	"2008"	"1"	"0"	"CTD_human"
"51181"	"DCXR"	"0.743"	"0.276"	"C0268162"	"Pentosuria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2012"	"2017"	"2"	"1"	"CTD_human;ORPHANET"
"51181"	"DCXR"	"0.743"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2008"	"1"	"0"	"CTD_human"
"51182"	"HSPA14"	"0.565"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51182"	"HSPA14"	"0.565"	"0.759"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51185"	"CRBN"	"0.743"	"0.414"	"C0000771"	"Abnormalities, Drug-Induced"	"phenotype"	"C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51185"	"CRBN"	"0.743"	"0.414"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.60"	"0.7857143"	"2012"	"2016"	"1"	"0"	"CGI;CTD_human"
"51185"	"CRBN"	"0.743"	"0.414"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51185"	"CRBN"	"0.743"	"0.414"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51185"	"CRBN"	"0.743"	"0.414"	"C1843942"	"Mental Retardation, Autosomal Recessive 2"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2000"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"51185"	"CRBN"	"0.743"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2004"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"51191"	"HERC5"	"0.713"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51191"	"HERC5"	"0.713"	"0.345"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"51191"	"HERC5"	"0.713"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51191"	"HERC5"	"0.713"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"51192"	"CKLF"	"0.743"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51194"	"IPO11"	"0.886"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"51194"	"IPO11"	"0.886"	"0.103"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"0"	"2010"	"2013"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0019100"	"Severe Dengue"	"disease"	"C02"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2017"	"1"	"3"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.39"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"	"0.9444444"	"2010"	"2016"	"2"	"1"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C0376300"	"Dengue Shock Syndrome"	"disease"	"C02"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51196"	"PLCE1"	"0.616"	"0.517"	"C1853124"	"NEPHROTIC SYNDROME, TYPE 3"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.61"	"1"	"2007"	"2010"	"1"	"11"	"CTD_human;UNIPROT"
"51196"	"PLCE1"	"0.616"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51199"	"NIN"	"0.672"	"0.586"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51199"	"NIN"	"0.672"	"0.586"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51199"	"NIN"	"0.672"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51199"	"NIN"	"0.672"	"0.586"	"C3553870"	"SECKEL SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"1"	"3"	"ORPHANET;UNIPROT"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2000"	"2000"	"1"	"1"	"UNIPROT"
"51201"	"ZDHHC2"	"0.752"	"0.241"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"UNIPROT"
"51203"	"NUSAP1"	"0.752"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51203"	"NUSAP1"	"0.752"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51203"	"NUSAP1"	"0.752"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51204"	"TACO1"	"0.685"	"0.414"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"51204"	"TACO1"	"0.685"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51204"	"TACO1"	"0.685"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51204"	"TACO1"	"0.685"	"0.414"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51204"	"TACO1"	"0.685"	"0.414"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51204"	"TACO1"	"0.685"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51204"	"TACO1"	"0.685"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"51206"	"GP6"	"0.639"	"0.448"	"C3280120"	"BLEEDING DISORDER, PLATELET-TYPE, 11"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2009"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51218"	"GLRX5"	"0.663"	"0.414"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"51218"	"GLRX5"	"0.663"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2007"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"51218"	"GLRX5"	"0.663"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"51218"	"GLRX5"	"0.663"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51218"	"GLRX5"	"0.663"	"0.414"	"C2673914"	"Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2007"	"2010"	"0"	"1"	"CTD_human;ORPHANET"
"51218"	"GLRX5"	"0.663"	"0.414"	"C4225155"	"ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY"	"disease"		"Disease or Syndrome"	"0.40"		"2007"	"2016"	"4"	"2"	"UNIPROT"
"51218"	"GLRX5"	"0.663"	"0.414"	"C4225178"	"SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2016"	"0"	"2"	"ORPHANET"
"51224"	"ELOA2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51225"	"ABI3"	"0.743"	"0.207"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51225"	"ABI3"	"0.743"	"0.207"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51227"	"PIGP"	"0.815"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51227"	"PIGP"	"0.815"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51227"	"PIGP"	"0.815"	"0.138"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51227"	"PIGP"	"0.815"	"0.138"	"C4539843"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"51232"	"CRIM1"	"0.857"	"0.207"	"C1865286"	"MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"51244"	"CCDC174"	"0.799"	"0.241"	"C4225196"	"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"51247"	"PAIP2"	"0.886"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51247"	"PAIP2"	"0.886"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51247"	"PAIP2"	"0.886"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C0002882"	"Anemia, Hemolytic, Congenital Nonspherocytic"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C1849507"	"Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.70"		"1983"	"2015"	"8"	"9"	"CTD_human;ORPHANET;UNIPROT"
"51251"	"NT5C3A"	"0.659"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51256"	"TBC1D7"	"0.773"	"0.241"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"51256"	"TBC1D7"	"0.773"	"0.241"	"C0221355"	"Macrocephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"51259"	"TMEM216"	"0.582"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2012"	"3"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"2002"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51259"	"TMEM216"	"0.582"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C1842577"	"JOUBERT SYNDROME 2"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2016"	"3"	"11"	"CTD_human;UNIPROT"
"51259"	"TMEM216"	"0.582"	"0.552"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51259"	"TMEM216"	"0.582"	"0.552"	"C1864148"	"MECKEL SYNDROME, TYPE 2"	"disease"	"C08;C09;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2014"	"1"	"9"	"CTD_human;UNIPROT"
"51259"	"TMEM216"	"0.582"	"0.552"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51259"	"TMEM216"	"0.582"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"51259"	"TMEM216"	"0.582"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0282526"	"Hyperpipecolic Acidemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"1989"	"2000"	"1"	"0"	"CTD_human"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0751708"	"Peroxisomal Dysfunction, General"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0751709"	"Peroxisomal Dysfunction, Multiple"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51268"	"PIPOX"	"0.773"	"0.138"	"C0751710"	"Peroxisomal Dysfunction, Single"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"51280"	"GOLM1"	"0.681"	"0.414"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51284"	"TLR7"	"0.542"	"0.759"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"51284"	"TLR7"	"0.542"	"0.759"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51284"	"TLR7"	"0.542"	"0.759"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"51284"	"TLR7"	"0.542"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51291"	"GMIP"	"0.928"	"0.034"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"51291"	"GMIP"	"0.928"	"0.034"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51292"	"GMPR2"	"0.762"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51293"	"CD320"	"0.752"	"0.31"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51293"	"CD320"	"0.752"	"0.31"	"C3150900"	"METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"51294"	"PCDH12"	"0.785"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"51294"	"PCDH12"	"0.785"	"0.207"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51294"	"PCDH12"	"0.785"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51294"	"PCDH12"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51294"	"PCDH12"	"0.785"	"0.207"	"C4538630"	"MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"2"	"0"	"UNIPROT"
"51295"	"ECSIT"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51296"	"SLC15A3"	"0.886"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51297"	"BPIFA1"	"0.69"	"0.448"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51297"	"BPIFA1"	"0.69"	"0.448"	"C0814154"	"Alcohol Related Neurodevelopmental Disorder"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51297"	"BPIFA1"	"0.69"	"0.448"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51297"	"BPIFA1"	"0.69"	"0.448"	"C3146244"	"Alcohol Related Birth Defect"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51297"	"BPIFA1"	"0.69"	"0.448"	"C3661483"	"Partial Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51299"	"NRN1"	"0.762"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"51300"	"TIMMDC1"	"0.639"	"0.483"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"51300"	"TIMMDC1"	"0.639"	"0.483"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51303"	"FKBP11"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51305"	"KCNK9"	"0.69"	"0.379"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51305"	"KCNK9"	"0.69"	"0.379"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2005"	"1"	"0"	"CTD_human"
"51305"	"KCNK9"	"0.69"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51305"	"KCNK9"	"0.69"	"0.379"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51305"	"KCNK9"	"0.69"	"0.379"	"C2676770"	"Birk-Barel Mental Retardation Dysmorphism Syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"51305"	"KCNK9"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1993"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"51305"	"KCNK9"	"0.69"	"0.379"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51305"	"KCNK9"	"0.69"	"0.379"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"51308"	"REEP2"	"0.834"	"0.207"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51308"	"REEP2"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51308"	"REEP2"	"0.834"	"0.207"	"C3810160"	"SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51308"	"REEP2"	"0.834"	"0.207"	"C3810161"	"SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"51309"	"ARMCX1"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51311"	"TLR8"	"0.611"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51311"	"TLR8"	"0.611"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51311"	"TLR8"	"0.611"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51311"	"TLR8"	"0.611"	"0.655"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51312"	"SLC25A37"	"0.681"	"0.483"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51313"	"FAM198B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51314"	"NME8"	"0.713"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51314"	"NME8"	"0.713"	"0.414"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2008"	"0"	"0"	"ORPHANET"
"51314"	"NME8"	"0.713"	"0.414"	"C1970506"	"CILIARY DYSKINESIA, PRIMARY, 6"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2007"	"0"	"1"	"CTD_human"
"51314"	"NME8"	"0.713"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51314"	"NME8"	"0.713"	"0.414"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51316"	"PLAC8"	"0.735"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51317"	"PHF21A"	"0.762"	"0.241"	"C1832588"	"Chromosome 11p11.2 Deletion Syndrome"	"disease"	"C04;C05;C16;C23"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"51317"	"PHF21A"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"1993"	"2017"	"11"	"0"	"GENOMICS_ENGLAND"
"51320"	"MEX3C"	"0.815"	"0.207"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51320"	"MEX3C"	"0.815"	"0.207"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51320"	"MEX3C"	"0.815"	"0.207"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51322"	"WAC"	"0.713"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51322"	"WAC"	"0.713"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51322"	"WAC"	"0.713"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51322"	"WAC"	"0.713"	"0.552"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51322"	"WAC"	"0.713"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"51322"	"WAC"	"0.713"	"0.552"	"C4225239"	"DESANTO-SHINAWI SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"0"	"7"	"CTD_human;ORPHANET"
"51322"	"WAC"	"0.713"	"0.552"	"C4225431"	"CHROMOSOME 10p12-p11 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"51324"	"SPG21"	"0.727"	"0.448"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2000"	"1"	"0"	"PSYGENET"
"51324"	"SPG21"	"0.727"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51324"	"SPG21"	"0.727"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51324"	"SPG21"	"0.727"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"51324"	"SPG21"	"0.727"	"0.448"	"C1855346"	"MAST SYNDROME"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.64"	"1"	"1967"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"51324"	"SPG21"	"0.727"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"51330"	"TNFRSF12A"	"0.547"	"0.586"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"51330"	"TNFRSF12A"	"0.547"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51330"	"TNFRSF12A"	"0.547"	"0.586"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51330"	"TNFRSF12A"	"0.547"	"0.586"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51330"	"TNFRSF12A"	"0.547"	"0.586"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2018"	"1"	"2"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51338"	"MS4A4A"	"0.762"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51339"	"DACT1"	"0.619"	"0.414"	"C0014067"	"Occipital Encephalocele"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"51339"	"DACT1"	"0.619"	"0.414"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"51339"	"DACT1"	"0.619"	"0.414"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"51339"	"DACT1"	"0.619"	"0.414"	"C0265246"	"Townes syndrome"	"disease"	"C06;C09;C10;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2018"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"51339"	"DACT1"	"0.619"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"51339"	"DACT1"	"0.619"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"51339"	"DACT1"	"0.619"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"51339"	"DACT1"	"0.619"	"0.414"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"51339"	"DACT1"	"0.619"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2009"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51341"	"ZBTB7A"	"0.59"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51343"	"FZR1"	"0.735"	"0.207"	"C0032578"	"Polyploidy"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51347"	"TAOK3"	"0.799"	"0.241"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51347"	"TAOK3"	"0.799"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51350"	"KRT76"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C0343057"	"Keratosis pilaris decalvans"	"disease"		"Congenital Abnormality"	"0.43"	"1"	"1996"	"2014"	"0"	"1"	"ORPHANET"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C1839988"	"Ichthyosis follicularis atrichia photophobia syndrome"	"disease"	"C10;C11;C16;C17;C23"	"Disease or Syndrome"	"0.74"	"1"	"2000"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C2609071"	"Olmsted syndrome"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C3502469"	"Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia"	"disease"	"C06;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"ORPHANET"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2014"	"6"	"0"	"GENOMICS_ENGLAND"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C3806745"	"PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"51360"	"MBTPS2"	"0.547"	"0.621"	"C3887525"	"Keratosis Follicularis Spinulosa Decalvans, X-Linked"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.53"	"1"	"2011"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"51361"	"HOOK1"	"0.834"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51363"	"CHST15"	"0.762"	"0.172"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51363"	"CHST15"	"0.762"	"0.172"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51364"	"ZMYND10"	"0.607"	"0.517"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.43"	"1"	"1993"	"2016"	"0"	"2"	"ORPHANET"
"51364"	"ZMYND10"	"0.607"	"0.517"	"C3809543"	"CILIARY DYSKINESIA, PRIMARY, 22"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2018"	"4"	"8"	"CTD_human;UNIPROT"
"51364"	"ZMYND10"	"0.607"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51364"	"ZMYND10"	"0.607"	"0.517"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51366"	"UBR5"	"0.667"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0153943"	"Benign neoplasm of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0154060"	"Carcinoma in situ of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0496905"	"Neoplasm of uncertain or unknown behavior of stomach"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"CGI"
"51366"	"UBR5"	"0.667"	"0.483"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51371"	"POMP"	"0.72"	"0.207"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2010"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51371"	"POMP"	"0.72"	"0.207"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51371"	"POMP"	"0.72"	"0.207"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51371"	"POMP"	"0.72"	"0.207"	"C1866029"	"Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2010"	"0"	"1"	"CTD_human;ORPHANET"
"51375"	"SNX7"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51380"	"CSAD"	"0.773"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51382"	"ATP6V1D"	"0.785"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51384"	"WNT16"	"0.735"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51388"	"NIP7"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51412"	"ACTL6B"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9375"	"2001"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0032915"	"Preexcitation Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.36"	"1"	"2001"	"2014"	"3"	"2"	"UNIPROT"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0043202"	"Wolff-Parkinson-White Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"	"0.9166667"	"1999"	"2015"	"3"	"3"	"CTD_human;UNIPROT"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0264897"	"Accessory Atrioventricular Bundle (disorder)"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2004"	"3"	"2"	"UNIPROT"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C1833236"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"1995"	"2017"	"15"	"10"	"CLINGEN;CTD_human;UNIPROT"
"51422"	"PRKAG2"	"0.614"	"0.414"	"C1849813"	"Glycogen Storage Disease of Heart, Lethal Congenital"	"disease"	"C14;C16;C18"	"Disease or Syndrome"	"0.70"		"1999"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51426"	"POLK"	"0.743"	"0.207"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"51426"	"POLK"	"0.743"	"0.207"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51426"	"POLK"	"0.743"	"0.207"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51428"	"DDX41"	"0.815"	"0.276"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51428"	"DDX41"	"0.815"	"0.276"	"C4225174"	"MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.70"		"2015"	"2016"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"51433"	"ANAPC5"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51438"	"MAGEC2"	"0.676"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"51441"	"YTHDF2"	"1"	"0.069"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51447"	"IP6K2"	"0.773"	"0.241"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51447"	"IP6K2"	"0.773"	"0.241"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51447"	"IP6K2"	"0.773"	"0.241"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51447"	"IP6K2"	"0.773"	"0.241"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51449"	"PCYOX1"			"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51451"	"LCMT1"	"0.928"	"0.103"	"C0012684"	"Blastocyst Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51451"	"LCMT1"	"0.928"	"0.103"	"C0752351"	"Embryo Loss"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51451"	"LCMT1"	"0.928"	"0.103"	"C1136082"	"Embryo Disintegration"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51454"	"GULP1"	"0.886"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51454"	"GULP1"	"0.886"	"0.207"	"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2011"	"2"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"51466"	"EVL"	"0.785"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.52"	"1"	"2006"	"2016"	"3"	"1"	"CTD_human;UNIPROT"
"51473"	"DCDC2"	"0.648"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"51473"	"DCDC2"	"0.648"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"51473"	"DCDC2"	"0.648"	"0.31"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"51473"	"DCDC2"	"0.648"	"0.31"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2015"	"3"	"0"	"CLINGEN"
"51473"	"DCDC2"	"0.648"	"0.31"	"C1857750"	"DEAFNESS, AUTOSOMAL RECESSIVE 66"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2006"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"51473"	"DCDC2"	"0.648"	"0.31"	"C4015542"	"NEPHRONOPHTHISIS 19"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"5"	"CTD_human"
"51473"	"DCDC2"	"0.648"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"51473"	"DCDC2"	"0.648"	"0.31"	"C4479344"	"SCLEROSING CHOLANGITIS, NEONATAL"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"51475"	"CABP2"	"0.834"	"0.172"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2017"	"5"	"0"	"CLINGEN"
"51475"	"CABP2"	"0.834"	"0.172"	"C3888355"	"DEAFNESS, AUTOSOMAL RECESSIVE 93"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"0"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51477"	"ISYNA1"	"0.548"	"0.69"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51479"	"ANKFY1"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51479"	"ANKFY1"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51491"	"NOP16"	"0.886"	"0.103"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51491"	"NOP16"	"0.886"	"0.103"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51491"	"NOP16"	"0.886"	"0.103"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51491"	"NOP16"	"0.886"	"0.103"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51501"	"HIKESHI"	"0.799"	"0.241"	"C4225170"	"LEUKODYSTROPHY, HYPOMYELINATING, 13"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"51510"	"CHMP5"	"0.857"	"0.069"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"51510"	"CHMP5"	"0.857"	"0.069"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51510"	"CHMP5"	"0.857"	"0.069"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51514"	"DTL"	"0.707"	"0.379"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51514"	"DTL"	"0.707"	"0.379"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51514"	"DTL"	"0.707"	"0.379"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51520"	"LARS"	"0.707"	"0.483"	"C3809522"	"INFANTILE LIVER FAILURE SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"51524"	"TMEM138"	"0.72"	"0.345"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"51524"	"TMEM138"	"0.72"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51524"	"TMEM138"	"0.72"	"0.345"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51524"	"TMEM138"	"0.72"	"0.345"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51524"	"TMEM138"	"0.72"	"0.345"	"C3280906"	"JOUBERT SYNDROME 16"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"1"	"4"	"UNIPROT"
"51524"	"TMEM138"	"0.72"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51527"	"GSKIP"	"0.928"	"0.034"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51527"	"GSKIP"	"0.928"	"0.034"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51527"	"GSKIP"	"0.928"	"0.034"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51530"	"ZC3HC1"	"0.773"	"0.207"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51530"	"ZC3HC1"	"0.773"	"0.207"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2011"	"2017"	"1"	"1"	"CTD_human"
"51530"	"ZC3HC1"	"0.773"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51530"	"ZC3HC1"	"0.773"	"0.207"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2018"	"1"	"1"	"CTD_human"
"51533"	"PHF7"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51535"	"PPHLN1"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51542"	"VPS54"	"0.773"	"0.138"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51547"	"SIRT7"	"0.645"	"0.379"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"51547"	"SIRT7"	"0.645"	"0.379"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51547"	"SIRT7"	"0.645"	"0.379"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51547"	"SIRT7"	"0.645"	"0.379"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"51548"	"SIRT6"	"0.588"	"0.586"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51548"	"SIRT6"	"0.588"	"0.586"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51550"	"CINP"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51554"	"ACKR4"	"0.785"	"0.241"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51554"	"ACKR4"	"0.785"	"0.241"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51555"	"PEX5L"	"0.815"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"51555"	"PEX5L"	"0.815"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"51555"	"PEX5L"	"0.815"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51555"	"PEX5L"	"0.815"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51561"	"IL23A"	"0.479"	"0.724"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"	"0.9375"	"2001"	"2016"	"1"	"0"	"CTD_human"
"51561"	"IL23A"	"0.479"	"0.724"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"51561"	"IL23A"	"0.479"	"0.724"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.9333333"	"2004"	"2017"	"2"	"0"	"CTD_human"
"51564"	"HDAC7"	"0.672"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"51567"	"TDP2"	"0.676"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51567"	"TDP2"	"0.676"	"0.414"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51567"	"TDP2"	"0.676"	"0.414"	"C4310780"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"2"	"ORPHANET"
"51569"	"UFM1"	"0.834"	"0.241"	"C2676244"	"Leukodystrophy, Hypomyelinating, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51571"	"FAM49B"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51573"	"GDE1"	"0.524"	"0.724"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"51573"	"GDE1"	"0.524"	"0.724"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"51574"	"LARP7"	"0.713"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51574"	"LARP7"	"0.713"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51574"	"LARP7"	"0.713"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51574"	"LARP7"	"0.713"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"51574"	"LARP7"	"0.713"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"51574"	"LARP7"	"0.713"	"0.414"	"C3554439"	"ALAZAMI SYNDROME"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2013"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"51574"	"LARP7"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"51586"	"MED15"	"0.672"	"0.448"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"51586"	"MED15"	"0.672"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2003"	"2005"	"2"	"0"	"PSYGENET"
"51592"	"TRIM33"	"0.707"	"0.379"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51592"	"TRIM33"	"0.707"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"51592"	"TRIM33"	"0.707"	"0.379"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51593"	"SRRT"	"0.834"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51593"	"SRRT"	"0.834"	"0.138"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51593"	"SRRT"	"0.834"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51593"	"SRRT"	"0.834"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51594"	"NBAS"	"0.659"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51594"	"NBAS"	"0.659"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51594"	"NBAS"	"0.659"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51594"	"NBAS"	"0.659"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51594"	"NBAS"	"0.659"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51594"	"NBAS"	"0.659"	"0.448"	"C3541319"	"SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2010"	"2016"	"1"	"3"	"ORPHANET;UNIPROT"
"51594"	"NBAS"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51594"	"NBAS"	"0.659"	"0.448"	"C3809651"	"INFANTILE LIVER FAILURE SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2017"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"51599"	"LSR"	"0.752"	"0.172"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51599"	"LSR"	"0.752"	"0.172"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2006"	"2"	"0"	"CTD_human"
"51601"	"LIPT1"	"0.735"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51601"	"LIPT1"	"0.735"	"0.276"	"C4225379"	"LIPOYLTRANSFERASE 1 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"51602"	"NOP58"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51604"	"PIGT"	"0.648"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51604"	"PIGT"	"0.648"	"0.483"	"C0019050"	"Hemoglobinuria, Paroxysmal"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51604"	"PIGT"	"0.648"	"0.483"	"C0024790"	"Paroxysmal nocturnal hemoglobinuria"	"disease"	"C15"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"51604"	"PIGT"	"0.648"	"0.483"	"C0086774"	"Cold paroxysmal hemoglobinuria"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51604"	"PIGT"	"0.648"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51604"	"PIGT"	"0.648"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51604"	"PIGT"	"0.648"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51604"	"PIGT"	"0.648"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51604"	"PIGT"	"0.648"	"0.483"	"C3809356"	"MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2014"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51614"	"ERGIC3"	"0.799"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51621"	"KLF13"	"0.799"	"0.414"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"51621"	"KLF13"	"0.799"	"0.414"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51621"	"KLF13"	"0.799"	"0.414"	"C2677613"	"Chromosome 15q13.3 Microdeletion Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0013903"	"Ellis-Van Creveld Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"51626"	"DYNC2LI1"	"0.672"	"0.483"	"C4310724"	"SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"1997"	"2018"	"2"	"9"	"UNIPROT"
"51633"	"OTUD6B"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51633"	"OTUD6B"	"0.713"	"0.379"	"C4479520"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"51635"	"DHRS7"	"0.743"	"0.138"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51635"	"DHRS7"	"0.743"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51643"	"TMBIM4"	"0.799"	"0.241"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51643"	"TMBIM4"	"0.799"	"0.241"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51649"	"MRPS23"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51649"	"MRPS23"	"0.886"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51649"	"MRPS23"	"0.886"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"51649"	"MRPS23"	"0.886"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51649"	"MRPS23"	"0.886"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"51651"	"PTRH2"	"0.659"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51651"	"PTRH2"	"0.659"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51651"	"PTRH2"	"0.659"	"0.517"	"C4015728"	"NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"51655"	"RASD1"	"0.72"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51655"	"RASD1"	"0.72"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51659"	"GINS2"	"0.762"	"0.31"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51659"	"GINS2"	"0.762"	"0.31"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51659"	"GINS2"	"0.762"	"0.31"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51660"	"MPC1"	"0.762"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51660"	"MPC1"	"0.762"	"0.276"	"C3553607"	"MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.70"		"2003"	"2012"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"51660"	"MPC1"	"0.762"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0004779"	"Basal Cell Nevus Syndrome"	"disease"	"C04;C05;C07;C16"	"Neoplastic Process"	"0.85"	"1"	"2002"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"51684"	"SUFU"	"0.565"	"0.621"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"0.8888889"	"2002"	"2017"	"0"	"5"	"CGI;CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51684"	"SUFU"	"0.565"	"0.621"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0205834"	"Meningiomas, Multiple"	"disease"	"C04;C10"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.64"	"1"	"2002"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C0796147"	"Acrocallosal Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C0812437"	"Oculo-dento-digital syndrome"	"disease"	"C05;C07;C11;C16"	"Congenital Abnormality"	"0.33"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C1333989"	"Familial meningioma"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C1334970"	"Medulloblastoma with extensive nodularity"	"disease"		"Neoplastic Process"	"0.40"		"2010"	"2010"	"0"	"1"	"ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C2931760"	"Acrocallosal syndrome, Schinzel type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51684"	"SUFU"	"0.565"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51684"	"SUFU"	"0.565"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51684"	"SUFU"	"0.565"	"0.621"	"C4540342"	"JOUBERT SYNDROME 32"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"UNIPROT"
"51692"	"CPSF3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51701"	"NLK"	"0.672"	"0.379"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51702"	"PADI3"	"0.834"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51702"	"PADI3"	"0.834"	"0.138"	"C0432347"	"Uncombable hair syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.70"		"2012"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"51703"	"ACSL5"	"0.707"	"0.31"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51703"	"ACSL5"	"0.707"	"0.31"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51703"	"ACSL5"	"0.707"	"0.31"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51703"	"ACSL5"	"0.707"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2018"	"0"	"0"	"UNIPROT"
"51715"	"RAB23"	"0.584"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"0.5"	"2007"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"51715"	"RAB23"	"0.584"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51715"	"RAB23"	"0.584"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51715"	"RAB23"	"0.584"	"0.621"	"C1275078"	"Acrocephalopolysyndactyly type 2"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.74"	"1"	"2007"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"51715"	"RAB23"	"0.584"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"51715"	"RAB23"	"0.584"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"51725"	"FBXO40"			"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51726"	"DNAJB11"	"0.886"	"0.207"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"51728"	"POLR3K"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51728"	"POLR3K"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51728"	"POLR3K"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51728"	"POLR3K"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0025517"	"Metabolic Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0393698"	"Cryptogenic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0393699"	"Symptomatic Infantile Spasms"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0546878"	"Nodding spasm"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0553558"	"Jackknife Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C0684276"	"Hypsarrhythmia"	"phenotype"	"C10"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C1291512"	"Beta-Ureidopropionase Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"51733"	"UPB1"	"0.735"	"0.276"	"C1527306"	"spasmus nutans"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C1527366"	"Salaam Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51733"	"UPB1"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"51734"	"MSRB1"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"51735"	"RAPGEF6"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2009"	"2"	"0"	"PSYGENET"
"51738"	"GHRL"	"0.511"	"0.655"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0006625"	"Cachexia"	"phenotype"	"C23"	"Sign or Symptom"	"0.32"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0009319"	"Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.9375"	"2001"	"2017"	"0"	"2"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"51738"	"GHRL"	"0.511"	"0.655"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0038358"	"Gastric ulcer"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2006"	"2"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"51738"	"GHRL"	"0.511"	"0.655"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51738"	"GHRL"	"0.511"	"0.655"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51741"	"WWOX"	"0.489"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2000"	"2016"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.44"	"1"	"2002"	"2012"	"1"	"1"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51741"	"WWOX"	"0.489"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2007"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0042076"	"Urologic Neoplasms"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2018"	"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0152018"	"Esophageal carcinoma"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"51741"	"WWOX"	"0.489"	"0.655"	"C0153942"	"Benign neoplasm of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51741"	"WWOX"	"0.489"	"0.655"	"C0154059"	"Carcinoma in situ of esophagus"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51741"	"WWOX"	"0.489"	"0.655"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.53"	"1"	"2002"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"51741"	"WWOX"	"0.489"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"2"	"GENOMICS_ENGLAND"
"51741"	"WWOX"	"0.489"	"0.655"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CGI"
"51741"	"WWOX"	"0.489"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9444444"	"2000"	"2016"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0751571"	"Cancer of Urinary Tract"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C3280452"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2017"	"2"	"6"	"ORPHANET;UNIPROT"
"51741"	"WWOX"	"0.489"	"0.655"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"51741"	"WWOX"	"0.489"	"0.655"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"51741"	"WWOX"	"0.489"	"0.655"	"C4015519"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"51741"	"WWOX"	"0.489"	"0.655"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51742"	"ARID4B"	"0.707"	"0.379"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"51744"	"CD244"	"0.701"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.44"	"0.5"	"2008"	"2011"	"1"	"1"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2013"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2009"	"2017"	"2"	"1"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.46"	"1"	"2013"	"2015"	"0"	"7"	"ORPHANET"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51750"	"RTEL1"	"0.509"	"0.621"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"51750"	"RTEL1"	"0.509"	"0.621"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"9"	"CTD_human;ORPHANET"
"51750"	"RTEL1"	"0.509"	"0.621"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.39"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"51750"	"RTEL1"	"0.509"	"0.621"	"C3554656"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"5"	"12"	"CTD_human;UNIPROT"
"51750"	"RTEL1"	"0.509"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51750"	"RTEL1"	"0.509"	"0.621"	"C3808802"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2014"	"5"	"9"	"CTD_human;UNIPROT"
"51750"	"RTEL1"	"0.509"	"0.621"	"C4225346"	"PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"1"	"8"	"CTD_human;UNIPROT"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"2013"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2006"	"1"	"0"	"CTD_human"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2014"	"4"	"0"	"CTD_human"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"1"	"2010"	"2017"	"4"	"8"	"CTD_human"
"51752"	"ERAP1"	"0.627"	"0.517"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.969697"	"2008"	"2018"	"4"	"11"	"CTD_human"
"51755"	"CDK12"	"0.743"	"0.241"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.34"	"1"	"2011"	"2017"	"0"	"0"	"CGI"
"51755"	"CDK12"	"0.743"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"51755"	"CDK12"	"0.743"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"51755"	"CDK12"	"0.743"	"0.241"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51755"	"CDK12"	"0.743"	"0.241"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"51755"	"CDK12"	"0.743"	"0.241"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"0"	"0"	"CGI"
"51755"	"CDK12"	"0.743"	"0.241"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51761"	"ATP8A2"	"0.676"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51761"	"ATP8A2"	"0.676"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51761"	"ATP8A2"	"0.676"	"0.414"	"C0394006"	"Dysequilibrium syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.71"	"1"	"1969"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"51761"	"ATP8A2"	"0.676"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"51761"	"ATP8A2"	"0.676"	"0.414"	"C3808977"	"CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.60"		"1969"	"2015"	"1"	"2"	"UNIPROT"
"51762"	"RAB8B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"51763"	"INPP5K"	"0.652"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51763"	"INPP5K"	"0.652"	"0.379"	"C0024814"	"Marinesco-Sjogren syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"51763"	"INPP5K"	"0.652"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51763"	"INPP5K"	"0.652"	"0.379"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51763"	"INPP5K"	"0.652"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"51763"	"INPP5K"	"0.652"	"0.379"	"C4479410"	"MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"2"	"8"	"CTD_human;UNIPROT"
"51765"	"STK26"	"0.834"	"0.103"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"51776"	"MAP3K20"	"0.645"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"51776"	"MAP3K20"	"0.645"	"0.448"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"51776"	"MAP3K20"	"0.645"	"0.448"	"C4225167"	"SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"51778"	"MYOZ2"	"0.834"	"0.138"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"51778"	"MYOZ2"	"0.834"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51778"	"MYOZ2"	"0.834"	"0.138"	"C3151204"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"51780"	"KDM3B"	"0.727"	"0.379"	"C0274869"	"Toxic effect of heavy metal"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"51780"	"KDM3B"	"0.727"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51804"	"SIX4"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"51807"	"TUBA8"	"0.685"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"51807"	"TUBA8"	"0.685"	"0.414"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51807"	"TUBA8"	"0.685"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"51807"	"TUBA8"	"0.685"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51807"	"TUBA8"	"0.685"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"51807"	"TUBA8"	"0.685"	"0.414"	"C2750798"	"Polymicrogyria With Optic Nerve Hypoplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"2009"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"51807"	"TUBA8"	"0.685"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"51816"	"ADA2"	"0.633"	"0.655"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1986"	"1986"	"1"	"0"	"GENOMICS_ENGLAND"
"51816"	"ADA2"	"0.633"	"0.655"	"C0282492"	"Sneddon Syndrome"	"disease"	"C10;C14;C17"	"Disease or Syndrome"	"0.70"		"2003"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"51816"	"ADA2"	"0.633"	"0.655"	"C3887654"	"POLYARTERITIS NODOSA, CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2014"	"2017"	"2"	"9"	"ORPHANET;UNIPROT"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0003635"	"Apraxias"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2016"	"1"	"1"	"PSYGENET"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0234526"	"Ideational Apraxia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0234527"	"Apraxia, Motor"	"phenotype"	"C10;C23;F01"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0234529"	"Dressing Apraxia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0264611"	"Apraxia of Phonation"	"disease"	"C10;C23;F01"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0349391"	"Apraxia, Verbal"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0422892"	"Apraxia, Gestural"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0454608"	"Apraxia, Oral"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0750927"	"Apraxia, Developmental Verbal"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0750928"	"Apraxia, Facial-Oral"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C3495144"	"Apraxia, Articulatory"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53335"	"BCL11A"	"0.572"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"53335"	"BCL11A"	"0.572"	"0.621"	"C4310833"	"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"53336"	"CPXCR1"	"1"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"53339"	"BTBD1"			"C0520757"	"Delayed Emergence from Anesthesia"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"53339"	"BTBD1"			"C4042763"	"Postoperative Residual Curarization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"53345"	"TM6SF2"	"0.685"	"0.414"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"53345"	"TM6SF2"	"0.685"	"0.414"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"53345"	"TM6SF2"	"0.685"	"0.414"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9130435"	"2014"	"2018"	"1"	"0"	"CTD_human"
"53345"	"TM6SF2"	"0.685"	"0.414"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"53346"	"TM6SF1"	"0.886"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"53347"	"UBASH3A"	"0.696"	"0.414"	"C0008313"	"Cholangitis, Sclerosing"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2013"	"2017"	"1"	"2"	"CTD_human"
"53347"	"UBASH3A"	"0.696"	"0.414"	"C0566602"	"Primary sclerosing cholangitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53353"	"LRP1B"	"0.672"	"0.414"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53373"	"TPCN1"	"0.752"	"0.138"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"53405"	"CLIC5"	"0.815"	"0.207"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2015"	"3"	"0"	"CLINGEN"
"53405"	"CLIC5"	"0.815"	"0.207"	"C4015050"	"DEAFNESS, AUTOSOMAL RECESSIVE 103"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"53615"	"MBD3"	"0.735"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"53630"	"BCO1"	"0.752"	"0.241"	"C2676023"	"Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant"	"disease"	"C18"	"Disease or Syndrome"	"0.70"		"1970"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"53630"	"BCO1"	"0.752"	"0.241"	"C2676024"	"CAROTENOIDS, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.50"		"2008"	"2008"	"1"	"1"	"ORPHANET;UNIPROT"
"53632"	"PRKAG3"	"0.928"	"0.172"	"C0007001"	"Carbohydrate Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2000"	"2010"	"2"	"0"	"CTD_human"
"53632"	"PRKAG3"	"0.928"	"0.172"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"53635"	"PTOV1"	"0.69"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53635"	"PTOV1"	"0.69"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53635"	"PTOV1"	"0.69"	"0.448"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53635"	"PTOV1"	"0.69"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53637"	"S1PR5"	"0.773"	"0.207"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53637"	"S1PR5"	"0.773"	"0.207"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53637"	"S1PR5"	"0.773"	"0.207"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"53637"	"S1PR5"	"0.773"	"0.207"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"53826"	"FXYD6"	"0.785"	"0.138"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53826"	"FXYD6"	"0.785"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"53826"	"FXYD6"	"0.785"	"0.138"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53826"	"FXYD6"	"0.785"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.4"	"2007"	"2011"	"5"	"0"	"PSYGENET"
"53826"	"FXYD6"	"0.785"	"0.138"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53827"	"FXYD5"	"0.672"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"53832"	"IL20RA"	"0.815"	"0.138"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"53832"	"IL20RA"	"0.815"	"0.138"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"53834"	"FGFRL1"	"0.621"	"0.586"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"53834"	"FGFRL1"	"0.621"	"0.586"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53834"	"FGFRL1"	"0.621"	"0.586"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"53834"	"FGFRL1"	"0.621"	"0.586"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"0"	"0"	"CTD_human"
"53834"	"FGFRL1"	"0.621"	"0.586"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.50"		"2009"	"2009"	"0"	"0"	"CTD_human"
"53836"	"GPR87"	"0.785"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"53904"	"MYO3A"	"0.785"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"53904"	"MYO3A"	"0.785"	"0.241"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"53904"	"MYO3A"	"0.785"	"0.241"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"53904"	"MYO3A"	"0.785"	"0.241"	"C1846784"	"Deafness, Autosomal Recessive 30"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2002"	"2011"	"0"	"3"	"CTD_human"
"53916"	"RAB4B"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53916"	"RAB4B"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"53919"	"SLCO1C1"	"0.815"	"0.207"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"53919"	"SLCO1C1"	"0.815"	"0.207"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"53944"	"CSNK1G1"	"1"	"0.034"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"53944"	"CSNK1G1"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"53947"	"A4GALT"	"0.815"	"0.207"	"C0006413"	"Burkitt Lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"53947"	"A4GALT"	"0.815"	"0.207"	"C0343640"	"African Burkitt's lymphoma"	"disease"	"C02;C04;C15;C20"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"54014"	"BRWD1"	"0.857"	"0.138"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54084"	"TSPEAR"	"0.857"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"54084"	"TSPEAR"	"0.857"	"0.172"	"C3553932"	"DEAFNESS, AUTOSOMAL RECESSIVE 98"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54093"	"SETD4"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54101"	"RIPK4"	"0.616"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"54101"	"RIPK4"	"0.616"	"0.69"	"C1849718"	"POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE"	"disease"	"C05;C07;C11;C16"	"Disease or Syndrome"	"0.78"	"1"	"2000"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"54101"	"RIPK4"	"0.616"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54106"	"TLR9"	"0.453"	"0.862"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2009"	"2"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0018193"	"Granuloma, Foreign-Body"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0018200"	"Granuloma, Respiratory Tract"	"phenotype"	"C08;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0036330"	"Schistosomiasis mansoni"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0242497"	"Intestinal schistosomiasis"	"disease"	"C03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54106"	"TLR9"	"0.453"	"0.862"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"2"	"UNIPROT"
"54106"	"TLR9"	"0.453"	"0.862"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"54112"	"GPR88"	"0.834"	"0.172"	"C4310787"	"CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"54187"	"NANS"	"0.63"	"0.379"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54187"	"NANS"	"0.63"	"0.379"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54187"	"NANS"	"0.63"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54187"	"NANS"	"0.63"	"0.379"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54187"	"NANS"	"0.63"	"0.379"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54187"	"NANS"	"0.63"	"0.379"	"C1864872"	"Spondyloepimetaphyseal dysplasia, Genevieve type"	"disease"	"C05;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1993"	"2016"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"54187"	"NANS"	"0.63"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54205"	"CYCS"	"0.667"	"0.483"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"54205"	"CYCS"	"0.667"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0022116"	"Ischemia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.44"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"54205"	"CYCS"	"0.667"	"0.483"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"54205"	"CYCS"	"0.667"	"0.483"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54205"	"CYCS"	"0.667"	"0.483"	"C2677608"	"Thrombocytopenia 4"	"disease"	"C15"	"Disease or Syndrome"	"0.61"	"1"	"2008"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"54205"	"CYCS"	"0.667"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"54206"	"ERRFI1"	"0.63"	"0.448"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54206"	"ERRFI1"	"0.63"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54206"	"ERRFI1"	"0.63"	"0.448"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"54206"	"ERRFI1"	"0.63"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54206"	"ERRFI1"	"0.63"	"0.448"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.50"	"0.962963"	"2007"	"2018"	"2"	"1"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.48"	"0.875"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"54209"	"TREM2"	"0.572"	"0.552"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2003"	"2017"	"2"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54209"	"TREM2"	"0.572"	"0.552"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2017"	"2"	"0"	"CTD_human;ORPHANET"
"54209"	"TREM2"	"0.572"	"0.552"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"54209"	"TREM2"	"0.572"	"0.552"	"C0338630"	"Senile Paranoid Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2013"	"2017"	"2"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0497327"	"Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"2"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0751071"	"Familial Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54209"	"TREM2"	"0.572"	"0.552"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"54209"	"TREM2"	"0.572"	"0.552"	"C1857316"	"POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY"	"disease"	"C02;C05;C10;C16;C17;C18"	"Disease or Syndrome"	"0.80"	"1"	"1983"	"2018"	"1"	"13"	"CTD_human;ORPHANET;UNIPROT"
"54209"	"TREM2"	"0.572"	"0.552"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54210"	"TREM1"	"0.562"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"54210"	"TREM1"	"0.562"	"0.621"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"54210"	"TREM1"	"0.562"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"54210"	"TREM1"	"0.562"	"0.621"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"54212"	"SNTG1"	"0.886"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54221"	"SNTG2"	"0.928"	"0.069"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"54221"	"SNTG2"	"0.928"	"0.069"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54332"	"GDAP1"	"0.645"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54332"	"GDAP1"	"0.645"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9777778"	"1993"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"54332"	"GDAP1"	"0.645"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1842197"	"Charcot-Marie-Tooth Disease, Recessive Intermediate A"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2003"	"2015"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1842983"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.91"	"1"	"1993"	"2018"	"5"	"15"	"CTD_human;ORPHANET;UNIPROT"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1842984"	"Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2005"	"2018"	"5"	"8"	"ORPHANET;UNIPROT"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1843173"	"Charcot-Marie-Tooth disease, Type 2H"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1843183"	"Charcot-Marie-Tooth disease, Type 4A, axonal form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2005"	"2"	"2"	"CTD_human;UNIPROT"
"54332"	"GDAP1"	"0.645"	"0.31"	"C1859198"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.78"	"1"	"1993"	"2017"	"3"	"11"	"CTD_human;ORPHANET;UNIPROT"
"54332"	"GDAP1"	"0.645"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54344"	"DPM3"	"0.815"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54344"	"DPM3"	"0.815"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"54344"	"DPM3"	"0.815"	"0.241"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"54344"	"DPM3"	"0.815"	"0.241"	"C2752007"	"Congenital Disorder of Glycosylation, Type Io"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"54344"	"DPM3"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"54345"	"SOX18"	"0.624"	"0.586"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.40"		"2003"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"54345"	"SOX18"	"0.624"	"0.586"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C0039445"	"Hereditary hemorrhagic telangiectasia"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54345"	"SOX18"	"0.624"	"0.586"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C1841989"	"Glomerulonephritis sparse hair telangiectases"	"disease"	"C12;C13;C14;C17;C20;C23"	"Disease or Syndrome"	"0.40"		"1990"	"2015"	"0"	"1"	"CTD_human"
"54345"	"SOX18"	"0.624"	"0.586"	"C1843004"	"HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME"	"disease"	"C14;C15;C17"	"Disease or Syndrome"	"0.65"	"0.8"	"2001"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"54345"	"SOX18"	"0.624"	"0.586"	"C4317151"	"Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"54360"	"CYTL1"	"0.886"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"54361"	"WNT4"	"0.588"	"0.586"	"C0013336"	"Dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C1720887"	"Female Urogenital Diseases"	"group"	"C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54361"	"WNT4"	"0.588"	"0.586"	"C2675014"	"Mullerian Aplasia and Hyperandrogenism"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"		"2004"	"2008"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"54361"	"WNT4"	"0.588"	"0.586"	"C2678492"	"Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs"	"disease"	"C08;C12;C13;C16;C19"	"Disease or Syndrome"	"0.70"		"2008"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"54361"	"WNT4"	"0.588"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"54363"	"HAO1"	"0.815"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54363"	"HAO1"	"0.815"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54363"	"HAO1"	"0.815"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54386"	"TERF2IP"	"0.588"	"0.69"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"54407"	"SLC38A2"	"0.834"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"54413"	"NLGN3"	"0.799"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.95"	"2003"	"2016"	"2"	"0"	"CTD_human"
"54413"	"NLGN3"	"0.799"	"0.276"	"C1845341"	"ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"54413"	"NLGN3"	"0.799"	"0.276"	"C1845540"	"AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding)"	"phenotype"		"Finding"	"0.40"		"2003"	"2005"	"1"	"1"	"UNIPROT"
"54413"	"NLGN3"	"0.799"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"54414"	"SIAE"	"0.886"	"0.138"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2015"	"0"	"0"	"CTD_human"
"54414"	"SIAE"	"0.886"	"0.138"	"C3150797"	"AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6"	"phenotype"		"Finding"	"0.40"		"2010"	"2010"	"1"	"11"	"UNIPROT"
"54431"	"DNAJC10"	"0.886"	"0.138"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54431"	"DNAJC10"	"0.886"	"0.138"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54431"	"DNAJC10"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54431"	"DNAJC10"	"0.886"	"0.138"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54431"	"DNAJC10"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54433"	"GAR1"	"0.857"	"0.172"	"C0018939"	"Hematological Disease"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54433"	"GAR1"	"0.857"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54433"	"GAR1"	"0.857"	"0.172"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"54433"	"GAR1"	"0.857"	"0.172"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54436"	"SH3TC1"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54436"	"SH3TC1"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54436"	"SH3TC1"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2006"	"2011"	"2"	"1"	"CTD_human;UNIPROT"
"54437"	"SEMA5B"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"54440"	"SASH3"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54441"	"STAG3L1"	"0.928"	"0.069"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54441"	"STAG3L1"	"0.928"	"0.069"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54441"	"STAG3L1"	"0.928"	"0.069"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54443"	"ANLN"	"0.707"	"0.379"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"54443"	"ANLN"	"0.707"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54443"	"ANLN"	"0.707"	"0.379"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54443"	"ANLN"	"0.707"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54443"	"ANLN"	"0.707"	"0.379"	"C4014993"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"1"	"UNIPROT"
"54453"	"RIN2"	"0.676"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"54453"	"RIN2"	"0.676"	"0.483"	"C2751321"	"Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.62"	"1"	"2009"	"2014"	"0"	"3"	"CTD_human;ORPHANET"
"54457"	"TAF7L"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54458"	"PRR13"	"0.886"	"0.103"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"54458"	"PRR13"	"0.886"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0020071"	"Hereditary Sensory Autonomic Neuropathy, Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0020074"	"HSAN Type IV"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0020075"	"Hereditary Sensory Autonomic Neuropathy, Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0027889"	"Hereditary Sensory and Autonomic Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0086405"	"Hereditary Sensory Radicular Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0699739"	"Sensory Neuropathy, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C0751540"	"Morvan's Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C2751092"	"Neuropathy, Hereditary Sensory And Autonomic, Type IIB"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2014"	"0"	"3"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C2752089"	"Neuropathy, Hereditary Sensory And Autonomic, Type IIA"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"1993"	"0"	"4"	"CTD_human"
"54463"	"RETREG1"	"0.648"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54465"	"ETAA1"	"0.857"	"0.138"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54465"	"ETAA1"	"0.857"	"0.138"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54465"	"ETAA1"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54466"	"SPIN2A"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0520757"	"Delayed Emergence from Anesthesia"	"phenotype"	"C23"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54469"	"ZFAND6"	"0.834"	"0.069"	"C4042763"	"Postoperative Residual Curarization"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.40"	"0.9"	"1993"	"2015"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0007528"	"Cecal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0153437"	"Malignant neoplasm of cecum"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54474"	"KRT20"	"0.448"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9642857"	"1996"	"2014"	"0"	"0"	"UNIPROT"
"54474"	"KRT20"	"0.448"	"0.759"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54475"	"NLE1"	"0.928"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"54476"	"RNF216"	"0.696"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54476"	"RNF216"	"0.696"	"0.31"	"C1859305"	"Cerebellar Ataxia and Hypogonadotropic Hypogonadism"	"disease"	"C10;C19;C23"	"Disease or Syndrome"	"0.73"	"1"	"2002"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"54476"	"RNF216"	"0.696"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2014"	"3"	"0"	"PSYGENET"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54487"	"DGCR8"	"0.63"	"0.621"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54491"	"OTULINL"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54496"	"PRMT7"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"54496"	"PRMT7"	"0.672"	"0.379"	"C4310689"	"SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"5"	"ORPHANET;UNIPROT"
"54498"	"SMOX"	"0.701"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54498"	"SMOX"	"0.701"	"0.379"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54498"	"SMOX"	"0.701"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54498"	"SMOX"	"0.701"	"0.379"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0151491"	"Congenital musculoskeletal anomalies"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.35"	"0.8"	"2011"	"2016"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54499"	"TMCO1"	"0.667"	"0.345"	"C1859252"	"Cerebrofaciothoracic Dysplasia"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.42"	"0.5"	"2007"	"2015"	"0"	"4"	"ORPHANET"
"54499"	"TMCO1"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"54502"	"RBM47"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54502"	"RBM47"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54502"	"RBM47"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0002726"	"Amyloidosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54503"	"ZDHHC13"	"0.743"	"0.276"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C0013581"	"Ectopia Lentis"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.46"	"1"	"2009"	"2017"	"0"	"0"	"ORPHANET"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C1644196"	"Ectopia Lentis with Ectopia of Pupil"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2012"	"0"	"3"	"CTD_human"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C1851286"	"Ectopia lentis isolated"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.36"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C2746069"	"Familial ectopia lentis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54507"	"ADAMTSL4"	"0.696"	"0.483"	"C3541474"	"ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"0"	"0"	"CTD_human"
"54518"	"APBB1IP"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54520"	"CCDC93"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54531"	"MIER2"	"0.928"	"0.069"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54531"	"MIER2"	"0.928"	"0.069"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54531"	"MIER2"	"0.928"	"0.069"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54535"	"CCHCR1"	"0.621"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54538"	"ROBO4"	"0.752"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"54539"	"NDUFB11"	"0.659"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54539"	"NDUFB11"	"0.659"	"0.448"	"C0796070"	"MICROPHTHALMIA, SYNDROMIC 7"	"disease"	"C11;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"0"	"0"	"ORPHANET"
"54539"	"NDUFB11"	"0.659"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"54539"	"NDUFB11"	"0.659"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"54539"	"NDUFB11"	"0.659"	"0.448"	"C4225421"	"LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"54541"	"DDIT4"	"0.648"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54541"	"DDIT4"	"0.648"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54550"	"NECAB2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9166667"	"2000"	"2018"	"1"	"0"	"CTD_human"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"54551"	"MAGEL2"	"0.642"	"0.379"	"C3809877"	"SCHAAF-YANG SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2017"	"0"	"9"	"ORPHANET"
"54556"	"ING3"	"0.735"	"0.241"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"UNIPROT"
"54567"	"DLL4"	"0.535"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"54567"	"DLL4"	"0.535"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"54567"	"DLL4"	"0.535"	"0.69"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2015"	"2018"	"0"	"9"	"CTD_human;ORPHANET"
"54567"	"DLL4"	"0.535"	"0.69"	"C0282160"	"Aplasia Cutis Congenita"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"54567"	"DLL4"	"0.535"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"54567"	"DLL4"	"0.535"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54567"	"DLL4"	"0.535"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2010"	"1"	"0"	"CTD_human"
"54567"	"DLL4"	"0.535"	"0.69"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"54567"	"DLL4"	"0.535"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54567"	"DLL4"	"0.535"	"0.69"	"C4225271"	"ADAMS-OLIVER SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2018"	"1"	"9"	"UNIPROT"
"54578"	"UGT1A6"	"0.636"	"0.414"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54578"	"UGT1A6"	"0.636"	"0.414"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54583"	"EGLN1"	"0.594"	"0.552"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.38"	"0.875"	"2006"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"54583"	"EGLN1"	"0.594"	"0.552"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2015"	"6"	"0"	"CLINGEN"
"54583"	"EGLN1"	"0.594"	"0.552"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2015"	"6"	"0"	"CLINGEN"
"54583"	"EGLN1"	"0.594"	"0.552"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2015"	"6"	"0"	"CLINGEN"
"54583"	"EGLN1"	"0.594"	"0.552"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2006"	"2015"	"6"	"0"	"CLINGEN"
"54583"	"EGLN1"	"0.594"	"0.552"	"C1318533"	"Secondary polycythemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54583"	"EGLN1"	"0.594"	"0.552"	"C1853286"	"Erythrocytosis, Familial, 3"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2006"	"2009"	"2"	"3"	"CTD_human;UNIPROT"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2008"	"2012"	"4"	"0"	"PSYGENET"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54584"	"GNB1L"	"0.762"	"0.31"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"54584"	"GNB1L"	"0.762"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54585"	"LZTFL1"	"0.672"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"54585"	"LZTFL1"	"0.672"	"0.448"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2015"	"0"	"2"	"ORPHANET"
"54585"	"LZTFL1"	"0.672"	"0.448"	"C3714980"	"BARDET-BIEDL SYNDROME 17"	"disease"		"Disease or Syndrome"	"0.80"		"2007"	"2015"	"2"	"4"	"CTD_human;UNIPROT"
"54585"	"LZTFL1"	"0.672"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54600"	"UGT1A9"	"0.621"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54620"	"FBXL19"	"0.834"	"0.138"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"54620"	"FBXL19"	"0.834"	"0.138"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54620"	"FBXL19"	"0.834"	"0.138"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2016"	"1"	"1"	"CTD_human"
"54657"	"UGT1A4"	"0.72"	"0.345"	"C0010324"	"Crigler Najjar syndrome, type 1"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.46"	"1"	"1990"	"2005"	"1"	"21"	"UNIPROT"
"54657"	"UGT1A4"	"0.72"	"0.345"	"C2931132"	"Crigler Najjar syndrome, type 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"1975"	"2008"	"2"	"20"	"UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0010324"	"Crigler Najjar syndrome, type 1"	"disease"	"C16;C18"	"Disease or Syndrome"	"1.00"	"0.9666667"	"1990"	"2016"	"10"	"21"	"CTD_human;ORPHANET;UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0017551"	"Gilbert Disease (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"1990"	"2018"	"6"	"8"	"CTD_human;UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0019829"	"Hodgkin Disease"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0020433"	"Hyperbilirubinemia"	"disease"	"C23"	"Disease or Syndrome"	"0.40"	"0.9090909"	"1993"	"2018"	"5"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0022610"	"Kernicterus"	"disease"	"C10;C15;C16;C18;C20;C23"	"Disease or Syndrome"	"0.42"	"0"	"2002"	"2017"	"2"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9074074"	"2004"	"2017"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0152266"	"Mixed Cellularity Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0152267"	"Hodgkin lymphoma, lymphocyte depletion"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0220597"	"Adult Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0262584"	"Carcinoma, Small Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0270210"	"Lucey-Driscoll syndrome (disorder)"	"disease"	"C16;C18;C23"	"Disease or Syndrome"	"0.70"		"2000"	"2008"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0270215"	"Neonatal jaundice due to delayed conjugation from breast milk inhibitor"	"phenotype"		"Pathologic Function"	"0.30"		"2000"	"2000"	"1"	"2"	"UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C0857007"	"Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.50"	"0.96"	"1999"	"2017"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"GENOMICS_ENGLAND"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1266194"	"Lymphocyte Rich Classical Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1334968"	"Nodular Lymphocyte Predominant Hodgkin Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1565885"	"Direct Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C1565886"	"Indirect Hyperbilirubinemia, Neonatal"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"1985"	"1985"	"1"	"0"	"CTD_human"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C2931132"	"Crigler Najjar syndrome, type 2"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"1975"	"2017"	"15"	"19"	"CTD_human;ORPHANET;UNIPROT"
"54658"	"UGT1A1"	"0.491"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54659"	"UGT1A3"	"0.681"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54663"	"WDR74"	"1"	"0.034"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54663"	"WDR74"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54663"	"WDR74"	"1"	"0.034"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54663"	"WDR74"	"1"	"0.034"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54664"	"TMEM106B"	"0.624"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"54664"	"TMEM106B"	"0.624"	"0.379"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"54664"	"TMEM106B"	"0.624"	"0.379"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"54664"	"TMEM106B"	"0.624"	"0.379"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"54664"	"TMEM106B"	"0.624"	"0.379"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54674"	"LRRN3"	"0.928"	"0.103"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54676"	"GTPBP2"	"1"	"0.034"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54677"	"CROT"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54680"	"ZNHIT6"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54704"	"PDP1"	"0.713"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54704"	"PDP1"	"0.713"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54704"	"PDP1"	"0.713"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54704"	"PDP1"	"0.713"	"0.379"	"C1837429"	"Pyruvate dehydrogenase phosphatase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"54714"	"CNGB3"	"0.659"	"0.138"	"C0152200"	"Achromatopsia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.50"	"1"	"2000"	"2018"	"0"	"3"	"ORPHANET"
"54714"	"CNGB3"	"0.659"	"0.138"	"C0271092"	"Progressive cone dystrophy (without rod involvement)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54714"	"CNGB3"	"0.659"	"0.138"	"C0271093"	"Stargardt's disease"	"phenotype"	"C11"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"54714"	"CNGB3"	"0.659"	"0.138"	"C1849792"	"Achromatopsia 3"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2018"	"5"	"51"	"CTD_human;UNIPROT"
"54714"	"CNGB3"	"0.659"	"0.138"	"C1855465"	"STARGARDT DISEASE 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.61"	"0"	"2006"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"54714"	"CNGB3"	"0.659"	"0.138"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"54714"	"CNGB3"	"0.659"	"0.138"	"C4282180"	"Juvenile macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"1"	"CTD_human;UNIPROT"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.875"	"2007"	"2016"	"2"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54715"	"RBFOX1"	"0.604"	"0.552"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54716"	"SLC6A20"	"0.773"	"0.345"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54716"	"SLC6A20"	"0.773"	"0.345"	"C0268654"	"Iminoglycinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"54716"	"SLC6A20"	"0.773"	"0.345"	"C0543541"	"HYPERGLYCINURIA (disorder)"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"54719"	"RNANC"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54738"	"FEV"	"0.611"	"0.586"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54738"	"FEV"	"0.611"	"0.586"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54738"	"FEV"	"0.611"	"0.586"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"54738"	"FEV"	"0.611"	"0.586"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"54739"	"XAF1"	"0.619"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2015"	"2"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"		"2006"	"2008"	"2"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"54739"	"XAF1"	"0.619"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"54749"	"EPDR1"	"0.886"	"0.138"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2006"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54756"	"IL17RD"	"0.685"	"0.448"	"C3808975"	"HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"5"	"CTD_human;UNIPROT"
"54757"	"FAM20A"	"0.701"	"0.414"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.44"	"1"	"2011"	"2016"	"10"	"0"	"GENOMICS_ENGLAND"
"54757"	"FAM20A"	"0.701"	"0.414"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54757"	"FAM20A"	"0.701"	"0.414"	"C2931783"	"Amelogenesis imperfecta nephrocalcinosis"	"disease"	"C07;C12;C13;C16;C18"	"Disease or Syndrome"	"0.76"	"1"	"2008"	"2018"	"11"	"11"	"CTD_human;ORPHANET;UNIPROT"
"54757"	"FAM20A"	"0.701"	"0.414"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54757"	"FAM20A"	"0.701"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54757"	"FAM20A"	"0.701"	"0.414"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54765"	"TRIM44"	"0.72"	"0.31"	"C0003076"	"Aniridia"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"54765"	"TRIM44"	"0.72"	"0.31"	"C4310695"	"ANIRIDIA 3"	"disease"		"Congenital Abnormality"	"0.40"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.53"	"1"	"1973"	"2015"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.31"	"1"	"2004"	"2015"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2013"	"0"	"2"	"ORPHANET"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C1837615"	"Ciliary Dyskinesia, Primary, 5"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.40"		"2004"	"2013"	"0"	"3"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2004"	"2008"	"2"	"0"	"CTD_human"
"54768"	"HYDIN"	"0.701"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54768"	"HYDIN"	"0.701"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54768"	"HYDIN"	"0.701"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0001815"	"Primary Myelofibrosis"	"disease"	"C15"	"Neoplastic Process"	"0.38"	"0.875"	"1992"	"2017"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0002893"	"Refractory anemias"	"disease"	"C15"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0002894"	"Refractory anaemia with excess blasts"	"disease"	"C15"	"Neoplastic Process"	"0.32"	"1"	"1997"	"2005"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54790"	"TET2"	"0.499"	"0.586"	"C0020981"	"Angioimmunoblastic Lymphadenopathy"	"disease"	"C15;C20"	"Neoplastic Process"	"0.37"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9655172"	"1990"	"2017"	"0"	"0"	"UNIPROT"
"54790"	"TET2"	"0.499"	"0.586"	"C0023480"	"Leukemia, Myelomonocytic, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"1992"	"2017"	"1"	"7"	"UNIPROT"
"54790"	"TET2"	"0.499"	"0.586"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"1992"	"2016"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0026987"	"Myelofibrosis"	"disease"		"Neoplastic Process"	"0.44"	"1"	"1992"	"2010"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0032463"	"Polycythemia Vera"	"disease"	"C04;C15"	"Neoplastic Process"	"0.37"	"0.8571429"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0040028"	"Thrombocythemia, Essential"	"disease"	"C15"	"Disease or Syndrome"	"0.35"	"1"	"2009"	"2015"	"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C0079774"	"Peripheral T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54790"	"TET2"	"0.499"	"0.586"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C0280449"	"secondary acute myeloid leukemia"	"disease"		"Neoplastic Process"	"0.36"	"1"	"2002"	"2013"	"2"	"1"	"UNIPROT"
"54790"	"TET2"	"0.499"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"0.6666667"	"2013"	"2017"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C1264195"	"Refractory anemia with ringed sideroblasts"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C1292773"	"Acute myeloid leukemia with multilineage dysplasia"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"54790"	"TET2"	"0.499"	"0.586"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2009"	"2017"	"2"	"0"	"CTD_human"
"54790"	"TET2"	"0.499"	"0.586"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.70"	"0.9888889"	"1990"	"2018"	"2"	"0"	"CGI;CTD_human"
"54795"	"TRPM4"	"0.69"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54795"	"TRPM4"	"0.69"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"54795"	"TRPM4"	"0.69"	"0.379"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"54795"	"TRPM4"	"0.69"	"0.379"	"C1879286"	"Hereditary bundle branch system defect"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2017"	"0"	"0"	"ORPHANET"
"54795"	"TRPM4"	"0.69"	"0.379"	"C1970298"	"Progressive Familial Heart Block, Type Ib"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.60"		"1977"	"2015"	"3"	"11"	"CTD_human;UNIPROT"
"54796"	"BNC2"	"0.701"	"0.414"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54796"	"BNC2"	"0.701"	"0.414"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54796"	"BNC2"	"0.701"	"0.414"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54796"	"BNC2"	"0.701"	"0.414"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"54796"	"BNC2"	"0.701"	"0.414"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54798"	"DCHS2"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"54800"	"KLHL24"	"0.834"	"0.069"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54800"	"KLHL24"	"0.834"	"0.069"	"C4310631"	"EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"3"	"CTD_human"
"54802"	"TRIT1"	"0.707"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54802"	"TRIT1"	"0.707"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54802"	"TRIT1"	"0.707"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54802"	"TRIT1"	"0.707"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54802"	"TRIT1"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2016"	"2"	"2"	"PSYGENET"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0037768"	"Spasmophilia"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0039621"	"Tetany"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0270224"	"Tetany, Neonatal"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C0917812"	"Tetanilla"	"disease"	"C10;C18;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C3151295"	"HYPOMAGNESEMIA 6, RENAL"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"54805"	"CNNM2"	"0.619"	"0.345"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4225333"	"HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54805"	"CNNM2"	"0.619"	"0.345"	"C4510731"	"Familial primary hypomagnesemia with normocalciuria and normocalcemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54806"	"AHI1"	"0.565"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"54806"	"AHI1"	"0.565"	"0.793"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54806"	"AHI1"	"0.565"	"0.793"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2017"	"0"	"3"	"ORPHANET"
"54806"	"AHI1"	"0.565"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54806"	"AHI1"	"0.565"	"0.793"	"C0162538"	"Immunoglobulin A deficiency (disorder)"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.50"	"0.95"	"2004"	"2017"	"0"	"2"	"ORPHANET"
"54806"	"AHI1"	"0.565"	"0.793"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54806"	"AHI1"	"0.565"	"0.793"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54806"	"AHI1"	"0.565"	"0.793"	"C1837713"	"JOUBERT SYNDROME 3"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.80"		"2004"	"2016"	"6"	"43"	"CTD_human;UNIPROT"
"54806"	"AHI1"	"0.565"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2004"	"2012"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"54806"	"AHI1"	"0.565"	"0.793"	"C4274118"	"Joubert syndrome with ocular defect"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54806"	"AHI1"	"0.565"	"0.793"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"54808"	"DYM"	"0.598"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54808"	"DYM"	"0.598"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54808"	"DYM"	"0.598"	"0.517"	"C0265286"	"Dyggve-Melchior-Clausen syndrome"	"disease"	"C05;C10;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.78"	"1"	"2002"	"2017"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"54808"	"DYM"	"0.598"	"0.517"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54808"	"DYM"	"0.598"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54808"	"DYM"	"0.598"	"0.517"	"C1844654"	"X-linked Dyggve-Melchior-Clausen syndrome"	"disease"	"C05;C10;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54808"	"DYM"	"0.598"	"0.517"	"C1846431"	"SMITH-MCCORT DYSPLASIA"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.82"	"1"	"2003"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"54808"	"DYM"	"0.598"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2005"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"54808"	"DYM"	"0.598"	"0.517"	"C3888088"	"SMITH-MCCORT DYSPLASIA 1"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2003"	"2009"	"3"	"2"	"UNIPROT"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.40"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0042063"	"Urogenital Abnormalities"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C1864861"	"Tumoral Calcinosis, Normophosphatemic, Familial"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.70"		"2006"	"2008"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"54809"	"SAMD9"	"0.639"	"0.655"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C3714514"	"Infection"	"group"	"C01"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"54809"	"SAMD9"	"0.639"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54809"	"SAMD9"	"0.639"	"0.655"	"C4284088"	"MIRAGE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"54820"	"NDE1"	"0.621"	"0.414"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54820"	"NDE1"	"0.621"	"0.414"	"C0020225"	"Hydranencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"54820"	"NDE1"	"0.621"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2011"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"54820"	"NDE1"	"0.621"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54820"	"NDE1"	"0.621"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2007"	"2016"	"4"	"0"	"PSYGENET"
"54820"	"NDE1"	"0.621"	"0.414"	"C0266463"	"Lissencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.42"	"1"	"2011"	"2013"	"0"	"0"	"CTD_human"
"54820"	"NDE1"	"0.621"	"0.414"	"C0266483"	"Pachygyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"54820"	"NDE1"	"0.621"	"0.414"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"54820"	"NDE1"	"0.621"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"54820"	"NDE1"	"0.621"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54820"	"NDE1"	"0.621"	"0.414"	"C1857977"	"MICROHYDRANENCEPHALY"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"54820"	"NDE1"	"0.621"	"0.414"	"C1879312"	"Agyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"54820"	"NDE1"	"0.621"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54820"	"NDE1"	"0.621"	"0.414"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"54820"	"NDE1"	"0.621"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54821"	"ERCC6L"	"0.886"	"0.241"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0009376"	"Colonic Polyps"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0022650"	"Kidney Calculi"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2009"	"2012"	"0"	"0"	"UNIPROT"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"54822"	"TRPM7"	"0.584"	"0.552"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54822"	"TRPM7"	"0.584"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54822"	"TRPM7"	"0.584"	"0.552"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"54826"	"GIN1"	"0.928"	"0.172"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"0.96"	"2005"	"2016"	"0"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0158252"	"Intervertebral disc disorder"	"group"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54829"	"ASPN"	"0.672"	"0.345"	"C0221775"	"Lumbar disc disease"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"54832"	"VPS13C"	"0.743"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54832"	"VPS13C"	"0.743"	"0.172"	"C4225186"	"PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"5"	"CTD_human;UNIPROT"
"54832"	"VPS13C"	"0.743"	"0.172"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54840"	"APTX"	"0.619"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54840"	"APTX"	"0.619"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54840"	"APTX"	"0.619"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"54840"	"APTX"	"0.619"	"0.414"	"C1859598"	"ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA"	"disease"	"C10;C15;C23;F01"	"Disease or Syndrome"	"0.80"	"1"	"2000"	"2018"	"8"	"13"	"CTD_human;ORPHANET;UNIPROT"
"54840"	"APTX"	"0.619"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54848"	"ARHGEF38"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54856"	"GON4L"	"0.834"	"0.241"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54856"	"GON4L"	"0.834"	"0.241"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54856"	"GON4L"	"0.834"	"0.241"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54856"	"GON4L"	"0.834"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"54861"	"SNRK"	"0.857"	"0.069"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"54861"	"SNRK"	"0.857"	"0.069"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54862"	"CC2D1A"	"0.743"	"0.31"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"54862"	"CC2D1A"	"0.743"	"0.31"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"54862"	"CC2D1A"	"0.743"	"0.31"	"C1838023"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"54862"	"CC2D1A"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2006"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"54863"	"TOR4A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54870"	"QRICH1"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"54872"	"PIGG"	"0.773"	"0.172"	"C4310794"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"54873"	"PALMD"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54877"	"ZCCHC2"	"0.928"	"0.172"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2013"	"2018"	"1"	"1"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"54880"	"BCOR"	"0.523"	"0.655"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"0"	"0"	"CGI"
"54880"	"BCOR"	"0.523"	"0.655"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0035335"	"Retinoblastoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"54880"	"BCOR"	"0.523"	"0.655"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54880"	"BCOR"	"0.523"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"54880"	"BCOR"	"0.523"	"0.655"	"C0206651"	"Clear Cell Sarcoma of Soft Tissue"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.36"	"1"	"2015"	"2017"	"0"	"0"	"ORPHANET"
"54880"	"BCOR"	"0.523"	"0.655"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C0796016"	"Microphthalmia, syndromic 1"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.54"	"1"	"2004"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"54880"	"BCOR"	"0.523"	"0.655"	"C1846265"	"Microphthalmia, syndromic 2"	"disease"	"C11;C14;C16"	"Disease or Syndrome"	"0.80"	"1"	"1993"	"2016"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"54880"	"BCOR"	"0.523"	"0.655"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54880"	"BCOR"	"0.523"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"54884"	"RETSAT"	"0.928"	"0.31"	"C0796154"	"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1"	"disease"	"C05;C10;C14;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54885"	"TBC1D8B"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54886"	"PLPPR1"	"0.727"	"0.069"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54887"	"UHRF1BP1"	"0.815"	"0.172"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2017"	"1"	"5"	"CTD_human"
"54887"	"UHRF1BP1"	"0.815"	"0.172"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"54888"	"NSUN2"	"0.659"	"0.586"	"C0175691"	"Dubowitz syndrome"	"disease"	"C05;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"54888"	"NSUN2"	"0.659"	"0.586"	"C1970199"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2007"	"2012"	"2"	"3"	"CTD_human;UNIPROT"
"54888"	"NSUN2"	"0.659"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"54894"	"RNF43"	"0.648"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2005"	"2015"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2012"	"2012"	"1"	"0"	"CGI;CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"0"	"2013"	"2013"	"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0347284"	"Benign tumor of pancreas"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54894"	"RNF43"	"0.648"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"54894"	"RNF43"	"0.648"	"0.276"	"C4310714"	"SESSILE SERRATED POLYPOSIS CANCER SYNDROME"	"disease"		"Neoplastic Process"	"0.40"		"2008"	"2017"	"6"	"1"	"CLINGEN"
"54897"	"CASZ1"	"0.659"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54897"	"CASZ1"	"0.659"	"0.552"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54897"	"CASZ1"	"0.659"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54897"	"CASZ1"	"0.659"	"0.552"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"54898"	"ELOVL2"	"0.886"	"0.069"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54898"	"ELOVL2"	"0.886"	"0.069"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54898"	"ELOVL2"	"0.886"	"0.069"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54899"	"PXK"	"0.815"	"0.207"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54899"	"PXK"	"0.815"	"0.207"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.47"	"0.8333333"	"2008"	"2015"	"1"	"2"	"CTD_human"
"54899"	"PXK"	"0.815"	"0.207"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54901"	"CDKAL1"	"0.639"	"0.483"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2013"	"2017"	"1"	"2"	"CTD_human"
"54901"	"CDKAL1"	"0.639"	"0.483"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"54901"	"CDKAL1"	"0.639"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.70"	"0.9873418"	"2007"	"2018"	"3"	"88"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54902"	"TTC19"	"0.659"	"0.345"	"C0021359"	"Infertility"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231686"	"Gait, Unsteady"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231687"	"Spastic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231688"	"Gait, Shuffling"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231689"	"Gait, Athetotic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231693"	"Charcot Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231694"	"Gait, Festinating"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231695"	"Cerebellar ataxic gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231696"	"Gait, Hemiplegic"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231698"	"Gait, Scissors"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0231712"	"Waddling gait"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0234996"	"Gait, Rigid"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0235000"	"Gait, Broadened"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0337210"	"Gait, Stumbling"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2013"	"2017"	"0"	"0"	"ORPHANET"
"54902"	"TTC19"	"0.659"	"0.345"	"C0427128"	"Rapid Fatigue of Gait"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0427149"	"Gait, Drop Foot"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0427169"	"Marche a Petit Pas"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0427177"	"Gait, Hysterical"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0729353"	"Subfertility"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751829"	"Gait Disorder, Sensorimotor"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751830"	"Gait Disorders, Neurologic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751831"	"Gait, Frontal"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C0751832"	"Gait, Widebased"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"54902"	"TTC19"	"0.659"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54902"	"TTC19"	"0.659"	"0.345"	"C4074771"	"Sterility, Reproductive"	"phenotype"	"C12;C13"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54903"	"MKS1"	"0.546"	"0.69"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54903"	"MKS1"	"0.546"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.43"	"1"	"2002"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"54903"	"MKS1"	"0.546"	"0.69"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2007"	"2017"	"0"	"3"	"ORPHANET"
"54903"	"MKS1"	"0.546"	"0.69"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.45"	"1"	"2006"	"2017"	"0"	"14"	"ORPHANET"
"54903"	"MKS1"	"0.546"	"0.69"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.54"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"54903"	"MKS1"	"0.546"	"0.69"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54903"	"MKS1"	"0.546"	"0.69"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54903"	"MKS1"	"0.546"	"0.69"	"C2673873"	"BARDET-BIEDL SYNDROME 13"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"54903"	"MKS1"	"0.546"	"0.69"	"C3714506"	"Meckel syndrome type 1"	"disease"	"C08;C09;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9473684"	"2004"	"2017"	"3"	"25"	"CTD_human;UNIPROT"
"54903"	"MKS1"	"0.546"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"54903"	"MKS1"	"0.546"	"0.69"	"C4274118"	"Joubert syndrome with ocular defect"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54903"	"MKS1"	"0.546"	"0.69"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"54916"	"TMEM260"	"0.752"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54919"	"DNAAF5"	"0.752"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"54919"	"DNAAF5"	"0.752"	"0.207"	"C3543825"	"CILIARY DYSKINESIA, PRIMARY, 18"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"2"	"1"	"CTD_human;UNIPROT"
"54919"	"DNAAF5"	"0.752"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54919"	"DNAAF5"	"0.752"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54927"	"CHCHD3"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"54928"	"IMPAD1"	"0.735"	"0.379"	"C3279757"	"CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2012"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"54928"	"IMPAD1"	"0.735"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54929"	"TMEM161A"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54931"	"TRMT10C"	"0.834"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54931"	"TRMT10C"	"0.834"	"0.207"	"C4310773"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"54938"	"SARS2"	"0.743"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"54938"	"SARS2"	"0.743"	"0.276"	"C3151209"	"HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"54941"	"RNF125"	"0.648"	"0.552"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"54941"	"RNF125"	"0.648"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"54941"	"RNF125"	"0.648"	"0.552"	"C4015710"	"TENORIO SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"54947"	"LPCAT2"	"0.815"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54947"	"LPCAT2"	"0.815"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0030421"	"Paraganglioma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"0"	"0"	"CGI"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"1982"	"2014"	"6"	"0"	"CLINGEN"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1982"	"2014"	"6"	"0"	"CLINGEN"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"1982"	"2014"	"6"	"0"	"CLINGEN"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"1982"	"2014"	"6"	"0"	"CLINGEN"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54949"	"SDHAF2"	"0.627"	"0.483"	"C1866552"	"PARAGANGLIOMAS 2 (disorder)"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.61"	"1"	"1982"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"54954"	"FAM120C"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"54959"	"ODAM"	"0.773"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0206669"	"Hepatocellular Adenoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"		"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"54968"	"TMEM70"	"0.656"	"0.586"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"54968"	"TMEM70"	"0.656"	"0.586"	"C3279699"	"Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.70"		"2008"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"54968"	"TMEM70"	"0.656"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"54970"	"TTC12"	"0.799"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2010"	"3"	"0"	"PSYGENET"
"54974"	"THG1L"	"0.857"	"0.172"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54974"	"THG1L"	"0.857"	"0.172"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"54974"	"THG1L"	"0.857"	"0.172"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C0002896"	"Sideroblastic anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C2673914"	"Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"0"	"5"	"CTD_human"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C4225425"	"ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"3"	"UNIPROT"
"54977"	"SLC25A38"	"0.727"	"0.241"	"C4274077"	"Autosomal recessive sideroblastic anemia"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"54982"	"CLN6"	"0.663"	"0.207"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54982"	"CLN6"	"0.663"	"0.207"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0022340"	"Late-Infantile Neuronal Ceroid Lipfuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"1998"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0022797"	"Adult Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"1988"	"2013"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"54982"	"CLN6"	"0.663"	"0.207"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0027877"	"Neuronal Ceroid-Lipofuscinoses"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"	"0.9090909"	"1998"	"2017"	"1"	"1"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54982"	"CLN6"	"0.663"	"0.207"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0268281"	"Infantile neuronal ceroid lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751383"	"Juvenile Neuronal Ceroid Lipofuscinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"1998"	"2016"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C1834207"	"Ceroid Lipofuscinosis, Neuronal, Parry Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C1866282"	"CEROID LIPOFUSCINOSIS, NEURONAL, 6"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.91"	"1"	"1993"	"2015"	"6"	"22"	"CTD_human;ORPHANET;UNIPROT"
"54982"	"CLN6"	"0.663"	"0.207"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"54982"	"CLN6"	"0.663"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"54986"	"ULK4"	"0.785"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54986"	"ULK4"	"0.785"	"0.276"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2012"	"2017"	"1"	"506"	"CTD_human"
"54986"	"ULK4"	"0.785"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"54995"	"OXSM"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"54996"	"MARC2"	"0.928"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54996"	"MARC2"	"0.928"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"54996"	"MARC2"	"0.928"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55005"	"RMND1"	"0.696"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55005"	"RMND1"	"0.696"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"9"	"GENOMICS_ENGLAND"
"55005"	"RMND1"	"0.696"	"0.345"	"C3554067"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2016"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"55005"	"RMND1"	"0.696"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55008"	"HERC6"	"1"	"0.069"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55014"	"STX17"	"0.886"	"0.069"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"1"	"CTD_human"
"55014"	"STX17"	"0.886"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"0.6666667"	"2008"	"2015"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55023"	"PHIP"	"0.785"	"0.379"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55023"	"PHIP"	"0.785"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55024"	"BANK1"	"0.701"	"0.31"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.50"	"0.8333333"	"2008"	"2016"	"1"	"3"	"CTD_human"
"55024"	"BANK1"	"0.701"	"0.31"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55033"	"FKBP14"	"0.696"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55033"	"FKBP14"	"0.696"	"0.448"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2017"	"7"	"0"	"GENOMICS_ENGLAND"
"55033"	"FKBP14"	"0.696"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"55033"	"FKBP14"	"0.696"	"0.448"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55033"	"FKBP14"	"0.696"	"0.448"	"C3281160"	"EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2012"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"55033"	"FKBP14"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55034"	"MOCOS"	"0.928"	"0.172"	"C1863688"	"Xanthinuria, Type II"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2001"	"2016"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"55036"	"CCDC40"	"0.815"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.63"	"1"	"2011"	"2013"	"1"	"2"	"CTD_human;ORPHANET"
"55036"	"CCDC40"	"0.815"	"0.138"	"C3151137"	"CILIARY DYSKINESIA, PRIMARY, 15"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2013"	"0"	"7"	"CTD_human"
"55036"	"CCDC40"	"0.815"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55036"	"CCDC40"	"0.815"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55036"	"CCDC40"	"0.815"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9266055"	"2001"	"2018"	"2"	"9"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.50"	"0.9565217"	"2007"	"2017"	"1"	"2"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2015"	"2"	"0"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"55054"	"ATG16L1"	"0.586"	"0.586"	"C1970207"	"Inflammatory Bowel Disease 10"	"disease"	"C06"	"Disease or Syndrome"	"0.70"		"2007"	"2016"	"11"	"1"	"CTD_human;UNIPROT"
"55055"	"ZWILCH"	"1"	"0.103"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55062"	"WIPI1"	"0.857"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55062"	"WIPI1"	"0.857"	"0.138"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"55065"	"SLC52A1"	"0.572"	"0.621"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55065"	"SLC52A1"	"0.572"	"0.621"	"C0035528"	"Riboflavin Deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"55066"	"PDPR"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"55072"	"RNF31"	"0.799"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55072"	"RNF31"	"0.799"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55076"	"TMEM45A"	"0.815"	"0.138"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55076"	"TMEM45A"	"0.815"	"0.138"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55083"	"KIF26B"	"0.773"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55084"	"SOBP"	"0.834"	"0.172"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"55084"	"SOBP"	"0.834"	"0.172"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"55084"	"SOBP"	"0.834"	"0.172"	"C3150924"	"MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2008"	"2011"	"0"	"1"	"CTD_human"
"55084"	"SOBP"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"55102"	"ATG2B"	"0.834"	"0.138"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55102"	"ATG2B"	"0.834"	"0.138"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55102"	"ATG2B"	"0.834"	"0.138"	"C0027022"	"Myeloproliferative disease"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55109"	"AGGF1"	"0.785"	"0.172"	"C0022739"	"Klippel-Trenaunay-Weber Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.57"	"1"	"2004"	"2013"	"1"	"1"	"ORPHANET;UNIPROT"
"55110"	"MAGOHB"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55110"	"MAGOHB"	"0.886"	"0.138"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55110"	"MAGOHB"	"0.886"	"0.138"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55112"	"WDR60"	"0.645"	"0.517"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55112"	"WDR60"	"0.645"	"0.517"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55112"	"WDR60"	"0.645"	"0.517"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"55112"	"WDR60"	"0.645"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"55112"	"WDR60"	"0.645"	"0.517"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.42"	"1"	"2013"	"2018"	"0"	"1"	"ORPHANET"
"55112"	"WDR60"	"0.645"	"0.517"	"C0432197"	"Short rib-polydactyly syndrome, Verma-Naumoff type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55112"	"WDR60"	"0.645"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"55112"	"WDR60"	"0.645"	"0.517"	"C3809691"	"SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2016"	"1"	"3"	"UNIPROT"
"55112"	"WDR60"	"0.645"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"55117"	"SLC6A15"	"0.785"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2011"	"2017"	"3"	"0"	"PSYGENET"
"55117"	"SLC6A15"	"0.785"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2017"	"2"	"0"	"PSYGENET"
"55120"	"FANCL"	"0.642"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"2003"	"2018"	"2"	"2"	"CTD_human;ORPHANET"
"55120"	"FANCL"	"0.642"	"0.586"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55120"	"FANCL"	"0.642"	"0.586"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55120"	"FANCL"	"0.642"	"0.586"	"C3469528"	"FANCONI ANEMIA, COMPLEMENTATION GROUP L"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2016"	"2018"	"0"	"2"	"CTD_human"
"55120"	"FANCL"	"0.642"	"0.586"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2003"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"55129"	"ANO10"	"0.676"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55129"	"ANO10"	"0.676"	"0.31"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55129"	"ANO10"	"0.676"	"0.31"	"C3150998"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2011"	"2015"	"1"	"10"	"ORPHANET;UNIPROT"
"55129"	"ANO10"	"0.676"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"55130"	"ARMC4"	"0.69"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2014"	"0"	"2"	"ORPHANET"
"55130"	"ARMC4"	"0.69"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55130"	"ARMC4"	"0.69"	"0.207"	"C3809548"	"CILIARY DYSKINESIA, PRIMARY, 23"	"disease"		"Disease or Syndrome"	"0.80"		"2013"	"2017"	"2"	"9"	"CTD_human;UNIPROT"
"55130"	"ARMC4"	"0.69"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55130"	"ARMC4"	"0.69"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55131"	"RBM28"	"0.727"	"0.345"	"C2677535"	"Alopecia, Neurologic Defects, and Endocrinopathy Syndrome"	"disease"	"C10;C17;C19;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"2008"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55131"	"RBM28"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"55135"	"WRAP53"	"0.672"	"0.31"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55135"	"WRAP53"	"0.672"	"0.31"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55135"	"WRAP53"	"0.672"	"0.31"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55135"	"WRAP53"	"0.672"	"0.31"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2013"	"0"	"0"	"ORPHANET"
"55135"	"WRAP53"	"0.672"	"0.31"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55135"	"WRAP53"	"0.672"	"0.31"	"C3151442"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2015"	"4"	"4"	"CLINGEN;CTD_human;UNIPROT"
"55135"	"WRAP53"	"0.672"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55140"	"ELP3"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55140"	"ELP3"	"0.815"	"0.172"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55140"	"ELP3"	"0.815"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55140"	"ELP3"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55140"	"ELP3"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55140"	"ELP3"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"	"0.9574468"	"1999"	"2018"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"55145"	"THAP1"	"0.648"	"0.379"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0393593"	"Dystonia Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.9565217"	"1999"	"2018"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0393598"	"Idiopathic familial dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"2013"	"2015"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0743332"	"Focal Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752197"	"Adult-Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752198"	"Adult-Onset Idiopathic Focal Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752199"	"Adult-Onset Idiopathic Torsion Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752200"	"Autosomal Dominant Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752201"	"Autosomal Recessive Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752202"	"Childhood Onset Dystonias"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752203"	"Dystonia, Primary"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2005"	"2015"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752205"	"Dystonia, Secondary"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752206"	"Dystonias, Sporadic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752207"	"Familial Dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C0752208"	"Pseudodystonia"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55145"	"THAP1"	"0.648"	"0.379"	"C1414216"	"Dystonia 6, torsion (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.95"	"1"	"2009"	"2018"	"19"	"16"	"CTD_human;ORPHANET;UNIPROT"
"55145"	"THAP1"	"0.648"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55145"	"THAP1"	"0.648"	"0.379"	"C4316810"	"Writer's Cramp"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55146"	"ZDHHC4"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55148"	"UBR7"	"0.886"	"0.138"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55148"	"UBR7"	"0.886"	"0.138"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55148"	"UBR7"	"0.886"	"0.138"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55148"	"UBR7"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55149"	"MTPAP"	"0.685"	"0.621"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55149"	"MTPAP"	"0.685"	"0.621"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55149"	"MTPAP"	"0.685"	"0.621"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55149"	"MTPAP"	"0.685"	"0.621"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55149"	"MTPAP"	"0.685"	"0.621"	"C3150925"	"SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55149"	"MTPAP"	"0.685"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.34"	"1"	"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C3554428"	"OSTEOGENESIS IMPERFECTA, TYPE XIV"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55151"	"TMEM38B"	"0.752"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55154"	"MSTO1"	"0.743"	"0.241"	"C4540096"	"MYOPATHY, MITOCHONDRIAL, AND ATAXIA"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2018"	"2"	"4"	"ORPHANET;UNIPROT"
"55157"	"DARS2"	"0.701"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55157"	"DARS2"	"0.701"	"0.31"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55157"	"DARS2"	"0.701"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55157"	"DARS2"	"0.701"	"0.31"	"C1970180"	"Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.74"	"1"	"1993"	"2016"	"1"	"15"	"CTD_human;ORPHANET;UNIPROT"
"55157"	"DARS2"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55159"	"RFWD3"	"0.762"	"0.414"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"55159"	"RFWD3"	"0.762"	"0.414"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2017"	"1"	"1"	"CTD_human"
"55160"	"ARHGEF10L"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55163"	"PNPO"	"0.69"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"55163"	"PNPO"	"0.69"	"0.276"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2005"	"2018"	"8"	"0"	"GENOMICS_ENGLAND"
"55163"	"PNPO"	"0.69"	"0.276"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55163"	"PNPO"	"0.69"	"0.276"	"C1864723"	"Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency"	"disease"	"C10;C14;C18;C23"	"Disease or Syndrome"	"0.70"		"2002"	"2017"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"55163"	"PNPO"	"0.69"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"55165"	"CEP55"	"0.636"	"0.414"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55165"	"CEP55"	"0.636"	"0.414"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55165"	"CEP55"	"0.636"	"0.414"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55165"	"CEP55"	"0.636"	"0.414"	"C1856053"	"Hydranencephaly with Renal Aplasia-Dysplasia"	"disease"	"C10;C12;C13;C16"	"Disease or Syndrome"	"0.41"	"1"	"2018"	"2018"	"0"	"2"	"ORPHANET"
"55165"	"CEP55"	"0.636"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55170"	"PRMT6"	"0.735"	"0.345"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55170"	"PRMT6"	"0.735"	"0.345"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55170"	"PRMT6"	"0.735"	"0.345"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55172"	"DNAAF2"	"0.752"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2014"	"0"	"3"	"ORPHANET"
"55172"	"DNAAF2"	"0.752"	"0.207"	"C2675867"	"CILIARY DYSKINESIA, PRIMARY, 10"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"0"	"2"	"CTD_human"
"55172"	"DNAAF2"	"0.752"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55172"	"DNAAF2"	"0.752"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55180"	"LINS1"	"0.799"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55180"	"LINS1"	"0.799"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55180"	"LINS1"	"0.799"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55180"	"LINS1"	"0.799"	"0.207"	"C3280538"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"3"	"4"	"CTD_human;UNIPROT"
"55180"	"LINS1"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55183"	"RIF1"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55187"	"VPS13D"	"1"	"0.069"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55187"	"VPS13D"	"1"	"0.069"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2011"	"2014"	"3"	"23"	"PSYGENET"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"0"	"0"	"CGI"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"2"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2017"	"1"	"1"	"PSYGENET"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0040100"	"Thymoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0205969"	"Thymic Carcinoma"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.70"	"1"	"2012"	"2018"	"2"	"1"	"CGI;CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"0"	"0"	"CGI"
"55193"	"PBRM1"	"0.59"	"0.517"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55193"	"PBRM1"	"0.59"	"0.517"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55193"	"PBRM1"	"0.59"	"0.517"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55193"	"PBRM1"	"0.59"	"0.517"	"C4518333"	"Clear cell papillary renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"55197"	"RPRD1A"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55198"	"APPL2"	"0.735"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55198"	"APPL2"	"0.735"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55205"	"ZNF532"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"55206"	"SBNO1"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55206"	"SBNO1"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55209"	"SETD5"	"0.611"	"0.69"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55209"	"SETD5"	"0.611"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55209"	"SETD5"	"0.611"	"0.69"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55209"	"SETD5"	"0.611"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2014"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"55209"	"SETD5"	"0.611"	"0.69"	"C3810406"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 23"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"55210"	"ATAD3A"	"0.652"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55210"	"ATAD3A"	"0.652"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55210"	"ATAD3A"	"0.652"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55210"	"ATAD3A"	"0.652"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55210"	"ATAD3A"	"0.652"	"0.448"	"C4310677"	"HAREL-YOON SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"55212"	"BBS7"	"0.713"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55212"	"BBS7"	"0.713"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55212"	"BBS7"	"0.713"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55212"	"BBS7"	"0.713"	"0.379"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.47"	"1"	"2003"	"2017"	"0"	"4"	"ORPHANET"
"55212"	"BBS7"	"0.713"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55212"	"BBS7"	"0.713"	"0.379"	"C1859565"	"BARDET-BIEDL SYNDROME 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2003"	"2016"	"4"	"12"	"CTD_human;UNIPROT"
"55212"	"BBS7"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55212"	"BBS7"	"0.713"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C1867332"	"Reticular Dystrophy Of Retinal Pigment Epithelium"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55213"	"RCBTB1"	"0.72"	"0.345"	"C4310680"	"RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"55214"	"P3H2"	"0.773"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"UNIPROT"
"55214"	"P3H2"	"0.773"	"0.207"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"55214"	"P3H2"	"0.773"	"0.207"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"55214"	"P3H2"	"0.773"	"0.207"	"C3280346"	"MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"55215"	"FANCI"	"0.701"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2001"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2017"	"0"	"7"	"ORPHANET"
"55215"	"FANCI"	"0.701"	"0.414"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C1836861"	"FANCONI ANEMIA, COMPLEMENTATION GROUP I"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.60"		"2007"	"2016"	"3"	"5"	"CTD_human;UNIPROT"
"55215"	"FANCI"	"0.701"	"0.414"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55215"	"FANCI"	"0.701"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55215"	"FANCI"	"0.701"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2001"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"55217"	"TMLHE"	"0.928"	"0.034"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2012"	"2016"	"0"	"0"	"CTD_human"
"55217"	"TMLHE"	"0.928"	"0.034"	"C3550875"	"AUTISM, SUSCEPTIBILITY TO, X-LINKED 6"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2016"	"2"	"4"	"UNIPROT"
"55217"	"TMLHE"	"0.928"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"55219"	"MACO1"	"1"	"0.034"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55219"	"MACO1"	"1"	"0.034"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55219"	"MACO1"	"1"	"0.034"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55229"	"PANK4"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"55237"	"VRTN"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"55240"	"STEAP3"	"0.696"	"0.31"	"C2673913"	"Anemia, Hypochromic Microcytic, With Iron Overload"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55240"	"STEAP3"	"0.696"	"0.31"	"C3808920"	"ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"ORPHANET"
"55244"	"SLC47A1"	"0.834"	"0.207"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55245"	"UQCC1"	"0.834"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55248"	"TMEM206"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"55249"	"YY1AP1"	"0.562"	"0.621"	"C1865267"	"Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly"	"disease"	"C05;C14;C16"	"Disease or Syndrome"	"0.60"		"1998"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"55250"	"ELP2"	"0.773"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55250"	"ELP2"	"0.773"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55250"	"ELP2"	"0.773"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55250"	"ELP2"	"0.773"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55250"	"ELP2"	"0.773"	"0.31"	"C4310641"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"55252"	"ASXL2"	"0.72"	"0.379"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55252"	"ASXL2"	"0.72"	"0.379"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55252"	"ASXL2"	"0.72"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55252"	"ASXL2"	"0.72"	"0.379"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"55252"	"ASXL2"	"0.72"	"0.379"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55252"	"ASXL2"	"0.72"	"0.379"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55252"	"ASXL2"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55254"	"TMEM39A"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55256"	"ADI1"	"0.713"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"55256"	"ADI1"	"0.713"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"55259"	"CASC1"	"0.785"	"0.138"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"55259"	"CASC1"	"0.785"	"0.138"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"55270"	"NUDT15"	"0.785"	"0.207"	"C4225160"	"THIOPURINES, POOR METABOLISM OF, 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55274"	"PHF10"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55275"	"VPS53"	"0.659"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"55275"	"VPS53"	"0.659"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"55275"	"VPS53"	"0.659"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1989"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"55275"	"VPS53"	"0.659"	"0.379"	"C4014488"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 2E"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"55278"	"QRSL1"	"0.579"	"0.552"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55280"	"CWF19L1"	"0.707"	"0.207"	"C4015301"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2017"	"0"	"3"	"ORPHANET"
"55281"	"TMEM140"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55286"	"C4orf19"	"1"	"0.034"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55289"	"ACOXL"	"0.735"	"0.379"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2017"	"1"	"5"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.60"	"1"	"2001"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0007103"	"Malignant neoplasm of endometrium"	"disease"		"Neoplastic Process"	"0.32"	"1"	"2002"	"2004"	"0"	"0"	"CGI"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2013"	"2016"	"1"	"2"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.35"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0346191"	"Carcinoma in situ of endometrium"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.54"	"1"	"2002"	"2013"	"1"	"0"	"CGI;CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2016"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C0919532"	"Genomic Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"CGI"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.42"	"0"	"2008"	"2016"	"1"	"4"	"CTD_human"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"2004"	"2018"	"0"	"0"	"UNIPROT"
"55294"	"FBXW7"	"0.511"	"0.759"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.8846154"	"2007"	"2018"	"2"	"0"	"CGI;CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55297"	"CCDC91"	"0.773"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55300"	"PI4K2B"	"0.857"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"55300"	"PI4K2B"	"0.857"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"55312"	"RFK"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55312"	"RFK"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.36"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0019618"	"Histiocytosis"	"disease"	"C15"	"Neoplastic Process"	"0.45"	"0.8"	"2010"	"2014"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0019625"	"Sinus histiocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.36"	"0.8333333"	"2010"	"2014"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0020555"	"Hypertrichosis"	"disease"	"C17"	"Disease or Syndrome"	"0.44"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0020619"	"Hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0162834"	"Hyperpigmentation"	"phenotype"	"C17"	"Pathologic Function"	"0.40"		"2009"	"2010"	"2"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0271623"	"Hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0432262"	"Dysosteosclerosis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C0948896"	"Primary hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C1864445"	"Histiocytosis with joint contractures and sensorineural deafness"	"disease"	"C05;C09;C10;C15;C23"	"Disease or Syndrome"	"0.80"	"1"	"2005"	"2017"	"9"	"16"	"CTD_human;ORPHANET;UNIPROT"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C3489396"	"Hypogonadism, Isolated Hypogonadotropic"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55315"	"SLC29A3"	"0.63"	"0.552"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"55325"	"UFSP2"	"0.857"	"0.069"	"C1840572"	"HIP DYSPLASIA, BEUKES TYPE"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1990"	"2018"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55328"	"RNLS"	"0.701"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55331"	"ACER3"	"0.928"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55331"	"ACER3"	"0.928"	"0.034"	"C4540358"	"LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55332"	"DRAM1"	"0.743"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55341"	"LSG1"	"1"	"0.069"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55341"	"LSG1"	"1"	"0.069"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55341"	"LSG1"	"1"	"0.069"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55341"	"LSG1"	"1"	"0.069"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55342"	"STRBP"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55342"	"STRBP"	"0.928"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55343"	"SLC35C1"	"0.773"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2004"	"2"	"0"	"GENOMICS_ENGLAND"
"55343"	"SLC35C1"	"0.773"	"0.414"	"C0398739"	"Congenital disorder of glycosylation, type 2C"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1992"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"55343"	"SLC35C1"	"0.773"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55344"	"PLCXD1"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55350"	"VNN3"	"0.815"	"0.138"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55350"	"VNN3"	"0.815"	"0.138"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human"
"55351"	"STK32B"	"0.785"	"0.379"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55356"	"SLC22A15"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55356"	"SLC22A15"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55356"	"SLC22A15"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55357"	"TBC1D2"	"0.886"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55357"	"TBC1D2"	"0.886"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55359"	"STYK1"	"0.727"	"0.241"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55364"	"IMPACT"	"0.762"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2013"	"1"	"0"	"PSYGENET"
"55364"	"IMPACT"	"0.762"	"0.31"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"55366"	"LGR4"	"0.713"	"0.552"	"C3714987"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17"	"phenotype"		"Finding"	"0.40"		"2013"	"2013"	"0"	"1"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55367"	"PIDD1"	"0.762"	"0.172"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55384"	"MEG3"	"0.573"	"0.69"	"C1842466"	"Uniparental disomy, paternal, chromosome 14"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55422"	"ZNF331"	"0.672"	"0.31"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55437"	"STRADB"	"1"	"0.034"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55486"	"PARL"	"0.762"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"55500"	"ETNK1"	"0.743"	"0.172"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55500"	"ETNK1"	"0.743"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55500"	"ETNK1"	"0.743"	"0.172"	"C1292772"	"Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative"	"disease"	"C04;C15"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CGI"
"55500"	"ETNK1"	"0.743"	"0.172"	"C1540912"	"Hypereosinophilic syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CGI"
"55500"	"ETNK1"	"0.743"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55500"	"ETNK1"	"0.743"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55502"	"HES6"	"0.701"	"0.241"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"55503"	"TRPV6"	"0.656"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55503"	"TRPV6"	"0.656"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55504"	"TNFRSF19"	"0.773"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"55504"	"TNFRSF19"	"0.773"	"0.207"	"C0027439"	"Nasopharyngeal Neoplasms"	"group"	"C04;C07;C09"	"Neoplastic Process"	"0.40"		"2010"	"2016"	"1"	"1"	"CTD_human"
"55504"	"TNFRSF19"	"0.773"	"0.207"	"C0238301"	"Cancer of Nasopharynx"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55505"	"NOP10"	"0.676"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"55505"	"NOP10"	"0.676"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"55505"	"NOP10"	"0.676"	"0.483"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2012"	"0"	"0"	"ORPHANET"
"55505"	"NOP10"	"0.676"	"0.483"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55505"	"NOP10"	"0.676"	"0.483"	"C1857144"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2007"	"1"	"1"	"UNIPROT"
"55505"	"NOP10"	"0.676"	"0.483"	"C3502105"	"Dyskeratosis Congenita, Autosomal Recessive"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human"
"55507"	"GPRC5D"	"0.713"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2010"	"3"	"0"	"PSYGENET"
"55507"	"GPRC5D"	"0.713"	"0.345"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"55507"	"GPRC5D"	"0.713"	"0.345"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2006"	"2"	"0"	"PSYGENET"
"55509"	"BATF3"	"0.886"	"0.069"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human"
"55512"	"SMPD3"	"0.701"	"0.379"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"55512"	"SMPD3"	"0.701"	"0.379"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55512"	"SMPD3"	"0.701"	"0.379"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55521"	"TRIM36"	"0.834"	"0.138"	"C0002902"	"Anencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.61"	"1"	"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"55521"	"TRIM36"	"0.834"	"0.138"	"C0302356"	"incomplete anencephaly, hemicrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"55521"	"TRIM36"	"0.834"	"0.138"	"C0431349"	"Aprosencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C1859817"	"2-AMINOADIPIC 2-OXOADIPIC ACIDURIA"	"disease"		"Finding"	"0.70"		"2013"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C3554366"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"55526"	"DHTKD1"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.43"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0020676"	"Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.50"		"1993"	"2015"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0032461"	"Polycythemia"	"disease"	"C15"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0271801"	"Central hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0677050"	"Manganese Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C1527405"	"Erythrocytosis"	"phenotype"	"C15"	"Finding"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C2750442"	"Hypermanganesemia with Dystonia Polycythemia and Cirrhosis"	"disease"	"C18"	"Disease or Syndrome"	"0.63"	"1"	"2012"	"2017"	"4"	"2"	"CTD_human;ORPHANET;UNIPROT"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C3665349"	"Secondary hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55532"	"SLC30A10"	"0.602"	"0.552"	"C4316995"	"Primary Hypothyroidism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C0205944"	"Sarcoma, Epithelioid"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C0205945"	"Sarcoma, Spindle Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C1261473"	"Sarcoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"55534"	"MAML3"	"0.696"	"0.414"	"C1710096"	"Sinonasal undifferentiated carcinoma"	"disease"	"C04;C08;C09"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55553"	"SOX6"	"0.713"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"55554"	"KLK15"	"0.727"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"UNIPROT"
"55558"	"PLXNA3"	"0.815"	"0.345"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55558"	"PLXNA3"	"0.815"	"0.345"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"55559"	"HAUS7"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55561"	"CDC42BPG"	"0.928"	"0.069"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"55567"	"DNAH3"	"0.886"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2010"	"2015"	"3"	"6"	"CTD_human;UNIPROT"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2010"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"55572"	"FOXRED1"	"0.616"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1998"	"2013"	"19"	"0"	"GENOMICS_ENGLAND"
"55576"	"STAB2"	"0.815"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55576"	"STAB2"	"0.815"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55576"	"STAB2"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55577"	"NAGK"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55577"	"NAGK"	"0.928"	"0.103"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55577"	"NAGK"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55577"	"NAGK"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55589"	"BMP2K"	"0.928"	"0.138"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"55596"	"ZCCHC8"	"0.815"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55596"	"ZCCHC8"	"0.815"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55596"	"ZCCHC8"	"0.815"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55596"	"ZCCHC8"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55599"	"RNPC3"	"0.656"	"0.586"	"C0342573"	"PITUITARY DWARFISM I"	"disease"	"C05;C10;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"55600"	"ITLN1"	"0.743"	"0.31"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"55600"	"ITLN1"	"0.743"	"0.31"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"55600"	"ITLN1"	"0.743"	"0.31"	"C0242698"	"Ventricular Dysfunction, Left"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55601"	"DDX60"	"1"	"0.069"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55605"	"KIF21A"	"0.727"	"0.345"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55605"	"KIF21A"	"0.727"	"0.345"	"C1302995"	"Congenital Fibrosis of the Extraocular Muscles"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.50"	"0.972973"	"2000"	"2017"	"0"	"0"	"ORPHANET"
"55605"	"KIF21A"	"0.727"	"0.345"	"C1851102"	"Fibrosis Of Extraocular Muscles, Congenital, 1"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.66"	"0.8333333"	"1993"	"2014"	"4"	"7"	"CTD_human;UNIPROT"
"55605"	"KIF21A"	"0.727"	"0.345"	"C2751105"	"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder)"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.60"		"2000"	"2014"	"4"	"7"	"CTD_human;UNIPROT"
"55605"	"KIF21A"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55612"	"FERMT1"	"0.602"	"0.483"	"C0014527"	"Epidermolysis Bullosa"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2003"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"55612"	"FERMT1"	"0.602"	"0.483"	"C0406556"	"Hereditary acrokeratotic poikiloderma of Weary"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55612"	"FERMT1"	"0.602"	"0.483"	"C0406557"	"Poikiloderma of Kindler"	"disease"	"C07;C16;C17;C23"	"Disease or Syndrome"	"1.00"	"0.9354839"	"1993"	"2017"	"3"	"21"	"CTD_human;ORPHANET;UNIPROT"
"55613"	"MTMR8"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55613"	"MTMR8"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"55614"	"KIF16B"	"0.857"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55616"	"ASAP3"	"0.785"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"55619"	"DOCK10"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55621"	"TRMT1"	"0.886"	"0.138"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55621"	"TRMT1"	"0.886"	"0.138"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55621"	"TRMT1"	"0.886"	"0.138"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55621"	"TRMT1"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"55623"	"THUMPD1"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2003"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.74"	"1"	"2003"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.70"	"0.9444444"	"2002"	"2014"	"0"	"55"	"CTD_human;ORPHANET"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.33"	"0.6666667"	"2007"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2004"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C3150412"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2002"	"2017"	"3"	"6"	"CTD_human;UNIPROT"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C3150417"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3"	"disease"		"Disease or Syndrome"	"0.70"		"2002"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C3151519"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2015"	"7"	"13"	"UNIPROT"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"0"	"2003"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"55624"	"POMGNT1"	"0.557"	"0.483"	"C4310704"	"RETINITIS PIGMENTOSA 76"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2016"	"2"	"6"	"CTD_human;UNIPROT"
"55625"	"ZDHHC7"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55626"	"AMBRA1"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2017"	"1"	"5"	"PSYGENET"
"55627"	"SMPD4"	"0.928"	"0.138"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55627"	"SMPD4"	"0.928"	"0.138"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55627"	"SMPD4"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0001197"	"Acrodermatitis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"		"2002"	"2007"	"5"	"0"	"CTD_human"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0086468"	"Prenatal Injuries"	"group"	"C13"	"Injury or Poisoning"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0221036"	"Acrodermatitis enteropathica"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"2000"	"2014"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0263372"	"Gianotti-Crosti Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"5"	"0"	"CTD_human"
"55630"	"SLC39A4"	"0.652"	"0.517"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.42"	"1"	"1995"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.50"	"1"	"1991"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"55636"	"CHD7"	"0.504"	"0.724"	"C0265354"	"CHARGE Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"1.00"	"0.9902913"	"2004"	"2018"	"21"	"141"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"55636"	"CHD7"	"0.504"	"0.724"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55636"	"CHD7"	"0.504"	"0.724"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"55636"	"CHD7"	"0.504"	"0.724"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C2936502"	"Familial CHARGE Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.70"		"2004"	"2016"	"9"	"0"	"CLINGEN;CTD_human"
"55636"	"CHD7"	"0.504"	"0.724"	"C3552553"	"HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2015"	"3"	"9"	"UNIPROT"
"55636"	"CHD7"	"0.504"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1991"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"55640"	"FLVCR2"	"0.785"	"0.276"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"55640"	"FLVCR2"	"0.785"	"0.276"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"55640"	"FLVCR2"	"0.785"	"0.276"	"C1856972"	"Encephaloclastic Proliferative Vasculopathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2009"	"2016"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"55640"	"FLVCR2"	"0.785"	"0.276"	"C3203738"	"Fowler syndrome"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"55640"	"FLVCR2"	"0.785"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"55644"	"OSGEP"	"0.727"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55644"	"OSGEP"	"0.727"	"0.31"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"55644"	"OSGEP"	"0.727"	"0.31"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55644"	"OSGEP"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55644"	"OSGEP"	"0.727"	"0.31"	"C4540266"	"GALLOWAY-MOWAT SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2017"	"2"	"6"	"UNIPROT"
"55650"	"PIGV"	"0.785"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"55650"	"PIGV"	"0.785"	"0.31"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.73"	"1"	"2010"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"55650"	"PIGV"	"0.785"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"55651"	"NHP2"	"0.652"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"55651"	"NHP2"	"0.652"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"55651"	"NHP2"	"0.652"	"0.552"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2001"	"2015"	"4"	"0"	"CLINGEN;ORPHANET"
"55651"	"NHP2"	"0.652"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55651"	"NHP2"	"0.652"	"0.552"	"C1148551"	"X-Linked Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2001"	"2015"	"4"	"0"	"CLINGEN"
"55651"	"NHP2"	"0.652"	"0.552"	"C3151441"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"3"	"CTD_human;UNIPROT"
"55651"	"NHP2"	"0.652"	"0.552"	"C3502105"	"Dyskeratosis Congenita, Autosomal Recessive"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"55651"	"NHP2"	"0.652"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0031511"	"Pheochromocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2010"	"2015"	"2"	"19"	"CTD_human;UNIPROT"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2010"	"2013"	"8"	"0"	"CLINGEN"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2010"	"2013"	"8"	"0"	"CLINGEN"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0206695"	"Carcinoma, Neuroendocrine"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2010"	"2013"	"8"	"0"	"CLINGEN"
"55654"	"TMEM127"	"0.701"	"0.414"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2010"	"2013"	"8"	"0"	"CLINGEN"
"55654"	"TMEM127"	"0.701"	"0.414"	"C1257877"	"Pheochromocytoma, Extra-Adrenal"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55654"	"TMEM127"	"0.701"	"0.414"	"C3149711"	"PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2005"	"2010"	"1"	"11"	"UNIPROT"
"55656"	"INTS8"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55669"	"MFN1"	"0.72"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55669"	"MFN1"	"0.72"	"0.414"	"C2931673"	"Ceroid lipofuscinosis, neuronal 1, infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0043459"	"Zellweger Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.52"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"55670"	"PEX26"	"0.584"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0162309"	"Adrenoleukodystrophy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C0282525"	"Adrenoleukodystrophy, Neonatal"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55670"	"PEX26"	"0.584"	"0.552"	"C0282527"	"Infantile Refsum Disease (disorder)"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human;ORPHANET"
"55670"	"PEX26"	"0.584"	"0.552"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C0751594"	"Zellweger-Like Syndrome"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2016"	"2"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C1527231"	"Adrenomyeloneuropathy"	"disease"	"C10;C16;C18;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C1832200"	"Peroxisome biogenesis disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C3539168"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2014"	"2"	"6"	"CTD_human;UNIPROT"
"55670"	"PEX26"	"0.584"	"0.552"	"C3553950"	"PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2003"	"2009"	"2"	"2"	"CTD_human;UNIPROT"
"55670"	"PEX26"	"0.584"	"0.552"	"C3553951"	"PEROXISOME BIOGENESIS DISORDER 7B"	"disease"		"Disease or Syndrome"	"0.60"		"1997"	"2005"	"1"	"4"	"CTD_human;UNIPROT"
"55670"	"PEX26"	"0.584"	"0.552"	"C3658299"	"Zellweger Spectrum"	"disease"	"C06;C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"55670"	"PEX26"	"0.584"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55670"	"PEX26"	"0.584"	"0.552"	"C3888385"	"PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)"	"disease"		"Disease or Syndrome"	"0.50"		"2003"	"2009"	"2"	"2"	"CTD_human;UNIPROT"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55676"	"SLC30A6"	"0.735"	"0.207"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55679"	"LIMS2"	"0.799"	"0.207"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55679"	"LIMS2"	"0.799"	"0.207"	"C4225192"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"55681"	"SCYL2"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55684"	"RABL6"	"0.834"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55684"	"RABL6"	"0.834"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55684"	"RABL6"	"0.834"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55684"	"RABL6"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55687"	"TRMU"	"0.735"	"0.241"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55687"	"TRMU"	"0.735"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55687"	"TRMU"	"0.735"	"0.241"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2013"	"4"	"0"	"GENOMICS_ENGLAND"
"55687"	"TRMU"	"0.735"	"0.241"	"C1838854"	"DEAFNESS, AMINOGLYCOSIDE-INDUCED"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"55687"	"TRMU"	"0.735"	"0.241"	"C1857332"	"Deafness, Sensorineural, Autosomal-Mitochondrial Type"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55687"	"TRMU"	"0.735"	"0.241"	"C3151898"	"MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55687"	"TRMU"	"0.735"	"0.241"	"C3278664"	"LIVER FAILURE, INFANTILE, TRANSIENT"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2014"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"55690"	"PACS1"	"0.676"	"0.483"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55690"	"PACS1"	"0.676"	"0.483"	"C3554343"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 17"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"1"	"1"	"ORPHANET;UNIPROT"
"55690"	"PACS1"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"55690"	"PACS1"	"0.676"	"0.483"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C4225193"	"CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"55691"	"FRMD4A"	"0.696"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55697"	"VAC14"	"0.627"	"0.552"	"C1857663"	"Yunis Varon syndrome"	"disease"	"C05;C07;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55697"	"VAC14"	"0.627"	"0.552"	"C4310743"	"STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"55699"	"IARS2"	"0.667"	"0.483"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55699"	"IARS2"	"0.667"	"0.483"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55699"	"IARS2"	"0.667"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55699"	"IARS2"	"0.667"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55699"	"IARS2"	"0.667"	"0.483"	"C4014942"	"CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"1993"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55703"	"POLR3B"	"0.624"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55703"	"POLR3B"	"0.624"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.49"	"0.8888889"	"2012"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"55703"	"POLR3B"	"0.624"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55703"	"POLR3B"	"0.624"	"0.517"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55703"	"POLR3B"	"0.624"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55703"	"POLR3B"	"0.624"	"0.517"	"C1859301"	"Cerebellar hypoplasia with endosteal sclerosis"	"disease"	"C05;C10;C23"	"Disease or Syndrome"	"0.40"				"0"	"2"	"ORPHANET"
"55703"	"POLR3B"	"0.624"	"0.517"	"C2676243"	"Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism"	"disease"	"C07;C10;C16;C19;C23"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"55703"	"POLR3B"	"0.624"	"0.517"	"C3280644"	"LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2015"	"3"	"11"	"UNIPROT"
"55703"	"POLR3B"	"0.624"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55704"	"CCDC88A"	"0.642"	"0.483"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55704"	"CCDC88A"	"0.642"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55704"	"CCDC88A"	"0.642"	"0.483"	"C1850055"	"PEHO syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55704"	"CCDC88A"	"0.642"	"0.483"	"C1850056"	"PEHO-Like Syndrome"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.52"	"1"	"2004"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"55704"	"CCDC88A"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55706"	"NDC1"	"1"	"0.069"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55714"	"TENM3"	"0.667"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55714"	"TENM3"	"0.667"	"0.448"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"55714"	"TENM3"	"0.667"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55714"	"TENM3"	"0.667"	"0.448"	"C0264423"	"Asthma, Occupational"	"disease"	"C08;C20;C24"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55714"	"TENM3"	"0.667"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"55714"	"TENM3"	"0.667"	"0.448"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55714"	"TENM3"	"0.667"	"0.448"	"C3554592"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2018"	"0"	"3"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"55717"	"WDR11"	"0.577"	"0.69"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.53"	"1"	"2010"	"2014"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55717"	"WDR11"	"0.577"	"0.69"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55717"	"WDR11"	"0.577"	"0.69"	"C3540450"	"HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"5"	"CTD_human;UNIPROT"
"55717"	"WDR11"	"0.577"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55717"	"WDR11"	"0.577"	"0.69"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"55717"	"WDR11"	"0.577"	"0.69"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55721"	"IQCC"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55721"	"IQCC"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55726"	"INTS13"	"0.834"	"0.241"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55726"	"INTS13"	"0.834"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55728"	"N4BP2"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0039590"	"Testicular Neoplasms"	"group"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0153594"	"Malignant neoplasm of testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55729"	"ATF7IP"	"0.594"	"0.655"	"C1720811"	"Tumor of Rete Testis"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55733"	"HHAT"	"0.616"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2013"	"1"	"1"	"PSYGENET"
"55733"	"HHAT"	"0.616"	"0.655"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"55733"	"HHAT"	"0.616"	"0.655"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55733"	"HHAT"	"0.616"	"0.655"	"C1838654"	"Nivelon Nivelon Mabille syndrome"	"disease"	"C05;C12;C13;C16;C19"	"Disease or Syndrome"	"0.50"		"2012"	"2014"	"0"	"0"	"ORPHANET"
"55733"	"HHAT"	"0.616"	"0.655"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55734"	"ZFP64"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55737"	"VPS35"	"0.713"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.60"	"0.9230769"	"2011"	"2018"	"9"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55737"	"VPS35"	"0.713"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55737"	"VPS35"	"0.713"	"0.379"	"C3280133"	"PARKINSON DISEASE 17"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2016"	"6"	"1"	"CTD_human;UNIPROT"
"55737"	"VPS35"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55737"	"VPS35"	"0.713"	"0.379"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.33"	"0.6666667"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"55738"	"ARFGAP1"	"0.928"	"0.103"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55738"	"ARFGAP1"	"0.928"	"0.103"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55738"	"ARFGAP1"	"0.928"	"0.103"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55738"	"ARFGAP1"	"0.928"	"0.103"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55739"	"NAXD"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55739"	"NAXD"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55739"	"NAXD"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55739"	"NAXD"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55740"	"ENAH"	"0.773"	"0.172"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55740"	"ENAH"	"0.773"	"0.172"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55740"	"ENAH"	"0.773"	"0.172"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55741"	"EDEM2"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55742"	"PARVA"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55743"	"CHFR"	"0.639"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.55"	"0.8"	"2008"	"2016"	"1"	"0"	"CTD_human;UNIPROT"
"55743"	"CHFR"	"0.639"	"0.448"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55743"	"CHFR"	"0.639"	"0.448"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"55743"	"CHFR"	"0.639"	"0.448"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"55743"	"CHFR"	"0.639"	"0.448"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55743"	"CHFR"	"0.639"	"0.448"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55744"	"COA1"	"0.928"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55745"	"AP5M1"	"0.762"	"0.172"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55745"	"AP5M1"	"0.762"	"0.172"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55745"	"AP5M1"	"0.762"	"0.172"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55745"	"AP5M1"	"0.762"	"0.172"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55745"	"AP5M1"	"0.762"	"0.172"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55745"	"AP5M1"	"0.762"	"0.172"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55746"	"NUP133"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55748"	"CNDP2"	"0.701"	"0.379"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"55748"	"CNDP2"	"0.701"	"0.379"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55748"	"CNDP2"	"0.701"	"0.379"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55748"	"CNDP2"	"0.701"	"0.379"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55749"	"CCAR1"	"0.735"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55750"	"AGK"	"0.659"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2012"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"55750"	"AGK"	"0.659"	"0.483"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"55750"	"AGK"	"0.659"	"0.483"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55750"	"AGK"	"0.659"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55750"	"AGK"	"0.659"	"0.483"	"C1859317"	"Cataract and cardiomyopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.68"	"1"	"1986"	"2018"	"1"	"8"	"CTD_human;ORPHANET"
"55750"	"AGK"	"0.659"	"0.483"	"C3553494"	"CATARACT 38"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"55750"	"AGK"	"0.659"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55752"	"SEPT11"	"0.752"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"55752"	"SEPT11"	"0.752"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"55752"	"SEPT11"	"0.752"	"0.241"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55752"	"SEPT11"	"0.752"	"0.241"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55755"	"CDK5RAP2"	"0.701"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.57"	"1"	"2005"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"55755"	"CDK5RAP2"	"0.701"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.34"	"1"	"2013"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"55755"	"CDK5RAP2"	"0.701"	"0.448"	"C1858108"	"Microcephaly, Primary Autosomal Recessive, 3"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2016"	"0"	"13"	"CTD_human"
"55755"	"CDK5RAP2"	"0.701"	"0.448"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"55755"	"CDK5RAP2"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"55759"	"WDR12"	"0.834"	"0.034"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"55759"	"WDR12"	"0.834"	"0.034"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55759"	"WDR12"	"0.834"	"0.034"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2016"	"2"	"1"	"CTD_human"
"55759"	"WDR12"	"0.834"	"0.034"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55759"	"WDR12"	"0.834"	"0.034"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human"
"55760"	"DHX32"	"0.762"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55764"	"IFT122"	"0.586"	"0.448"	"C0008780"	"Ciliary Motility Disorders"	"group"	"C08;C09;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2010"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55764"	"IFT122"	"0.586"	"0.448"	"C0013608"	"Edema, Cardiac"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55764"	"IFT122"	"0.586"	"0.448"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0037932"	"Curvature of spine"	"phenotype"	"C05"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0432198"	"Short rib-polydactyly syndrome, Beemer type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"55764"	"IFT122"	"0.586"	"0.448"	"C0432235"	"Cranioectodermal Dysplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"55764"	"IFT122"	"0.586"	"0.448"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55764"	"IFT122"	"0.586"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55764"	"IFT122"	"0.586"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2010"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"55765"	"INAVA"			"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2017"	"1"	"2"	"CTD_human"
"55768"	"NGLY1"	"0.815"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55768"	"NGLY1"	"0.815"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55768"	"NGLY1"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"55768"	"NGLY1"	"0.815"	"0.207"	"C3808991"	"NGLY1 deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2013"	"2018"	"7"	"16"	"CLINGEN;CTD_human;ORPHANET"
"55773"	"TBC1D23"	"0.886"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"55773"	"TBC1D23"	"0.886"	"0.034"	"C4540164"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 11"	"disease"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"2"	"0"	"UNIPROT"
"55775"	"TDP1"	"0.69"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55775"	"TDP1"	"0.69"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55775"	"TDP1"	"0.69"	"0.345"	"C1846574"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.96"	"0.8333333"	"2002"	"2007"	"5"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55777"	"MBD5"	"0.58"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55777"	"MBD5"	"0.58"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55777"	"MBD5"	"0.58"	"0.552"	"C1969562"	"Mental Retardation, Autosomal Dominant 1"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.80"		"1993"	"2017"	"2"	"11"	"CTD_human;UNIPROT"
"55777"	"MBD5"	"0.58"	"0.552"	"C3277090"	"CHROMOSOME 2q23.1 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.50"		"2007"	"2012"	"2"	"5"	"UNIPROT"
"55777"	"MBD5"	"0.58"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.44"	"1"	"2011"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"55777"	"MBD5"	"0.58"	"0.552"	"C4304532"	"2q23.1 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55780"	"ERMARD"	"0.707"	"0.31"	"C1848213"	"Periventricular Heterotopia, X-Linked"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55780"	"ERMARD"	"0.707"	"0.31"	"C1868720"	"Periventricular Nodular Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"55780"	"ERMARD"	"0.707"	"0.31"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"55780"	"ERMARD"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"55780"	"ERMARD"	"0.707"	"0.31"	"C3809872"	"PERIVENTRICULAR NODULAR HETEROTOPIA 6"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"55780"	"ERMARD"	"0.707"	"0.31"	"C4304514"	"6q terminal deletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55781"	"RIOK2"	"0.928"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"55783"	"CMTR2"	"0.799"	"0.138"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55783"	"CMTR2"	"0.799"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55783"	"CMTR2"	"0.799"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55783"	"CMTR2"	"0.799"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55784"	"MCTP2"	"0.645"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"55784"	"MCTP2"	"0.645"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"55784"	"MCTP2"	"0.645"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"55784"	"MCTP2"	"0.645"	"0.517"	"C2675463"	"Chromosome 15q26-Qter Deletion Syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55785"	"FGD6"	"0.834"	"0.172"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55785"	"FGD6"	"0.834"	"0.172"	"C2237660"	"exudative macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"55788"	"LMBRD1"	"0.72"	"0.31"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55788"	"LMBRD1"	"0.72"	"0.31"	"C1848578"	"METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE (disorder)"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.53"	"1"	"2011"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"55788"	"LMBRD1"	"0.72"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55790"	"CSGALNACT1"	"0.815"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55796"	"MBNL3"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55799"	"CACNA2D3"	"0.752"	"0.345"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55799"	"CACNA2D3"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55800"	"SCN3B"	"0.752"	"0.172"	"C1142166"	"Brugada Syndrome (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.73"	"0.6666667"	"2008"	"2013"	"0"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"55800"	"SCN3B"	"0.752"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"55800"	"SCN3B"	"0.752"	"0.172"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55800"	"SCN3B"	"0.752"	"0.172"	"C2751088"	"Brugada Syndrome 7"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.70"		"2008"	"2011"	"2"	"3"	"CTD_human;UNIPROT"
"55800"	"SCN3B"	"0.752"	"0.172"	"C4013699"	"ATRIAL FIBRILLATION, FAMILIAL, 16"	"phenotype"		"Finding"	"0.60"		"2008"	"2011"	"2"	"3"	"UNIPROT"
"55806"	"HR"	"0.713"	"0.207"	"C0002170"	"Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.43"	"1"	"2002"	"2013"	"1"	"0"	"CTD_human"
"55806"	"HR"	"0.713"	"0.207"	"C0086873"	"Pseudopelade"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55806"	"HR"	"0.713"	"0.207"	"C0162311"	"Androgenetic Alopecia"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55806"	"HR"	"0.713"	"0.207"	"C0263477"	"Female pattern alopecia (disorder)"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55806"	"HR"	"0.713"	"0.207"	"C0263505"	"Alopecia universalis"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.61"	"1"	"1998"	"1998"	"0"	"0"	"CTD_human;ORPHANET"
"55806"	"HR"	"0.713"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"55806"	"HR"	"0.713"	"0.207"	"C1859592"	"ATRICHIA WITH PAPULAR LESIONS"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.80"		"1998"	"2005"	"0"	"2"	"CTD_human;ORPHANET"
"55806"	"HR"	"0.713"	"0.207"	"C1859877"	"Alopecia universalis congenita"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.80"		"1998"	"2014"	"4"	"3"	"CTD_human;UNIPROT"
"55806"	"HR"	"0.713"	"0.207"	"C2931059"	"Marie Unna congenital hypotrichosis"	"disease"	"C17"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human;ORPHANET"
"55806"	"HR"	"0.713"	"0.207"	"C4083212"	"Alopecia, Male Pattern"	"phenotype"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55808"	"ST6GALNAC1"	"0.743"	"0.241"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"55808"	"ST6GALNAC1"	"0.743"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"55808"	"ST6GALNAC1"	"0.743"	"0.241"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"55809"	"TRERF1"	"0.886"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"55809"	"TRERF1"	"0.886"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"55809"	"TRERF1"	"0.886"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55809"	"TRERF1"	"0.886"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2009"	"1"	"0"	"CTD_human"
"55811"	"ADCY10"	"0.743"	"0.379"	"C0342639"	"Familial idiopathic hypercalciuria"	"disease"	"C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"55811"	"ADCY10"	"0.743"	"0.379"	"C0543800"	"Idiopathic hypercalciuria"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55812"	"SPATA7"	"0.652"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.53"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"55812"	"SPATA7"	"0.652"	"0.414"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.66"	"1"	"2006"	"2015"	"1"	"2"	"CTD_human;ORPHANET"
"55812"	"SPATA7"	"0.652"	"0.414"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55812"	"SPATA7"	"0.652"	"0.414"	"C1858677"	"LEBER CONGENITAL AMAUROSIS 3 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"0"	"6"	"CTD_human"
"55812"	"SPATA7"	"0.652"	"0.414"	"C2751780"	"Retinitis Pigmentosa, Juvenile, SPATA7-Related"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"0"	"0"	"CTD_human"
"55812"	"SPATA7"	"0.652"	"0.414"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55814"	"BDP1"	"0.799"	"0.207"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CLINGEN"
"55814"	"BDP1"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"55816"	"DOK5"	"0.886"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"55818"	"KDM3A"	"0.663"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"UNIPROT"
"55819"	"RNF130"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55819"	"RNF130"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55823"	"VPS11"	"0.667"	"0.552"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"55823"	"VPS11"	"0.667"	"0.552"	"C4225247"	"LEUKODYSTROPHY, HYPOMYELINATING, 12"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"55824"	"PAG1"	"0.564"	"0.655"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55824"	"PAG1"	"0.564"	"0.655"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55824"	"PAG1"	"0.564"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"55824"	"PAG1"	"0.564"	"0.655"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55825"	"PECR"	"0.857"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55825"	"PECR"	"0.857"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55825"	"PECR"	"0.857"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55825"	"PECR"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55827"	"DCAF6"	"0.815"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55827"	"DCAF6"	"0.815"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"1"	"2001"	"2015"	"1"	"0"	"CTD_human"
"55829"	"SELENOS"	"0.672"	"0.448"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"55829"	"SELENOS"	"0.672"	"0.448"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"55829"	"SELENOS"	"0.672"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55829"	"SELENOS"	"0.672"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55830"	"GLT8D1"	"0.834"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55830"	"GLT8D1"	"0.834"	"0.069"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2014"	"2014"	"1"	"7"	"PSYGENET"
"55830"	"GLT8D1"	"0.834"	"0.069"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55833"	"UBAP2"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"55835"	"CENPJ"	"0.596"	"0.586"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55835"	"CENPJ"	"0.596"	"0.586"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2005"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"55835"	"CENPJ"	"0.596"	"0.586"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"55835"	"CENPJ"	"0.596"	"0.586"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.32"	"1"	"2006"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"55835"	"CENPJ"	"0.596"	"0.586"	"C1842109"	"Microcephaly, Primary Autosomal Recessive, 6"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2013"	"2"	"7"	"CTD_human;UNIPROT"
"55835"	"CENPJ"	"0.596"	"0.586"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"55835"	"CENPJ"	"0.596"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55835"	"CENPJ"	"0.596"	"0.586"	"C3888212"	"SECKEL SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.60"		"2008"	"2015"	"0"	"11"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2017"	"1"	"0"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2015"	"1"	"0"	"CTD_human"
"55840"	"EAF2"	"0.735"	"0.31"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55841"	"WWC3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55851"	"PSENEN"	"0.752"	"0.241"	"C1840560"	"Hidradenitis suppurativa, familial"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.50"		"2010"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"55851"	"PSENEN"	"0.752"	"0.241"	"C3714534"	"dowling-degos disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55857"	"KIZ"	"0.713"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"55857"	"KIZ"	"0.713"	"0.31"	"C4014312"	"RETINITIS PIGMENTOSA 69"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"3"	"CTD_human"
"55858"	"TMEM165"	"0.762"	"0.241"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"55858"	"TMEM165"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55858"	"TMEM165"	"0.762"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.36"	"1"	"2012"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"55858"	"TMEM165"	"0.762"	"0.241"	"C3553571"	"Carbohydrate deficient glycoprotein syndrome type 2k"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2014"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"55858"	"TMEM165"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55861"	"DBNDD2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55862"	"ECHDC1"	"0.773"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55863"	"TMEM126B"	"0.676"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"GENOMICS_ENGLAND"
"55863"	"TMEM126B"	"0.676"	"0.379"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"CTD_human"
"55863"	"TMEM126B"	"0.676"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"55863"	"TMEM126B"	"0.676"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55869"	"HDAC8"	"0.546"	"0.828"	"C0270972"	"Cornelia De Lange Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"55869"	"HDAC8"	"0.546"	"0.828"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"55869"	"HDAC8"	"0.546"	"0.828"	"C1839736"	"WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME"	"disease"	"C10;C16;C17;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55869"	"HDAC8"	"0.546"	"0.828"	"C3550903"	"CORNELIA DE LANGE SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2017"	"1"	"17"	"UNIPROT"
"55869"	"HDAC8"	"0.546"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"55869"	"HDAC8"	"0.546"	"0.828"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55870"	"ASH1L"	"0.72"	"0.414"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55870"	"ASH1L"	"0.72"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55870"	"ASH1L"	"0.72"	"0.414"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"55870"	"ASH1L"	"0.72"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"55870"	"ASH1L"	"0.72"	"0.414"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55870"	"ASH1L"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"55872"	"PBK"	"0.607"	"0.621"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55872"	"PBK"	"0.607"	"0.621"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"55876"	"GSDMB"	"0.713"	"0.379"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.50"	"0.9565217"	"2007"	"2018"	"1"	"12"	"CTD_human"
"55876"	"GSDMB"	"0.713"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"55879"	"GABRQ"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"55901"	"THSD1"	"0.785"	"0.31"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55904"	"KMT2E"	"0.773"	"0.103"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"0.5"	"2002"	"2011"	"1"	"0"	"CTD_human"
"55904"	"KMT2E"	"0.773"	"0.103"	"C0023466"	"Leukemia, Monocytic, Chronic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"55904"	"KMT2E"	"0.773"	"0.103"	"C0023470"	"Myeloid Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2009"	"1"	"0"	"CTD_human"
"55904"	"KMT2E"	"0.773"	"0.103"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"55904"	"KMT2E"	"0.773"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55905"	"RNF114"	"0.886"	"0.034"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55905"	"RNF114"	"0.886"	"0.034"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.45"	"1"	"2008"	"2016"	"1"	"2"	"CTD_human"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C0796200"	"Wieacker-Wolff syndrome"	"disease"	"C05;C10;C11;C16;C23;F01"	"Disease or Syndrome"	"0.62"	"1"	"1985"	"2017"	"1"	"8"	"ORPHANET;UNIPROT"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C1839735"	"MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C1844934"	"Arthrogryposis multiplex congenita, distal, X-linked"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1985"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"55906"	"ZC4H2"	"0.701"	"0.276"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55914"	"ERBIN"	"0.735"	"0.172"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"55917"	"CTTNBP2NL"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55930"	"MYO5C"	"0.799"	"0.103"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"55958"	"KLHL9"			"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"55959"	"SULF2"	"0.609"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2006"	"2013"	"0"	"0"	"UNIPROT"
"55959"	"SULF2"	"0.609"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"55959"	"SULF2"	"0.609"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"CTD_human"
"55967"	"NDUFA12"	"0.676"	"0.345"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"55967"	"NDUFA12"	"0.676"	"0.345"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55967"	"NDUFA12"	"0.676"	"0.345"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55967"	"NDUFA12"	"0.676"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55967"	"NDUFA12"	"0.676"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"55971"	"BAIAP2L1"	"0.815"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"55972"	"SLC25A40"	"1"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55975"	"KLHL7"	"0.611"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"55975"	"KLHL7"	"0.611"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55975"	"KLHL7"	"0.611"	"0.621"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2017"	"0"	"0"	"ORPHANET"
"55975"	"KLHL7"	"0.611"	"0.621"	"C0796232"	"Bohring syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55975"	"KLHL7"	"0.611"	"0.621"	"C1832409"	"Crisponi syndrome"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55975"	"KLHL7"	"0.611"	"0.621"	"C1848947"	"COLD-INDUCED SWEATING SYNDROME 1"	"disease"	"C05;C10;C16;C17;C23"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"ORPHANET"
"55975"	"KLHL7"	"0.611"	"0.621"	"C2751986"	"RETINITIS PIGMENTOSA 42"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1991"	"2012"	"4"	"3"	"CTD_human;UNIPROT"
"55975"	"KLHL7"	"0.611"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"55975"	"KLHL7"	"0.611"	"0.621"	"C4310742"	"COLD-INDUCED SWEATING SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"55997"	"CFC1"	"0.572"	"0.552"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.62"	"1"	"1999"	"2008"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C0040761"	"Transposition of Great Vessels"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"55997"	"CFC1"	"0.572"	"0.552"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"55997"	"CFC1"	"0.572"	"0.552"	"C1415817"	"HETEROTAXY, VISCERAL, 2, AUTOSOMAL"	"disease"		"Disease or Syndrome"	"0.80"		"2000"	"2002"	"2"	"3"	"CTD_human;UNIPROT"
"55997"	"CFC1"	"0.572"	"0.552"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C1956410"	"Double Outlet Right Ventricle, Noncommitted VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C1956411"	"Double Outlet Right Ventricle, Subaortic VSD"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C1956412"	"Double Outlet Right Ventricle, Subpulmonary VSD"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C1956413"	"Taussig-Bing Anomaly"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"55997"	"CFC1"	"0.572"	"0.552"	"C4274029"	"Biliary atresia with splenic malformation syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"55997"	"CFC1"	"0.572"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"55998"	"NXF5"	"0.815"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2002"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"55999"	"NXF4"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"56005"	"MYDGF"	"0.535"	"0.759"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56006"	"SMG9"	"0.735"	"0.207"	"C4310793"	"HEART AND BRAIN MALFORMATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"2"	"CTD_human"
"56033"	"BARX1"	"0.857"	"0.172"	"C0279628"	"Adenocarcinoma Of Esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.42"	"1"	"2014"	"2016"	"1"	"1"	"CTD_human"
"56034"	"PDGFC"	"0.648"	"0.448"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56052"	"ALG1"	"0.696"	"0.621"	"C2931005"	"Congenital disorder of glycosylation type 1K"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"2004"	"2016"	"4"	"20"	"CTD_human;ORPHANET;UNIPROT"
"56100"	"PCDHGB6"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56100"	"PCDHGB6"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56100"	"PCDHGB6"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56100"	"PCDHGB6"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56121"	"PCDHB15"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56128"	"PCDHB8"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56136"	"PCDHA13"	"1"	"0.069"	"C0152101"	"Hypoplastic Left Heart Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56145"	"PCDHA3"	"0.886"	"0.172"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56145"	"PCDHA3"	"0.886"	"0.172"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56155"	"TEX14"	"0.834"	"0.172"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56159"	"TEX11"	"0.834"	"0.034"	"C1839841"	"SPERMATOGENIC FAILURE, X-LINKED, 2"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"56160"	"NSMCE3"	"0.785"	"0.241"	"C4310653"	"LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"56164"	"STK31"	"0.752"	"0.138"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56172"	"ANKH"	"0.636"	"0.517"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56172"	"ANKH"	"0.636"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56172"	"ANKH"	"0.636"	"0.517"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56172"	"ANKH"	"0.636"	"0.517"	"C0265292"	"Schwartz-Lelek syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.37"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"56172"	"ANKH"	"0.636"	"0.517"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56172"	"ANKH"	"0.636"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56172"	"ANKH"	"0.636"	"0.517"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56172"	"ANKH"	"0.636"	"0.517"	"C0553730"	"Calcium pyrophosphate deposition disease"	"disease"	"C05"	"Disease or Syndrome"	"0.40"	"0.9375"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"56172"	"ANKH"	"0.636"	"0.517"	"C0856830"	"Calcium pyrophosphate arthropathy"	"disease"	"C05"	"Disease or Syndrome"	"0.75"	"1"	"1989"	"2013"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"56172"	"ANKH"	"0.636"	"0.517"	"C1852502"	"CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT"	"disease"	"C05;C07"	"Disease or Syndrome"	"0.88"	"1"	"1965"	"2016"	"1"	"6"	"CTD_human;UNIPROT"
"56172"	"ANKH"	"0.636"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56180"	"MOSPD1"	"0.886"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56203"	"LMOD3"	"0.799"	"0.172"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"56203"	"LMOD3"	"0.799"	"0.172"	"C0206157"	"Myopathies, Nemaline"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"56203"	"LMOD3"	"0.799"	"0.172"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.32"	"1"	"2015"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"56203"	"LMOD3"	"0.799"	"0.172"	"C4015360"	"NEMALINE MYOPATHY 10"	"disease"		"Disease or Syndrome"	"0.80"		"2015"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"56244"	"BTNL2"	"0.619"	"0.621"	"C0005138"	"Berylliosis"	"disease"	"C08;C24"	"Injury or Poisoning"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56244"	"BTNL2"	"0.619"	"0.621"	"C0036202"	"Sarcoidosis"	"disease"	"C15"	"Disease or Syndrome"	"0.70"	"1"	"2005"	"2017"	"0"	"25"	"CTD_human;ORPHANET"
"56244"	"BTNL2"	"0.619"	"0.621"	"C2350873"	"Beryllium Disease"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56246"	"MRAP"	"0.773"	"0.241"	"C0342482"	"X-linked Adrenal Hypoplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56246"	"MRAP"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56246"	"MRAP"	"0.773"	"0.241"	"C4049650"	"Familial Glucocorticoid Deficiency Type 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.40"				"0"	"1"	"ORPHANET"
"56246"	"MRAP"	"0.773"	"0.241"	"C4049714"	"Familial Glucocorticoid Deficiency Type 2"	"disease"	"C19"	"Disease or Syndrome"	"0.40"		"2005"	"2013"	"0"	"1"	"CTD_human"
"56247"	"FMR3"	"0.928"	"0.172"	"C0751157"	"FRAXE Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56261"	"GPCPD1"	"1"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"56262"	"LRRC8A"	"0.743"	"0.414"	"C0001768"	"Agammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"56262"	"LRRC8A"	"0.743"	"0.414"	"C0086438"	"Hypogammaglobulinemia"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56262"	"LRRC8A"	"0.743"	"0.414"	"C1832241"	"Agammaglobulinemia, non-Bruton type"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56267"	"KYAT3"	"0.785"	"0.276"	"C0024517"	"Major depression, single episode"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"56267"	"KYAT3"	"0.785"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"56267"	"KYAT3"	"0.785"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"56270"	"WDR45B"	"0.834"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56270"	"WDR45B"	"0.834"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56270"	"WDR45B"	"0.834"	"0.172"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"56270"	"WDR45B"	"0.834"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"56270"	"WDR45B"	"0.834"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56270"	"WDR45B"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2018"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"56271"	"BEX4"	"0.886"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.31"		"2005"	"2008"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"0"	"2005"	"2005"	"0"	"0"	"UNIPROT"
"56287"	"GKN1"	"0.69"	"0.241"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2017"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56287"	"GKN1"	"0.69"	"0.241"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56288"	"PARD3"	"0.69"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56288"	"PARD3"	"0.69"	"0.414"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"1"	"UNIPROT"
"56288"	"PARD3"	"0.69"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"56288"	"PARD3"	"0.69"	"0.414"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2018"	"2018"	"1"	"1"	"UNIPROT"
"56301"	"SLC7A10"	"0.785"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2008"	"2014"	"2"	"0"	"PSYGENET"
"56311"	"ANKRD7"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"56342"	"PPAN"	"0.886"	"0.138"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56474"	"CTPS2"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"56475"	"RPRM"	"0.785"	"0.069"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56475"	"RPRM"	"0.785"	"0.069"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56475"	"RPRM"	"0.785"	"0.069"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56475"	"RPRM"	"0.785"	"0.069"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56479"	"KCNQ5"	"0.762"	"0.345"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56479"	"KCNQ5"	"0.762"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"56479"	"KCNQ5"	"0.762"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56479"	"KCNQ5"	"0.762"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"56479"	"KCNQ5"	"0.762"	"0.345"	"C4539851"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 46"	"disease"		"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"4"	"UNIPROT"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56521"	"DNAJC12"	"0.727"	"0.345"	"C4479270"	"HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"56547"	"MMP26"	"0.659"	"0.448"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56547"	"MMP26"	"0.659"	"0.448"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56547"	"MMP26"	"0.659"	"0.448"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2006"	"1"	"0"	"CTD_human"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0026636"	"Mouth Diseases"	"group"	"C07"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.11"	"1"	"2010"	"2016"	"1"	"1"	"PSYGENET"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"56603"	"CYP26B1"	"0.701"	"0.379"	"C3280729"	"RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"2"	"ORPHANET;UNIPROT"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.40"		"2008"	"2017"	"2"	"6"	"CTD_human"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C0473219"	"Renal hypouricemia"	"disease"	"C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.70"	"0.9166667"	"2008"	"2016"	"2"	"1"	"CTD_human;ORPHANET"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C0740394"	"Hyperuricemia"	"disease"	"C23"	"Disease or Syndrome"	"0.37"	"0.8571429"	"2008"	"2018"	"1"	"0"	"CTD_human"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C2677549"	"Hypouricemia, Renal, 2"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2008"	"2014"	"3"	"6"	"CTD_human;UNIPROT"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C2677550"	"URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.40"		"2008"	"2012"	"3"	"8"	"UNIPROT"
"56606"	"SLC2A9"	"0.642"	"0.552"	"C2677551"	"GOUT SUSCEPTIBILITY 2"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2012"	"3"	"5"	"UNIPROT"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0007786"	"Brain Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0020179"	"Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0393574"	"Huntington Disease, Late Onset"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0751207"	"Akinetic-Rigid Variant of Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0751208"	"Juvenile Huntington Disease"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C0917798"	"Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"56616"	"DIABLO"	"0.596"	"0.552"	"C3279948"	"DEAFNESS, AUTOSOMAL DOMINANT 64"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0008780"	"Ciliary Motility Disorders"	"group"	"C08;C09;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0015398"	"Eye Diseases, Hereditary"	"group"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2009"	"2013"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0030846"	"Penile Diseases"	"group"	"C12"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.76"	"1"	"2003"	"2018"	"3"	"19"	"CTD_human;ORPHANET;UNIPROT"
"56623"	"INPP5E"	"0.63"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56623"	"INPP5E"	"0.63"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56623"	"INPP5E"	"0.63"	"0.552"	"C1857662"	"COACH syndrome"	"disease"	"C06;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56623"	"INPP5E"	"0.63"	"0.552"	"C1857802"	"MORM syndrome"	"disease"	"C10;C11;C12;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"2009"	"2009"	"0"	"1"	"CTD_human;ORPHANET"
"56623"	"INPP5E"	"0.63"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2009"	"2016"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"56623"	"INPP5E"	"0.63"	"0.552"	"C4274118"	"Joubert syndrome with ocular defect"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56623"	"INPP5E"	"0.63"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2009"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"56624"	"ASAH2"	"0.886"	"0.241"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56624"	"ASAH2"	"0.886"	"0.241"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56649"	"TMPRSS4"	"0.659"	"0.276"	"C0235946"	"Cerebral atrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56652"	"TWNK"	"0.567"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56652"	"TWNK"	"0.567"	"0.517"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56652"	"TWNK"	"0.567"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56652"	"TWNK"	"0.567"	"0.517"	"C0685838"	"Gonadal dysgenesis XX type deafness"	"disease"	"C09;C10;C12;C13;C16;C19;C23"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"56652"	"TWNK"	"0.567"	"0.517"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.45"	"1"	"2010"	"2017"	"0"	"4"	"GENOMICS_ENGLAND"
"56652"	"TWNK"	"0.567"	"0.517"	"C1834846"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"	"disease"	"C10;C11;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56652"	"TWNK"	"0.567"	"0.517"	"C1836439"	"Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.60"		"1999"	"2011"	"12"	"12"	"CTD_human;UNIPROT"
"56652"	"TWNK"	"0.567"	"0.517"	"C1843851"	"Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"56652"	"TWNK"	"0.567"	"0.517"	"C1849096"	"Infantile onset spinocerebellar ataxia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.77"	"1"	"1993"	"2016"	"5"	"8"	"CTD_human;ORPHANET;UNIPROT"
"56652"	"TWNK"	"0.567"	"0.517"	"C4015307"	"PERRAULT SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"4"	"UNIPROT"
"56654"	"NPDC1"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56660"	"KCNK12"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56666"	"PANX2"	"0.799"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"56666"	"PANX2"	"0.799"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.02"	"0.5"	"2007"	"2017"	"1"	"0"	"PSYGENET"
"56683"	"CFAP298"	"0.735"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2014"	"0"	"3"	"ORPHANET"
"56683"	"CFAP298"	"0.735"	"0.207"	"C3809684"	"CILIARY DYSKINESIA, PRIMARY, 26"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"4"	"CTD_human"
"56683"	"CFAP298"	"0.735"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"56704"	"JPH1"	"0.815"	"0.138"	"C1842983"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2001"	"2015"	"0"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0019337"	"Heroin Dependence"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0403447"	"Chronic Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9166667"	"2003"	"2015"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C1561643"	"Chronic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"56729"	"RETN"	"0.542"	"0.759"	"C4505390"	"Heroin Smoking"	"disease"	"C25"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56776"	"FMN2"	"0.69"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"56776"	"FMN2"	"0.69"	"0.345"	"C4015444"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"CTD_human"
"56833"	"SLAMF8"	"0.928"	"0.034"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0238281"	"Middle Cerebral Artery Syndrome"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0740376"	"Middle Cerebral Artery Thrombosis"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0740391"	"Middle Cerebral Artery Occlusion"	"phenotype"	"C10;C14"	"Acquired Abnormality"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0740392"	"Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751845"	"Middle Cerebral Artery Embolus"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751846"	"Left Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751847"	"Embolic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751848"	"Thrombotic Infarction, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56848"	"SPHK2"	"0.609"	"0.483"	"C0751849"	"Right Middle Cerebral Artery Infarction"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56849"	"TCEAL7"	"0.773"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"56849"	"TCEAL7"	"0.773"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"56882"	"CDC42SE1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56884"	"FSTL5"	"0.857"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"56891"	"LGALS14"	"0.735"	"0.345"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56891"	"LGALS14"	"0.735"	"0.345"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56894"	"AGPAT3"	"1"	"0.034"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56894"	"AGPAT3"	"1"	"0.034"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56894"	"AGPAT3"	"1"	"0.034"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"56899"	"ANKS1B"	"0.743"	"0.276"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56899"	"ANKS1B"	"0.743"	"0.276"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56901"	"NDUFA4L2"	"1"	"0.103"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"56915"	"EXOSC5"	"0.799"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56915"	"EXOSC5"	"0.799"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56915"	"EXOSC5"	"0.799"	"0.103"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56915"	"EXOSC5"	"0.799"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C0406707"	"Basan syndrome"	"disease"	"C16;C17;C23"	"Disease or Syndrome"	"0.60"		"2011"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"56916"	"SMARCAD1"	"0.752"	"0.241"	"C1852150"	"Fingerprints, Absence of"	"phenotype"	"C16;C17"	"Finding"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"56922"	"MCCC1"	"0.743"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"56922"	"MCCC1"	"0.743"	"0.276"	"C0268600"	"3-methylcrotonyl CoA carboxylase 1 deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2001"	"2017"	"11"	"22"	"CTD_human;ORPHANET;UNIPROT"
"56922"	"MCCC1"	"0.743"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"56923"	"NMUR2"	"0.857"	"0.207"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"56924"	"PAK6"	"0.773"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"56924"	"PAK6"	"0.773"	"0.241"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56924"	"PAK6"	"0.773"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.35"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"56924"	"PAK6"	"0.773"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"56925"	"LXN"	"0.681"	"0.517"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human"
"56925"	"LXN"	"0.681"	"0.517"	"C1257806"	"Chromosomal Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56929"	"FEM1C"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56937"	"PMEPA1"	"0.676"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56938"	"ARNTL2"	"0.72"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2010"	"2"	"0"	"PSYGENET"
"56938"	"ARNTL2"	"0.72"	"0.414"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"56942"	"CMC2"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56942"	"CMC2"	"0.857"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56942"	"CMC2"	"0.857"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56942"	"CMC2"	"0.857"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56944"	"OLFML3"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56945"	"MRPS22"	"0.773"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56945"	"MRPS22"	"0.773"	"0.345"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56945"	"MRPS22"	"0.773"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"56945"	"MRPS22"	"0.773"	"0.345"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56945"	"MRPS22"	"0.773"	"0.345"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56945"	"MRPS22"	"0.773"	"0.345"	"C2673642"	"Combined Oxidative Phosphorylation Deficiency 5"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2008"	"2011"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"56945"	"MRPS22"	"0.773"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56946"	"EMSY"	"0.676"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.8571429"	"2004"	"2014"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"56946"	"EMSY"	"0.676"	"0.379"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"56947"	"MFF"	"0.72"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56947"	"MFF"	"0.72"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56947"	"MFF"	"0.72"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"56947"	"MFF"	"0.72"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56947"	"MFF"	"0.72"	"0.345"	"C4310726"	"ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"56950"	"SMYD2"	"0.707"	"0.31"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56950"	"SMYD2"	"0.707"	"0.31"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"56952"	"PRTFDC1"	"0.785"	"0.31"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"56955"	"MEPE"	"0.672"	"0.483"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56955"	"MEPE"	"0.672"	"0.483"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"56955"	"MEPE"	"0.672"	"0.483"	"C3887650"	"Adult Rickets"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.33"	"1"	"2001"	"2014"	"1"	"0"	"CTD_human"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2017"	"11"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2000"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56975"	"FAM20C"	"0.619"	"0.586"	"C1850106"	"RAINE SYNDROME"	"disease"	"C05;C07;C10;C11;C16"	"Disease or Syndrome"	"0.80"	"1"	"1991"	"2017"	"3"	"13"	"CTD_human;ORPHANET;UNIPROT"
"56975"	"FAM20C"	"0.619"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56978"	"PRDM8"	"0.707"	"0.241"	"C4225258"	"EPILEPSY, PROGRESSIVE MYOCLONIC, 10"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"ORPHANET;UNIPROT"
"56981"	"PRDM11"	"0.834"	"0.172"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"56981"	"PRDM11"	"0.834"	"0.172"	"C1332201"	"Adult Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"56981"	"PRDM11"	"0.834"	"0.172"	"C1332967"	"Childhood Diffuse Large B-Cell Lymphoma"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"2"	"UNIPROT"
"56983"	"POGLUT1"	"0.815"	"0.103"	"C0406811"	"Reticulate acropigmentation of Kitamura"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"56983"	"POGLUT1"	"0.815"	"0.103"	"C3714534"	"dowling-degos disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"56983"	"POGLUT1"	"0.815"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56983"	"POGLUT1"	"0.815"	"0.103"	"C3810313"	"DOWLING-DEGOS DISEASE 4"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2017"	"2"	"5"	"UNIPROT"
"56983"	"POGLUT1"	"0.815"	"0.103"	"C4310660"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"56990"	"CDC42SE2"	"0.773"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2012"	"2"	"0"	"PSYGENET"
"56992"	"KIF15"	"0.785"	"0.414"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"56992"	"KIF15"	"0.785"	"0.414"	"C2931364"	"Thrombocytopenia Robin sequence"	"disease"	"C05;C07;C10;C15;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"56994"	"CHPT1"	"0.524"	"0.655"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"56997"	"COQ8A"	"0.727"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56997"	"COQ8A"	"0.727"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56997"	"COQ8A"	"0.727"	"0.276"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56997"	"COQ8A"	"0.727"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"56997"	"COQ8A"	"0.727"	"0.276"	"C2677589"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2017"	"9"	"30"	"CTD_human;ORPHANET;UNIPROT"
"56997"	"COQ8A"	"0.727"	"0.276"	"C3551954"	"COENZYME Q10 DEFICIENCY, PRIMARY, 1"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"56997"	"COQ8A"	"0.727"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"56999"	"ADAMTS9"	"0.69"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.35"	"1"	"2008"	"2014"	"2"	"0"	"CTD_human"
"57001"	"SDHAF3"	"0.857"	"0.103"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"1999"	"2010"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.962963"	"2005"	"2017"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57007"	"ACKR3"	"0.494"	"0.759"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"57010"	"CABP4"	"0.727"	"0.138"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.43"	"1"	"2006"	"2013"	"0"	"0"	"ORPHANET"
"57010"	"CABP4"	"0.727"	"0.138"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"1"	"1"	"CTD_human;UNIPROT"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0011616"	"Contact Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0162351"	"Contact hypersensitivity"	"phenotype"	"C17"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"57016"	"AKR1B10"	"0.588"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1999"	"2016"	"1"	"0"	"CTD_human"
"57017"	"COQ9"	"0.676"	"0.345"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57017"	"COQ9"	"0.676"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57017"	"COQ9"	"0.676"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"57017"	"COQ9"	"0.676"	"0.345"	"C3553374"	"COENZYME Q10 DEFICIENCY, PRIMARY, 5"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"57017"	"COQ9"	"0.676"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2010"	"2"	"0"	"PSYGENET"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.25"	"2004"	"2013"	"4"	"0"	"PSYGENET"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0178417"	"Anhedonia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2013"	"2"	"0"	"PSYGENET"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57030"	"SLC17A7"	"0.645"	"0.207"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57035"	"RSRP1"	"0.886"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57038"	"RARS2"	"0.672"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57038"	"RARS2"	"0.672"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57038"	"RARS2"	"0.672"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2007"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"57038"	"RARS2"	"0.672"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57038"	"RARS2"	"0.672"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57038"	"RARS2"	"0.672"	"0.379"	"C1843504"	"Pontocerebellar Hypoplasia Type 1"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"57038"	"RARS2"	"0.672"	"0.379"	"C1969084"	"Pontocerebellar Hypoplasia Type 6"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.65"	"1"	"2010"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"57038"	"RARS2"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0022360"	"Jaw Abnormalities"	"group"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0078982"	"Arhinencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2011"	"1"	"0"	"CTD_human"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57045"	"TWSG1"	"0.598"	"0.586"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57047"	"PLSCR2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57054"	"DAZ3"	"0.815"	"0.172"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"57054"	"DAZ3"	"0.815"	"0.172"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57054"	"DAZ3"	"0.815"	"0.172"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57055"	"DAZ2"	"0.785"	"0.172"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"57055"	"DAZ2"	"0.785"	"0.172"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57055"	"DAZ2"	"0.785"	"0.172"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57057"	"TBX20"	"0.743"	"0.069"	"C0344724"	"Ostium secundum atrial septal defect"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57057"	"TBX20"	"0.743"	"0.069"	"C1969657"	"Atrial Septal Defect 4"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2007"	"2010"	"2"	"3"	"CTD_human;UNIPROT"
"57057"	"TBX20"	"0.743"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57061"	"HYMAI"	"0.696"	"0.414"	"C1832386"	"Diabetes Mellitus, Transient Neonatal, 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.52"	"1"	"2000"	"2004"	"0"	"0"	"CTD_human;ORPHANET"
"57082"	"KNL1"	"0.696"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"57082"	"KNL1"	"0.696"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.33"	"1"	"2010"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"57082"	"KNL1"	"0.696"	"0.414"	"C1858516"	"MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2013"	"2016"	"2"	"5"	"CTD_human;UNIPROT"
"57082"	"KNL1"	"0.696"	"0.414"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"57082"	"KNL1"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0025261"	"Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2010"	"3"	"0"	"PSYGENET"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0233794"	"Memory impairment"	"phenotype"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751292"	"Age-Related Memory Disorders"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751293"	"Memory Disorder, Semantic"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751294"	"Memory Disorder, Spatial"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C0751295"	"Memory Loss"	"phenotype"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"57084"	"SLC17A6"	"0.707"	"0.276"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57088"	"PLSCR4"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"57088"	"PLSCR4"	"0.815"	"0.172"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57094"	"CPA6"	"0.735"	"0.172"	"C3280730"	"EPILEPSY, FAMILIAL TEMPORAL LOBE, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"57094"	"CPA6"	"0.735"	"0.172"	"C3280734"	"FEBRILE SEIZURES, FAMILIAL, 11"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"57094"	"CPA6"	"0.735"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0028738"	"Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.41"	"1"	"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.59"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0155380"	"Dissociated Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0240595"	"Rotary Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271382"	"Periodic Alternating Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271383"	"Symptomatic Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271384"	"Spontaneous Ocular Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271385"	"Horizontal Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271386"	"Vertical Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271387"	"Rebound Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271388"	"Pendular Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0271389"	"Jerk Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"1"	"2001"	"2018"	"2"	"4"	"CTD_human;ORPHANET"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0344243"	"See-Saw Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0520731"	"Retraction Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521753"	"Temporary Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521754"	"Permanent Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521755"	"Unidirectional Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521756"	"Multidirectional Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521757"	"Conjugate Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521759"	"Convergence Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521760"	"Fatigable Positional Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0521761"	"Non-Fatigable Positional Nystagmus"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C0854723"	"Retinal Dystrophies"	"group"	"C11"	"Disease or Syndrome"	"0.43"	"1"	"2003"	"2013"	"1"	"5"	"CTD_human"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C1854260"	"LEBER CONGENITAL AMAUROSIS 6 (disorder)"	"disease"	"C11"	"Congenital Abnormality; Disease or Syndrome"	"0.80"		"2001"	"2017"	"5"	"11"	"CTD_human;UNIPROT"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C2750720"	"Cone-Rod Dystrophy 13"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"2"	"5"	"CTD_human;UNIPROT"
"57096"	"RPGRIP1"	"0.567"	"0.448"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"2"	"0"	"CTD_human"
"57099"	"AVEN"	"0.785"	"0.207"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"57102"	"C12orf4"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"2"	"0"	"CTD_human"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57104"	"PNPLA2"	"0.559"	"0.69"	"C1853136"	"Neutral Lipid Storage Disease with Myopathy"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"2007"	"2016"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0220633"	"Uveal melanoma"	"disease"	"C04;C11"	"Neoplastic Process"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0346373"	"Malignant melanoma of iris"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C0346388"	"Malignant melanoma of choroid"	"disease"		"Neoplastic Process"	"0.40"				"0"	"0"	"ORPHANET"
"57105"	"CYSLTR2"	"0.69"	"0.345"	"C1319853"	"Asthma, Aspirin-Induced"	"disease"	"C08;C20;C25"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2010"	"2"	"0"	"CTD_human"
"57107"	"PDSS2"	"0.642"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57107"	"PDSS2"	"0.642"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57107"	"PDSS2"	"0.642"	"0.448"	"C3553358"	"COENZYME Q10 DEFICIENCY, PRIMARY, 3"	"disease"		"Disease or Syndrome"	"0.80"		"1971"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"57107"	"PDSS2"	"0.642"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57113"	"TRPC7"	"0.815"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"57113"	"TRPC7"	"0.815"	"0.103"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"57120"	"GOPC"	"0.63"	"0.483"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57122"	"NUP107"	"0.645"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"57122"	"NUP107"	"0.645"	"0.379"	"C0685837"	"Pure Gonadal Dysgenesis, 46, XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57122"	"NUP107"	"0.645"	"0.379"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57122"	"NUP107"	"0.645"	"0.379"	"C0949595"	"Gonadal Dysgenesis, 46,XX"	"disease"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"57122"	"NUP107"	"0.645"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57122"	"NUP107"	"0.645"	"0.379"	"C4225228"	"NEPHROTIC SYNDROME, TYPE 11"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"57124"	"CD248"	"0.69"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"UNIPROT"
"57128"	"LYRM4"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"57128"	"LYRM4"	"0.773"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57128"	"LYRM4"	"0.773"	"0.207"	"C3810055"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"57132"	"CHMP1B"	"0.799"	"0.345"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2005"	"2007"	"2"	"0"	"PSYGENET"
"57135"	"DAZ4"	"0.857"	"0.172"	"C1507149"	"Partial chromosome Y deletion"	"phenotype"	"C12;C13;C16;C19;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"57135"	"DAZ4"	"0.857"	"0.172"	"C2931163"	"Male sterility due to Y-chromosome deletions"	"disease"	"C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57136"	"APMAP"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57140"	"RNPEPL1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57142"	"RTN4"	"0.667"	"0.448"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"57142"	"RTN4"	"0.667"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57142"	"RTN4"	"0.667"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.875"	"2003"	"2012"	"1"	"0"	"CTD_human"
"57142"	"RTN4"	"0.667"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57144"	"PAK5"	"0.672"	"0.345"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"57144"	"PAK5"	"0.672"	"0.345"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57144"	"PAK5"	"0.672"	"0.345"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57144"	"PAK5"	"0.672"	"0.345"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"57144"	"PAK5"	"0.672"	"0.345"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"57152"	"SLURP1"	"0.636"	"0.345"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.56"	"1"	"1999"	"2017"	"17"	"0"	"CTD_human;GENOMICS_ENGLAND"
"57152"	"SLURP1"	"0.636"	"0.345"	"C0025221"	"Meleda Disease"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"1.00"	"0.9166667"	"1999"	"2018"	"10"	"9"	"CTD_human;ORPHANET;UNIPROT"
"57152"	"SLURP1"	"0.636"	"0.345"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"1999"	"2017"	"16"	"0"	"GENOMICS_ENGLAND"
"57152"	"SLURP1"	"0.636"	"0.345"	"C1855644"	"Keratoderma, Palmoplantar, Norrbotten Recessive Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57153"	"SLC44A2"	"0.834"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57158"	"JPH2"	"0.815"	"0.138"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.56"	"1"	"2007"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"57158"	"JPH2"	"0.815"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57158"	"JPH2"	"0.815"	"0.138"	"C3151264"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17"	"disease"		"Disease or Syndrome"	"0.70"		"2004"	"2017"	"9"	"2"	"CLINGEN;CTD_human;UNIPROT"
"57162"	"PELI1"	"0.752"	"0.379"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57162"	"PELI1"	"0.752"	"0.379"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57162"	"PELI1"	"0.752"	"0.379"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57162"	"PELI1"	"0.752"	"0.379"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57162"	"PELI1"	"0.752"	"0.379"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57162"	"PELI1"	"0.752"	"0.379"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57165"	"GJC2"	"0.619"	"0.517"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57165"	"GJC2"	"0.619"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2011"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"57165"	"GJC2"	"0.619"	"0.517"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57165"	"GJC2"	"0.619"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"57165"	"GJC2"	"0.619"	"0.517"	"C1704423"	"Milroy Disease"	"disease"	"C15"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2011"	"0"	"0"	"ORPHANET"
"57165"	"GJC2"	"0.619"	"0.517"	"C1837355"	"Leukodystrophy, Hypomyelinating, 2"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.92"	"1"	"2004"	"2015"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"57165"	"GJC2"	"0.619"	"0.517"	"C2750784"	"SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"57165"	"GJC2"	"0.619"	"0.517"	"C3150732"	"LYMPHEDEMA, HEREDITARY, IC"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2011"	"1"	"2"	"CTD_human;UNIPROT"
"57165"	"GJC2"	"0.619"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57167"	"SALL4"	"0.524"	"0.69"	"C0008297"	"Choanal Atresia"	"disease"	"C08;C09;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57167"	"SALL4"	"0.524"	"0.69"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"57167"	"SALL4"	"0.524"	"0.69"	"C0013261"	"Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.49"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"57167"	"SALL4"	"0.524"	"0.69"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57167"	"SALL4"	"0.524"	"0.69"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57167"	"SALL4"	"0.524"	"0.69"	"C0751083"	"Duane Retraction Syndrome, Type 2"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57167"	"SALL4"	"0.524"	"0.69"	"C0751084"	"Duane Retraction Syndrome, Type 3"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.70"		"2003"	"2007"	"3"	"1"	"CTD_human;UNIPROT"
"57167"	"SALL4"	"0.524"	"0.69"	"C0994516"	"Type 1 Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57167"	"SALL4"	"0.524"	"0.69"	"C1327918"	"Oculootoradial syndrome"	"disease"	"C05;C06;C09;C10;C11;C15;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2007"	"0"	"0"	"CTD_human;ORPHANET"
"57167"	"SALL4"	"0.524"	"0.69"	"C1623209"	"Okihiro Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"1.00"	"1"	"1977"	"2016"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"57167"	"SALL4"	"0.524"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57167"	"SALL4"	"0.524"	"0.69"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57172"	"CAMK1G"	"0.857"	"0.138"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"57172"	"CAMK1G"	"0.857"	"0.138"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57172"	"CAMK1G"	"0.857"	"0.138"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57172"	"CAMK1G"	"0.857"	"0.138"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57175"	"CORO1B"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"57176"	"VARS2"	"0.762"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"57176"	"VARS2"	"0.762"	"0.448"	"C4014660"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2015"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"57178"	"ZMIZ1"	"0.63"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"UNIPROT"
"57178"	"ZMIZ1"	"0.63"	"0.414"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"		"2010"	"2015"	"1"	"2"	"CTD_human"
"57178"	"ZMIZ1"	"0.63"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57178"	"ZMIZ1"	"0.63"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57178"	"ZMIZ1"	"0.63"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57181"	"SLC39A10"	"0.857"	"0.138"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57185"	"NIPAL3"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57185"	"NIPAL3"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57187"	"THOC2"	"0.762"	"0.172"	"C0796218"	"MENTAL RETARDATION, X-LINKED 12"	"disease"		"Disease or Syndrome"	"0.70"		"1992"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"57187"	"THOC2"	"0.762"	"0.172"	"C0796242"	"MENTAL RETARDATION, X-LINKED 35"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"57187"	"THOC2"	"0.762"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"1996"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"57188"	"ADAMTSL3"	"0.785"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2017"	"1"	"2"	"PSYGENET"
"57188"	"ADAMTSL3"	"0.785"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"2"	"UNIPROT"
"57190"	"SELENON"	"0.636"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"57190"	"SELENON"	"0.636"	"0.379"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.48"	"1"	"2002"	"2008"	"1"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.34"	"1"	"2005"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"57190"	"SELENON"	"0.636"	"0.379"	"C0410180"	"Eichsfeld type congenital muscular dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"1.00"	"1"	"1999"	"2017"	"6"	"19"	"CTD_human;ORPHANET;UNIPROT"
"57190"	"SELENON"	"0.636"	"0.379"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.75"	"1"	"1993"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"57190"	"SELENON"	"0.636"	"0.379"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2001"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"57190"	"SELENON"	"0.636"	"0.379"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57190"	"SELENON"	"0.636"	"0.379"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0020725"	"Type II Mucolipidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0023806"	"Lipomucopolysaccharidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0026697"	"Mucolipidoses"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"2002"	"2016"	"2"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0033788"	"Pseudo-Hurler Polydystrophy"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0238286"	"Mucolipidosis Type IV"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.80"	"0.952381"	"1993"	"2017"	"14"	"33"	"CTD_human;ORPHANET;UNIPROT"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C0268226"	"Type I Mucolipidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"57192"	"MCOLN1"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57194"	"ATP10A"	"0.815"	"0.241"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2001"	"2011"	"1"	"0"	"CTD_human"
"57205"	"ATP10D"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57211"	"ADGRG6"	"0.785"	"0.241"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"57211"	"ADGRG6"	"0.785"	"0.241"	"C2700406"	"SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)"	"phenotype"		"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57211"	"ADGRG6"	"0.785"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57211"	"ADGRG6"	"0.785"	"0.241"	"C4225303"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 9"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0028945"	"oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0279070"	"Adult Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0280475"	"Childhood Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0280793"	"Mixed Oligodendroglioma-Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0334590"	"Anaplastic Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0344461"	"Oligodendroblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0751395"	"Mixed Oligodendroglioma-Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57212"	"TP73-AS1"	"0.743"	"0.172"	"C0751396"	"Well Differentiated Oligodendroglioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0002902"	"Anencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.39"	"1"	"1990"	"2016"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0038219"	"Status Dysraphicus"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.51"	"1"	"2010"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.34"	"0.75"	"1990"	"2014"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0266452"	"Hemicephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0266508"	"Rachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0266672"	"Amyelencephalus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0302356"	"incomplete anencephaly, hemicrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0685896"	"Acephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.50"		"1990"	"1990"	"1"	"0"	"CTD_human;ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57216"	"VANGL2"	"0.607"	"0.414"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57216"	"VANGL2"	"0.607"	"0.414"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2010"	"2010"	"1"	"2"	"UNIPROT"
"57217"	"TTC7A"	"0.743"	"0.345"	"C0220744"	"Multiple gastrointestinal atresias (disorder)"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.75"	"1"	"2013"	"2017"	"8"	"20"	"CTD_human;ORPHANET;UNIPROT"
"57217"	"TTC7A"	"0.743"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57231"	"SNX14"	"0.656"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57231"	"SNX14"	"0.656"	"0.241"	"C0007758"	"Cerebellar Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.43"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0234162"	"Cerebellar Dysmetria"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0234357"	"Adiadochokinesis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"57231"	"SNX14"	"0.656"	"0.241"	"C0750994"	"Cerebellar Hemiataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C3668822"	"Hypermetria (finding)"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57231"	"SNX14"	"0.656"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.52"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"57231"	"SNX14"	"0.656"	"0.241"	"C4225355"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2017"	"0"	"9"	"ORPHANET"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0085541"	"Epilepsy, Frontal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0151740"	"Intracranial Hypertension"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0393671"	"Frontal Epilepsy, Benign, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0393683"	"Epilepsy, Supplementary Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0393684"	"Epilepsy, Cingulate"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0393688"	"Epilepsy, Opercular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0751642"	"Epilepsy, Anterior Fronto-Polar"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0751643"	"Epilepsy, Orbito-Frontal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57282"	"SLC4A10"	"0.69"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"57309"	"SPG14"	"0.886"	"0.172"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57309"	"SPG14"	"0.886"	"0.172"	"C1854568"	"SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57333"	"RCN3"	"0.928"	"0.034"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57333"	"RCN3"	"0.928"	"0.034"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57338"	"JPH3"	"0.619"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57338"	"JPH3"	"0.619"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57338"	"JPH3"	"0.619"	"0.414"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57338"	"JPH3"	"0.619"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57338"	"JPH3"	"0.619"	"0.414"	"C1847987"	"HUNTINGTON DISEASE-LIKE 2"	"disease"	"C10;C16;C23;F03"	"Disease or Syndrome"	"0.57"	"1"	"2001"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"57369"	"GJD2"	"0.773"	"0.276"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.35"	"0.8"	"2012"	"2018"	"1"	"0"	"CTD_human"
"57369"	"GJD2"	"0.773"	"0.276"	"C0034951"	"Refractive Errors"	"group"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"57369"	"GJD2"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"57369"	"GJD2"	"0.773"	"0.276"	"C0036344"	"Schizophrenia, Catatonic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"57369"	"GJD2"	"0.773"	"0.276"	"C1527310"	"Ametropia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C0004364"	"Autoimmune Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C0005699"	"Blast Phase"	"disease"	"C04;C15;C23"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C0272236"	"Hyperimmunoglobulin M syndrome"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2011"	"0"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C1720956"	"Hyper-IgM Immunodeficiency Syndrome, Type 2"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.73"	"1"	"2000"	"2016"	"5"	"12"	"CTD_human;ORPHANET;UNIPROT"
"57379"	"AICDA"	"0.484"	"0.862"	"C1720957"	"Hyper-IgM Immunodeficiency Syndrome, Type 3"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57379"	"AICDA"	"0.484"	"0.862"	"C1720958"	"Hyper-IgM Immunodeficiency Syndrome, Type 5"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57381"	"RHOJ"	"0.727"	"0.276"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57381"	"RHOJ"	"0.727"	"0.276"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57381"	"RHOJ"	"0.727"	"0.276"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57381"	"RHOJ"	"0.727"	"0.276"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57381"	"RHOJ"	"0.727"	"0.276"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57410"	"SCYL1"	"0.621"	"0.483"	"C4225236"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0027660"	"Neoplasms, Glandular and Epithelial"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0205854"	"Glandular Neoplasms"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2015"	"2"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2015"	"1"	"1"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57412"	"AS3MT"	"0.672"	"0.31"	"C1368683"	"Epithelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57419"	"SLC24A3"	"0.834"	"0.138"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57419"	"SLC24A3"	"0.834"	"0.138"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57419"	"SLC24A3"	"0.834"	"0.138"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2004"	"2008"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0007787"	"Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0472381"	"Posterior Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0524524"	"Pseudoaphakia"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0751019"	"Carotid Circulation Transient Ischemic Attack"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0751020"	"Transient Ischemic Attack, Vertebrobasilar Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0751021"	"Crescendo Transient Ischemic Attacks"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0751022"	"Brain Stem Ischemia, Transient"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C0917805"	"Transient Cerebral Ischemia"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C1510497"	"Lens Opacities"	"phenotype"	"C11"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57447"	"NDRG2"	"0.558"	"0.621"	"C1527335"	"Transient Ischemic Attack, Anterior Circulation"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57448"	"BIRC6"	"0.681"	"0.345"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57448"	"BIRC6"	"0.681"	"0.345"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57448"	"BIRC6"	"0.681"	"0.345"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57449"	"PLEKHG5"	"0.735"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"57449"	"PLEKHG5"	"0.735"	"0.241"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57449"	"PLEKHG5"	"0.735"	"0.241"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57449"	"PLEKHG5"	"0.735"	"0.241"	"C1970211"	"Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2006"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"57449"	"PLEKHG5"	"0.735"	"0.241"	"C3809309"	"CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2017"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"57451"	"TENM2"	"0.773"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57451"	"TENM2"	"0.773"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57453"	"DSCAML1"	"0.928"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"57453"	"DSCAML1"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57455"	"REXO1"	"0.713"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57455"	"REXO1"	"0.713"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57459"	"GATAD2B"	"0.69"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57459"	"GATAD2B"	"0.69"	"0.448"	"C3554448"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 18"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"57459"	"GATAD2B"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CLINGEN"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0795927"	"Deafness, congenital onychodystrophy, recessive form"	"disease"	"C05;C09;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0795934"	"Digitorenocerebral Syndrome"	"disease"	"C05;C09;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.34"	"0.75"	"2014"	"2015"	"1"	"5"	"UNIPROT"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.66"	"1"	"1993"	"2017"	"2"	"5"	"ORPHANET;UNIPROT"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CLINGEN"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C2829265"	"DEAFNESS, AUTOSOMAL RECESSIVE 86"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C3809173"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"2"	"6"	"UNIPROT"
"57465"	"TBC1D24"	"0.614"	"0.483"	"C3892048"	"DEAFNESS, AUTOSOMAL DOMINANT 65"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.56"	"1"	"2002"	"2018"	"2"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0014556"	"Epilepsy, Temporal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0014558"	"Uncinate Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2011"	"2012"	"3"	"0"	"PSYGENET"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2008"	"2"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2002"	"2008"	"2"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0270850"	"Idiopathic generalized epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0393672"	"Epilepsy, Benign Psychomotor, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0393682"	"Epilepsy, Lateral Temporal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2002"	"2008"	"2"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"UNIPROT"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4225245"	"EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14"	"phenotype"		"Finding"	"0.40"		"2015"	"2015"	"3"	"2"	"UNIPROT"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4225257"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57468"	"SLC12A5"	"0.584"	"0.414"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57470"	"LRRC47"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57475"	"PLEKHH1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57477"	"SHROOM4"	"0.752"	"0.345"	"C1845530"	"Stocco dos Santos syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"		"2004"	"2006"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"57477"	"SHROOM4"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"57480"	"PLEKHG1"	"0.834"	"0.103"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57480"	"PLEKHG1"	"0.834"	"0.103"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57480"	"PLEKHG1"	"0.834"	"0.103"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57480"	"PLEKHG1"	"0.834"	"0.103"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57489"	"ODF2L"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"				"0"	"0"	"CGI;UNIPROT"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.66"	"1"	"2012"	"2016"	"2"	"2"	"CTD_human;ORPHANET"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"57492"	"ARID1B"	"0.561"	"0.655"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"57492"	"ARID1B"	"0.561"	"0.655"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"57492"	"ARID1B"	"0.561"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.51"	"1"	"2012"	"2018"	"1"	"0"	"CGI;CTD_human"
"57492"	"ARID1B"	"0.561"	"0.655"	"C3150215"	"CHROMOSOME 6q24-q25 DELETION SYNDROME"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57492"	"ARID1B"	"0.561"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2012"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"57496"	"MKL2"	"0.834"	"0.207"	"C0008074"	"Child Development Disorders, Pervasive"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57496"	"MKL2"	"0.834"	"0.207"	"C0524528"	"Pervasive Development Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57498"	"KIDINS220"	"0.579"	"0.655"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57498"	"KIDINS220"	"0.579"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.875"	"2003"	"2016"	"1"	"0"	"CTD_human"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8666667"	"2003"	"2016"	"1"	"0"	"CTD_human"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C1845334"	"ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"57502"	"NLGN4X"	"0.743"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.45"	"0.6"	"1999"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"57505"	"AARS2"	"0.663"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"57505"	"AARS2"	"0.663"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2015"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"57505"	"AARS2"	"0.663"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"57505"	"AARS2"	"0.663"	"0.379"	"C1847967"	"OVARIOLEUKODYSTROPHY"	"disease"	"C10;C13;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57505"	"AARS2"	"0.663"	"0.379"	"C3279793"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2014"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"57505"	"AARS2"	"0.663"	"0.379"	"C3711381"	"Hereditary Diffuse Leukoencephalopathy with Spheroids"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57505"	"AARS2"	"0.663"	"0.379"	"C4014588"	"LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"57509"	"MTUS1"	"0.659"	"0.448"	"C0206624"	"Hepatoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"57509"	"MTUS1"	"0.659"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"57509"	"MTUS1"	"0.659"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"3"	"UNIPROT"
"57509"	"MTUS1"	"0.659"	"0.448"	"C2676033"	"Hepatoblastoma Caused By Somatic Mutation"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"3"	"UNIPROT"
"57510"	"XPO5"	"0.681"	"0.31"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57510"	"XPO5"	"0.681"	"0.31"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57510"	"XPO5"	"0.681"	"0.31"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57510"	"XPO5"	"0.681"	"0.31"	"C1868672"	"NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57510"	"XPO5"	"0.681"	"0.31"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57511"	"COG6"	"0.685"	"0.379"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"57511"	"COG6"	"0.685"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57511"	"COG6"	"0.685"	"0.379"	"C3553230"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2010"	"2016"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"57511"	"COG6"	"0.685"	"0.379"	"C3809160"	"SHAHEEN SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2016"	"0"	"1"	"ORPHANET"
"57514"	"ARHGAP31"	"0.602"	"0.621"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"2011"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"57514"	"ARHGAP31"	"0.602"	"0.621"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"57514"	"ARHGAP31"	"0.602"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"57520"	"HECW2"	"0.701"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57520"	"HECW2"	"0.701"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57520"	"HECW2"	"0.701"	"0.345"	"C4310643"	"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"57521"	"RPTOR"	"0.676"	"0.552"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57521"	"RPTOR"	"0.676"	"0.552"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57521"	"RPTOR"	"0.676"	"0.552"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57521"	"RPTOR"	"0.676"	"0.552"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57522"	"SRGAP1"	"0.785"	"0.31"	"C2931367"	"Thyroid cancer, follicular"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"57522"	"SRGAP1"	"0.785"	"0.31"	"C4225426"	"THYROID CANCER, NONMEDULLARY, 2"	"disease"		"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"4"	"UNIPROT"
"57523"	"NYNRIN"	"1"	"0.069"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9722222"	"2008"	"2018"	"1"	"0"	"CTD_human"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57526"	"PCDH19"	"0.656"	"0.207"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"57526"	"PCDH19"	"0.656"	"0.207"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57526"	"PCDH19"	"0.656"	"0.207"	"C1848137"	"EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION (disorder)"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.72"	"1"	"1990"	"2017"	"12"	"20"	"CTD_human;ORPHANET;UNIPROT"
"57526"	"PCDH19"	"0.656"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"1971"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"57529"	"RTL9"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57531"	"HACE1"	"0.701"	"0.448"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.61"	"1"	"2012"	"2012"	"1"	"5"	"CTD_human;ORPHANET"
"57531"	"HACE1"	"0.701"	"0.448"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57531"	"HACE1"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57531"	"HACE1"	"0.701"	"0.448"	"C4225215"	"SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"8"	"ORPHANET"
"57532"	"NUFIP2"	"0.713"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"57534"	"MIB1"	"0.478"	"0.69"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"57534"	"MIB1"	"0.478"	"0.69"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C3554496"	"LEFT VENTRICULAR NONCOMPACTION 7"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"57534"	"MIB1"	"0.478"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"57534"	"MIB1"	"0.478"	"0.69"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"57534"	"MIB1"	"0.478"	"0.69"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57534"	"MIB1"	"0.478"	"0.69"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57535"	"KIAA1324"	"0.713"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57537"	"SORCS2"	"0.815"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"PSYGENET"
"57538"	"ALPK3"	"0.834"	"0.276"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"4"	"0"	"CLINGEN"
"57538"	"ALPK3"	"0.834"	"0.276"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57538"	"ALPK3"	"0.834"	"0.276"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57538"	"ALPK3"	"0.834"	"0.276"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.40"		"2001"	"2016"	"4"	"1"	"CLINGEN"
"57539"	"WDR35"	"0.58"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"57539"	"WDR35"	"0.58"	"0.552"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57539"	"WDR35"	"0.58"	"0.552"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"57539"	"WDR35"	"0.58"	"0.552"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C0432197"	"Short rib-polydactyly syndrome, Verma-Naumoff type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57539"	"WDR35"	"0.58"	"0.552"	"C0432235"	"Cranioectodermal Dysplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.56"	"1"	"2010"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"57539"	"WDR35"	"0.58"	"0.552"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57539"	"WDR35"	"0.58"	"0.552"	"C3150874"	"CRANIOECTODERMAL DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"1"	"13"	"UNIPROT"
"57539"	"WDR35"	"0.58"	"0.552"	"C3279792"	"SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.82"	"1"	"2011"	"2018"	"1"	"4"	"ORPHANET;UNIPROT"
"57539"	"WDR35"	"0.58"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57539"	"WDR35"	"0.58"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2008"	"2017"	"0"	"7"	"ORPHANET"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C1857662"	"COACH syndrome"	"disease"	"C06;C10;C11;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"2010"	"2012"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C2676788"	"JOUBERT SYNDROME 9 (disorder)"	"disease"	"C10;C11;C12;C13;C16;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2008"	"2016"	"7"	"47"	"CTD_human;UNIPROT"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C2676790"	"MECKEL SYNDROME, TYPE 6 (disorder)"	"disease"	"C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.60"		"2008"	"2015"	"3"	"24"	"CTD_human;UNIPROT"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C3280898"	"JOUBERT SYNDROME 9/15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2016"	"7"	"20"	"UNIPROT"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2008"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"57545"	"CC2D2A"	"0.559"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2008"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"57546"	"PDP2"	"1"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57547"	"ZNF624"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57551"	"TAOK1"	"0.886"	"0.172"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57551"	"TAOK1"	"0.886"	"0.172"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57551"	"TAOK1"	"0.886"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57554"	"LRRC7"	"0.785"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57554"	"LRRC7"	"0.785"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57554"	"LRRC7"	"0.785"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57554"	"LRRC7"	"0.785"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57555"	"NLGN2"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"57560"	"IFT80"	"0.642"	"0.517"	"C0004044"	"Asphyxia"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57560"	"IFT80"	"0.642"	"0.517"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0039978"	"Thoracic Diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"		"2007"	"2007"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"57560"	"IFT80"	"0.642"	"0.517"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2007"	"2018"	"0"	"1"	"ORPHANET"
"57560"	"IFT80"	"0.642"	"0.517"	"C0432197"	"Short rib-polydactyly syndrome, Verma-Naumoff type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"0"	"0"	"ORPHANET"
"57560"	"IFT80"	"0.642"	"0.517"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"57560"	"IFT80"	"0.642"	"0.517"	"C1970005"	"Asphyxiating Thoracic Dystrophy 2"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.80"		"2007"	"2011"	"1"	"6"	"CTD_human;UNIPROT"
"57560"	"IFT80"	"0.642"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57560"	"IFT80"	"0.642"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57561"	"ARRDC3"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"57561"	"ARRDC3"	"0.886"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"57561"	"ARRDC3"	"0.886"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57561"	"ARRDC3"	"0.886"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57562"	"CEP126"	"0.928"	"0.069"	"C1865384"	"Amyotrophy, monomelic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57570"	"TRMT5"	"0.799"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"57570"	"TRMT5"	"0.799"	"0.241"	"C4225290"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26"	"disease"		"Disease or Syndrome"	"0.70"		"1989"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"57572"	"DOCK6"	"0.672"	"0.483"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.65"	"1"	"2011"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"57572"	"DOCK6"	"0.672"	"0.483"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"57572"	"DOCK6"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"1993"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"57573"	"ZNF471"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57575"	"PCDH10"	"0.648"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"57575"	"PCDH10"	"0.648"	"0.586"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57575"	"PCDH10"	"0.648"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57576"	"KIF17"	"0.928"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2016"	"2"	"0"	"PSYGENET"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0014547"	"Epilepsies, Partial"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0085541"	"Epilepsy, Frontal Lobe"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0086240"	"Epilepsy, Simple Partial"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0234974"	"Simple Partial Seizures"	"phenotype"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0270820"	"Gelastic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0270847"	"Benign Focal Epilepsy, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393671"	"Frontal Epilepsy, Benign, Childhood"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393675"	"Childhood Benign Occipital Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393679"	"Amygdalo-Hippocampal Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393681"	"Rhinencephalic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393683"	"Epilepsy, Supplementary Motor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393684"	"Epilepsy, Cingulate"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393688"	"Epilepsy, Opercular"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0393691"	"Occipital Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0751112"	"Subclinical Seizure"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0751113"	"Uncinate Seizures"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0751115"	"Digestive Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0751642"	"Epilepsy, Anterior Fronto-Polar"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C0751643"	"Epilepsy, Orbito-Frontal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C1851549"	"Benign Occipital Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57582"	"KCNT1"	"0.621"	"0.172"	"C3554195"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"6"	"11"	"CTD_human;UNIPROT"
"57582"	"KCNT1"	"0.621"	"0.172"	"C3554306"	"EPILEPSY, NOCTURNAL FRONTAL LOBE, 5"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"9"	"CTD_human;UNIPROT"
"57582"	"KCNT1"	"0.621"	"0.172"	"C3696898"	"Autosomal Dominant Nocturnal Frontal Lobe Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.35"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"57582"	"KCNT1"	"0.621"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57586"	"SYT13"	"0.928"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57586"	"SYT13"	"0.928"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57586"	"SYT13"	"0.928"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57592"	"ZNF687"	"0.834"	"0.103"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"57592"	"ZNF687"	"0.834"	"0.103"	"C4085250"	"PAGET DISEASE OF BONE 6"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2016"	"1"	"2"	"UNIPROT"
"57595"	"PDZD4"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"57596"	"BEGAIN"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57596"	"BEGAIN"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57596"	"BEGAIN"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57599"	"WDR48"	"0.707"	"0.414"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57608"	"JCAD"	"0.752"	"0.241"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"57608"	"JCAD"	"0.752"	"0.241"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2018"	"1"	"4"	"CTD_human"
"57609"	"DIP2B"	"0.834"	"0.241"	"C1969893"	"Mental Retardation, Fra12a Type"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57609"	"DIP2B"	"0.834"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"57610"	"RANBP10"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57610"	"RANBP10"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57610"	"RANBP10"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57610"	"RANBP10"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57616"	"TSHZ3"	"0.773"	"0.241"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"57616"	"TSHZ3"	"0.773"	"0.241"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57617"	"VPS18"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57620"	"STIM2"	"0.727"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57620"	"STIM2"	"0.727"	"0.345"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57620"	"STIM2"	"0.727"	"0.345"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57623"	"ZFAT"	"0.857"	"0.103"	"C0920350"	"Autoimmune thyroiditis"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57628"	"DPP10"	"0.752"	"0.345"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57628"	"DPP10"	"0.752"	"0.345"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57628"	"DPP10"	"0.752"	"0.345"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57628"	"DPP10"	"0.752"	"0.345"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"57628"	"DPP10"	"0.752"	"0.345"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"57636"	"ARHGAP23"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57636"	"ARHGAP23"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57644"	"MYH7B"	"0.799"	"0.241"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57646"	"USP28"	"0.785"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"57646"	"USP28"	"0.785"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"2"	"0"	"CTD_human"
"57654"	"UVSSA"	"0.799"	"0.276"	"C0020241"	"Hydroa Vacciniforme"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"57654"	"UVSSA"	"0.799"	"0.276"	"C1833561"	"UV-Sensitive Syndrome"	"disease"	"C17"	"Disease or Syndrome"	"0.54"	"1"	"2012"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"57654"	"UVSSA"	"0.799"	"0.276"	"C3553328"	"UV-SENSITIVE SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"1985"	"2012"	"3"	"2"	"UNIPROT"
"57654"	"UVSSA"	"0.799"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57657"	"HCN3"	"0.928"	"0.138"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57659"	"ZBTB4"	"0.799"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57661"	"PHRF1"	"0.752"	"0.276"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2008"	"2014"	"1"	"2"	"CTD_human"
"57661"	"PHRF1"	"0.752"	"0.276"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0004114"	"Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0205768"	"Subependymal Giant Cell Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0280783"	"Juvenile Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0280785"	"Diffuse Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0334579"	"Anaplastic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0334580"	"Protoplasmic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0334581"	"Gemistocytic astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0334582"	"Fibrillary Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0334583"	"Pilocytic Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.60"	"0.96"	"2009"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0338070"	"Childhood Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0547065"	"Mixed oligoastrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0750935"	"Cerebral Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C0750936"	"Intracranial Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57670"	"KIAA1549"	"0.676"	"0.138"	"C1704230"	"Grade I Astrocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57674"	"RNF213"	"0.72"	"0.345"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.32"	"1"	"2016"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"57674"	"RNF213"	"0.72"	"0.345"	"C0026654"	"Moyamoya Disease"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"	"1"	"2011"	"2018"	"0"	"5"	"ORPHANET"
"57674"	"RNF213"	"0.72"	"0.345"	"C1846689"	"MOYAMOYA DISEASE 2"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.60"		"2011"	"2017"	"9"	"4"	"CTD_human;UNIPROT"
"57674"	"RNF213"	"0.72"	"0.345"	"C2931384"	"Moyamoya disease 1"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.50"	"1"	"2011"	"2018"	"0"	"5"	"ORPHANET"
"57678"	"GPAM"	"0.773"	"0.207"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"57678"	"GPAM"	"0.773"	"0.207"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"57678"	"GPAM"	"0.773"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57678"	"GPAM"	"0.773"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57678"	"GPAM"	"0.773"	"0.207"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"1998"	"1998"	"1"	"0"	"CTD_human"
"57679"	"ALS2"	"0.663"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"57679"	"ALS2"	"0.663"	"0.31"	"C1853396"	"Primary lateral sclerosis juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2014"	"0"	"4"	"CTD_human;ORPHANET"
"57679"	"ALS2"	"0.663"	"0.31"	"C1859807"	"AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.49"	"1"	"1990"	"2014"	"0"	"4"	"CTD_human"
"57679"	"ALS2"	"0.663"	"0.31"	"C2931441"	"Hereditary spastic paralysis, infantile onset ascending"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9166667"	"1993"	"2017"	"0"	"13"	"CTD_human;ORPHANET"
"57679"	"ALS2"	"0.663"	"0.31"	"C3468114"	"Juvenile amyotrophic lateral sclerosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57679"	"ALS2"	"0.663"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"57680"	"CHD8"	"0.727"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C0017178"	"Gastrointestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C0221355"	"Macrocephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.35"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C0559031"	"Functional Gastrointestinal Disorders"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2013"	"2017"	"2"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C1565321"	"Cholera Infantum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57680"	"CHD8"	"0.727"	"0.31"	"C3554373"	"AUTISM, SUSCEPTIBILITY TO, 18"	"phenotype"		"Finding"	"0.40"		"2013"	"2016"	"2"	"10"	"UNIPROT"
"57680"	"CHD8"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"57683"	"ZDBF2"	"1"	"0.069"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57688"	"ZSWIM6"	"0.681"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57688"	"ZSWIM6"	"0.681"	"0.379"	"C0796182"	"Acromelic frontonasal dysplasia"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57688"	"ZSWIM6"	"0.681"	"0.379"	"C1863616"	"ACROMELIC FRONTONASAL DYSOSTOSIS"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"2014"	"2018"	"1"	"1"	"CTD_human;UNIPROT"
"57688"	"ZSWIM6"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"57692"	"MAGEE1"	"0.685"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"57692"	"MAGEE1"	"0.685"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57697"	"FANCM"	"0.672"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"0.952381"	"2005"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"57697"	"FANCM"	"0.672"	"0.414"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"57697"	"FANCM"	"0.672"	"0.414"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57697"	"FANCM"	"0.672"	"0.414"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2005"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"57700"	"FAM160B1"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57704"	"GBA2"	"0.69"	"0.448"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57704"	"GBA2"	"0.69"	"0.448"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2018"	"0"	"2"	"GENOMICS_ENGLAND"
"57704"	"GBA2"	"0.69"	"0.448"	"C2828721"	"SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2015"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"57704"	"GBA2"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"57709"	"SLC7A14"	"0.69"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"57709"	"SLC7A14"	"0.69"	"0.345"	"C3810380"	"RETINITIS PIGMENTOSA 68"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"7"	"CTD_human;UNIPROT"
"57716"	"PRX"	"0.696"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"57716"	"PRX"	"0.696"	"0.31"	"C0011195"	"Dejerine-Sottas Disease (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"2000"	"2016"	"0"	"3"	"CTD_human;ORPHANET"
"57716"	"PRX"	"0.696"	"0.31"	"C0019816"	"Hereditary, Type VII, Motor and Sensory Neuropathy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57716"	"PRX"	"0.696"	"0.31"	"C0027888"	"Hereditary Motor and Sensory Neuropathies"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"57716"	"PRX"	"0.696"	"0.31"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"57716"	"PRX"	"0.696"	"0.31"	"C3540453"	"CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"1993"	"2016"	"1"	"9"	"CTD_human;ORPHANET;UNIPROT"
"57716"	"PRX"	"0.696"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57724"	"EPG5"	"0.624"	"0.69"	"C0003257"	"Antibody Deficiency Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"1"	"UNIPROT"
"57724"	"EPG5"	"0.624"	"0.69"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.40"		"2013"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"57724"	"EPG5"	"0.624"	"0.69"	"C0021051"	"Immunologic Deficiency Syndromes"	"group"	"C20"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C0162835"	"Hypopigmentation disorder"	"group"	"C17"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2013"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"57724"	"EPG5"	"0.624"	"0.69"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"57724"	"EPG5"	"0.624"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"57724"	"EPG5"	"0.624"	"0.69"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57724"	"EPG5"	"0.624"	"0.69"	"C1855772"	"Absent corpus callosum cataract immunodeficiency"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.79"	"1"	"1988"	"2018"	"1"	"12"	"CTD_human;ORPHANET;UNIPROT"
"57724"	"EPG5"	"0.624"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1988"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"57728"	"WDR19"	"0.584"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57728"	"WDR19"	"0.584"	"0.586"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2015"	"2018"	"0"	"5"	"ORPHANET"
"57728"	"WDR19"	"0.584"	"0.586"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"57728"	"WDR19"	"0.584"	"0.586"	"C0432235"	"Cranioectodermal Dysplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"57728"	"WDR19"	"0.584"	"0.586"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57728"	"WDR19"	"0.584"	"0.586"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57728"	"WDR19"	"0.584"	"0.586"	"C3280598"	"SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2018"	"1"	"2"	"UNIPROT"
"57728"	"WDR19"	"0.584"	"0.586"	"C3280612"	"NEPHRONOPHTHISIS 13"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2012"	"2016"	"1"	"4"	"UNIPROT"
"57728"	"WDR19"	"0.584"	"0.586"	"C3280616"	"CRANIOECTODERMAL DYSPLASIA 4"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2012"	"1"	"2"	"UNIPROT"
"57728"	"WDR19"	"0.584"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57728"	"WDR19"	"0.584"	"0.586"	"C4225376"	"SENIOR-LOKEN SYNDROME 8"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2018"	"2"	"11"	"UNIPROT"
"57728"	"WDR19"	"0.584"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.53"	"1"	"2012"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57731"	"SPTBN4"	"0.752"	"0.276"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57733"	"GBA3"	"0.752"	"0.483"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57760"	"SPG16"	"0.773"	"0.138"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"57760"	"SPG16"	"0.773"	"0.138"	"C1846046"	"SPASTIC PARAPLEGIA 16, X-LINKED (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57761"	"TRIB3"	"0.627"	"0.517"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57761"	"TRIB3"	"0.627"	"0.517"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"57761"	"TRIB3"	"0.627"	"0.517"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2009"	"1"	"0"	"CTD_human"
"57761"	"TRIB3"	"0.627"	"0.517"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"57761"	"TRIB3"	"0.627"	"0.517"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"57787"	"MARK4"	"0.773"	"0.241"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"57798"	"GATAD1"	"0.799"	"0.172"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"57798"	"GATAD1"	"0.799"	"0.172"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57798"	"GATAD1"	"0.799"	"0.172"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57798"	"GATAD1"	"0.799"	"0.172"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"57798"	"GATAD1"	"0.799"	"0.172"	"C3553409"	"CARDIOMYOPATHY, DILATED, 2B"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"57805"	"CCAR2"	"0.672"	"0.448"	"C0043020"	"Wallerian Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"57817"	"HAMP"	"0.499"	"0.759"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.70"	"0.9701493"	"2003"	"2017"	"3"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2006"	"2017"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0005411"	"Biliary Atresia"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.32"	"1"	"2006"	"2009"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"57817"	"HAMP"	"0.499"	"0.759"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57817"	"HAMP"	"0.499"	"0.759"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9230769"	"2002"	"2016"	"6"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0019202"	"Hepatolenticular Degeneration"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.55"	"0.75"	"2007"	"2017"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57817"	"HAMP"	"0.499"	"0.759"	"C0268060"	"Juvenile hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2015"	"0"	"0"	"ORPHANET"
"57817"	"HAMP"	"0.499"	"0.759"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0282193"	"Iron Overload"	"disease"	"C18"	"Disease or Syndrome"	"0.40"	"0.9615385"	"2002"	"2017"	"2"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57817"	"HAMP"	"0.499"	"0.759"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9361702"	"2002"	"2017"	"6"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"57817"	"HAMP"	"0.499"	"0.759"	"C1527352"	"Hepatic Form of Wilson Disease"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C1865616"	"HEMOCHROMATOSIS, TYPE 2B"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2003"	"2004"	"5"	"3"	"CTD_human;UNIPROT"
"57817"	"HAMP"	"0.499"	"0.759"	"C3489571"	"Familial Extrahepatic Biliary Atresia"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57817"	"HAMP"	"0.499"	"0.759"	"C3489572"	"Idiopathic Extrahepatic Biliary Atresia"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0015927"	"Fetal Death"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"1983"	"2013"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0175697"	"Van der Woude syndrome"	"disease"	"C04;C05;C07;C16;C23"	"Disease or Syndrome"	"0.65"	"1"	"2014"	"2017"	"0"	"1"	"ORPHANET"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0266122"	"Cleft uvula"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0432090"	"Cleft of hard palate"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0432098"	"Cleft Soft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0432103"	"Submucous cleft of hard palate"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"57822"	"GRHL3"	"0.656"	"0.379"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"1983"	"1983"	"1"	"0"	"CTD_human"
"57822"	"GRHL3"	"0.656"	"0.379"	"C1847604"	"Van der Woude syndrome 2"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2014"	"1"	"6"	"CTD_human;UNIPROT"
"57822"	"GRHL3"	"0.656"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"58157"	"NGB"	"0.681"	"0.31"	"C0751870"	"Heredodegenerative Disorders, Nervous System"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"58189"	"WFDC1"	"0.752"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"58189"	"WFDC1"	"0.752"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"58191"	"CXCL16"	"0.58"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"58473"	"PLEKHB1"	"0.815"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C0014356"	"Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C0268390"	"Muckle-Wells Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C0343068"	"Familial cold urticaria"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"58484"	"NLRC4"	"0.6"	"0.552"	"C0409818"	"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"58484"	"NLRC4"	"0.6"	"0.552"	"C0751422"	"Hereditary Autoinflammatory Diseases"	"group"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"2"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C1096155"	"Macrophage Activation Syndrome"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C2316212"	"Cryopyrin-Associated Periodic Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"58484"	"NLRC4"	"0.6"	"0.552"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"58484"	"NLRC4"	"0.6"	"0.552"	"C4015067"	"AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"58484"	"NLRC4"	"0.6"	"0.552"	"C4015276"	"FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"58485"	"TRAPPC1"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"58495"	"OVOL2"	"0.713"	"0.241"	"C0206711"	"Pilomatrixoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"58495"	"OVOL2"	"0.713"	"0.241"	"C0339284"	"Polymorphous corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.66"	"1"	"2003"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"58495"	"OVOL2"	"0.713"	"0.241"	"C1562689"	"Congenital hereditary endothelial dystrophy"	"disease"		"Disease or Syndrome"	"0.36"	"1"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"58495"	"OVOL2"	"0.713"	"0.241"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"58497"	"PRUNE1"	"0.762"	"0.207"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"58497"	"PRUNE1"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"58497"	"PRUNE1"	"0.762"	"0.207"	"C4479566"	"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"3"	"7"	"UNIPROT"
"58498"	"MYL7"	"0.834"	"0.207"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2001"	"1"	"0"	"CTD_human"
"58505"	"OSTC"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2004"	"2018"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0023897"	"Liver Diseases, Parasitic"	"group"	"C03;C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0206698"	"Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0345905"	"Intrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C0795833"	"Kleefstra Syndrome"	"disease"	"C05;C10;C14;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"58508"	"KMT2C"	"0.604"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2017"	"0"	"0"	"UNIPROT"
"58508"	"KMT2C"	"0.604"	"0.621"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"58508"	"KMT2C"	"0.604"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"58508"	"KMT2C"	"0.604"	"0.621"	"C3805278"	"Extrahepatic Cholangiocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"58510"	"PRODH2"	"0.886"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"58510"	"PRODH2"	"0.886"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2002"	"2002"	"1"	"0"	"PSYGENET"
"58513"	"EPS15L1"	"0.886"	"0.207"	"C0265554"	"Ectrodactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"58524"	"DMRT3"	"0.652"	"0.414"	"C4510744"	"46,XY partial gonadal dysgenesis"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"58526"	"MID1IP1"	"0.928"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.40"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"0"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2014"	"0"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"59067"	"IL21"	"0.504"	"0.759"	"C4014258"	"IMMUNODEFICIENCY, COMMON VARIABLE, 11"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"59082"	"CARD18"	"0.857"	"0.138"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59082"	"CARD18"	"0.857"	"0.138"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59084"	"ENPP5"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59084"	"ENPP5"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59269"	"HIVEP3"	"0.727"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"59269"	"HIVEP3"	"0.727"	"0.345"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2003"	"2016"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.60"	"0.9655172"	"2004"	"2017"	"4"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C0553980"	"Endomyocardial Fibrosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"59272"	"ACE2"	"0.542"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"59283"	"CACNG8"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"59335"	"PRDM12"	"0.785"	"0.241"	"C0002768"	"Congenital Pain Insensitivity"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"59335"	"PRDM12"	"0.785"	"0.241"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59335"	"PRDM12"	"0.785"	"0.241"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"59335"	"PRDM12"	"0.785"	"0.241"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"59335"	"PRDM12"	"0.785"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59335"	"PRDM12"	"0.785"	"0.241"	"C4225308"	"NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"1"	"6"	"CTD_human;UNIPROT"
"59338"	"PLEKHA1"	"0.886"	"0.103"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2014"	"2017"	"1"	"2"	"CTD_human"
"59338"	"PLEKHA1"	"0.886"	"0.103"	"C1864205"	"Macular Degeneration, Age-Related, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0033774"	"Pruritus"	"phenotype"	"C17;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59340"	"HRH4"	"0.676"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2011"	"2012"	"2"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.65"	"1"	"1993"	"2016"	"3"	"4"	"CTD_human;GENOMICS_ENGLAND"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0013366"	"Dyschondroplasias"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0015814"	"Femur Head Necrosis"	"disease"	"C05;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0020625"	"Hyponatremia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.33"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0025237"	"Melnick-Needles Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0026760"	"Multiple Epiphyseal Dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0026847"	"Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0029422"	"Osteochondrodysplasias"	"group"	"C05;C16"	"Disease or Syndrome"	"0.47"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0036391"	"Schwartz-Jampel Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0038015"	"Spondyloepiphyseal Dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0042035"	"Urination Disorders"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0206085"	"Kleine-Levin Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0265280"	"Spondylometaphyseal dysplasia, Kozlowski type"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.76"	"0.8333333"	"2009"	"2017"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0265281"	"Metatropic dwarfism"	"disease"	"C05;C16;C19"	"Congenital Abnormality"	"0.80"	"1"	"2004"	"2017"	"5"	"17"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0270765"	"Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"1998"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0393541"	"Distal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0393546"	"Oculopharyngeal Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0393547"	"Bulbospinal Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0410480"	"Avascular Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0432227"	"Brachyolmia Type 3"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.76"	"1"	"2008"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0432272"	"Van Buchem disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0524595"	"Aseptic Necrosis of Femur Head"	"phenotype"	"C05;C23"	"Pathologic Function"	"0.30"				"0"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751334"	"Progressive Proximal Myelopathic Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0751335"	"Scapuloperoneal Form of Spinal Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.74"	"1"	"1992"	"2017"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C0917981"	"Progressive Muscular Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C1838492"	"SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"1985"	"2014"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C1847406"	"Digital Arthropathy-Brachydactyly, Familial"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"1993"	"2011"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C1853710"	"HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.63"	"1"	"2010"	"2014"	"7"	"7"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C1868616"	"Parastremmatic dwarfism"	"disease"	"C05;C10;C16;C19;C23;F01;F03"	"Congenital Abnormality"	"0.73"	"1"	"2009"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"59341"	"TRPV4"	"0.519"	"0.759"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3150755"	"SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3159322"	"SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2004"	"2011"	"0"	"4"	"CTD_human;ORPHANET"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3541456"	"Spondyloepiphyseal Dysplasia Tarda, X-Linked"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3661519"	"Hereditary Motor Neuronopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3711162"	"Metatropic Dysplasia Type 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"59341"	"TRPV4"	"0.519"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59341"	"TRPV4"	"0.519"	"0.759"	"C4479260"	"AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.57"	"0.8571429"	"2005"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.65"	"1"	"2007"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C1847849"	"ICHTHYOSIS, LAMELLAR, 5"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2002"	"2015"	"0"	"5"	"CTD_human"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C1855789"	"Self-Healing Collodion Baby"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C1855792"	"ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2006"	"2017"	"1"	"1"	"CTD_human;ORPHANET"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C3539888"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2010"	"5"	"5"	"UNIPROT"
"59344"	"ALOXE3"	"0.656"	"0.483"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"59345"	"GNB4"	"0.785"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"59345"	"GNB4"	"0.785"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59345"	"GNB4"	"0.785"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59345"	"GNB4"	"0.785"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"59345"	"GNB4"	"0.785"	"0.276"	"C3554654"	"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"59350"	"RXFP1"	"0.762"	"0.172"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2011"	"1"	"0"	"CTD_human"
"59350"	"RXFP1"	"0.762"	"0.172"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2013"	"2"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2016"	"2"	"2"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2013"	"2"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2013"	"2"	"0"	"CTD_human"
"59352"	"LGR6"	"0.652"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2008"	"2011"	"2"	"0"	"CTD_human;UNIPROT"
"60370"	"AVPI1"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"60370"	"AVPI1"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"60385"	"TSKS"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2002"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C1846648"	"MICROCEPHALY, AMISH TYPE (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.71"	"0"	"2002"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C3150973"	"THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY TYPE)"	"disease"		"Disease or Syndrome"	"0.70"		"2009"	"2009"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"60386"	"SLC25A19"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"60401"	"EDA2R"	"0.735"	"0.31"	"C0162359"	"Christ-Siemens-Touraine syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60412"	"EXOC4"	"0.773"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"60468"	"BACH2"	"0.596"	"0.586"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2016"	"1"	"3"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.43"	"1"	"2008"	"2016"	"1"	"3"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"2"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"60468"	"BACH2"	"0.596"	"0.586"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60481"	"ELOVL5"	"0.663"	"0.31"	"C4014812"	"SPINOCEREBELLAR ATAXIA 38"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2014"	"2017"	"1"	"2"	"ORPHANET;UNIPROT"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0221480"	"Recurrent depression"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2017"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C1834703"	"Neuropathy, Distal Hereditary Motor, Type VIIA"	"disease"	"C08;C09;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60482"	"SLC5A7"	"0.659"	"0.448"	"C4310694"	"MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"6"	"UNIPROT"
"60493"	"FASTKD5"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"60495"	"HPSE2"	"0.621"	"0.552"	"C0403555"	"Ochoa syndrome"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.88"	"1"	"1993"	"2016"	"1"	"5"	"CTD_human;ORPHANET"
"60495"	"HPSE2"	"0.621"	"0.552"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60495"	"HPSE2"	"0.621"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60506"	"NYX"	"0.685"	"0.207"	"C0028077"	"Night Blindness"	"disease"	"C11"	"Disease or Syndrome"	"0.67"	"1"	"1998"	"2013"	"1"	"14"	"UNIPROT"
"60506"	"NYX"	"0.685"	"0.207"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.70"	"0.9230769"	"2000"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"60506"	"NYX"	"0.685"	"0.207"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"	"1"	"1993"	"2016"	"0"	"0"	"CTD_human"
"60506"	"NYX"	"0.685"	"0.207"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60506"	"NYX"	"0.685"	"0.207"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60506"	"NYX"	"0.685"	"0.207"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.81"	"1"	"1998"	"2014"	"1"	"19"	"CTD_human;UNIPROT"
"60506"	"NYX"	"0.685"	"0.207"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60506"	"NYX"	"0.685"	"0.207"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.34"	"1"	"1998"	"2009"	"0"	"0"	"CTD_human"
"60506"	"NYX"	"0.685"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60506"	"NYX"	"0.685"	"0.207"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60509"	"AGBL5"	"0.701"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"60509"	"AGBL5"	"0.701"	"0.31"	"C4310759"	"RETINITIS PIGMENTOSA 75"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"4"	"3"	"CTD_human;UNIPROT"
"60526"	"LDAH"	"0.857"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"60526"	"LDAH"	"0.857"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"60528"	"ELAC2"	"0.707"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"60528"	"ELAC2"	"0.707"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9705882"	"2000"	"2016"	"1"	"0"	"CTD_human"
"60528"	"ELAC2"	"0.707"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60528"	"ELAC2"	"0.707"	"0.276"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.60"	"1"	"2001"	"2016"	"1"	"0"	"GENOMICS_ENGLAND;ORPHANET"
"60528"	"ELAC2"	"0.707"	"0.276"	"C3539120"	"PROSTATE CANCER, HEREDITARY, 2"	"disease"		"Neoplastic Process"	"0.40"		"2001"	"2008"	"9"	"8"	"UNIPROT"
"60528"	"ELAC2"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"60528"	"ELAC2"	"0.707"	"0.276"	"C3809526"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"60529"	"ALX4"	"0.58"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"60529"	"ALX4"	"0.58"	"0.552"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"60529"	"ALX4"	"0.58"	"0.552"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C1832588"	"Chromosome 11p11.2 Deletion Syndrome"	"disease"	"C04;C05;C16;C23"	"Disease or Syndrome"	"0.36"	"1"	"1999"	"2016"	"0"	"0"	"ORPHANET"
"60529"	"ALX4"	"0.58"	"0.552"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C1865044"	"PARIETAL FORAMINA 2"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"2"	"9"	"CTD_human;UNIPROT"
"60529"	"ALX4"	"0.58"	"0.552"	"C1868598"	"PARIETAL FORAMINA"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.59"	"0.8888889"	"2000"	"2016"	"0"	"0"	"ORPHANET"
"60529"	"ALX4"	"0.58"	"0.552"	"C1876203"	"Frontonasal dysplasia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60529"	"ALX4"	"0.58"	"0.552"	"C3150703"	"FRONTONASAL DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2014"	"0"	"4"	"ORPHANET"
"60529"	"ALX4"	"0.58"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"60529"	"ALX4"	"0.58"	"0.552"	"C3809819"	"CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"60558"	"GUF1"	"0.762"	"0.138"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60558"	"GUF1"	"0.762"	"0.138"	"C4310737"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"60561"	"RINT1"	"0.785"	"0.241"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2001"	"2016"	"5"	"0"	"CLINGEN"
"60561"	"RINT1"	"0.785"	"0.241"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CLINGEN"
"60673"	"ATG101"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"60673"	"ATG101"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"60674"	"GAS5"	"0.598"	"0.448"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0020429"	"Hyperalgesia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"60675"	"PROK2"	"0.592"	"0.552"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"60675"	"PROK2"	"0.592"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.34"	"1"	"2006"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"60675"	"PROK2"	"0.592"	"0.552"	"C0458247"	"Allodynia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"PSYGENET"
"60675"	"PROK2"	"0.592"	"0.552"	"C0751211"	"Hyperalgesia, Primary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0751212"	"Hyperalgesia, Secondary"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0751213"	"Tactile Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C0751214"	"Hyperalgesia, Thermal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2012"	"2"	"0"	"PSYGENET"
"60675"	"PROK2"	"0.592"	"0.552"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C2936719"	"Mechanical Allodynia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"60675"	"PROK2"	"0.592"	"0.552"	"C3552343"	"HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2015"	"4"	"4"	"UNIPROT"
"60678"	"EEFSEC"	"0.886"	"0.103"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"60678"	"EEFSEC"	"0.886"	"0.103"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"60681"	"FKBP10"	"0.639"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"60681"	"FKBP10"	"0.639"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.37"	"1"	"2010"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"60681"	"FKBP10"	"0.639"	"0.414"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"60681"	"FKBP10"	"0.639"	"0.414"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60681"	"FKBP10"	"0.639"	"0.414"	"C0432253"	"Bruck syndrome"	"disease"		"Disease or Syndrome"	"0.38"	"0.875"	"2011"	"2017"	"0"	"0"	"ORPHANET"
"60681"	"FKBP10"	"0.639"	"0.414"	"C1836602"	"Bruck syndrome 2"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60681"	"FKBP10"	"0.639"	"0.414"	"C1850168"	"Bruck syndrome 1"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.70"		"1997"	"2014"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"60681"	"FKBP10"	"0.639"	"0.414"	"C1859709"	"Kuskokwim disease"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2013"	"2"	"3"	"ORPHANET;UNIPROT"
"60681"	"FKBP10"	"0.639"	"0.414"	"C3151218"	"OSTEOGENESIS IMPERFECTA, TYPE XI"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"0"	"3"	"CTD_human"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C0271742"	"Glucocorticoid deficiency with achalasia"	"disease"	"C06;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"60684"	"TRAPPC11"	"0.713"	"0.345"	"C3809236"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2017"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"60685"	"ZFAND3"	"0.834"	"0.172"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2018"	"1"	"1"	"CTD_human"
"60685"	"ZFAND3"	"0.834"	"0.172"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"60685"	"ZFAND3"	"0.834"	"0.172"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"60685"	"ZFAND3"	"0.834"	"0.172"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"63027"	"SLC22A23"	"0.834"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"63035"	"BCORL1"	"0.713"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"63035"	"BCORL1"	"0.713"	"0.345"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"63035"	"BCORL1"	"0.713"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63035"	"BCORL1"	"0.713"	"0.345"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"63035"	"BCORL1"	"0.713"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63035"	"BCORL1"	"0.713"	"0.345"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"63035"	"BCORL1"	"0.713"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"63036"	"CELA2A"	"1"	"0.069"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63826"	"SRR"	"0.681"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"63826"	"SRR"	"0.681"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"0.75"	"2005"	"2018"	"4"	"1"	"PSYGENET"
"63826"	"SRR"	"0.681"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"63876"	"PKNOX2"	"0.815"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"PSYGENET"
"63876"	"PKNOX2"	"0.815"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"63891"	"RNF123"	"0.834"	"0.138"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"63891"	"RNF123"	"0.834"	"0.138"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0.5"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"63892"	"THADA"	"0.707"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.45"	"1"	"2008"	"2018"	"1"	"5"	"CTD_human"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C1859722"	"Arthrogryposis renal dysfunction cholestasis syndrome"	"disease"	"C05;C06;C12;C13;C16"	"Disease or Syndrome"	"0.76"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63894"	"VIPAS39"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C0220666"	"ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C0796033"	"MARDEN-WALKER SYNDROME"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.71"	"1"	"2014"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C1862472"	"Oculomelic amyoplasia"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.73"	"1"	"1991"	"2016"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"63895"	"PIEZO2"	"0.573"	"0.655"	"C4310692"	"ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"8"	"CTD_human;UNIPROT"
"63901"	"FAM111A"	"0.645"	"0.414"	"C0265291"	"Kenny-Caffey syndrome"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.61"	"1"	"2014"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"63901"	"FAM111A"	"0.645"	"0.414"	"C1865639"	"Gracile bone dysplasia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"2014"	"2014"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"63901"	"FAM111A"	"0.645"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"63901"	"FAM111A"	"0.645"	"0.414"	"C4316787"	"Kenny-Caffey syndrome, type 2"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.70"		"2014"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"63904"	"DUSP21"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"63910"	"SLC17A9"	"0.886"	"0.069"	"C0265970"	"Porokeratosis, Disseminated Superficial Actinic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"63910"	"SLC17A9"	"0.886"	"0.069"	"C4015128"	"POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"63916"	"ELMO2"	"0.886"	"0.345"	"C0796133"	"Ramon Syndrome"	"disease"	"C05;C07;C10;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"63916"	"ELMO2"	"0.886"	"0.345"	"C1847197"	"Vascular Malformation, Primary Intraosseous"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"63924"	"CIDEC"	"0.676"	"0.379"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"63924"	"CIDEC"	"0.676"	"0.379"	"C0271694"	"Familial partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"63924"	"CIDEC"	"0.676"	"0.379"	"C1720859"	"Familial Partial Lipodystrophy, Type 1"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"63924"	"CIDEC"	"0.676"	"0.379"	"C1720860"	"Familial Partial Lipodystrophy, Type 2"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"63924"	"CIDEC"	"0.676"	"0.379"	"C1720861"	"Familial Partial Lipodystrophy, Type 3"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"63924"	"CIDEC"	"0.676"	"0.379"	"C3808940"	"LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5"	"disease"		"Disease or Syndrome"	"0.40"		"2008"	"2010"	"0"	"1"	"ORPHANET"
"63925"	"ZNF335"	"0.707"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63925"	"ZNF335"	"0.707"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"63925"	"ZNF335"	"0.707"	"0.379"	"C3554499"	"MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"63925"	"ZNF335"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"63926"	"ANKEF1"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"63929"	"XPNPEP3"	"0.799"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"63929"	"XPNPEP3"	"0.799"	"0.207"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63929"	"XPNPEP3"	"0.799"	"0.207"	"C3150419"	"NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"63929"	"XPNPEP3"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"63929"	"XPNPEP3"	"0.799"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2010"	"2010"	"0"	"0"	"GENOMICS_ENGLAND"
"63939"	"FAM217B"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"63943"	"FKBPL"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"63943"	"FKBPL"	"0.799"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"63943"	"FKBPL"	"0.799"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"63943"	"FKBPL"	"0.799"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"63943"	"FKBPL"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"63951"	"DMRTA1"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"63967"	"CLSPN"	"0.743"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2010"	"0"	"0"	"UNIPROT"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2011"	"2017"	"1"	"4"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"63976"	"PRDM16"	"0.573"	"0.621"	"C1842870"	"Chromosome 1p36 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"63976"	"PRDM16"	"0.573"	"0.621"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"63976"	"PRDM16"	"0.573"	"0.621"	"C3809288"	"LEFT VENTRICULAR NONCOMPACTION 8"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"5"	"CTD_human;UNIPROT"
"63976"	"PRDM16"	"0.573"	"0.621"	"C3809289"	"CARDIOMYOPATHY, DILATED, 1LL"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"63976"	"PRDM16"	"0.573"	"0.621"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"63978"	"PRDM14"	"0.735"	"0.31"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"63978"	"PRDM14"	"0.735"	"0.31"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"63978"	"PRDM14"	"0.735"	"0.31"	"C1336708"	"Testicular Germ Cell Tumor"	"disease"	"C04;C12;C19"	"Neoplastic Process"	"0.40"		"2013"	"2017"	"1"	"1"	"CTD_human"
"63978"	"PRDM14"	"0.735"	"0.31"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"63979"	"FIGNL1"	"0.886"	"0.138"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"63979"	"FIGNL1"	"0.886"	"0.138"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"63982"	"ANO3"	"0.735"	"0.31"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"				"0"	"0"	"CTD_human"
"63982"	"ANO3"	"0.735"	"0.31"	"C3554374"	"DYSTONIA 24"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2001"	"2015"	"1"	"2"	"ORPHANET;UNIPROT"
"63982"	"ANO3"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64005"	"MYO1G"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"64061"	"TSPYL2"	"0.663"	"0.552"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64061"	"TSPYL2"	"0.663"	"0.552"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64062"	"RBM26"	"1"	"0.034"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"64067"	"NPAS3"	"0.735"	"0.241"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2014"	"3"	"0"	"PSYGENET"
"64067"	"NPAS3"	"0.735"	"0.241"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"PSYGENET"
"64067"	"NPAS3"	"0.735"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2003"	"2016"	"4"	"0"	"PSYGENET"
"64067"	"NPAS3"	"0.735"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"64067"	"NPAS3"	"0.735"	"0.241"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"1"	"0"	"PSYGENET"
"64067"	"NPAS3"	"0.735"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"64072"	"CDH23"	"0.577"	"0.552"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64072"	"CDH23"	"0.577"	"0.552"	"C0010481"	"Cushing Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64072"	"CDH23"	"0.577"	"0.552"	"C0033375"	"Prolactinoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C0221406"	"Pituitary-dependent Cushing's disease"	"disease"	"C10;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C0346303"	"Thyrotroph adenoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.69"	"0.8888889"	"1993"	"2013"	"6"	"2"	"CLINGEN;ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C1832394"	"Deafness, Autosomal Recessive 12"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.82"	"1"	"2001"	"2016"	"8"	"17"	"CTD_human;UNIPROT"
"64072"	"CDH23"	"0.577"	"0.552"	"C1832845"	"USHER SYNDROME, TYPE ID"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.67"	"0.8571429"	"1966"	"2016"	"6"	"45"	"UNIPROT"
"64072"	"CDH23"	"0.577"	"0.552"	"C1848638"	"USHER SYNDROME, TYPE IB (disorder)"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"		"2001"	"2012"	"6"	"0"	"CLINGEN"
"64072"	"CDH23"	"0.577"	"0.552"	"C1848639"	"USHER SYNDROME, TYPE IA, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2012"	"6"	"0"	"CLINGEN"
"64072"	"CDH23"	"0.577"	"0.552"	"C1848640"	"USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"2001"	"2012"	"6"	"0"	"CLINGEN"
"64072"	"CDH23"	"0.577"	"0.552"	"C1863340"	"PITUITARY ADENOMA PREDISPOSITION (disorder)"	"phenotype"	"C04;C10;C19"	"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"64072"	"CDH23"	"0.577"	"0.552"	"C2931208"	"Usher syndrome, type 1D"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.39"	"1"	"2001"	"2016"	"0"	"0"	"CTD_human"
"64072"	"CDH23"	"0.577"	"0.552"	"C3152102"	"USH1D/F, CDH23/PCDH15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.50"		"1966"	"2008"	"6"	"3"	"UNIPROT"
"64072"	"CDH23"	"0.577"	"0.552"	"C3275872"	"USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.50"		"1966"	"2008"	"6"	"3"	"UNIPROT"
"64072"	"CDH23"	"0.577"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64072"	"CDH23"	"0.577"	"0.552"	"C4539685"	"PITUITARY ADENOMA 5, MULTIPLE TYPES"	"disease"		"Neoplastic Process"	"0.40"		"2017"	"2017"	"1"	"3"	"UNIPROT"
"64077"	"LHPP"	"0.834"	"0.241"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2015"	"2"	"0"	"PSYGENET"
"64077"	"LHPP"	"0.834"	"0.241"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2015"	"2"	"0"	"PSYGENET"
"64081"	"PBLD"	"0.886"	"0.069"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64081"	"PBLD"	"0.886"	"0.069"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64084"	"CLSTN2"	"0.762"	"0.31"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64084"	"CLSTN2"	"0.762"	"0.31"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64084"	"CLSTN2"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"64087"	"MCCC2"	"0.685"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64087"	"MCCC2"	"0.685"	"0.448"	"C0268600"	"3-methylcrotonyl CoA carboxylase 1 deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2012"	"0"	"0"	"ORPHANET"
"64087"	"MCCC2"	"0.685"	"0.448"	"C1859499"	"3-methylcrotonyl CoA carboxylase 2 deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.60"		"1982"	"2017"	"11"	"42"	"CTD_human;UNIPROT"
"64087"	"MCCC2"	"0.685"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64093"	"SMOC1"	"0.592"	"0.759"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64093"	"SMOC1"	"0.592"	"0.759"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64093"	"SMOC1"	"0.592"	"0.759"	"C0599973"	"Waardenburg Anophthalmia Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.96"	"1"	"2009"	"2018"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"64093"	"SMOC1"	"0.592"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64094"	"SMOC2"	"0.72"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64094"	"SMOC2"	"0.72"	"0.241"	"C0399379"	"Dentin dysplasia, type 1"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"64101"	"LRRC4"	"0.713"	"0.345"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64108"	"RTP4"	"0.886"	"0.138"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64109"	"CRLF2"	"0.639"	"0.483"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"64109"	"CRLF2"	"0.639"	"0.483"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"64109"	"CRLF2"	"0.639"	"0.483"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64109"	"CRLF2"	"0.639"	"0.483"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64109"	"CRLF2"	"0.639"	"0.483"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"0.95"	"2009"	"2017"	"1"	"0"	"CGI;CTD_human"
"64109"	"CRLF2"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64114"	"TMBIM1"	"0.857"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64115"	"VSIR"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64116"	"SLC39A8"	"0.667"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64116"	"SLC39A8"	"0.667"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"64116"	"SLC39A8"	"0.667"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"64116"	"SLC39A8"	"0.667"	"0.483"	"C4225234"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"64118"	"DUS1L"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C0024301"	"Lymphoma, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C0079745"	"Lymphoma, Large-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C0079758"	"Lymphoma, Mixed-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C0079765"	"Lymphoma, Small Cleaved-Cell, Follicular"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C1956130"	"Lymphoma, Follicular, Grade 1"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C1956131"	"Lymphoma, Follicular, Grade 3"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64121"	"RRAGC"	"0.799"	"0.103"	"C1956132"	"Lymphoma, Follicular, Grade 2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64123"	"ADGRL4"	"0.857"	"0.103"	"C3160814"	"Cannabis use"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"64127"	"NOD2"	"0.458"	"0.862"	"C0003872"	"Arthritis, Psoriatic"	"disease"	"C05;C17"	"Disease or Syndrome"	"0.40"	"0.8"	"2003"	"2012"	"0"	"0"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"64127"	"NOD2"	"0.458"	"0.862"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.90"	"0.8266667"	"1998"	"2017"	"6"	"41"	"CTD_human;UNIPROT"
"64127"	"NOD2"	"0.458"	"0.862"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.90"	"0.9088"	"1998"	"2018"	"12"	"57"	"CTD_human;UNIPROT"
"64127"	"NOD2"	"0.458"	"0.862"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"2003"	"2013"	"1"	"0"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.50"	"0.9014085"	"1998"	"2018"	"2"	"3"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2001"	"2010"	"8"	"0"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2015"	"8"	"0"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2001"	"2017"	"8"	"3"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2010"	"8"	"0"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C1836122"	"SARCOIDOSIS, EARLY-ONSET"	"disease"	"C15"	"Disease or Syndrome"	"0.48"	"1"	"2005"	"2014"	"2"	"6"	"CTD_human"
"64127"	"NOD2"	"0.458"	"0.862"	"C1861303"	"SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)"	"disease"	"C05;C11"	"Disease or Syndrome"	"0.80"	"0.9848485"	"1994"	"2018"	"14"	"17"	"CTD_human;ORPHANET;UNIPROT"
"64127"	"NOD2"	"0.458"	"0.862"	"C2675113"	"CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.50"		"2001"	"2014"	"5"	"39"	"UNIPROT"
"64127"	"NOD2"	"0.458"	"0.862"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"1993"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"64127"	"NOD2"	"0.458"	"0.862"	"C4310620"	"YAO SYNDROME"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0033847"	"Pseudoxanthoma Elasticum"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2006"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0376359"	"Gronblad-Strandberg Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0432242"	"Desbuquois syndrome"	"disease"	"C05;C16;C19;C23"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"64131"	"XYLT1"	"0.645"	"0.621"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C1867450"	"Pseudoxanthoma Elasticum, Incomplete"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64131"	"XYLT1"	"0.645"	"0.621"	"C3279392"	"PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C3279393"	"PXE, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C4014294"	"DESBUQUOIS DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"3"	"6"	"UNIPROT"
"64131"	"XYLT1"	"0.645"	"0.621"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64132"	"XYLT2"	"0.636"	"0.655"	"C0033847"	"Pseudoxanthoma Elasticum"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.52"	"1"	"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"64132"	"XYLT2"	"0.636"	"0.655"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"64132"	"XYLT2"	"0.636"	"0.655"	"C0376359"	"Gronblad-Strandberg Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"64132"	"XYLT2"	"0.636"	"0.655"	"C1853925"	"Spondyloocular Syndrome, Autosomal Recessive"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"ORPHANET"
"64132"	"XYLT2"	"0.636"	"0.655"	"C1867450"	"Pseudoxanthoma Elasticum, Incomplete"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64132"	"XYLT2"	"0.636"	"0.655"	"C3279392"	"PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"64132"	"XYLT2"	"0.636"	"0.655"	"C3279393"	"PXE, MODIFIER OF SEVERITY OF"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.34"	"0.5"	"2007"	"2014"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.70"	"1"	"2006"	"2017"	"2"	"1"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2017"	"1"	"4"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0162538"	"Immunoglobulin A deficiency (disorder)"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"		"2010"	"2016"	"2"	"1"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"2"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"2014"	"2017"	"0"	"0"	"ORPHANET"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0432254"	"Singleton Merten syndrome"	"disease"	"C05;C07;C10;C14;C16;C18"	"Disease or Syndrome"	"0.54"	"1"	"2015"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64135"	"IFIH1"	"0.524"	"0.759"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.37"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64135"	"IFIH1"	"0.524"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"64135"	"IFIH1"	"0.524"	"0.759"	"C3888244"	"AICARDI-GOUTIERES SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"2"	"8"	"UNIPROT"
"64135"	"IFIH1"	"0.524"	"0.759"	"C4225427"	"SINGLETON-MERTEN SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2015"	"1"	"1"	"UNIPROT"
"64150"	"DIO3OS"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64150"	"DIO3OS"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64150"	"DIO3OS"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64151"	"NCAPG"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64167"	"ERAP2"	"0.685"	"0.345"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2017"	"1"	"4"	"CTD_human"
"64167"	"ERAP2"	"0.685"	"0.345"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64167"	"ERAP2"	"0.685"	"0.345"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64167"	"ERAP2"	"0.685"	"0.345"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64167"	"ERAP2"	"0.685"	"0.345"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64170"	"CARD9"	"0.624"	"0.448"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"2008"	"2017"	"1"	"5"	"CTD_human"
"64170"	"CARD9"	"0.624"	"0.448"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"1"	"CTD_human"
"64170"	"CARD9"	"0.624"	"0.448"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.46"	"0.8333333"	"2008"	"2018"	"1"	"2"	"CTD_human"
"64170"	"CARD9"	"0.624"	"0.448"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.44"	"1"	"2011"	"2017"	"1"	"3"	"CTD_human"
"64170"	"CARD9"	"0.624"	"0.448"	"C1859353"	"Candidiasis, Familial, 2"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.70"		"1998"	"2013"	"3"	"5"	"CTD_human;ORPHANET;UNIPROT"
"64175"	"P3H1"	"0.727"	"0.241"	"C0023931"	"Lobstein Disease"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64175"	"P3H1"	"0.727"	"0.241"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.80"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"64175"	"P3H1"	"0.727"	"0.241"	"C0268358"	"Osteogenesis imperfecta, dominant perinatal lethal"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"64175"	"P3H1"	"0.727"	"0.241"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64175"	"P3H1"	"0.727"	"0.241"	"C1970458"	"Osteogenesis imperfecta, type VIII"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"2007"	"2017"	"0"	"9"	"CTD_human"
"64175"	"P3H1"	"0.727"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64211"	"LHX5"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"PSYGENET"
"64215"	"DNAJC1"	"0.886"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64216"	"TFB2M"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CLINGEN"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"ORPHANET"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2017"	"2"	"0"	"CLINGEN"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2017"	"2"	"0"	"CLINGEN"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C1846529"	"CONE-ROD DYSTROPHY 10"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"2"	"CTD_human;UNIPROT"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C1853214"	"RETINITIS PIGMENTOSA 35"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2012"	"2"	"2"	"CTD_human;UNIPROT"
"64218"	"SEMA4A"	"0.616"	"0.517"	"C3896578"	"Familial Colorectal Cancer Type X"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"64219"	"PJA1"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"64220"	"STRA6"	"0.614"	"0.655"	"C0003119"	"Anophthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.48"	"0.875"	"2007"	"2014"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"64220"	"STRA6"	"0.614"	"0.655"	"C0018798"	"Congenital Heart Defects"	"group"	"C14;C16"	"Congenital Abnormality"	"0.41"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0019284"	"Diaphragmatic Hernia"	"phenotype"	"C23"	"Anatomical Abnormality"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.44"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C1832661"	"ANOPHTHALMIA AND PULMONARY HYPOPLASIA"	"disease"	"C08;C11;C16"	"Disease or Syndrome"	"0.77"	"1"	"2007"	"2018"	"4"	"14"	"CTD_human;ORPHANET;UNIPROT"
"64220"	"STRA6"	"0.614"	"0.655"	"C2677362"	"Alveolar capillary dysplasia"	"disease"	"C08;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64220"	"STRA6"	"0.614"	"0.655"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64220"	"STRA6"	"0.614"	"0.655"	"C3540845"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8"	"disease"		"Disease or Syndrome"	"0.40"		"2007"	"2012"	"4"	"6"	"UNIPROT"
"64220"	"STRA6"	"0.614"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.62"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"64221"	"ROBO3"	"0.557"	"0.793"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"64221"	"ROBO3"	"0.557"	"0.793"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"64221"	"ROBO3"	"0.557"	"0.793"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2004"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"64221"	"ROBO3"	"0.557"	"0.793"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"64221"	"ROBO3"	"0.557"	"0.793"	"C1846496"	"Gaze Palsy, Familial Horizontal, with Progressive Scoliosis"	"disease"	"C05;C10;C11;C18;C23"	"Disease or Syndrome"	"0.80"	"1"	"2004"	"2017"	"1"	"10"	"CTD_human;ORPHANET;UNIPROT"
"64221"	"ROBO3"	"0.557"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64224"	"HERPUD2"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64224"	"HERPUD2"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64224"	"HERPUD2"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64231"	"MS4A6A"	"0.857"	"0.172"	"C0017661"	"IGA Glomerulonephritis"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64232"	"MS4A5"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0004153"	"Atherosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2014"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2001"	"2"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2015"	"1"	"1"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0043325"	"Xanthomatosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0302314"	"Xanthoma"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0342907"	"Sitosterolemia"	"disease"	"C06;C16;C18"	"Congenital Abnormality"	"0.80"	"0.95"	"2000"	"2018"	"5"	"10"	"CTD_human;ORPHANET;UNIPROT"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"64240"	"ABCG5"	"0.602"	"0.414"	"C1563937"	"Atherogenesis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"0.5"	"2000"	"2015"	"2"	"0"	"CTD_human"
"64240"	"ABCG5"	"0.602"	"0.414"	"C2749759"	"Macrothrombocytopenia-Stomatocytosis, Mediterranean"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.50"		"2000"	"2004"	"5"	"4"	"CTD_human;UNIPROT"
"64240"	"ABCG5"	"0.602"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2005"	"1"	"0"	"CTD_human"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64241"	"ABCG8"	"0.584"	"0.448"	"C0342907"	"Sitosterolemia"	"disease"	"C06;C16;C18"	"Congenital Abnormality"	"0.80"	"1"	"1974"	"2018"	"3"	"20"	"CTD_human;ORPHANET;UNIPROT"
"64241"	"ABCG8"	"0.584"	"0.448"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"64241"	"ABCG8"	"0.584"	"0.448"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.45"	"0.8"	"2000"	"2018"	"1"	"2"	"CTD_human"
"64241"	"ABCG8"	"0.584"	"0.448"	"C1969115"	"GALLBLADDER DISEASE 4"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64241"	"ABCG8"	"0.584"	"0.448"	"C2749759"	"Macrothrombocytopenia-Stomatocytosis, Mediterranean"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.50"		"2000"	"2004"	"3"	"9"	"CTD_human;UNIPROT"
"64288"	"ZSCAN31"	"0.815"	"0.207"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"64288"	"ZSCAN31"	"0.815"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2016"	"1"	"2"	"PSYGENET"
"64288"	"ZSCAN31"	"0.815"	"0.207"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"64321"	"SOX17"	"0.609"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"64321"	"SOX17"	"0.609"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64321"	"SOX17"	"0.609"	"0.414"	"C0042580"	"Vesico-Ureteral Reflux"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.61"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"64321"	"SOX17"	"0.609"	"0.414"	"C0232910"	"Teratogenesis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64321"	"SOX17"	"0.609"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"64321"	"SOX17"	"0.609"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64321"	"SOX17"	"0.609"	"0.414"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"64321"	"SOX17"	"0.609"	"0.414"	"C3150927"	"VESICOURETERAL REFLUX 3"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"64321"	"SOX17"	"0.609"	"0.414"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"64321"	"SOX17"	"0.609"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64324"	"NSD1"	"0.546"	"0.655"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.42"	"1"	"2003"	"2017"	"0"	"21"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64324"	"NSD1"	"0.546"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C0175695"	"Sotos' syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.70"	"0.9701493"	"2002"	"2018"	"16"	"7"	"CTD_human;ORPHANET;UNIPROT"
"64324"	"NSD1"	"0.546"	"0.655"	"C0265210"	"Weaver syndrome"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.55"	"0.8"	"2003"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"64324"	"NSD1"	"0.546"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64324"	"NSD1"	"0.546"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"64324"	"NSD1"	"0.546"	"0.655"	"C2931574"	"Chromosome 5, monosomy 5q35"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"				"0"	"0"	"ORPHANET"
"64324"	"NSD1"	"0.546"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.63"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"64324"	"NSD1"	"0.546"	"0.655"	"C4304526"	"5q35 microduplication syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64326"	"COP1"	"0.696"	"0.379"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.45"	"1"	"2002"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0241397"	"Triphalangeal thumb"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"2000"	"2018"	"0"	"5"	"CTD_human"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0265559"	"Acheiropodia"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.72"	"1"	"2001"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0265581"	"Longitudinal deficiency of radius"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0265596"	"Talipomanus"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C0265598"	"Manus vara"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C1851100"	"LAURIN-SANDROW SYNDROME"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C1851101"	"Laurin-Sandrow Syndrome, Segmental"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64327"	"LMBR1"	"0.624"	"0.103"	"C1861099"	"Absence of tibia with polydactyly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"1999"	"2015"	"0"	"2"	"CTD_human"
"64327"	"LMBR1"	"0.624"	"0.103"	"C1861355"	"Syndactyly, Type IV"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.51"	"1"	"2000"	"2000"	"0"	"0"	"CTD_human;ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C1868114"	"POLYDACTYLY, PREAXIAL II (disorder)"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.62"	"1"	"1994"	"2015"	"0"	"10"	"CTD_human;ORPHANET"
"64327"	"LMBR1"	"0.624"	"0.103"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64332"	"NFKBIZ"	"0.735"	"0.31"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"64332"	"NFKBIZ"	"0.735"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64332"	"NFKBIZ"	"0.735"	"0.31"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"64332"	"NFKBIZ"	"0.735"	"0.31"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"64333"	"ARHGAP9"	"0.928"	"0.069"	"C0010073"	"Coronary Artery Vasospasm"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"64333"	"ARHGAP9"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64359"	"NXN"	"0.672"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64359"	"NXN"	"0.672"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"64359"	"NXN"	"0.672"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2014"	"2017"	"1"	"1"	"CTD_human"
"64359"	"NXN"	"0.672"	"0.414"	"C1849334"	"Robinow syndrome, autosomal recessive"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64374"	"SIL1"	"0.604"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64374"	"SIL1"	"0.604"	"0.586"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"64374"	"SIL1"	"0.604"	"0.586"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64374"	"SIL1"	"0.604"	"0.586"	"C0024814"	"Marinesco-Sjogren syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"2000"	"2017"	"0"	"10"	"CTD_human;ORPHANET"
"64374"	"SIL1"	"0.604"	"0.586"	"C0033132"	"Cerebellar Degenerations, Primary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"64374"	"SIL1"	"0.604"	"0.586"	"C0037952"	"Spinocerebellar Degeneration"	"group"	"C10;C16"	"Disease or Syndrome"	"0.32"		"2006"	"2008"	"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64374"	"SIL1"	"0.604"	"0.586"	"C0270749"	"Marie Cerebellar Ataxia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0270755"	"Corticostriatal-Spinal Degeneration"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0393519"	"Cerebellar Ataxia, Early Onset"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C0393524"	"Cerebellar Ataxia, Late Onset"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64374"	"SIL1"	"0.604"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"0"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"64375"	"IKZF4"	"0.857"	"0.172"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"1"	"CTD_human"
"64375"	"IKZF4"	"0.857"	"0.172"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"4"	"CTD_human"
"64377"	"CHST8"	"0.834"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64377"	"CHST8"	"0.834"	"0.172"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"64377"	"CHST8"	"0.834"	"0.172"	"C4015729"	"PEELING SKIN SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"1"	"ORPHANET;UNIPROT"
"64388"	"GREM2"	"0.834"	"0.241"	"C4310638"	"TOOTH AGENESIS, SELECTIVE, 9"	"disease"		"Congenital Abnormality"	"0.60"		"2013"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"64393"	"ZMAT3"	"0.727"	"0.276"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64396"	"GMCL2"	"0.834"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64399"	"HHIP"	"0.619"	"0.345"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64399"	"HHIP"	"0.619"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"64399"	"HHIP"	"0.619"	"0.345"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64400"	"AKTIP"	"0.773"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64405"	"CDH22"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64405"	"CDH22"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64405"	"CDH22"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64411"	"ARAP3"	"0.773"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2018"	"1"	"1"	"UNIPROT"
"64411"	"ARAP3"	"0.773"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"64411"	"ARAP3"	"0.773"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64411"	"ARAP3"	"0.773"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"64412"	"GZF1"	"0.928"	"0.241"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"2006"	"2006"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"64419"	"MTMR14"	"0.785"	"0.069"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64419"	"MTMR14"	"0.785"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C1865370"	"Severe combined immunodeficiency with sensitivity to ionizing radiation"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.81"	"1"	"2001"	"2017"	"5"	"5"	"CTD_human;UNIPROT"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C1865371"	"SEVERE COMBINED IMMUNODEFICIENCY, ATHABASKAN-TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2009"	"5"	"1"	"UNIPROT"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C1865372"	"Athabaskan severe combined immunodeficiency"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.70"		"2001"	"2009"	"5"	"0"	"ORPHANET;UNIPROT"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C1865373"	"SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2009"	"5"	"1"	"UNIPROT"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C2700553"	"Omenn Syndrome"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.55"	"1"	"1997"	"2010"	"1"	"1"	"ORPHANET;UNIPROT"
"64421"	"DCLRE1C"	"0.575"	"0.724"	"C2931884"	"Reticuloendotheliosis, familial, with eosinophilia"	"disease"	"C15;C16;C18;C20"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"64423"	"INF2"	"0.701"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"2011"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"64423"	"INF2"	"0.701"	"0.207"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.50"	"0.9545455"	"2010"	"2017"	"1"	"1"	"CTD_human"
"64423"	"INF2"	"0.701"	"0.207"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64423"	"INF2"	"0.701"	"0.207"	"C2750475"	"Focal Segmental Glomerulosclerosis 5"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2010"	"2014"	"6"	"7"	"CTD_human;UNIPROT"
"64423"	"INF2"	"0.701"	"0.207"	"C3280845"	"CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E"	"disease"		"Disease or Syndrome"	"0.70"		"1967"	"2016"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"64423"	"INF2"	"0.701"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"64434"	"NOM1"	"1"	"0.103"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64446"	"DNAI2"	"0.743"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.64"	"1"	"1993"	"2014"	"0"	"2"	"ORPHANET"
"64446"	"DNAI2"	"0.743"	"0.207"	"C2676235"	"CILIARY DYSKINESIA, PRIMARY, 9"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2013"	"0"	"4"	"CTD_human"
"64446"	"DNAI2"	"0.743"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64446"	"DNAI2"	"0.743"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2015"	"1"	"2"	"PSYGENET"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2013"	"1"	"2"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2011"	"2017"	"5"	"6"	"PSYGENET"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64478"	"CSMD1"	"0.639"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64499"	"TPSB2"	"1"	"0.103"	"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64506"	"CPEB1"	"0.727"	"0.379"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64577"	"ALDH8A1"	"1"	"0.034"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64579"	"NDST4"	"0.815"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"64579"	"NDST4"	"0.815"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"64581"	"CLEC7A"	"0.6"	"0.655"	"C0004030"	"Aspergillosis"	"disease"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"64581"	"CLEC7A"	"0.6"	"0.655"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"64581"	"CLEC7A"	"0.6"	"0.655"	"C1859353"	"Candidiasis, Familial, 2"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"64644"	"GINGF2"	"0.928"	"0.103"	"C0399440"	"Hereditary gingival fibromatosis"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.32"	"1"	"2002"	"2005"	"0"	"0"	"ORPHANET"
"64651"	"CSRNP1"	"0.886"	"0.172"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"64651"	"CSRNP1"	"0.886"	"0.172"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"64682"	"ANAPC1"	"0.857"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"64699"	"TMPRSS3"	"0.685"	"0.448"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64699"	"TMPRSS3"	"0.685"	"0.448"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64699"	"TMPRSS3"	"0.685"	"0.448"	"C1832827"	"DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2001"	"2015"	"6"	"10"	"UNIPROT"
"64699"	"TMPRSS3"	"0.685"	"0.448"	"C1854414"	"Deafness, Autosomal Recessive 10"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.32"	"1"	"2001"	"2005"	"6"	"6"	"UNIPROT"
"64711"	"HS3ST6"	"0.928"	"0.069"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64711"	"HS3ST6"	"0.928"	"0.069"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64743"	"WDR13"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"64748"	"PLPPR2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64754"	"SMYD3"	"0.676"	"0.483"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64754"	"SMYD3"	"0.676"	"0.483"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64754"	"SMYD3"	"0.676"	"0.483"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64755"	"C16orf58"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64756"	"ATPAF1"	"0.799"	"0.207"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64756"	"ATPAF1"	"0.799"	"0.207"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64757"	"MARC1"	"0.928"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64757"	"MARC1"	"0.928"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64757"	"MARC1"	"0.928"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"64761"	"PARP12"	"0.886"	"0.138"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64764"	"CREB3L2"	"0.743"	"0.103"	"C3714524"	"Fibromyxosarcoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"64768"	"IPPK"	"1"	"0.034"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64777"	"RMND5B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0022578"	"Keratoconus"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"64778"	"FNDC3B"	"0.762"	"0.138"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"64780"	"MICAL1"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64781"	"CERK"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64782"	"AEN"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64788"	"LMF1"	"0.72"	"0.241"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64788"	"LMF1"	"0.72"	"0.241"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.39"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"64788"	"LMF1"	"0.72"	"0.241"	"C1274228"	"Chylomicronemia syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64788"	"LMF1"	"0.72"	"0.241"	"C1855498"	"Lipase deficiency combined"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.43"	"1"	"2007"	"2011"	"0"	"2"	"CTD_human"
"64799"	"IQCH"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64801"	"ARV1"	"0.799"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64801"	"ARV1"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"64801"	"ARV1"	"0.799"	"0.138"	"C4310762"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0029124"	"Optic Atrophy"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0043020"	"Wallerian Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.70"	"1"	"2003"	"2017"	"4"	"4"	"CTD_human;ORPHANET"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C0876926"	"Traumatic Brain Injury"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C1837873"	"LEBER CONGENITAL AMAUROSIS 9 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.81"	"1"	"1993"	"2017"	"4"	"19"	"CTD_human;UNIPROT"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C1852767"	"Hereditary macular coloboma"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C3540662"	"Congenital Amaurosis of Retinal Origin"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"4"	"0"	"CTD_human"
"64802"	"NMNAT1"	"0.696"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"0"	"2008"	"2010"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.50"		"2007"	"2010"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"64805"	"P2RY12"	"0.642"	"0.379"	"C1853278"	"Bleeding Disorder Due To P2RY12 Defect"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.90"		"2001"	"2015"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"64816"	"CYP3A43"	"0.799"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2005"	"2005"	"1"	"0"	"CTD_human"
"64816"	"CYP3A43"	"0.799"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.36"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"64837"	"KLC2"	"0.785"	"0.241"	"C1836010"	"Spastic Paraplegia, Optic Atrophy, and Neuropathy"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"64838"	"FNDC4"	"0.928"	"0.103"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"64840"	"PORCN"	"0.557"	"0.586"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"64840"	"PORCN"	"0.557"	"0.586"	"C0016395"	"Focal Dermal Hypoplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"2007"	"2018"	"8"	"7"	"CTD_human;ORPHANET;UNIPROT"
"64840"	"PORCN"	"0.557"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64840"	"PORCN"	"0.557"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"64841"	"GNPNAT1"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64850"	"ETNPPL"	"0.799"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2012"	"2"	"0"	"PSYGENET"
"64853"	"AIDA"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"64854"	"USP46"	"0.799"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"64854"	"USP46"	"0.799"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"64854"	"USP46"	"0.799"	"0.103"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"64857"	"PLEKHG2"	"0.762"	"0.345"	"C4225213"	"LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"64859"	"NABP1"	"0.928"	"0.069"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64866"	"CDCP1"	"0.619"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"64881"	"PCDH20"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64901"	"RANBP17"	"1"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"64902"	"AGXT2"	"0.785"	"0.345"	"C0025521"	"Inborn Errors of Metabolism"	"group"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64902"	"AGXT2"	"0.785"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"64919"	"BCL11B"	"0.624"	"0.483"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.34"	"0.75"	"2003"	"2015"	"1"	"0"	"CTD_human"
"64919"	"BCL11B"	"0.624"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"64919"	"BCL11B"	"0.624"	"0.483"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"64919"	"BCL11B"	"0.624"	"0.483"	"C4310656"	"IMMUNODEFICIENCY 49"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"64946"	"CENPH"	"0.752"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2006"	"1"	"1"	"UNIPROT"
"64963"	"MRPS11"	"0.886"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64963"	"MRPS11"	"0.886"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64963"	"MRPS11"	"0.886"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64963"	"MRPS11"	"0.886"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64968"	"MRPS6"	"0.928"	"0.034"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64968"	"MRPS6"	"0.928"	"0.034"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"64969"	"MRPS5"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"64976"	"MRPL40"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65005"	"MRPL9"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"65005"	"MRPL9"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"65005"	"MRPL9"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"65005"	"MRPL9"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"65012"	"SLC26A10"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65018"	"PINK1"	"0.577"	"0.586"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.36"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"0.9652174"	"2002"	"2018"	"5"	"0"	"CTD_human;GENOMICS_ENGLAND"
"65018"	"PINK1"	"0.577"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.6666667"	"2007"	"2015"	"3"	"0"	"PSYGENET"
"65018"	"PINK1"	"0.577"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"65018"	"PINK1"	"0.577"	"0.586"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.50"	"0.9861111"	"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"65018"	"PINK1"	"0.577"	"0.586"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"65018"	"PINK1"	"0.577"	"0.586"	"C1853833"	"Parkinson Disease 6, Autosomal Recessive Early-Onset"	"disease"	"C10"	"Disease or Syndrome"	"0.81"	"1"	"2004"	"2017"	"26"	"19"	"CTD_human;UNIPROT"
"65018"	"PINK1"	"0.577"	"0.586"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.53"	"1"	"2001"	"2016"	"6"	"0"	"CTD_human"
"65018"	"PINK1"	"0.577"	"0.586"	"C1970035"	"PARKINSON DISEASE 6, LATE-ONSET, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.60"		"2004"	"2015"	"23"	"15"	"UNIPROT"
"65018"	"PINK1"	"0.577"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65018"	"PINK1"	"0.577"	"0.586"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.40"	"0.975"	"2005"	"2018"	"0"	"0"	"ORPHANET"
"65055"	"REEP1"	"0.707"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65055"	"REEP1"	"0.707"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"1"	"2006"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"65055"	"REEP1"	"0.707"	"0.31"	"C1833308"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"65055"	"REEP1"	"0.707"	"0.31"	"C1853247"	"SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2017"	"6"	"9"	"CTD_human;ORPHANET;UNIPROT"
"65055"	"REEP1"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65057"	"ACD"	"0.624"	"0.69"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"65057"	"ACD"	"0.624"	"0.69"	"C1846142"	"HOYERAAL-HREIDARSSON SYNDROME"	"disease"	"C05;C10;C13;C16;C17;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"65057"	"ACD"	"0.624"	"0.69"	"C2314896"	"Familial Atypical Mole Melanoma Syndrome"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"65057"	"ACD"	"0.624"	"0.69"	"C4225283"	"DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7"	"phenotype"		"Finding"	"0.50"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"65057"	"ACD"	"0.624"	"0.69"	"C4225284"	"DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"65059"	"RAPH1"	"0.621"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2012"	"0"	"0"	"UNIPROT"
"65059"	"RAPH1"	"0.621"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"65059"	"RAPH1"	"0.621"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"65061"	"CDK15"	"0.727"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65061"	"CDK15"	"0.727"	"0.448"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65062"	"TMEM237"	"0.652"	"0.345"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"65062"	"TMEM237"	"0.652"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65062"	"TMEM237"	"0.652"	"0.345"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2012"	"0"	"1"	"ORPHANET"
"65062"	"TMEM237"	"0.652"	"0.345"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65062"	"TMEM237"	"0.652"	"0.345"	"C1846790"	"JOUBERT SYNDROME 4 (disorder)"	"disease"	"C10;C11;C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"65062"	"TMEM237"	"0.652"	"0.345"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"65062"	"TMEM237"	"0.652"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"65062"	"TMEM237"	"0.652"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"65078"	"RTN4R"	"0.696"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.57"	"1"	"2005"	"2018"	"3"	"6"	"CTD_human;UNIPROT"
"65078"	"RTN4R"	"0.696"	"0.31"	"C4538533"	"SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2018"	"3"	"6"	"UNIPROT"
"65080"	"MRPL44"	"0.857"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65080"	"MRPL44"	"0.857"	"0.103"	"C3809339"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2014"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"65082"	"VPS33A"	"0.727"	"0.414"	"C4310627"	"MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"65084"	"TMEM135"	"0.834"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65084"	"TMEM135"	"0.834"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65084"	"TMEM135"	"0.834"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65084"	"TMEM135"	"0.834"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"65109"	"UPF3B"	"0.701"	"0.31"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65109"	"UPF3B"	"0.701"	"0.31"	"C0796022"	"Lujan Fryns syndrome"	"disease"	"C05;C10;C14;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"65109"	"UPF3B"	"0.701"	"0.31"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2010"	"1"	"0"	"CTD_human"
"65109"	"UPF3B"	"0.701"	"0.31"	"C1970822"	"Mental Retardation, X-Linked, Syndromic 14"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2007"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"65109"	"UPF3B"	"0.701"	"0.31"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"65109"	"UPF3B"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2007"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"65125"	"WNK1"	"0.472"	"0.793"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2005"	"2016"	"0"	"0"	"UNIPROT"
"65125"	"WNK1"	"0.472"	"0.793"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65125"	"WNK1"	"0.472"	"0.793"	"C0013364"	"Dysautonomia, Familial"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2004"	"2008"	"4"	"0"	"GENOMICS_ENGLAND"
"65125"	"WNK1"	"0.472"	"0.793"	"C0020072"	"Hereditary Sensory Autonomic Neuropathy, Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2013"	"0"	"0"	"ORPHANET"
"65125"	"WNK1"	"0.472"	"0.793"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.9473684"	"2004"	"2016"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"65125"	"WNK1"	"0.472"	"0.793"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2017"	"0"	"0"	"ORPHANET"
"65125"	"WNK1"	"0.472"	"0.793"	"C0391976"	"Pain Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2011"	"7"	"0"	"GENOMICS_ENGLAND"
"65125"	"WNK1"	"0.472"	"0.793"	"C0751540"	"Morvan's Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"	"0.9375"	"2004"	"2013"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2013"	"0"	"0"	"UNIPROT"
"65125"	"WNK1"	"0.472"	"0.793"	"C1840391"	"Pseudohypoaldosteronism, Type IIc"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2004"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"65125"	"WNK1"	"0.472"	"0.793"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65125"	"WNK1"	"0.472"	"0.793"	"C2752089"	"Neuropathy, Hereditary Sensory And Autonomic, Type IIA"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"1993"	"2017"	"0"	"7"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0009197"	"Cochlear Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.41"		"2000"	"2008"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0271097"	"Usher Syndrome"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.47"	"1"	"2001"	"2015"	"1"	"1"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.49"	"0.8888889"	"1993"	"2015"	"0"	"3"	"ORPHANET"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1832845"	"USHER SYNDROME, TYPE ID"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"		"2003"	"2017"	"2"	"3"	"UNIPROT"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1836027"	"Deafness, Autosomal Recessive 23"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.82"	"1"	"2003"	"2017"	"3"	"6"	"CTD_human;UNIPROT"
"65217"	"PCDH15"	"0.627"	"0.448"	"C1865885"	"Usher Syndrome, Type IF"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.87"	"1"	"2001"	"2017"	"9"	"49"	"CLINGEN;UNIPROT"
"65217"	"PCDH15"	"0.627"	"0.448"	"C2931205"	"Usher syndrome, type 1A"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C2931208"	"Usher syndrome, type 1D"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C2931210"	"Usher syndrome, type 1F"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.38"	"0.875"	"2001"	"2016"	"0"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C3152102"	"USH1D/F, CDH23/PCDH15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"0"	"UNIPROT"
"65217"	"PCDH15"	"0.627"	"0.448"	"C3275872"	"USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.30"		"2005"	"2008"	"2"	"0"	"UNIPROT"
"65217"	"PCDH15"	"0.627"	"0.448"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"65217"	"PCDH15"	"0.627"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"65250"	"CPLANE1"	"0.633"	"0.586"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.46"	"1"	"2012"	"2018"	"0"	"1"	"ORPHANET"
"65250"	"CPLANE1"	"0.633"	"0.586"	"C1865384"	"Amyotrophy, monomelic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"65250"	"CPLANE1"	"0.633"	"0.586"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"2013"	"2018"	"0"	"12"	"CTD_human;ORPHANET"
"65258"	"MPPE1"	"0.886"	"0.103"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"65260"	"COA7"	"0.72"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.50"	"0.9142857"	"2003"	"2016"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"65266"	"WNK4"	"0.685"	"0.379"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65266"	"WNK4"	"0.685"	"0.379"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65266"	"WNK4"	"0.685"	"0.379"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"	"0.96"	"2003"	"2015"	"1"	"0"	"CTD_human"
"65266"	"WNK4"	"0.685"	"0.379"	"C1840390"	"Pseudohypoaldosteronism, Type IIb"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"		"1978"	"2013"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"65266"	"WNK4"	"0.685"	"0.379"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"65267"	"WNK3"	"0.815"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"65267"	"WNK3"	"0.815"	"0.241"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65267"	"WNK3"	"0.815"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65267"	"WNK3"	"0.815"	"0.241"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65267"	"WNK3"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"65975"	"STK33"	"0.815"	"0.207"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"65980"	"BRD9"	"1"	"0.103"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"65992"	"DDRGK1"	"0.815"	"0.172"	"C1865185"	"Spondyloepimetaphyseal Dysplasia, Shohat Type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"65993"	"MRPS34"	"0.928"	"0.103"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"65993"	"MRPS34"	"0.928"	"0.103"	"C4540029"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"3"	"UNIPROT"
"65998"	"C11orf95"	"0.857"	"0.034"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2017"	"0"	"0"	"ORPHANET"
"66008"	"TRAK2"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"66037"	"BOLL"	"0.762"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"66037"	"BOLL"	"0.762"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"66037"	"BOLL"	"0.762"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"78987"	"CRELD1"	"0.743"	"0.207"	"C0344735"	"Partial atrioventricular canal"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"78987"	"CRELD1"	"0.743"	"0.207"	"C1853508"	"ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.40"		"2003"	"2013"	"2"	"5"	"UNIPROT"
"78987"	"CRELD1"	"0.743"	"0.207"	"C1853509"	"Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.50"		"2003"	"2005"	"2"	"4"	"CTD_human;UNIPROT"
"78987"	"CRELD1"	"0.743"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0022283"	"Incontinentia Pigmenti Achromians"	"disease"	"C17;C23"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0036305"	"Schamberg Disease"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0549567"	"Pigmentation Disorders"	"group"	"C17;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0796032"	"Malpuech facial clefting syndrome"	"disease"	"C05;C14;C16;F03"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0796059"	"Oculopalatoskeletal syndrome"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"78989"	"COLEC11"	"0.663"	"0.621"	"C0796279"	"Carnevale syndrome"	"disease"	"C05;C10;C11;C12;C16;C19"	"Disease or Syndrome"	"0.60"		"2011"	"2017"	"3"	"2"	"CTD_human;UNIPROT"
"78989"	"COLEC11"	"0.663"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"78989"	"COLEC11"	"0.663"	"0.621"	"C4303860"	"Craniofacial ulnar renal syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"78990"	"OTUB2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"78996"	"CYREN"	"0.773"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"78997"	"GDAP1L1"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0003496"	"Aortic Rupture"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0005779"	"Blood Coagulation Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"0.75"	"2006"	"2013"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2015"	"2"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2008"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0741160"	"Aortic Aneurysm, Ruptured"	"disease"	"C14;C26"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0750384"	"Coumarin Resistance"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.60"	"1"	"2004"	"2016"	"1"	"7"	"CTD_human;UNIPROT"
"79001"	"VKORC1"	"0.639"	"0.655"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79001"	"VKORC1"	"0.639"	"0.655"	"C1843832"	"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.60"		"2001"	"2005"	"2"	"1"	"CTD_human;UNIPROT"
"79001"	"VKORC1"	"0.639"	"0.655"	"C1848534"	"VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79001"	"VKORC1"	"0.639"	"0.655"	"C2608079"	"WARFARIN SENSITIVITY (disorder)"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2014"	"1"	"7"	"UNIPROT"
"79001"	"VKORC1"	"0.639"	"0.655"	"C2675747"	"Coumarin Sensitivity"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2011"	"1"	"7"	"UNIPROT"
"79003"	"MIS12"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79012"	"CAMKV"	"0.928"	"0.069"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79012"	"CAMKV"	"0.928"	"0.069"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79026"	"AHNAK"	"0.727"	"0.241"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79026"	"AHNAK"	"0.727"	"0.241"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79039"	"DDX54"	"0.834"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0011168"	"Deglutition Disorders"	"group"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0267071"	"Oropharyngeal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0267072"	"Esophageal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C2676465"	"Pontocerebellar Hypoplasia Type 2C"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"79042"	"TSEN34"	"0.685"	"0.31"	"C2932714"	"Pontocerebellar Hypoplasia Type 2"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79042"	"TSEN34"	"0.685"	"0.31"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79042"	"TSEN34"	"0.685"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"79042"	"TSEN34"	"0.685"	"0.31"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79047"	"KCTD15"	"0.815"	"0.207"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.38"	"0.75"	"2009"	"2015"	"1"	"0"	"CTD_human"
"79048"	"SECISBP2"	"0.799"	"0.172"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79048"	"SECISBP2"	"0.799"	"0.172"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79048"	"SECISBP2"	"0.799"	"0.172"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79048"	"SECISBP2"	"0.799"	"0.172"	"C1864761"	"Thyroid Hormone Metabolism, Abnormal"	"disease"	"C19"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2012"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"79048"	"SECISBP2"	"0.799"	"0.172"	"C2940786"	"Thyroid Hormone Resistance Syndrome"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2006"	"2014"	"7"	"0"	"GENOMICS_ENGLAND"
"79053"	"ALG8"	"0.815"	"0.241"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"79053"	"ALG8"	"0.815"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79053"	"ALG8"	"0.815"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79053"	"ALG8"	"0.815"	"0.241"	"C2931002"	"Congenital disorder of glycosylation type 1H"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"2003"	"2016"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"79053"	"ALG8"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.47"	"0.7142857"	"2011"	"2016"	"1"	"4"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79054"	"TRPM8"	"0.598"	"0.517"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79057"	"PRRG3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79058"	"ASPSCR1"	"0.815"	"0.103"	"C0206657"	"Alveolar Soft Part Sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.70"	"1"	"2001"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"79058"	"ASPSCR1"	"0.815"	"0.103"	"C4518356"	"MiT family translocation renal cell carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"79068"	"FTO"	"0.519"	"0.828"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2015"	"3"	"0"	"PSYGENET"
"79068"	"FTO"	"0.519"	"0.828"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2008"	"2012"	"2"	"3"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2012"	"2016"	"2"	"0"	"PSYGENET"
"79068"	"FTO"	"0.519"	"0.828"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.6666667"	"2012"	"2016"	"3"	"0"	"PSYGENET"
"79068"	"FTO"	"0.519"	"0.828"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9195402"	"2007"	"2017"	"1"	"17"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.43"	"1"	"2013"	"2017"	"1"	"1"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"	"0.9529086"	"2007"	"2018"	"6"	"58"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"79068"	"FTO"	"0.519"	"0.828"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.47"	"1"	"2013"	"2018"	"1"	"4"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C2362324"	"Pediatric Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2007"	"2016"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C2675914"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C2752001"	"Growth Retardation, Developmental Delay, Coarse Facies, And Early Death"	"disease"	"C05;C16;C19;C23;F03"	"Congenital Abnormality"	"0.70"		"2009"	"2016"	"4"	"3"	"CTD_human;ORPHANET;UNIPROT"
"79068"	"FTO"	"0.519"	"0.828"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79068"	"FTO"	"0.519"	"0.828"	"C4317171"	"Adolescent Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79068"	"FTO"	"0.519"	"0.828"	"C4521075"	"Childhood Overweight"	"phenotype"	"C18;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79071"	"ELOVL6"	"0.69"	"0.345"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79072"	"FASTKD3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79080"	"CCDC86"	"0.928"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"79080"	"CCDC86"	"0.928"	"0.138"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79083"	"MLPH"	"0.799"	"0.276"	"C1836573"	"GRISCELLI SYNDROME, TYPE 3"	"disease"	"C16;C17;C18;C23"	"Disease or Syndrome"	"0.70"		"2003"	"2003"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"79084"	"WDR77"	"0.707"	"0.31"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79084"	"WDR77"	"0.707"	"0.31"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79087"	"ALG12"	"0.799"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"79087"	"ALG12"	"0.799"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79087"	"ALG12"	"0.799"	"0.207"	"C2931001"	"Congenital disorder of glycosylation type 1G"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2002"	"2014"	"4"	"8"	"CTD_human;ORPHANET;UNIPROT"
"79087"	"ALG12"	"0.799"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2003"	"3"	"0"	"GENOMICS_ENGLAND"
"79090"	"TRAPPC6A"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"79092"	"CARD14"	"0.616"	"0.483"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79092"	"CARD14"	"0.616"	"0.483"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2014"	"2"	"0"	"CTD_human"
"79092"	"CARD14"	"0.616"	"0.483"	"C0032027"	"Pityriasis Rubra Pilaris"	"disease"	"C17"	"Disease or Syndrome"	"0.76"	"0.8333333"	"2012"	"2017"	"6"	"2"	"CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT"
"79092"	"CARD14"	"0.616"	"0.483"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.9047619"	"2003"	"2018"	"2"	"1"	"CTD_human"
"79092"	"CARD14"	"0.616"	"0.483"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.34"	"1"	"2012"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"79092"	"CARD14"	"0.616"	"0.483"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79092"	"CARD14"	"0.616"	"0.483"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79092"	"CARD14"	"0.616"	"0.483"	"C1864497"	"PSORIASIS 2"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1994"	"2017"	"5"	"13"	"UNIPROT"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79101"	"TAF1D"	"0.834"	"0.069"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2008"	"2012"	"1"	"3"	"CTD_human;UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2012"	"2"	"2"	"UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"79133"	"NDUFAF5"	"0.645"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"79137"	"RETREG2"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"79139"	"DERL1"	"0.6"	"0.517"	"C0014518"	"Toxic Epidermal Necrolysis"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79139"	"DERL1"	"0.6"	"0.517"	"C0038325"	"Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79139"	"DERL1"	"0.6"	"0.517"	"C1274933"	"Drug-Induced Stevens Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79139"	"DERL1"	"0.6"	"0.517"	"C3658301"	"Mycoplasma-Induced Stevens-Johnson Syndrome"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79139"	"DERL1"	"0.6"	"0.517"	"C3658302"	"Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum"	"disease"	"C07;C17;C20;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79140"	"CCDC28B"	"0.857"	"0.138"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79140"	"CCDC28B"	"0.857"	"0.138"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79140"	"CCDC28B"	"0.857"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"79143"	"MBOAT7"	"0.752"	"0.172"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"CTD_human"
"79143"	"MBOAT7"	"0.752"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79143"	"MBOAT7"	"0.752"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79143"	"MBOAT7"	"0.752"	"0.172"	"C4310673"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"5"	"CTD_human"
"79147"	"FKRP"	"0.514"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2004"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"79147"	"FKRP"	"0.514"	"0.586"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"2009"	"2018"	"0"	"1"	"CTD_human"
"79147"	"FKRP"	"0.514"	"0.586"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.53"	"1"	"2009"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"79147"	"FKRP"	"0.514"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"2002"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.70"	"1"	"2002"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79147"	"FKRP"	"0.514"	"0.586"	"C1846672"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.95"	"1"	"2002"	"2016"	"5"	"27"	"CTD_human;ORPHANET;UNIPROT"
"79147"	"FKRP"	"0.514"	"0.586"	"C1847759"	"MUSCULAR DYSTROPHY, CONGENITAL, 1C"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.86"	"1"	"2002"	"2015"	"4"	"11"	"CTD_human;UNIPROT"
"79147"	"FKRP"	"0.514"	"0.586"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79147"	"FKRP"	"0.514"	"0.586"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"0"	"0"	"CTD_human"
"79147"	"FKRP"	"0.514"	"0.586"	"C3150413"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2015"	"1"	"8"	"UNIPROT"
"79147"	"FKRP"	"0.514"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2004"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"79149"	"ZSCAN5A"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79152"	"FA2H"	"0.633"	"0.517"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"2009"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"79152"	"FA2H"	"0.633"	"0.517"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2010"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"79152"	"FA2H"	"0.633"	"0.517"	"C3496228"	"Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.83"	"1"	"2009"	"2012"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"79152"	"FA2H"	"0.633"	"0.517"	"C3668943"	"Fatty Acid Hydroxylase-Associated Neurodegeneration"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2014"	"0"	"8"	"ORPHANET"
"79152"	"FA2H"	"0.633"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"79153"	"GDPD3"	"1"	"0.069"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2007"	"3"	"0"	"CTD_human"
"79156"	"PLEKHF1"	"0.857"	"0.138"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79156"	"PLEKHF1"	"0.857"	"0.138"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"4"	"0"	"GENOMICS_ENGLAND"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0020725"	"Type II Mucolipidosis"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"2005"	"2017"	"15"	"12"	"CTD_human;ORPHANET;UNIPROT"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0033788"	"Pseudo-Hurler Polydystrophy"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2017"	"15"	"55"	"CTD_human;ORPHANET;UNIPROT"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C2673375"	"Mucolipidosis III Alpha Beta, Atypical"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.70"		"2005"	"2017"	"15"	"20"	"CTD_human;ORPHANET;UNIPROT"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C2673377"	"MUCOLIPIDOSIS II ALPHA/BETA (disorder)"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.83"	"1"	"1993"	"2017"	"15"	"110"	"CTD_human;UNIPROT"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C2931894"	"Mucolipidosis 2"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79158"	"GNPTAB"	"0.624"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"79184"	"BRCC3"	"0.785"	"0.138"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"79184"	"BRCC3"	"0.785"	"0.138"	"C3151857"	"MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79187"	"FSD1"	"0.53"	"0.69"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"79187"	"FSD1"	"0.53"	"0.69"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79187"	"FSD1"	"0.53"	"0.69"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0085298"	"Sudden Cardiac Death"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0349788"	"Arrhythmogenic Right Ventricular Dysplasia"	"disease"	"C14;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.48"	"1"	"2008"	"2016"	"0"	"2"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0410189"	"Muscular Dystrophy, Emery-Dreifuss"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"0"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0410190"	"Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79188"	"TMEM43"	"0.69"	"0.276"	"C0751337"	"X-Linked Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C1450051"	"Autosomal Recessive Emery-Dreifuss Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C1720824"	"Sudden Cardiac Arrest"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79188"	"TMEM43"	"0.69"	"0.276"	"C1858379"	"ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"79188"	"TMEM43"	"0.69"	"0.276"	"C3553060"	"EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"2"	"UNIPROT"
"79191"	"IRX3"	"0.928"	"0.103"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79192"	"IRX1"	"0.72"	"0.345"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79228"	"THOC6"	"0.735"	"0.379"	"C3150939"	"BEAULIEU-BOYCOTT-INNES SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"79228"	"THOC6"	"0.735"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"79258"	"MMEL1"	"0.672"	"0.517"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.44"	"1"	"2008"	"2018"	"1"	"2"	"CTD_human"
"79258"	"MMEL1"	"0.672"	"0.517"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human;ORPHANET"
"79258"	"MMEL1"	"0.672"	"0.517"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79258"	"MMEL1"	"0.672"	"0.517"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2008"	"2017"	"1"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"0.5"	"2007"	"2017"	"1"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0751508"	"Long Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0751509"	"Short Sleeper Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"1"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0751510"	"Sleep-Related Neurogenic Tachypnea"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0751511"	"Subwakefullness Syndrome"	"disease"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C0851578"	"Sleep Disorders"	"group"	"C10;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79365"	"BHLHE41"	"0.663"	"0.414"	"C4042891"	"Sleep Wake Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"79366"	"HMGN5"	"0.69"	"0.241"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79443"	"FYCO1"	"0.815"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79443"	"FYCO1"	"0.815"	"0.172"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"79443"	"FYCO1"	"0.815"	"0.172"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79443"	"FYCO1"	"0.815"	"0.172"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79443"	"FYCO1"	"0.815"	"0.172"	"C1864908"	"Cataract, autosomal recessive congenital 2"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2001"	"2011"	"1"	"6"	"CTD_human;UNIPROT"
"79443"	"FYCO1"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79444"	"BIRC7"	"0.645"	"0.31"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"79444"	"BIRC7"	"0.645"	"0.31"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"2"	"0"	"CTD_human"
"79444"	"BIRC7"	"0.645"	"0.31"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"79444"	"BIRC7"	"0.645"	"0.31"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"79444"	"BIRC7"	"0.645"	"0.31"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"79444"	"BIRC7"	"0.645"	"0.31"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"79465"	"ULBP3"	"1"	"0.034"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79570"	"NKAIN1"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"79571"	"GCC1"	"0.799"	"0.069"	"C0006868"	"Cannabis Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0018614"	"Hashish Abuse"	"disease"	"C25;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0031391"	"Phencyclidine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0236735"	"Cannabis-Related Disorder"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0236742"	"Phencyclidine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79571"	"GCC1"	"0.799"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79572"	"ATP13A3"	"0.886"	"0.103"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"79572"	"ATP13A3"	"0.886"	"0.103"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"79574"	"EPS8L3"	"0.857"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79574"	"EPS8L3"	"0.857"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"79574"	"EPS8L3"	"0.857"	"0.138"	"C2931059"	"Marie Unna congenital hypotrichosis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"79576"	"NKAP"	"0.928"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79577"	"CDC73"	"0.609"	"0.448"	"C0018671"	"Head and Neck Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79577"	"CDC73"	"0.609"	"0.448"	"C0030521"	"Parathyroid Neoplasms"	"group"	"C04;C19"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2013"	"0"	"0"	"CTD_human"
"79577"	"CDC73"	"0.609"	"0.448"	"C0262587"	"Parathyroid Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.69"	"0.6666667"	"2003"	"2013"	"0"	"0"	"CGI;CTD_human"
"79577"	"CDC73"	"0.609"	"0.448"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79577"	"CDC73"	"0.609"	"0.448"	"C0687150"	"Parathyroid Gland Adenocarcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.80"	"0.9148936"	"1993"	"2017"	"0"	"12"	"CTD_human;GENOMICS_ENGLAND;ORPHANET"
"79577"	"CDC73"	"0.609"	"0.448"	"C1704981"	"Hyperparathyroidism-Jaw Tumor Syndrome"	"disease"	"C04;C05;C07;C19"	"Neoplastic Process"	"0.70"	"0.9803922"	"1995"	"2017"	"3"	"6"	"ORPHANET;UNIPROT"
"79577"	"CDC73"	"0.609"	"0.448"	"C1840394"	"Parathyroid Adenomatosis, Familial Cystic"	"disease"	"C04;C05;C07;C19"	"Disease or Syndrome"	"0.30"		"2003"	"2006"	"3"	"1"	"UNIPROT"
"79577"	"CDC73"	"0.609"	"0.448"	"C1840402"	"HYPERPARATHYROIDISM 1"	"disease"	"C19"	"Disease or Syndrome"	"0.70"	"0.95"	"1998"	"2015"	"5"	"5"	"ORPHANET;UNIPROT"
"79577"	"CDC73"	"0.609"	"0.448"	"C1840403"	"Parathyroid Adenoma, Familial"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2003"	"2009"	"5"	"1"	"UNIPROT"
"79577"	"CDC73"	"0.609"	"0.448"	"C3887461"	"Head and Neck Carcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79581"	"SLC52A2"	"0.528"	"0.759"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79581"	"SLC52A2"	"0.528"	"0.759"	"C0796274"	"Brown-Vialetto-Van Laere syndrome"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.54"	"1"	"2013"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"79581"	"SLC52A2"	"0.528"	"0.759"	"C1849094"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79581"	"SLC52A2"	"0.528"	"0.759"	"C3553538"	"BROWN-VIALETTO-VAN LAERE SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2017"	"5"	"18"	"UNIPROT"
"79583"	"TMEM231"	"0.611"	"0.552"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"79583"	"TMEM231"	"0.611"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79583"	"TMEM231"	"0.611"	"0.552"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79583"	"TMEM231"	"0.611"	"0.552"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2015"	"0"	"1"	"ORPHANET"
"79583"	"TMEM231"	"0.611"	"0.552"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79583"	"TMEM231"	"0.611"	"0.552"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79583"	"TMEM231"	"0.611"	"0.552"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79583"	"TMEM231"	"0.611"	"0.552"	"C3554235"	"JOUBERT SYNDROME 20"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"2"	"3"	"UNIPROT"
"79583"	"TMEM231"	"0.611"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79583"	"TMEM231"	"0.611"	"0.552"	"C3809352"	"MECKEL SYNDROME, TYPE 11"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2017"	"1"	"4"	"UNIPROT"
"79583"	"TMEM231"	"0.611"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"79587"	"CARS2"	"0.727"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79587"	"CARS2"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79587"	"CARS2"	"0.727"	"0.31"	"C4225251"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"79595"	"SAP130"	"0.886"	"0.138"	"C0152101"	"Hypoplastic Left Heart Syndrome"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"79600"	"TCTN1"	"0.685"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.52"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"79600"	"TCTN1"	"0.685"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79600"	"TCTN1"	"0.685"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79600"	"TCTN1"	"0.685"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79600"	"TCTN1"	"0.685"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79600"	"TCTN1"	"0.685"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79602"	"ADIPOR2"	"0.594"	"0.586"	"C0021361"	"Female infertility"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79602"	"ADIPOR2"	"0.594"	"0.586"	"C0038279"	"Sterility, Postpartum"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79602"	"ADIPOR2"	"0.594"	"0.586"	"C0341869"	"Subfertility, Female"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79602"	"ADIPOR2"	"0.594"	"0.586"	"C0917730"	"Female sterility"	"phenotype"	"C13"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79605"	"PGBD5"	"1"	"0.034"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79605"	"PGBD5"	"1"	"0.034"	"C0206743"	"Rhabdoid Tumor"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79608"	"RIC3"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2006"	"2017"	"0"	"1"	"ORPHANET"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C0796126"	"AICARDI-GOUTIERES SYNDROME 1"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.36"	"1"	"2006"	"2017"	"0"	"0"	"CTD_human"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C3489724"	"Aicardi-Goutieres Syndrome 2"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.60"		"2006"	"2017"	"4"	"15"	"CTD_human;UNIPROT"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79621"	"RNASEH2B"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79625"	"NDNF"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79625"	"NDNF"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79628"	"SH3TC2"	"0.672"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"2004"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"79628"	"SH3TC2"	"0.672"	"0.414"	"C1866636"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.96"	"1"	"1993"	"2016"	"1"	"23"	"CTD_human;ORPHANET;UNIPROT"
"79628"	"SH3TC2"	"0.672"	"0.414"	"C3150596"	"MONONEUROPATHY OF THE MEDIAN NERVE, MILD"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"79628"	"SH3TC2"	"0.672"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79631"	"EFL1"	"0.735"	"0.345"	"C0272170"	"Shwachman syndrome"	"disease"	"C06;C15;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79632"	"FAM184A"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"79633"	"FAT4"	"0.572"	"0.724"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C0340834"	"Hennekam lymphangiectasia lymphedema syndrome"	"disease"	"C05;C15;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"79633"	"FAT4"	"0.572"	"0.724"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C1832390"	"Van Maldergem Wetzburger Verloes syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human;ORPHANET"
"79633"	"FAT4"	"0.572"	"0.724"	"C1842563"	"Heterotopia, Periventricular, Autosomal Recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"79633"	"FAT4"	"0.572"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"79633"	"FAT4"	"0.572"	"0.724"	"C3809875"	"VAN MALDERGEM SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2014"	"1"	"6"	"UNIPROT"
"79633"	"FAT4"	"0.572"	"0.724"	"C4014939"	"HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2003"	"2014"	"1"	"5"	"UNIPROT"
"79641"	"ROGDI"	"0.735"	"0.276"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.40"		"1989"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"79641"	"ROGDI"	"0.735"	"0.276"	"C0406740"	"Kohlschutter Tonz syndrome"	"disease"	"C07;C10;C16;F03"	"Disease or Syndrome"	"0.62"	"1"	"1974"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"79641"	"ROGDI"	"0.735"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79641"	"ROGDI"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C2675185"	"Kahrizi Syndrome"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2011"	"0"	"1"	"CTD_human"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C3150191"	"Coloboma, Ocular, And Ichthyosis, Brain Malformations, And Endocrine Abnormalities"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2008"	"2018"	"0"	"7"	"CTD_human;ORPHANET"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"79644"	"SRD5A3"	"0.652"	"0.414"	"C4317224"	"Congenital disorder of glycosylation type 1q"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79648"	"MCPH1"	"0.584"	"0.621"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.60"	"1"	"2002"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"79648"	"MCPH1"	"0.584"	"0.621"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2016"	"7"	"0"	"CLINGEN"
"79648"	"MCPH1"	"0.584"	"0.621"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.40"	"1"	"2002"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"79648"	"MCPH1"	"0.584"	"0.621"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2013"	"0"	"0"	"CLINGEN"
"79648"	"MCPH1"	"0.584"	"0.621"	"C1855081"	"MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.66"	"1"	"1993"	"2015"	"3"	"8"	"CTD_human;UNIPROT"
"79648"	"MCPH1"	"0.584"	"0.621"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.37"	"1"	"2000"	"2015"	"0"	"0"	"ORPHANET"
"79648"	"MCPH1"	"0.584"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"79649"	"MAP7D3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1989"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79650"	"USB1"	"0.672"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79650"	"USB1"	"0.672"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79650"	"USB1"	"0.672"	"0.414"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"79650"	"USB1"	"0.672"	"0.414"	"C1858723"	"Poikiloderma with Neutropenia"	"disease"	"C15;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2018"	"0"	"8"	"CTD_human;ORPHANET"
"79650"	"USB1"	"0.672"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79651"	"RHBDF2"	"0.672"	"0.276"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2012"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"79651"	"RHBDF2"	"0.672"	"0.276"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"79651"	"RHBDF2"	"0.672"	"0.276"	"C1835664"	"TYLOSIS WITH ESOPHAGEAL CANCER"	"disease"	"C04;C06;C16;C17"	"Neoplastic Process"	"0.72"	"1"	"1954"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"2012"	"2018"	"1"	"1"	"CTD_human;ORPHANET"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"		"2009"	"2013"	"4"	"22"	"CTD_human;ORPHANET;UNIPROT"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2012"	"1"	"0"	"CTD_human"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.33"	"1"	"2012"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.44"	"1"	"2009"	"2018"	"0"	"32"	"ORPHANET"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0432197"	"Short rib-polydactyly syndrome, Verma-Naumoff type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"2009"	"2016"	"4"	"22"	"ORPHANET;UNIPROT"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79659"	"DYNC2H1"	"0.624"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.33"	"1"	"2011"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"79660"	"PPP1R3B"	"0.762"	"0.31"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.50"		"2006"	"2011"	"2"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0524620"	"Metabolic Syndrome X"	"disease"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2007"	"2"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C1257963"	"Endogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C1257964"	"Exogenous Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C1257965"	"Compensatory Hyperinsulinemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79661"	"NEIL1"	"0.636"	"0.586"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2011"	"2"	"0"	"CTD_human"
"79663"	"HSPBAP1"	"0.857"	"0.138"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"79664"	"ICE2"	"0.886"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79664"	"ICE2"	"0.886"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79664"	"ICE2"	"0.886"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79664"	"ICE2"	"0.886"	"0.069"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79668"	"PARP8"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79677"	"SMC6"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"79685"	"SAP30L"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79685"	"SAP30L"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79689"	"STEAP4"	"0.713"	"0.379"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79689"	"STEAP4"	"0.713"	"0.379"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"79689"	"STEAP4"	"0.713"	"0.379"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79694"	"MANEA"	"0.762"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2009"	"2"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79694"	"MANEA"	"0.762"	"0.207"	"C1456784"	"Paranoia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79695"	"GALNT12"	"0.752"	"0.241"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2014"	"0"	"0"	"CTD_human"
"79695"	"GALNT12"	"0.752"	"0.241"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2004"	"2004"	"0"	"0"	"CTD_human"
"79695"	"GALNT12"	"0.752"	"0.241"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2004"	"2009"	"2"	"0"	"CLINGEN"
"79695"	"GALNT12"	"0.752"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79695"	"GALNT12"	"0.752"	"0.241"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2004"	"2009"	"2"	"0"	"CLINGEN"
"79695"	"GALNT12"	"0.752"	"0.241"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2004"	"2009"	"2"	"0"	"CLINGEN"
"79695"	"GALNT12"	"0.752"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2014"	"0"	"0"	"CTD_human"
"79695"	"GALNT12"	"0.752"	"0.241"	"C1837315"	"COLORECTAL CANCER, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.40"		"2009"	"2014"	"3"	"5"	"UNIPROT"
"79705"	"LRRK1"	"0.857"	"0.034"	"C3554665"	"OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2015"	"2017"	"0"	"1"	"ORPHANET"
"79705"	"LRRK1"	"0.857"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79710"	"MORC4"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79711"	"IPO4"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0024305"	"Lymphoma, Non-Hodgkin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0154017"	"Benign neoplasm of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0154091"	"Carcinoma in situ of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0496930"	"Neoplasm of uncertain or unknown behavior of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C0742472"	"Central nervous system lymphoma"	"group"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C1865644"	"Plantar Lipomatosis, Unusual Facies, and Developmental Delay"	"disease"	"C17;C18;C23;F03"	"Disease or Syndrome"	"0.71"	"1"	"1998"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"79718"	"TBL1XR1"	"0.567"	"0.69"	"C4310784"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 41"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2017"	"4"	"2"	"CTD_human;UNIPROT"
"79719"	"AAGAB"	"0.701"	"0.448"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2013"	"2015"	"4"	"1"	"CTD_human;GENOMICS_ENGLAND"
"79719"	"AAGAB"	"0.701"	"0.448"	"C0025221"	"Meleda Disease"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79719"	"AAGAB"	"0.701"	"0.448"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"79719"	"AAGAB"	"0.701"	"0.448"	"C1835662"	"Keratosis palmoplantaris papulosa"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2013"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"79722"	"ANKRD55"	"0.659"	"0.345"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2014"	"1"	"3"	"CTD_human"
"79722"	"ANKRD55"	"0.659"	"0.345"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79722"	"ANKRD55"	"0.659"	"0.345"	"C2931171"	"Juvenile pauciarticular chronic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79723"	"SUV39H2"	"0.773"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79727"	"LIN28A"	"0.561"	"0.586"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"79727"	"LIN28A"	"0.561"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79727"	"LIN28A"	"0.561"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79727"	"LIN28A"	"0.561"	"0.586"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"79727"	"LIN28A"	"0.561"	"0.586"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2007"	"2011"	"1"	"1"	"PSYGENET"
"79728"	"PALB2"	"0.569"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9684211"	"2007"	"2018"	"4"	"1"	"CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT"
"79728"	"PALB2"	"0.569"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2017"	"2018"	"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0007112"	"Adenocarcinoma of prostate"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0009405"	"Hereditary Nonpolyposis Colorectal Neoplasms"	"group"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.30"		"2013"	"2018"	"7"	"0"	"CLINGEN"
"79728"	"PALB2"	"0.569"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2007"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.50"	"1"	"2007"	"2018"	"0"	"1"	"ORPHANET"
"79728"	"PALB2"	"0.569"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.39"	"0.7777778"	"2008"	"2015"	"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"		"2007"	"2018"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"79728"	"PALB2"	"0.569"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.80"	"0.9642857"	"2006"	"2018"	"10"	"163"	"CLINGEN;ORPHANET;UNIPROT"
"79728"	"PALB2"	"0.569"	"0.552"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.40"	"0.9375"	"2009"	"2018"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.44"	"1"	"2007"	"2018"	"0"	"11"	"ORPHANET"
"79728"	"PALB2"	"0.569"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9571429"	"2007"	"2018"	"1"	"0"	"CGI;CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2008"	"2008"	"0"	"1"	"CGI"
"79728"	"PALB2"	"0.569"	"0.552"	"C1112155"	"Hereditary non-polyposis colorectal cancer syndrome"	"disease"		"Congenital Abnormality"	"0.30"		"2013"	"2018"	"7"	"0"	"CLINGEN"
"79728"	"PALB2"	"0.569"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.68"	"0.75"	"2006"	"2016"	"3"	"0"	"CGI;CLINGEN"
"79728"	"PALB2"	"0.569"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C1333990"	"Hereditary Nonpolyposis Colorectal Cancer"	"disease"	"C04;C06;C16;C18"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2018"	"7"	"0"	"CLINGEN"
"79728"	"PALB2"	"0.569"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"	"1"	"2006"	"2017"	"1"	"1"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C1835817"	"FANCONI ANEMIA, COMPLEMENTATION GROUP N"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2015"	"0"	"11"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"CTD_human"
"79728"	"PALB2"	"0.569"	"0.552"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2017"	"3"	"1"	"UNIPROT"
"79728"	"PALB2"	"0.569"	"0.552"	"C2931038"	"Pancreatic carcinoma, familial"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.39"	"0.8888889"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"79728"	"PALB2"	"0.569"	"0.552"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79728"	"PALB2"	"0.569"	"0.552"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2007"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"79730"	"NSUN7"	"1"	"0.034"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"79730"	"NSUN7"	"1"	"0.034"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79730"	"NSUN7"	"1"	"0.034"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79731"	"NARS2"	"0.681"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79731"	"NARS2"	"0.681"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"3"	"0"	"GENOMICS_ENGLAND"
"79731"	"NARS2"	"0.681"	"0.483"	"C1838951"	"LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C1850597"	"Leigh Syndrome Due To Mitochondrial Complex II Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C1850598"	"Leigh Syndrome due to Mitochondrial Complex III Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C1850599"	"Leigh Syndrome due to Mitochondrial Complex IV Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C1850600"	"Leigh Syndrome due to Mitochondrial Complex V Deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C2931891"	"Necrotizing encephalopathy, infantile subacute, of Leigh"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"UNIPROT"
"79731"	"NARS2"	"0.681"	"0.483"	"C4015643"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2015"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"79734"	"KCTD17"	"0.735"	"0.241"	"C1834570"	"Myoclonic dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"79734"	"KCTD17"	"0.735"	"0.241"	"C4225341"	"DYSTONIA 26, MYOCLONIC"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"79738"	"BBS10"	"0.676"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"79738"	"BBS10"	"0.676"	"0.414"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2017"	"0"	"11"	"ORPHANET"
"79738"	"BBS10"	"0.676"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79738"	"BBS10"	"0.676"	"0.414"	"C1859568"	"BARDET-BIEDL SYNDROME 10"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.80"		"2006"	"2017"	"7"	"52"	"CTD_human;UNIPROT"
"79738"	"BBS10"	"0.676"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79738"	"BBS10"	"0.676"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79742"	"CXorf36"	"0.886"	"0.172"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"79742"	"CXorf36"	"0.886"	"0.172"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"2"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79750"	"ZNF385D"	"0.762"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79751"	"SLC25A22"	"0.701"	"0.207"	"C0270855"	"Early myoclonic encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"2005"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"79751"	"SLC25A22"	"0.701"	"0.207"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"ORPHANET"
"79751"	"SLC25A22"	"0.701"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2009"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"79751"	"SLC25A22"	"0.701"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79751"	"SLC25A22"	"0.701"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79753"	"SNIP1"	"0.685"	"0.345"	"C3281055"	"PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"79753"	"SNIP1"	"0.685"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"79755"	"ZNF750"	"0.762"	"0.241"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"79755"	"ZNF750"	"0.762"	"0.241"	"C1853258"	"Seborrhea-Like Dermatitis with Psoriasiform Elements"	"disease"	"C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"79759"	"ZNF668"	"0.773"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"UNIPROT"
"79759"	"ZNF668"	"0.773"	"0.069"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79759"	"ZNF668"	"0.773"	"0.069"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79759"	"ZNF668"	"0.773"	"0.069"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79759"	"ZNF668"	"0.773"	"0.069"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79759"	"ZNF668"	"0.773"	"0.069"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79763"	"ISOC2"	"0.928"	"0.034"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79763"	"ISOC2"	"0.928"	"0.034"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79770"	"TXNDC15"	"0.857"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"0"	"0"	"UNIPROT"
"79770"	"TXNDC15"	"0.857"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79776"	"ZFHX4"	"0.815"	"0.138"	"C0266573"	"Congenital ptosis"	"disease"		"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"79776"	"ZFHX4"	"0.815"	"0.138"	"C1867438"	"PTOSIS, HEREDITARY CONGENITAL 1 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79776"	"ZFHX4"	"0.815"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79777"	"ACBD4"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0007852"	"Cervical Migraine Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0018984"	"Hemicrania migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0042331"	"Migraine Variant"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0149931"	"Migraine Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.41"	"0"	"2013"	"2017"	"1"	"3"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0270858"	"Abdominal Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0338489"	"Status Migrainosus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0342873"	"Glutaric Aciduria III"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1991"	"2014"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0521664"	"Acute Confusional Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79783"	"SUGCT"	"0.735"	"0.276"	"C0700438"	"Sick Headaches"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79784"	"MYH14"	"0.69"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79784"	"MYH14"	"0.69"	"0.414"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79784"	"MYH14"	"0.69"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79784"	"MYH14"	"0.69"	"0.414"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79784"	"MYH14"	"0.69"	"0.414"	"C0345218"	"Low anorectal malformation"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"79784"	"MYH14"	"0.69"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79784"	"MYH14"	"0.69"	"0.414"	"C1833503"	"Deafness, Autosomal Dominant 4"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2004"	"2006"	"2"	"5"	"CTD_human;UNIPROT"
"79784"	"MYH14"	"0.69"	"0.414"	"C3280556"	"PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2011"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"79791"	"FBXO31"	"0.752"	"0.345"	"C4014864"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"79796"	"ALG9"	"0.681"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"79796"	"ALG9"	"0.681"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79796"	"ALG9"	"0.681"	"0.448"	"C1849762"	"Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia"	"disease"	"C05;C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"79796"	"ALG9"	"0.681"	"0.448"	"C2931006"	"Congenital disorder of glycosylation type 1L"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2004"	"2005"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"79796"	"ALG9"	"0.681"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"79797"	"ZNF408"	"0.663"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"79797"	"ZNF408"	"0.663"	"0.414"	"C0339539"	"Familial Exudative Vitreoretinopathy"	"disease"	"C11"	"Congenital Abnormality"	"0.34"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"79797"	"ZNF408"	"0.663"	"0.414"	"C1851402"	"Exudative vitreoretinopathy 1"	"disease"	"C05;C11;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79797"	"ZNF408"	"0.663"	"0.414"	"C4225315"	"RETINITIS PIGMENTOSA 72"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"79797"	"ZNF408"	"0.663"	"0.414"	"C4225316"	"EXUDATIVE VITREORETINOPATHY 6"	"disease"		"Disease or Syndrome"	"0.60"		"1982"	"2013"	"1"	"2"	"CTD_human;UNIPROT"
"79798"	"ARMC5"	"0.667"	"0.414"	"C1857451"	"Acth-Independent Macronodular Adrenal Hyperplasia"	"disease"	"C19"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"79798"	"ARMC5"	"0.667"	"0.414"	"C4014803"	"ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2"	"disease"		"Disease or Syndrome"	"0.47"	"1"	"2013"	"2018"	"10"	"10"	"UNIPROT"
"79801"	"SHCBP1"	"0.727"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79801"	"SHCBP1"	"0.727"	"0.448"	"C0039101"	"synovial sarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"79803"	"HPS6"	"0.857"	"0.172"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"79807"	"GSTCD"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79807"	"GSTCD"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"2"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2011"	"2018"	"1"	"2"	"CTD_human;ORPHANET"
"79809"	"TTC21B"	"0.696"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79809"	"TTC21B"	"0.696"	"0.379"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79809"	"TTC21B"	"0.696"	"0.379"	"C1865872"	"NEPHRONOPHTHISIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79809"	"TTC21B"	"0.696"	"0.379"	"C3151185"	"SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2016"	"1"	"4"	"UNIPROT"
"79809"	"TTC21B"	"0.696"	"0.379"	"C3151186"	"NEPHRONOPHTHISIS 12"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2017"	"2"	"9"	"CTD_human;UNIPROT"
"79809"	"TTC21B"	"0.696"	"0.379"	"C3279203"	"JOUBERT SYNDROME 11"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2012"	"2"	"7"	"CTD_human;UNIPROT"
"79809"	"TTC21B"	"0.696"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"79809"	"TTC21B"	"0.696"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79812"	"MMRN2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C0795833"	"Kleefstra Syndrome"	"disease"	"C05;C10;C14;C16;C23;F01;F03"	"Disease or Syndrome"	"0.99"	"1"	"1993"	"2017"	"2"	"20"	"CTD_human;ORPHANET;UNIPROT"
"79813"	"EHMT1"	"0.579"	"0.586"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79813"	"EHMT1"	"0.579"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"79815"	"NIPAL2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79816"	"TLE6"	"0.886"	"0.069"	"C4225197"	"PREIMPLANTATION EMBRYONIC LETHALITY 1"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"79822"	"ARHGAP28"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79822"	"ARHGAP28"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0011757"	"Developmental Coordination Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0026613"	"Motor Skills Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0151786"	"Muscle Weakness"	"phenotype"	"C05;C10;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0162668"	"Megaconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0162669"	"Pleoconial Myopathies"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0162670"	"Mitochondrial Myopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C0949496"	"Luft Disease"	"disease"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C1848030"	"Hypotonia-Cystinuria Syndrome"	"disease"	"C05;C10;C12;C13;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"79823"	"CAMKMT"	"0.565"	"0.69"	"C4304537"	"2p21 microdeletion syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79827"	"CLMP"	"0.743"	"0.207"	"C0021847"	"Intestinal Pseudo-Obstruction"	"disease"	"C06"	"Disease or Syndrome"	"0.72"	"1"	"2006"	"2018"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"79827"	"CLMP"	"0.743"	"0.207"	"C0030446"	"Paralytic Ileus"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79827"	"CLMP"	"0.743"	"0.207"	"C0042781"	"Visceral Myopathy"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79834"	"PEAK1"	"0.785"	"0.207"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79834"	"PEAK1"	"0.785"	"0.207"	"C0699885"	"Carcinoma of bladder"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79836"	"LONRF3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"79837"	"PIP4K2C"	"0.857"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"79837"	"PIP4K2C"	"0.857"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2005"	"2016"	"2"	"0"	"PSYGENET"
"79840"	"NHEJ1"	"0.762"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2007"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"79840"	"NHEJ1"	"0.762"	"0.345"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"79840"	"NHEJ1"	"0.762"	"0.345"	"C1969799"	"Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation"	"disease"	"C05;C10;C16;C18;C20;C23"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2012"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"79840"	"NHEJ1"	"0.762"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79842"	"ZBTB3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"79848"	"CSPP1"	"0.63"	"0.586"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79848"	"CSPP1"	"0.63"	"0.586"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2015"	"0"	"1"	"ORPHANET"
"79848"	"CSPP1"	"0.63"	"0.586"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.35"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"79848"	"CSPP1"	"0.63"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"79848"	"CSPP1"	"0.63"	"0.586"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"79848"	"CSPP1"	"0.63"	"0.586"	"C4518774"	"Joubert syndrome with Jeune asphyxiating thoracic dystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79852"	"EPHX3"	"0.834"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79852"	"EPHX3"	"0.834"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79852"	"EPHX3"	"0.834"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79852"	"EPHX3"	"0.834"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79853"	"TM4SF20"	"1"		"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"79853"	"TM4SF20"	"1"		"C3809483"	"SPECIFIC LANGUAGE IMPAIRMENT 5"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79858"	"NEK11"	"0.815"	"0.138"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"3"	"UNIPROT"
"79861"	"TUBAL3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"79867"	"TCTN2"	"0.63"	"0.517"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79867"	"TCTN2"	"0.63"	"0.517"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79867"	"TCTN2"	"0.63"	"0.517"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"79867"	"TCTN2"	"0.63"	"0.517"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2016"	"0"	"7"	"ORPHANET"
"79867"	"TCTN2"	"0.63"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"79867"	"TCTN2"	"0.63"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79868"	"ALG13"	"0.72"	"0.241"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"79868"	"ALG13"	"0.72"	"0.241"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"79868"	"ALG13"	"0.72"	"0.241"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79868"	"ALG13"	"0.72"	"0.241"	"C3550904"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2018"	"5"	"3"	"CTD_human;UNIPROT"
"79868"	"ALG13"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"79868"	"ALG13"	"0.72"	"0.241"	"C4317295"	"Congenital disorder of glycosylation type 1s"	"disease"		"Disease or Syndrome"	"0.50"		"2012"	"2016"	"5"	"2"	"CTD_human;UNIPROT"
"79870"	"BAALC"	"0.696"	"0.241"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"79870"	"BAALC"	"0.696"	"0.241"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79870"	"BAALC"	"0.696"	"0.241"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79875"	"THSD4"	"0.799"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"79876"	"UBA5"	"0.639"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79876"	"UBA5"	"0.639"	"0.379"	"C4310699"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2016"	"1"	"4"	"UNIPROT"
"79876"	"UBA5"	"0.639"	"0.379"	"C4310700"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"12"	"CTD_human;UNIPROT"
"79879"	"CCDC134"	"0.857"	"0.103"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79879"	"CCDC134"	"0.857"	"0.103"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79879"	"CCDC134"	"0.857"	"0.103"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79879"	"CCDC134"	"0.857"	"0.103"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"79882"	"ZC3H14"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"79882"	"ZC3H14"	"0.857"	"0.172"	"C4310703"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"0"	"2"	"CTD_human"
"79887"	"PLBD1"	"1"	"0.069"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79890"	"RIN3"	"0.834"	"0.207"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2016"	"1"	"1"	"CTD_human"
"79906"	"MORN1"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79906"	"MORN1"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"79912"	"PYROXD1"	"0.773"	"0.276"	"C2678065"	"Myofibrillar Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79912"	"PYROXD1"	"0.773"	"0.276"	"C4310645"	"MYOPATHY, MYOFIBRILLAR, 8"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"5"	"UNIPROT"
"79915"	"ATAD5"	"0.752"	"0.345"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2017"	"1"	"1"	"CTD_human"
"79917"	"MAGIX"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"79923"	"NANOG"	"0.579"	"0.448"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.33"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2008"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79923"	"NANOG"	"0.579"	"0.448"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"79924"	"ADM2"	"0.815"	"0.276"	"C0042373"	"Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79924"	"ADM2"	"0.815"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"79930"	"DOK3"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"79930"	"DOK3"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"79932"	"KIAA0319L"	"0.773"	"0.31"	"C0206138"	"CREST Syndrome"	"disease"	"C06;C14;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79932"	"KIAA0319L"	"0.773"	"0.31"	"C0748540"	"Scleroderma, Limited"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79934"	"COQ8B"	"0.785"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"79934"	"COQ8B"	"0.785"	"0.172"	"C3809965"	"NEPHROTIC SYNDROME, TYPE 9"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2016"	"2"	"11"	"CTD_human;UNIPROT"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C1855995"	"L-2-HYDROXYGLUTARIC ACIDURIA"	"disease"		"Disease or Syndrome"	"0.89"	"1"	"2005"	"2015"	"2"	"11"	"ORPHANET;UNIPROT"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C2746066"	"Combined D-2- and L-2-hydroxyglutaric aciduria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.38"	"1"	"2005"	"2015"	"3"	"0"	"CTD_human"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"79944"	"L2HGDH"	"0.656"	"0.414"	"C3888081"	"L-2-hydroxyglutaric acidemia"	"disease"		"Disease or Syndrome"	"0.80"		"2005"	"2015"	"2"	"6"	"ORPHANET;UNIPROT"
"79947"	"DHDDS"	"0.514"	"0.724"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"79947"	"DHDDS"	"0.514"	"0.724"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"79947"	"DHDDS"	"0.514"	"0.724"	"C3151227"	"RETINITIS PIGMENTOSA 59"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"79949"	"PLEKHS1"			"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79949"	"PLEKHS1"			"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79949"	"PLEKHS1"			"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79953"	"SYNDIG1"	"1"	"0.034"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"79955"	"PDZD7"	"0.735"	"0.172"	"C0339534"	"Usher syndrome type 2"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"79955"	"PDZD7"	"0.735"	"0.172"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79955"	"PDZD7"	"0.735"	"0.172"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2017"	"10"	"0"	"CLINGEN"
"79955"	"PDZD7"	"0.735"	"0.172"	"C1848634"	"USHER SYNDROME, TYPE IIA"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"79955"	"PDZD7"	"0.735"	"0.172"	"C2931213"	"Usher syndrome, type 2C"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79971"	"WLS"	"0.541"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"79971"	"WLS"	"0.541"	"0.69"	"C0858355"	"Addicted to cocaine"	"phenotype"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"79973"	"ZNF442"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"79974"	"CPED1"	"0.815"	"0.276"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79974"	"CPED1"	"0.815"	"0.276"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79974"	"CPED1"	"0.815"	"0.276"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"79977"	"GRHL2"	"0.633"	"0.517"	"C1837640"	"Deafness, Autosomal Dominant 28"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.41"	"0"	"2003"	"2013"	"0"	"3"	"CTD_human"
"79977"	"GRHL2"	"0.633"	"0.517"	"C4014987"	"ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"79983"	"POF1B"	"0.815"	"0.172"	"C1845105"	"Premature Ovarian Failure 2b"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.50"		"2006"	"2012"	"2"	"1"	"CTD_human;UNIPROT"
"79991"	"STN1"	"0.648"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79991"	"STN1"	"0.648"	"0.483"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"79991"	"STN1"	"0.648"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79991"	"STN1"	"0.648"	"0.483"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"79991"	"STN1"	"0.648"	"0.483"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"79991"	"STN1"	"0.648"	"0.483"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"79991"	"STN1"	"0.648"	"0.483"	"C2677299"	"CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder)"	"disease"	"C04;C05;C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"79991"	"STN1"	"0.648"	"0.483"	"C4479220"	"CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"80000"	"GREB1L"	"0.799"	"0.207"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80000"	"GREB1L"	"0.799"	"0.207"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80013"	"MINDY3"	"0.752"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80018"	"NAA25"	"0.642"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1993"	"1993"	"0"	"0"	"UNIPROT"
"80025"	"PANK2"	"0.648"	"0.379"	"C0018523"	"Hallervorden-Spatz Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"0.9791667"	"2001"	"2018"	"7"	"30"	"CTD_human;UNIPROT"
"80025"	"PANK2"	"0.648"	"0.379"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.40"		"2010"	"2015"	"1"	"2"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80025"	"PANK2"	"0.648"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"80025"	"PANK2"	"0.648"	"0.379"	"C0270715"	"Degenerative Diseases, Central Nervous System"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C0524851"	"Neurodegenerative Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.45"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80025"	"PANK2"	"0.648"	"0.379"	"C0751733"	"Degenerative Diseases, Spinal Cord"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C1846582"	"Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"1992"	"2006"	"0"	"5"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C2931845"	"Neurodegeneration with brain iron accumulation (NBIA)"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"80025"	"PANK2"	"0.648"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80031"	"SEMA6D"	"0.727"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0000786"	"Spontaneous abortion"	"phenotype"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0000822"	"Abortion, Tubal"	"disease"	"C13"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80034"	"CSRNP3"	"0.799"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80036"	"TRPM3"	"0.727"	"0.31"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"80036"	"TRPM3"	"0.727"	"0.31"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"80036"	"TRPM3"	"0.727"	"0.31"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"80054"	"CEBPA-DT"	"0.857"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80054"	"CEBPA-DT"	"0.857"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80054"	"CEBPA-DT"	"0.857"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80055"	"PGAP1"	"0.72"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80055"	"PGAP1"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2014"	"2016"	"7"	"0"	"GENOMICS_ENGLAND"
"80055"	"PGAP1"	"0.72"	"0.379"	"C4014343"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2017"	"0"	"9"	"CTD_human"
"80067"	"DCAF17"	"0.672"	"0.483"	"C0342286"	"Woodhouse Sakati syndrome"	"disease"	"C10;C14;C17;C18;C19;C23;F01;F03"	"Disease or Syndrome"	"0.65"	"1"	"1983"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"80067"	"DCAF17"	"0.672"	"0.483"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"80067"	"DCAF17"	"0.672"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"80070"	"ADAMTS20"	"0.928"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80095"	"ZNF606"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80114"	"BICC1"	"0.685"	"0.448"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2016"	"2"	"0"	"PSYGENET"
"80114"	"BICC1"	"0.685"	"0.448"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2010"	"2016"	"2"	"0"	"PSYGENET"
"80114"	"BICC1"	"0.685"	"0.448"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"80114"	"BICC1"	"0.685"	"0.448"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80114"	"BICC1"	"0.685"	"0.448"	"C3275898"	"RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2012"	"2012"	"1"	"1"	"UNIPROT"
"80127"	"BBOF1"	"0.886"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80127"	"BBOF1"	"0.886"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80142"	"PTGES2"	"0.713"	"0.379"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80142"	"PTGES2"	"0.713"	"0.379"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80142"	"PTGES2"	"0.713"	"0.379"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80144"	"FRAS1"	"0.562"	"0.552"	"C0024433"	"Macrostomia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"80144"	"FRAS1"	"0.562"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80144"	"FRAS1"	"0.562"	"0.552"	"C0265233"	"Cryptophthalmos syndrome"	"disease"	"C05;C11;C12;C13;C16"	"Disease or Syndrome"	"0.90"	"0.8666667"	"2003"	"2018"	"1"	"16"	"CTD_human;ORPHANET"
"80144"	"FRAS1"	"0.562"	"0.552"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"80144"	"FRAS1"	"0.562"	"0.552"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80144"	"FRAS1"	"0.562"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2007"	"3"	"0"	"GENOMICS_ENGLAND"
"80146"	"UXS1"	"0.834"	"0.138"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80148"	"PQLC1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80149"	"ZC3H12A"	"0.636"	"0.552"	"C0003838"	"Arterial Occlusive Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80150"	"ASRGL1"	"0.609"	"0.483"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"80153"	"EDC3"	"0.857"	"0.172"	"C4225319"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50"	"disease"		"Mental or Behavioral Dysfunction"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"80155"	"NAA15"	"0.773"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80155"	"NAA15"	"0.773"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80155"	"NAA15"	"0.773"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80155"	"NAA15"	"0.773"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2016"	"2018"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80157"	"CWH43"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80157"	"CWH43"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0006111"	"Brain Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2012"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"80169"	"CTC1"	"0.659"	"0.414"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0085584"	"Encephalopathies"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0154832"	"Exudative retinopathy"	"disease"	"C11;C14"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"80169"	"CTC1"	"0.659"	"0.414"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0265965"	"Dyskeratosis Congenita"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2017"	"0"	"5"	"ORPHANET"
"80169"	"CTC1"	"0.659"	"0.414"	"C0267211"	"Gastric Antral Vascular Ectasia"	"phenotype"	"C06;C14"	"Acquired Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"80169"	"CTC1"	"0.659"	"0.414"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80169"	"CTC1"	"0.659"	"0.414"	"C2677299"	"CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder)"	"disease"	"C04;C05;C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.75"	"1"	"2004"	"2018"	"2"	"15"	"CTD_human;ORPHANET;UNIPROT"
"80169"	"CTC1"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"80173"	"IFT74"	"0.72"	"0.379"	"C4310707"	"BARDET-BIEDL SYNDROME 20"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"80184"	"CEP290"	"0.546"	"0.724"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"80184"	"CEP290"	"0.546"	"0.724"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80184"	"CEP290"	"0.546"	"0.724"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.44"	"1"	"2006"	"2017"	"0"	"17"	"ORPHANET"
"80184"	"CEP290"	"0.546"	"0.724"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"1"	"2006"	"2017"	"0"	"1"	"ORPHANET"
"80184"	"CEP290"	"0.546"	"0.724"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2013"	"0"	"0"	"ORPHANET"
"80184"	"CEP290"	"0.546"	"0.724"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.68"	"1"	"2008"	"2014"	"1"	"1"	"CTD_human;ORPHANET"
"80184"	"CEP290"	"0.546"	"0.724"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80184"	"CEP290"	"0.546"	"0.724"	"C1855675"	"Arima syndrome"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80184"	"CEP290"	"0.546"	"0.724"	"C1857779"	"SENIOR-LOKEN SYNDROME 6"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2015"	"1"	"23"	"CTD_human;UNIPROT"
"80184"	"CEP290"	"0.546"	"0.724"	"C1857780"	"JOUBERT SYNDROME 5"	"disease"	"C10;C11;C12;C13;C23"	"Disease or Syndrome"	"0.80"		"2006"	"2016"	"5"	"47"	"CTD_human;UNIPROT"
"80184"	"CEP290"	"0.546"	"0.724"	"C1857821"	"LEBER CONGENITAL AMAUROSIS 10 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"0"	"27"	"CTD_human"
"80184"	"CEP290"	"0.546"	"0.724"	"C1970161"	"MECKEL SYNDROME, TYPE 4"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.41"	"1"	"2007"	"2015"	"0"	"34"	"CTD_human"
"80184"	"CEP290"	"0.546"	"0.724"	"C2673874"	"BARDET-BIEDL SYNDROME 14 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2015"	"0"	"4"	"CTD_human"
"80184"	"CEP290"	"0.546"	"0.724"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"80184"	"CEP290"	"0.546"	"0.724"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.40"	"1"	"2006"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"80185"	"TTI2"	"0.752"	"0.241"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80185"	"TTI2"	"0.752"	"0.241"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80185"	"TTI2"	"0.752"	"0.241"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80185"	"TTI2"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80185"	"TTI2"	"0.752"	"0.241"	"C3809853"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"80196"	"RNF34"	"0.685"	"0.414"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80196"	"RNF34"	"0.685"	"0.414"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0003803"	"Arnold Chiari Malformation"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.36"	"0.8333333"	"1999"	"2012"	"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0300948"	"Caudal Regression Syndrome"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C0344490"	"Sacral agenesis"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C0555206"	"Chiari malformation type II"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"80199"	"FUZ"	"0.624"	"0.483"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80199"	"FUZ"	"0.624"	"0.483"	"C1867774"	"Sacral Agenesis Syndrome"	"disease"	"C04;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80199"	"FUZ"	"0.624"	"0.483"	"C2609260"	"Caudal dysplasia syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80204"	"FBXO11"	"0.815"	"0.207"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CGI"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80206"	"FHOD3"	"0.785"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80207"	"OPA3"	"0.652"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"1993"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.45"	"1"	"2005"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C0574084"	"3-Methylglutaconic aciduria type 3"	"disease"	"C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.89"	"1"	"1993"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"80207"	"OPA3"	"0.652"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80207"	"OPA3"	"0.652"	"0.276"	"C1833809"	"OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.70"		"1961"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"80207"	"OPA3"	"0.652"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.70"	"1"	"2004"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C1858479"	"Spastic paraplegia 11, autosomal recessive"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.96"	"0.8333333"	"1993"	"2017"	"4"	"110"	"CTD_human;ORPHANET;UNIPROT"
"80208"	"SPG11"	"0.586"	"0.483"	"C1865864"	"AMYOTROPHIC LATERAL SCLEROSIS 5"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.40"		"2007"	"2016"	"0"	"6"	"CTD_human"
"80208"	"SPG11"	"0.586"	"0.483"	"C2931821"	"Nakamura Osame syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80208"	"SPG11"	"0.586"	"0.483"	"C3468114"	"Juvenile amyotrophic lateral sclerosis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80208"	"SPG11"	"0.586"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"		"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"80208"	"SPG11"	"0.586"	"0.483"	"C4225253"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2017"	"0"	"7"	"CTD_human;ORPHANET"
"80210"	"ARMC9"	"0.676"	"0.655"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"80210"	"ARMC9"	"0.676"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2017"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"80212"	"CCDC92"	"0.886"	"0.103"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80212"	"CCDC92"	"0.886"	"0.103"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C0027719"	"Nephrosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C1262477"	"Weight decreased"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80216"	"ALPK1"	"0.773"	"0.379"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80222"	"TARS2"	"0.773"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"80222"	"TARS2"	"0.773"	"0.345"	"C4014668"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"80224"	"NUBPL"	"0.648"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80224"	"NUBPL"	"0.648"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80224"	"NUBPL"	"0.648"	"0.414"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80224"	"NUBPL"	"0.648"	"0.414"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80224"	"NUBPL"	"0.648"	"0.414"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80224"	"NUBPL"	"0.648"	"0.414"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.61"	"1"	"2010"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"80224"	"NUBPL"	"0.648"	"0.414"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"2010"	"2013"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"80224"	"NUBPL"	"0.648"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80230"	"RUFY1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80232"	"WDR26"	"0.707"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"80232"	"WDR26"	"0.707"	"0.517"	"C4539927"	"SKRABAN-DEARDORFF SYNDROME"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"80243"	"PREX2"	"0.762"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80254"	"CEP63"	"0.648"	"0.414"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"80254"	"CEP63"	"0.648"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80254"	"CEP63"	"0.648"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"80254"	"CEP63"	"0.648"	"0.414"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80254"	"CEP63"	"0.648"	"0.414"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"80254"	"CEP63"	"0.648"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"80254"	"CEP63"	"0.648"	"0.414"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80264"	"ZNF430"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80264"	"ZNF430"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80270"	"HSD3B7"	"0.713"	"0.276"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80270"	"HSD3B7"	"0.713"	"0.276"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2000"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"80270"	"HSD3B7"	"0.713"	"0.276"	"C1843116"	"Bile acid synthesis defect, congenital, 1"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.70"		"1987"	"2014"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"80270"	"HSD3B7"	"0.713"	"0.276"	"C2931067"	"Cholestasis, progressive familial intrahepatic 4"	"disease"	"C06;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"80270"	"HSD3B7"	"0.713"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80271"	"ITPKC"	"0.799"	"0.241"	"C0010051"	"Coronary Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"80271"	"ITPKC"	"0.799"	"0.241"	"C0026691"	"Mucocutaneous Lymph Node Syndrome"	"disease"	"C14;C15;C17"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2015"	"1"	"1"	"CTD_human"
"80273"	"GRPEL1"	"0.928"	"0.138"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"80273"	"GRPEL1"	"0.928"	"0.138"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"80303"	"EFHD1"	"0.857"	"0.103"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"80303"	"EFHD1"	"0.857"	"0.103"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"80303"	"EFHD1"	"0.857"	"0.103"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"80304"	"WDCP"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80306"	"MED28"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"80306"	"MED28"	"0.815"	"0.138"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80306"	"MED28"	"0.815"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"80306"	"MED28"	"0.815"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80306"	"MED28"	"0.815"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2007"	"2012"	"1"	"0"	"CTD_human"
"80308"	"FLAD1"	"0.713"	"0.414"	"C0410214"	"Myopathy with Abnormal Lipid Metabolism"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"80308"	"FLAD1"	"0.713"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"80308"	"FLAD1"	"0.713"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80308"	"FLAD1"	"0.713"	"0.414"	"C4310822"	"LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2016"	"1"	"6"	"UNIPROT"
"80310"	"PDGFD"	"0.616"	"0.483"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80310"	"PDGFD"	"0.616"	"0.483"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80310"	"PDGFD"	"0.616"	"0.483"	"C0273115"	"Lung Injury"	"disease"	"C08;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80310"	"PDGFD"	"0.616"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80310"	"PDGFD"	"0.616"	"0.483"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80310"	"PDGFD"	"0.616"	"0.483"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"80310"	"PDGFD"	"0.616"	"0.483"	"C2350344"	"Chronic Lung Injury"	"disease"	"C08;C26"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80311"	"KLHL15"	"0.773"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"80311"	"KLHL15"	"0.773"	"0.276"	"C4310818"	"MENTAL RETARDATION, X-LINKED 103"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"80312"	"TET1"	"0.611"	"0.414"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"80312"	"TET1"	"0.611"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"80312"	"TET1"	"0.611"	"0.414"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"80312"	"TET1"	"0.611"	"0.414"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"80317"	"ZKSCAN3"	"0.713"	"0.414"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"80317"	"ZKSCAN3"	"0.713"	"0.414"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"80317"	"ZKSCAN3"	"0.713"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"80323"	"CCDC68"	"0.886"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"80324"	"PUS1"	"0.676"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80324"	"PUS1"	"0.676"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80324"	"PUS1"	"0.676"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"80324"	"PUS1"	"0.676"	"0.483"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80324"	"PUS1"	"0.676"	"0.483"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80324"	"PUS1"	"0.676"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"80324"	"PUS1"	"0.676"	"0.483"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80324"	"PUS1"	"0.676"	"0.483"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"80324"	"PUS1"	"0.676"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"80324"	"PUS1"	"0.676"	"0.483"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80324"	"PUS1"	"0.676"	"0.483"	"C1838103"	"MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.95"	"1"	"1995"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"80324"	"PUS1"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2009"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"80326"	"WNT10A"	"0.588"	"0.517"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.50"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"80326"	"WNT10A"	"0.588"	"0.517"	"C0334634"	"Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80326"	"WNT10A"	"0.588"	"0.517"	"C0406702"	"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"80326"	"WNT10A"	"0.588"	"0.517"	"C0751958"	"Lymphoma, Lymphocytic, Intermediate"	"disease"	"C04;C15;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80326"	"WNT10A"	"0.588"	"0.517"	"C0796093"	"Odontoonychodermal dysplasia"	"disease"	"C07;C16;C17"	"Disease or Syndrome"	"0.72"	"0.5"	"2007"	"2017"	"4"	"9"	"CTD_human;ORPHANET;UNIPROT"
"80326"	"WNT10A"	"0.588"	"0.517"	"C1275074"	"Odonto-onycho-dermal dysplasia"	"disease"		"Congenital Abnormality"	"0.35"	"1"	"2007"	"2015"	"0"	"0"	"ORPHANET"
"80326"	"WNT10A"	"0.588"	"0.517"	"C1835492"	"TOOTH AGENESIS, SELECTIVE, 4 (disorder)"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2018"	"8"	"18"	"CTD_human;UNIPROT"
"80326"	"WNT10A"	"0.588"	"0.517"	"C1835493"	"Succedaneous Teeth, Agenesis Of"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2018"	"8"	"15"	"CTD_human;UNIPROT"
"80326"	"WNT10A"	"0.588"	"0.517"	"C1857069"	"SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)"	"disease"	"C04;C07;C11;C16;C17"	"Disease or Syndrome"	"0.76"	"1"	"2009"	"2015"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"80326"	"WNT10A"	"0.588"	"0.517"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.46"	"1"	"2009"	"2016"	"0"	"0"	"ORPHANET"
"80328"	"ULBP2"	"0.72"	"0.31"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80328"	"ULBP2"	"0.72"	"0.31"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80328"	"ULBP2"	"0.72"	"0.31"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80331"	"DNAJC5"	"0.735"	"0.207"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"80331"	"DNAJC5"	"0.735"	"0.207"	"C1834207"	"Ceroid Lipofuscinosis, Neuronal, Parry Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"1971"	"2013"	"5"	"2"	"ORPHANET;UNIPROT"
"80332"	"ADAM33"	"0.681"	"0.31"	"C0085129"	"Bronchial Hyperreactivity"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"0.9333333"	"2002"	"2012"	"1"	"0"	"CTD_human"
"80332"	"ADAM33"	"0.681"	"0.31"	"C1321872"	"Stage IV Skin Melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9454545"	"2008"	"2018"	"1"	"0"	"CTD_human"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.49"	"0.7777778"	"2010"	"2016"	"2"	"1"	"CTD_human"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C0023896"	"Alcoholic Liver Diseases"	"group"	"C06;C25"	"Disease or Syndrome"	"0.40"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.954955"	"2008"	"2018"	"3"	"3"	"CTD_human"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9195402"	"2009"	"2018"	"1"	"0"	"CTD_human"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C2750440"	"FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1"	"disease"		"Finding"	"0.30"		"2008"	"2016"	"4"	"2"	"UNIPROT"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C2750441"	"LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"		"2008"	"2016"	"4"	"2"	"UNIPROT"
"80339"	"PNPLA3"	"0.584"	"0.552"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2008"	"2018"	"3"	"1"	"CTD_human"
"80341"	"BPIFB2"	"0.928"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80342"	"TRAF3IP3"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80345"	"ZSCAN16"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80347"	"COASY"	"0.621"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"80347"	"COASY"	"0.621"	"0.448"	"C3810230"	"NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"80351"	"TNKS2"	"0.72"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"80352"	"RNF39"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80381"	"CD276"	"0.569"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80381"	"CD276"	"0.569"	"0.552"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"80381"	"CD276"	"0.569"	"0.552"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C0004782"	"Basal Ganglia Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C0015371"	"Extrapyramidal Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C0750951"	"Lenticulostriate Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C1843807"	"Basal ganglia disease, biotin-responsive"	"disease"	"C10"	"Disease or Syndrome"	"0.80"	"1"	"2005"	"2018"	"1"	"10"	"CTD_human;ORPHANET;UNIPROT"
"80704"	"SLC19A3"	"0.681"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"80712"	"ESX1"	"0.834"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80714"	"PBX4"	"0.857"	"0.207"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80714"	"PBX4"	"0.857"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80723"	"SLC35G2"	"0.928"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"80725"	"SRCIN1"	"0.72"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80725"	"SRCIN1"	"0.72"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80725"	"SRCIN1"	"0.72"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80731"	"THSD7B"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"1"	"1"	"PSYGENET"
"80736"	"SLC44A4"	"0.727"	"0.414"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"80736"	"SLC44A4"	"0.727"	"0.414"	"C4539886"	"DEAFNESS, AUTOSOMAL DOMINANT 72"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"80739"	"MPIG6B"	"0.735"	"0.414"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"80739"	"MPIG6B"	"0.735"	"0.414"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"80739"	"MPIG6B"	"0.735"	"0.414"	"C4479504"	"THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"1"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0011168"	"Deglutition Disorders"	"group"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2009"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0267071"	"Oropharyngeal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0267072"	"Esophageal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C2676466"	"Pontocerebellar Hypoplasia Type 2B"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"1"	"7"	"CTD_human;UNIPROT"
"80746"	"TSEN2"	"0.685"	"0.31"	"C2932714"	"Pontocerebellar Hypoplasia Type 2"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"80746"	"TSEN2"	"0.685"	"0.31"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80746"	"TSEN2"	"0.685"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80746"	"TSEN2"	"0.685"	"0.31"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"80774"	"LIMD2"	"0.785"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"80774"	"LIMD2"	"0.785"	"0.172"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80774"	"LIMD2"	"0.785"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"80774"	"LIMD2"	"0.785"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80774"	"LIMD2"	"0.785"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"80776"	"B9D2"	"0.663"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80776"	"B9D2"	"0.663"	"0.448"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"80776"	"B9D2"	"0.663"	"0.448"	"C3280036"	"MECKEL SYNDROME, TYPE 10"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"UNIPROT"
"80776"	"B9D2"	"0.663"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80776"	"B9D2"	"0.663"	"0.448"	"C4539386"	"JOUBERT SYNDROME 34"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"UNIPROT"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0006663"	"Calcinosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0018824"	"Heart valve disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0018923"	"Hemangiosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0263628"	"Tumoral calcinosis"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0521174"	"Microcalcification"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80781"	"COL18A1"	"0.489"	"0.759"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"80781"	"COL18A1"	"0.489"	"0.759"	"C1849409"	"Knobloch syndrome"	"disease"	"C10;C11;C16;C23"	"Disease or Syndrome"	"0.70"	"1"	"1992"	"2017"	"0"	"6"	"CTD_human;ORPHANET"
"80781"	"COL18A1"	"0.489"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"80790"	"CMIP"	"0.752"	"0.31"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"3"	"CTD_human"
"80816"	"ASXL3"	"0.762"	"0.345"	"C0079772"	"T-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"80816"	"ASXL3"	"0.762"	"0.345"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"80816"	"ASXL3"	"0.762"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"80816"	"ASXL3"	"0.762"	"0.345"	"C3809650"	"BAINBRIDGE-ROPERS SYNDROME"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2013"	"2018"	"0"	"11"	"CTD_human;ORPHANET"
"80818"	"ZNF436"	"0.63"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"80821"	"DDHD1"	"0.773"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"80821"	"DDHD1"	"0.773"	"0.276"	"C1836295"	"SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.51"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"80821"	"DDHD1"	"0.773"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"80824"	"DUSP16"	"0.785"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"80830"	"APOL6"	"0.886"	"0.103"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"80832"	"APOL4"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"80863"	"PRRT1"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"80896"	"NPL"	"0.681"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"81027"	"TUBB1"	"0.834"	"0.103"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81027"	"TUBB1"	"0.834"	"0.103"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81027"	"TUBB1"	"0.834"	"0.103"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81027"	"TUBB1"	"0.834"	"0.103"	"C2751259"	"Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;UNIPROT"
"81027"	"TUBB1"	"0.834"	"0.103"	"C4304021"	"Autosomal dominant macrothrombocytopenia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"81029"	"WNT5B"	"0.743"	"0.276"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81029"	"WNT5B"	"0.743"	"0.276"	"C0023267"	"Fibroid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"81029"	"WNT5B"	"0.743"	"0.276"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81029"	"WNT5B"	"0.743"	"0.276"	"C0042133"	"Uterine Fibroids"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"81029"	"WNT5B"	"0.743"	"0.276"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0024796"	"Marfan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"		"2003"	"2010"	"2"	"0"	"CLINGEN"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2006"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C1859726"	"ARTERIAL TORTUOSITY SYNDROME"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.78"	"0.875"	"1993"	"2018"	"2"	"19"	"CTD_human;ORPHANET;UNIPROT"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C3279191"	"Arterial tortuosity"	"phenotype"		"Finding"	"0.40"		"2006"	"2008"	"2"	"8"	"UNIPROT"
"81031"	"SLC2A10"	"0.594"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81033"	"KCNH6"	"0.834"	"0.103"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"81033"	"KCNH6"	"0.834"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"81033"	"KCNH6"	"0.834"	"0.103"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"81034"	"SLC25A32"	"1"		"C4225187"	"EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81035"	"COLEC12"	"0.762"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2012"	"0"	"0"	"UNIPROT"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0007117"	"Basal cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"		"2009"	"2016"	"1"	"2"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0007873"	"Uterine Cervical Neoplasm"	"disease"	"C04;C13"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0023448"	"Lymphoid leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2014"	"3"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.43"	"1"	"2009"	"2016"	"1"	"2"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9565217"	"2008"	"2017"	"3"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C1368275"	"Pigmented Basal Cell Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81037"	"CLPTM1L"	"0.602"	"0.517"	"C4048328"	"cervical cancer"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"0"	"2009"	"2013"	"1"	"0"	"CTD_human"
"81494"	"CFHR5"	"0.676"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"81494"	"CFHR5"	"0.676"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"81494"	"CFHR5"	"0.676"	"0.345"	"C1305904"	"Familial hematuria"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"81494"	"CFHR5"	"0.676"	"0.345"	"C3553720"	"CFHR5 DEFICIENCY"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0029401"	"Osteitis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2017"	"1"	"1"	"CTD_human"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81501"	"DCSTAMP"	"0.799"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81545"	"FBXO38"	"0.799"	"0.103"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"81545"	"FBXO38"	"0.799"	"0.103"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"81545"	"FBXO38"	"0.799"	"0.103"	"C3711384"	"Distal Hereditary Motor Neuropathy, Type II"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1995"	"2017"	"0"	"1"	"ORPHANET"
"81545"	"FBXO38"	"0.799"	"0.103"	"C3888271"	"NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID"	"disease"		"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"1"	"CTD_human;UNIPROT"
"81552"	"VOPP1"	"0.815"	"0.138"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81552"	"VOPP1"	"0.815"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81552"	"VOPP1"	"0.815"	"0.138"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81552"	"VOPP1"	"0.815"	"0.138"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81553"	"FAM49A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2013"	"2017"	"1"	"2"	"PSYGENET"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81562"	"LMAN2L"	"0.72"	"0.31"	"C4225168"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"81565"	"NDEL1"	"0.752"	"0.276"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2011"	"2012"	"2"	"0"	"PSYGENET"
"81565"	"NDEL1"	"0.752"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.75"	"2007"	"2016"	"4"	"0"	"PSYGENET"
"81565"	"NDEL1"	"0.752"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81565"	"NDEL1"	"0.752"	"0.276"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"81565"	"NDEL1"	"0.752"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.33"	"1"	"1991"	"2009"	"1"	"0"	"CTD_human"
"81565"	"NDEL1"	"0.752"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81567"	"TXNDC5"	"0.639"	"0.414"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"81570"	"CLPB"	"0.707"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"81570"	"CLPB"	"0.707"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"81570"	"CLPB"	"0.707"	"0.379"	"C4225393"	"3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2016"	"1"	"18"	"CTD_human;ORPHANET;UNIPROT"
"81572"	"PDRG1"	"0.857"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81572"	"PDRG1"	"0.857"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"81578"	"COL21A1"	"0.928"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81578"	"COL21A1"	"0.928"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81578"	"COL21A1"	"0.928"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81579"	"PLA2G12A"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81603"	"TRIM8"	"0.799"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81605"	"URM1"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81605"	"URM1"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81605"	"URM1"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81605"	"URM1"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81606"	"LBH"	"0.815"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81607"	"NECTIN4"	"0.636"	"0.448"	"C3150807"	"ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2010"	"2015"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C0206141"	"Idiopathic Hypereosinophilic Syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.972973"	"2003"	"2017"	"1"	"0"	"CTD_human"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C0206142"	"Eosinophilic leukemia"	"disease"	"C15"	"Neoplastic Process"	"0.38"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C0206143"	"Loeffler's Endocarditis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C0346421"	"Chronic eosinophilic leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2015"	"0"	"0"	"ORPHANET"
"81608"	"FIP1L1"	"0.63"	"0.276"	"C1540912"	"Hypereosinophilic syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.40"	"0.9411765"	"2003"	"2017"	"1"	"0"	"CTD_human"
"81620"	"CDT1"	"0.645"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81620"	"CDT1"	"0.645"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"81620"	"CDT1"	"0.645"	"0.517"	"C1868684"	"EAR, PATELLA, SHORT STATURE SYNDROME"	"disease"	"C05;C07;C09;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"81620"	"CDT1"	"0.645"	"0.517"	"C3151120"	"MEIER-GORLIN SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2011"	"2"	"6"	"UNIPROT"
"81620"	"CDT1"	"0.645"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0001338"	"Herpetic Acute Necrotizing Encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.54"	"1"	"2008"	"2010"	"0"	"0"	"CTD_human;ORPHANET"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81622"	"UNC93B1"	"0.727"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81624"	"DIAPH3"	"0.707"	"0.31"	"C1836743"	"AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.51"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"81628"	"TSC22D4"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81631"	"MAP1LC3B"	"0.607"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81689"	"ISCA1"	"0.928"	"0.034"	"C4539919"	"MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2018"	"2018"	"1"	"1"	"UNIPROT"
"81693"	"AMN"	"0.701"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"81693"	"AMN"	"0.701"	"0.517"	"C0013604"	"Edema"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C0015378"	"Extravasation of Contrast Media"	"phenotype"	"C23;C26"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C0015379"	"Extravasation of Diagnostic and Therapeutic Materials"	"disease"	"C23;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C0151603"	"Anasarca"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"81693"	"AMN"	"0.701"	"0.517"	"C0600467"	"Neurogenic Inflammation"	"disease"	"C10;C23"	"Injury or Poisoning"	"0.30"		"2007"	"2008"	"2"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C1306856"	"Megaloblastic anemia due to inborn errors of metabolism"	"disease"	"C06;C12;C13;C15;C18;C23"	"Disease or Syndrome"	"0.76"	"1"	"2003"	"2014"	"1"	"19"	"CTD_human;ORPHANET;UNIPROT"
"81693"	"AMN"	"0.701"	"0.517"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81693"	"AMN"	"0.701"	"0.517"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81704"	"DOCK8"	"0.611"	"0.586"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C1968689"	"Hyper-Immunoglobulin E Syndrome, Autosomal Recessive"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.80"	"1"	"2004"	"2018"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"81704"	"DOCK8"	"0.611"	"0.586"	"C2936739"	"Hyper-Immunoglobulin E Syndrome, Autosomal Dominant"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C3279842"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 2"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"81704"	"DOCK8"	"0.611"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"81704"	"DOCK8"	"0.611"	"0.586"	"C3887645"	"Job Syndrome"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.40"	"1"	"2010"	"2016"	"0"	"0"	"CTD_human"
"81788"	"NUAK2"	"0.834"	"0.172"	"C0346163"	"Endometrioid carcinoma ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"81790"	"RNF170"	"0.928"	"0.069"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"GENOMICS_ENGLAND"
"81790"	"RNF170"	"0.928"	"0.069"	"C1837015"	"ATAXIA, SENSORY, AUTOSOMAL DOMINANT"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.60"		"2007"	"2011"	"1"	"2"	"CTD_human;UNIPROT"
"81792"	"ADAMTS12"	"0.752"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"81793"	"TLR10"	"0.672"	"0.586"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"		"2005"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C0265313"	"Weill-Marchesani syndrome"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2009"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C1869114"	"Weill-Marchesani Syndrome, Autosomal Recessive"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.62"	"1"	"2005"	"2016"	"2"	"7"	"CTD_human;UNIPROT"
"81794"	"ADAMTS10"	"0.667"	"0.345"	"C1869115"	"Weill-Marchesani Syndrome, Autosomal Dominant"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"81797"	"OR12D3"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"81831"	"NETO2"	"0.928"	"0.069"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81831"	"NETO2"	"0.928"	"0.069"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81831"	"NETO2"	"0.928"	"0.069"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.40"	"1"	"2007"	"2017"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0037205"	"Sirenomelia"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0080178"	"Spina Bifida"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"5"	"UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2014"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0300948"	"Caudal Regression Syndrome"	"disease"		"Congenital Abnormality"	"0.60"		"2007"	"2007"	"1"	"1"	"ORPHANET;UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0344490"	"Sacral agenesis"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0431415"	"Lumbosacral agenesis"	"disease"	"C10;C16;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2009"	"2"	"0"	"CTD_human"
"81839"	"VANGL1"	"0.6"	"0.483"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81839"	"VANGL1"	"0.6"	"0.483"	"C1838568"	"Sacral defect and anterior sacral meningocele"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C1838569"	"Caudal Dysgenesis Syndrome"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"81839"	"VANGL1"	"0.6"	"0.483"	"C1867774"	"Sacral Agenesis Syndrome"	"disease"	"C04;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"81839"	"VANGL1"	"0.6"	"0.483"	"C1960883"	"Spina bifida aperta of cervical spine"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"81839"	"VANGL1"	"0.6"	"0.483"	"C2609260"	"Caudal dysplasia syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"81839"	"VANGL1"	"0.6"	"0.483"	"C3891448"	"NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2007"	"2009"	"2"	"5"	"UNIPROT"
"81846"	"SBF2"	"0.672"	"0.379"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.58"	"1"	"2003"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"81846"	"SBF2"	"0.672"	"0.379"	"C1858278"	"Charcot-Marie-Tooth disease, Type 4B2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"2005"	"2008"	"0"	"1"	"CTD_human;ORPHANET"
"81846"	"SBF2"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81848"	"SPRY4"	"0.602"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"81848"	"SPRY4"	"0.602"	"0.552"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81848"	"SPRY4"	"0.602"	"0.552"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"81848"	"SPRY4"	"0.602"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"81848"	"SPRY4"	"0.602"	"0.552"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"81848"	"SPRY4"	"0.602"	"0.552"	"C3808971"	"HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"8"	"CTD_human;UNIPROT"
"81849"	"ST6GALNAC5"	"0.785"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"2"	"0"	"CTD_human"
"81857"	"MED25"	"0.672"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"81857"	"MED25"	"0.672"	"0.552"	"C1854150"	"Charcot-Marie-Tooth disease, Type 2B2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"81857"	"MED25"	"0.672"	"0.552"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"81857"	"MED25"	"0.672"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"81857"	"MED25"	"0.672"	"0.552"	"C4225323"	"BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"81858"	"SHARPIN"	"0.713"	"0.276"	"C0011603"	"Dermatitis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"81858"	"SHARPIN"	"0.713"	"0.276"	"C0014457"	"Eosinophilia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81858"	"SHARPIN"	"0.713"	"0.276"	"C0014458"	"Eosinophilia, Tropical"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"81876"	"RAB1B"	"0.713"	"0.276"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"81887"	"LAS1L"	"0.696"	"0.552"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"81887"	"LAS1L"	"0.696"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"81887"	"LAS1L"	"0.696"	"0.552"	"C1839736"	"WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME"	"disease"	"C10;C16;C17;C18;C23"	"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"81887"	"LAS1L"	"0.696"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"81889"	"FAHD1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83259"	"PCDH11Y"	"0.857"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2002"	"2006"	"1"	"0"	"CTD_human"
"83259"	"PCDH11Y"	"0.857"	"0.138"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"83259"	"PCDH11Y"	"0.857"	"0.138"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"83259"	"PCDH11Y"	"0.857"	"0.138"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"83259"	"PCDH11Y"	"0.857"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"83394"	"PITPNM3"	"0.785"	"0.138"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.33"	"0.6666667"	"1998"	"2010"	"0"	"0"	"ORPHANET"
"83394"	"PITPNM3"	"0.785"	"0.138"	"C1832976"	"Cone-Rod Dystrophy 5"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.52"	"1"	"2003"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"83416"	"FCRL5"	"0.799"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"83439"	"TCF7L1"	"0.762"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"83439"	"TCF7L1"	"0.762"	"0.241"	"C0040136"	"Thyroid Neoplasm"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"83439"	"TCF7L1"	"0.762"	"0.241"	"C0151468"	"Thyroid Gland Follicular Adenoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"83439"	"TCF7L1"	"0.762"	"0.241"	"C0549473"	"Thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"83442"	"SH3BGRL3"	"0.815"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83452"	"RAB33B"	"0.857"	"0.103"	"C1846431"	"SMITH-MCCORT DYSPLASIA"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2017"	"0"	"0"	"ORPHANET"
"83452"	"RAB33B"	"0.857"	"0.103"	"C3714896"	"SMITH-MCCORT DYSPLASIA 2"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2017"	"2"	"6"	"UNIPROT"
"83473"	"KATNAL2"			"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83473"	"KATNAL2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83479"	"DDX59"	"0.713"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"83479"	"DDX59"	"0.713"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83479"	"DDX59"	"0.713"	"0.345"	"C1868118"	"Orofaciodigital syndrome 5"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"83479"	"DDX59"	"0.713"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83480"	"PUS3"	"0.762"	"0.31"	"C4310745"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"83481"	"EPPK1"	"1"	"0.034"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"83481"	"EPPK1"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83538"	"TTC25"	"0.773"	"0.241"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83538"	"TTC25"	"0.773"	"0.241"	"C4310721"	"CILIARY DYSKINESIA, PRIMARY, 35"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"2"	"CTD_human"
"83538"	"TTC25"	"0.773"	"0.241"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83544"	"DNAL1"	"0.752"	"0.207"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2011"	"0"	"1"	"ORPHANET"
"83544"	"DNAL1"	"0.752"	"0.207"	"C3151460"	"CILIARY DYSKINESIA, PRIMARY, 16"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"83544"	"DNAL1"	"0.752"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83544"	"DNAL1"	"0.752"	"0.207"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83546"	"RTBDN"	"0.834"	"0.034"	"C0014474"	"Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83546"	"RTBDN"	"0.834"	"0.034"	"C0205769"	"Myxopapillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83546"	"RTBDN"	"0.834"	"0.034"	"C0280788"	"Anaplastic Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83546"	"RTBDN"	"0.834"	"0.034"	"C0334578"	"Papillary ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83546"	"RTBDN"	"0.834"	"0.034"	"C1384403"	"Cellular Ependymoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83548"	"COG3"	"0.886"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"83550"	"GPR101"	"0.672"	"0.379"	"C0001206"	"Acromegaly"	"disease"	"C05;C10;C19"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"83550"	"GPR101"	"0.672"	"0.379"	"C0346302"	"Growth Hormone-Secreting Pituitary Adenoma"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"83550"	"GPR101"	"0.672"	"0.379"	"C3489630"	"Somatotrophinoma, Familial"	"disease"	"C04;C10;C19"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"83550"	"GPR101"	"0.672"	"0.379"	"C3891556"	"CHROMOSOME Xq26.3 DUPLICATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2016"	"2017"	"0"	"0"	"ORPHANET"
"83550"	"GPR101"	"0.672"	"0.379"	"C4012409"	"PITUITARY ADENOMA 2, GROWTH HORMONE-SECRETING"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"83552"	"MFRP"	"0.676"	"0.207"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.50"	"0.9333333"	"2005"	"2016"	"0"	"0"	"ORPHANET"
"83552"	"MFRP"	"0.676"	"0.207"	"C0266524"	"Dysplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"83552"	"MFRP"	"0.676"	"0.207"	"C0266527"	"Hypoplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"83552"	"MFRP"	"0.676"	"0.207"	"C0311249"	"Cryptophthalmos"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"83552"	"MFRP"	"0.676"	"0.207"	"C1836006"	"NANOPHTHALMOS 2 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2005"	"1"	"6"	"CTD_human;UNIPROT"
"83552"	"MFRP"	"0.676"	"0.207"	"C1970236"	"Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2017"	"0"	"11"	"CTD_human;ORPHANET"
"83552"	"MFRP"	"0.676"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83592"	"AKR1E2"	"0.773"	"0.241"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83593"	"RASSF5"	"0.659"	"0.379"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83593"	"RASSF5"	"0.659"	"0.379"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"83593"	"RASSF5"	"0.659"	"0.379"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83597"	"RTP3"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83597"	"RTP3"	"0.886"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"83597"	"RTP3"	"0.886"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"83597"	"RTP3"	"0.886"	"0.069"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"1993"	"1993"	"1"	"0"	"GENOMICS_ENGLAND"
"83605"	"CCM2"	"0.676"	"0.345"	"C0752160"	"Hemangioma, Cavernous, Central Nervous System"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C0752161"	"Cavernous Hemangioma, Extracerebral"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C0752164"	"Cavernous Hemangioma, Intracerebral"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C1140710"	"Cerebral Cavernous Hemangioma"	"disease"	"C04;C10;C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C1864041"	"CEREBRAL CAVERNOUS MALFORMATIONS 2"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.89"	"1"	"1993"	"2017"	"3"	"5"	"CTD_human;UNIPROT"
"83605"	"CCM2"	"0.676"	"0.345"	"C1956260"	"Cavernous Angioma, Central Nervous System"	"disease"	"C04;C10;C14;C15;C16"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C2919945"	"Cavernous Hemangioma of Brain"	"phenotype"	"C04;C10;C14;C15;C16"	"Anatomical Abnormality"	"0.40"	"0.975"	"2004"	"2016"	"1"	"0"	"CTD_human"
"83605"	"CCM2"	"0.676"	"0.345"	"C2931263"	"Familial cerebral cavernous malformation"	"disease"	"C04;C10;C14;C15;C16"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"83606"	"GUCD1"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83606"	"GUCD1"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83636"	"C19orf12"	"0.667"	"0.379"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83636"	"C19orf12"	"0.667"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2018"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"83636"	"C19orf12"	"0.667"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83636"	"C19orf12"	"0.667"	"0.379"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"83636"	"C19orf12"	"0.667"	"0.379"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"83636"	"C19orf12"	"0.667"	"0.379"	"C2680446"	"SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"83636"	"C19orf12"	"0.667"	"0.379"	"C3280371"	"NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2016"	"10"	"11"	"CTD_human;ORPHANET;UNIPROT"
"83636"	"C19orf12"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"83638"	"C11orf68"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83667"	"SESN2"	"0.542"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83696"	"TRAPPC9"	"0.642"	"0.483"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2010"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"83696"	"TRAPPC9"	"0.642"	"0.483"	"C2750791"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"2008"	"2012"	"0"	"3"	"CTD_human"
"83696"	"TRAPPC9"	"0.642"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.47"	"1"	"2010"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"83699"	"SH3BGRL2"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83699"	"SH3BGRL2"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83699"	"SH3BGRL2"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83700"	"JAM3"	"0.659"	"0.448"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"83700"	"JAM3"	"0.659"	"0.448"	"C3151000"	"HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS"	"disease"		"Disease or Syndrome"	"0.70"		"2011"	"2013"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"83700"	"JAM3"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83706"	"FERMT3"	"0.663"	"0.379"	"C0005818"	"Blood Platelet Disorders"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83706"	"FERMT3"	"0.663"	"0.379"	"C0019080"	"Hemorrhage"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83706"	"FERMT3"	"0.663"	"0.379"	"C0029454"	"Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"83706"	"FERMT3"	"0.663"	"0.379"	"C2748536"	"Leukocyte Adhesion Deficiency, Type III"	"disease"	"C20"	"Disease or Syndrome"	"0.92"	"1"	"2008"	"2016"	"6"	"4"	"CTD_human;ORPHANET;UNIPROT"
"83706"	"FERMT3"	"0.663"	"0.379"	"C3179239"	"Osteopetrosis Autosomal Dominant Type 2"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83706"	"FERMT3"	"0.663"	"0.379"	"C3645711"	"Congenital Osteopetrosis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C1837007"	"DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2017"	"3"	"3"	"CTD_human;UNIPROT"
"83715"	"ESPN"	"0.72"	"0.207"	"C3149566"	"DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2017"	"3"	"3"	"CTD_human;UNIPROT"
"83715"	"ESPN"	"0.72"	"0.207"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83715"	"ESPN"	"0.72"	"0.207"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0149504"	"Encephalopathy, Toxic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0154659"	"Toxic Encephalitis"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83716"	"CRISPLD2"	"0.642"	"0.483"	"C0235032"	"Neurotoxicity Syndromes"	"group"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83719"	"YPEL3"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83729"	"INHBE"	"0.609"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"83729"	"INHBE"	"0.609"	"0.552"	"C0023794"	"Lipoidosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"83729"	"INHBE"	"0.609"	"0.552"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2007"	"2015"	"2"	"0"	"CTD_human"
"83737"	"ITCH"	"0.619"	"0.517"	"C3150649"	"AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"0"	"1"	"CTD_human;ORPHANET"
"83737"	"ITCH"	"0.619"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83741"	"TFAP2D"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"83743"	"GRWD1"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83746"	"L3MBTL2"	"0.762"	"0.138"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83756"	"TAS1R3"	"0.886"	"0.172"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"83756"	"TAS1R3"	"0.886"	"0.172"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"83756"	"TAS1R3"	"0.886"	"0.172"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"83795"	"KCNK16"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2017"	"1"	"2"	"CTD_human"
"83852"	"SETDB2"	"0.886"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83854"	"ANGPTL6"	"0.773"	"0.241"	"C1862932"	"ANEURYSM, INTRACRANIAL BERRY, 1 (disorder)"	"disease"	"C10;C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83858"	"ATAD3B"	"0.815"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83861"	"RSPH3"	"0.857"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2015"	"0"	"1"	"ORPHANET"
"83861"	"RSPH3"	"0.857"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83861"	"RSPH3"	"0.857"	"0.138"	"C4225311"	"CILIARY DYSKINESIA, PRIMARY, 32"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"0"	"5"	"CTD_human"
"83861"	"RSPH3"	"0.857"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83872"	"HMCN1"	"0.815"	"0.31"	"C1864205"	"Macular Degeneration, Age-Related, 1"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2004"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"83876"	"MRO"	"0.834"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83879"	"CDCA7"	"0.69"	"0.586"	"C4310799"	"IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"1991"	"2016"	"1"	"4"	"CTD_human;UNIPROT"
"83893"	"SPATA16"	"0.928"	"0.034"	"C0403825"	"Globozoospermia"	"phenotype"	"C12"	"Finding"	"0.60"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"83931"	"STK40"	"0.886"	"0.172"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"2"	"UNIPROT"
"83932"	"SPRTN"	"0.762"	"0.345"	"C0033300"	"Progeria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83932"	"SPRTN"	"0.762"	"0.345"	"C0919532"	"Genomic Instability"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83932"	"SPRTN"	"0.762"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"83932"	"SPRTN"	"0.762"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83932"	"SPRTN"	"0.762"	"0.345"	"C4015461"	"RUIJS-AALFS SYNDROME"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2003"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"83937"	"RASSF4"	"0.799"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"2013"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83938"	"LRMDA"	"0.735"	"0.345"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2013"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"83938"	"LRMDA"	"0.735"	"0.345"	"C3808786"	"ALBINISM, OCULOCUTANEOUS, TYPE VII"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"83938"	"LRMDA"	"0.735"	"0.345"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"83939"	"EIF2A"	"0.834"	"0.241"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83939"	"EIF2A"	"0.834"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"83940"	"TATDN1"	"0.928"	"0.103"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"83943"	"IMMP2L"	"0.72"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C0016781"	"Fuchs Endothelial Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2006"	"2008"	"3"	"0"	"GENOMICS_ENGLAND"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C1857569"	"CORNEAL ENDOTHELIAL DYSTROPHY 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"1.00"	"1"	"2006"	"2016"	"12"	"16"	"CTD_human;ORPHANET;UNIPROT"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C1857572"	"CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.80"	"1"	"2002"	"2016"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C1861453"	"Pseudohyperkalemia Cardiff"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C2750450"	"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2015"	"4"	"10"	"CTD_human;UNIPROT"
"83959"	"SLC4A11"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83986"	"FAM234A"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"CTD_human"
"83987"	"CCDC8"	"0.672"	"0.414"	"C1848862"	"Miller-McKusick-Malvaux-Syndrome (3M Syndrome)"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.35"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"83987"	"CCDC8"	"0.672"	"0.414"	"C1851996"	"Dwarfism tall vertebrae"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83987"	"CCDC8"	"0.672"	"0.414"	"C2678312"	"Three M Syndrome 1"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9767442"	"2001"	"2017"	"2"	"1"	"CGI;CTD_human;UNIPROT"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.60"	"0.9444444"	"2005"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0029925"	"Ovarian Carcinoma"	"disease"		"Neoplastic Process"	"0.47"	"1"	"2006"	"2016"	"0"	"2"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0278996"	"Malignant Head and Neck Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.65"	"1"	"2001"	"2017"	"6"	"67"	"CLINGEN;GENOMICS_ENGLAND;UNIPROT"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0496920"	"Neoplasm of uncertain or unknown behavior of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0496956"	"Neoplasm of uncertain or unknown behavior of breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0677776"	"Hereditary Breast and Ovarian Cancer Syndrome"	"disease"	"C04;C13;C16;C17;C19"	"Neoplastic Process"	"0.42"	"1"	"2005"	"2017"	"0"	"8"	"ORPHANET"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.70"	"0.9705882"	"2004"	"2017"	"0"	"0"	"CGI;CTD_human"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0858252"	"Breast adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"83990"	"BRIP1"	"0.586"	"0.552"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.60"		"2005"	"2018"	"1"	"28"	"CGI;CTD_human"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.76"	"1"	"2001"	"2018"	"14"	"0"	"CGI;CLINGEN;CTD_human;UNIPROT"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2009"	"0"	"0"	"CTD_human"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1836860"	"FANCONI ANEMIA, COMPLEMENTATION GROUP J"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.66"	"1"	"2005"	"2018"	"3"	"64"	"CTD_human;UNIPROT"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"83990"	"BRIP1"	"0.586"	"0.552"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2001"	"2004"	"2"	"1"	"UNIPROT"
"83990"	"BRIP1"	"0.586"	"0.552"	"C2931456"	"Prostate cancer, familial"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"83990"	"BRIP1"	"0.586"	"0.552"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2004"	"2005"	"4"	"0"	"GENOMICS_ENGLAND"
"83992"	"CTTNBP2"	"0.799"	"0.241"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"83992"	"CTTNBP2"	"0.799"	"0.241"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"83992"	"CTTNBP2"	"0.799"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2002"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"83998"	"REG4"	"0.642"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2004"	"2012"	"1"	"0"	"CTD_human"
"83998"	"REG4"	"0.642"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"83998"	"REG4"	"0.642"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"83999"	"KREMEN1"	"0.762"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"83999"	"KREMEN1"	"0.762"	"0.379"	"C4479322"	"ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"84033"	"OBSCN"	"0.799"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84033"	"OBSCN"	"0.799"	"0.31"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"84033"	"OBSCN"	"0.799"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"2"	"5"	"UNIPROT"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C0339534"	"Usher syndrome type 2"	"disease"		"Disease or Syndrome"	"0.55"	"1"	"2004"	"2016"	"8"	"0"	"CLINGEN;ORPHANET"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C1568249"	"Usher Syndrome, Type II"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2004"	"2016"	"8"	"0"	"CLINGEN;ORPHANET"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C1858493"	"FEBRILE CONVULSIONS, FAMILIAL, 4"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.42"	"0.5"	"2002"	"2011"	"0"	"1"	"CTD_human"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C2931213"	"Usher syndrome, type 2C"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.62"	"1"	"1999"	"2017"	"0"	"40"	"CTD_human"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84059"	"ADGRV1"	"0.639"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84061"	"MAGT1"	"0.6"	"0.586"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"0"	"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"84061"	"MAGT1"	"0.6"	"0.586"	"C3275445"	"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2011"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"84061"	"MAGT1"	"0.6"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0004930"	"Behavior Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0004936"	"Mental disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.8"	"2008"	"2016"	"1"	"0"	"CTD_human"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2016"	"5"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"4"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2014"	"4"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0033937"	"Psychoses, Drug"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9206349"	"2002"	"2018"	"1"	"0"	"CTD_human"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2011"	"5"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"0"	"0"	"CTD_human"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0270458"	"Severe major depression with psychotic features"	"disease"		"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2016"	"2"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0376338"	"Diagnosis, Psychiatric"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2005"	"2011"	"3"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2011"	"5"	"0"	"PSYGENET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C3279756"	"HERMANSKY-PUDLAK SYNDROME 7"	"disease"		"Disease or Syndrome"	"0.60"		"1991"	"2017"	"0"	"2"	"ORPHANET"
"84062"	"DTNBP1"	"0.619"	"0.379"	"C4046029"	"Mental Disorders, Severe"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84064"	"HDHD2"			"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84068"	"SLC10A7"	"0.773"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84075"	"FSCB"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84085"	"FBXO30"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84100"	"ARL6"	"0.659"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.61"	"1"	"2009"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"84100"	"ARL6"	"0.659"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84100"	"ARL6"	"0.659"	"0.414"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.48"	"1"	"1998"	"2013"	"0"	"1"	"ORPHANET"
"84100"	"ARL6"	"0.659"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84100"	"ARL6"	"0.659"	"0.414"	"C1859564"	"Bardet-Biedl syndrome 3"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.62"	"1"	"1994"	"2013"	"2"	"6"	"CTD_human;UNIPROT"
"84100"	"ARL6"	"0.659"	"0.414"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84100"	"ARL6"	"0.659"	"0.414"	"C3150808"	"RETINITIS PIGMENTOSA 55"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"84100"	"ARL6"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84100"	"ARL6"	"0.659"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84126"	"ATRIP"	"0.72"	"0.414"	"C0265202"	"Seckel syndrome"	"disease"	"C05;C10;C16;C19;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"84126"	"ATRIP"	"0.72"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84131"	"CEP78"	"0.773"	"0.172"	"C1568248"	"Usher Syndrome, Type III"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84131"	"CEP78"	"0.773"	"0.172"	"C4310657"	"CONE-ROD DYSTROPHY AND HEARING LOSS"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"4"	"7"	"CLINGEN;CTD_human"
"84133"	"ZNRF3"	"0.752"	"0.31"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"84133"	"ZNRF3"	"0.752"	"0.31"	"C0206686"	"Adrenocortical carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"84133"	"ZNRF3"	"0.752"	"0.31"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"84133"	"ZNRF3"	"0.752"	"0.31"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"84134"	"TOMM40L"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84140"	"FAM161A"	"0.696"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"0.9090909"	"2004"	"2016"	"0"	"0"	"ORPHANET"
"84140"	"FAM161A"	"0.696"	"0.31"	"C1419614"	"RETINITIS PIGMENTOSA 28"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1999"	"2016"	"0"	"6"	"CTD_human"
"84140"	"FAM161A"	"0.696"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84142"	"ABRAXAS1"	"0.799"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2009"	"2015"	"2"	"1"	"UNIPROT"
"84142"	"ABRAXAS1"	"0.799"	"0.138"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"2"	"1"	"UNIPROT"
"84142"	"ABRAXAS1"	"0.799"	"0.138"	"C1861906"	"Breast Cancer, Familial Male"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2015"	"2"	"1"	"UNIPROT"
"84146"	"ZNF644"	"0.834"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84146"	"ZNF644"	"0.834"	"0.172"	"C3279997"	"MYOPIA 21, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2015"	"4"	"9"	"CTD_human;UNIPROT"
"84148"	"KAT8"	"0.672"	"0.345"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"84148"	"KAT8"	"0.672"	"0.345"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84148"	"KAT8"	"0.672"	"0.345"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2007"	"2017"	"4"	"0"	"PSYGENET"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0007370"	"Catalepsy"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0013384"	"Dyskinetic syndrome"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2007"	"2017"	"5"	"0"	"PSYGENET"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0152115"	"Lingual-Facial-Buccal Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0221169"	"Hemiballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0232766"	"Asterixis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0233612"	"Waxy flexibility"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0427086"	"Involuntary Movements"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0454606"	"Oral Dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C0752196"	"Ballismus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84152"	"PPP1R1B"	"0.624"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C0263666"	"Dermatomyositis, Childhood Type"	"disease"	"C05;C10;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C0393591"	"AICARDI-GOUTIERES SYNDROME"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C1835916"	"AICARDI-GOUTIERES SYNDROME 3"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.60"		"2006"	"2013"	"3"	"7"	"CTD_human;UNIPROT"
"84153"	"RNASEH2C"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2014"	"2"	"3"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"84159"	"ARID5B"	"0.672"	"0.345"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.44"	"1"	"2009"	"2018"	"2"	"9"	"CTD_human"
"84162"	"KIAA1109"	"0.696"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"84162"	"KIAA1109"	"0.696"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"84162"	"KIAA1109"	"0.696"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84162"	"KIAA1109"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"84166"	"NLRC5"	"0.752"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84166"	"NLRC5"	"0.752"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84168"	"ANTXR1"	"0.642"	"0.379"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84168"	"ANTXR1"	"0.642"	"0.379"	"C0406723"	"Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy"	"disease"	"C07;C10;C11;C16;C17;C23"	"Disease or Syndrome"	"0.63"	"1"	"1991"	"2015"	"0"	"6"	"CTD_human;ORPHANET"
"84168"	"ANTXR1"	"0.642"	"0.379"	"C1865871"	"HEMANGIOMA, CAPILLARY INFANTILE"	"disease"	"C04;C16"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"0"	"1"	"CTD_human"
"84168"	"ANTXR1"	"0.642"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84171"	"LOXL4"	"0.752"	"0.276"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"84171"	"LOXL4"	"0.752"	"0.276"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"84173"	"ELMOD3"	"0.886"	"0.172"	"C2829267"	"DEAFNESS, AUTOSOMAL RECESSIVE 88"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2014"	"1"	"1"	"CLINGEN;CTD_human;UNIPROT"
"84181"	"CHD6"	"0.834"	"0.241"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84181"	"CHD6"	"0.834"	"0.241"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84181"	"CHD6"	"0.834"	"0.241"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84181"	"CHD6"	"0.834"	"0.241"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84181"	"CHD6"	"0.834"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84181"	"CHD6"	"0.834"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84187"	"TMEM164"	"0.799"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84187"	"TMEM164"	"0.799"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84188"	"FAR1"	"0.762"	"0.241"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84188"	"FAR1"	"0.762"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84188"	"FAR1"	"0.762"	"0.241"	"C4015344"	"PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"ORPHANET;UNIPROT"
"84189"	"SLITRK6"	"0.743"	"0.345"	"C1857342"	"Deafness, Cochlear, with Myopia and Intellectual Impairment"	"disease"	"C09;C10;C11;C23;F01;F03"	"Disease or Syndrome"	"0.40"		"1993"	"2014"	"2"	"3"	"CLINGEN"
"84189"	"SLITRK6"	"0.743"	"0.345"	"C3806275"	"DEAFNESS AND MYOPIA"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2018"	"2"	"0"	"CLINGEN;CTD_human;ORPHANET"
"84196"	"USP48"	"0.834"	"0.103"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84196"	"USP48"	"0.834"	"0.103"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84196"	"USP48"	"0.834"	"0.103"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84197"	"POMK"	"0.616"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2013"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84197"	"POMK"	"0.616"	"0.414"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"84197"	"POMK"	"0.616"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84197"	"POMK"	"0.616"	"0.414"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84197"	"POMK"	"0.616"	"0.414"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84197"	"POMK"	"0.616"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84197"	"POMK"	"0.616"	"0.414"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84197"	"POMK"	"0.616"	"0.414"	"C3808964"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"4"	"5"	"UNIPROT"
"84197"	"POMK"	"0.616"	"0.414"	"C4015184"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"84215"	"ZNF541"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84216"	"TMEM117"	"0.799"	"0.069"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84216"	"TMEM117"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"84217"	"ZMYND12"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"84225"	"ZMYND15"	"0.857"	"0.034"	"C4014454"	"SPERMATOGENIC FAILURE 14"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"84231"	"TRAF7"	"0.886"	"0.103"	"C0025286"	"Meningioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2013"	"0"	"0"	"CGI"
"84231"	"TRAF7"	"0.886"	"0.103"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84233"	"TMEM126A"	"0.857"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84233"	"TMEM126A"	"0.857"	"0.138"	"C2751812"	"OPTIC ATROPHY 7 (disorder)"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"84247"	"RTL6"	"0.834"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84247"	"RTL6"	"0.834"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84249"	"PSD2"			"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84249"	"PSD2"			"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84251"	"SGIP1"	"0.928"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2012"	"2"	"0"	"PSYGENET"
"84254"	"CAMKK1"	"0.886"	"0.069"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84258"	"SYT3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84260"	"TCHP"	"0.52"	"0.759"	"C0235974"	"Pancreatic carcinoma"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"1"	"UNIPROT"
"84260"	"TCHP"	"0.52"	"0.759"	"C0699791"	"Stomach Carcinoma"	"disease"		"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"1"	"UNIPROT"
"84263"	"HSDL2"	"0.886"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84263"	"HSDL2"	"0.886"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84265"	"POLR3GL"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84265"	"POLR3GL"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84273"	"NOA1"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84274"	"COQ5"	"0.886"	"0.138"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84274"	"COQ5"	"0.886"	"0.138"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84274"	"COQ5"	"0.886"	"0.138"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84274"	"COQ5"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2009"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"84281"	"C2orf88"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84281"	"C2orf88"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84281"	"C2orf88"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C0023186"	"Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C0751262"	"Adult Learning Disorders"	"group"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C0751263"	"Learning Disturbance"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C0751265"	"Learning Disabilities"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C1330966"	"Developmental Academic Disorder"	"phenotype"	"C10;C23;F03"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84282"	"RNF135"	"0.785"	"0.172"	"C3280095"	"MACROCEPHALY, MACROSOMIA, AND FACIAL DYSMORPHISM SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"84282"	"RNF135"	"0.785"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84285"	"EIF1AD"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84295"	"PHF6"	"0.639"	"0.586"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"84295"	"PHF6"	"0.639"	"0.586"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"84295"	"PHF6"	"0.639"	"0.586"	"C0265339"	"Borjeson-Forssman-Lehmann syndrome"	"disease"	"C10;C16;C18;C19;C23"	"Disease or Syndrome"	"0.80"	"1"	"1962"	"2017"	"8"	"11"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"84295"	"PHF6"	"0.639"	"0.586"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.57"	"0.8571429"	"2010"	"2015"	"1"	"0"	"CGI;CTD_human"
"84295"	"PHF6"	"0.639"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2014"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"84300"	"UQCC2"	"0.743"	"0.345"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"84300"	"UQCC2"	"0.743"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84300"	"UQCC2"	"0.743"	"0.345"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84314"	"TMEM107"	"0.663"	"0.414"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84314"	"TMEM107"	"0.663"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"84314"	"TMEM107"	"0.663"	"0.414"	"C4539729"	"OROFACIODIGITAL SYNDROME XVI"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"2"	"1"	"UNIPROT"
"84315"	"MON1A"			"C0012715"	"Iron Metabolism Disorders"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84317"	"CCDC115"	"0.815"	"0.172"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"84317"	"CCDC115"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"84317"	"CCDC115"	"0.815"	"0.172"	"C4225191"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo"	"disease"		"Congenital Abnormality"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"84320"	"ACBD6"	"0.857"	"0.241"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84320"	"ACBD6"	"0.857"	"0.241"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84320"	"ACBD6"	"0.857"	"0.241"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84320"	"ACBD6"	"0.857"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"84334"	"APOPT1"	"0.69"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"4"	"CTD_human"
"84334"	"APOPT1"	"0.69"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"84334"	"APOPT1"	"0.69"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0037929"	"Spinal Cord Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0433895"	"Spinal Cord Contusion"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0433900"	"Spinal Cord Laceration"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0433905"	"Spinal Cord transection injury"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84335"	"AKT1S1"	"0.676"	"0.345"	"C0751515"	"Post-Traumatic Myelopathy"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84340"	"GFM2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"GENOMICS_ENGLAND"
"84342"	"COG8"	"0.773"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"84342"	"COG8"	"0.773"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84342"	"COG8"	"0.773"	"0.207"	"C1970021"	"Congenital Disorder Of Glycosylation, Type IIH"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.62"	"1"	"2007"	"2007"	"0"	"1"	"CTD_human;ORPHANET"
"84342"	"COG8"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84343"	"HPS3"	"0.785"	"0.31"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"2"	"0"	"GENOMICS_ENGLAND"
"84343"	"HPS3"	"0.785"	"0.31"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.34"	"1"	"2001"	"2005"	"0"	"0"	"CTD_human"
"84343"	"HPS3"	"0.785"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84343"	"HPS3"	"0.785"	"0.31"	"C3888001"	"HERMANSKY-PUDLAK SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1988"	"2014"	"1"	"6"	"UNIPROT"
"84364"	"ARFGAP2"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84364"	"ARFGAP2"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84364"	"ARFGAP2"	"0.928"	"0.069"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84364"	"ARFGAP2"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84376"	"HOOK3"	"0.785"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84376"	"HOOK3"	"0.785"	"0.276"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84376"	"HOOK3"	"0.785"	"0.276"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84418"	"CYSTM1"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0023493"	"Adult T-Cell Lymphoma/Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0036920"	"Sezary Syndrome"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"2"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0079744"	"Diffuse Large B-Cell Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.60"	"1"	"2006"	"2017"	"2"	"0"	"CGI;CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84433"	"CARD11"	"0.633"	"0.517"	"C1847973"	"Persistent Polyclonal B-Cell Lymphocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2013"	"2017"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"84433"	"CARD11"	"0.633"	"0.517"	"C3554686"	"IMMUNODEFICIENCY 11"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"84433"	"CARD11"	"0.633"	"0.517"	"C4539957"	"IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"84439"	"HHIPL1"	"0.857"	"0.034"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84439"	"HHIPL1"	"0.857"	"0.034"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.40"		"2011"	"2018"	"1"	"2"	"CTD_human"
"84441"	"MAML2"	"0.645"	"0.31"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84441"	"MAML2"	"0.645"	"0.31"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84441"	"MAML2"	"0.645"	"0.31"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84444"	"DOT1L"	"0.659"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84445"	"LZTS2"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"UNIPROT"
"84445"	"LZTS2"	"0.799"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84446"	"BRSK1"	"0.799"	"0.276"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"84446"	"BRSK1"	"0.799"	"0.276"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84446"	"BRSK1"	"0.799"	"0.276"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84448"	"ABLIM2"	"1"	"0.103"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84456"	"L3MBTL3"	"0.773"	"0.241"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84464"	"SLX4"	"0.672"	"0.517"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C0015625"	"Fanconi Anemia"	"disease"	"C15;C16;C18"	"Disease or Syndrome"	"0.70"	"1"	"2011"	"2017"	"3"	"3"	"CTD_human;ORPHANET"
"84464"	"SLX4"	"0.672"	"0.517"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2017"	"8"	"0"	"CLINGEN"
"84464"	"SLX4"	"0.672"	"0.517"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CLINGEN"
"84464"	"SLX4"	"0.672"	"0.517"	"C1861028"	"Esophageal atresia with or without tracheoesophageal fistula"	"disease"	"C06;C08;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84464"	"SLX4"	"0.672"	"0.517"	"C3469542"	"FANCONI ANEMIA, COMPLEMENTATION GROUP P"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84464"	"SLX4"	"0.672"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"84464"	"SLX4"	"0.672"	"0.517"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0011168"	"Deglutition Disorders"	"group"	"C06;C09"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.34"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0035220"	"Respiratory Distress Syndrome, Newborn"	"disease"	"C08;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0267071"	"Oropharyngeal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0267072"	"Esophageal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84466"	"MEGF10"	"0.696"	"0.414"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84466"	"MEGF10"	"0.696"	"0.414"	"C3280679"	"MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2007"	"2017"	"5"	"11"	"ORPHANET;UNIPROT"
"84466"	"MEGF10"	"0.696"	"0.414"	"C3541476"	"MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"5"	"3"	"ORPHANET;UNIPROT"
"84466"	"MEGF10"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84504"	"NKX6-2"	"0.815"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"84504"	"NKX6-2"	"0.815"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"84504"	"NKX6-2"	"0.815"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"84504"	"NKX6-2"	"0.815"	"0.379"	"C4479653"	"SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"2"	"UNIPROT"
"84515"	"MCM8"	"0.735"	"0.345"	"C2752067"	"MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3"	"phenotype"		"Finding"	"0.60"		"2015"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"84515"	"MCM8"	"0.735"	"0.345"	"C4225402"	"PREMATURE OVARIAN FAILURE 10"	"disease"		"Disease or Syndrome"	"0.50"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"84516"	"DCTN5"	"0.834"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"84519"	"ACRBP"	"0.773"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84519"	"ACRBP"	"0.773"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84519"	"ACRBP"	"0.773"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84519"	"ACRBP"	"0.773"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84519"	"ACRBP"	"0.773"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84522"	"JAGN1"	"0.857"	"0.069"	"C0027947"	"Neutropenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"84522"	"JAGN1"	"0.857"	"0.069"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"84522"	"JAGN1"	"0.857"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84522"	"JAGN1"	"0.857"	"0.069"	"C4014954"	"NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"84525"	"HOPX"	"0.642"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84527"	"ZNF559"	"0.886"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"84527"	"ZNF559"	"0.886"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84527"	"ZNF559"	"0.886"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84529"	"C15orf41"	"0.785"	"0.103"	"C0002876"	"Congenital dyserythropoietic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84529"	"C15orf41"	"0.785"	"0.103"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1997"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"84529"	"C15orf41"	"0.785"	"0.103"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1997"	"2014"	"3"	"0"	"GENOMICS_ENGLAND"
"84529"	"C15orf41"	"0.785"	"0.103"	"C0271933"	"Congenital dyserythropoietic anemia, type I"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"84529"	"C15orf41"	"0.785"	"0.103"	"C0271934"	"Congenital dyserythropoietic anemia, type III"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84529"	"C15orf41"	"0.785"	"0.103"	"C1306589"	"Congenital dyserythropoietic anemia, type II"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84529"	"C15orf41"	"0.785"	"0.103"	"C3810185"	"ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2015"	"1"	"2"	"UNIPROT"
"84530"	"SRRM4"	"0.886"	"0.138"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84530"	"SRRM4"	"0.886"	"0.138"	"C0155536"	"Paracousis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84530"	"SRRM4"	"0.886"	"0.138"	"C0260662"	"Hearing problem"	"group"	"C09;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84530"	"SRRM4"	"0.886"	"0.138"	"C0877848"	"Distorted hearing"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84530"	"SRRM4"	"0.886"	"0.138"	"C1510450"	"Dysacusis"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84539"	"MCHR2"	"0.69"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"84539"	"MCHR2"	"0.69"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"84541"	"KBTBD8"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84547"	"PGBD1"	"0.815"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2014"	"1"	"2"	"CTD_human"
"84548"	"TMEM185A"	"0.857"	"0.172"	"C4274329"	"FRAXF syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84557"	"MAP1LC3A"	"0.696"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84560"	"MT4"	"0.928"	"0.103"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84560"	"MT4"	"0.928"	"0.103"	"C0023176"	"Lead Poisoning"	"disease"	"C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84570"	"COL25A1"	"0.713"	"0.379"	"C0013261"	"Duane Retraction Syndrome"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84570"	"COL25A1"	"0.713"	"0.379"	"C0266573"	"Congenital ptosis"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"84570"	"COL25A1"	"0.713"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84570"	"COL25A1"	"0.713"	"0.379"	"C4015552"	"FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"84572"	"GNPTG"	"0.735"	"0.345"	"C1854896"	"Mucolipidosis III Gamma"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2016"	"6"	"20"	"CTD_human;ORPHANET;UNIPROT"
"84572"	"GNPTG"	"0.735"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2000"	"2010"	"4"	"0"	"GENOMICS_ENGLAND"
"84617"	"TUBB6"	"0.785"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84617"	"TUBB6"	"0.785"	"0.241"	"C4540277"	"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"UNIPROT"
"84623"	"KIRREL3"	"0.799"	"0.241"	"C2675487"	"Mental Retardation, Autosomal Dominant 4"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2009"	"2015"	"0"	"4"	"CTD_human;UNIPROT"
"84623"	"KIRREL3"	"0.799"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0010034"	"Corneal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2014"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0022410"	"Joint Instability"	"phenotype"	"C05"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0086437"	"Joint laxity"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0268344"	"Ehlers-Danlos syndrome 6B"	"disease"	"C05;C11;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"1968"	"2017"	"1"	"5"	"CTD_human;ORPHANET"
"84627"	"ZNF469"	"0.672"	"0.483"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84627"	"ZNF469"	"0.672"	"0.483"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2008"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"84628"	"NTNG2"	"0.773"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.52"	"0.5"	"2008"	"2010"	"2"	"0"	"CTD_human;PSYGENET"
"84628"	"NTNG2"	"0.773"	"0.207"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84628"	"NTNG2"	"0.773"	"0.207"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84628"	"NTNG2"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"84628"	"NTNG2"	"0.773"	"0.207"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84630"	"TTBK1"	"0.815"	"0.207"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"84630"	"TTBK1"	"0.815"	"0.207"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84631"	"SLITRK2"	"0.928"	"0.138"	"C0015923"	"Fetal Alcohol Syndrome"	"disease"	"C13;C16;C25"	"Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"84631"	"SLITRK2"	"0.928"	"0.138"	"C2985290"	"Fetal Alcohol Spectrum Disorders"	"group"	"C13;C16;C25"	"Congenital Abnormality; Disease or Syndrome"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0034012"	"Delayed Puberty"	"phenotype"	"C19"	"Pathologic Function"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.54"	"1"	"2003"	"2016"	"0"	"0"	"ORPHANET"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.40"	"1"	"2003"	"2015"	"5"	"0"	"GENOMICS_ENGLAND"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0342543"	"Central Precocious Puberty"	"disease"	"C19"	"Disease or Syndrome"	"0.48"	"0.875"	"2007"	"2016"	"0"	"1"	"CTD_human"
"84634"	"KISS1R"	"0.554"	"0.552"	"C0342544"	"Idiopathic central precocious puberty"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"84634"	"KISS1R"	"0.554"	"0.552"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84634"	"KISS1R"	"0.554"	"0.552"	"C3553841"	"HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.80"		"2003"	"2015"	"6"	"6"	"CTD_human;UNIPROT"
"84634"	"KISS1R"	"0.554"	"0.552"	"C3805879"	"PRECOCIOUS PUBERTY, CENTRAL, 1"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"84648"	"LCE3D"	"0.928"	"0.034"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"84648"	"LCE3D"	"0.928"	"0.034"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84649"	"DGAT2"	"0.72"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84654"	"SPZ1"	"0.538"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84654"	"SPZ1"	"0.538"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"0"	"2006"	"2013"	"1"	"0"	"CTD_human"
"84654"	"SPZ1"	"0.538"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"84660"	"CCDC62"	"0.785"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84662"	"GLIS2"	"0.648"	"0.31"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"84662"	"GLIS2"	"0.648"	"0.31"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84662"	"GLIS2"	"0.648"	"0.31"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84662"	"GLIS2"	"0.648"	"0.31"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84662"	"GLIS2"	"0.648"	"0.31"	"C1969092"	"NEPHRONOPHTHISIS 7"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2007"	"2014"	"0"	"1"	"CTD_human"
"84662"	"GLIS2"	"0.648"	"0.31"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84662"	"GLIS2"	"0.648"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2015"	"0"	"1"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0007196"	"Restrictive cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"84665"	"MYPN"	"0.69"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84665"	"MYPN"	"0.69"	"0.276"	"C0348616"	"Other restrictive cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84665"	"MYPN"	"0.69"	"0.276"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84665"	"MYPN"	"0.69"	"0.276"	"C3710589"	"Cap Myopathy"	"disease"	"C05;C10"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"84665"	"MYPN"	"0.69"	"0.276"	"C3714995"	"CARDIOMYOPATHY, DILATED, 1KK"	"disease"		"Disease or Syndrome"	"0.70"		"2001"	"2013"	"4"	"16"	"CLINGEN;CTD_human;UNIPROT"
"84665"	"MYPN"	"0.69"	"0.276"	"C3714998"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2013"	"4"	"16"	"CLINGEN;CTD_human;UNIPROT"
"84665"	"MYPN"	"0.69"	"0.276"	"C3808963"	"CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4"	"disease"		"Disease or Syndrome"	"0.70"		"2001"	"2013"	"4"	"17"	"CLINGEN;CTD_human;UNIPROT"
"84665"	"MYPN"	"0.69"	"0.276"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84665"	"MYPN"	"0.69"	"0.276"	"C4479186"	"NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"4"	"CTD_human"
"84667"	"HES7"	"0.713"	"0.207"	"C0265343"	"Jarcho-Levin syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2014"	"0"	"0"	"ORPHANET"
"84667"	"HES7"	"0.713"	"0.207"	"C1837549"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"84667"	"HES7"	"0.713"	"0.207"	"C1853296"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84667"	"HES7"	"0.713"	"0.207"	"C3150942"	"SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2010"	"2"	"3"	"UNIPROT"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84668"	"FAM126A"	"0.681"	"0.379"	"C1864663"	"HYPOMYELINATION AND CONGENITAL CATARACT"	"disease"	"C10;C11;C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.72"	"1"	"1993"	"2016"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"84668"	"FAM126A"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"84668"	"FAM126A"	"0.681"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.51"		"2001"	"2011"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0033141"	"Cardiomyopathies, Primary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0036529"	"Myocardial Diseases, Secondary"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0333641"	"Atrophic"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C0878544"	"Cardiomyopathies"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84676"	"TRIM63"	"0.676"	"0.483"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84678"	"KDM2B"	"0.713"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84680"	"ACCS"	"0.785"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84687"	"PPP1R9B"	"0.713"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2004"	"2009"	"2"	"0"	"PSYGENET"
"84687"	"PPP1R9B"	"0.713"	"0.241"	"C0037199"	"Sinusitis"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84693"	"MCEE"	"0.834"	"0.172"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84693"	"MCEE"	"0.834"	"0.172"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"		"2006"	"2015"	"4"	"0"	"GENOMICS_ENGLAND"
"84693"	"MCEE"	"0.834"	"0.172"	"C1855100"	"Methylmalonyl-CoA Epimerase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"1993"	"2006"	"0"	"1"	"CTD_human;ORPHANET"
"84693"	"MCEE"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"84695"	"LOXL3"	"0.785"	"0.31"	"C2020284"	"Stickler syndrome, type 1"	"disease"	"C05;C09;C10;C11;C17;C23"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84699"	"CREB3L3"	"0.834"	"0.172"	"C0020481"	"Hyperlipoproteinemia Type V"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.31"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"UNIPROT"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"84700"	"MYO18B"	"0.681"	"0.448"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84700"	"MYO18B"	"0.681"	"0.448"	"C4225285"	"KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"84701"	"COX4I2"	"0.696"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"84701"	"COX4I2"	"0.696"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"84701"	"COX4I2"	"0.696"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84701"	"COX4I2"	"0.696"	"0.379"	"C2675184"	"Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis"	"disease"	"C05;C06;C15;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"84705"	"GTPBP3"	"0.785"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84705"	"GTPBP3"	"0.785"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84705"	"GTPBP3"	"0.785"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84705"	"GTPBP3"	"0.785"	"0.138"	"C4015447"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"2"	"9"	"CTD_human;ORPHANET;UNIPROT"
"84706"	"GPT2"	"0.743"	"0.379"	"C4225388"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49"	"disease"		"Mental or Behavioral Dysfunction"	"0.70"		"2016"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"84709"	"MGARP"	"0.928"	"0.172"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84720"	"PIGO"	"0.727"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"84720"	"PIGO"	"0.727"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2014"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"84720"	"PIGO"	"0.727"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84720"	"PIGO"	"0.727"	"0.31"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.62"	"1"	"2012"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"84720"	"PIGO"	"0.727"	"0.31"	"C3553637"	"HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2018"	"4"	"8"	"UNIPROT"
"84720"	"PIGO"	"0.727"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"84725"	"PLEKHA8"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84733"	"CBX2"	"0.743"	"0.172"	"C0018054"	"Gonadal Dysgenesis, 46,XY"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84733"	"CBX2"	"0.743"	"0.172"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2009"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"84733"	"CBX2"	"0.743"	"0.172"	"C2751317"	"46, XY Sex Reversal 5"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"84733"	"CBX2"	"0.743"	"0.172"	"C2936694"	"Swyer Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84734"	"FAM167B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2016"	"3"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2007"	"2012"	"3"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1973"	"1973"	"2"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1973"	"1973"	"2"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0027854"	"Neurologic Manifestations"	"group"	"C10;C23"	"Finding"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0235031"	"Neurologic Symptoms"	"group"	"C10;C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0268632"	"Homocarnosinosis"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1968"	"1968"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0422837"	"Neurological observations"	"group"	"C10;C23"	"Finding"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0521654"	"Neurologic Deficits"	"group"	"C10;C23"	"Finding"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0746857"	"Focal Neurologic Deficits"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0751377"	"Neurologic Dysfunction"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0751378"	"Neurologic Signs"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"1973"	"1973"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1973"	"1973"	"2"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C3495554"	"Homocarnosinase deficiency"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1968"	"1968"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C3495555"	"Carnosinemia"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"1968"	"1968"	"1"	"0"	"CTD_human"
"84735"	"CNDP1"	"0.685"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1973"	"1973"	"2"	"0"	"CTD_human"
"84740"	"AFAP1-AS1"	"0.696"	"0.276"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84740"	"AFAP1-AS1"	"0.696"	"0.276"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84740"	"AFAP1-AS1"	"0.696"	"0.276"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84740"	"AFAP1-AS1"	"0.696"	"0.276"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"84752"	"B3GNT9"	"1"	"0.103"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84790"	"TUBA1C"	"0.735"	"0.276"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84790"	"TUBA1C"	"0.735"	"0.276"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84790"	"TUBA1C"	"0.735"	"0.276"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84790"	"TUBA1C"	"0.735"	"0.276"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84804"	"MFSD9"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84816"	"RTN4IP1"	"0.799"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84816"	"RTN4IP1"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1970"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"84816"	"RTN4IP1"	"0.799"	"0.138"	"C4225227"	"OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"84817"	"TXNDC17"	"1"	"0.069"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"84818"	"IL17RC"	"0.743"	"0.276"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"84818"	"IL17RC"	"0.743"	"0.276"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"84818"	"IL17RC"	"0.743"	"0.276"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2007"	"1"	"0"	"CTD_human"
"84818"	"IL17RC"	"0.743"	"0.276"	"C4225324"	"CANDIDIASIS, FAMILIAL, 9"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"2"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0220989"	"Acquired partial lipodystrophy"	"disease"	"C17;C18"	"Disease or Syndrome"	"0.63"	"1"	"2006"	"2012"	"0"	"2"	"CTD_human;ORPHANET"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84823"	"LMNB2"	"0.659"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84823"	"LMNB2"	"0.659"	"0.483"	"C3887501"	"LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO"	"disease"		"Finding"	"0.30"		"2006"	"2012"	"2"	"1"	"UNIPROT"
"84823"	"LMNB2"	"0.659"	"0.483"	"C4225289"	"EPILEPSY, PROGRESSIVE MYOCLONIC, 9"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"ORPHANET;UNIPROT"
"84830"	"ADTRP"	"0.834"	"0.172"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"84830"	"ADTRP"	"0.834"	"0.172"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"84839"	"RAX2"	"0.727"	"0.207"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"84839"	"RAX2"	"0.727"	"0.207"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84839"	"RAX2"	"0.727"	"0.207"	"C1835865"	"Cone-Rod Dystrophy 11"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"84839"	"RAX2"	"0.727"	"0.207"	"C1854023"	"Spinal muscular atrophy, Jerash type"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84839"	"RAX2"	"0.727"	"0.207"	"C3151060"	"Macular Degeneration, Age-Related, 6"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"2"	"CTD_human;UNIPROT"
"84864"	"RIOX2"	"0.727"	"0.207"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"84864"	"RIOX2"	"0.727"	"0.207"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2005"	"2011"	"1"	"0"	"CTD_human"
"84866"	"TMEM25"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84866"	"TMEM25"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84866"	"TMEM25"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84866"	"TMEM25"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84867"	"PTPN5"	"0.743"	"0.379"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84867"	"PTPN5"	"0.743"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2016"	"2"	"0"	"PSYGENET"
"84870"	"RSPO3"	"0.762"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84870"	"RSPO3"	"0.762"	"0.276"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84870"	"RSPO3"	"0.762"	"0.276"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84870"	"RSPO3"	"0.762"	"0.276"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84871"	"AGBL4"	"0.785"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2013"	"1"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.55"	"1"	"2014"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C1861451"	"Stormorken Syndrome"	"disease"	"C10;C11;C15;C16;C17;C23;F03"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"84876"	"ORAI1"	"0.565"	"0.655"	"C2748568"	"Immune dysfunction with T-cell inactivation due to calcium entry defect 1"	"disease"	"C16;C18;C20"	"Disease or Syndrome"	"0.70"		"1994"	"2010"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"84876"	"ORAI1"	"0.565"	"0.655"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84876"	"ORAI1"	"0.565"	"0.655"	"C4014557"	"MYOPATHY, TUBULAR AGGREGATE, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2018"	"2"	"3"	"UNIPROT"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0009090"	"Cluttering"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.53"	"1"	"2015"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0037822"	"Speech Disorders"	"group"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0233726"	"Aprosodia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0751512"	"Dysglossia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0751513"	"Rhinolalia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0751514"	"Verbal Fluency Disorders"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C3495145"	"Dyslalia"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2015"	"2015"	"2"	"0"	"CTD_human"
"84879"	"MFSD2A"	"0.645"	"0.379"	"C4225310"	"MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.52"	"1"	"2012"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C3553813"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"84892"	"POMGNT2"	"0.63"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84894"	"LINGO1"	"0.752"	"0.207"	"C0270736"	"Essential Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2009"	"2017"	"1"	"1"	"CTD_human"
"84894"	"LINGO1"	"0.752"	"0.207"	"C0393615"	"Familial Tremor"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84896"	"ATAD1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"84899"	"TMTC4"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84902"	"CEP89"	"0.928"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"84908"	"FAM136A"	"0.928"	"0.034"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"84909"	"C9orf3"	"0.785"	"0.345"	"C0004238"	"Atrial Fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.42"	"0.5"	"2012"	"2017"	"1"	"2"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C0235480"	"Paroxysmal atrial fibrillation"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C2585653"	"Persistent atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C3468561"	"familial atrial fibrillation"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84909"	"C9orf3"	"0.785"	"0.345"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84913"	"ATOH8"	"0.727"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"84916"	"UTP4"	"0.752"	"0.207"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84916"	"UTP4"	"0.752"	"0.207"	"C1858051"	"NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS"	"disease"	"C06"	"Disease or Syndrome"	"0.57"	"1"	"2000"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"84919"	"PPP1R15B"	"0.727"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"84919"	"PPP1R15B"	"0.727"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"84919"	"PPP1R15B"	"0.727"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"84919"	"PPP1R15B"	"0.727"	"0.448"	"C4225195"	"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"84920"	"ALG10"	"0.834"	"0.172"	"C0023976"	"Long QT Syndrome"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"84920"	"ALG10"	"0.834"	"0.172"	"C3150943"	"Long Qt Syndrome 2"	"disease"	"C14;C16;C23"	"Disease or Syndrome"	"0.40"		"2004"	"2004"	"0"	"1"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.46"	"0.8333333"	"2002"	"2016"	"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"CTD_human"
"84925"	"DIRC2"	"0.762"	"0.172"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"84930"	"MASTL"	"0.785"	"0.276"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"84930"	"MASTL"	"0.785"	"0.276"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2004"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"84930"	"MASTL"	"0.785"	"0.276"	"C1861185"	"THROMBOCYTOPENIA 2 (disorder)"	"disease"	"C15;C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"CTD_human"
"84942"	"WDR73"	"0.614"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"84942"	"WDR73"	"0.614"	"0.414"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"84942"	"WDR73"	"0.614"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"84942"	"WDR73"	"0.614"	"0.414"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.56"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"84942"	"WDR73"	"0.614"	"0.414"	"C1847114"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"84942"	"WDR73"	"0.614"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0013421"	"Dystonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.42"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0023772"	"Lipid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"		"2006"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0393588"	"Dystonia, Paroxysmal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0393610"	"Dystonia, Diurnal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0751093"	"Dystonia, Limb"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"84947"	"SERAC1"	"0.672"	"0.379"	"C3553597"	"3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2006"	"2018"	"3"	"9"	"CTD_human;ORPHANET;UNIPROT"
"84947"	"SERAC1"	"0.672"	"0.379"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84947"	"SERAC1"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2018"	"7"	"0"	"GENOMICS_ENGLAND"
"84947"	"SERAC1"	"0.672"	"0.379"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"84951"	"TNS4"	"0.69"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2011"	"1"	"1"	"UNIPROT"
"84952"	"CGNL1"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"84962"	"AJUBA"	"0.743"	"0.172"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"84966"	"IGSF21"	"0.886"	"0.172"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84966"	"IGSF21"	"0.886"	"0.172"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84966"	"IGSF21"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"84976"	"DISP1"	"0.815"	"0.207"	"C0079541"	"Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.33"	"1"	"2007"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"84976"	"DISP1"	"0.815"	"0.207"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84976"	"DISP1"	"0.815"	"0.207"	"C0431362"	"Lobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"84976"	"DISP1"	"0.815"	"0.207"	"C0431363"	"Alobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"84976"	"DISP1"	"0.815"	"0.207"	"C0751617"	"Semilobar Holoprosencephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"84976"	"DISP1"	"0.815"	"0.207"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"84981"	"MIR22HG"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84981"	"MIR22HG"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84981"	"MIR22HG"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"84984"	"CEP19"	"0.785"	"0.138"	"C3810324"	"MORBID OBESITY AND SPERMATOGENIC FAILURE"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"84987"	"COX14"	"0.72"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2012"	"2012"	"0"	"1"	"CTD_human;ORPHANET"
"84987"	"COX14"	"0.72"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84987"	"COX14"	"0.72"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"84991"	"RBM17"	"0.743"	"0.276"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84991"	"RBM17"	"0.743"	"0.276"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"84992"	"PIGY"	"0.707"	"0.345"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"84992"	"PIGY"	"0.707"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"84992"	"PIGY"	"0.707"	"0.345"	"C4225201"	"HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"85007"	"PHYKPL"	"0.928"	"0.138"	"C3554344"	"PHOSPHOHYDROXYLYSINURIA"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2012"	"2014"	"1"	"2"	"UNIPROT"
"85012"	"TCEAL3"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"85236"	"HIST1H2BK"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85236"	"HIST1H2BK"	"0.886"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85236"	"HIST1H2BK"	"0.886"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85236"	"HIST1H2BK"	"0.886"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85300"	"ATCAY"	"0.773"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85300"	"ATCAY"	"0.773"	"0.241"	"C1832585"	"CEREBELLAR ATAXIA, CAYMAN TYPE"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.81"	"1"	"2003"	"2006"	"1"	"0"	"CTD_human;ORPHANET;UNIPROT"
"85300"	"ATCAY"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"85301"	"COL27A1"	"0.834"	"0.138"	"C3554594"	"STEEL SYNDROME"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"2015"	"2018"	"1"	"1"	"ORPHANET;UNIPROT"
"85320"	"ABCC11"	"0.611"	"0.517"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.70"	"1"	"2005"	"2018"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2006"	"2016"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2006"	"2007"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2010"	"2018"	"0"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2009"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0564408"	"Manic mood"	"phenotype"		"Finding"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2007"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.969697"	"2007"	"2018"	"2"	"0"	"CTD_human"
"85358"	"SHANK3"	"0.594"	"0.448"	"C1853490"	"22q13.3 Deletion Syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.80"	"1"	"2003"	"2018"	"4"	"5"	"CTD_human;ORPHANET;UNIPROT"
"85358"	"SHANK3"	"0.594"	"0.448"	"C3151380"	"SCHIZOPHRENIA 15"	"disease"		"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"2"	"UNIPROT"
"85358"	"SHANK3"	"0.594"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"85360"	"SYDE1"	"1"	"0.103"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"85363"	"TRIM5"	"0.799"	"0.241"	"C0019693"	"HIV Infections"	"group"	"C02;C20"	"Disease or Syndrome"	"0.36"	"1"	"2004"	"2015"	"1"	"0"	"CTD_human"
"85363"	"TRIM5"	"0.799"	"0.241"	"C4505456"	"HIV Coinfection"	"disease"	"C02;C20"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85365"	"ALG2"	"0.676"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85365"	"ALG2"	"0.676"	"0.31"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"85365"	"ALG2"	"0.676"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85365"	"ALG2"	"0.676"	"0.31"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"85365"	"ALG2"	"0.676"	"0.31"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"85365"	"ALG2"	"0.676"	"0.31"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"85365"	"ALG2"	"0.676"	"0.31"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"85365"	"ALG2"	"0.676"	"0.31"	"C1842836"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2003"	"2003"	"0"	"2"	"CTD_human;ORPHANET"
"85365"	"ALG2"	"0.676"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"85365"	"ALG2"	"0.676"	"0.31"	"C4015597"	"MYASTHENIC SYNDROME, CONGENITAL, 14"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2015"	"1"	"2"	"UNIPROT"
"85366"	"MYLK2"	"0.785"	"0.103"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.50"		"2000"	"2012"	"6"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"85366"	"MYLK2"	"0.785"	"0.103"	"C0205700"	"Asymmetric Septal Hypertrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2001"	"2001"	"1"	"2"	"UNIPROT"
"85366"	"MYLK2"	"0.785"	"0.103"	"C0700053"	"Idiopathic hypertrophic subaortic stenosis"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2001"	"2001"	"1"	"2"	"UNIPROT"
"85366"	"MYLK2"	"0.785"	"0.103"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2000"	"2012"	"6"	"2"	"CLINGEN;UNIPROT"
"85366"	"MYLK2"	"0.785"	"0.103"	"C3495498"	"Cardiomyopathy, Familial Hypertrophic, 1 (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.50"		"2001"	"2001"	"1"	"2"	"CTD_human;UNIPROT"
"85377"	"MICALL1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"85378"	"TUBGCP6"	"0.685"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85378"	"TUBGCP6"	"0.685"	"0.276"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"85378"	"TUBGCP6"	"0.685"	"0.276"	"C3502492"	"Microcephaly with Chorioretinopathy, Autosomal Recessive"	"disease"	"C05;C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"85378"	"TUBGCP6"	"0.685"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"85413"	"SLC22A16"	"0.707"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"85413"	"SLC22A16"	"0.707"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"85413"	"SLC22A16"	"0.707"	"0.276"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"85413"	"SLC22A16"	"0.707"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"85413"	"SLC22A16"	"0.707"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"85415"	"RHPN2"	"0.815"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"85415"	"RHPN2"	"0.815"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85415"	"RHPN2"	"0.815"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.42"	"1"	"2008"	"2016"	"1"	"2"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0011999"	"Diastematomyelia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0027794"	"Neural Tube Defects"	"group"	"C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2013"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0027806"	"Neurenteric Cyst"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0080218"	"Tethered Cord Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0152234"	"Iniencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0152426"	"Craniorachischisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0266453"	"Exencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0344479"	"Spinal Cord Myelodysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85416"	"ZIC5"	"0.762"	"0.103"	"C0702169"	"Acrania"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"85417"	"CCNB3"	"0.785"	"0.069"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"85417"	"CCNB3"	"0.785"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"85417"	"CCNB3"	"0.785"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"85439"	"STON2"	"0.886"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"85439"	"STON2"	"0.886"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2014"	"2"	"0"	"PSYGENET"
"85439"	"STON2"	"0.886"	"0.069"	"C1842605"	"SCHIZOPHRENIA 11"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"85440"	"DOCK7"	"0.727"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"85440"	"DOCK7"	"0.727"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"85440"	"DOCK7"	"0.727"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"85440"	"DOCK7"	"0.727"	"0.345"	"C4014492"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"85443"	"DCLK3"	"0.72"	"0.448"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"85443"	"DCLK3"	"0.72"	"0.448"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"85443"	"DCLK3"	"0.72"	"0.448"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"85443"	"DCLK3"	"0.72"	"0.448"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"85443"	"DCLK3"	"0.72"	"0.448"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0024713"	"Manic Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0338831"	"Manic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85458"	"DIXDC1"	"0.681"	"0.207"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"85463"	"ZC3H12C"	"0.928"	"0.034"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"85463"	"ZC3H12C"	"0.928"	"0.034"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"1"	"CTD_human"
"85465"	"SELENOI"	"0.928"	"0.138"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85465"	"SELENOI"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85476"	"GFM1"	"0.663"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85476"	"GFM1"	"0.663"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85476"	"GFM1"	"0.663"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"85476"	"GFM1"	"0.663"	"0.414"	"C1836797"	"Combined Oxidative Phosphorylation Deficiency 1"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.70"		"2004"	"2016"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"85476"	"GFM1"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"85478"	"CCDC65"	"0.762"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2014"	"0"	"1"	"ORPHANET"
"85478"	"CCDC65"	"0.762"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85478"	"CCDC65"	"0.762"	"0.138"	"C3809701"	"CILIARY DYSKINESIA, PRIMARY, 27"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"85478"	"CCDC65"	"0.762"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"85478"	"CCDC65"	"0.762"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"85480"	"TSLP"	"0.547"	"0.69"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2018"	"1"	"2"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.60"	"1"	"2002"	"2018"	"3"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0017662"	"Glomerulonephritis, Membranoproliferative"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2007"	"2018"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0035228"	"Respiratory Hypersensitivity"	"phenotype"	"C08;C20"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2006"	"2014"	"3"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0268742"	"Membranoproliferative Glomerulonephritis, Type I"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0268743"	"Membranoproliferative Glomerulonephritis, Type II"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C0341106"	"Eosinophilic esophagitis"	"disease"	"C06;C15;C20"	"Disease or Syndrome"	"0.37"	"1"	"2010"	"2016"	"1"	"2"	"CTD_human"
"85480"	"TSLP"	"0.547"	"0.69"	"C1720821"	"Membranoproliferative Glomerulonephritis, Type III"	"disease"	"C12;C13;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"85481"	"PSKH2"	"1"	"0.069"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"86123"	"YWHAZP5"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"86614"	"HSFY1"	"0.815"	"0.069"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"87178"	"PNPT1"	"0.696"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"87178"	"PNPT1"	"0.696"	"0.448"	"C1824925"	"DEAFNESS, AUTOSOMAL RECESSIVE 70"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CLINGEN;CTD_human;UNIPROT"
"87178"	"PNPT1"	"0.696"	"0.448"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"87178"	"PNPT1"	"0.696"	"0.448"	"C3554129"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"87178"	"PNPT1"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89765"	"RSPH1"	"0.743"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.45"	"1"	"1993"	"2015"	"0"	"6"	"ORPHANET"
"89765"	"RSPH1"	"0.743"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89765"	"RSPH1"	"0.743"	"0.138"	"C3809634"	"CILIARY DYSKINESIA, PRIMARY, 24"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"1"	"6"	"CTD_human;UNIPROT"
"89765"	"RSPH1"	"0.743"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89765"	"RSPH1"	"0.743"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"89780"	"WNT3A"	"0.598"	"0.621"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"89780"	"WNT3A"	"0.598"	"0.621"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"89780"	"WNT3A"	"0.598"	"0.621"	"C0264080"	"Juvenile osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"89781"	"HPS4"	"0.762"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"2"	"0"	"PSYGENET"
"89781"	"HPS4"	"0.762"	"0.31"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.40"		"2002"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"89781"	"HPS4"	"0.762"	"0.31"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.44"	"1"	"2002"	"2015"	"0"	"1"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89795"	"NAV3"	"0.69"	"0.483"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"89796"	"NAV1"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"89797"	"NAV2"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"89832"	"CHRFAM7A"	"0.672"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"2006"	"2016"	"5"	"0"	"PSYGENET"
"89832"	"CHRFAM7A"	"0.672"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"1998"	"2016"	"1"	"0"	"PSYGENET"
"89866"	"SEC16B"	"0.886"	"0.207"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2009"	"2012"	"2"	"1"	"CTD_human"
"89869"	"PLCZ1"	"0.857"	"0.241"	"C4310666"	"SPERMATOGENIC FAILURE 17"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"89884"	"LHX4"	"0.639"	"0.414"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"		"2001"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"89884"	"LHX4"	"0.639"	"0.414"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89884"	"LHX4"	"0.639"	"0.414"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2001"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"89884"	"LHX4"	"0.639"	"0.414"	"C2678408"	"PITUITARY HORMONE DEFICIENCY, COMBINED, 4"	"disease"	"C05;C10;C16;C19"	"Disease or Syndrome"	"0.70"		"2008"	"2013"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"89884"	"LHX4"	"0.639"	"0.414"	"C2751608"	"Pituitary Hormone Deficiency, Combined, 1"	"disease"	"C16;C19;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"89884"	"LHX4"	"0.639"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"89884"	"LHX4"	"0.639"	"0.414"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"89885"	"FATE1"	"0.762"	"0.414"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"89886"	"SLAMF9"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"89891"	"WDR34"	"0.659"	"0.448"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"89891"	"WDR34"	"0.659"	"0.448"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"89891"	"WDR34"	"0.659"	"0.448"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"89891"	"WDR34"	"0.659"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89891"	"WDR34"	"0.659"	"0.448"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.42"	"1"	"2013"	"2018"	"0"	"3"	"ORPHANET"
"89891"	"WDR34"	"0.659"	"0.448"	"C0432197"	"Short rib-polydactyly syndrome, Verma-Naumoff type"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"89891"	"WDR34"	"0.659"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89891"	"WDR34"	"0.659"	"0.448"	"C3810200"	"SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2013"	"2"	"9"	"UNIPROT"
"89891"	"WDR34"	"0.659"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89910"	"UBE3B"	"0.624"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"89910"	"UBE3B"	"0.624"	"0.552"	"C1855663"	"Kaufman oculocerebrofacial syndrome"	"disease"	"C05;C10;C11;C16;C23;F01;F03"	"Disease or Syndrome"	"0.75"	"1"	"2011"	"2018"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"89910"	"UBE3B"	"0.624"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"89970"	"RSPRY1"	"0.743"	"0.31"	"C4225232"	"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"ORPHANET;UNIPROT"
"90121"	"TSR2"	"0.743"	"0.345"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"1993"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"90121"	"TSR2"	"0.743"	"0.345"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"1993"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"90121"	"TSR2"	"0.743"	"0.345"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"90121"	"TSR2"	"0.743"	"0.345"	"C1260899"	"Anemia, Diamond-Blackfan"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"90121"	"TSR2"	"0.743"	"0.345"	"C2931850"	"Aase Smith syndrome 2"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"90121"	"TSR2"	"0.743"	"0.345"	"C4225422"	"DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"90139"	"TSPAN18"	"0.857"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2016"	"1"	"3"	"CTD_human"
"90141"	"EFCAB11"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"90161"	"HS6ST2"	"0.834"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90167"	"FRMD7"	"0.701"	"0.31"	"C1839580"	"Nystagmus 1, congenital, X- linked"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"13"	"10"	"CTD_human;UNIPROT"
"90167"	"FRMD7"	"0.701"	"0.31"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2007"	"2015"	"6"	"0"	"GENOMICS_ENGLAND"
"90167"	"FRMD7"	"0.701"	"0.31"	"C3151880"	"NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED (disorder)"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2013"	"12"	"6"	"UNIPROT"
"90167"	"FRMD7"	"0.701"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2011"	"6"	"0"	"GENOMICS_ENGLAND"
"90226"	"UCN2"	"0.696"	"0.379"	"C0003123"	"Anorexia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C0018801"	"Heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C0018802"	"Congestive heart failure"	"disease"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C0023212"	"Left-Sided Heart Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C0235527"	"Heart Failure, Right-Sided"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C1959583"	"Myocardial Failure"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"90226"	"UCN2"	"0.696"	"0.379"	"C1961112"	"Heart Decompensation"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"90268"	"OTULIN"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90268"	"OTULIN"	"0.815"	"0.207"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"90268"	"OTULIN"	"0.815"	"0.207"	"C4310614"	"AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"90273"	"CEACAM21"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2012"	"2012"	"1"	"1"	"PSYGENET"
"90326"	"THAP3"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90326"	"THAP3"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90332"	"EXOC3L2"	"0.834"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90338"	"ZNF160"	"0.886"	"0.103"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"90338"	"ZNF160"	"0.886"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"90338"	"ZNF160"	"0.886"	"0.103"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"90338"	"ZNF160"	"0.886"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"90338"	"ZNF160"	"0.886"	"0.103"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"1994"	"2017"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"90353"	"CTU1"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"90362"	"FAM110B"	"0.886"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"90381"	"TICRR"	"1"	"0.069"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90411"	"MCFD2"	"0.72"	"0.207"	"C1856883"	"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.37"	"1"	"2003"	"2014"	"0"	"0"	"ORPHANET"
"90411"	"MCFD2"	"0.72"	"0.207"	"C3150889"	"FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2"	"disease"		"Disease or Syndrome"	"0.60"		"1954"	"2011"	"4"	"6"	"CTD_human;UNIPROT"
"90417"	"KNSTRN"	"0.799"	"0.207"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"90427"	"BMF"	"0.743"	"0.241"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.41"	"1"	"2013"	"2017"	"1"	"1"	"CTD_human"
"90427"	"BMF"	"0.743"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"90529"	"STPG1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"90624"	"LYRM7"	"0.69"	"0.345"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2016"	"2018"	"0"	"0"	"ORPHANET"
"90624"	"LYRM7"	"0.69"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"90624"	"LYRM7"	"0.69"	"0.345"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"90624"	"LYRM7"	"0.69"	"0.345"	"C4014440"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2016"	"1"	"5"	"UNIPROT"
"90627"	"STARD13"	"0.69"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"90668"	"CARMIL3"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90668"	"CARMIL3"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.85"	"1"	"1993"	"2017"	"1"	"2"	"CTD_human;GENOMICS_ENGLAND"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2010"	"2013"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C1837805"	"Charcot-Marie-Tooth disease, axonal, Type 2G"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C1843183"	"Charcot-Marie-Tooth disease, Type 4A, axonal form"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2017"	"2"	"0"	"CTD_human"
"90678"	"LRSAM1"	"0.681"	"0.276"	"C3280797"	"CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P"	"disease"		"Disease or Syndrome"	"0.90"		"1986"	"2017"	"4"	"6"	"CTD_human;ORPHANET;UNIPROT"
"90693"	"CCDC126"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"90826"	"PRMT9"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"90853"	"SPOCD1"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"90865"	"IL33"	"0.503"	"0.793"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.50"	"0.974359"	"2009"	"2018"	"4"	"3"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0020523"	"Immediate hypersensitivity"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"90865"	"IL33"	"0.503"	"0.793"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"90952"	"ESAM"	"0.857"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"90993"	"CREB3L1"	"0.707"	"0.241"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2014"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"90993"	"CREB3L1"	"0.707"	"0.241"	"C0268362"	"Osteogenesis imperfecta type III (disorder)"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"90993"	"CREB3L1"	"0.707"	"0.241"	"C3714524"	"Fibromyxosarcoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"91039"	"DPP9"	"0.72"	"0.31"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"91039"	"DPP9"	"0.72"	"0.31"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"91074"	"ANKRD30A"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2001"	"2016"	"0"	"0"	"UNIPROT"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0029124"	"Optic Atrophy"	"disease"	"C10;C11"	"Disease or Syndrome"	"0.42"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0205713"	"Roussy-Levy Syndrome (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0270911"	"Charcot-Marie-Tooth Disease, Type Ia (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0270912"	"Charcot-Marie-Tooth Disease, Type Ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0270914"	"Hereditary Motor and Sensory-Neuropathy Type II"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0393807"	"Hereditary motor and sensory neuropathy with optic atrophy (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0751036"	"Hereditary Motor and Sensory Neuropathy Type I"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"91137"	"SLC25A46"	"0.72"	"0.31"	"C4225302"	"NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"1"	"9"	"CTD_human;UNIPROT"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"	"1"	"2009"	"2016"	"1"	"2"	"GENOMICS_ENGLAND"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.60"		"2009"	"2015"	"1"	"2"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.42"	"1"	"2002"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.43"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0265215"	"Meckel-Gruber syndrome"	"disease"		"Disease or Syndrome"	"0.42"	"1"	"2002"	"2018"	"0"	"8"	"ORPHANET"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.47"	"0.8571429"	"2002"	"2018"	"0"	"8"	"ORPHANET"
"91147"	"TMEM67"	"0.559"	"0.655"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"2006"	"2015"	"1"	"2"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2010"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"91147"	"TMEM67"	"0.559"	"0.655"	"C1846357"	"Meckel syndrome type 3"	"disease"	"C08;C09;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.63"	"1"	"2006"	"2016"	"4"	"36"	"CTD_human;UNIPROT"
"91147"	"TMEM67"	"0.559"	"0.655"	"C1853153"	"JOUBERT SYNDROME 6"	"disease"	"C10;C11;C12;C13"	"Disease or Syndrome"	"0.80"		"1989"	"2016"	"5"	"44"	"CTD_human;UNIPROT"
"91147"	"TMEM67"	"0.559"	"0.655"	"C1857662"	"COACH syndrome"	"disease"	"C06;C10;C11;C16;C23"	"Disease or Syndrome"	"0.73"	"1"	"1989"	"2017"	"3"	"24"	"CTD_human;ORPHANET;UNIPROT"
"91147"	"TMEM67"	"0.559"	"0.655"	"C2673874"	"BARDET-BIEDL SYNDROME 14 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"91147"	"TMEM67"	"0.559"	"0.655"	"C3150796"	"NEPHRONOPHTHISIS 11"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2009"	"2015"	"1"	"4"	"CTD_human;UNIPROT"
"91147"	"TMEM67"	"0.559"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"91147"	"TMEM67"	"0.559"	"0.655"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.39"	"1"	"2008"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"91179"	"SCARF2"	"0.743"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"91179"	"SCARF2"	"0.743"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"91179"	"SCARF2"	"0.743"	"0.31"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"91179"	"SCARF2"	"0.743"	"0.31"	"C1833136"	"Marden Walker like syndrome"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.72"	"1"	"2010"	"2015"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"91179"	"SCARF2"	"0.743"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0005940"	"Bone Diseases"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0009782"	"Connective Tissue Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.53"	"1"	"2008"	"2017"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0022821"	"Kyphosis deformity of spine"	"phenotype"	"C05"	"Anatomical Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0040427"	"Tooth Abnormalities"	"group"	"C07;C16"	"Anatomical Abnormality"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0268338"	"Ehlers-Danlos Syndrome, Type IV"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C0524730"	"Odontome"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2012"	"2"	"0"	"CTD_human"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C2676510"	"Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like"	"disease"	"C05;C14;C15;C16;C17"	"Disease or Syndrome"	"0.61"	"1"	"2009"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"91252"	"SLC39A13"	"0.727"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91289"	"LMF2"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"91368"	"CDKN2AIPNL"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91404"	"SESTD1"	"1"	"0.034"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"91452"	"ACBD5"	"0.928"	"0.138"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91522"	"COL23A1"			"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91522"	"COL23A1"			"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91543"	"RSAD2"	"0.799"	"0.207"	"C0021400"	"Influenza"	"disease"	"C02;C08"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2013"	"1"	"0"	"CTD_human"
"91543"	"RSAD2"	"0.799"	"0.207"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"91574"	"C12orf65"	"0.701"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91574"	"C12orf65"	"0.701"	"0.276"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91574"	"C12orf65"	"0.701"	"0.276"	"C0162666"	"Mitochondrial Encephalomyopathies"	"group"	"C05;C10;C18"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91574"	"C12orf65"	"0.701"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91574"	"C12orf65"	"0.701"	"0.276"	"C3150801"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2015"	"0"	"2"	"CTD_human;ORPHANET"
"91574"	"C12orf65"	"0.701"	"0.276"	"C3539506"	"SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"1988"	"2015"	"0"	"5"	"ORPHANET"
"91574"	"C12orf65"	"0.701"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"91608"	"RASL10B"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"91608"	"RASL10B"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"91608"	"RASL10B"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"91614"	"DEPDC7"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91624"	"NEXN"	"0.743"	"0.138"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2009"	"2009"	"0"	"0"	"GENOMICS_ENGLAND"
"91624"	"NEXN"	"0.743"	"0.138"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.51"	"1"	"2009"	"2017"	"3"	"0"	"CLINGEN;GENOMICS_ENGLAND"
"91624"	"NEXN"	"0.743"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91624"	"NEXN"	"0.743"	"0.138"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91624"	"NEXN"	"0.743"	"0.138"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"91624"	"NEXN"	"0.743"	"0.138"	"C0949658"	"Cardiomyopathy, Hypertrophic, Familial"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2017"	"3"	"0"	"CLINGEN"
"91624"	"NEXN"	"0.743"	"0.138"	"C2751084"	"Cardiomyopathy, Dilated, 1CC"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"2009"	"2009"	"1"	"2"	"CTD_human;UNIPROT"
"91624"	"NEXN"	"0.743"	"0.138"	"C3151267"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20"	"disease"		"Disease or Syndrome"	"0.80"		"2011"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C0342779"	"Complex V deficiency"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"0"	"0"	"ORPHANET"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2010"	"2"	"0"	"GENOMICS_ENGLAND"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C2700431"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"91647"	"ATPAF2"	"0.743"	"0.31"	"C3276276"	"MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1"	"disease"		"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"91653"	"BOC"	"0.752"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"91653"	"BOC"	"0.752"	"0.31"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"91653"	"BOC"	"0.752"	"0.31"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91661"	"ZNF765"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"91662"	"NLRP12"	"0.656"	"0.552"	"C2673198"	"Familial Cold Autoinflammatory Syndrome 2"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.60"		"2008"	"2017"	"0"	"5"	"CTD_human;ORPHANET"
"91662"	"NLRP12"	"0.656"	"0.552"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"91663"	"MYADM"	"0.799"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2009"	"2018"	"5"	"1"	"PSYGENET"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"	"0.9473684"	"2009"	"2018"	"1"	"5"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2011"	"2"	"0"	"PSYGENET"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"91752"	"ZNF804A"	"0.639"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"91754"	"NEK9"	"0.69"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2011"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"91754"	"NEK9"	"0.69"	"0.414"	"C0265987"	"Nevus comedonicus"	"disease"		"Neoplastic Process"	"0.70"		"2017"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"91754"	"NEK9"	"0.69"	"0.414"	"C3280309"	"ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"91754"	"NEK9"	"0.69"	"0.414"	"C4310760"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 10"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"1"	"CTD_human;ORPHANET"
"91768"	"CABLES1"	"0.696"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"91768"	"CABLES1"	"0.696"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"91768"	"CABLES1"	"0.696"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"91801"	"ALKBH8"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91801"	"ALKBH8"	"0.886"	"0.138"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91801"	"ALKBH8"	"0.886"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91801"	"ALKBH8"	"0.886"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91801"	"ALKBH8"	"0.886"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91807"	"MYLK3"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"91833"	"WDR20"	"0.667"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91833"	"WDR20"	"0.667"	"0.379"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91833"	"WDR20"	"0.667"	"0.379"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"91851"	"CHRDL1"	"0.834"	"0.172"	"C0344530"	"Congenital keratoglobus"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.65"	"1"	"2012"	"2017"	"1"	"7"	"ORPHANET;UNIPROT"
"91851"	"CHRDL1"	"0.834"	"0.172"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"91851"	"CHRDL1"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91869"	"RFT1"	"0.69"	"0.448"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2009"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"91869"	"RFT1"	"0.69"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91869"	"RFT1"	"0.69"	"0.448"	"C2677590"	"Congenital Disorder Of Glycosylation, Type In"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.71"	"1"	"2008"	"2018"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"91869"	"RFT1"	"0.69"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"91937"	"TIMD4"	"0.713"	"0.414"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"91937"	"TIMD4"	"0.713"	"0.414"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"0"	"1"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0752107"	"Brain Diseases, Metabolic, Inherited"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0752109"	"Brain Diseases, Metabolic, Inborn"	"group"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C0752110"	"Central Nervous System Inborn Metabolic Diseases"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2005"	"2009"	"0"	"2"	"CTD_human"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"91942"	"NDUFAF2"	"0.607"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2010"	"3"	"0"	"GENOMICS_ENGLAND"
"91949"	"COG7"	"0.815"	"0.207"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91949"	"COG7"	"0.815"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"91949"	"COG7"	"0.815"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91949"	"COG7"	"0.815"	"0.207"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"91949"	"COG7"	"0.815"	"0.207"	"C2931010"	"Congenital disorder of glycosylation type 2E"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"				"0"	"1"	"CTD_human;ORPHANET"
"91949"	"COG7"	"0.815"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92002"	"CCNQ"	"0.696"	"0.345"	"C2678045"	"TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS"	"disease"	"C05;C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.54"	"1"	"2014"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"92014"	"SLC25A51"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"92086"	"GGTLC1"	"0.63"	"0.552"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"92105"	"INTS4"	"0.785"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"92105"	"INTS4"	"0.785"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"92126"	"DSEL"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"92140"	"MTDH"	"0.554"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2016"	"1"	"0"	"CTD_human"
"92140"	"MTDH"	"0.554"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human"
"92140"	"MTDH"	"0.554"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"92140"	"MTDH"	"0.554"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"92140"	"MTDH"	"0.554"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2004"	"2009"	"1"	"0"	"CTD_human"
"92211"	"CDHR1"	"0.681"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"92211"	"CDHR1"	"0.681"	"0.31"	"C3150912"	"CONE-ROD DYSTROPHY 15"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2016"	"2"	"1"	"CTD_human;UNIPROT"
"92211"	"CDHR1"	"0.681"	"0.31"	"C3552852"	"RETINITIS PIGMENTOSA 65"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2016"	"2"	"0"	"CTD_human;UNIPROT"
"92241"	"RCSD1"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"92304"	"SCGB3A1"	"0.639"	"0.448"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92304"	"SCGB3A1"	"0.639"	"0.448"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2007"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"92335"	"STRADA"	"0.701"	"0.379"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92335"	"STRADA"	"0.701"	"0.379"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92335"	"STRADA"	"0.701"	"0.379"	"C1970203"	"Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy"	"disease"	"C05;C10;C13;C16;C23;F01"	"Disease or Syndrome"	"0.60"		"2017"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"92335"	"STRADA"	"0.701"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2007"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"92344"	"GORAB"	"0.663"	"0.552"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"92344"	"GORAB"	"0.663"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2008"	"2009"	"2"	"0"	"GENOMICS_ENGLAND"
"92344"	"GORAB"	"0.663"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92344"	"GORAB"	"0.663"	"0.552"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.42"	"1"	"2001"	"2008"	"1"	"0"	"CTD_human"
"92344"	"GORAB"	"0.663"	"0.552"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"92344"	"GORAB"	"0.663"	"0.552"	"C0037268"	"Skin Abnormalities"	"group"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"92344"	"GORAB"	"0.663"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"92344"	"GORAB"	"0.663"	"0.552"	"C0432255"	"Geroderma osteodysplastica"	"disease"	"C05;C16;C17;C19"	"Disease or Syndrome"	"0.65"	"1"	"1978"	"2015"	"1"	"5"	"CTD_human;ORPHANET"
"92344"	"GORAB"	"0.663"	"0.552"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"92344"	"GORAB"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"92345"	"NAF1"	"0.773"	"0.241"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"92369"	"SPSB4"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"92421"	"CHMP4C"	"0.785"	"0.138"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92421"	"CHMP4C"	"0.785"	"0.138"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"92482"	"BBIP1"	"0.701"	"0.379"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2014"	"0"	"1"	"ORPHANET"
"92482"	"BBIP1"	"0.701"	"0.379"	"C3806174"	"BARDET-BIEDL SYNDROME 18"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human"
"92483"	"LDHAL6B"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92483"	"LDHAL6B"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92483"	"LDHAL6B"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92483"	"LDHAL6B"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"92552"	"ATXN3L"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"92579"	"G6PC3"	"0.616"	"0.655"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"92579"	"G6PC3"	"0.616"	"0.655"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"92579"	"G6PC3"	"0.616"	"0.655"	"C2675526"	"Neutropenia, Severe Congenital, Autosomal Recessive 4"	"disease"	"C15"	"Disease or Syndrome"	"0.71"	"1"	"1993"	"2015"	"11"	"15"	"CTD_human;ORPHANET;UNIPROT"
"92579"	"G6PC3"	"0.616"	"0.655"	"C2751630"	"Dursun Syndrome"	"disease"	"C08;C14;C15;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"11"	"11"	"UNIPROT"
"92579"	"G6PC3"	"0.616"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92609"	"TIMM50"	"0.799"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92609"	"TIMM50"	"0.799"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92609"	"TIMM50"	"0.799"	"0.207"	"C4540171"	"3-METHYLGLUTACONIC ACIDURIA, TYPE IX"	"disease"		"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"ORPHANET;UNIPROT"
"92667"	"MGME1"	"0.735"	"0.345"	"C0013911"	"Emaciation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0029089"	"Ophthalmoplegia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0035229"	"Respiratory Insufficiency"	"phenotype"	"C08"	"Pathologic Function"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0162292"	"External Ophthalmoplegia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0235063"	"Respiratory Depression"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0339693"	"Internal Ophthalmoplegia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0751401"	"Ophthalmoparesis"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"92667"	"MGME1"	"0.735"	"0.345"	"C0949855"	"Electron Transport Chain Deficiencies, Mitochondrial"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0949856"	"Oxidative Phosphorylation Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C0949857"	"Mitochondrial Respiratory Chain Deficiencies"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C1145670"	"Respiratory Failure"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"92667"	"MGME1"	"0.735"	"0.345"	"C3554462"	"MITOCHONDRIAL DNA DEPLETION SYNDROME 11"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"92736"	"OTOP2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"92749"	"DRC1"	"0.696"	"0.379"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.81"	"1"	"1993"	"2013"	"1"	"2"	"CTD_human;ORPHANET"
"92749"	"DRC1"	"0.696"	"0.379"	"C3809087"	"CILIARY DYSKINESIA, PRIMARY, 21"	"disease"		"Disease or Syndrome"	"0.60"		"2003"	"2013"	"0"	"2"	"CTD_human"
"92749"	"DRC1"	"0.696"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92749"	"DRC1"	"0.696"	"0.379"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"92840"	"REEP6"	"0.681"	"0.379"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"92840"	"REEP6"	"0.681"	"0.379"	"C4310626"	"RETINITIS PIGMENTOSA 77"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"92935"	"MARS2"	"0.69"	"0.379"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"92935"	"MARS2"	"0.69"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"92935"	"MARS2"	"0.69"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"92935"	"MARS2"	"0.69"	"0.379"	"C1969645"	"Ataxia, Spastic, 3, Autosomal Recessive"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.51"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human;ORPHANET"
"92935"	"MARS2"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"92935"	"MARS2"	"0.69"	"0.379"	"C4225329"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"93058"	"COQ10A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"93099"	"DMKN"	"0.815"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"93145"	"OLFM2"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"93166"	"PRDM6"	"0.752"	"0.276"	"C0013274"	"Patent ductus arteriosus"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"93166"	"PRDM6"	"0.752"	"0.276"	"C2936170"	"Patent Ductus Arteriosus Familial"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"93166"	"PRDM6"	"0.752"	"0.276"	"C4310753"	"PATENT DUCTUS ARTERIOSUS 3"	"disease"		"Congenital Abnormality"	"0.40"		"1965"	"2017"	"1"	"3"	"UNIPROT"
"93183"	"PIGM"	"0.685"	"0.138"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.41"	"1"	"2006"	"2007"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0042487"	"Venous Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0149871"	"Deep Vein Thrombosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"93183"	"PIGM"	"0.685"	"0.138"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C1853205"	"Glycosylphosphatidylinositol deficiency"	"disease"		"Disease or Syndrome"	"0.52"	"1"	"2006"	"2007"	"0"	"1"	"CTD_human;ORPHANET"
"93183"	"PIGM"	"0.685"	"0.138"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93183"	"PIGM"	"0.685"	"0.138"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93210"	"PGAP3"	"0.72"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"93210"	"PGAP3"	"0.72"	"0.483"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"93210"	"PGAP3"	"0.72"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"93210"	"PGAP3"	"0.72"	"0.483"	"C3810354"	"HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2015"	"1"	"11"	"UNIPROT"
"93233"	"CCDC114"	"0.785"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2013"	"0"	"1"	"ORPHANET"
"93233"	"CCDC114"	"0.785"	"0.138"	"C3540844"	"CILIARY DYSKINESIA, PRIMARY, 20"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"5"	"CTD_human"
"93233"	"CCDC114"	"0.785"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"93233"	"CCDC114"	"0.785"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"93233"	"CCDC114"	"0.785"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"93426"	"SYCE1"	"0.752"	"0.276"	"C4310779"	"SPERMATOGENIC FAILURE 15"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"0"	"1"	"CTD_human"
"93426"	"SYCE1"	"0.752"	"0.276"	"C4310782"	"PREMATURE OVARIAN FAILURE 12"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"0"	"1"	"CTD_human"
"93517"	"SDR42E1"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C0020459"	"Hyperinsulinism"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2015"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2016"	"5"	"0"	"GENOMICS_ENGLAND"
"93587"	"TRMT10A"	"0.752"	"0.345"	"C4014997"	"MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"4"	"2"	"CTD_human;UNIPROT"
"93589"	"CACNA2D4"	"0.743"	"0.241"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"93589"	"CACNA2D4"	"0.743"	"0.241"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"0"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"93589"	"CACNA2D4"	"0.743"	"0.241"	"C1864849"	"RETINAL CONE DYSTROPHY 4"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"93611"	"FBXO44"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"93611"	"FBXO44"	"0.886"	"0.138"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"93611"	"FBXO44"	"0.886"	"0.138"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"93611"	"FBXO44"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"93627"	"TBCK"	"0.773"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"93627"	"TBCK"	"0.773"	"0.207"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"93627"	"TBCK"	"0.773"	"0.207"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"93627"	"TBCK"	"0.773"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"93627"	"TBCK"	"0.773"	"0.207"	"C4225161"	"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"93649"	"MYOCD"	"0.659"	"0.483"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93649"	"MYOCD"	"0.659"	"0.483"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93650"	"ACP4"	"0.886"	"0.069"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"93650"	"ACP4"	"0.886"	"0.069"	"C0399367"	"Amelogenesis imperfecta local hypoplastic form"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"93650"	"ACP4"	"0.886"	"0.069"	"C4310630"	"AMELOGENESIS IMPERFECTA, TYPE IJ"	"disease"		"Congenital Abnormality"	"0.60"		"2017"	"2017"	"1"	"7"	"CTD_human;UNIPROT"
"93659"	"CGB5"	"0.648"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2014"	"1"	"0"	"CTD_human"
"93659"	"CGB5"	"0.648"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"93663"	"ARHGAP18"	"0.785"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"PSYGENET"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.56"	"1"	"2003"	"2012"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93664"	"CADPS2"	"0.72"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"93983"	"DYT13"	"0.785"	"0.207"	"C1843264"	"DYSTONIA 13, TORSION"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0003635"	"Apraxias"	"group"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2003"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9230769"	"2002"	"2015"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0023012"	"Language Delay"	"phenotype"	"C10;C23"	"Finding"	"0.40"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0023014"	"Language Development Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8"	"2005"	"2018"	"5"	"0"	"PSYGENET"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0234526"	"Ideational Apraxia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0234527"	"Apraxia, Motor"	"phenotype"	"C10;C23;F01"	"Pathologic Function"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0234529"	"Dressing Apraxia"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0241210"	"Speech Delay"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0264611"	"Apraxia of Phonation"	"disease"	"C10;C23;F01"	"Disease or Syndrome"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0349391"	"Apraxia, Verbal"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0422892"	"Apraxia, Gestural"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0454608"	"Apraxia, Oral"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0454655"	"Semantic-Pragmatic Disorder"	"disease"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0750927"	"Apraxia, Developmental Verbal"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.80"	"1"	"1990"	"2018"	"3"	"6"	"CTD_human;ORPHANET;UNIPROT"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0750928"	"Apraxia, Facial-Oral"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C0751257"	"Auditory Processing Disorder, Central"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"93986"	"FOXP2"	"0.598"	"0.517"	"C3495144"	"Apraxia, Articulatory"	"disease"	"C10;C23;F01"	"Mental or Behavioral Dysfunction"	"0.30"		"2006"	"2017"	"2"	"0"	"CTD_human"
"93986"	"FOXP2"	"0.598"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"94005"	"PIGS"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"94025"	"MUC16"	"0.58"	"0.517"	"C0033687"	"Proteinuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"94025"	"MUC16"	"0.58"	"0.517"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.8823529"	"1988"	"2016"	"1"	"0"	"CTD_human"
"94025"	"MUC16"	"0.58"	"0.517"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.40"	"0.95"	"1987"	"2018"	"1"	"0"	"CTD_human"
"94081"	"SFXN1"	"0.69"	"0.483"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94081"	"SFXN1"	"0.69"	"0.483"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94081"	"SFXN1"	"0.69"	"0.483"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94081"	"SFXN1"	"0.69"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94103"	"ORMDL3"	"0.727"	"0.276"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2007"	"2017"	"2"	"3"	"CTD_human"
"94103"	"ORMDL3"	"0.727"	"0.276"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"94121"	"SYTL4"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"94122"	"SYTL5"	"0.928"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"94137"	"RP1L1"	"0.799"	"0.103"	"C3150833"	"OCCULT MACULAR DYSTROPHY"	"disease"		"Disease or Syndrome"	"0.79"	"1"	"2010"	"2017"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"94160"	"ABCC12"	"0.928"	"0.069"	"C0005956"	"Bone Marrow Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"94160"	"ABCC12"	"0.928"	"0.069"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"94160"	"ABCC12"	"0.928"	"0.069"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"94233"	"OPN4"	"0.672"	"0.448"	"C0085159"	"Seasonal Affective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.75"	"2009"	"2013"	"4"	"0"	"PSYGENET"
"94234"	"FOXQ1"	"0.663"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"94234"	"FOXQ1"	"0.663"	"0.414"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"94234"	"FOXQ1"	"0.663"	"0.414"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94234"	"FOXQ1"	"0.663"	"0.414"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"94235"	"GNG8"	"0.886"	"0.103"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"94235"	"GNG8"	"0.886"	"0.103"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"94274"	"PPP1R14A"	"0.799"	"0.207"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"94274"	"PPP1R14A"	"0.799"	"0.207"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"94274"	"PPP1R14A"	"0.799"	"0.207"	"C0025500"	"Mesothelioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"94274"	"PPP1R14A"	"0.799"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"95681"	"CEP41"	"0.727"	"0.379"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"95681"	"CEP41"	"0.727"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"95681"	"CEP41"	"0.727"	"0.379"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"95681"	"CEP41"	"0.727"	"0.379"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"95681"	"CEP41"	"0.727"	"0.379"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"95681"	"CEP41"	"0.727"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"95681"	"CEP41"	"0.727"	"0.379"	"C4274118"	"Joubert syndrome with ocular defect"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"95681"	"CEP41"	"0.727"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"112398"	"EGLN2"	"0.624"	"0.586"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"112398"	"EGLN2"	"0.624"	"0.586"	"C0154040"	"Benign neoplasm of adrenal gland"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"112398"	"EGLN2"	"0.624"	"0.586"	"C0154045"	"Benign neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"112398"	"EGLN2"	"0.624"	"0.586"	"C0344456"	"Malignant Adrenal Medulla Neoplasm"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"112398"	"EGLN2"	"0.624"	"0.586"	"C0438413"	"Malignant neoplasm of aortic body and other paraganglia"	"disease"		"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"112398"	"EGLN2"	"0.624"	"0.586"	"C1861063"	"TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"112399"	"EGLN3"	"0.596"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"112399"	"EGLN3"	"0.596"	"0.552"	"C0152264"	"Familial erythrocytosis"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"112399"	"EGLN3"	"0.596"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0220669"	"Familial benign neonatal epilepsy"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.38"	"0.875"	"2012"	"2015"	"0"	"0"	"ORPHANET"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0270862"	"Hemiplegic migraine"	"disease"		"Disease or Syndrome"	"0.39"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112476"	"PRRT2"	"0.491"	"0.793"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"112476"	"PRRT2"	"0.491"	"0.793"	"C1842534"	"DYSTONIA 18 (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2000"	"2000"	"0"	"0"	"ORPHANET"
"112476"	"PRRT2"	"0.491"	"0.793"	"C1853995"	"SEIZURES, BENIGN FAMILIAL INFANTILE, 2"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"1993"	"2016"	"3"	"7"	"UNIPROT"
"112476"	"PRRT2"	"0.491"	"0.793"	"C1865926"	"Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.70"	"0.9333333"	"1993"	"2017"	"2"	"9"	"ORPHANET;UNIPROT"
"112476"	"PRRT2"	"0.491"	"0.793"	"C1868682"	"Paroxysmal kinesigenic choreoathetosis"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.80"	"0.9636364"	"1993"	"2018"	"6"	"14"	"CTD_human;ORPHANET;UNIPROT"
"112476"	"PRRT2"	"0.491"	"0.793"	"C1869117"	"Paroxysmal nonkinesigenic dyskinesia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"112476"	"PRRT2"	"0.491"	"0.793"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.55"	"1"	"2012"	"2016"	"4"	"0"	"CTD_human;GENOMICS_ENGLAND"
"112479"	"ERI2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"112574"	"SNX18"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112574"	"SNX18"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112574"	"SNX18"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112574"	"SNX18"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112574"	"SNX18"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112574"	"SNX18"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"112609"	"MRAP2"	"0.834"	"0.241"	"C3714940"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18"	"phenotype"		"Finding"	"0.40"		"2013"	"2013"	"0"	"1"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112724"	"RDH13"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"112744"	"IL17F"	"0.546"	"0.724"	"C0006845"	"Candidiasis, Chronic Mucocutaneous"	"disease"	"C01;C17"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2013"	"0"	"0"	"ORPHANET"
"112744"	"IL17F"	"0.546"	"0.724"	"C3151405"	"CANDIDIASIS, FAMILIAL, 6"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"CTD_human;UNIPROT"
"112752"	"IFT43"	"0.672"	"0.345"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112752"	"IFT43"	"0.672"	"0.345"	"C0432235"	"Cranioectodermal Dysplasia"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human;ORPHANET"
"112752"	"IFT43"	"0.672"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112752"	"IFT43"	"0.672"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112755"	"STX1B"	"0.713"	"0.103"	"C0009952"	"Febrile Convulsions"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.43"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0149886"	"Seizure, Febrile, Simple"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"112755"	"STX1B"	"0.713"	"0.103"	"C0751057"	"Seizure, Febrile, Complex"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112755"	"STX1B"	"0.713"	"0.103"	"C3502809"	"Generalized Epilepsy with Febrile Seizures Plus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"112755"	"STX1B"	"0.713"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"112755"	"STX1B"	"0.713"	"0.103"	"C4015395"	"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9"	"disease"		"Disease or Syndrome"	"0.60"		"2001"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"112802"	"KRT71"	"0.799"	"0.103"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.42"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C0343073"	"Wooly hair"	"phenotype"		"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"112802"	"KRT71"	"0.799"	"0.103"	"C0345427"	"Woolly hair, congenital"	"disease"	"C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"112802"	"KRT71"	"0.799"	"0.103"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"112802"	"KRT71"	"0.799"	"0.103"	"C4014616"	"HYPOTRICHOSIS 13"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"1"	"UNIPROT"
"112812"	"FDX2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112817"	"HOGA1"	"0.815"	"0.172"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"112817"	"HOGA1"	"0.815"	"0.172"	"C0282528"	"Peroxisomal Disorders"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112817"	"HOGA1"	"0.815"	"0.172"	"C3150878"	"Primary hyperoxaluria type III"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"1993"	"2017"	"1"	"30"	"CTD_human;ORPHANET;UNIPROT"
"112849"	"L3HYPDH"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112858"	"TP53RK"	"0.743"	"0.31"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"112858"	"TP53RK"	"0.743"	"0.31"	"C0795949"	"Galloway Mowat syndrome"	"disease"	"C05;C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.50"		"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"112858"	"TP53RK"	"0.743"	"0.31"	"C4540270"	"GALLOWAY-MOWAT SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"112869"	"SGF29"	"0.773"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112869"	"SGF29"	"0.773"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112869"	"SGF29"	"0.773"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112869"	"SGF29"	"0.773"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112869"	"SGF29"	"0.773"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112869"	"SGF29"	"0.773"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"112939"	"NACC1"	"0.663"	"0.414"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"112939"	"NACC1"	"0.663"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"112939"	"NACC1"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"112939"	"NACC1"	"0.663"	"0.414"	"C4479333"	"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"113179"	"ADAT3"	"0.815"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"113179"	"ADAT3"	"0.815"	"0.31"	"C3809039"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36"	"disease"		"Disease or Syndrome"	"0.70"		"2014"	"2017"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"113189"	"CHST14"	"0.659"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"113189"	"CHST14"	"0.659"	"0.552"	"C0009081"	"Congenital clubfoot"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"1997"	"2017"	"18"	"0"	"GENOMICS_ENGLAND"
"113189"	"CHST14"	"0.659"	"0.552"	"C0022410"	"Joint Instability"	"phenotype"	"C05"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113189"	"CHST14"	"0.659"	"0.552"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0086437"	"Joint laxity"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"113189"	"CHST14"	"0.659"	"0.552"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113189"	"CHST14"	"0.659"	"0.552"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0431886"	"Thumb in palm deformity"	"disease"	"C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C1866294"	"EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.74"	"1"	"1997"	"2016"	"3"	"10"	"CTD_human;ORPHANET;UNIPROT"
"113189"	"CHST14"	"0.659"	"0.552"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"113189"	"CHST14"	"0.659"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113201"	"CASC4"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0024523"	"Malabsorption Syndrome"	"group"	"C06;C18"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2008"	"2"	"0"	"CTD_human"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0030312"	"Pancytopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0342705"	"Folate Malabsorption, Hereditary"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.80"	"1"	"1985"	"2018"	"5"	"15"	"CTD_human;ORPHANET;UNIPROT"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C0598608"	"Hyperhomocysteinemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"113235"	"SLC46A1"	"0.624"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2001"	"2011"	"6"	"0"	"GENOMICS_ENGLAND"
"113246"	"C12orf57"	"0.639"	"0.483"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"113246"	"C12orf57"	"0.639"	"0.483"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"113246"	"C12orf57"	"0.639"	"0.483"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"113246"	"C12orf57"	"0.639"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113246"	"C12orf57"	"0.639"	"0.483"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"113246"	"C12orf57"	"0.639"	"0.483"	"C1857512"	"Temtamy syndrome"	"disease"	"C05;C10;C11;C16;C23"	"Disease or Syndrome"	"0.70"		"2012"	"2017"	"3"	"4"	"CTD_human;ORPHANET;UNIPROT"
"113246"	"C12orf57"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"113251"	"LARP4"	"0.857"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113251"	"LARP4"	"0.857"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113277"	"TMEM106A"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0015708"	"Fazio-Londe Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0030442"	"Progressive bulbar palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.38"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0393540"	"Childhood Progressive Bulbar Palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C0796274"	"Brown-Vialetto-Van Laere syndrome"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.69"	"0.8888889"	"2010"	"2017"	"8"	"15"	"CTD_human;ORPHANET;UNIPROT"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2011"	"4"	"0"	"GENOMICS_ENGLAND"
"113278"	"SLC52A3"	"0.656"	"0.448"	"C4082299"	"Bulbar palsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"113510"	"HELQ"	"0.752"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"113612"	"CYP2U1"	"0.799"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113612"	"CYP2U1"	"0.799"	"0.241"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"113612"	"CYP2U1"	"0.799"	"0.241"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.32"	"1"	"2017"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"113612"	"CYP2U1"	"0.799"	"0.241"	"C3539507"	"SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"113612"	"CYP2U1"	"0.799"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"113828"	"FAM83F"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"113878"	"DTX2"	"0.834"	"0.069"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"113878"	"DTX2"	"0.834"	"0.069"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"114034"	"TOE1"	"0.701"	"0.414"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"114034"	"TOE1"	"0.701"	"0.414"	"C0266468"	"Congenital pontocerebellar hypoplasia"	"disease"	"C10"	"Congenital Abnormality"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"114034"	"TOE1"	"0.701"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"114034"	"TOE1"	"0.701"	"0.414"	"C3554226"	"Congenital pontocerebellar hypoplasia type 7"	"disease"		"Disease or Syndrome"	"0.70"		"2017"	"2017"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"114034"	"TOE1"	"0.701"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"114131"	"UCN3"	"0.659"	"0.586"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114131"	"UCN3"	"0.659"	"0.586"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114131"	"UCN3"	"0.659"	"0.586"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"114131"	"UCN3"	"0.659"	"0.586"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114134"	"SLC2A13"	"0.785"	"0.207"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114294"	"LACTB"	"1"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"114294"	"LACTB"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0001890"	"Akinetic Petit Mal"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0014553"	"Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.43"	"0.6666667"	"1994"	"2009"	"0"	"2"	"CTD_human"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0270853"	"Juvenile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.90"	"0.9210526"	"1993"	"2018"	"6"	"18"	"CTD_human;ORPHANET;UNIPROT"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0393676"	"Panayiotopoulos Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"114327"	"EFHC1"	"0.701"	"0.207"	"C0751124"	"Epilepsy, Absence, Atypical"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114327"	"EFHC1"	"0.701"	"0.207"	"C1850778"	"MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.40"		"2004"	"2018"	"6"	"18"	"UNIPROT"
"114327"	"EFHC1"	"0.701"	"0.207"	"C2750892"	"EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"ORPHANET"
"114327"	"EFHC1"	"0.701"	"0.207"	"C4281785"	"Childhood Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114327"	"EFHC1"	"0.701"	"0.207"	"C4317339"	"Juvenile Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0002792"	"anaphylaxis"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0003949"	"Asbestosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.8571429"	"2004"	"2015"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0013182"	"Drug Allergy"	"phenotype"	"C20;C25"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0016470"	"Food Allergy"	"group"	"C20"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.31"		"2002"	"2012"	"2"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0026769"	"Multiple Sclerosis"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0268390"	"Muckle-Wells Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"2000"	"2016"	"8"	"8"	"CTD_human;ORPHANET;UNIPROT"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0343068"	"Familial cold urticaria"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"1"	"1971"	"2016"	"10"	"18"	"CTD_human;ORPHANET;UNIPROT"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0409818"	"Chronic Infantile Neurological, Cutaneous, and Articular Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"1.00"	"0.9285714"	"2002"	"2016"	"9"	"18"	"CTD_human;ORPHANET;UNIPROT"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0751324"	"Multiple Sclerosis, Acute Fulminating"	"disease"	"C10;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C2316212"	"Cryopyrin-Associated Periodic Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"	"0.96875"	"2002"	"2018"	"3"	"2"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C2930617"	"Pulmonary Fibrosis - from Asbestos Exposure"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"114548"	"NLRP3"	"0.435"	"0.862"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"114548"	"NLRP3"	"0.435"	"0.862"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2007"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"114571"	"SLC22A9"	"0.886"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"114571"	"SLC22A9"	"0.886"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0004610"	"Bacteremia"	"disease"	"C01;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2009"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0032269"	"Pneumococcal Infections"	"group"	"C01"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0041296"	"Tuberculosis"	"disease"	"C01"	"Disease or Syndrome"	"0.35"	"0.75"	"2007"	"2016"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C1835828"	"Invasive Pneumococcal Disease, Recurrent Isolated, 1"	"disease"	"C01;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114609"	"TIRAP"	"0.652"	"0.586"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"114757"	"CYGB"	"0.639"	"0.448"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114757"	"CYGB"	"0.639"	"0.448"	"C0751870"	"Heredodegenerative Disorders, Nervous System"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"114781"	"BTBD9"	"0.743"	"0.345"	"C0035258"	"Restless Legs Syndrome"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.70"	"0.9444444"	"2007"	"2017"	"1"	"8"	"CTD_human"
"114781"	"BTBD9"	"0.743"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"114784"	"CSMD2"	"0.785"	"0.138"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"114784"	"CSMD2"	"0.785"	"0.138"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"114784"	"CSMD2"	"0.785"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"114786"	"XKR4"	"0.834"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114786"	"XKR4"	"0.834"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2013"	"2"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114788"	"CSMD3"	"0.713"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2014"	"1"	"2"	"UNIPROT"
"114788"	"CSMD3"	"0.713"	"0.276"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"114795"	"TMEM132B"	"0.857"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"114798"	"SLITRK1"	"0.799"	"0.207"	"C0040517"	"Gilles de la Tourette syndrome"	"disease"	"C10;C16;F03"	"Disease or Syndrome"	"0.70"	"0.8333333"	"2005"	"2016"	"0"	"2"	"CTD_human"
"114798"	"SLITRK1"	"0.799"	"0.207"	"C0040953"	"Trichotillomania"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2005"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"114805"	"GALNT13"	"0.928"	"0.103"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"114814"	"GNRHR2"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"114814"	"GNRHR2"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"114815"	"SORCS1"	"0.785"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"114822"	"RHPN1"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"114822"	"RHPN1"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C0025149"	"Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C0205833"	"Medullomyoblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C0278510"	"Childhood Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C0278876"	"Adult Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C0751291"	"Desmoplastic Medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114826"	"SMYD4"	"0.785"	"0.069"	"C1275668"	"Melanotic medulloblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"114879"	"OSBPL5"	"0.857"	"0.172"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"114882"	"OSBPL8"	"0.886"	"0.103"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"114885"	"OSBPL11"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"114899"	"C1QTNF3"	"0.857"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"114902"	"C1QTNF5"	"0.752"	"0.172"	"C0023308"	"Lens Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"114902"	"C1QTNF5"	"0.752"	"0.172"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.36"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"114902"	"C1QTNF5"	"0.752"	"0.172"	"C1854065"	"LATE-ONSET RETINAL DEGENERATION (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.97"	"1"	"2004"	"2016"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"114904"	"C1QTNF6"	"0.743"	"0.276"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2015"	"1"	"3"	"CTD_human"
"114904"	"C1QTNF6"	"0.743"	"0.276"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"114904"	"C1QTNF6"	"0.743"	"0.276"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"114904"	"C1QTNF6"	"0.743"	"0.276"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"114907"	"FBXO32"	"0.69"	"0.448"	"C0026846"	"Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.54"		"2001"	"2011"	"1"	"0"	"CTD_human"
"114907"	"FBXO32"	"0.69"	"0.448"	"C0270948"	"Neurogenic Muscular Atrophy"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"114990"	"VASN"	"0.834"	"0.103"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"115019"	"SLC26A9"	"0.762"	"0.207"	"C0021843"	"Intestinal Obstruction"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"115019"	"SLC26A9"	"0.762"	"0.207"	"C1859047"	"CYSTIC FIBROSIS MODIFIER 1"	"disease"		"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"115019"	"SLC26A9"	"0.762"	"0.207"	"C3276246"	"MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"115019"	"SLC26A9"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"115111"	"SLC26A7"	"0.834"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"115207"	"KCTD12"	"0.928"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"115207"	"KCTD12"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"115207"	"KCTD12"	"0.928"	"0.034"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"115209"	"OMA1"	"0.815"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"115265"	"DDIT4L"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"115286"	"SLC25A26"	"0.762"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"115286"	"SLC25A26"	"0.762"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"115286"	"SLC25A26"	"0.762"	"0.207"	"C4225206"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"115352"	"FCRL3"	"0.642"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"115352"	"FCRL3"	"0.642"	"0.552"	"C0018213"	"Graves Disease"	"disease"	"C11;C19;C20"	"Disease or Syndrome"	"0.47"	"1"	"2006"	"2016"	"1"	"2"	"CTD_human"
"115352"	"FCRL3"	"0.642"	"0.552"	"C0920350"	"Autoimmune thyroiditis"	"disease"	"C19;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"115361"	"GBP4"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"115426"	"UHRF2"	"0.773"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2012"	"1"	"1"	"UNIPROT"
"115548"	"FCHO2"	"1"	"0.034"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C0009447"	"Common Variable Immunodeficiency"	"disease"	"C20"	"Disease or Syndrome"	"0.60"	"1"	"2006"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C2936664"	"Acquired Hypogammaglobulinemia"	"disease"	"C20"	"Disease or Syndrome"	"0.33"	"1"	"2006"	"2015"	"0"	"0"	"CTD_human"
"115650"	"TNFRSF13C"	"0.575"	"0.724"	"C2936665"	"Immunoglobulin Deficiency, Late-Onset"	"disease"	"C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"115701"	"ALPK2"	"0.762"	"0.207"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"115701"	"ALPK2"	"0.762"	"0.207"	"C0346167"	"Undifferentiated carcinoma of ovary"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"115761"	"ARL11"	"0.672"	"0.345"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2007"	"0"	"0"	"ORPHANET"
"115761"	"ARL11"	"0.672"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"115761"	"ARL11"	"0.672"	"0.345"	"C0855095"	"Small Lymphocytic Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"115761"	"ARL11"	"0.672"	"0.345"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"115761"	"ARL11"	"0.672"	"0.345"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"115761"	"ARL11"	"0.672"	"0.345"	"C1868683"	"B-CELL MALIGNANCY, LOW-GRADE"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"115908"	"CTHRC1"	"0.642"	"0.448"	"C0004763"	"Barrett Esophagus"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"115908"	"CTHRC1"	"0.642"	"0.448"	"C1258085"	"Barrett Epithelium"	"disease"	"C04;C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"115948"	"CCDC151"	"0.735"	"0.276"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2015"	"0"	"2"	"ORPHANET"
"115948"	"CCDC151"	"0.735"	"0.276"	"C4015016"	"CILIARY DYSKINESIA, PRIMARY, 30"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"0"	"2"	"CTD_human"
"115948"	"CCDC151"	"0.735"	"0.276"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"115948"	"CCDC151"	"0.735"	"0.276"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"116039"	"OSR2"	"0.799"	"0.345"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116039"	"OSR2"	"0.799"	"0.345"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116068"	"LYSMD3"	"0.834"	"0.069"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116068"	"LYSMD3"	"0.834"	"0.069"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116068"	"LYSMD3"	"0.834"	"0.069"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116068"	"LYSMD3"	"0.834"	"0.069"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116071"	"BATF2"	"0.773"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"116085"	"SLC22A12"	"0.701"	"0.379"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.41"	"1"	"2004"	"2004"	"1"	"0"	"CTD_human"
"116085"	"SLC22A12"	"0.701"	"0.379"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"116085"	"SLC22A12"	"0.701"	"0.379"	"C0473219"	"Renal hypouricemia"	"disease"	"C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.80"	"0.9047619"	"2002"	"2017"	"8"	"11"	"CTD_human;ORPHANET;UNIPROT"
"116085"	"SLC22A12"	"0.701"	"0.379"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"116085"	"SLC22A12"	"0.701"	"0.379"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.40"		"2004"	"2004"	"1"	"0"	"CTD_human"
"116113"	"FOXP4"	"0.773"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"116113"	"FOXP4"	"0.773"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116113"	"FOXP4"	"0.773"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"116115"	"ZNF526"	"0.857"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"116115"	"ZNF526"	"0.857"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"116115"	"ZNF526"	"0.857"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"116115"	"ZNF526"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2016"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116135"	"LRRC3B"	"0.834"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"116150"	"NUS1"	"0.713"	"0.379"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"116150"	"NUS1"	"0.713"	"0.379"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"116150"	"NUS1"	"0.713"	"0.379"	"C4310727"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"116228"	"COX20"	"0.72"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"116228"	"COX20"	"0.72"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.71"	"1"	"2013"	"2018"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"116228"	"COX20"	"0.72"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"116285"	"ACSM1"	"0.815"	"0.172"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"116285"	"ACSM1"	"0.815"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2015"	"2"	"0"	"PSYGENET"
"116285"	"ACSM1"	"0.815"	"0.172"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"116285"	"ACSM1"	"0.815"	"0.172"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"116285"	"ACSM1"	"0.815"	"0.172"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"116328"	"C8orf34"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"116369"	"SLC26A8"	"0.743"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116369"	"SLC26A8"	"0.743"	"0.241"	"C1847540"	"Azoospermia, Nonobstructive"	"disease"	"C12"	"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.33"	"1"	"1989"	"2017"	"6"	"0"	"GENOMICS_ENGLAND"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0796195"	"Waisman syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1985"	"2017"	"7"	"2"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"116442"	"RAB39B"	"0.676"	"0.276"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"116442"	"RAB39B"	"0.676"	"0.276"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"116442"	"RAB39B"	"0.676"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.64"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"116443"	"GRIN3A"	"0.762"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"116443"	"GRIN3A"	"0.762"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2016"	"3"	"0"	"PSYGENET"
"116443"	"GRIN3A"	"0.762"	"0.276"	"C0242350"	"Erectile dysfunction"	"disease"	"C12;F03"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116449"	"CLNK"	"0.857"	"0.103"	"C0042900"	"Vitiligo"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"1"	"CTD_human"
"116461"	"TSEN15"	"0.815"	"0.207"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"116461"	"TSEN15"	"0.815"	"0.207"	"C2932714"	"Pontocerebellar Hypoplasia Type 2"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"116461"	"TSEN15"	"0.815"	"0.207"	"C4310757"	"PONTOCEREBELLAR HYPOPLASIA, TYPE 2F"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"2"	"3"	"CTD_human;UNIPROT"
"116496"	"FAM129A"	"0.785"	"0.207"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9130435"	"2001"	"2018"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C0020479"	"Hyperlipoproteinemia Type III"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.33"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C0020480"	"Hyperlipoproteinemia Type IV"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C0020481"	"Hyperlipoproteinemia Type V"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2005"	"2005"	"0"	"1"	"CTD_human;ORPHANET"
"116519"	"APOA5"	"0.609"	"0.483"	"C0020557"	"Hypertriglyceridemia"	"phenotype"	"C18"	"Disease or Syndrome"	"0.40"	"0.9545455"	"2003"	"2016"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.9411765"	"2001"	"2018"	"1"	"2"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C2362324"	"Pediatric Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C3489395"	"Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C4317171"	"Adolescent Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"116519"	"APOA5"	"0.609"	"0.483"	"C4521075"	"Childhood Overweight"	"phenotype"	"C18;C23"	"Sign or Symptom"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"116833"	"ANIB1"	"0.648"	"0.31"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"116840"	"CNTROB"	"0.857"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116840"	"CNTROB"	"0.857"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"116844"	"LRG1"	"0.696"	"0.31"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"116844"	"LRG1"	"0.696"	"0.31"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"116844"	"LRG1"	"0.696"	"0.31"	"C0032580"	"Adenomatous Polyposis Coli"	"disease"	"C04;C06;C16"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"116844"	"LRG1"	"0.696"	"0.31"	"C2713442"	"Polyposis, Adenomatous Intestinal"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"116844"	"LRG1"	"0.696"	"0.31"	"C2713443"	"Familial Intestinal Polyposis"	"disease"	"C04;C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"116966"	"WDR17"	"0.886"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116966"	"WDR17"	"0.886"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"116986"	"AGAP2"	"0.762"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"116987"	"AGAP1"	"0.886"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"117144"	"CATSPER1"	"0.857"	"0.034"	"C2751811"	"Spermatogenic Failure 7"	"disease"	"C12"	"Disease or Syndrome"	"0.40"		"1993"	"2009"	"0"	"2"	"CTD_human"
"117145"	"THEM4"	"0.727"	"0.241"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"117155"	"CATSPER2"	"0.785"	"0.138"	"C1970187"	"Deafness, Sensorineural, And Male Infertility"	"disease"	"C09;C10;C12;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"117155"	"CATSPER2"	"0.785"	"0.138"	"C2751811"	"Spermatogenic Failure 7"	"disease"	"C12"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"117156"	"SCGB3A2"	"0.713"	"0.414"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.8181818"	"2002"	"2018"	"0"	"0"	"CTD_human"
"117156"	"SCGB3A2"	"0.713"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"117159"	"DCD"	"0.701"	"0.414"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2010"	"1"	"0"	"CTD_human"
"117159"	"DCD"	"0.701"	"0.414"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2010"	"2013"	"2"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"117289"	"TAGAP"	"0.727"	"0.31"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"117531"	"TMC1"	"0.735"	"0.345"	"C1832978"	"Deafness, Autosomal Recessive 7"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.90"		"1980"	"2015"	"6"	"9"	"CLINGEN;CTD_human;UNIPROT"
"117531"	"TMC1"	"0.735"	"0.345"	"C1847626"	"Deafness, Autosomal Dominant 36"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.81"	"1"	"1980"	"2016"	"1"	"3"	"CTD_human;UNIPROT"
"117579"	"RLN3"	"0.928"	"0.069"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"117579"	"RLN3"	"0.928"	"0.069"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"117581"	"TWIST2"	"0.57"	"0.586"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"117581"	"TWIST2"	"0.57"	"0.586"	"C1319466"	"Barber Say syndrome"	"disease"	"C05;C07;C11;C16;C17;C23"	"Disease or Syndrome"	"0.71"	"1"	"1991"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"117581"	"TWIST2"	"0.57"	"0.586"	"C1744559"	"Congenital ectodermal dysplasia of face"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.75"	"1"	"1963"	"2016"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"117581"	"TWIST2"	"0.57"	"0.586"	"C1860224"	"ABLEPHARON-MACROSTOMIA SYNDROME"	"disease"	"C07;C11;C16"	"Disease or Syndrome"	"0.71"	"1"	"1991"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"117581"	"TWIST2"	"0.57"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"117583"	"PARD3B"	"0.857"	"0.103"	"C1535926"	"Neurodevelopmental Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"1993"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0009917"	"Contracture"	"group"	"C05"	"Anatomical Abnormality"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0016045"	"fibroma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0016048"	"Fibromatosis"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0017567"	"Gingival Hypertrophy"	"disease"	"C07"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"2"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.49"	"0.8888889"	"2010"	"2017"	"2"	"3"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0205766"	"Myxofibroma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"2"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0221204"	"Lytic lesion"	"phenotype"	"C05"	"Pathologic Function"	"0.40"		"2003"	"2003"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"118429"	"ANTXR2"	"0.609"	"0.621"	"C2745948"	"Hyalinosis, Systemic"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.80"	"1"	"2003"	"2017"	"3"	"12"	"CTD_human;ORPHANET;UNIPROT"
"118490"	"MSS51"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"118813"	"ZFYVE27"	"0.834"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"118813"	"ZFYVE27"	"0.834"	"0.138"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"118813"	"ZFYVE27"	"0.834"	"0.138"	"C1853251"	"Spastic Paraplegia 33, Autosomal Dominant"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2006"	"2014"	"4"	"1"	"CTD_human;UNIPROT"
"118856"	"MMP21"	"0.636"	"0.31"	"C0002991"	"Cutaneous Fibrous Histiocytoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"118856"	"MMP21"	"0.636"	"0.31"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C0175707"	"Asplenia Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C0206644"	"Histiocytoma, Benign Fibrous"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C0265357"	"Polysplenia Syndrome"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.62"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"118856"	"MMP21"	"0.636"	"0.31"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"118856"	"MMP21"	"0.636"	"0.31"	"C3178805"	"Heterotaxy Syndrome"	"disease"	"C14;C15;C16"	"Disease or Syndrome"	"0.40"		"2013"	"2016"	"1"	"1"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C3178806"	"Right Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C3178807"	"Left Atrial Isomerism"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"118856"	"MMP21"	"0.636"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"118856"	"MMP21"	"0.636"	"0.31"	"C4225217"	"HETEROTAXY, VISCERAL, 7, AUTOSOMAL"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"3"	"7"	"CTD_human;UNIPROT"
"119391"	"GSTO2"	"0.685"	"0.517"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"119391"	"GSTO2"	"0.685"	"0.517"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"119559"	"SFXN4"	"0.785"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"119559"	"SFXN4"	"0.785"	"0.276"	"C3810001"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"3"	"CTD_human;ORPHANET"
"119749"	"OR4C46"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"120114"	"FAT3"	"0.886"	"0.138"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C0268689"	"Vitamin D-dependent rickets, type 1"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"120227"	"CYP2R1"	"0.607"	"0.586"	"C1838657"	"Vitamin D Hydroxylation-Deficient Rickets, Type 1B"	"disease"	"C05;C12;C13;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"1994"	"2018"	"2"	"1"	"CTD_human;UNIPROT"
"120237"	"DBX1"	"0.928"	"0.069"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"120237"	"DBX1"	"0.928"	"0.069"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"120526"	"DNAJC24"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"120534"	"ARL14EP"	"0.886"	"0.138"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120534"	"ARL14EP"	"0.886"	"0.138"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120534"	"ARL14EP"	"0.886"	"0.138"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120534"	"ARL14EP"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0027746"	"Nerve Degeneration"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.70"	"0.9664122"	"2002"	"2018"	"16"	"4"	"CTD_human;GENOMICS_ENGLAND"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0242422"	"Parkinsonian Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.40"	"0.9367089"	"2004"	"2017"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0242423"	"Ramsay Hunt Paralysis Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752097"	"Autosomal Dominant Juvenile Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752098"	"Autosomal Dominant Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2004"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752100"	"Autosomal Recessive Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752101"	"Parkinsonism, Experimental"	"disease"	"C10"	"Experimental Model of Disease"	"0.30"		"2013"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752104"	"Familial Juvenile Parkinsonism"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C0752105"	"Parkinsonism, Juvenile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1846862"	"PARKINSON DISEASE 8 (disorder)"	"disease"		"Disease or Syndrome"	"0.83"	"1"	"1993"	"2017"	"33"	"29"	"CTD_human;UNIPROT"
"120892"	"LRRK2"	"0.545"	"0.69"	"C1868675"	"PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2009"	"2016"	"3"	"0"	"CTD_human"
"120892"	"LRRK2"	"0.545"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"120892"	"LRRK2"	"0.545"	"0.69"	"C4274355"	"Autosomal dominant late onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.35"	"1"	"2005"	"2015"	"0"	"0"	"ORPHANET"
"120892"	"LRRK2"	"0.545"	"0.69"	"C4275179"	"Young onset Parkinson disease"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2005"	"2013"	"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121214"	"SDR9C7"	"0.752"	"0.207"	"C4539772"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13"	"disease"		"Congenital Abnormality"	"0.40"		"2016"	"2016"	"1"	"3"	"UNIPROT"
"121256"	"TMEM132D"	"0.659"	"0.448"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"1997"	"2009"	"1"	"0"	"CTD_human"
"121256"	"TMEM132D"	"0.659"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121256"	"TMEM132D"	"0.659"	"0.448"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"121256"	"TMEM132D"	"0.659"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121256"	"TMEM132D"	"0.659"	"0.448"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121260"	"SLC15A4"	"0.928"	"0.069"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.43"	"1"	"2009"	"2016"	"1"	"4"	"CTD_human"
"121260"	"SLC15A4"	"0.928"	"0.069"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2009"	"2016"	"1"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2016"	"5"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2005"	"2016"	"5"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0011573"	"Endogenous depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2008"	"2013"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"1"	"2005"	"2016"	"6"	"0"	"CTD_human;PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0025193"	"Melancholia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2006"	"2015"	"2"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.5"	"2005"	"2015"	"2"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0036349"	"Paranoid Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0041671"	"Attention Deficit Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.80"	"0.8"	"2005"	"2018"	"6"	"0"	"CTD_human;PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0085762"	"Alcohol abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0086133"	"Depressive Syndrome"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0282126"	"Depression, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"0.8"	"2005"	"2016"	"5"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2006"	"2015"	"2"	"0"	"PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C1263846"	"Attention deficit hyperactivity disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9230769"	"2005"	"2016"	"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.60"	"0.8"	"2005"	"2018"	"5"	"0"	"CTD_human;PSYGENET"
"121278"	"TPH2"	"0.562"	"0.552"	"C1321905"	"Minimal Brain Dysfunction"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"121278"	"TPH2"	"0.562"	"0.552"	"C2751802"	"ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7"	"phenotype"		"Finding"	"0.40"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"121278"	"TPH2"	"0.562"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"121340"	"SP7"	"0.727"	"0.276"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"121340"	"SP7"	"0.727"	"0.276"	"C0268363"	"Osteogenesis imperfecta type IV (disorder)"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121340"	"SP7"	"0.727"	"0.276"	"C3151433"	"OSTEOGENESIS IMPERFECTA, TYPE XII"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"121391"	"KRT74"	"0.752"	"0.103"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.42"	"1"	"2011"	"2014"	"0"	"0"	"CTD_human"
"121391"	"KRT74"	"0.752"	"0.103"	"C0343073"	"Wooly hair"	"phenotype"		"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"121391"	"KRT74"	"0.752"	"0.103"	"C0345427"	"Woolly hair, congenital"	"disease"	"C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"121391"	"KRT74"	"0.752"	"0.103"	"C1840299"	"Hypotrichosis Simplex of Scalp"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121391"	"KRT74"	"0.752"	"0.103"	"C1860238"	"WOOLLY HAIR, AUTOSOMAL DOMINANT"	"disease"		"Finding"	"0.60"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"121391"	"KRT74"	"0.752"	"0.103"	"C1865951"	"Ectodermal Dysplasia, Pure Hair-Nail Type"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"121391"	"KRT74"	"0.752"	"0.103"	"C3151432"	"HYPOTRICHOSIS 3"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"121391"	"KRT74"	"0.752"	"0.103"	"C3554117"	"ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"121512"	"FGD4"	"0.735"	"0.276"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2007"	"2012"	"0"	"0"	"GENOMICS_ENGLAND"
"121512"	"FGD4"	"0.735"	"0.276"	"C1836336"	"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.95"	"1"	"1993"	"2018"	"2"	"7"	"CTD_human;ORPHANET;UNIPROT"
"121512"	"FGD4"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"121551"	"BTBD11"	"0.886"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121551"	"BTBD11"	"0.886"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"121601"	"ANO4"	"0.785"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"122011"	"CSNK1A1L"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"122042"	"RXFP2"	"0.72"	"0.31"	"C0010417"	"Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.80"	"0.8823529"	"2003"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"122042"	"RXFP2"	"0.72"	"0.31"	"C0431663"	"Bilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.32"	"1"	"2004"	"2011"	"0"	"0"	"CTD_human"
"122042"	"RXFP2"	"0.72"	"0.31"	"C0431664"	"Unilateral Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"122042"	"RXFP2"	"0.72"	"0.31"	"C1563730"	"Abdominal Cryptorchidism"	"disease"	"C12;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"122042"	"RXFP2"	"0.72"	"0.31"	"C1563731"	"Inguinal Cryptorchidism"	"phenotype"	"C12;C16;C19"	"Finding"	"0.30"				"0"	"0"	"CTD_human"
"122258"	"SPACA7"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"122416"	"ANKRD9"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"122416"	"ANKRD9"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"122416"	"ANKRD9"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"122525"	"C14orf28"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"122553"	"TRAPPC6B"	"0.928"	"0.103"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"122553"	"TRAPPC6B"	"0.928"	"0.103"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"122553"	"TRAPPC6B"	"0.928"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2018"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"122618"	"PLD4"	"0.886"	"0.138"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2012"	"2014"	"1"	"2"	"CTD_human"
"122618"	"PLD4"	"0.886"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"122622"	"ADSSL1"	"0.762"	"0.276"	"C4310754"	"MYOPATHY, DISTAL, 5"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"122809"	"SOCS4"	"0.815"	"0.241"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"122809"	"SOCS4"	"0.815"	"0.241"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"122953"	"JDP2"	"0.785"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"122953"	"JDP2"	"0.785"	"0.172"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"122961"	"ISCA2"	"0.834"	"0.172"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"		"2018"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"122961"	"ISCA2"	"0.834"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"122961"	"ISCA2"	"0.834"	"0.172"	"C3502075"	"Multiple Mitochondrial Dysfunctions Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.40"		"2015"	"2016"	"0"	"1"	"CTD_human"
"122961"	"ISCA2"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"122961"	"ISCA2"	"0.834"	"0.172"	"C4225348"	"MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2018"	"1"	"2"	"ORPHANET;UNIPROT"
"123016"	"TTC8"	"0.642"	"0.414"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"123016"	"TTC8"	"0.642"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"123016"	"TTC8"	"0.642"	"0.414"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.64"	"1"	"2003"	"2017"	"0"	"1"	"ORPHANET"
"123016"	"TTC8"	"0.642"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"123016"	"TTC8"	"0.642"	"0.414"	"C1859566"	"BARDET-BIEDL SYNDROME 8"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2003"	"2011"	"0"	"3"	"CTD_human"
"123016"	"TTC8"	"0.642"	"0.414"	"C3150715"	"RETINITIS PIGMENTOSA 51"	"disease"		"Disease or Syndrome"	"0.40"		"2010"	"2016"	"0"	"2"	"CTD_human"
"123016"	"TTC8"	"0.642"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"123016"	"TTC8"	"0.642"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"123041"	"SLC24A4"	"0.773"	"0.276"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.41"	"1"	"2013"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"123041"	"SLC24A4"	"0.773"	"0.276"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"123041"	"SLC24A4"	"0.773"	"0.276"	"C0399376"	"Amelogenesis Imperfecta, Type III"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"123041"	"SLC24A4"	"0.773"	"0.276"	"C4014578"	"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2015"	"2"	"3"	"CTD_human;UNIPROT"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123096"	"SLC25A29"	"0.799"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123263"	"MTFMT"	"0.743"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"123263"	"MTFMT"	"0.743"	"0.241"	"C3554182"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2017"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"123263"	"MTFMT"	"0.743"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"123264"	"SLC51B"	"0.773"	"0.241"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123264"	"SLC51B"	"0.773"	"0.241"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"123264"	"SLC51B"	"0.773"	"0.241"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123264"	"SLC51B"	"0.773"	"0.241"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"123355"	"LRRC28"	"0.886"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123606"	"NIPA1"	"0.681"	"0.379"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.46"	"1"	"2007"	"2018"	"0"	"1"	"GENOMICS_ENGLAND"
"123606"	"NIPA1"	"0.681"	"0.379"	"C1838192"	"SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.72"	"1"	"1995"	"2017"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"123606"	"NIPA1"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2006"	"3"	"0"	"GENOMICS_ENGLAND"
"123624"	"AGBL1"	"0.834"	"0.138"	"C0016781"	"Fuchs Endothelial Dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"123624"	"AGBL1"	"0.834"	"0.138"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"123624"	"AGBL1"	"0.834"	"0.138"	"C3809798"	"CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"123688"	"HYKK"	"0.773"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"123872"	"DNAAF1"	"0.743"	"0.31"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.43"	"1"	"1993"	"2013"	"0"	"2"	"ORPHANET"
"123872"	"DNAAF1"	"0.743"	"0.31"	"C2750790"	"CILIARY DYSKINESIA, PRIMARY, 13"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"3"	"5"	"CTD_human;UNIPROT"
"123872"	"DNAAF1"	"0.743"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"123872"	"DNAAF1"	"0.743"	"0.31"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"123879"	"DCUN1D3"			"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"123920"	"CMTM3"	"0.785"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0175709"	"Centronuclear myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0410203"	"X-linked centronuclear myopathy"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0410207"	"Tubular Aggregate Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0546264"	"Congenital Fiber Type Disproportion"	"disease"	"C05;C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C0752282"	"Congenital Structural Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C1834558"	"Myopathy, Centronuclear, Autosomal Dominant"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C3553709"	"MYOPATHY, CENTRONUCLEAR, 4"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"124093"	"CCDC78"	"0.743"	"0.138"	"C3645536"	"Autosomal Recessive Centronuclear Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C3661489"	"Autosomal Dominant Myotubular Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"124093"	"CCDC78"	"0.743"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"124222"	"PAQR4"	"1"	"0.069"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"124222"	"PAQR4"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"124222"	"PAQR4"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"124401"	"ANKS3"	"0.886"	"0.103"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"124404"	"SEPT12"	"0.886"	"0.034"	"C3553793"	"SPERMATOGENIC FAILURE 10"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2016"	"3"	"2"	"CTD_human;UNIPROT"
"124454"	"EARS2"	"0.663"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124454"	"EARS2"	"0.663"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124454"	"EARS2"	"0.663"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124454"	"EARS2"	"0.663"	"0.414"	"C3554079"	"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12"	"disease"		"Disease or Syndrome"	"0.74"	"1"	"2012"	"2017"	"3"	"13"	"CTD_human;ORPHANET;UNIPROT"
"124512"	"METTL23"	"0.785"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124512"	"METTL23"	"0.785"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124512"	"METTL23"	"0.785"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124512"	"METTL23"	"0.785"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"124512"	"METTL23"	"0.785"	"0.172"	"C4014745"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2015"	"0"	"3"	"CTD_human"
"124583"	"CANT1"	"0.645"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124583"	"CANT1"	"0.645"	"0.621"	"C0432242"	"Desbuquois syndrome"	"disease"	"C05;C16;C19;C23"	"Disease or Syndrome"	"0.68"	"1"	"2009"	"2015"	"6"	"8"	"CTD_human;ORPHANET;UNIPROT"
"124583"	"CANT1"	"0.645"	"0.621"	"C3278482"	"DESBUQUOIS DYSPLASIA, KIM VARIANT"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2012"	"6"	"8"	"UNIPROT"
"124583"	"CANT1"	"0.645"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"124583"	"CANT1"	"0.645"	"0.621"	"C4012146"	"DESBUQUOIS DYSPLASIA 1"	"disease"		"Disease or Syndrome"	"0.40"		"2009"	"2015"	"6"	"18"	"UNIPROT"
"124583"	"CANT1"	"0.645"	"0.621"	"C4540251"	"EPIPHYSEAL DYSPLASIA, MULTIPLE, 7"	"disease"		"Congenital Abnormality"	"0.40"		"2017"	"2017"	"1"	"2"	"UNIPROT"
"124590"	"USH1G"	"0.69"	"0.241"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.65"	"1"	"1993"	"2017"	"9"	"3"	"CLINGEN;ORPHANET"
"124590"	"USH1G"	"0.69"	"0.241"	"C1847089"	"USHER SYNDROME, TYPE IG"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.81"	"1"	"1992"	"2016"	"2"	"7"	"CTD_human;UNIPROT"
"124590"	"USH1G"	"0.69"	"0.241"	"C1848638"	"USHER SYNDROME, TYPE IB (disorder)"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"		"2002"	"2017"	"9"	"0"	"CLINGEN"
"124590"	"USH1G"	"0.69"	"0.241"	"C1848639"	"USHER SYNDROME, TYPE IA, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2017"	"9"	"0"	"CLINGEN"
"124590"	"USH1G"	"0.69"	"0.241"	"C1848640"	"USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2017"	"9"	"0"	"CLINGEN"
"124842"	"TMEM132E"	"0.857"	"0.172"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CLINGEN"
"124842"	"TMEM132E"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"124872"	"B4GALNT2"	"0.752"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"124925"	"SEZ6"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124935"	"SLC43A2"	"0.857"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"124936"	"CYB5D2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"124989"	"EFCAB13"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"124997"	"WDR81"	"0.69"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"124997"	"WDR81"	"0.69"	"0.276"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"124997"	"WDR81"	"0.69"	"0.276"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"124997"	"WDR81"	"0.69"	"0.276"	"C0394006"	"Dysequilibrium syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"124997"	"WDR81"	"0.69"	"0.276"	"C2750234"	"Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.60"		"2006"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"124997"	"WDR81"	"0.69"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"125228"	"FAM210A"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"125228"	"FAM210A"	"0.928"	"0.103"	"C0016658"	"Fracture"	"group"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"125228"	"FAM210A"	"0.928"	"0.103"	"C0332712"	"Fracture, spiral"	"disease"	"C26"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"125336"	"LOXHD1"	"0.857"	"0.172"	"C2746083"	"DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2009"	"2015"	"0"	"9"	"CTD_human"
"125336"	"LOXHD1"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"125893"	"ZNF816"	"0.857"	"0.069"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2014"	"2"	"0"	"CTD_human"
"125893"	"ZNF816"	"0.857"	"0.069"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2014"	"2"	"0"	"CTD_human"
"125958"	"OR7D4"	"0.928"	"0.069"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"125958"	"OR7D4"	"0.928"	"0.069"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"125972"	"CALR3"	"0.857"	"0.138"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"125972"	"CALR3"	"0.857"	"0.138"	"C3151266"	"CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 19"	"disease"		"Disease or Syndrome"	"0.50"		"2007"	"2007"	"1"	"1"	"CTD_human;UNIPROT"
"125988"	"C19orf70"	"0.785"	"0.241"	"C0574084"	"3-Methylglutaconic aciduria type 3"	"disease"	"C10;C11;C16;C18;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"125997"	"MBD3L2"	"0.928"	"0.069"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"125997"	"MBD3L2"	"0.928"	"0.069"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"125997"	"MBD3L2"	"0.928"	"0.069"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"126129"	"CPT1C"	"0.762"	"0.31"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"126129"	"CPT1C"	"0.762"	"0.31"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"CTD_human"
"126129"	"CPT1C"	"0.762"	"0.31"	"C4225387"	"SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"126133"	"ALDH16A1"	"0.857"	"0.207"	"C0018099"	"Gout"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"126133"	"ALDH16A1"	"0.857"	"0.207"	"C0268117"	"Gout, HPRT-Related"	"disease"	"C05;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"126133"	"ALDH16A1"	"0.857"	"0.207"	"C0740394"	"Hyperuricemia"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"126205"	"NLRP8"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"126205"	"NLRP8"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"126248"	"WDR88"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"126306"	"JSRP1"	"0.857"	"0.207"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"126306"	"JSRP1"	"0.857"	"0.207"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"126308"	"MOB3A"	"0.928"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"126326"	"GIPC3"	"0.799"	"0.241"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2012"	"2"	"0"	"CLINGEN"
"126326"	"GIPC3"	"0.799"	"0.241"	"C1866094"	"DEAFNESS, AUTOSOMAL RECESSIVE 15"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1997"	"2012"	"2"	"6"	"CTD_human;UNIPROT"
"126328"	"NDUFA11"	"0.667"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"126328"	"NDUFA11"	"0.667"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"126328"	"NDUFA11"	"0.667"	"0.379"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"126328"	"NDUFA11"	"0.667"	"0.379"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"126328"	"NDUFA11"	"0.667"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"126393"	"HSPB6"	"0.752"	"0.276"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"126393"	"HSPB6"	"0.752"	"0.276"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2008"	"2012"	"1"	"0"	"CTD_human"
"126393"	"HSPB6"	"0.752"	"0.276"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C1858133"	"Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"5"	"UNIPROT"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C1858142"	"ICHTHYOSIS, LAMELLAR, 3"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"5"	"UNIPROT"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"126410"	"CYP4F22"	"0.735"	"0.172"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"126695"	"KDF1"	"0.785"	"0.241"	"C0265331"	"Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"126695"	"KDF1"	"0.785"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"126695"	"KDF1"	"0.785"	"0.241"	"C4310616"	"ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2017"	"4"	"0"	"GENOMICS_ENGLAND"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C0432243"	"Spondyloepimetaphyseal Dysplasia With Joint Laxity"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.71"	"1"	"2014"	"2016"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C1869122"	"EHLERS-DANLOS SYNDROME, PROGEROID FORM"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"126792"	"B3GALT6"	"0.63"	"0.517"	"C3809210"	"EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"5"	"UNIPROT"
"127534"	"GJB4"	"0.752"	"0.207"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"127534"	"GJB4"	"0.752"	"0.207"	"C0079153"	"Hyperkeratosis, Epidermolytic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"127534"	"GJB4"	"0.752"	"0.207"	"C0265961"	"Erythrokeratodermia variabilis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.67"	"0.8571429"	"1985"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"127534"	"GJB4"	"0.752"	"0.207"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2012"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"127534"	"GJB4"	"0.752"	"0.207"	"C1851480"	"Greither Disease"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"127534"	"GJB4"	"0.752"	"0.207"	"C4479618"	"ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2"	"disease"		"Disease or Syndrome"	"0.40"		"1978"	"2009"	"2"	"6"	"UNIPROT"
"127795"	"C1orf87"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"127829"	"ARL8A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"127833"	"SYT2"	"0.743"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"127833"	"SYT2"	"0.743"	"0.207"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"127833"	"SYT2"	"0.743"	"0.207"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2016"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"127833"	"SYT2"	"0.743"	"0.207"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"127833"	"SYT2"	"0.743"	"0.207"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"127833"	"SYT2"	"0.743"	"0.207"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"127833"	"SYT2"	"0.743"	"0.207"	"C4015038"	"MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"127933"	"UHMK1"	"0.735"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"127933"	"UHMK1"	"0.735"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.5"	"2007"	"2012"	"4"	"0"	"PSYGENET"
"128077"	"LIX1L"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128077"	"LIX1L"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128178"	"EDARADD"	"0.648"	"0.345"	"C0020608"	"Hypodontia"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.42"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"128178"	"EDARADD"	"0.648"	"0.345"	"C0265331"	"Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"128178"	"EDARADD"	"0.648"	"0.345"	"C0406702"	"Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.61"	"1"	"1993"	"2011"	"0"	"2"	"CTD_human;ORPHANET"
"128178"	"EDARADD"	"0.648"	"0.345"	"C1720965"	"Ectodermal Dysplasia 3, Anhidrotic"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.40"		"1993"	"2007"	"0"	"1"	"CTD_human"
"128178"	"EDARADD"	"0.648"	"0.345"	"C3539920"	"ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.48"	"0.875"	"1997"	"2017"	"3"	"3"	"UNIPROT"
"128178"	"EDARADD"	"0.648"	"0.345"	"C3541517"	"ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.68"	"0.875"	"2005"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"128178"	"EDARADD"	"0.648"	"0.345"	"C4082304"	"Oligodontia"	"disease"		"Congenital Abnormality"	"0.42"	"1"	"2011"	"2014"	"0"	"0"	"ORPHANET"
"128218"	"TMEM125"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"128239"	"IQGAP3"	"0.834"	"0.138"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"128240"	"NAXE"	"0.743"	"0.276"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128240"	"NAXE"	"0.743"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128240"	"NAXE"	"0.743"	"0.276"	"C4310675"	"ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"2"	"7"	"CTD_human;UNIPROT"
"128338"	"DRAM2"	"0.799"	"0.172"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"128338"	"DRAM2"	"0.799"	"0.172"	"C4049066"	"Retinal dystrophy with early macular involvement"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"128439"	"SNHG11"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"128439"	"SNHG11"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"128611"	"ZNF831"	"0.799"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"128637"	"TBC1D20"	"0.607"	"0.448"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128637"	"TBC1D20"	"0.607"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"128637"	"TBC1D20"	"0.607"	"0.448"	"C1838625"	"Warburg Sjo Fledelius syndrome"	"disease"	"C05;C10;C11;C16;C19;C23;F01;F03"	"Disease or Syndrome"	"0.52"	"1"	"2014"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.60"	"0.9090909"	"2006"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0338503"	"Septo-Optic Dysplasia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2013"	"0"	"0"	"ORPHANET"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.43"	"1"	"2006"	"2015"	"1"	"1"	"GENOMICS_ENGLAND"
"128674"	"PROKR2"	"0.567"	"0.621"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2009"	"2010"	"3"	"0"	"PSYGENET"
"128674"	"PROKR2"	"0.567"	"0.621"	"C1563719"	"Kallmann Syndrome 1"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C1563720"	"Kallmann Syndrome 2 (disorder)"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C2930927"	"Kallmann syndrome, type 3, recessive"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.40"		"2006"	"2015"	"0"	"6"	"CTD_human"
"128674"	"PROKR2"	"0.567"	"0.621"	"C3550478"	"HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2015"	"6"	"18"	"UNIPROT"
"128674"	"PROKR2"	"0.567"	"0.621"	"C4053775"	"Pituitary stalk interruption syndrome"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"128859"	"BPIFB6"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"128866"	"CHMP4B"	"0.785"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"128866"	"CHMP4B"	"0.785"	"0.172"	"C0858617"	"Posterior subcapsular cataract"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"128866"	"CHMP4B"	"0.785"	"0.172"	"C1854311"	"Cataract, posterior polar, 3"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2000"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"128989"	"TANGO2"	"0.727"	"0.379"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"128989"	"TANGO2"	"0.727"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"128989"	"TANGO2"	"0.727"	"0.379"	"C4225171"	"METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2016"	"2"	"4"	"ORPHANET;UNIPROT"
"129563"	"DIS3L2"	"0.701"	"0.517"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.46"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"129563"	"DIS3L2"	"0.701"	"0.517"	"C0796113"	"Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor"	"disease"	"C04;C12;C13;C16;C19;C23"	"Disease or Syndrome"	"0.76"	"1"	"2012"	"2017"	"3"	"3"	"CTD_human;ORPHANET;UNIPROT"
"129563"	"DIS3L2"	"0.701"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"129642"	"MBOAT2"			"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"129787"	"TMEM18"	"0.762"	"0.276"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"129787"	"TMEM18"	"0.762"	"0.276"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.8823529"	"2009"	"2016"	"1"	"0"	"CTD_human"
"129880"	"BBS5"	"0.696"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"129880"	"BBS5"	"0.696"	"0.379"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.46"	"1"	"1999"	"2017"	"0"	"3"	"ORPHANET"
"129880"	"BBS5"	"0.696"	"0.379"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"129880"	"BBS5"	"0.696"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"129880"	"BBS5"	"0.696"	"0.379"	"C3892039"	"BARDET-BIEDL SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2004"	"2016"	"2"	"3"	"CTD_human;UNIPROT"
"129880"	"BBS5"	"0.696"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"130120"	"REG3G"	"0.834"	"0.138"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"130340"	"AP1S3"	"0.834"	"0.069"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"130340"	"AP1S3"	"0.834"	"0.069"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"130340"	"AP1S3"	"0.834"	"0.069"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"130340"	"AP1S3"	"0.834"	"0.069"	"C0392439"	"Acrodermatitis continua of Hallopeau"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"130340"	"AP1S3"	"0.834"	"0.069"	"C4015235"	"PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO"	"phenotype"		"Finding"	"0.40"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"130399"	"ACVR1C"	"0.773"	"0.276"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"130540"	"ALS2CR12"	"0.785"	"0.207"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"130557"	"ZNF513"	"0.69"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"130557"	"ZNF513"	"0.69"	"0.345"	"C3150879"	"RETINITIS PIGMENTOSA 58"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"1"	"1"	"CTD_human;UNIPROT"
"130749"	"CPO"	"0.834"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"130814"	"PQLC3"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"130814"	"PQLC3"	"0.928"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"130814"	"PQLC3"	"0.928"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"130872"	"AHSA2P"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2006"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.44"	"1"	"2006"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2006"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C1857776"	"3-@METHYLGLUTACONIC ACIDURIA, TYPE V"	"disease"	"C10;C14;C16;C18;C23"	"Disease or Syndrome"	"0.63"	"1"	"2006"	"2014"	"0"	"2"	"CTD_human;ORPHANET"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"131118"	"DNAJC19"	"0.743"	"0.414"	"C4021133"	"Left ventricular noncompaction cardiomyopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"131177"	"FAM3D"	"0.928"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"131377"	"KLHL40"	"0.785"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"131377"	"KLHL40"	"0.785"	"0.207"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"131377"	"KLHL40"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"131377"	"KLHL40"	"0.785"	"0.207"	"C3809209"	"NEMALINE MYOPATHY 8"	"disease"		"Disease or Syndrome"	"0.80"		"2013"	"2017"	"4"	"12"	"CTD_human;UNIPROT"
"131408"	"FAM131A"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"131450"	"CD200R1"	"0.707"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"131566"	"DCBLD2"	"0.773"	"0.172"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"131566"	"DCBLD2"	"0.773"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"131566"	"DCBLD2"	"0.773"	"0.172"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131566"	"DCBLD2"	"0.773"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"131566"	"DCBLD2"	"0.773"	"0.172"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"131583"	"FAM43A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0268514"	"Urocanase deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2009"	"2009"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"131669"	"UROC1"	"0.785"	"0.207"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.40"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"131669"	"UROC1"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"131870"	"NUDT16"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"131890"	"GRK7"	"0.785"	"0.172"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"131965"	"METTL6"	"0.834"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"131965"	"METTL6"	"0.834"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"131965"	"METTL6"	"0.834"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"131965"	"METTL6"	"0.834"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"132112"	"RTP1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"132158"	"GLYCTK"	"0.735"	"0.207"	"C0342765"	"D-Glyceric aciduria"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2011"	"2018"	"1"	"1"	"UNIPROT"
"132158"	"GLYCTK"	"0.735"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"1987"	"1987"	"1"	"0"	"GENOMICS_ENGLAND"
"132158"	"GLYCTK"	"0.735"	"0.207"	"C1291386"	"D-glycericacidemia"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.71"	"1"	"2011"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"132158"	"GLYCTK"	"0.735"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"132158"	"GLYCTK"	"0.735"	"0.207"	"C3887877"	"Deficiency of glycerate kinase"	"disease"		"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"132320"	"SCLT1"	"0.696"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.52"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"132332"	"TMEM155"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"132671"	"SPATA18"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"132671"	"SPATA18"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"132789"	"GNPDA2"	"0.857"	"0.172"	"C0005910"	"Body Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"132789"	"GNPDA2"	"0.857"	"0.172"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2009"	"2016"	"1"	"0"	"CTD_human"
"132884"	"EVC2"	"0.607"	"0.621"	"C0013903"	"Ellis-Van Creveld Syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"1.00"	"0.9333333"	"2003"	"2017"	"5"	"11"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"132884"	"EVC2"	"0.607"	"0.621"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"132884"	"EVC2"	"0.607"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"132884"	"EVC2"	"0.607"	"0.621"	"C0457013"	"Weyers acrofacial dysostosis"	"disease"	"C05;C07;C16"	"Disease or Syndrome"	"0.64"	"1"	"2007"	"2013"	"0"	"1"	"CTD_human;ORPHANET"
"132884"	"EVC2"	"0.607"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"132884"	"EVC2"	"0.607"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"132884"	"EVC2"	"0.607"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0268397"	"Amyloidosis, Primary Cutaneous"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.42"	"0.5"	"2010"	"2016"	"0"	"0"	"CTD_human"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0268398"	"Familial lichen amyloidosis"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"ORPHANET"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"133396"	"IL31RA"	"0.645"	"0.517"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"133396"	"IL31RA"	"0.645"	"0.517"	"C3151404"	"AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"UNIPROT"
"133396"	"IL31RA"	"0.645"	"0.517"	"C3889979"	"Periodic Fever Syndrome"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"133418"	"EMB"	"0.701"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"133418"	"EMB"	"0.701"	"0.345"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C0020473"	"Hyperlipidemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"1"	"2000"	"2015"	"0"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"		"2006"	"2011"	"1"	"0"	"CTD_human"
"133522"	"PPARGC1B"	"0.642"	"0.552"	"C1706412"	"Lipidemias"	"phenotype"	"C18"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"133686"	"NADK2"	"0.713"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"133686"	"NADK2"	"0.713"	"0.207"	"C1857252"	"2,4-Dienoyl-CoA Reductase Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"133686"	"NADK2"	"0.713"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C0272170"	"Shwachman syndrome"	"disease"	"C06;C15;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C2931245"	"Bone Marrow failure syndromes"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C3808553"	"Bone marrow failure syndrome 1"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C3810350"	"Bone marrow failure syndrome 2"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"134218"	"DNAJC21"	"0.69"	"0.379"	"C4310744"	"BONE MARROW FAILURE SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"4"	"UNIPROT"
"134430"	"WDR36"	"0.762"	"0.172"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"0"	"2009"	"2016"	"1"	"1"	"CTD_human"
"134430"	"WDR36"	"0.762"	"0.172"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.44"	"1"	"2005"	"2012"	"1"	"0"	"CTD_human"
"134430"	"WDR36"	"0.762"	"0.172"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"134430"	"WDR36"	"0.762"	"0.172"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.95"	"2005"	"2017"	"1"	"0"	"CTD_human"
"134430"	"WDR36"	"0.762"	"0.172"	"C1835933"	"Glaucoma 1, Open Angle, G"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"2005"	"2008"	"2"	"5"	"CTD_human;UNIPROT"
"134701"	"RIPPLY2"	"0.762"	"0.103"	"C0265343"	"Jarcho-Levin syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"0"	"0"	"ORPHANET"
"134701"	"RIPPLY2"	"0.762"	"0.103"	"C1837549"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"	"disease"	"C05"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"0"	"0"	"CTD_human"
"134701"	"RIPPLY2"	"0.762"	"0.103"	"C1853296"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05"	"Disease or Syndrome"	"0.50"		"2007"	"2007"	"0"	"0"	"CTD_human"
"134728"	"IRAK1BP1"	"0.928"	"0.172"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"134728"	"IRAK1BP1"	"0.928"	"0.172"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"134829"	"CLVS2"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"134864"	"TAAR1"	"0.799"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"135112"	"NCOA7"	"0.886"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"135112"	"NCOA7"	"0.886"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"135152"	"B3GAT2"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"135228"	"CD109"	"0.707"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2011"	"2"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"135228"	"CD109"	"0.707"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2008"	"2011"	"2"	"0"	"CTD_human;UNIPROT"
"135228"	"CD109"	"0.707"	"0.31"	"C3853779"	"Neonatal Alloimmune Thrombocytopenia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"135228"	"CD109"	"0.707"	"0.31"	"C3854603"	"FNAITP"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"135644"	"TRIM40"	"0.886"	"0.172"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"135656"	"MUCL3"	"0.857"	"0.138"	"C0878555"	"Diffuse panbronchiolitis"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.51"	"1"	"2002"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"135932"	"TMEM139"			"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"135935"	"NOBOX"	"0.834"	"0.207"	"C1969060"	"Premature Ovarian Failure 5"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.60"		"2007"	"2017"	"4"	"10"	"CTD_human;UNIPROT"
"136259"	"KLF14"	"0.743"	"0.172"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.38"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"136259"	"KLF14"	"0.743"	"0.172"	"C0021655"	"Insulin Resistance"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"136259"	"KLF14"	"0.743"	"0.172"	"C0242339"	"Dyslipidemias"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"136259"	"KLF14"	"0.743"	"0.172"	"C0598784"	"Dyslipoproteinemias"	"group"	"C18"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"136259"	"KLF14"	"0.743"	"0.172"	"C0920563"	"Insulin Sensitivity"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"136371"	"ASB10"	"0.834"	"0.103"	"C1863926"	"GLAUCOMA 1, OPEN ANGLE, F (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1999"	"2012"	"1"	"18"	"CTD_human;UNIPROT"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C0432267"	"Tricho-thiodystrophy disorder"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C1313961"	"Trichorrhexis nodosa syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"1"	"UNIPROT"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C1866504"	"Photosensitive Trichothiodystrophy"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.55"	"1"	"2005"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C3495483"	"Amish Brittle Hair Brain Syndrome"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"136647"	"MPLKIP"	"0.72"	"0.276"	"C4083251"	"Trichothiodystrophy, Nonphotosensitive 1"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.50"		"2005"	"2005"	"1"	"1"	"CTD_human;UNIPROT"
"136991"	"ASZ1"	"0.799"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"136991"	"ASZ1"	"0.799"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"137196"	"CCDC26"	"0.713"	"0.31"	"C0017638"	"Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.50"	"1"	"2009"	"2018"	"1"	"1"	"CTD_human"
"137196"	"CCDC26"	"0.713"	"0.31"	"C0259783"	"mixed gliomas"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"137196"	"CCDC26"	"0.713"	"0.31"	"C0555198"	"Malignant Glioma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"137209"	"ZNF572"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"137492"	"VPS37A"	"0.752"	"0.31"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"137492"	"VPS37A"	"0.752"	"0.31"	"C3539494"	"SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.70"		"2013"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2015"	"0"	"1"	"CTD_human"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2008"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"2"	"6"	"UNIPROT"
"137682"	"NDUFAF6"	"0.656"	"0.483"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2012"	"2016"	"2"	"6"	"UNIPROT"
"137735"	"ABRA"	"1"	"0.034"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"137735"	"ABRA"	"1"	"0.034"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C0013069"	"Double Outlet Right Ventricle"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.60"		"2005"	"2015"	"4"	"1"	"CTD_human;UNIPROT"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C0041207"	"Truncus Arteriosus, Persistent"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.70"		"2005"	"2015"	"4"	"1"	"CTD_human;ORPHANET;UNIPROT"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C0152419"	"Interrupted aortic arch"	"disease"		"Congenital Abnormality"	"0.50"		"2005"	"2015"	"4"	"1"	"CTD_human;UNIPROT"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.50"		"2005"	"2015"	"4"	"1"	"CTD_human;UNIPROT"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"137814"	"NKX2-6"	"0.667"	"0.345"	"C1857586"	"CONOTRUNCAL HEART MALFORMATIONS (disorder)"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"4"	"2"	"CTD_human;UNIPROT"
"137868"	"SGCZ"	"0.799"	"0.172"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"137868"	"SGCZ"	"0.799"	"0.172"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"137868"	"SGCZ"	"0.799"	"0.172"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"137868"	"SGCZ"	"0.799"	"0.172"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"137872"	"ADHFE1"	"0.799"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"137872"	"ADHFE1"	"0.799"	"0.276"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"138046"	"RALYL"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"138046"	"RALYL"	"0.857"	"0.138"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"138046"	"RALYL"	"0.857"	"0.138"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"138046"	"RALYL"	"0.857"	"0.138"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0026706"	"Mucopolysaccharidosis III"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.60"		"2006"	"2016"	"0"	"2"	"CTD_human"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0086647"	"Mucopolysaccharidosis Type IIIA"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"0"	"0"	"CTD_human"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0086648"	"MPS III B"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"0"	"0"	"CTD_human"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0086649"	"MPS III C"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.77"	"1"	"2006"	"2018"	"8"	"15"	"CTD_human;ORPHANET;UNIPROT"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0086650"	"MPS III D"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2013"	"5"	"0"	"GENOMICS_ENGLAND"
"138050"	"HGSNAT"	"0.639"	"0.483"	"C4225287"	"RETINITIS PIGMENTOSA 73"	"disease"		"Disease or Syndrome"	"0.60"		"2006"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"138428"	"PTRH1"	"0.727"	"0.345"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"138474"	"TAF1L"	"0.857"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"138474"	"TAF1L"	"0.857"	"0.103"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"138474"	"TAF1L"	"0.857"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"138474"	"TAF1L"	"0.857"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"138474"	"TAF1L"	"0.857"	"0.103"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"138883"	"OR1N1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"139081"	"MAGEC3"	"0.928"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"139105"	"BEND2"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"139105"	"BEND2"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"139105"	"BEND2"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"139135"	"PASD1"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"139189"	"DGKK"	"0.886"	"0.138"	"C0848558"	"Hypospadias"	"group"	"C12;C13;C16"	"Congenital Abnormality"	"0.43"	"1"	"2011"	"2016"	"2"	"1"	"CTD_human"
"139212"	"PIH1D3"	"0.773"	"0.241"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"139212"	"PIH1D3"	"0.773"	"0.241"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"139212"	"PIH1D3"	"0.773"	"0.241"	"C4478372"	"CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"0"	"2"	"CTD_human"
"139285"	"AMER1"	"0.598"	"0.586"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.40"	"0.9444444"	"2007"	"2017"	"1"	"0"	"CTD_human"
"139285"	"AMER1"	"0.598"	"0.586"	"C0432268"	"Osteopathia striata cranial sclerosis"	"disease"	"C05"	"Disease or Syndrome"	"0.86"	"1"	"1996"	"2014"	"1"	"5"	"CTD_human;ORPHANET"
"139285"	"AMER1"	"0.598"	"0.586"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"139285"	"AMER1"	"0.598"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"139378"	"ADGRG4"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"1"	"2008"	"2016"	"2"	"0"	"CTD_human"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"139411"	"PTCHD1"	"0.743"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.65"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"139422"	"MAGEB10"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"139599"	"MAGEE2"	"0.928"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"139628"	"FOXR2"	"0.743"	"0.207"	"C0206727"	"Nerve Sheath Tumors"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"139628"	"FOXR2"	"0.743"	"0.207"	"C0751689"	"Peripheral Nerve Sheath Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"139628"	"FOXR2"	"0.743"	"0.207"	"C0751691"	"Perineurioma"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"139716"	"GAB3"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"139818"	"DOCK11"	"0.72"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"140032"	"RPS4Y2"	"0.928"	"0.069"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"140465"	"MYL6B"			"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140606"	"SELENOM"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"140609"	"NEK7"	"0.815"	"0.207"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"140609"	"NEK7"	"0.815"	"0.207"	"C1335177"	"Ovarian Serous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"140625"	"ACTRT2"			"C0022548"	"Keloid"	"phenotype"	"C17;C23"	"Acquired Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140628"	"GATA5"	"0.596"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"140628"	"GATA5"	"0.596"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2009"	"1"	"0"	"CTD_human"
"140628"	"GATA5"	"0.596"	"0.552"	"C0039685"	"Tetralogy of Fallot"	"disease"	"C14;C16"	"Congenital Abnormality"	"0.42"	"1"	"2013"	"2014"	"0"	"0"	"ORPHANET"
"140628"	"GATA5"	"0.596"	"0.552"	"C0149630"	"Bicuspid aortic valve"	"disease"	"C14"	"Congenital Abnormality"	"0.44"	"1"	"2011"	"2015"	"0"	"0"	"ORPHANET"
"140628"	"GATA5"	"0.596"	"0.552"	"C0162872"	"Aortic Aneurysm, Thoracic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"140628"	"GATA5"	"0.596"	"0.552"	"C0428791"	"Aortic valve calcification"	"disease"	"C14;C18"	"Disease or Syndrome"	"0.40"				"0"	"0"	"ORPHANET"
"140628"	"GATA5"	"0.596"	"0.552"	"C1260873"	"Aortic valve disorder"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"ORPHANET"
"140628"	"GATA5"	"0.596"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"140628"	"GATA5"	"0.596"	"0.552"	"C1843687"	"ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"140628"	"GATA5"	"0.596"	"0.552"	"C3887892"	"Aortic Valve Disease 1"	"disease"	"C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"140679"	"SLC32A1"	"0.799"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140683"	"BPIFA2"	"0.773"	"0.448"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140691"	"TRIM69"	"0.659"	"0.517"	"C0344315"	"Depressed mood"	"phenotype"		"Finding"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"140732"	"SUN5"	"0.857"	"0.103"	"C4310674"	"SPERMATOGENIC FAILURE 16"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2017"	"2018"	"4"	"7"	"CTD_human;UNIPROT"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2011"	"2015"	"1"	"4"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140733"	"MACROD2"	"0.727"	"0.241"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140738"	"TMEM37"	"0.886"	"0.069"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"140767"	"NRSN1"	"0.652"	"0.655"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"140767"	"NRSN1"	"0.652"	"0.655"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"140803"	"TRPM6"	"0.707"	"0.448"	"C0001126"	"Renal tubular acidosis"	"phenotype"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"140803"	"TRPM6"	"0.707"	"0.448"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"140803"	"TRPM6"	"0.707"	"0.448"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"140803"	"TRPM6"	"0.707"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"140803"	"TRPM6"	"0.707"	"0.448"	"C1321780"	"Hypomagnesmic tetany"	"disease"		"Disease or Syndrome"	"0.30"		"2002"	"2014"	"3"	"1"	"UNIPROT"
"140803"	"TRPM6"	"0.707"	"0.448"	"C1865974"	"Hypomagnesemia 1, Intestinal"	"disease"	"C18"	"Disease or Syndrome"	"0.80"	"0.9333333"	"2002"	"2017"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"140885"	"SIRPA"	"0.652"	"0.586"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"140885"	"SIRPA"	"0.652"	"0.586"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"140886"	"PABPC5"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"140902"	"R3HDML"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"140902"	"R3HDML"	"1"	"0.034"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"140907"	"SPG19"	"0.928"	"0.069"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2002"	"2002"	"0"	"0"	"GENOMICS_ENGLAND"
"140907"	"SPG19"	"0.928"	"0.069"	"C1846685"	"SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"140947"	"DCANP1"	"0.857"	"0.069"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"140947"	"DCANP1"	"0.857"	"0.069"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.6666667"	"2010"	"2014"	"3"	"0"	"PSYGENET"
"140947"	"DCANP1"	"0.857"	"0.069"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2010"	"2014"	"3"	"0"	"PSYGENET"
"142678"	"MIB2"	"0.815"	"0.207"	"C1960469"	"Left ventricular noncompaction"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"142680"	"SLC34A3"	"0.701"	"0.31"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"142680"	"SLC34A3"	"0.701"	"0.31"	"C1853271"	"HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY"	"disease"	"C05;C12;C13;C16;C18;C23"	"Disease or Syndrome"	"0.71"	"1"	"1985"	"2007"	"2"	"14"	"CTD_human;ORPHANET;UNIPROT"
"142685"	"ASB15"	"0.799"	"0.207"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142685"	"ASB15"	"0.799"	"0.207"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142685"	"ASB15"	"0.799"	"0.207"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142685"	"ASB15"	"0.799"	"0.207"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142685"	"ASB15"	"0.799"	"0.207"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142685"	"ASB15"	"0.799"	"0.207"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"142689"	"ASB12"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"143098"	"MPP7"	"0.799"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143098"	"MPP7"	"0.799"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143162"	"FRMPD2"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0001418"	"Adenocarcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0205641"	"Adenocarcinoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0205642"	"Adenocarcinoma, Oxyphilic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0205643"	"Carcinoma, Cribriform"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0205644"	"Carcinoma, Granular Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C0205645"	"Adenocarcinoma, Tubular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"143187"	"VTI1A"	"0.743"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.42"	"1"	"2011"	"2018"	"1"	"2"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143379"	"C10orf82"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143384"	"CACUL1"	"0.727"	"0.379"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"143384"	"CACUL1"	"0.727"	"0.379"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"143384"	"CACUL1"	"0.727"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"143425"	"SYT9"	"0.834"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143458"	"LDLRAD3"	"0.834"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143503"	"OR51E1"	"0.799"	"0.172"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"143686"	"SESN3"	"0.815"	"0.207"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"143686"	"SESN3"	"0.815"	"0.207"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"143689"	"PIWIL4"	"0.667"	"0.379"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"143941"	"TTC36"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"144100"	"PLEKHA7"	"0.773"	"0.241"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2018"	"2"	"1"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144132"	"DNHD1"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"144165"	"PRICKLE1"	"0.645"	"0.621"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"144165"	"PRICKLE1"	"0.645"	"0.621"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"144165"	"PRICKLE1"	"0.645"	"0.621"	"C0751785"	"Unverricht-Lundborg Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"144165"	"PRICKLE1"	"0.645"	"0.621"	"C2676254"	"Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"1993"	"2011"	"2"	"3"	"CTD_human;UNIPROT"
"144165"	"PRICKLE1"	"0.645"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"144568"	"A2ML1"	"0.639"	"0.621"	"C0028326"	"Noonan Syndrome"	"disease"	"C05;C14;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"144568"	"A2ML1"	"0.639"	"0.621"	"C0029882"	"Otitis Media"	"disease"	"C09"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"144568"	"A2ML1"	"0.639"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"144577"	"C12orf66"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"144577"	"C12orf66"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"144717"	"PHETA1"	"0.743"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2005"	"2007"	"1"	"0"	"PSYGENET"
"144717"	"PHETA1"	"0.743"	"0.276"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"144717"	"PHETA1"	"0.743"	"0.276"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"144717"	"PHETA1"	"0.743"	"0.276"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"144717"	"PHETA1"	"0.743"	"0.276"	"C1839839"	"MAJOR AFFECTIVE DISORDER 2"	"disease"	"C16;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"144811"	"LACC1"	"0.752"	"0.241"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"144811"	"LACC1"	"0.752"	"0.241"	"C1384600"	"Systemic onset juvenile chronic arthritis"	"disease"		"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"ORPHANET"
"144811"	"LACC1"	"0.752"	"0.241"	"C1858558"	"Rheumatoid Arthritis, Systemic Juvenile"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2006"	"2008"	"2"	"0"	"GENOMICS_ENGLAND"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2015"	"2"	"0"	"GENOMICS_ENGLAND"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C0796012"	"Krause-Kivlin syndrome"	"disease"	"C05;C07;C16;C23"	"Disease or Syndrome"	"0.70"	"1"	"1993"	"2017"	"1"	"6"	"CTD_human;ORPHANET"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2006"	"2009"	"3"	"0"	"GENOMICS_ENGLAND"
"145173"	"B3GLCT"	"0.58"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"145226"	"RDH12"	"0.652"	"0.345"	"C0035304"	"Retinal Degeneration"	"phenotype"	"C11"	"Pathologic Function"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"145226"	"RDH12"	"0.652"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.66"	"1"	"2004"	"2013"	"1"	"2"	"CTD_human;ORPHANET"
"145226"	"RDH12"	"0.652"	"0.345"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.38"	"1"	"2004"	"2018"	"0"	"0"	"ORPHANET"
"145226"	"RDH12"	"0.652"	"0.345"	"C0854723"	"Retinal Dystrophies"	"group"	"C11"	"Disease or Syndrome"	"0.46"	"1"	"2004"	"2017"	"1"	"2"	"CTD_human"
"145226"	"RDH12"	"0.652"	"0.345"	"C2675186"	"LEBER CONGENITAL AMAUROSIS 13"	"disease"	"C11"	"Disease or Syndrome"	"0.60"		"1993"	"2017"	"5"	"18"	"CTD_human;UNIPROT"
"145226"	"RDH12"	"0.652"	"0.345"	"C3150208"	"RETINITIS PIGMENTOSA 53"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2009"	"4"	"9"	"UNIPROT"
"145258"	"GSC"	"0.645"	"0.483"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"145258"	"GSC"	"0.645"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"1999"	"1999"	"1"	"0"	"CTD_human"
"145258"	"GSC"	"0.645"	"0.483"	"C1865361"	"SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES"	"disease"	"C05"	"Disease or Syndrome"	"0.43"	"1"	"1998"	"2014"	"0"	"3"	"ORPHANET"
"145270"	"PRIMA1"	"0.63"	"0.517"	"C0026850"	"Muscular Dystrophy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"145270"	"PRIMA1"	"0.63"	"0.517"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"145270"	"PRIMA1"	"0.63"	"0.517"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"145270"	"PRIMA1"	"0.63"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"UNIPROT"
"145282"	"MIPOL1"	"0.886"	"0.241"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"145447"	"ABHD12B"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"145624"	"PWAR1"	"0.528"	"0.69"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"0.75"	"1996"	"2001"	"0"	"0"	"CTD_human"
"145624"	"PWAR1"	"0.528"	"0.69"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"145741"	"C2CD4A"	"0.928"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"145864"	"HAPLN3"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"145873"	"MESP2"	"0.752"	"0.241"	"C0265343"	"Jarcho-Levin syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.33"	"1"	"2004"	"2010"	"0"	"0"	"ORPHANET"
"145873"	"MESP2"	"0.752"	"0.241"	"C1837549"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"	"disease"	"C05"	"Disease or Syndrome"	"0.40"		"1993"	"2008"	"0"	"7"	"CTD_human"
"145873"	"MESP2"	"0.752"	"0.241"	"C1853296"	"SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3"	"disease"	"C05"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"145873"	"MESP2"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146057"	"TTBK2"	"0.676"	"0.345"	"C1858351"	"SPINOCEREBELLAR ATAXIA 11"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2007"	"0"	"3"	"CTD_human;ORPHANET"
"146057"	"TTBK2"	"0.676"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"146059"	"CDAN1"	"0.659"	"0.483"	"C0002876"	"Congenital dyserythropoietic anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.38"	"1"	"1994"	"2014"	"0"	"0"	"CTD_human"
"146059"	"CDAN1"	"0.659"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"146059"	"CDAN1"	"0.659"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"146059"	"CDAN1"	"0.659"	"0.483"	"C0271933"	"Congenital dyserythropoietic anemia, type I"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.75"	"1"	"1993"	"2013"	"2"	"11"	"CTD_human;ORPHANET;UNIPROT"
"146059"	"CDAN1"	"0.659"	"0.483"	"C0271934"	"Congenital dyserythropoietic anemia, type III"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"146059"	"CDAN1"	"0.659"	"0.483"	"C1306589"	"Congenital dyserythropoietic anemia, type II"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"146167"	"SLC38A8"	"0.785"	"0.241"	"C1836603"	"Foveal Hypoplasia and Anterior Segment Dysgenesis"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"2011"	"2015"	"0"	"3"	"CTD_human"
"146167"	"SLC38A8"	"0.785"	"0.241"	"C3807873"	"FOVEAL HYPOPLASIA 2"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"4"	"ORPHANET;UNIPROT"
"146177"	"VWA3A"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"146177"	"VWA3A"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"146183"	"OTOA"	"0.857"	"0.103"	"C1846896"	"Deafness, Autosomal Recessive 22"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2013"	"2015"	"0"	"6"	"CTD_human"
"146225"	"CMTM2"	"0.857"	"0.138"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"146225"	"CMTM2"	"0.857"	"0.138"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"146225"	"CMTM2"	"0.857"	"0.138"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"146227"	"BEAN1"	"0.701"	"0.241"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"146227"	"BEAN1"	"0.701"	"0.241"	"C1861736"	"SPINOCEREBELLAR ATAXIA 31 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"146227"	"BEAN1"	"0.701"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"GENOMICS_ENGLAND"
"146279"	"TEKT5"	"0.834"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"146433"	"IL34"	"0.72"	"0.483"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"146433"	"IL34"	"0.72"	"0.483"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"146664"	"MGAT5B"	"0.799"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"146664"	"MGAT5B"	"0.799"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"146664"	"MGAT5B"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"146705"	"TEPSIN"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"146845"	"CFAP52"	"0.886"	"0.138"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0234544"	"Todd Paralysis"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0392557"	"Nuclear cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"146862"	"UNC45B"	"0.834"	"0.103"	"C0522224"	"Paralysed"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"146862"	"UNC45B"	"0.834"	"0.103"	"C1112705"	"Nuclear non-senile cataract"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"146862"	"UNC45B"	"0.834"	"0.103"	"C4225389"	"CATARACT 43"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"147007"	"TMEM199"	"0.886"	"0.069"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"147007"	"TMEM199"	"0.886"	"0.069"	"C4225190"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.70"		"2012"	"2016"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"147138"	"TMC8"	"0.707"	"0.172"	"C0014522"	"Epidermodysplasia Verruciformis"	"disease"	"C02;C17"	"Neoplastic Process"	"0.70"	"1"	"2003"	"2018"	"0"	"1"	"CTD_human;ORPHANET"
"147183"	"KRT25"	"0.799"	"0.069"	"C0343073"	"Wooly hair"	"phenotype"		"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"147183"	"KRT25"	"0.799"	"0.069"	"C0345427"	"Woolly hair, congenital"	"disease"	"C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"147183"	"KRT25"	"0.799"	"0.069"	"C3502073"	"Woolly Hair, Autosomal Recessive"	"disease"	"C17"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"147183"	"KRT25"	"0.799"	"0.069"	"C4225214"	"WOOLLY HAIR, AUTOSOMAL RECESSIVE 3"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2018"	"3"	"2"	"UNIPROT"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.51"	"0"	"2004"	"2014"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0024228"	"Lymphatic Diseases"	"group"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0340834"	"Hennekam lymphangiectasia lymphedema syndrome"	"disease"	"C05;C15;C16"	"Disease or Syndrome"	"0.70"		"2010"	"2010"	"2"	"6"	"CTD_human;ORPHANET;UNIPROT"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0455988"	"Hydrops Fetalis, Non-Immune"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0455990"	"Immune Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147372"	"CCBE1"	"0.611"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.61"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"147372"	"CCBE1"	"0.611"	"0.655"	"C4012050"	"HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2010"	"2"	"5"	"UNIPROT"
"147381"	"CBLN2"	"0.815"	"0.241"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"147381"	"CBLN2"	"0.815"	"0.241"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"147381"	"CBLN2"	"0.815"	"0.241"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"147409"	"DSG4"	"0.735"	"0.207"	"C0546966"	"Monilethrix"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.36"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"147409"	"DSG4"	"0.735"	"0.207"	"C1842839"	"HYPOTRICHOSIS 6"	"disease"	"C17"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"0"	"4"	"CTD_human"
"147409"	"DSG4"	"0.735"	"0.207"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"147463"	"ANKRD29"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"147495"	"APCDD1"	"0.696"	"0.345"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"147495"	"APCDD1"	"0.696"	"0.345"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.72"	"1"	"2000"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"147657"	"ZNF480"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"147657"	"ZNF480"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147685"	"C19orf18"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"147741"	"ZNF560"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"147906"	"DACT3"	"0.785"	"0.241"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"147906"	"DACT3"	"0.785"	"0.241"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"147912"	"SIX5"	"0.681"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.31"	"1"	"1999"	"1999"	"0"	"0"	"GENOMICS_ENGLAND"
"147912"	"SIX5"	"0.681"	"0.379"	"C0265234"	"Branchio-Oto-Renal Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.53"	"1"	"2007"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"147912"	"SIX5"	"0.681"	"0.379"	"C0376524"	"Branchio-Oculo-Facial Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"147912"	"SIX5"	"0.681"	"0.379"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"147912"	"SIX5"	"0.681"	"0.379"	"C1970479"	"Branchiootorenal Syndrome 2"	"disease"	"C16"	"Disease or Syndrome"	"0.60"		"1993"	"2007"	"1"	"4"	"CTD_human;UNIPROT"
"147912"	"SIX5"	"0.681"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"147929"	"ZNF565"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"148014"	"TTC9B"	"0.928"	"0.103"	"C0221074"	"Depression, Postpartum"	"disease"	"C13;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"PSYGENET"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0001338"	"Herpetic Acute Necrotizing Encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0004681"	"Bagassosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0019385"	"Herpetic meningoencephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0032273"	"Pneumoconiosis"	"disease"	"C08;C24"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0035126"	"Reperfusion Injury"	"disease"	"C14;C23"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0035235"	"Respiratory Syncytial Virus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"148022"	"TICAM1"	"0.639"	"0.586"	"C0276226"	"Herpes encephalitis"	"disease"	"C02;C10"	"Disease or Syndrome"	"0.53"	"0.6666667"	"2012"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"148022"	"TICAM1"	"0.639"	"0.586"	"C3553869"	"HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 4"	"phenotype"		"Finding"	"0.40"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"148103"	"ZNF599"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"148266"	"ZNF569"	"0.624"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"148266"	"ZNF569"	"0.624"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"148266"	"ZNF569"	"0.624"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"148266"	"ZNF569"	"0.624"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"148327"	"CREB3L4"	"0.762"	"0.31"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"148327"	"CREB3L4"	"0.762"	"0.31"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"148327"	"CREB3L4"	"0.762"	"0.31"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2002"	"2017"	"1"	"0"	"CTD_human"
"148398"	"SAMD11"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"148738"	"HJV"	"0.685"	"0.414"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"148738"	"HJV"	"0.685"	"0.414"	"C0018995"	"Hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2000"	"2017"	"4"	"0"	"CTD_human"
"148738"	"HJV"	"0.685"	"0.414"	"C0268060"	"Juvenile hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.80"	"1"	"2000"	"2017"	"0"	"8"	"CTD_human;ORPHANET"
"148738"	"HJV"	"0.685"	"0.414"	"C0392514"	"Hereditary hemochromatosis"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.37"	"1"	"2005"	"2017"	"4"	"0"	"CTD_human"
"148738"	"HJV"	"0.685"	"0.414"	"C1865614"	"HEMOCHROMATOSIS, TYPE 2A"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.60"		"2003"	"2017"	"0"	"12"	"CTD_human"
"148741"	"ANKRD35"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"148741"	"ANKRD35"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"UNIPROT"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.33"	"1"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C3554638"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"8"	"UNIPROT"
"148789"	"B3GALNT2"	"0.607"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"148867"	"SLC30A7"	"0.834"	"0.207"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"148867"	"SLC30A7"	"0.834"	"0.207"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"149111"	"CNIH3"	"0.815"	"0.138"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"149111"	"CNIH3"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"149111"	"CNIH3"	"0.815"	"0.138"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.40"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"149233"	"IL23R"	"0.505"	"0.724"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9756098"	"2006"	"2017"	"3"	"9"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9230769"	"2006"	"2017"	"2"	"23"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.50"	"0.9166667"	"2006"	"2017"	"3"	"3"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2014"	"3"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.50"	"0.9333333"	"2007"	"2017"	"3"	"10"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.50"	"0.9487179"	"2008"	"2017"	"2"	"6"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"2"	"0"	"CTD_human"
"149233"	"IL23R"	"0.505"	"0.724"	"C2677091"	"Inflammatory Bowel Disease 17"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149420"	"PDIK1L"	"0.573"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2014"	"2"	"0"	"PSYGENET"
"149461"	"CLDN19"	"0.685"	"0.379"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"149461"	"CLDN19"	"0.685"	"0.379"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"149461"	"CLDN19"	"0.685"	"0.379"	"C1855466"	"Hypomagnesemia 5, Renal, with Ocular Involvement"	"disease"	"C11;C12;C13;C16;C18"	"Disease or Syndrome"	"0.70"		"2006"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"149461"	"CLDN19"	"0.685"	"0.379"	"C2931121"	"Meier Blumberg Imahorn syndrome"	"disease"	"C10;C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"149461"	"CLDN19"	"0.685"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"149563"	"SRARP"	"0.886"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2018"	"0"	"0"	"UNIPROT"
"149628"	"PYHIN1"	"0.857"	"0.172"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.43"	"0.6666667"	"2011"	"2016"	"1"	"1"	"CTD_human"
"149628"	"PYHIN1"	"0.857"	"0.172"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"149628"	"PYHIN1"	"0.857"	"0.172"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C0033805"	"Pseudohypoaldosteronism"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C0268436"	"Pseudohypoaldosteronism, Type I"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C1449842"	"Pseudohypoaldosteronism, Type I, Autosomal Dominant"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C1449843"	"Pseudohypoaldosteronism, Type I, Autosomal Recessive"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C1449844"	"Pseudohypoaldosteronism, Type II"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149775"	"GNAS-AS1"	"0.743"	"0.241"	"C2713447"	"Hyperpotassemia and Hypertension, Familial"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"149998"	"LIPI"	"0.928"	"0.103"	"C0020480"	"Hyperlipoproteinemia Type IV"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.50"		"2004"	"2004"	"1"	"1"	"CTD_human;UNIPROT"
"150000"	"ABCC13"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"150000"	"ABCC13"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"150000"	"ABCC13"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"150084"	"IGSF5"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150084"	"IGSF5"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"150094"	"SIK1"	"0.636"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C0270855"	"Early myoclonic encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"150094"	"SIK1"	"0.636"	"0.552"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"150094"	"SIK1"	"0.636"	"0.552"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"150094"	"SIK1"	"0.636"	"0.552"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"150094"	"SIK1"	"0.636"	"0.552"	"C1449563"	"Cardiomyopathy, Familial Idiopathic"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"150094"	"SIK1"	"0.636"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"150094"	"SIK1"	"0.636"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"150094"	"SIK1"	"0.636"	"0.552"	"C4225360"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"150094"	"SIK1"	"0.636"	"0.552"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"150356"	"CHADL"	"0.928"	"0.034"	"C0029410"	"Osteoarthritis of hip"	"disease"	"C05"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"150468"	"CKAP2L"	"0.672"	"0.379"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"150468"	"CKAP2L"	"0.672"	"0.379"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"150468"	"CKAP2L"	"0.672"	"0.379"	"C0795940"	"Filippi syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.61"	"1"	"1996"	"2015"	"0"	"5"	"CTD_human;ORPHANET"
"150468"	"CKAP2L"	"0.672"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"150483"	"TEKT4"	"0.857"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0013221"	"Drug toxicity"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0019189"	"Hepatitis, Chronic"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0041755"	"Adverse reaction to drug"	"group"	"C25"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0149519"	"Chronic Persistent Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0520463"	"Chronic active hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C0524611"	"Cryptogenic Chronic Hepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2015"	"2"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"150684"	"COMMD1"	"0.676"	"0.345"	"C1876165"	"Copper-Overload Cirrhosis"	"disease"	"C06;C10;C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"150962"	"PUS10"	"0.762"	"0.31"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"151056"	"PLB1"	"0.532"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"151254"	"C2CD6"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"151295"	"SLC23A3"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0009806"	"Constipation"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0237326"	"Dyschezia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"151306"	"GPBAR1"	"0.624"	"0.586"	"C1257861"	"Colonic Inertia"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151354"	"FAM84A"	"0.857"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"151354"	"FAM84A"	"0.857"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"151393"	"RMDN2"	"0.604"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151507"	"MSL3P1"	"0.886"	"0.069"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151507"	"MSL3P1"	"0.886"	"0.069"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151507"	"MSL3P1"	"0.886"	"0.069"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151531"	"UPP2"	"0.857"	"0.138"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"151556"	"GPR155"	"0.928"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"151556"	"GPR155"	"0.928"	"0.103"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"151636"	"DTX3L"	"0.834"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"151647"	"FAM19A4"	"0.815"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"151647"	"FAM19A4"	"0.815"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"151647"	"FAM19A4"	"0.815"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"151647"	"FAM19A4"	"0.815"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C0003811"	"Cardiac Arrhythmia"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C0021831"	"Intestinal Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C0236811"	"Chronobiology Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C0813142"	"Circadian Rhythm Disorders"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C0887800"	"Psychogenic Inversion of Circadian Rhythm"	"disease"	"C10"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151648"	"SGO1"	"0.696"	"0.31"	"C4015474"	"Chronic atrial and intestinal dysrhythmia"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"151742"	"PPM1L"	"0.886"	"0.207"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"151790"	"WDR49"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"151887"	"CCDC80"	"0.707"	"0.345"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"151887"	"CCDC80"	"0.707"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"152110"	"NEK10"	"0.743"	"0.241"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"152110"	"NEK10"	"0.743"	"0.241"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"152137"	"CCDC50"	"0.857"	"0.207"	"C1843895"	"Deafness, Autosomal Dominant 44"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"152273"	"FGD5"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"152273"	"FGD5"	"0.886"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"152273"	"FGD5"	"0.886"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"152273"	"FGD5"	"0.886"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2014"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0008073"	"Developmental Disabilities"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0085996"	"Child Development Deviations"	"phenotype"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0085997"	"Child Development Disorders, Specific"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"152330"	"CNTN4"	"0.685"	"0.483"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"152330"	"CNTN4"	"0.685"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"152518"	"NFXL1"	"0.785"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152518"	"NFXL1"	"0.785"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"152573"	"SHISA3"	"0.799"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"152789"	"JAKMIP1"	"0.886"	"0.172"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2007"	"2015"	"1"	"0"	"CTD_human"
"152789"	"JAKMIP1"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"152816"	"ODAPH"	"0.857"	"0.069"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"152816"	"ODAPH"	"0.857"	"0.069"	"C3553830"	"AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2012"	"0"	"1"	"CTD_human"
"152926"	"PPM1K"	"0.785"	"0.241"	"C0024776"	"Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.52"	"0.5"	"2009"	"2013"	"0"	"0"	"CTD_human"
"152926"	"PPM1K"	"0.785"	"0.241"	"C0268568"	"Classic Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"152926"	"PPM1K"	"0.785"	"0.241"	"C0268569"	"Intermittent Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"152926"	"PPM1K"	"0.785"	"0.241"	"C0751285"	"Maple Syrup Urine Disease, Thiamine Responsive"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"152926"	"PPM1K"	"0.785"	"0.241"	"C1621920"	"Intermediate Maple Syrup Urine Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"153020"	"RASGEF1B"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"153020"	"RASGEF1B"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"153020"	"RASGEF1B"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"		"2004"	"2012"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2003"	"2007"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0034065"	"Pulmonary Embolism"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0085096"	"Peripheral Vascular Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"153090"	"DAB2IP"	"0.648"	"0.414"	"C0524702"	"Pulmonary Thromboembolisms"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"153129"	"SLC38A9"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"153129"	"SLC38A9"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"153201"	"SLC36A2"	"0.799"	"0.276"	"C0268654"	"Iminoglycinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.61"	"1"	"2008"	"2008"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"153201"	"SLC36A2"	"0.799"	"0.276"	"C0543541"	"HYPERGLYCINURIA (disorder)"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.60"		"2008"	"2008"	"1"	"1"	"CTD_human;UNIPROT"
"153241"	"CEP120"	"0.663"	"0.448"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"153241"	"CEP120"	"0.663"	"0.448"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"153241"	"CEP120"	"0.663"	"0.448"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"153241"	"CEP120"	"0.663"	"0.448"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"153241"	"CEP120"	"0.663"	"0.448"	"C0265275"	"Jeune thoracic dystrophy"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"153241"	"CEP120"	"0.663"	"0.448"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"153241"	"CEP120"	"0.663"	"0.448"	"C4225378"	"SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2016"	"1"	"2"	"UNIPROT"
"153241"	"CEP120"	"0.663"	"0.448"	"C4274118"	"Joubert syndrome with ocular defect"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"153241"	"CEP120"	"0.663"	"0.448"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"153241"	"CEP120"	"0.663"	"0.448"	"C4540355"	"JOUBERT SYNDROME 31"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"2"	"UNIPROT"
"153562"	"MARVELD2"	"0.773"	"0.241"	"C1857811"	"DEAFNESS, AUTOSOMAL RECESSIVE 49"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.51"	"1"	"2007"	"2015"	"0"	"0"	"CTD_human"
"153562"	"MARVELD2"	"0.773"	"0.241"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"153572"	"IRX2"	"0.857"	"0.138"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"153572"	"IRX2"	"0.857"	"0.138"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"154064"	"RAET1L"	"0.928"	"0.069"	"C0002171"	"Alopecia Areata"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"154141"	"MBOAT1"	"0.928"	"0.103"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"154215"	"NKAIN2"	"0.727"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"154288"	"KHDC3L"	"0.785"	"0.103"	"C0020217"	"Hydatidiform Mole"	"disease"	"C04;C13"	"Neoplastic Process"	"0.37"	"0.8571429"	"2011"	"2016"	"0"	"0"	"CTD_human"
"154288"	"KHDC3L"	"0.785"	"0.103"	"C0334529"	"Hydatidiform Mole, Partial"	"disease"	"C04;C13"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"154288"	"KHDC3L"	"0.785"	"0.103"	"C0678213"	"Complete hydatidiform mole"	"disease"	"C04;C13"	"Neoplastic Process"	"0.62"	"1"	"2002"	"2014"	"0"	"5"	"CTD_human;ORPHANET"
"154664"	"ABCA13"	"0.773"	"0.207"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"154664"	"ABCA13"	"0.773"	"0.207"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"154664"	"ABCA13"	"0.773"	"0.207"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"154664"	"ABCA13"	"0.773"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2010"	"2015"	"1"	"1"	"PSYGENET"
"154664"	"ABCA13"	"0.773"	"0.207"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"154664"	"ABCA13"	"0.773"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154796"	"AMOT"	"0.701"	"0.276"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"154865"	"IQUB"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"154881"	"KCTD7"	"0.735"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"154881"	"KCTD7"	"0.735"	"0.276"	"C2673257"	"EPILEPSY, PROGRESSIVE MYOCLONIC 3"	"disease"	"C10"	"Disease or Syndrome"	"0.70"		"1990"	"2017"	"4"	"7"	"CTD_human;ORPHANET;UNIPROT"
"154881"	"KCTD7"	"0.735"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"155054"	"ZNF425"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"157378"	"TMEM65"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"157506"	"RDH10"	"0.857"	"0.172"	"C0015927"	"Fetal Death"	"phenotype"	"C13;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157506"	"RDH10"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"157506"	"RDH10"	"0.857"	"0.172"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157570"	"ESCO2"	"0.6"	"0.552"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"157570"	"ESCO2"	"0.6"	"0.552"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157570"	"ESCO2"	"0.6"	"0.552"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"157570"	"ESCO2"	"0.6"	"0.552"	"C0392475"	"Roberts-SC phocomelia syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.80"	"0.9333333"	"1979"	"2017"	"4"	"28"	"CTD_human;ORPHANET;UNIPROT"
"157570"	"ESCO2"	"0.6"	"0.552"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157570"	"ESCO2"	"0.6"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"157570"	"ESCO2"	"0.6"	"0.552"	"C4025414"	"Radial club hand"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"157657"	"C8orf37"	"0.639"	"0.483"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.83"	"1"	"2013"	"2018"	"0"	"0"	"CTD_human;ORPHANET"
"157657"	"C8orf37"	"0.639"	"0.483"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"157657"	"C8orf37"	"0.639"	"0.483"	"C3281045"	"CONE-ROD DYSTROPHY 16"	"disease"		"Disease or Syndrome"	"0.80"		"2012"	"2018"	"1"	"4"	"CTD_human;UNIPROT"
"157657"	"C8orf37"	"0.639"	"0.483"	"C3281046"	"RETINITIS PIGMENTOSA 64"	"disease"		"Disease or Syndrome"	"0.80"		"2012"	"2018"	"1"	"5"	"CTD_human;UNIPROT"
"157657"	"C8orf37"	"0.639"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"157657"	"C8orf37"	"0.639"	"0.483"	"C4049066"	"Retinal dystrophy with early macular involvement"	"disease"		"Disease or Syndrome"	"0.70"		"2012"	"2018"	"1"	"2"	"CTD_human;UNIPROT"
"157657"	"C8orf37"	"0.639"	"0.483"	"C4319932"	"BARDET-BIEDL SYNDROME 21"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2017"	"2"	"2"	"CTD_human;UNIPROT"
"157680"	"VPS13B"	"0.624"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"157680"	"VPS13B"	"0.624"	"0.621"	"C0265223"	"Cohen syndrome"	"disease"	"C05;C10;C11;C16;C18;C23;F01;F03"	"Congenital Abnormality"	"0.80"	"0.9615385"	"1993"	"2017"	"7"	"187"	"CTD_human;ORPHANET;UNIPROT"
"157680"	"VPS13B"	"0.624"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"157697"	"ERICH1"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"157855"	"KCNU1"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157869"	"SBSPON"	"1"	"0.034"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"157922"	"CAMSAP1"	"0.857"	"0.207"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"157922"	"CAMSAP1"	"0.857"	"0.207"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"157922"	"CAMSAP1"	"0.857"	"0.207"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"158038"	"LINGO2"	"0.773"	"0.414"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"158038"	"LINGO2"	"0.773"	"0.414"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"158038"	"LINGO2"	"0.773"	"0.414"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"158038"	"LINGO2"	"0.773"	"0.414"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"158038"	"LINGO2"	"0.773"	"0.414"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"158056"	"MAMDC4"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"158314"	"LINC00475"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"158314"	"LINC00475"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;GENOMICS_ENGLAND"
"158326"	"FREM1"	"0.619"	"0.414"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0030044"	"Acrocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0221356"	"Brachycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0221363"	"Bifid nose"	"phenotype"	"C08;C09"	"Anatomical Abnormality"	"0.42"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0235833"	"Congenital diaphragmatic hernia"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2016"	"2"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0265534"	"Scaphycephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0265535"	"Trigonocephaly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.60"				"0"	"0"	"CTD_human;ORPHANET"
"158326"	"FREM1"	"0.619"	"0.414"	"C0265699"	"Congenital hernia of foramen of Morgagni"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0265700"	"Congenital hernia of foramen of Bochdalek"	"disease"	"C16;C23"	"Congenital Abnormality"	"0.30"		"2013"	"2016"	"2"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"158326"	"FREM1"	"0.619"	"0.414"	"C1609433"	"Congenital absence of kidneys syndrome"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2013"	"1"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C1833340"	"Synostotic Posterior Plagiocephaly"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C1855425"	"Marles Greenberg Persaud syndrome"	"disease"	"C05;C11;C16"	"Disease or Syndrome"	"0.75"	"0.8"	"2007"	"2017"	"3"	"2"	"CTD_human;ORPHANET;UNIPROT"
"158326"	"FREM1"	"0.619"	"0.414"	"C1860819"	"Metopic synostosis"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"158326"	"FREM1"	"0.619"	"0.414"	"C2750433"	"Bifid Nose With Or Without Anorectal And Renal Anomalies"	"disease"	"C06;C12;C13"	"Disease or Syndrome"	"0.73"	"0.6666667"	"2009"	"2013"	"2"	"2"	"CTD_human;ORPHANET;UNIPROT"
"158326"	"FREM1"	"0.619"	"0.414"	"C2751431"	"Bifid Nose, Autosomal Dominant"	"disease"	"C08;C09"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C2931150"	"Synostotic Anterior Plagiocephaly"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"158326"	"FREM1"	"0.619"	"0.414"	"C3280974"	"TRIGONOCEPHALY 2"	"disease"		"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"2"	"UNIPROT"
"158326"	"FREM1"	"0.619"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2007"	"2"	"0"	"GENOMICS_ENGLAND"
"158326"	"FREM1"	"0.619"	"0.414"	"C3887497"	"Bifid Nose, Autosomal Recessive"	"disease"	"C08;C09"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"158471"	"PRUNE2"	"0.762"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"158584"	"FAAH2"	"0.815"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"158763"	"ARHGAP36"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"158835"	"AWAT2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"158866"	"ZDHHC15"	"0.735"	"0.241"	"C1845142"	"MENTAL RETARDATION, X-LINKED 91 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"158866"	"ZDHHC15"	"0.735"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"0"	"2005"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"159195"	"USP54"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2015"	"3"	"1"	"CTD_human"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"	"0.9285714"	"2007"	"2015"	"3"	"2"	"CTD_human"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"3"	"0"	"CTD_human"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"3"	"0"	"CTD_human"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"3"	"0"	"CTD_human"
"159296"	"NKX2-3"	"0.762"	"0.069"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2008"	"3"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160335"	"TMTC2"	"0.785"	"0.241"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"160364"	"CLEC12A"	"0.743"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"160418"	"TMTC3"	"0.72"	"0.31"	"C0266463"	"Lissencephaly"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"160418"	"TMTC3"	"0.72"	"0.31"	"C0266483"	"Pachygyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"160418"	"TMTC3"	"0.72"	"0.31"	"C1868720"	"Periventricular Nodular Heterotopia"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2018"	"2018"	"0"	"0"	"ORPHANET"
"160418"	"TMTC3"	"0.72"	"0.31"	"C1879312"	"Agyria"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"160418"	"TMTC3"	"0.72"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2018"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"160418"	"TMTC3"	"0.72"	"0.31"	"C4310646"	"LISSENCEPHALY 8"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"5"	"UNIPROT"
"160428"	"ALDH1L2"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160492"	"LMNTD1"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"160492"	"LMNTD1"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"160728"	"SLC5A8"	"0.636"	"0.345"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2003"	"2011"	"2"	"0"	"CTD_human"
"160728"	"SLC5A8"	"0.636"	"0.345"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2006"	"2"	"0"	"CTD_human"
"160728"	"SLC5A8"	"0.636"	"0.345"	"C0740394"	"Hyperuricemia"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160760"	"PPTC7"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"160762"	"CCDC63"	"0.928"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"160851"	"DGKH"	"0.707"	"0.276"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.49"	"1"	"2008"	"2015"	"5"	"1"	"PSYGENET"
"160851"	"DGKH"	"0.707"	"0.276"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"160851"	"DGKH"	"0.707"	"0.276"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"160851"	"DGKH"	"0.707"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"160851"	"DGKH"	"0.707"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"160851"	"DGKH"	"0.707"	"0.276"	"C2678248"	"Mood instability"	"phenotype"		"Finding"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"160851"	"DGKH"	"0.707"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"160897"	"GPR180"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"161291"	"TMEM30B"	"0.834"	"0.138"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"161424"	"NOP9"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.50"		"2006"	"2008"	"2"	"1"	"CTD_human;UNIPROT"
"161424"	"NOP9"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"161424"	"NOP9"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"161424"	"NOP9"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"161436"	"EML5"	"0.815"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2009"	"2011"	"1"	"1"	"PSYGENET"
"161497"	"STRC"	"0.735"	"0.138"	"C1863561"	"Deafness, Autosomal Recessive 16"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.61"	"1"	"2001"	"2015"	"0"	"6"	"CTD_human"
"161497"	"STRC"	"0.735"	"0.138"	"C1970187"	"Deafness, Sensorineural, And Male Infertility"	"disease"	"C09;C10;C12;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"161497"	"STRC"	"0.735"	"0.138"	"C2751811"	"Spermatogenic Failure 7"	"disease"	"C12"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0002018"	"Alexia"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.52"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0476254"	"Dyslexia"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9615385"	"2003"	"2016"	"0"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C0920296"	"Developmental reading disorder"	"disease"	"C10;C23;F03"	"Mental or Behavioral Dysfunction"	"0.39"	"0.8888889"	"2003"	"2012"	"0"	"0"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C3809641"	"CILIARY DYSKINESIA, PRIMARY, 25"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"0"	"2"	"CTD_human"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"161582"	"DNAAF4"	"0.667"	"0.552"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"161742"	"SPRED1"	"0.672"	"0.517"	"C0027831"	"Neurofibromatosis 1"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.60"	"0.8461538"	"2007"	"2017"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"161742"	"SPRED1"	"0.672"	"0.517"	"C0221263"	"Cafe-au-Lait Spots"	"phenotype"	"C17;C23"	"Finding"	"0.40"		"2007"	"2007"	"1"	"0"	"CTD_human"
"161742"	"SPRED1"	"0.672"	"0.517"	"C0265541"	"Cranioschisis"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"161742"	"SPRED1"	"0.672"	"0.517"	"C0497552"	"Congenital neurologic anomalies"	"group"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"161742"	"SPRED1"	"0.672"	"0.517"	"C0553586"	"Cafe-au-lait macules with pulmonary stenosis"	"disease"	"C04;C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"161742"	"SPRED1"	"0.672"	"0.517"	"C1969623"	"NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.80"	"0.9090909"	"2005"	"2017"	"4"	"12"	"CTD_human;ORPHANET;UNIPROT"
"161742"	"SPRED1"	"0.672"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"162387"	"MFSD6L"	"1"	"0.034"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"162417"	"NAGS"	"0.834"	"0.172"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.68"	"1"	"2002"	"2015"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"162417"	"NAGS"	"0.834"	"0.172"	"C0268543"	"Hyperammonemia, type III"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.74"	"1"	"1998"	"2017"	"4"	"13"	"CTD_human;ORPHANET;UNIPROT"
"162417"	"NAGS"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"162466"	"PHOSPHO1"	"0.928"	"0.103"	"C0005944"	"Metabolic Bone Disorder"	"group"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"162466"	"PHOSPHO1"	"0.928"	"0.103"	"C0029453"	"Osteopenia"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"162514"	"TRPV3"	"0.659"	"0.379"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"162514"	"TRPV3"	"0.659"	"0.379"	"C0343055"	"Generalized pustular psoriasis"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"162514"	"TRPV3"	"0.659"	"0.379"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"162514"	"TRPV3"	"0.659"	"0.379"	"C1849193"	"PEELING SKIN SYNDROME"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"162514"	"TRPV3"	"0.659"	"0.379"	"C2609071"	"Olmsted syndrome"	"disease"		"Disease or Syndrome"	"0.80"	"1"	"2012"	"2018"	"2"	"3"	"CTD_human;ORPHANET;UNIPROT"
"162514"	"TRPV3"	"0.659"	"0.379"	"C2931923"	"Hyperkeratosis of the palms and soles and esophageal papillomas"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"162514"	"TRPV3"	"0.659"	"0.379"	"C4225339"	"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"163175"	"LGI4"	"0.72"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.41"	"1"	"2005"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"163175"	"LGI4"	"0.72"	"0.276"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2005"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"163175"	"LGI4"	"0.72"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2005"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"163175"	"LGI4"	"0.72"	"0.276"	"C4479539"	"ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"6"	"CTD_human;UNIPROT"
"163183"	"SYNE4"	"0.886"	"0.103"	"C3147083"	"DEAFNESS, AUTOSOMAL RECESSIVE 76"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"1"	"CTD_human"
"163223"	"ZNF676"			"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"163255"	"ZNF540"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2016"	"1"	"2"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2010"	"2017"	"1"	"4"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"1"	"3"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"163486"	"DENND1B"	"0.727"	"0.172"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"163702"	"IFNLR1"	"0.727"	"0.31"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"163702"	"IFNLR1"	"0.727"	"0.31"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"163786"	"SASS6"	"0.743"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"163786"	"SASS6"	"0.743"	"0.276"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"163786"	"SASS6"	"0.743"	"0.276"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"163786"	"SASS6"	"0.743"	"0.276"	"C4225338"	"MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"163882"	"CNST"			"C0040128"	"Thyroid Diseases"	"group"	"C19"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"164045"	"HFM1"	"0.785"	"0.276"	"C3810376"	"PREMATURE OVARIAN FAILURE 9"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"4"	"CTD_human;UNIPROT"
"164395"	"TTLL9"	"0.886"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"164395"	"TTLL9"	"0.886"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"164395"	"TTLL9"	"0.886"	"0.138"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"164395"	"TTLL9"	"0.886"	"0.138"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"164395"	"TTLL9"	"0.886"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"164395"	"TTLL9"	"0.886"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2014"	"1"	"1"	"UNIPROT"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C0085576"	"Iron-Refractory Iron Deficiency Anemia"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.80"	"1"	"2008"	"2018"	"12"	"22"	"CTD_human;ORPHANET;UNIPROT"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C0162316"	"Iron deficiency anemia"	"disease"	"C15;C18"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2017"	"2"	"0"	"CTD_human"
"164656"	"TMPRSS6"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"164781"	"DAW1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"164832"	"LONRF2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"165530"	"CLEC4F"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"165904"	"XIRP1"	"0.815"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"165904"	"XIRP1"	"0.815"	"0.207"	"C0032343"	"Poisoning"	"group"	"C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"165918"	"RNF168"	"0.785"	"0.414"	"C2677792"	"Riddle Syndrome"	"disease"	"C05;C10;C16;C20;C23;F03"	"Disease or Syndrome"	"0.83"	"1"	"2009"	"2011"	"0"	"1"	"CTD_human;ORPHANET"
"165918"	"RNF168"	"0.785"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"166336"	"PRICKLE2"	"0.886"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"166378"	"SPATA5"	"0.735"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"166378"	"SPATA5"	"0.735"	"0.31"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2015"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"166378"	"SPATA5"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"166378"	"SPATA5"	"0.735"	"0.31"	"C4225276"	"EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2017"	"1"	"13"	"CTD_human;ORPHANET;UNIPROT"
"166379"	"BBS12"	"0.696"	"0.414"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"166379"	"BBS12"	"0.696"	"0.414"	"C0752166"	"Bardet-Biedl Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.45"	"1"	"2009"	"2017"	"0"	"3"	"ORPHANET"
"166379"	"BBS12"	"0.696"	"0.414"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"166379"	"BBS12"	"0.696"	"0.414"	"C1859570"	"BARDET-BIEDL SYNDROME 12"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2007"	"2015"	"4"	"14"	"CTD_human;UNIPROT"
"166379"	"BBS12"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"166379"	"BBS12"	"0.696"	"0.414"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"166752"	"FREM3"	"0.815"	"0.207"	"C0011574"	"Involutional Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"166752"	"FREM3"	"0.815"	"0.207"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"166752"	"FREM3"	"0.815"	"0.207"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.51"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human;PSYGENET"
"166752"	"FREM3"	"0.815"	"0.207"	"C1571983"	"Involutional paraphrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"166752"	"FREM3"	"0.815"	"0.207"	"C1571984"	"Psychosis, Involutional"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"166785"	"MMAA"	"0.72"	"0.379"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"		"2003"	"2005"	"2"	"0"	"GENOMICS_ENGLAND"
"166785"	"MMAA"	"0.72"	"0.379"	"C1855109"	"Methylmalonic aciduria cblA type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"1993"	"2018"	"6"	"28"	"CTD_human;ORPHANET;UNIPROT"
"166785"	"MMAA"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"167127"	"UGT3A2"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"167359"	"NIM1K"	"0.834"	"0.207"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.51"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"		"2010"	"2011"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.50"		"2010"	"2011"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167465"	"ZNF366"	"0.799"	"0.31"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"167681"	"PRSS35"	"0.886"	"0.207"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0155003"	"Blindness, Transient"	"phenotype"	"C10;C11;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0221473"	"Blindness, Hysterical"	"disease"	"C10;C11;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0271215"	"Blindness, Legal"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.47"	"1"	"1993"	"2017"	"0"	"3"	"ORPHANET"
"167691"	"LCA5"	"0.672"	"0.241"	"C0339730"	"Blindness, Acquired"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0376288"	"Amaurosis"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0456909"	"Blindness"	"phenotype"	"C10;C11;C23"	"Finding"	"0.32"		"2007"	"2008"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C0750958"	"Blindness, Monocular"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C1858080"	"Retinal Dystrophy, Early Onset Severe"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"167691"	"LCA5"	"0.672"	"0.241"	"C1858301"	"LEBER CONGENITAL AMAUROSIS 5"	"disease"	"C11"	"Disease or Syndrome"	"0.62"	"1"	"1993"	"2017"	"0"	"4"	"CTD_human"
"167691"	"LCA5"	"0.672"	"0.241"	"C1879328"	"Blindness both eyes NOS (disorder)"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"168002"	"DACT2"	"0.707"	"0.172"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"168002"	"DACT2"	"0.707"	"0.172"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"168391"	"GALNTL5"	"0.928"	"0.034"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"168400"	"DDX53"	"0.58"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"168507"	"PKD1L1"	"0.799"	"0.138"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"ORPHANET"
"168507"	"PKD1L1"	"0.799"	"0.138"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.40"		"2017"	"2017"	"0"	"2"	"ORPHANET"
"168507"	"PKD1L1"	"0.799"	"0.138"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"168507"	"PKD1L1"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"168507"	"PKD1L1"	"0.799"	"0.138"	"C4310668"	"HETEROTAXY, VISCERAL, 8, AUTOSOMAL"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"168667"	"BMPER"	"0.676"	"0.483"	"C0027412"	"Opioid-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"168667"	"BMPER"	"0.676"	"0.483"	"C0029095"	"Opioid abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"168667"	"BMPER"	"0.676"	"0.483"	"C0524662"	"Opiate Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"168667"	"BMPER"	"0.676"	"0.483"	"C1842691"	"Diaphanospondylodysostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.73"	"1"	"2010"	"2016"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"168667"	"BMPER"	"0.676"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"168667"	"BMPER"	"0.676"	"0.483"	"C4274732"	"Ischio-vertebral syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"169026"	"SLC30A8"	"0.663"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9605263"	"2007"	"2018"	"6"	"3"	"CTD_human"
"169026"	"SLC30A8"	"0.663"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"169044"	"COL22A1"	"0.928"	"0.172"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"169166"	"SNX31"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"169436"	"STKLD1"	"0.928"	"0.069"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"169522"	"KCNV2"	"0.785"	"0.103"	"C1835897"	"Retinal Cone Dystrophy 3B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.71"	"1"	"2006"	"2013"	"1"	"11"	"CTD_human;ORPHANET;UNIPROT"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.45"	"0.8"	"2006"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.42"	"1"	"2010"	"2018"	"1"	"3"	"CTD_human"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.48"	"1"	"2011"	"2018"	"1"	"5"	"CTD_human"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"169792"	"GLIS3"	"0.633"	"0.483"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2006"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"169792"	"GLIS3"	"0.633"	"0.483"	"C1857775"	"Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism"	"disease"	"C05;C16;C18;C19"	"Disease or Syndrome"	"0.80"		"2004"	"2016"	"0"	"4"	"CTD_human;ORPHANET"
"169792"	"GLIS3"	"0.633"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"169792"	"GLIS3"	"0.633"	"0.483"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"169841"	"ZNF169"	"0.928"	"0.138"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"170062"	"FAM47B"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170261"	"ZCCHC12"	"0.928"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.31"		"2004"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0037769"	"West Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"1"	"2002"	"2016"	"0"	"0"	"ORPHANET"
"170302"	"ARX"	"0.541"	"0.448"	"C0393706"	"Early infantile epileptic encephalopathy with suppression bursts"	"disease"		"Disease or Syndrome"	"0.37"	"1"	"2007"	"2012"	"0"	"0"	"ORPHANET"
"170302"	"ARX"	"0.541"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C0796124"	"Proud Syndrome"	"disease"	"C10;C12;C13;C16;C23;F01;F03"	"Disease or Syndrome"	"0.70"		"1992"	"2012"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"170302"	"ARX"	"0.541"	"0.448"	"C0796244"	"MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"170302"	"ARX"	"0.541"	"0.448"	"C0796250"	"PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME"	"disease"	"C10;C16;C23"	"Disease or Syndrome"	"0.54"	"1"	"1996"	"2015"	"0"	"0"	"CTD_human;ORPHANET"
"170302"	"ARX"	"0.541"	"0.448"	"C1846171"	"Lissencephaly, X-Linked, 2"	"disease"	"C10;C12;C13;C16"	"Disease or Syndrome"	"0.73"	"1"	"2002"	"2016"	"2"	"24"	"CTD_human;ORPHANET;UNIPROT"
"170302"	"ARX"	"0.541"	"0.448"	"C1846172"	"Hydranencephaly and Abnormal Genitalia"	"disease"	"C10;C12;C13;C16"	"Disease or Syndrome"	"0.60"		"2002"	"2004"	"2"	"4"	"CTD_human;UNIPROT"
"170302"	"ARX"	"0.541"	"0.448"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170302"	"ARX"	"0.541"	"0.448"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"0"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"170302"	"ARX"	"0.541"	"0.448"	"C3463992"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.90"		"1997"	"2017"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"170302"	"ARX"	"0.541"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"	"1"	"2002"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"170394"	"PWWP2B"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"170394"	"PWWP2B"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"170572"	"HTR3C"	"0.799"	"0.172"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2009"	"2009"	"1"	"0"	"CTD_human"
"170572"	"HTR3C"	"0.799"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"170575"	"GIMAP1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"170589"	"GPHA2"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"170679"	"PSORS1C1"	"0.667"	"0.621"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"7"	"CTD_human"
"170679"	"PSORS1C1"	"0.667"	"0.621"	"C0036421"	"Systemic Scleroderma"	"disease"	"C17"	"Disease or Syndrome"	"0.42"	"1"	"2012"	"2013"	"1"	"1"	"CTD_human"
"170680"	"PSORS1C2"	"0.799"	"0.207"	"C0026764"	"Multiple Myeloma"	"disease"	"C04;C14;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"3"	"CTD_human"
"170689"	"ADAMTS15"	"0.799"	"0.207"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2006"	"2010"	"1"	"1"	"UNIPROT"
"170691"	"ADAMTS17"	"0.752"	"0.31"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"170691"	"ADAMTS17"	"0.752"	"0.31"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"170691"	"ADAMTS17"	"0.752"	"0.31"	"C2750787"	"Weill-Marchesani-Like Syndrome"	"disease"	"C05;C11;C16;C19"	"Disease or Syndrome"	"0.62"	"0.5"	"2009"	"2016"	"0"	"2"	"CTD_human;ORPHANET"
"170692"	"ADAMTS18"	"0.713"	"0.379"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"170692"	"ADAMTS18"	"0.713"	"0.379"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2012"	"2014"	"2"	"0"	"GENOMICS_ENGLAND"
"170692"	"ADAMTS18"	"0.713"	"0.379"	"C3809567"	"MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"2012"	"2014"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"170712"	"COX7B2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"170825"	"GSX2"	"0.886"	"0.138"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"170825"	"GSX2"	"0.886"	"0.138"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"170954"	"PPP1R18"	"0.834"	"0.241"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"171019"	"ADAMTS19"	"0.886"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2010"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0023473"	"Myeloid Leukemia, Chronic"	"disease"	"C04;C15"	"Neoplastic Process"	"0.36"	"0.8333333"	"2002"	"2017"	"0"	"0"	"CGI"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2002"	"2016"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2017"	"3"	"0"	"GENOMICS_ENGLAND"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0349639"	"Juvenile Myelomonocytic Leukemia"	"disease"	"C04;C15"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C0796232"	"Bohring syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.68"	"0.875"	"2011"	"2017"	"1"	"7"	"CTD_human;ORPHANET"
"171023"	"ASXL1"	"0.532"	"0.69"	"C2713368"	"Hematopoetic Myelodysplasia"	"disease"	"C15"	"Pathologic Function"	"0.50"		"2014"	"2017"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C3463824"	"MYELODYSPLASTIC SYNDROME"	"group"	"C15"	"Neoplastic Process"	"0.70"	"1"	"1990"	"2017"	"1"	"0"	"CGI;CTD_human"
"171023"	"ASXL1"	"0.532"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"171024"	"SYNPO2"	"0.857"	"0.207"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human"
"171511"	"ADIPQTL2"			"C1847530"	"ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"171512"	"ADIPQTL3"	"0.928"	"0.069"	"C1847529"	"ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3"	"phenotype"		"Finding"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"171558"	"PTCRA"	"0.743"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"171558"	"PTCRA"	"0.743"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"192286"	"HIGD2A"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"192286"	"HIGD2A"	"1"	"0.069"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"192286"	"HIGD2A"	"1"	"0.069"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"192286"	"HIGD2A"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"192683"	"SCAMP5"	"1"	"0.069"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"196403"	"DTX3"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"196403"	"DTX3"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"196403"	"DTX3"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"196403"	"DTX3"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"196441"	"ZFC3H1"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"196441"	"ZFC3H1"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"196441"	"ZFC3H1"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"196475"	"RMST"	"1"	"0.069"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"1"	"CTD_human"
"196527"	"ANO6"	"0.857"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"196527"	"ANO6"	"0.857"	"0.172"	"C0038013"	"Ankylosing spondylitis"	"disease"	"C05"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2013"	"1"	"1"	"CTD_human"
"196527"	"ANO6"	"0.857"	"0.172"	"C0796149"	"Scott Syndrome"	"disease"	"C15"	"Disease or Syndrome"	"0.55"	"0.8"	"2011"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"196528"	"ARID2"	"0.645"	"0.621"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"196528"	"ARID2"	"0.645"	"0.621"	"C0265338"	"Coffin-Siris syndrome"	"disease"	"C05;C07;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"196528"	"ARID2"	"0.645"	"0.621"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"196528"	"ARID2"	"0.645"	"0.621"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.58"	"1"	"2011"	"2017"	"2"	"0"	"CGI;CTD_human"
"196528"	"ARID2"	"0.645"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2016"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"196740"	"VSTM4"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"196743"	"PAOX"	"0.785"	"0.31"	"C0038454"	"Cerebrovascular accident"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"196743"	"PAOX"	"0.785"	"0.31"	"C0751956"	"Acute Cerebrovascular Accidents"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"197131"	"UBR1"	"0.636"	"0.621"	"C0175692"	"Johanson-Blizzard syndrome"	"disease"	"C06;C09;C10;C16;C17;C19;C23;F01;F03"	"Disease or Syndrome"	"1.00"	"1"	"2002"	"2018"	"5"	"5"	"CTD_human;ORPHANET;UNIPROT"
"197131"	"UBR1"	"0.636"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2006"	"2006"	"0"	"0"	"GENOMICS_ENGLAND"
"197135"	"PATL2"	"1"		"C4540284"	"OOCYTE MATURATION DEFECT 4"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"2"	"4"	"UNIPROT"
"197259"	"MLKL"	"0.752"	"0.276"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"197322"	"ACSF3"	"0.815"	"0.172"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"197322"	"ACSF3"	"0.815"	"0.172"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"197322"	"ACSF3"	"0.815"	"0.172"	"C0342793"	"Malonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"197322"	"ACSF3"	"0.815"	"0.172"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"CTD_human"
"197322"	"ACSF3"	"0.815"	"0.172"	"C3280314"	"Combined Malonic and Methylmalonic Aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"2011"	"2017"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"197322"	"ACSF3"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2012"	"2"	"0"	"GENOMICS_ENGLAND"
"199221"	"DZIP1L"	"0.785"	"0.241"	"C0085548"	"Autosomal Recessive Polycystic Kidney Disease"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.71"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"199221"	"DZIP1L"	"0.785"	"0.241"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"199221"	"DZIP1L"	"0.785"	"0.241"	"C4539903"	"POLYCYSTIC KIDNEY DISEASE 5"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"4"	"UNIPROT"
"199713"	"NLRP7"	"0.72"	"0.241"	"C0020217"	"Hydatidiform Mole"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.8888889"	"2006"	"2016"	"0"	"0"	"CTD_human"
"199713"	"NLRP7"	"0.72"	"0.241"	"C0334529"	"Hydatidiform Mole, Partial"	"disease"	"C04;C13"	"Neoplastic Process"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"199713"	"NLRP7"	"0.72"	"0.241"	"C0678213"	"Complete hydatidiform mole"	"disease"	"C04;C13"	"Neoplastic Process"	"0.66"	"0.6666667"	"2006"	"2015"	"2"	"8"	"CTD_human;ORPHANET;UNIPROT"
"199713"	"NLRP7"	"0.72"	"0.241"	"C2931618"	"Gestational trophoblastic disease"	"disease"	"C04;C13"	"Disease or Syndrome"	"0.40"		"1991"	"2016"	"2"	"13"	"UNIPROT"
"199713"	"NLRP7"	"0.72"	"0.241"	"C3463897"	"HYDATIDIFORM MOLE, RECURRENT, 1"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2006"	"2016"	"2"	"8"	"UNIPROT"
"199857"	"ALG14"	"0.815"	"0.103"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"199857"	"ALG14"	"0.815"	"0.103"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2013"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"199857"	"ALG14"	"0.815"	"0.103"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.51"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"199857"	"ALG14"	"0.815"	"0.103"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"199857"	"ALG14"	"0.815"	"0.103"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"199857"	"ALG14"	"0.815"	"0.103"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"199857"	"ALG14"	"0.815"	"0.103"	"C4015596"	"MYASTHENIC SYNDROME, CONGENITAL, 15"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"2"	"UNIPROT"
"200150"	"PLD5"			"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"200162"	"SPAG17"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"200205"	"IBA57"	"0.713"	"0.207"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"200205"	"IBA57"	"0.713"	"0.207"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"200205"	"IBA57"	"0.713"	"0.207"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"200205"	"IBA57"	"0.713"	"0.207"	"C3502075"	"Multiple Mitochondrial Dysfunctions Syndrome"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200205"	"IBA57"	"0.713"	"0.207"	"C3809165"	"MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"1"	"1"	"ORPHANET;UNIPROT"
"200205"	"IBA57"	"0.713"	"0.207"	"C4225322"	"SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0027671"	"Neoplastic Processes"	"group"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"200315"	"APOBEC3A"	"0.696"	"0.448"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"200403"	"VWA3B"	"0.713"	"0.207"	"C4310781"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22"	"disease"		"Disease or Syndrome"	"0.40"		"2017"	"2017"	"1"	"1"	"UNIPROT"
"200424"	"TET3"	"0.72"	"0.345"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"200576"	"PIKFYVE"	"0.857"	"0.138"	"C1562113"	"Fleck corneal dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.75"	"1"	"2005"	"2016"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"200576"	"PIKFYVE"	"0.857"	"0.138"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2005"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"200728"	"TMEM17"	"1"	"0.069"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"200728"	"TMEM17"	"1"	"0.069"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"200734"	"SPRED2"	"0.752"	"0.448"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2010"	"2014"	"2"	"4"	"CTD_human"
"200879"	"LIPH"	"0.743"	"0.103"	"C0020678"	"Hypotrichosis"	"disease"	"C17"	"Congenital Abnormality"	"0.50"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"200879"	"LIPH"	"0.743"	"0.103"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"200879"	"LIPH"	"0.743"	"0.103"	"C0343073"	"Wooly hair"	"phenotype"		"Finding"	"0.40"				"0"	"0"	"ORPHANET"
"200879"	"LIPH"	"0.743"	"0.103"	"C0345427"	"Woolly hair, congenital"	"disease"	"C17"	"Congenital Abnormality"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"200879"	"LIPH"	"0.743"	"0.103"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"200879"	"LIPH"	"0.743"	"0.103"	"C1836672"	"Total Hypotrichosis, Mari type"	"disease"	"C17;C23"	"Disease or Syndrome"	"0.49"	"1"	"2006"	"2016"	"3"	"2"	"UNIPROT"
"200879"	"LIPH"	"0.743"	"0.103"	"C1854310"	"Hypotrichosis simplex"	"disease"	"C17"	"Disease or Syndrome"	"0.34"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"200879"	"LIPH"	"0.743"	"0.103"	"C3148823"	"WOOLLY HAIR, AUTOSOMAL RECESSIVE 2, WITH OR WITHOUT HYPOTRICHOSIS"	"disease"		"Disease or Syndrome"	"0.40"		"2006"	"2011"	"3"	"2"	"UNIPROT"
"200879"	"LIPH"	"0.743"	"0.103"	"C3148824"	"WH/HT"	"disease"		"Disease or Syndrome"	"0.30"		"2006"	"2009"	"3"	"1"	"UNIPROT"
"200894"	"ARL13B"	"0.752"	"0.345"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"200894"	"ARL13B"	"0.752"	"0.345"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.40"	"1"	"2008"	"2016"	"0"	"0"	"ORPHANET"
"200894"	"ARL13B"	"0.752"	"0.345"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"200894"	"ARL13B"	"0.752"	"0.345"	"C2676771"	"JOUBERT SYNDROME 8 (disorder)"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2016"	"2"	"7"	"CTD_human;UNIPROT"
"200894"	"ARL13B"	"0.752"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2008"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"200894"	"ARL13B"	"0.752"	"0.345"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.32"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"200909"	"HTR3D"	"0.857"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"200931"	"SLC51A"	"0.799"	"0.172"	"C0008312"	"Primary biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"200931"	"SLC51A"	"0.799"	"0.172"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2014"	"2"	"0"	"CTD_human"
"200931"	"SLC51A"	"0.799"	"0.172"	"C0023892"	"Biliary cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"200931"	"SLC51A"	"0.799"	"0.172"	"C0238065"	"Biliary Cirrhosis, Secondary"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"200933"	"FBXO45"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"200942"	"KLHDC8B"	"0.857"	"0.138"	"C0152268"	"Nodular Sclerosis Classical Hodgkin Lymphoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"200942"	"KLHDC8B"	"0.857"	"0.138"	"C1855523"	"Leg, Absence Deformity of, with Congenital Cataract"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"201163"	"FLCN"	"0.567"	"0.655"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.50"	"0.9375"	"2003"	"2016"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"		"2003"	"2003"	"0"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0010709"	"Cyst"	"phenotype"	"C04;C23"	"Disease or Syndrome"	"0.32"	"1"	"2007"	"2016"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0013720"	"Ehlers-Danlos Syndrome"	"disease"	"C14;C15;C16;C17"	"Disease or Syndrome"	"0.30"		"2005"	"2011"	"7"	"0"	"GENOMICS_ENGLAND"
"201163"	"FLCN"	"0.567"	"0.655"	"C0018552"	"Hamartoma"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2016"	"2"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0022665"	"Kidney Neoplasm"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.39"	"1"	"2003"	"2017"	"0"	"0"	"CGI"
"201163"	"FLCN"	"0.567"	"0.655"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0032326"	"Pneumothorax"	"phenotype"	"C08"	"Disease or Syndrome"	"0.46"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0149781"	"Spontaneous pneumothorax"	"disease"	"C08"	"Disease or Syndrome"	"0.46"	"1"	"2003"	"2018"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0264558"	"Tension Pneumothorax"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.73"	"1"	"2003"	"2014"	"2"	"1"	"CTD_human;UNIPROT"
"201163"	"FLCN"	"0.567"	"0.655"	"C0345050"	"Congenital aneurysm of ascending aorta"	"disease"	"C14"	"Congenital Abnormality"	"0.30"		"2003"	"2016"	"9"	"0"	"GENOMICS_ENGLAND"
"201163"	"FLCN"	"0.567"	"0.655"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0346010"	"Multiple fibrofolliculomas"	"disease"	"C04;C16"	"Disease or Syndrome"	"1.00"	"0.9074074"	"1993"	"2018"	"9"	"64"	"CLINGEN;CTD_human;ORPHANET;UNIPROT"
"201163"	"FLCN"	"0.567"	"0.655"	"C0346255"	"Oncocytoma, renal"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.32"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C0740457"	"Malignant neoplasm of kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.60"	"1"	"2003"	"2017"	"0"	"0"	"CGI;GENOMICS_ENGLAND"
"201163"	"FLCN"	"0.567"	"0.655"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.31"	"1"	"2003"	"2004"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"201163"	"FLCN"	"0.567"	"0.655"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"201163"	"FLCN"	"0.567"	"0.655"	"C1378703"	"Renal carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2003"	"2017"	"0"	"0"	"CGI"
"201163"	"FLCN"	"0.567"	"0.655"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"201163"	"FLCN"	"0.567"	"0.655"	"C1868193"	"PNEUMOTHORAX, PRIMARY SPONTANEOUS"	"disease"	"C08"	"Disease or Syndrome"	"0.75"	"0.8"	"2003"	"2016"	"3"	"8"	"CTD_human;ORPHANET;UNIPROT"
"201163"	"FLCN"	"0.567"	"0.655"	"C2750825"	"NONPAPILLARY RENAL CARCINOMA 1 LOCUS"	"phenotype"		"Finding"	"0.50"		"2008"	"2008"	"1"	"1"	"UNIPROT"
"201163"	"FLCN"	"0.567"	"0.655"	"C2931246"	"Potocki-Lupski syndrome"	"disease"	"C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"201229"	"LYRM9"	"1"	"0.069"	"C0149925"	"Small cell carcinoma of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"201283"	"AMZ2P1"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"201283"	"AMZ2P1"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"201283"	"AMZ2P1"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"201294"	"UNC13D"	"0.696"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"201294"	"UNC13D"	"0.696"	"0.414"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"201294"	"UNC13D"	"0.696"	"0.414"	"C0272199"	"Familial Hemophagocytic Lymphocytosis"	"phenotype"	"C15"	"Disease or Syndrome"	"0.40"		"2004"	"2015"	"0"	"2"	"ORPHANET"
"201294"	"UNC13D"	"0.696"	"0.414"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"201294"	"UNC13D"	"0.696"	"0.414"	"C1837174"	"HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3"	"disease"	"C15"	"Disease or Syndrome"	"0.64"	"1"	"2004"	"2017"	"0"	"11"	"CTD_human"
"201305"	"SPNS3"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"201475"	"RAB12"	"1"	"0.034"	"C0151744"	"Myocardial Ischemia"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"201595"	"STT3B"	"0.743"	"0.345"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"201595"	"STT3B"	"0.743"	"0.345"	"C2931007"	"Congenital disorder of glycosylation type 1X"	"disease"	"C15;C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;ORPHANET"
"201595"	"STT3B"	"0.743"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"201626"	"PDE12"	"1"	"0.034"	"C0035235"	"Respiratory Syncytial Virus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"201626"	"PDE12"	"1"	"0.034"	"C0206617"	"Cardiovirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"201973"	"PRIMPOL"	"0.857"	"0.103"	"C3809464"	"MYOPIA 22, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"0"	"1"	"CTD_human;UNIPROT"
"202018"	"TAPT1"	"0.681"	"0.517"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"202018"	"TAPT1"	"0.681"	"0.517"	"C4225162"	"OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE"	"disease"		"Disease or Syndrome"	"0.70"		"2016"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"202018"	"TAPT1"	"0.681"	"0.517"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"202333"	"CMYA5"	"0.785"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2012"	"2015"	"3"	"0"	"PSYGENET"
"202333"	"CMYA5"	"0.785"	"0.345"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"202333"	"CMYA5"	"0.785"	"0.345"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"202374"	"STK32A"	"1"	"0.034"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"202559"	"KHDRBS2"	"0.857"	"0.172"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"203062"	"TSNARE1"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2013"	"2018"	"1"	"4"	"PSYGENET"
"203068"	"TUBB"	"0.611"	"0.655"	"C0473586"	"Michelin tire baby syndrome"	"disease"	"C04;C16;C17"	"Disease or Syndrome"	"0.60"		"2002"	"2016"	"1"	"2"	"ORPHANET;UNIPROT"
"203068"	"TUBB"	"0.611"	"0.655"	"C4014283"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.70"	"0.9667897"	"2010"	"2018"	"1"	"9"	"CTD_human;ORPHANET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.8"	"2013"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.6666667"	"2012"	"2016"	"3"	"0"	"PSYGENET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"PSYGENET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.37"	"0.5"	"2013"	"2016"	"2"	"0"	"PSYGENET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0338462"	"Semantic Dementia"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.40"	"0.6666667"	"2012"	"2016"	"3"	"0"	"PSYGENET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0393554"	"Amyotrophic Lateral Sclerosis With Dementia"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0543859"	"Amyotrophic Lateral Sclerosis, Guam Form"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.31"	"0"	"2013"	"2018"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0751072"	"Frontotemporal Lobar Degeneration"	"disease"	"C10;C18;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9583333"	"2012"	"2018"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C0751706"	"Primary Progressive Nonfluent Aphasia"	"disease"	"C10;C18;C23;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C1862937"	"AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2013"	"0"	"1"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"203228"	"C9orf72"	"0.536"	"0.552"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"203228"	"C9orf72"	"0.536"	"0.552"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.59"	"0.8888889"	"2012"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"203228"	"C9orf72"	"0.536"	"0.552"	"C4011788"	"Behavioral variant of frontotemporal dementia"	"disease"		"Disease or Syndrome"	"0.40"	"1"	"2012"	"2016"	"0"	"0"	"ORPHANET"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0022679"	"Cystic kidney"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0085413"	"Polycystic Kidney, Autosomal Dominant"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.31"	"1"	"1997"	"2002"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0243050"	"Cardiovascular Abnormalities"	"group"	"C14;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C0887850"	"Polycystic Kidney, Type 1 Autosomal Dominant Disease"	"disease"	"C12;C13;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"203286"	"ANKS6"	"0.681"	"0.276"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"203286"	"ANKS6"	"0.681"	"0.276"	"C1865872"	"NEPHRONOPHTHISIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"203286"	"ANKS6"	"0.681"	"0.276"	"C2751306"	"Polycystic kidney disease, type 2"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"203286"	"ANKS6"	"0.681"	"0.276"	"C3809320"	"NEPHRONOPHTHISIS 16"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"5"	"CTD_human;UNIPROT"
"203286"	"ANKS6"	"0.681"	"0.276"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"203328"	"SUSD3"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"UNIPROT"
"203447"	"NRK"	"0.834"	"0.172"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"203447"	"NRK"	"0.834"	"0.172"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"203447"	"NRK"	"0.834"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"203522"	"INTS6L"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"203547"	"VMA21"	"0.834"	"0.172"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"203547"	"VMA21"	"0.834"	"0.172"	"C1839615"	"X-linked myopathy with excessive autophagy"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2015"	"0"	"7"	"CTD_human;ORPHANET"
"203547"	"VMA21"	"0.834"	"0.172"	"C2931230"	"Vacuolar myopathy"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2014"	"0"	"0"	"ORPHANET"
"203859"	"ANO5"	"0.645"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2007"	"2018"	"1"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2009"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.56"	"1"	"2010"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"203859"	"ANO5"	"0.645"	"0.448"	"C1833736"	"Osteogenesis imperfecta, Levin type"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.76"	"0.8333333"	"1969"	"2017"	"3"	"12"	"CTD_human;ORPHANET;UNIPROT"
"203859"	"ANO5"	"0.645"	"0.448"	"C1969785"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.92"	"1"	"1993"	"2017"	"4"	"42"	"CTD_human;ORPHANET;UNIPROT"
"203859"	"ANO5"	"0.645"	"0.448"	"C2750076"	"Miyoshi Muscular Dystrophy 3"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2014"	"2"	"16"	"CTD_human;ORPHANET;UNIPROT"
"203859"	"ANO5"	"0.645"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"204219"	"CERS3"	"0.72"	"0.414"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2013"	"2018"	"0"	"0"	"ORPHANET"
"204219"	"CERS3"	"0.72"	"0.414"	"C2750787"	"Weill-Marchesani-Like Syndrome"	"disease"	"C05;C11;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"204219"	"CERS3"	"0.72"	"0.414"	"C3554349"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"2"	"CTD_human"
"204474"	"PDILT"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"204851"	"HIPK1"	"0.785"	"0.138"	"C0238198"	"Gastrointestinal Stromal Tumors"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"204851"	"HIPK1"	"0.785"	"0.138"	"C3179349"	"Gastrointestinal Stromal Sarcoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"205428"	"C3orf58"	"0.785"	"0.345"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"205428"	"C3orf58"	"0.785"	"0.345"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"205428"	"C3orf58"	"0.785"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"207063"	"DHRSX"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"219285"	"SAMD9L"	"0.72"	"0.379"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"219285"	"SAMD9L"	"0.72"	"0.379"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"219285"	"SAMD9L"	"0.72"	"0.379"	"C0376545"	"Hematologic Neoplasms"	"group"	"C04;C15"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"219285"	"SAMD9L"	"0.72"	"0.379"	"C1327919"	"Myelocerebellar Disorder"	"disease"	"C10;C15;C23"	"Disease or Syndrome"	"0.70"		"1978"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"219287"	"AMER2"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"219621"	"CABCOCO1"	"1"	"0.034"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"219736"	"STOX1"	"0.834"	"0.172"	"C0032914"	"Pre-Eclampsia"	"phenotype"	"C13"	"Pathologic Function"	"0.61"		"2009"	"2009"	"0"	"0"	"CTD_human;ORPHANET"
"219736"	"STOX1"	"0.834"	"0.172"	"C1836255"	"Preeclampsia Eclampsia 4"	"disease"	"C13"	"Disease or Syndrome"	"0.40"		"2005"	"2007"	"1"	"4"	"UNIPROT"
"219749"	"ZNF25"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"219770"	"GJD4"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"219771"	"CCNY"	"0.72"	"0.207"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2011"	"1"	"1"	"CTD_human"
"219771"	"CCNY"	"0.72"	"0.207"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.42"	"1"	"2008"	"2011"	"1"	"2"	"CTD_human"
"219771"	"CCNY"	"0.72"	"0.207"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"219771"	"CCNY"	"0.72"	"0.207"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"219771"	"CCNY"	"0.72"	"0.207"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"219771"	"CCNY"	"0.72"	"0.207"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"219790"	"RTKN2"	"0.815"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2016"	"1"	"1"	"PSYGENET"
"219844"	"HYLS1"	"0.645"	"0.552"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"219844"	"HYLS1"	"0.645"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"219844"	"HYLS1"	"0.645"	"0.552"	"C0431399"	"Familial aplasia of the vermis"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"219844"	"HYLS1"	"0.645"	"0.552"	"C1856016"	"HYDROLETHALUS SYNDROME 1"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"2005"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"219844"	"HYLS1"	"0.645"	"0.552"	"C2931104"	"Hydrolethalus syndrome"	"disease"	"C05;C10;C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"2005"	"2009"	"0"	"1"	"ORPHANET"
"219844"	"HYLS1"	"0.645"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"219844"	"HYLS1"	"0.645"	"0.552"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"219902"	"TMEM136"	"1"	"0.034"	"C0206368"	"Exfoliation Syndrome"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"219972"	"MPEG1"	"0.672"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"219972"	"MPEG1"	"0.672"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"219972"	"MPEG1"	"0.672"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"219972"	"MPEG1"	"0.672"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"220074"	"LRTOMT"	"0.799"	"0.172"	"C1969621"	"DEAFNESS, AUTOSOMAL RECESSIVE 63"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.90"		"2008"	"2017"	"5"	"8"	"CLINGEN;CTD_human;UNIPROT"
"220136"	"CFAP53"	"0.799"	"0.138"	"C0037221"	"Situs Inversus"	"disease"	"C16"	"Congenital Abnormality"	"0.41"	"1"	"2015"	"2015"	"0"	"0"	"ORPHANET"
"220136"	"CFAP53"	"0.799"	"0.138"	"C0266642"	"Situs ambiguus"	"disease"	"C14;C15;C16"	"Congenital Abnormality"	"0.33"	"1"	"2013"	"2016"	"0"	"0"	"ORPHANET"
"220136"	"CFAP53"	"0.799"	"0.138"	"C1167664"	"Situs ambiguous"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"220136"	"CFAP53"	"0.799"	"0.138"	"C3553676"	"HETEROTAXY, VISCERAL, 6, AUTOSOMAL"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"220136"	"CFAP53"	"0.799"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"220202"	"ATOH7"	"0.762"	"0.172"	"C0266568"	"Persistent Hyperplastic Primary Vitreous"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"220202"	"ATOH7"	"0.762"	"0.172"	"C1857299"	"RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL"	"disease"	"C11"	"Congenital Abnormality"	"0.60"		"2001"	"2013"	"3"	"3"	"ORPHANET;UNIPROT"
"220202"	"ATOH7"	"0.762"	"0.172"	"C1867315"	"Retinal Nonattachment And Falciform Detachment"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"220202"	"ATOH7"	"0.762"	"0.172"	"C1969783"	"Persistent Hyperplastic Primary Vitreous, Autosomal Recessive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2013"	"3"	"2"	"UNIPROT"
"220202"	"ATOH7"	"0.762"	"0.172"	"C3151617"	"ANTERIOR SEGMENT DYSGENESIS 7"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C1854416"	"MACROCEPHALY/AUTISM SYNDROME"	"disease"	"C05;C10;C16;C23;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C1858854"	"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS"	"disease"	"C04;C10;C16;C18;C23"	"Congenital Abnormality"	"0.60"	"1"	"2011"	"2017"	"0"	"0"	"CTD_human;ORPHANET"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C3151355"	"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A"	"disease"		"Disease or Syndrome"	"0.40"		"1993"	"2011"	"1"	"6"	"UNIPROT"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C3151356"	"MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"4"	"CTD_human;UNIPROT"
"220296"	"HEPACAM"	"0.645"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"220929"	"ZNF438"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"220929"	"ZNF438"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"220972"	"MARCH8"	"0.672"	"0.552"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"220972"	"MARCH8"	"0.672"	"0.552"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"220988"	"HNRNPA3"	"0.773"	"0.276"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"CTD_human"
"221035"	"REEP3"	"0.886"	"0.103"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0012236"	"DiGeorge Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2012"	"1"	"9"	"CTD_human"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0220704"	"Shprintzen syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0431406"	"Asymmetric crying face association"	"disease"	"C07;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C0795907"	"CONOTRUNCAL ANOMALY FACE SYNDROME"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C1333813"	"Central Nervous System Germinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C2936346"	"22q11 Deletion Syndrome"	"disease"	"C05;C14;C15;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C3266101"	"22q11 partial monosomy syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2012"	"1"	"9"	"CTD_human"
"221037"	"JMJD1C"	"0.596"	"0.621"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.40"		"2009"	"2012"	"1"	"9"	"CTD_human"
"221074"	"SLC39A12"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"221074"	"SLC39A12"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"221078"	"NSUN6"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"221078"	"NSUN6"	"0.928"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"221078"	"NSUN6"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"221078"	"NSUN6"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"221078"	"NSUN6"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"221079"	"ARL5B"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"221264"	"AK9"	"1"	"0.069"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221294"	"NT5DC1"	"0.857"	"0.207"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"221322"	"TBC1D32"	"0.773"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"221357"	"GSTA5"			"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"221393"	"ADGRF4"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"221393"	"ADGRF4"	"0.928"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"221421"	"RSPH9"	"0.785"	"0.172"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.45"	"0.8"	"1993"	"2015"	"0"	"1"	"ORPHANET"
"221421"	"RSPH9"	"0.785"	"0.172"	"C2675228"	"CILIARY DYSKINESIA, PRIMARY, 12"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.40"		"2009"	"2013"	"0"	"3"	"CTD_human"
"221421"	"RSPH9"	"0.785"	"0.172"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"221421"	"RSPH9"	"0.785"	"0.172"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"221458"	"KIF6"	"0.752"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"221458"	"KIF6"	"0.752"	"0.241"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"221472"	"FGD2"	"0.928"	"0.103"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"221472"	"FGD2"	"0.928"	"0.103"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"221496"	"LEMD2"	"0.815"	"0.207"	"C0220721"	"CATARACT 46, JUVENILE-ONSET"	"disease"		"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"1"	"CTD_human;UNIPROT"
"221496"	"LEMD2"	"0.815"	"0.207"	"C0266539"	"Congenital total cataract"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"221687"	"RNF182"	"0.857"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221687"	"RNF182"	"0.857"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2008"	"2008"	"1"	"0"	"CTD_human;UNIPROT"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.34"	"1"	"2011"	"2017"	"3"	"0"	"CTD_human"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.47"	"1"	"2009"	"2017"	"2"	"2"	"CTD_human"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C0338480"	"Common Migraine"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2012"	"2017"	"1"	"1"	"CTD_human"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C0751814"	"Cerebrovascular Trauma"	"disease"	"C10;C14;C26"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.48"	"0.875"	"2011"	"2018"	"3"	"2"	"CTD_human"
"221692"	"PHACTR1"	"0.752"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"221749"	"PXDC1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"221833"	"SP8"	"0.928"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"221833"	"SP8"	"0.928"	"0.034"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"221833"	"SP8"	"0.928"	"0.034"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.50"	"0.9375"	"2008"	"2018"	"1"	"4"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.43"	"0.6666667"	"2009"	"2016"	"1"	"3"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0206630"	"Endometrial Stromal Sarcoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.40"	"0.9"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.37"	"0.8571429"	"2008"	"2015"	"1"	"0"	"CTD_human"
"221895"	"JAZF1"	"0.616"	"0.448"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"221914"	"GPC2"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2001"	"2001"	"0"	"0"	"UNIPROT"
"221927"	"BRAT1"	"0.785"	"0.069"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"221927"	"BRAT1"	"0.785"	"0.069"	"C3281029"	"RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2017"	"0"	"8"	"ORPHANET"
"221927"	"BRAT1"	"0.785"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"222256"	"CDHR3"	"0.886"	"0.069"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2015"	"1"	"1"	"CTD_human"
"222389"	"BEND7"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"222537"	"HS3ST5"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"222546"	"RFX6"	"0.713"	"0.241"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"222546"	"RFX6"	"0.713"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"222546"	"RFX6"	"0.713"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"222546"	"RFX6"	"0.713"	"0.241"	"C2748662"	"Mitchell-Riley Syndrome"	"disease"	"C06;C16;C18;C19"	"Disease or Syndrome"	"0.72"	"1"	"2005"	"2017"	"2"	"10"	"CTD_human;ORPHANET;UNIPROT"
"222546"	"RFX6"	"0.713"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"222643"	"UNC5CL"	"0.928"	"0.069"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"222662"	"LHFPL5"	"0.886"	"0.103"	"C1853223"	"Deafness, Autosomal Recessive 67"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2006"	"2017"	"3"	"4"	"CTD_human;UNIPROT"
"222698"	"NKAPL"	"0.928"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.43"	"1"	"2012"	"2015"	"1"	"1"	"CTD_human"
"222894"	"FERD3L"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"223075"	"CCDC129"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"223117"	"SEMA3D"	"0.713"	"0.345"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.41"	"1"	"2012"	"2012"	"0"	"0"	"ORPHANET"
"223117"	"SEMA3D"	"0.713"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"223117"	"SEMA3D"	"0.713"	"0.345"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"223117"	"SEMA3D"	"0.713"	"0.345"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2018"	"2"	"0"	"GENOMICS_ENGLAND"
"225689"	"MAPK15"	"0.834"	"0.172"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"225689"	"MAPK15"	"0.834"	"0.172"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"245806"	"VGLL2"	"0.886"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"245812"	"CNPY4"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"245972"	"ATP6V0D2"	"0.834"	"0.207"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"245972"	"ATP6V0D2"	"0.834"	"0.207"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"245972"	"ATP6V0D2"	"0.834"	"0.207"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"245972"	"ATP6V0D2"	"0.834"	"0.207"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"245972"	"ATP6V0D2"	"0.834"	"0.207"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"246213"	"SLC17A8"	"0.735"	"0.31"	"C1854158"	"DEAFNESS, AUTOSOMAL DOMINANT 25 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"2008"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"246243"	"RNASEH1"	"0.743"	"0.276"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"246243"	"RNASEH1"	"0.743"	"0.276"	"C4225312"	"PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"246243"	"RNASEH1"	"0.743"	"0.276"	"C4511138"	"Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"246269"	"AFG1L"	"1"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"246329"	"STAC3"	"0.696"	"0.414"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"246329"	"STAC3"	"0.696"	"0.414"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"246329"	"STAC3"	"0.696"	"0.414"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"246329"	"STAC3"	"0.696"	"0.414"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"246329"	"STAC3"	"0.696"	"0.414"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"246329"	"STAC3"	"0.696"	"0.414"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"246329"	"STAC3"	"0.696"	"0.414"	"C1850625"	"Native American myopathy"	"disease"	"C05;C07;C10;C16;C23"	"Disease or Syndrome"	"0.73"	"1"	"2013"	"2018"	"2"	"1"	"CTD_human;ORPHANET;UNIPROT"
"246744"	"STH"	"0.735"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"PSYGENET"
"246778"	"IL27"	"0.532"	"0.724"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2013"	"1"	"1"	"CTD_human"
"246778"	"IL27"	"0.532"	"0.724"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2014"	"2"	"0"	"CTD_human"
"246778"	"IL27"	"0.532"	"0.724"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"246778"	"IL27"	"0.532"	"0.724"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"246778"	"IL27"	"0.532"	"0.724"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2015"	"2"	"0"	"CTD_human"
"246778"	"IL27"	"0.532"	"0.724"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253012"	"HEPACAM2"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"253017"	"TECRL"	"0.799"	"0.172"	"C0340485"	"Familial ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"253017"	"TECRL"	"0.799"	"0.172"	"C1631597"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"253017"	"TECRL"	"0.799"	"0.172"	"C2677794"	"Stress-induced polymorphic ventricular tachycardia"	"disease"	"C14;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"253017"	"TECRL"	"0.799"	"0.172"	"C3151463"	"VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3"	"disease"		"Disease or Syndrome"	"0.40"		"2007"	"2017"	"1"	"2"	"UNIPROT"
"253260"	"RICTOR"	"0.656"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"253260"	"RICTOR"	"0.656"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"253260"	"RICTOR"	"0.656"	"0.379"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"CGI"
"253512"	"SLC25A30"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"253650"	"ANKRD18A"	"1"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"253650"	"ANKRD18A"	"1"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"253738"	"EBF3"	"0.645"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"253738"	"EBF3"	"0.645"	"0.517"	"C4310618"	"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"3"	"10"	"CTD_human;UNIPROT"
"253782"	"CERS6"	"0.696"	"0.379"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253782"	"CERS6"	"0.696"	"0.379"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"253827"	"MSRB3"	"0.799"	"0.241"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"253827"	"MSRB3"	"0.799"	"0.241"	"C2239351"	"DEAFNESS, AUTOSOMAL RECESSIVE 74"	"disease"		"Disease or Syndrome"	"0.81"	"1"	"2010"	"2014"	"1"	"2"	"CTD_human;UNIPROT"
"254065"	"BRWD3"	"0.743"	"0.379"	"C1970841"	"MENTAL RETARDATION, X-LINKED 93 (disorder)"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"		"1994"	"2014"	"1"	"5"	"CTD_human;UNIPROT"
"254065"	"BRWD3"	"0.743"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"254158"	"CXorf58"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"254173"	"TTLL10"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"254251"	"LCORL"			"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.40"		"2013"	"2017"	"1"	"2"	"CTD_human"
"254394"	"MCM9"	"0.785"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"254394"	"MCM9"	"0.785"	"0.276"	"C4015409"	"OVARIAN DYSGENESIS 4"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2017"	"0"	"3"	"CTD_human;ORPHANET"
"254428"	"SLC41A1"	"0.834"	"0.172"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.45"	"1"	"2011"	"2017"	"3"	"2"	"GENOMICS_ENGLAND"
"254528"	"MEIOB"	"0.886"	"0.034"	"C4540179"	"SPERMATOGENIC FAILURE 22"	"disease"		"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"UNIPROT"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"254887"	"ZDHHC23"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"255022"	"CALHM1"	"0.815"	"0.207"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"255022"	"CALHM1"	"0.815"	"0.207"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"255082"	"CASC2"	"0.707"	"0.207"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2004"	"2015"	"0"	"0"	"UNIPROT"
"255101"	"CFAP65"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8"	"2005"	"2015"	"5"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2011"	"2012"	"3"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0006870"	"Cannabis Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2014"	"2"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0023015"	"Language Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0024809"	"Marijuana Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.02"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.38"	"1"	"2007"	"2016"	"2"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0345958"	"Large cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0454560"	"Acquired Language Disorders"	"group"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"255239"	"ANKK1"	"0.624"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"255239"	"ANKK1"	"0.624"	"0.414"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"255738"	"PCSK9"	"0.572"	"0.552"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.40"	"0.9545455"	"2005"	"2016"	"2"	"0"	"CTD_human"
"255738"	"PCSK9"	"0.572"	"0.552"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.50"	"0.9166667"	"2003"	"2017"	"1"	"0"	"CTD_human"
"255738"	"PCSK9"	"0.572"	"0.552"	"C0342881"	"Familial hypercholesterolemia - homozygous"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"255738"	"PCSK9"	"0.572"	"0.552"	"C1863551"	"HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3"	"disease"	"C18"	"Disease or Syndrome"	"0.60"		"1993"	"2018"	"3"	"9"	"CTD_human;UNIPROT"
"255738"	"PCSK9"	"0.572"	"0.552"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.50"	"0.969697"	"2006"	"2018"	"2"	"1"	"CTD_human"
"255738"	"PCSK9"	"0.572"	"0.552"	"C3276239"	"LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1"	"phenotype"		"Finding"	"0.40"		"2003"	"2014"	"3"	"9"	"UNIPROT"
"255758"	"TCTEX1D2"	"0.799"	"0.103"	"C0024507"	"Majewski Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255758"	"TCTEX1D2"	"0.799"	"0.103"	"C0036069"	"Saldino-Noonan Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255758"	"TCTEX1D2"	"0.799"	"0.103"	"C0036996"	"Short Rib-Polydactyly Syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"255758"	"TCTEX1D2"	"0.799"	"0.103"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"255758"	"TCTEX1D2"	"0.799"	"0.103"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"255928"	"SYT14"	"0.727"	"0.138"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"255928"	"SYT14"	"0.727"	"0.138"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"255928"	"SYT14"	"0.727"	"0.138"	"C3280226"	"SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11"	"disease"		"Disease or Syndrome"	"0.60"		"2011"	"2011"	"1"	"1"	"ORPHANET;UNIPROT"
"255928"	"SYT14"	"0.727"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2007"	"2007"	"1"	"0"	"GENOMICS_ENGLAND"
"256297"	"PTF1A"	"0.663"	"0.414"	"C0007760"	"Cerebellar Diseases"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2005"	"2009"	"2"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2005"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"256297"	"PTF1A"	"0.663"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"256297"	"PTF1A"	"0.663"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C1836780"	"PANCREATIC AND CEREBELLAR AGENESIS"	"disease"	"C13;C16;C18;C19;C23"	"Disease or Syndrome"	"0.61"	"1"	"1999"	"2009"	"2"	"1"	"CTD_human;ORPHANET"
"256297"	"PTF1A"	"0.663"	"0.414"	"C1850096"	"Pancreatic Agenesis, Congenital"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"2005"	"2014"	"2"	"0"	"CTD_human;ORPHANET"
"256297"	"PTF1A"	"0.663"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"1999"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"256297"	"PTF1A"	"0.663"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256297"	"PTF1A"	"0.663"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256471"	"MFSD8"	"0.672"	"0.172"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"256471"	"MFSD8"	"0.672"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"256471"	"MFSD8"	"0.672"	"0.172"	"C1838571"	"Ceroid Lipofuscinosis, Neuronal, 7"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.95"	"1"	"1993"	"2018"	"7"	"15"	"CTD_human;ORPHANET;UNIPROT"
"256471"	"MFSD8"	"0.672"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"256471"	"MFSD8"	"0.672"	"0.172"	"C4015371"	"MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"256472"	"TMEM151A"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256472"	"TMEM151A"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256536"	"TCERG1L"	"0.815"	"0.172"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"256536"	"TCERG1L"	"0.815"	"0.172"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256536"	"TCERG1L"	"0.815"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.51"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human;UNIPROT"
"256646"	"NUTM1"	"0.762"	"0.138"	"C1707291"	"NUT midline carcinoma"	"disease"		"Neoplastic Process"	"0.40"	"1"	"2010"	"2018"	"0"	"0"	"ORPHANET"
"256714"	"MAP7D2"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"256764"	"WDR72"	"0.785"	"0.069"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.63"	"1"	"2009"	"2017"	"7"	"1"	"GENOMICS_ENGLAND"
"256764"	"WDR72"	"0.785"	"0.069"	"C0399372"	"Amelogenesis Imperfecta hypomaturation type"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"256764"	"WDR72"	"0.785"	"0.069"	"C2750771"	"Amelogenesis Imperfecta, Hypomaturation Type, Iia3"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2015"	"0"	"4"	"CTD_human"
"256933"	"NPB"	"0.886"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256933"	"NPB"	"0.886"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"256957"	"HEATR9"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"257019"	"FRMD3"	"0.727"	"0.345"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"257044"	"CATSPERE"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"257101"	"ZNF683"	"0.886"	"0.103"	"C0263454"	"Chloracne"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"257106"	"ARHGAP30"	"0.834"	"0.138"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"257106"	"ARHGAP30"	"0.834"	"0.138"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"257106"	"ARHGAP30"	"0.834"	"0.138"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"257194"	"NEGR1"	"0.815"	"0.276"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.40"	"0.9230769"	"2009"	"2016"	"1"	"0"	"CTD_human"
"257202"	"GPX6"	"0.834"	"0.276"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"257240"	"KLHL34"	"0.886"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"259173"	"ALS2CL"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"259173"	"ALS2CL"	"0.857"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"259197"	"NCR3"	"0.735"	"0.483"	"C0024530"	"Malaria"	"disease"	"C03"	"Disease or Syndrome"	"0.33"	"1"	"2007"	"2017"	"0"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2005"	"2005"	"1"	"0"	"PSYGENET"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259217"	"HSPA12A"	"0.773"	"0.138"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"259232"	"NALCN"	"0.609"	"0.586"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"259232"	"NALCN"	"0.609"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"259232"	"NALCN"	"0.609"	"0.586"	"C0220662"	"ARTHROGRYPOSIS, DISTAL, TYPE 1"	"disease"	"C05;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"259232"	"NALCN"	"0.609"	"0.586"	"C0265224"	"Freeman-Sheldon syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"259232"	"NALCN"	"0.609"	"0.586"	"C1834523"	"ARTHROGRYPOSIS, DISTAL, TYPE 2B"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"259232"	"NALCN"	"0.609"	"0.586"	"C1852085"	"Digitotalar Dysmorphism"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"259232"	"NALCN"	"0.609"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"259232"	"NALCN"	"0.609"	"0.586"	"C3809454"	"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2014"	"2"	"3"	"CTD_human;UNIPROT"
"259232"	"NALCN"	"0.609"	"0.586"	"C4225398"	"CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2015"	"2017"	"1"	"17"	"CTD_human;UNIPROT"
"259236"	"TMIE"	"0.857"	"0.172"	"C1832992"	"DEAFNESS, AUTOSOMAL RECESSIVE 6"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"1996"	"2009"	"1"	"6"	"CTD_human;UNIPROT"
"259266"	"ASPM"	"0.586"	"0.69"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.59"	"1"	"2004"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"259266"	"ASPM"	"0.586"	"0.69"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C0036095"	"Salivary Gland Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C0220636"	"Malignant neoplasm of salivary gland"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.37"	"1"	"2004"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"259266"	"ASPM"	"0.586"	"0.69"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C1837501"	"Microcephaly, Primary Autosomal Recessive, 5"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2018"	"0"	"127"	"CTD_human"
"259266"	"ASPM"	"0.586"	"0.69"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"259266"	"ASPM"	"0.586"	"0.69"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"	"1"	"2001"	"2015"	"0"	"1"	"ORPHANET"
"259266"	"ASPM"	"0.586"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2004"	"2004"	"0"	"0"	"GENOMICS_ENGLAND"
"259282"	"BOD1L1"	"0.886"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"261734"	"NPHP4"	"0.681"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"261734"	"NPHP4"	"0.681"	"0.31"	"C0403553"	"Renal dysplasia and retinal aplasia (disorder)"	"disease"	"C10;C11;C12;C13;C16"	"Disease or Syndrome"	"0.33"	"1"	"2002"	"2007"	"0"	"0"	"ORPHANET"
"261734"	"NPHP4"	"0.681"	"0.31"	"C1112213"	"Cholestasis in newborn"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"261734"	"NPHP4"	"0.681"	"0.31"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"261734"	"NPHP4"	"0.681"	"0.31"	"C1846979"	"SENIOR-LOKEN SYNDROME 4"	"disease"	"C11;C12;C13;C16"	"Disease or Syndrome"	"0.60"		"1976"	"2015"	"4"	"7"	"CTD_human;UNIPROT"
"261734"	"NPHP4"	"0.681"	"0.31"	"C1847013"	"NEPHRONOPHTHISIS 4"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.80"		"2002"	"2015"	"6"	"16"	"CTD_human;UNIPROT"
"261734"	"NPHP4"	"0.681"	"0.31"	"C1855681"	"Nephronophthisis, familial juvenile"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"261734"	"NPHP4"	"0.681"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"261734"	"NPHP4"	"0.681"	"0.31"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"GENOMICS_ENGLAND"
"266553"	"OFCC1"	"0.857"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"266727"	"MDGA1"	"0.815"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"266727"	"MDGA1"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2011"	"2"	"0"	"PSYGENET"
"266727"	"MDGA1"	"0.815"	"0.138"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"266727"	"MDGA1"	"0.815"	"0.138"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"266743"	"NPAS4"	"0.815"	"0.138"	"C0005587"	"Depression, Bipolar"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"266743"	"NPAS4"	"0.815"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"266812"	"NAP1L5"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"267004"	"PGBD3"	"0.676"	"0.414"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"267012"	"DAOA"	"0.681"	"0.172"	"C0001723"	"Affective Disorders, Psychotic"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2010"	"2011"	"2"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2014"	"5"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2009"	"2016"	"2"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.8780488"	"2002"	"2018"	"0"	"0"	"CTD_human"
"267012"	"DAOA"	"0.681"	"0.172"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"0.8"	"2010"	"2015"	"5"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"2006"	"2011"	"5"	"0"	"PSYGENET"
"267012"	"DAOA"	"0.681"	"0.172"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.8"	"2011"	"2015"	"5"	"0"	"PSYGENET"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0009714"	"Hepatic Fibrosis, Congenital"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0016470"	"Food Allergy"	"group"	"C20"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0019196"	"Hepatitis C"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"0.960452"	"2009"	"2018"	"0"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"282617"	"IFNL3"	"0.557"	"0.793"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"0"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"282706"	"DAOA-AS1"	"0.713"	"0.138"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.36"	"1"	"2003"	"2014"	"5"	"0"	"PSYGENET"
"282706"	"DAOA-AS1"	"0.713"	"0.138"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"0.5"	"2009"	"2010"	"2"	"0"	"PSYGENET"
"282706"	"DAOA-AS1"	"0.713"	"0.138"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"282706"	"DAOA-AS1"	"0.713"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"1"	"2004"	"2014"	"4"	"0"	"PSYGENET"
"282775"	"OR5J2"			"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C0009241"	"Cognition Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C0282631"	"Facies"	"group"	"C23"	"Organism Attribute"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C1845285"	"Martin-Probst Deafness-Mental Retardation Syndrome"	"disease"	"C09;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"1"	"CTD_human;UNIPROT"
"282808"	"RAB40AL"	"0.834"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2000"	"2016"	"6"	"0"	"GENOMICS_ENGLAND"
"282809"	"POC1B"	"0.752"	"0.241"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2015"	"0"	"0"	"ORPHANET"
"282809"	"POC1B"	"0.752"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"282809"	"POC1B"	"0.752"	"0.241"	"C4014856"	"CONE-ROD DYSTROPHY 20"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"3"	"3"	"CTD_human;UNIPROT"
"282809"	"POC1B"	"0.752"	"0.241"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"GENOMICS_ENGLAND"
"282973"	"JAKMIP3"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"282974"	"STK32C"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"282991"	"BLOC1S2"	"0.785"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"282996"	"RBM20"	"0.785"	"0.138"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2009"	"2017"	"0"	"5"	"GENOMICS_ENGLAND"
"282996"	"RBM20"	"0.785"	"0.138"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"282996"	"RBM20"	"0.785"	"0.138"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"282996"	"RBM20"	"0.785"	"0.138"	"C0340427"	"Familial dilated cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2016"	"0"	"1"	"ORPHANET"
"282996"	"RBM20"	"0.785"	"0.138"	"C2750995"	"Cardiomyopathy, Dilated, 1DD"	"disease"	"C14"	"Disease or Syndrome"	"0.60"		"1990"	"2017"	"4"	"7"	"CTD_human;UNIPROT"
"283008"	"NUTM2E"	"1"	"0.103"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"283092"	"OR4C13"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283092"	"OR4C13"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283092"	"OR4C13"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283092"	"OR4C13"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283092"	"OR4C13"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283092"	"OR4C13"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"283106"	"CSNK2A3"	"0.834"	"0.069"	"C0684249"	"Carcinoma of lung"	"disease"		"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"1"	"1"	"UNIPROT"
"283120"	"H19"	"0.525"	"0.759"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.40"	"0.952381"	"1994"	"2016"	"0"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"0.8"	"1996"	"2018"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0019188"	"Hepatitis, Animal"	"disease"	"C06;C22"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0027708"	"Nephroblastoma"	"disease"	"C04;C12;C13;C16"	"Neoplastic Process"	"0.66"	"0.8333333"	"1993"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"283120"	"H19"	"0.525"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2001"	"2001"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C0175693"	"Russell-Silver syndrome"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"	"0.9285714"	"1997"	"2015"	"3"	"0"	"CTD_human;GENOMICS_ENGLAND"
"283120"	"H19"	"0.525"	"0.759"	"C0332890"	"Congenital hemihypertrophy"	"disease"		"Congenital Abnormality"	"0.41"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"283120"	"H19"	"0.525"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.37"	"0.8571429"	"1996"	"2018"	"1"	"1"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"1996"	"2018"	"1"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C1853800"	"Familial Wilms tumor 2"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"283120"	"H19"	"0.525"	"0.759"	"C1856184"	"HEMIHYPERPLASIA, ISOLATED"	"disease"	"C23"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2016"	"0"	"0"	"ORPHANET"
"283120"	"H19"	"0.525"	"0.759"	"C2930471"	"Bilateral Wilms Tumor"	"disease"	"C04;C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"283130"	"SLC25A45"	"0.886"	"0.103"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2018"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283131"	"NEAT1"	"0.645"	"0.517"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283234"	"CCDC88B"	"0.928"	"0.069"	"C0023343"	"Leprosy"	"disease"	"C01"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human"
"283237"	"TTC9C"	"0.928"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"283237"	"TTC9C"	"0.928"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"283238"	"SLC22A24"	"0.886"	"0.069"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"283238"	"SLC22A24"	"0.886"	"0.069"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"283238"	"SLC22A24"	"0.886"	"0.069"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2014"	"2016"	"2"	"0"	"CTD_human"
"283310"	"OTOGL"	"0.815"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"283310"	"OTOGL"	"0.815"	"0.241"	"C3554159"	"DEAFNESS, AUTOSOMAL RECESSIVE 84B"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"5"	"CTD_human"
"283310"	"OTOGL"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283316"	"CD163L1"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"283375"	"SLC39A5"	"0.886"	"0.034"	"C4014762"	"MYOPIA 24, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.60"		"2015"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"283417"	"DPY19L2"	"0.928"	"0.034"	"C3151407"	"SPERMATOGENIC FAILURE 9"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"5"	"CTD_human"
"283446"	"MYO1H"	"0.886"	"0.138"	"C1275808"	"Congenital central hypoventilation"	"disease"	"C08;C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"283450"	"HECTD4"	"0.743"	"0.276"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"283450"	"HECTD4"	"0.743"	"0.276"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"283455"	"KSR2"	"0.752"	"0.241"	"C0028756"	"Obesity, Morbid"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"283455"	"KSR2"	"0.752"	"0.241"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"283459"	"GATC"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283463"	"MUC19"	"0.799"	"0.31"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.40"		"2011"	"2012"	"1"	"1"	"CTD_human"
"283489"	"CHAMP1"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2015"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"283489"	"CHAMP1"	"0.735"	"0.31"	"C4225275"	"MENTAL RETARDATION, AUTOSOMAL DOMINANT 40"	"disease"		"Disease or Syndrome"	"0.40"		"2012"	"2015"	"0"	"6"	"CTD_human"
"283571"	"PROX2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283652"	"SLC24A5"	"0.762"	"0.31"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"2013"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"283652"	"SLC24A5"	"0.762"	"0.31"	"C2673809"	"Infantile nystagmus"	"phenotype"		"Finding"	"0.30"		"2013"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"283652"	"SLC24A5"	"0.762"	"0.31"	"C2676042"	"Skin-Hair-Eye Pigmentation, Variation In, 4"	"phenotype"	"C16;C17;C23"	"Finding"	"0.40"		"2005"	"2017"	"0"	"2"	"CTD_human"
"283652"	"SLC24A5"	"0.762"	"0.31"	"C3695272"	"Oculocutaneous albinism type 6"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"283659"	"PRTG"	"0.857"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"283748"	"PLA2G4D"	"0.886"	"0.138"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"283849"	"EXOC3L1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"2"	"UNIPROT"
"283871"	"PGP"	"0.672"	"0.379"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"1994"	"1995"	"2"	"0"	"PSYGENET"
"283927"	"NUDT7"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"283927"	"NUDT7"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0011168"	"Deglutition Disorders"	"group"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0018975"	"Hemeralopia"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0026650"	"Movement Disorders"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0035410"	"Rhabdomyolysis"	"phenotype"	"C05"	"Pathologic Function"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0042790"	"Vision Disorders"	"group"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0233769"	"Micropsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0233771"	"Macropsia"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2009"	"2015"	"4"	"1"	"GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0266487"	"Etat Marbre"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0267071"	"Oropharyngeal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0267072"	"Esophageal Dysphagia"	"disease"	"C06;C09"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0271185"	"Metamorphopsia"	"phenotype"	"C10;C11;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C1843504"	"Pontocerebellar Hypoplasia Type 1"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"283989"	"TSEN54"	"0.667"	"0.345"	"C1848526"	"Pontocerebellar Hypoplasia Type 2A"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2015"	"2"	"5"	"CTD_human;UNIPROT"
"283989"	"TSEN54"	"0.667"	"0.345"	"C1856974"	"PONTOCEREBELLAR HYPOPLASIA TYPE 4 (disorder)"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.71"	"1"	"1993"	"2015"	"2"	"5"	"CTD_human;ORPHANET;UNIPROT"
"283989"	"TSEN54"	"0.667"	"0.345"	"C1857762"	"Olivopontocerebellar hypoplasia, fetal-onset"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.41"	"1"	"2006"	"2011"	"0"	"2"	"ORPHANET"
"283989"	"TSEN54"	"0.667"	"0.345"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C2932714"	"Pontocerebellar Hypoplasia Type 2"	"disease"	"C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.33"	"1"	"2010"	"2014"	"0"	"0"	"ORPHANET"
"283989"	"TSEN54"	"0.667"	"0.345"	"C3489704"	"Vision Disability"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C3665347"	"Visual Impairment"	"phenotype"	"C10;C11;C23"	"Finding"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"283989"	"TSEN54"	"0.667"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2009"	"2009"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"283989"	"TSEN54"	"0.667"	"0.345"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284013"	"VMO1"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0026825"	"Flaccid Muscle Tone"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0026827"	"Muscle hypotonia"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0427201"	"Floppy Muscles"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0427202"	"Muscle Tone Atonic"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0751330"	"Unilateral Hypotonia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C1860789"	"Leukemia, Megakaryoblastic, of Down Syndrome"	"disease"	"C04;C10;C16"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C1864871"	"Chromosome 17q21.31 Deletion Syndrome"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.64"	"0.75"	"1993"	"2018"	"0"	"9"	"CTD_human;ORPHANET"
"284058"	"KANSL1"	"0.624"	"0.552"	"C2267233"	"Neonatal Hypotonia"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C2931713"	"Chromosome 17 deletion"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C3683846"	"Chromosome 17p Deletion Syndrome"	"disease"	"C10;C16;C23"	"Cell or Molecular Dysfunction"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"284058"	"KANSL1"	"0.624"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.65"	"1"	"2012"	"2018"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"284086"	"NEK8"	"0.685"	"0.379"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"284086"	"NEK8"	"0.685"	"0.379"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.34"	"1"	"2008"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"284086"	"NEK8"	"0.685"	"0.379"	"C1865872"	"NEPHRONOPHTHISIS 2"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284086"	"NEK8"	"0.685"	"0.379"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284086"	"NEK8"	"0.685"	"0.379"	"C2673883"	"RENAL-HEPATIC-PANCREATIC DYSPLASIA"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284086"	"NEK8"	"0.685"	"0.379"	"C3151188"	"NEPHRONOPHTHISIS 9"	"disease"		"Disease or Syndrome"	"0.62"	"1"	"2008"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"284086"	"NEK8"	"0.685"	"0.379"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.34"	"1"	"2010"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"284098"	"PIGW"	"0.785"	"0.207"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"284098"	"PIGW"	"0.785"	"0.207"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284098"	"PIGW"	"0.785"	"0.207"	"C1853205"	"Glycosylphosphatidylinositol deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284098"	"PIGW"	"0.785"	"0.207"	"C1855923"	"Hyperphosphatasia with Mental Retardation"	"disease"	"C10;C16;C18;C23;F01;F03"	"Disease or Syndrome"	"0.51"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human;ORPHANET"
"284098"	"PIGW"	"0.785"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"284098"	"PIGW"	"0.785"	"0.207"	"C4014958"	"HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"1"	"2"	"UNIPROT"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C0406740"	"Kohlschutter Tonz syndrome"	"disease"	"C07;C10;C16;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2014"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C1291560"	"Deficiency of glutamate decarboxylase"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C1849508"	"EPILEPSY, PYRIDOXINE-DEPENDENT"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"284111"	"SLC13A5"	"0.659"	"0.414"	"C4014621"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"2"	"10"	"CTD_human;UNIPROT"
"284119"	"CAVIN1"	"0.621"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"284119"	"CAVIN1"	"0.621"	"0.552"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"284119"	"CAVIN1"	"0.621"	"0.552"	"C0268583"	"Methylmalonic acidemia"	"phenotype"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"284119"	"CAVIN1"	"0.621"	"0.552"	"C1855119"	"Methylmalonic aciduria"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"284119"	"CAVIN1"	"0.621"	"0.552"	"C2750069"	"Lipodystrophy, Congenital Generalized, Type 4"	"disease"	"C16;C17;C18"	"Disease or Syndrome"	"0.73"	"1"	"2008"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"284207"	"METRNL"	"0.928"	"0.103"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0400966"	"Non-alcoholic Fatty Liver Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C3241937"	"Nonalcoholic Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284217"	"LAMA1"	"0.663"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"284217"	"LAMA1"	"0.663"	"0.552"	"C4014821"	"PORETTI-BOLTSHAUSER SYNDROME"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2014"	"0"	"8"	"ORPHANET"
"284252"	"KCTD1"	"0.713"	"0.586"	"C1867020"	"SCALP-EAR-NIPPLE SYNDROME"	"disease"	"C10;C12;C13;C16;C23"	"Disease or Syndrome"	"0.71"	"1"	"1992"	"2013"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"284252"	"KCTD1"	"0.713"	"0.586"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284276"	"LINC00908"			"C0005612"	"Birth Weight"	"phenotype"	"C23"	"Organism Attribute"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"284276"	"LINC00908"			"C0015934"	"Fetal Growth Retardation"	"phenotype"	"C13;C16;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"284382"	"ACTL9"	"0.886"	"0.172"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.32"	"0.5"	"2013"	"2015"	"1"	"0"	"CTD_human"
"284382"	"ACTL9"	"0.886"	"0.172"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284382"	"ACTL9"	"0.886"	"0.172"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"284403"	"WDR62"	"0.619"	"0.517"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.56"	"0.8333333"	"2010"	"2015"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.32"	"1"	"2014"	"2017"	"0"	"0"	"GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C1858535"	"MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 2 (disorder)"	"disease"		"Disease or Syndrome"	"0.40"		"2000"	"2015"	"4"	"23"	"UNIPROT"
"284403"	"WDR62"	"0.619"	"0.517"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C3501830"	"Microcephaly, Primary Autosomal Recessive, 2"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"284403"	"WDR62"	"0.619"	"0.517"	"C3711387"	"Autosomal Recessive Primary Microcephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.35"	"1"	"2000"	"2014"	"0"	"0"	"ORPHANET"
"284403"	"WDR62"	"0.619"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.60"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"284403"	"WDR62"	"0.619"	"0.517"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"284439"	"SLC25A42"	"1"	"0.069"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"284439"	"SLC25A42"	"1"	"0.069"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"284439"	"SLC25A42"	"1"	"0.069"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284611"	"FAM102B"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"284615"	"ANKRD34A"	"1"	"0.069"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284615"	"ANKRD34A"	"1"	"0.069"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284654"	"RSPO1"	"0.645"	"0.414"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2008"	"0"	"0"	"GENOMICS_ENGLAND"
"284654"	"RSPO1"	"0.645"	"0.414"	"C0036875"	"Disorders of Sex Development"	"group"	"C12;C13;C16;C19"	"Congenital Abnormality"	"0.31"	"1"	"2007"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"284654"	"RSPO1"	"0.645"	"0.414"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"284654"	"RSPO1"	"0.645"	"0.414"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.41"	"1"	"2015"	"2017"	"1"	"2"	"CTD_human"
"284654"	"RSPO1"	"0.645"	"0.414"	"C2674504"	"Palmoplantar Hyperkeratosis And True Hermaphroditism"	"disease"	"C12;C13;C16;C17;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"284654"	"RSPO1"	"0.645"	"0.414"	"C3149931"	"PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"284654"	"RSPO1"	"0.645"	"0.414"	"C3502495"	"Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal"	"disease"	"C04;C12;C13;C16;C17;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"284656"	"EPHA10"	"0.815"	"0.138"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"284656"	"EPHA10"	"0.815"	"0.138"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"284996"	"RNF149"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"285025"	"CCDC141"	"0.762"	"0.241"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"285025"	"CCDC141"	"0.762"	"0.241"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"CTD_human"
"285172"	"FAM126B"	"0.928"	"0.138"	"C0043094"	"Weight Gain"	"phenotype"	"C23"	"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"285175"	"UNC80"	"0.696"	"0.276"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285175"	"UNC80"	"0.696"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285175"	"UNC80"	"0.696"	"0.276"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"285175"	"UNC80"	"0.696"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2018"	"3"	"0"	"GENOMICS_ENGLAND"
"285175"	"UNC80"	"0.696"	"0.276"	"C4225203"	"HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2018"	"2"	"13"	"CTD_human;UNIPROT"
"285195"	"SLC9A9"	"0.707"	"0.31"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"285195"	"SLC9A9"	"0.707"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285203"	"EOGT"	"0.696"	"0.448"	"C0265268"	"Adams Oliver syndrome"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.64"	"1"	"2013"	"2016"	"0"	"1"	"CTD_human;ORPHANET"
"285203"	"EOGT"	"0.696"	"0.448"	"C2931779"	"Congenital defect of skull and scalp"	"disease"	"C05;C16;C17"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"285203"	"EOGT"	"0.696"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285203"	"EOGT"	"0.696"	"0.448"	"C3809092"	"ADAMS-OLIVER SYNDROME 4"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"1"	"3"	"UNIPROT"
"285242"	"HTR3E"	"0.857"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"285362"	"SUMF1"	"0.642"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2003"	"2003"	"2"	"0"	"GENOMICS_ENGLAND"
"285362"	"SUMF1"	"0.642"	"0.448"	"C0020305"	"Hydrops Fetalis"	"disease"	"C13;C15;C16;C20;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"285362"	"SUMF1"	"0.642"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285362"	"SUMF1"	"0.642"	"0.448"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285362"	"SUMF1"	"0.642"	"0.448"	"C0268263"	"Multiple Sulfatase Deficiency Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"1987"	"2018"	"6"	"22"	"CTD_human;ORPHANET;UNIPROT"
"285362"	"SUMF1"	"0.642"	"0.448"	"C1720864"	"Sulfatidosis, Juvenile, Austin Type"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.70"		"2007"	"2007"	"1"	"0"	"CTD_human;ORPHANET"
"285362"	"SUMF1"	"0.642"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2003"	"2011"	"3"	"0"	"GENOMICS_ENGLAND"
"285440"	"CYP4V2"	"0.762"	"0.241"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285440"	"CYP4V2"	"0.762"	"0.241"	"C1859486"	"BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY"	"disease"	"C11;C16"	"Disease or Syndrome"	"1.00"	"1"	"1993"	"2018"	"2"	"32"	"CTD_human;ORPHANET;UNIPROT"
"285489"	"DOK7"	"0.607"	"0.552"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.40"		"2006"	"2006"	"1"	"0"	"GENOMICS_ENGLAND"
"285489"	"DOK7"	"0.607"	"0.552"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"	"0.95"	"1993"	"2014"	"4"	"1"	"GENOMICS_ENGLAND"
"285489"	"DOK7"	"0.607"	"0.552"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"285489"	"DOK7"	"0.607"	"0.552"	"C1276035"	"Pena-Shokeir syndrome type I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.61"	"1"	"1990"	"2017"	"0"	"4"	"CTD_human;ORPHANET"
"285489"	"DOK7"	"0.607"	"0.552"	"C1850792"	"Congenital myasthenic syndrome ib"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.81"	"1"	"1990"	"2017"	"5"	"22"	"CTD_human;UNIPROT"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0010278"	"Craniosynostosis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C1855305"	"Ter Haar syndrome"	"disease"	"C05;C14;C16;F03"	"Disease or Syndrome"	"0.76"	"1"	"1983"	"2017"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C1859406"	"Borrone Di Rocco Crovato syndrome"	"disease"	"C05;C14;C17"	"Disease or Syndrome"	"0.40"		"2010"	"2010"	"1"	"2"	"UNIPROT"
"285590"	"SH3PXD2B"	"0.648"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"285601"	"GPR150"	"0.886"	"0.103"	"C0919267"	"ovarian neoplasm"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"285601"	"GPR150"	"0.886"	"0.103"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"285704"	"RGMB"	"0.799"	"0.241"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"285704"	"RGMB"	"0.799"	"0.241"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"285704"	"RGMB"	"0.799"	"0.241"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"285761"	"DCBLD1"	"0.928"	"0.069"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"285848"	"PNPLA1"	"0.713"	"0.345"	"C0020757"	"Ichthyoses"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"		"2012"	"2012"	"1"	"0"	"CTD_human"
"285848"	"PNPLA1"	"0.713"	"0.345"	"C0043345"	"Xeroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"285848"	"PNPLA1"	"0.713"	"0.345"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.34"	"1"	"2012"	"2018"	"0"	"0"	"ORPHANET"
"285848"	"PNPLA1"	"0.713"	"0.345"	"C3554355"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2017"	"1"	"4"	"CTD_human;UNIPROT"
"286053"	"NSMCE2"	"0.681"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"UNIPROT"
"286053"	"NSMCE2"	"0.681"	"0.448"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"286077"	"FAM83H"	"0.834"	"0.138"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.68"	"1"	"2008"	"2016"	"16"	"0"	"CTD_human;GENOMICS_ENGLAND"
"286077"	"FAM83H"	"0.834"	"0.138"	"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"286077"	"FAM83H"	"0.834"	"0.138"	"C0399376"	"Amelogenesis Imperfecta, Type III"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.73"	"1"	"2008"	"2016"	"2"	"14"	"CTD_human;ORPHANET;UNIPROT"
"286204"	"CRB2"	"0.713"	"0.207"	"C0017668"	"Focal glomerulosclerosis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.40"				"0"	"0"	"CTD_human"
"286204"	"CRB2"	"0.713"	"0.207"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"286204"	"CRB2"	"0.713"	"0.207"	"C0086432"	"Hyalinosis, Segmental Glomerular"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"286204"	"CRB2"	"0.713"	"0.207"	"C1857423"	"Cystic Kidney Disease with Ventriculomegaly"	"disease"	"C10;C12;C13"	"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"286204"	"CRB2"	"0.713"	"0.207"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"286204"	"CRB2"	"0.713"	"0.207"	"C4015555"	"FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"5"	"UNIPROT"
"286204"	"CRB2"	"0.713"	"0.207"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"286262"	"TPRN"	"0.834"	"0.103"	"C2750082"	"Deafness, Autosomal Recessive 79"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.60"		"2010"	"2017"	"0"	"5"	"CTD_human"
"286343"	"LURAP1L"	"0.735"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"286410"	"ATP11C"	"0.928"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"286464"	"CFAP47"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"286530"	"P2RY8"	"0.72"	"0.31"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"286530"	"P2RY8"	"0.72"	"0.31"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"286530"	"P2RY8"	"0.72"	"0.31"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"286530"	"P2RY8"	"0.72"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"286676"	"ILDR1"	"0.785"	"0.138"	"C1864818"	"DEAFNESS, AUTOSOMAL RECESSIVE 42 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"2005"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"286827"	"TRIM59"	"0.752"	"0.207"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"286887"	"KRT6C"	"0.834"	"0.103"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"286887"	"KRT6C"	"0.834"	"0.103"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"286887"	"KRT6C"	"0.834"	"0.103"	"C3810394"	"PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2014"	"3"	"1"	"CTD_human;ORPHANET;UNIPROT"
"317649"	"EIF4E3"	"0.815"	"0.172"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"317714"	"DYT15"	"0.928"	"0.103"	"C1834570"	"Myoclonic dystonia"	"disease"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"0"	"0"	"ORPHANET"
"317719"	"KLHL10"	"0.857"	"0.034"	"C3554453"	"SPERMATOGENIC FAILURE 11"	"disease"		"Disease or Syndrome"	"0.60"		"2007"	"2007"	"1"	"2"	"CTD_human;UNIPROT"
"317772"	"HIST2H2AB"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"317781"	"DDX51"	"0.886"	"0.138"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"319100"	"TAAR6"	"0.857"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"1"	"2008"	"2010"	"3"	"0"	"PSYGENET"
"319100"	"TAAR6"	"0.857"	"0.034"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"319101"	"KRT73"	"0.857"	"0.138"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"319101"	"KRT73"	"0.857"	"0.138"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"319101"	"KRT73"	"0.857"	"0.138"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"319101"	"KRT73"	"0.857"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"326625"	"MMAB"	"0.735"	"0.31"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"326625"	"MMAB"	"0.735"	"0.31"	"C0220994"	"Hyperammonemia"	"phenotype"	"C23"	"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"326625"	"MMAB"	"0.735"	"0.31"	"C1855102"	"Methylmalonic aciduria cblB type"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.72"	"1"	"1993"	"2016"	"2"	"18"	"CTD_human;ORPHANET;UNIPROT"
"326625"	"MMAB"	"0.735"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2003"	"2003"	"1"	"0"	"GENOMICS_ENGLAND"
"333929"	"SNAI3"	"0.928"	"0.069"	"C0520459"	"Necrotizing Enterocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"337867"	"UBAC2"	"0.735"	"0.345"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2013"	"0"	"0"	"ORPHANET"
"337975"	"KRTAP20-1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"337977"	"KRTAP21-1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"338090"	"SPG24"	"0.886"	"0.103"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"338090"	"SPG24"	"0.886"	"0.103"	"C1843569"	"SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"338321"	"NLRP9"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"338323"	"NLRP14"	"0.886"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"338324"	"S100A7A"	"0.727"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338324"	"S100A7A"	"0.727"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338328"	"GPIHBP1"	"0.72"	"0.241"	"C0020445"	"Hypercholesterolemia, Familial"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"338328"	"GPIHBP1"	"0.72"	"0.241"	"C1274228"	"Chylomicronemia syndrome"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"338328"	"GPIHBP1"	"0.72"	"0.241"	"C4014767"	"HYPERLIPOPROTEINEMIA, TYPE ID"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2016"	"8"	"9"	"CTD_human;UNIPROT"
"338339"	"CLEC4D"	"0.676"	"0.345"	"C0024115"	"Lung diseases"	"group"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338382"	"RAB7B"	"0.656"	"0.552"	"C0001787"	"Osteoporosis, Age-Related"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"338382"	"RAB7B"	"0.656"	"0.552"	"C0029456"	"Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"338382"	"RAB7B"	"0.656"	"0.552"	"C0029459"	"Osteoporosis, Senile"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"338382"	"RAB7B"	"0.656"	"0.552"	"C0751406"	"Post-Traumatic Osteoporosis"	"disease"	"C05;C18"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"338382"	"RAB7B"	"0.656"	"0.552"	"C0948089"	"Acute Coronary Syndrome"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338398"	"TAS2R60"	"1"	"0.034"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338433"	"SNORD115-1"	"0.707"	"0.276"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"		"2006"	"2006"	"0"	"0"	"CTD_human"
"338433"	"SNORD115-1"	"0.707"	"0.276"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"338435"	"SCA25"	"1"	"0.069"	"C1837518"	"Spinocerebellar ataxia 25"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"ORPHANET"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0007114"	"Malignant neoplasm of skin"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0016382"	"Flushing"	"phenotype"	"C23"	"Sign or Symptom"	"0.35"	"1"	"2006"	"2014"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"CTD_human"
"338442"	"HCAR2"	"0.676"	"0.483"	"C0037286"	"Skin Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"338557"	"FFAR4"	"0.752"	"0.276"	"C2675659"	"BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10"	"phenotype"		"Finding"	"0.40"		"2012"	"2017"	"0"	"1"	"CTD_human"
"338567"	"KCNK18"	"0.834"	"0.138"	"C3150908"	"MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13"	"phenotype"		"Finding"	"0.40"		"2010"	"2015"	"0"	"2"	"CTD_human"
"338917"	"VSX2"	"0.735"	"0.172"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.41"	"1"	"2000"	"2005"	"1"	"0"	"GENOMICS_ENGLAND"
"338917"	"VSX2"	"0.735"	"0.172"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.41"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"338917"	"VSX2"	"0.735"	"0.172"	"C1855052"	"MICROPHTHALMIA, ISOLATED 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"338917"	"VSX2"	"0.735"	"0.172"	"C1864720"	"MICROPHTHALMIA, ISOLATED 2"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2001"	"2012"	"2"	"2"	"CTD_human;UNIPROT"
"338917"	"VSX2"	"0.735"	"0.172"	"C1864721"	"Microphthalmia, Isolated, with Coloboma 3"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"		"2000"	"2015"	"3"	"2"	"CTD_human;UNIPROT"
"338917"	"VSX2"	"0.735"	"0.172"	"C1864722"	"Microphthalmia, Cataracts, and Iris Abnormalities"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.40"		"2000"	"2015"	"3"	"2"	"UNIPROT"
"338917"	"VSX2"	"0.735"	"0.172"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"338917"	"VSX2"	"0.735"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"339145"	"FAM92B"	"0.834"	"0.034"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.33"	"0.3333333"	"2008"	"2012"	"1"	"0"	"CTD_human"
"339145"	"FAM92B"	"0.834"	"0.034"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"339145"	"FAM92B"	"0.834"	"0.034"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"339145"	"FAM92B"	"0.834"	"0.034"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"339145"	"FAM92B"	"0.834"	"0.034"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"339230"	"CCDC137"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"339327"	"ZNF546"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"339345"	"NANOS2"	"0.69"	"0.379"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"339345"	"NANOS2"	"0.69"	"0.379"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"339345"	"NANOS2"	"0.69"	"0.379"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"339453"	"TMEM240"	"0.735"	"0.172"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"339453"	"TMEM240"	"0.735"	"0.172"	"C1843891"	"SPINOCEREBELLAR ATAXIA 21"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.71"	"1"	"2001"	"2015"	"1"	"7"	"CTD_human;ORPHANET;UNIPROT"
"339453"	"TMEM240"	"0.735"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"339487"	"ZBTB8OS"	"1"	"0.138"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"339487"	"ZBTB8OS"	"1"	"0.138"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"339829"	"CCDC39"	"0.713"	"0.276"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.55"	"1"	"2011"	"2016"	"0"	"0"	"ORPHANET"
"339829"	"CCDC39"	"0.713"	"0.276"	"C3151136"	"CILIARY DYSKINESIA, PRIMARY, 14"	"disease"		"Disease or Syndrome"	"0.80"		"1993"	"2015"	"3"	"6"	"CTD_human;UNIPROT"
"339829"	"CCDC39"	"0.713"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"339829"	"CCDC39"	"0.713"	"0.276"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"339829"	"CCDC39"	"0.713"	"0.276"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"339855"	"KY"	"0.834"	"0.172"	"C2678065"	"Myofibrillar Myopathy"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"339855"	"KY"	"0.834"	"0.172"	"C4310711"	"MYOPATHY, MYOFIBRILLAR, 7"	"disease"		"Disease or Syndrome"	"0.40"		"2016"	"2017"	"0"	"2"	"ORPHANET"
"339896"	"GADL1"	"0.696"	"0.552"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"339896"	"GADL1"	"0.696"	"0.552"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"339896"	"GADL1"	"0.696"	"0.552"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"339970"	"GCOM2"	"1"	"0.034"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"339976"	"TRIML1"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"340024"	"SLC6A19"	"0.69"	"0.379"	"C0018609"	"Hartnup Disease"	"disease"	"C10;C12;C13;C16;C18"	"Disease or Syndrome"	"1.00"	"1"	"2004"	"2015"	"1"	"4"	"CTD_human;ORPHANET;UNIPROT"
"340024"	"SLC6A19"	"0.69"	"0.379"	"C0268654"	"Iminoglycinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.51"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human;ORPHANET"
"340024"	"SLC6A19"	"0.69"	"0.379"	"C0543541"	"HYPERGLYCINURIA (disorder)"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.41"	"1"	"2008"	"2008"	"0"	"0"	"CTD_human"
"340024"	"SLC6A19"	"0.69"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2009"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"340024"	"SLC6A19"	"0.69"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"340061"	"TMEM173"	"0.616"	"0.621"	"C0024145"	"Chilblain lupus 1"	"disease"	"C17;C26"	"Disease or Syndrome"	"0.50"		"2016"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"340061"	"TMEM173"	"0.616"	"0.621"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"		"2015"	"2015"	"1"	"1"	"CTD_human"
"340061"	"TMEM173"	"0.616"	"0.621"	"C4014722"	"STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET"	"disease"		"Disease or Syndrome"	"0.72"	"1"	"2014"	"2017"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"340075"	"ARSI"	"0.834"	"0.241"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"340156"	"MYLK4"	"0.928"	"0.103"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"340156"	"MYLK4"	"0.928"	"0.103"	"C3165106"	"Infiltrating duct carcinoma of female breast"	"disease"		"Neoplastic Process"	"0.30"				"0"	"1"	"UNIPROT"
"340205"	"TREML1"	"0.799"	"0.276"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"340205"	"TREML1"	"0.799"	"0.276"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"340205"	"TREML1"	"0.799"	"0.276"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"340205"	"TREML1"	"0.799"	"0.276"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"340267"	"COL28A1"	"0.928"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"340267"	"COL28A1"	"0.928"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"340267"	"COL28A1"	"0.928"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"340273"	"ABCB5"	"0.652"	"0.448"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"340273"	"ABCB5"	"0.652"	"0.448"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"340273"	"ABCB5"	"0.652"	"0.448"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"1"	"2004"	"2017"	"1"	"0"	"CTD_human"
"340273"	"ABCB5"	"0.652"	"0.448"	"C1335302"	"Pancreatic Ductal Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"340273"	"ABCB5"	"0.652"	"0.448"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;UNIPROT"
"340533"	"NEXMIF"	"0.685"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"340533"	"NEXMIF"	"0.685"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.43"	"0.6666667"	"2005"	"2016"	"0"	"0"	"GENOMICS_ENGLAND"
"340533"	"NEXMIF"	"0.685"	"0.276"	"C3806730"	"MENTAL RETARDATION, X-LINKED 98"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2017"	"0"	"11"	"CTD_human;ORPHANET"
"340665"	"CYP26C1"	"0.752"	"0.31"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"340665"	"CYP26C1"	"0.752"	"0.31"	"C2936827"	"Focal facial dermal dysplasia"	"disease"	"C16;C17"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"340665"	"CYP26C1"	"0.752"	"0.31"	"C3554246"	"FOCAL FACIAL DERMAL DYSPLASIA 4"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"340706"	"VWA2"	"0.857"	"0.241"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"340719"	"NANOS1"	"0.696"	"0.379"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"340719"	"NANOS1"	"0.696"	"0.379"	"C3809427"	"SPERMATOGENIC FAILURE 12"	"disease"		"Disease or Syndrome"	"0.40"		"2013"	"2013"	"0"	"2"	"CTD_human"
"340990"	"OTOG"	"0.815"	"0.207"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"1997"	"2017"	"6"	"0"	"CLINGEN"
"340990"	"OTOG"	"0.815"	"0.207"	"C1862939"	"AMYOTROPHIC LATERAL SCLEROSIS 1"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"340990"	"OTOG"	"0.815"	"0.207"	"C1862941"	"Amyotrophic Lateral Sclerosis, Sporadic"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"340990"	"OTOG"	"0.815"	"0.207"	"C3554163"	"DEAFNESS, AUTOSOMAL RECESSIVE 18B"	"disease"		"Disease or Syndrome"	"0.81"	"1"	"2013"	"2015"	"1"	"5"	"CTD_human;UNIPROT"
"341568"	"OR8S1"	"1"	"0.103"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341568"	"OR8S1"	"1"	"0.103"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"341640"	"FREM2"	"0.564"	"0.552"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"341640"	"FREM2"	"0.564"	"0.552"	"C0265233"	"Cryptophthalmos syndrome"	"disease"	"C05;C11;C12;C13;C16"	"Disease or Syndrome"	"0.90"	"0.9166667"	"2005"	"2014"	"1"	"1"	"CTD_human;ORPHANET"
"341640"	"FREM2"	"0.564"	"0.552"	"C0266294"	"Unilateral agenesis of kidney"	"disease"	"C12;C13;C23"	"Congenital Abnormality"	"0.40"		"2015"	"2015"	"0"	"1"	"ORPHANET"
"341640"	"FREM2"	"0.564"	"0.552"	"C1968949"	"Cakut"	"disease"	"C12;C13;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"341640"	"FREM2"	"0.564"	"0.552"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"341640"	"FREM2"	"0.564"	"0.552"	"C4540036"	"FRASER SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.40"		"2005"	"2008"	"1"	"2"	"UNIPROT"
"342035"	"GLDN"	"0.799"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"342035"	"GLDN"	"0.799"	"0.31"	"C4310670"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 11"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"7"	"CTD_human;UNIPROT"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"		"2005"	"2007"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"342371"	"ATXN1L"	"0.799"	"0.069"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"342510"	"CD300E"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"342618"	"SLFN14"	"1"		"C4310797"	"BLEEDING DISORDER, PLATELET-TYPE, 20"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2016"	"2"	"4"	"CTD_human;ORPHANET;UNIPROT"
"342945"	"ZSCAN22"	"1"	"0.069"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"342945"	"ZSCAN22"	"1"	"0.069"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"343035"	"RD3"	"0.735"	"0.172"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"343035"	"RD3"	"0.735"	"0.172"	"C1857743"	"LEBER CONGENITAL AMAUROSIS 12 (disorder)"	"disease"	"C11"	"Disease or Syndrome"	"0.61"	"1"	"1993"	"2014"	"0"	"5"	"CTD_human"
"343450"	"KCNT2"	"0.815"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"343637"	"RSPO4"	"0.886"	"0.069"	"C0265998"	"ANONYCHIA"	"disease"	"C23"	"Congenital Abnormality"	"0.45"	"1"	"1973"	"2017"	"0"	"8"	"CTD_human"
"343637"	"RSPO4"	"0.886"	"0.069"	"C3277900"	"NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4"	"disease"		"Disease or Syndrome"	"0.51"	"1"	"2007"	"2013"	"1"	"4"	"ORPHANET;UNIPROT"
"343637"	"RSPO4"	"0.886"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"343641"	"TGM6"	"0.685"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"343641"	"TGM6"	"0.685"	"0.276"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"343641"	"TGM6"	"0.685"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"343641"	"TGM6"	"0.685"	"0.276"	"C3888031"	"SPINOCEREBELLAR ATAXIA 35"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2011"	"2018"	"4"	"5"	"ORPHANET;UNIPROT"
"343930"	"MSGN1"	"0.815"	"0.103"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"343930"	"MSGN1"	"0.815"	"0.103"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"343930"	"MSGN1"	"0.815"	"0.103"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"343930"	"MSGN1"	"0.815"	"0.103"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"343930"	"MSGN1"	"0.815"	"0.103"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"343930"	"MSGN1"	"0.815"	"0.103"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"344018"	"FIGLA"	"0.886"	"0.138"	"C2676742"	"Premature Ovarian Failure 6"	"disease"	"C13;C19"	"Disease or Syndrome"	"0.40"		"2008"	"2008"	"0"	"1"	"CTD_human"
"344148"	"NCKAP5"	"0.857"	"0.069"	"C0086132"	"Depressive Symptoms"	"phenotype"	"F01"	"Sign or Symptom"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"344558"	"SH3RF3"	"0.886"	"0.069"	"C0236733"	"Amphetamine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"344558"	"SH3RF3"	"0.886"	"0.069"	"C0236804"	"Amphetamine Addiction"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"344558"	"SH3RF3"	"0.886"	"0.069"	"C0236807"	"Amphetamine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344805"	"TMPRSS7"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"344838"	"PAQR9"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.61"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"345193"	"LRIT3"	"0.713"	"0.103"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C3554399"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2014"	"1"	"4"	"UNIPROT"
"345193"	"LRIT3"	"0.713"	"0.103"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345193"	"LRIT3"	"0.713"	"0.103"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345557"	"PLCXD3"	"0.928"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"345611"	"IRGM"	"0.648"	"0.345"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.45"	"0.8"	"2009"	"2017"	"1"	"2"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0010346"	"Crohn Disease"	"disease"	"C06"	"Disease or Syndrome"	"0.50"	"0.9130435"	"2007"	"2018"	"4"	"5"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0021390"	"Inflammatory Bowel Diseases"	"group"	"C06"	"Disease or Syndrome"	"0.50"	"1"	"2009"	"2017"	"1"	"1"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0156147"	"Crohn's disease of large bowel"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"4"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0267380"	"Crohn's disease of the ileum"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"4"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0678202"	"Regional enteritis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"4"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C0949272"	"IIeocolitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2007"	"2011"	"4"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C1834752"	"MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)"	"phenotype"		"Finding"	"0.30"				"0"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C1969665"	"MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C2677078"	"Generalized Epilepsy With Febrile Seizures Plus, Type 6"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"345611"	"IRGM"	"0.648"	"0.345"	"C2677079"	"Inflammatory Bowel Disease 19"	"disease"	"C06"	"Disease or Syndrome"	"0.40"		"2007"	"2011"	"0"	"1"	"CTD_human"
"345643"	"MCIDAS"	"0.707"	"0.276"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.41"	"1"	"1993"	"2016"	"0"	"3"	"ORPHANET"
"345643"	"MCIDAS"	"0.707"	"0.276"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"345643"	"MCIDAS"	"0.707"	"0.276"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"345895"	"RSPH4A"	"0.785"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.43"	"1"	"1993"	"2015"	"0"	"2"	"ORPHANET"
"345895"	"RSPH4A"	"0.785"	"0.138"	"C2675229"	"CILIARY DYSKINESIA, PRIMARY, 11"	"disease"	"C08;C09;C16"	"Disease or Syndrome"	"0.60"		"1993"	"2015"	"3"	"9"	"CTD_human;UNIPROT"
"345895"	"RSPH4A"	"0.785"	"0.138"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"345895"	"RSPH4A"	"0.785"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"345930"	"ECT2L"	"0.928"	"0.138"	"C1961099"	"Precursor T-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"346007"	"EYS"	"0.685"	"0.345"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.70"	"1"	"2005"	"2018"	"1"	"23"	"CTD_human;ORPHANET"
"346007"	"EYS"	"0.685"	"0.345"	"C1864446"	"Retinitis Pigmentosa 25"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2008"	"2015"	"5"	"31"	"CTD_human;UNIPROT"
"346171"	"ZFP57"	"0.696"	"0.414"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"346171"	"ZFP57"	"0.696"	"0.414"	"C1832386"	"Diabetes Mellitus, Transient Neonatal, 1"	"disease"	"C16;C18;C19"	"Disease or Syndrome"	"0.72"	"1"	"2008"	"2016"	"1"	"8"	"CTD_human;ORPHANET;UNIPROT"
"346171"	"ZFP57"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2013"	"2013"	"1"	"0"	"GENOMICS_ENGLAND"
"346288"	"SEPT14"	"0.857"	"0.034"	"C0017636"	"Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"CTD_human"
"346288"	"SEPT14"	"0.857"	"0.034"	"C0206726"	"gliosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"346288"	"SEPT14"	"0.857"	"0.034"	"C0334588"	"Giant Cell Glioblastoma"	"disease"	"C04"	"Neoplastic Process"	"0.50"		"2013"	"2013"	"1"	"0"	"CTD_human;ORPHANET"
"346288"	"SEPT14"	"0.857"	"0.034"	"C1621958"	"Glioblastoma Multiforme"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"346389"	"MACC1"	"0.621"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"346562"	"GNAT3"	"0.857"	"0.138"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"346562"	"GNAT3"	"0.857"	"0.138"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"346562"	"GNAT3"	"0.857"	"0.138"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"347088"	"ADGRD2"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347088"	"ADGRD2"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347273"	"CAVIN4"	"1"	"0.034"	"C0007193"	"Cardiomyopathy, Dilated"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"347273"	"CAVIN4"	"1"	"0.034"	"C0264886"	"Conduction disorder of the heart"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"347344"	"ZNF81"	"0.799"	"0.172"	"C1845333"	"Mental Retardation, X-Linked 45"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"347344"	"ZNF81"	"0.799"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"347344"	"ZNF81"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"347365"	"ITIH6"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"347688"	"TUBB8"	"1"		"C4225210"	"OOCYTE MATURATION DEFECT 2"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"2"	"13"	"CTD_human;UNIPROT"
"347730"	"LRRTM1"	"0.857"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2008"	"2015"	"2"	"0"	"PSYGENET"
"347731"	"LRRTM3"	"0.834"	"0.103"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.32"	"1"	"2012"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0394006"	"Dysequilibrium syndrome"	"disease"	"C10;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0431380"	"Cortical Dysplasia"	"disease"	"C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2002"	"2002"	"1"	"0"	"CTD_human"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C1276035"	"Pena-Shokeir syndrome type I"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"1"	"UNIPROT"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C1302995"	"Congenital Fibrosis of the Extraocular Muscles"	"disease"	"C10;C11;C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.52"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C3552236"	"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7"	"disease"		"Disease or Syndrome"	"0.70"		"2010"	"2014"	"3"	"7"	"CTD_human;UNIPROT"
"347733"	"TUBB2B"	"0.633"	"0.345"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"347735"	"SERINC2"	"0.928"	"0.138"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2014"	"2014"	"1"	"1"	"PSYGENET"
"348180"	"CTU2"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348180"	"CTU2"	"0.928"	"0.069"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348180"	"CTU2"	"0.928"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348180"	"CTU2"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348180"	"CTU2"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348180"	"CTU2"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"348327"	"ZNF530"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"348654"	"GEN1"	"0.773"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"0"	"0"	"UNIPROT"
"348654"	"GEN1"	"0.773"	"0.207"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2011"	"2016"	"6"	"0"	"CLINGEN"
"348654"	"GEN1"	"0.773"	"0.207"	"C1140680"	"Malignant neoplasm of ovary"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"0"	"0"	"CLINGEN"
"348793"	"WDR53"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"348932"	"SLC6A18"	"0.886"	"0.172"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.32"	"0"	"2004"	"2008"	"1"	"0"	"CTD_human"
"348932"	"SLC6A18"	"0.886"	"0.172"	"C0268654"	"Iminoglycinuria"	"disease"	"C12;C13;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2008"	"2008"	"0"	"0"	"ORPHANET"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.43"	"1"	"2010"	"2017"	"0"	"0"	"ORPHANET"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C2677065"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6"	"disease"		"Disease or Syndrome"	"0.60"		"2005"	"2017"	"2"	"5"	"CTD_human;UNIPROT"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"348938"	"NIPAL4"	"0.69"	"0.379"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"348980"	"HCN1"	"0.6"	"0.379"	"C0004134"	"Ataxia"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"348980"	"HCN1"	"0.6"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2013"	"2"	"0"	"PSYGENET"
"348980"	"HCN1"	"0.6"	"0.379"	"C0014544"	"Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.38"	"1"	"2003"	"2014"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0022333"	"Jacksonian Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0036572"	"Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.32"	"0.5"	"2008"	"2014"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0086237"	"Epilepsy, Cryptogenic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0149958"	"Complex partial seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0234533"	"Generalized seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0234535"	"Seizures, Clonic"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0236018"	"Aura"	"phenotype"	"C10"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0240991"	"Ataxia, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0270824"	"Visual seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.50"		"2008"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0270844"	"Tonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0270846"	"Epileptic drop attack"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0278161"	"Ataxia, Motor"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0422850"	"Seizures, Somatosensory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0422852"	"Seizures, Auditory"	"phenotype"	"C10;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0422853"	"Olfactory seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0422854"	"Gustatory seizure"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0422855"	"Vertiginous seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0427190"	"Ataxia, Truncal"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0494475"	"Tonic - clonic seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0520966"	"Abnormal coordination"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2015"	"0"	"2"	"GENOMICS_ENGLAND"
"348980"	"HCN1"	"0.6"	"0.379"	"C0750937"	"Ataxia, Appendicular"	"phenotype"	"C10;C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0750940"	"Tremor, Rubral"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751056"	"Non-epileptic convulsion"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751110"	"Single Seizure"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751111"	"Awakening Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751123"	"Atonic Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751494"	"Convulsive Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751495"	"Seizures, Focal"	"phenotype"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C0751496"	"Seizures, Sensory"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C3463992"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C3495874"	"Nonepileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"348980"	"HCN1"	"0.6"	"0.379"	"C4014531"	"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2017"	"2"	"8"	"CTD_human;UNIPROT"
"348980"	"HCN1"	"0.6"	"0.379"	"C4048158"	"Convulsions"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C4316903"	"Absence Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C4317109"	"Epileptic Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C4317123"	"Myoclonic Seizures"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"348980"	"HCN1"	"0.6"	"0.379"	"C4505436"	"Generalized Absence Seizures"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"349075"	"ZNF713"	"1"	"0.034"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"349149"	"GJC3"	"0.928"	"0.138"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"349565"	"NMNAT3"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"349565"	"NMNAT3"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"352909"	"DNAAF3"	"0.659"	"0.483"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.84"	"1"	"1993"	"2015"	"1"	"3"	"CTD_human;ORPHANET"
"352909"	"DNAAF3"	"0.659"	"0.483"	"C1847554"	"CILIARY DYSKINESIA, PRIMARY, 2 (disorder)"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.80"		"2000"	"2012"	"1"	"3"	"CTD_human;UNIPROT"
"352909"	"DNAAF3"	"0.659"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"352909"	"DNAAF3"	"0.659"	"0.483"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"352909"	"DNAAF3"	"0.659"	"0.483"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;ORPHANET"
"353143"	"LCE3B"	"0.799"	"0.138"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"353143"	"LCE3B"	"0.799"	"0.138"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.9615385"	"2009"	"2017"	"1"	"0"	"CTD_human"
"353144"	"LCE3C"	"0.785"	"0.172"	"C0030246"	"Pustulosis of Palms and Soles"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"353144"	"LCE3C"	"0.785"	"0.172"	"C0033860"	"Psoriasis"	"disease"	"C17"	"Disease or Syndrome"	"0.40"	"0.9615385"	"2009"	"2017"	"1"	"0"	"CTD_human"
"353238"	"PADI6"	"0.815"	"0.138"	"C4310659"	"PREIMPLANTATION EMBRYONIC LETHALITY 2"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"5"	"CTD_human;UNIPROT"
"353293"	"SPG23"	"0.928"	"0.138"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2004"	"1"	"0"	"GENOMICS_ENGLAND"
"353293"	"SPG23"	"0.928"	"0.138"	"C0796019"	"SPASTIC PARAPLEGIA 23 (disorder)"	"disease"	"C10;C16;C17;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"353376"	"TICAM2"	"0.504"	"0.793"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"353376"	"TICAM2"	"0.504"	"0.793"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"353376"	"TICAM2"	"0.504"	"0.793"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"353376"	"TICAM2"	"0.504"	"0.793"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"353500"	"BMP8A"			"C1704436"	"Peripheral Arterial Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"1"	"CTD_human"
"353514"	"LILRA5"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"353514"	"LILRA5"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"353514"	"LILRA5"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0027654"	"Embryonal Neoplasm"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0027658"	"Neoplasms, Germ Cell and Embryonal"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0205851"	"Germ cell tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0205852"	"Neoplasms, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0740345"	"Germ Cell Cancer"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0751364"	"Cancer, Embryonal"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359787"	"DPPA3"	"0.857"	"0.034"	"C0751365"	"Cancer, Embryonal and Mixed"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"359845"	"RFLNB"	"1"	"0.034"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"359948"	"IRF2BP2"	"0.773"	"0.172"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"373156"	"GSTK1"	"0.441"	"0.828"	"C0029408"	"Degenerative polyarthritis"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"373156"	"GSTK1"	"0.441"	"0.828"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"373156"	"GSTK1"	"0.441"	"0.828"	"C0086743"	"Osteoarthrosis Deformans"	"disease"	"C05"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"373156"	"GSTK1"	"0.441"	"0.828"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"0.9411765"	"2001"	"2014"	"1"	"0"	"CTD_human"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0023264"	"Leigh Disease"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.35"	"1"	"1999"	"2007"	"0"	"0"	"CTD_human"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0751267"	"Encephalopathy, Subacute Necrotizing, Infantile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0751268"	"Encephalopathy, Subacute Necrotizing, Juvenile"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C1838979"	"MITOCHONDRIAL COMPLEX I DEFICIENCY"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"2"	"1"	"UNIPROT"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C2936907"	"NADH:Q(1) Oxidoreductase deficiency"	"disease"	"C18"	"Disease or Syndrome"	"0.50"		"1999"	"1999"	"2"	"1"	"ORPHANET;UNIPROT"
"374291"	"NDUFS7"	"0.63"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"374393"	"FAM111B"	"0.72"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"374393"	"FAM111B"	"0.72"	"0.31"	"C0007134"	"Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"374393"	"FAM111B"	"0.72"	"0.31"	"C0279702"	"Conventional (Clear Cell) Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C1266042"	"Chromophobe Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C1266043"	"Sarcomatoid Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C1266044"	"Collecting Duct Carcinoma of the Kidney"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C1306837"	"Papillary Renal Cell Carcinoma"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374393"	"FAM111B"	"0.72"	"0.31"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374393"	"FAM111B"	"0.72"	"0.31"	"C3810325"	"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS"	"disease"		"Disease or Syndrome"	"0.60"		"1993"	"2017"	"1"	"6"	"ORPHANET;UNIPROT"
"374407"	"DNAJB13"	"0.886"	"0.138"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"374407"	"DNAJB13"	"0.886"	"0.138"	"C4310722"	"CILIARY DYSKINESIA, PRIMARY, 34"	"disease"		"Disease or Syndrome"	"0.60"		"2017"	"2017"	"1"	"2"	"CTD_human;UNIPROT"
"374407"	"DNAJB13"	"0.886"	"0.138"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"374462"	"PTPRQ"	"0.815"	"0.241"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374462"	"PTPRQ"	"0.815"	"0.241"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2003"	"2016"	"8"	"0"	"CLINGEN"
"374462"	"PTPRQ"	"0.815"	"0.241"	"C3150654"	"DEAFNESS, AUTOSOMAL RECESSIVE 84A"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"2"	"3"	"CTD_human;UNIPROT"
"374569"	"ASPG"	"0.707"	"0.207"	"C0002792"	"anaphylaxis"	"disease"	"C20"	"Disease or Syndrome"	"0.30"		"1977"	"1977"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0002871"	"Anemia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0008350"	"Cholelithiasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0015967"	"Fever"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0018965"	"Hematuria"	"phenotype"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0023530"	"Leukopenia"	"disease"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0040034"	"Thrombocytopenia"	"phenotype"	"C15"	"Disease or Syndrome"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0042963"	"Vomiting"	"phenotype"	"C23"	"Sign or Symptom"	"0.30"		"1990"	"1990"	"1"	"0"	"CTD_human"
"374569"	"ASPG"	"0.707"	"0.207"	"C0701818"	"Choledocholithiasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C0008925"	"Cleft Palate"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"374654"	"KIF7"	"0.573"	"0.621"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"374654"	"KIF7"	"0.573"	"0.621"	"C0020796"	"Profound Mental Retardation"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C0025363"	"Mental Retardation, Psychosocial"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"374654"	"KIF7"	"0.573"	"0.621"	"C0796147"	"Acrocallosal Syndrome"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.95"	"1"	"2011"	"2018"	"3"	"16"	"CTD_human;ORPHANET;UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C0917816"	"Mental deficiency"	"disease"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C1691228"	"Cystic Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"374654"	"KIF7"	"0.573"	"0.621"	"C1837218"	"Cleft palate, isolated"	"disease"	"C05;C07;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C1846722"	"Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.70"		"1998"	"2013"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C1856016"	"HYDROLETHALUS SYNDROME 1"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human"
"374654"	"KIF7"	"0.573"	"0.621"	"C2745997"	"OROFACIODIGITAL SYNDROME VI"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"374654"	"KIF7"	"0.573"	"0.621"	"C2931104"	"Hydrolethalus syndrome"	"disease"	"C05;C10;C14;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2011"	"1"	"0"	"CTD_human;ORPHANET"
"374654"	"KIF7"	"0.573"	"0.621"	"C2931760"	"Acrocallosal syndrome, Schinzel type"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"		"2011"	"2016"	"3"	"5"	"ORPHANET;UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C2936862"	"Bardet-Biedl syndrome 1 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"3"	"UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C3277723"	"JOUBERT SYNDROME 12"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2016"	"3"	"7"	"UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C3280899"	"JOUBERT SYNDROME 12/15, DIGENIC"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2016"	"3"	"6"	"UNIPROT"
"374654"	"KIF7"	"0.573"	"0.621"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.50"		"2012"	"2012"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"374654"	"KIF7"	"0.573"	"0.621"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.51"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"374868"	"ATP9B"	"0.857"	"0.138"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"374868"	"ATP9B"	"0.857"	"0.138"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"374868"	"ATP9B"	"0.857"	"0.138"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"374879"	"ZNF699"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2006"	"2016"	"1"	"0"	"PSYGENET"
"374887"	"YJEFN3"	"0.928"	"0.138"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"374887"	"YJEFN3"	"0.928"	"0.138"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"374920"	"ZSWIM9"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374920"	"ZSWIM9"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374955"	"SPATA21"	"0.857"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"374955"	"SPATA21"	"0.857"	"0.172"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374955"	"SPATA21"	"0.857"	"0.172"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374955"	"SPATA21"	"0.857"	"0.172"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"374955"	"SPATA21"	"0.857"	"0.172"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"374969"	"SVBP"	"1"	"0.069"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"374977"	"MROH7"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"375056"	"MIA3"	"0.752"	"0.241"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"375056"	"MIA3"	"0.752"	"0.241"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.43"	"1"	"2009"	"2017"	"1"	"3"	"CTD_human"
"375056"	"MIA3"	"0.752"	"0.241"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2011"	"2018"	"1"	"4"	"CTD_human"
"375061"	"FAM89A"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"375298"	"CERKL"	"0.69"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"	"1"	"2004"	"2017"	"0"	"2"	"ORPHANET"
"375298"	"CERKL"	"0.69"	"0.31"	"C1842127"	"Retinitis Pigmentosa 26"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2004"	"2013"	"2"	"7"	"CTD_human;UNIPROT"
"375387"	"NRROS"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"375444"	"C5orf34"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"375449"	"MAST4"	"0.857"	"0.207"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C3151230"	"DEAFNESS, AUTOSOMAL RECESSIVE 61"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"2"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375611"	"SLC26A5"	"0.752"	"0.276"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"375612"	"LHFPL3"	"0.815"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"		"2014"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C2931245"	"Bone Marrow failure syndromes"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C3808553"	"Bone marrow failure syndrome 1"	"disease"	"C15"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"375748"	"ERCC6L2"	"0.785"	"0.138"	"C3810350"	"Bone marrow failure syndrome 2"	"disease"	"C15"	"Disease or Syndrome"	"0.60"		"2014"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"375790"	"AGRN"	"0.735"	"0.31"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"375790"	"AGRN"	"0.735"	"0.31"	"C0023467"	"Leukemia, Myelocytic, Acute"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"375790"	"AGRN"	"0.735"	"0.31"	"C0026998"	"Acute Myeloid Leukemia, M1"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"375790"	"AGRN"	"0.735"	"0.31"	"C0751882"	"Myasthenic Syndromes, Congenital"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.63"	"1"	"1993"	"2018"	"3"	"8"	"CTD_human;GENOMICS_ENGLAND"
"375790"	"AGRN"	"0.735"	"0.31"	"C0751883"	"Congenital Myasthenic Syndromes, Postsynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"375790"	"AGRN"	"0.735"	"0.31"	"C0751884"	"Congenital Myasthenic Syndromes, Presynaptic"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"375790"	"AGRN"	"0.735"	"0.31"	"C0751885"	"Myasthenic Syndromes, Congenital, Slow Channel"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"375790"	"AGRN"	"0.735"	"0.31"	"C1879321"	"Acute Myeloid Leukemia (AML-M2)"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"375790"	"AGRN"	"0.735"	"0.31"	"C3808739"	"MYASTHENIC SYNDROME, CONGENITAL, 8"	"disease"		"Disease or Syndrome"	"0.60"		"2009"	"2014"	"3"	"3"	"UNIPROT"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2003"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0271713"	"Ketotic hypoglycemia"	"phenotype"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751776"	"Atypical Inclusion-Body Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751777"	"Familial Progressive Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751778"	"Myoclonic Epilepsies, Progressive"	"disease"	"C10"	"Disease or Syndrome"	"0.44"	"1"	"2003"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751779"	"Action Myoclonus-Renal Failure Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751780"	"Biotin-Responsive Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751781"	"Dentatorubral-Pallidoluysian Atrophy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751782"	"May-White Syndrome"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751783"	"Lafora Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"1.00"	"0.962963"	"1993"	"2018"	"6"	"13"	"CTD_human;ORPHANET;UNIPROT"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C0751784"	"Lafora Body Disease, Late Onset"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C1850764"	"EPILEPSY, PROGRESSIVE MYOCLONIC 2B"	"disease"	"C10"	"Disease or Syndrome"	"0.40"		"2003"	"2011"	"6"	"14"	"UNIPROT"
"378884"	"NHLRC1"	"0.701"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9759036"	"2003"	"2018"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0236663"	"Alcohol withdrawal syndrome"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"0.8"	"2015"	"2018"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"378938"	"MALAT1"	"0.519"	"0.724"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"386653"	"IL31"	"0.727"	"0.276"	"C0011615"	"Dermatitis, Atopic"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.40"	"1"	"2005"	"2015"	"1"	"0"	"CTD_human"
"386653"	"IL31"	"0.727"	"0.276"	"C0086196"	"Eczema, Infantile"	"disease"	"C16;C17;C20"	"Disease or Syndrome"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"386681"	"KRTAP10-8"	"0.928"	"0.103"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"386681"	"KRTAP10-8"	"0.928"	"0.103"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"387032"	"ZKSCAN4"	"0.886"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.42"	"1"	"2012"	"2013"	"1"	"2"	"CTD_human"
"387082"	"SUMO4"	"0.659"	"0.517"	"C1838260"	"DIABETES MELLITUS, INSULIN-DEPENDENT, 5"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.40"		"2004"	"2005"	"0"	"1"	"CTD_human"
"387119"	"CEP85L"	"0.752"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"387129"	"NPSR1"	"0.639"	"0.379"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"387129"	"NPSR1"	"0.639"	"0.379"	"C0004096"	"Asthma"	"disease"	"C08;C20"	"Disease or Syndrome"	"0.40"	"0.9666667"	"2004"	"2017"	"3"	"0"	"CTD_human"
"387129"	"NPSR1"	"0.639"	"0.379"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"387129"	"NPSR1"	"0.639"	"0.379"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"387129"	"NPSR1"	"0.639"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.5"	"2007"	"2014"	"2"	"0"	"PSYGENET"
"387129"	"NPSR1"	"0.639"	"0.379"	"C1837811"	"ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2"	"disease"		"Disease or Syndrome"	"0.40"		"2004"	"2004"	"0"	"1"	"CTD_human"
"387357"	"THEMIS"	"0.815"	"0.276"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"387357"	"THEMIS"	"0.815"	"0.276"	"C0007570"	"Celiac Disease"	"disease"	"C06;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"387496"	"RASL11A"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"387496"	"RASL11A"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"387509"	"GPR153"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"387583"	"SPG25"	"0.928"	"0.138"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2002"	"2002"	"1"	"0"	"GENOMICS_ENGLAND"
"387583"	"SPG25"	"0.928"	"0.138"	"C2936860"	"Spastic paraplegia 25, autosomal recessive"	"disease"	"C05;C10;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"387700"	"SLC16A12"	"0.785"	"0.276"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.42"	"1"	"2010"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"387700"	"SLC16A12"	"0.785"	"0.276"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2008"	"2008"	"1"	"0"	"GENOMICS_ENGLAND"
"387700"	"SLC16A12"	"0.785"	"0.276"	"C2677587"	"Cataract, Juvenile, With Microcornea And Glucosuria"	"disease"	"C11;C12;C13;C16;C18"	"Disease or Syndrome"	"0.40"		"2007"	"2017"	"0"	"1"	"CTD_human"
"387700"	"SLC16A12"	"0.785"	"0.276"	"C4310806"	"CATARACT 47"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"387712"	"ENO4"	"1"	"0.034"	"C0021364"	"Male infertility"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"387712"	"ENO4"	"1"	"0.034"	"C0848676"	"Subfertility, Male"	"phenotype"	"C12"	"Sign or Symptom"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"387712"	"ENO4"	"1"	"0.034"	"C0917731"	"Male sterility"	"phenotype"	"C12"	"Finding"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"387715"	"ARMS2"	"0.681"	"0.276"	"C0242383"	"Age related macular degeneration"	"disease"	"C11"	"Disease or Syndrome"	"0.50"	"0.9725275"	"2006"	"2018"	"3"	"4"	"CTD_human"
"387715"	"ARMS2"	"0.681"	"0.276"	"C3151070"	"MACULAR DEGENERATION, AGE-RELATED, 8"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"387733"	"IFITM5"	"0.799"	"0.138"	"C0029434"	"Osteogenesis Imperfecta"	"disease"	"C05;C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.35"	"1"	"2014"	"2018"	"0"	"0"	"GENOMICS_ENGLAND"
"387733"	"IFITM5"	"0.799"	"0.138"	"C1970414"	"Osteogenesis Imperfecta, Type V"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.70"	"1"	"2012"	"2016"	"1"	"2"	"ORPHANET;UNIPROT"
"387733"	"IFITM5"	"0.799"	"0.138"	"C2931093"	"Osteogenesis imperfecta, type 5"	"disease"	"C05;C16;C17"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"387733"	"IFITM5"	"0.799"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"387787"	"LIPT2"	"0.886"	"0.034"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"387787"	"LIPT2"	"0.886"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"387787"	"LIPT2"	"0.886"	"0.034"	"C4540052"	"ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2017"	"1"	"2"	"UNIPROT"
"388015"	"RTL1"	"0.656"	"0.483"	"C1842466"	"Uniparental disomy, paternal, chromosome 14"	"disease"	"C23"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"388115"	"CCDC9B"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"388125"	"C2CD4B"	"0.928"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2010"	"2012"	"1"	"0"	"CTD_human"
"388228"	"SBK1"	"1"	"0.034"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"388389"	"CCDC103"	"0.799"	"0.172"	"C0022521"	"Kartagener Syndrome"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.42"	"1"	"1993"	"2015"	"0"	"2"	"ORPHANET"
"388389"	"CCDC103"	"0.799"	"0.172"	"C3542550"	"CILIARY DYSKINESIA, PRIMARY, 17"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2015"	"1"	"2"	"CTD_human;UNIPROT"
"388389"	"CCDC103"	"0.799"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"388389"	"CCDC103"	"0.799"	"0.172"	"C4277690"	"Ciliopathies"	"group"	"C16"	"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"388389"	"CCDC103"	"0.799"	"0.172"	"C4317124"	"Polynesian Bronchiectasis"	"disease"	"C08;C09;C14;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"388531"	"RGS9BP"	"0.928"	"0.103"	"C1842073"	"Prolonged Electroretinal Response Suppression"	"phenotype"	"C11;C16"	"Finding"	"0.60"		"2015"	"2015"	"0"	"1"	"CTD_human;ORPHANET"
"388551"	"CEACAM16"	"0.815"	"0.172"	"C0452138"	"Sensorineural hearing loss, bilateral"	"disease"		"Disease or Syndrome"	"0.50"		"2011"	"2016"	"4"	"0"	"CLINGEN"
"388551"	"CEACAM16"	"0.815"	"0.172"	"C1852282"	"DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2011"	"2016"	"4"	"0"	"CLINGEN"
"388551"	"CEACAM16"	"0.815"	"0.172"	"C3281297"	"DEAFNESS, AUTOSOMAL DOMINANT 4B"	"disease"		"Disease or Syndrome"	"0.60"		"1995"	"2016"	"2"	"2"	"CTD_human;UNIPROT"
"388552"	"BLOC1S3"	"0.773"	"0.379"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388552"	"BLOC1S3"	"0.773"	"0.379"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2008"	"2014"	"1"	"0"	"PSYGENET"
"388552"	"BLOC1S3"	"0.773"	"0.379"	"C0079504"	"Hermanski-Pudlak Syndrome"	"disease"	"C11;C15;C16;C17;C18"	"Disease or Syndrome"	"0.32"	"1"	"2006"	"2013"	"0"	"0"	"CTD_human"
"388552"	"BLOC1S3"	"0.773"	"0.379"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388552"	"BLOC1S3"	"0.773"	"0.379"	"C3888026"	"HERMANSKY-PUDLAK SYNDROME 8"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"1981"	"2013"	"0"	"2"	"ORPHANET"
"388585"	"HES5"	"0.707"	"0.31"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0027765"	"nervous system disorder"	"group"	"C10"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388585"	"HES5"	"0.707"	"0.31"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"388591"	"RNF207"	"1"	"0.034"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"388662"	"SLC6A17"	"0.773"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"388662"	"SLC6A17"	"0.773"	"0.241"	"C4225395"	"MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48"	"disease"		"Disease or Syndrome"	"0.70"		"2015"	"2015"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"388698"	"FLG2"	"0.834"	"0.103"	"C4015729"	"PEELING SKIN SYNDROME 3"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"388753"	"COA6"	"0.834"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"388753"	"COA6"	"0.834"	"0.172"	"C1858424"	"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"388753"	"COA6"	"0.834"	"0.172"	"C4225304"	"CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2016"	"3"	"2"	"UNIPROT"
"388939"	"PCARE"	"0.69"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.44"	"1"	"2010"	"2017"	"0"	"4"	"ORPHANET"
"388939"	"PCARE"	"0.69"	"0.31"	"C3150691"	"RETINITIS PIGMENTOSA 54"	"disease"		"Disease or Syndrome"	"0.60"		"1973"	"2015"	"0"	"11"	"CTD_human"
"388962"	"BOLA3"	"0.773"	"0.172"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"388962"	"BOLA3"	"0.773"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"388962"	"BOLA3"	"0.773"	"0.172"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"388962"	"BOLA3"	"0.773"	"0.172"	"C3280378"	"MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA"	"disease"		"Disease or Syndrome"	"0.70"		"2001"	"2016"	"4"	"4"	"CTD_human;ORPHANET;UNIPROT"
"388962"	"BOLA3"	"0.773"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2001"	"2001"	"1"	"0"	"GENOMICS_ENGLAND"
"389015"	"SLC9A4"	"0.928"	"0.069"	"C0001122"	"Acidosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"389015"	"SLC9A4"	"0.928"	"0.069"	"C0220981"	"Metabolic acidosis"	"phenotype"	"C18"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"389058"	"SP5"	"1"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"389058"	"SP5"	"1"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"389197"	"C4orf50"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389207"	"GRXCR1"	"0.857"	"0.172"	"C1414017"	"DEAFNESS, AUTOSOMAL RECESSIVE 25"	"disease"		"Disease or Syndrome"	"0.60"		"2010"	"2010"	"2"	"8"	"CTD_human;UNIPROT"
"389289"	"ANXA2R"	"0.928"	"0.207"	"C0005684"	"Malignant neoplasm of urinary bladder"	"disease"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"389289"	"ANXA2R"	"0.928"	"0.207"	"C0005695"	"Bladder Neoplasm"	"group"	"C04;C12;C13"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"389400"	"GFRAL"	"0.928"	"0.138"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389421"	"LIN28B"	"0.6"	"0.517"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"389421"	"LIN28B"	"0.6"	"0.517"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"389421"	"LIN28B"	"0.6"	"0.517"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"389421"	"LIN28B"	"0.6"	"0.517"	"C0027819"	"Neuroblastoma"	"group"	"C04"	"Neoplastic Process"	"0.68"	"1"	"2012"	"2017"	"2"	"1"	"CTD_human;ORPHANET"
"389421"	"LIN28B"	"0.6"	"0.517"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"389421"	"LIN28B"	"0.6"	"0.517"	"C2931189"	"Neural crest tumor"	"disease"	"C04;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"389434"	"IYD"	"0.696"	"0.483"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.33"	"1"	"2008"	"2018"	"4"	"0"	"GENOMICS_ENGLAND"
"389434"	"IYD"	"0.696"	"0.483"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"389434"	"IYD"	"0.696"	"0.483"	"C0342195"	"Thyroid Dyshormonogenesis 4"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.63"	"1"	"1954"	"2014"	"1"	"4"	"CTD_human;UNIPROT"
"389434"	"IYD"	"0.696"	"0.483"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2008"	"2014"	"4"	"0"	"GENOMICS_ENGLAND"
"389434"	"IYD"	"0.696"	"0.483"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"389549"	"FEZF1"	"0.727"	"0.31"	"C0162809"	"Kallmann Syndrome"	"disease"	"C12;C13;C16;C19"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"389549"	"FEZF1"	"0.727"	"0.31"	"C0342384"	"Idiopathic hypogonadotropic hypogonadism"	"disease"	"C19"	"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"0"	"CTD_human;GENOMICS_ENGLAND"
"389549"	"FEZF1"	"0.727"	"0.31"	"C4014988"	"HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA"	"disease"		"Disease or Syndrome"	"0.50"		"2014"	"2014"	"1"	"1"	"CTD_human;UNIPROT"
"389558"	"FAM180A"	"0.928"	"0.034"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"389558"	"FAM180A"	"0.928"	"0.034"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"389799"	"CFAP77"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"389827"	"MYMK"	"0.685"	"0.448"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"389827"	"MYMK"	"0.685"	"0.448"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"389827"	"MYMK"	"0.685"	"0.448"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"389827"	"MYMK"	"0.685"	"0.448"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"389827"	"MYMK"	"0.685"	"0.448"	"C1850746"	"Myopathy, congenital nonprogressive with Moebius and Robin sequences"	"disease"	"C05;C07;C10;C16"	"Disease or Syndrome"	"0.60"		"1982"	"2017"	"1"	"5"	"ORPHANET;UNIPROT"
"389840"	"MAP3K15"	"0.857"	"0.103"	"C0149782"	"Squamous cell carcinoma of lung"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389840"	"MAP3K15"	"0.857"	"0.103"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389840"	"MAP3K15"	"0.857"	"0.103"	"C0278883"	"Metastatic melanoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389840"	"MAP3K15"	"0.857"	"0.103"	"C1319315"	"Adenocarcinoma of large intestine"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"389840"	"MAP3K15"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"389856"	"USP27X"	"0.857"	"0.172"	"C2931498"	"Mental Retardation, X-Linked 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"389856"	"USP27X"	"0.857"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"389856"	"USP27X"	"0.857"	"0.172"	"C4310816"	"MENTAL RETARDATION, X-LINKED 105"	"disease"		"Disease or Syndrome"	"0.60"		"2016"	"2016"	"1"	"2"	"CTD_human;UNIPROT"
"390168"	"OR5M1"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"390594"	"KBTBD13"	"0.857"	"0.103"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"390594"	"KBTBD13"	"0.857"	"0.103"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"GENOMICS_ENGLAND"
"390594"	"KBTBD13"	"0.857"	"0.103"	"C0546125"	"Nemaline Myopathy, Childhood Onset"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"390594"	"KBTBD13"	"0.857"	"0.103"	"C1836472"	"Nemaline myopathy 6"	"disease"	"C05;C10"	"Disease or Syndrome"	"0.60"		"2003"	"2015"	"1"	"3"	"CTD_human;UNIPROT"
"390594"	"KBTBD13"	"0.857"	"0.103"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"391051"	"UOX"	"0.72"	"0.345"	"C0010093"	"Corpus Luteum Cyst"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C0028961"	"Oliguria"	"disease"	"C12;C13;C23"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C0029927"	"Ovarian Cysts"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C0041364"	"Tumor Lysis Syndrome"	"disease"	"C15;C20"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2005"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"391051"	"UOX"	"0.72"	"0.345"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"391356"	"PTRHD1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"392255"	"GDF6"	"0.614"	"0.414"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"392255"	"GDF6"	"0.614"	"0.414"	"C0022738"	"Klippel-Feil Syndrome"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.63"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human;ORPHANET"
"392255"	"GDF6"	"0.614"	"0.414"	"C0339527"	"Leber Congenital Amaurosis"	"disease"	"C11"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"392255"	"GDF6"	"0.614"	"0.414"	"C1531773"	"Currarino triad"	"disease"	"C06;C10;C16"	"Disease or Syndrome"	"0.30"		"1988"	"1988"	"1"	"0"	"GENOMICS_ENGLAND"
"392255"	"GDF6"	"0.614"	"0.414"	"C1861689"	"KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.63"	"1"	"1999"	"2013"	"1"	"4"	"CTD_human;UNIPROT"
"392255"	"GDF6"	"0.614"	"0.414"	"C2751307"	"MICROPHTHALMIA, ISOLATED 4 (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2009"	"2015"	"2"	"4"	"CTD_human;UNIPROT"
"392255"	"GDF6"	"0.614"	"0.414"	"C2931501"	"Microphthalmia associated with colobomatous cyst"	"disease"	"C04;C11;C16;C23"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"392255"	"GDF6"	"0.614"	"0.414"	"C3150968"	"MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"1"	"CTD_human"
"392255"	"GDF6"	"0.614"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"392255"	"GDF6"	"0.614"	"0.414"	"C3715164"	"LEBER CONGENITAL AMAUROSIS 17"	"disease"		"Disease or Syndrome"	"0.60"		"2013"	"2013"	"1"	"3"	"CTD_human;UNIPROT"
"392636"	"AGMO"	"0.857"	"0.276"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"399909"	"PCNX3"	"0.886"	"0.103"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"399909"	"PCNX3"	"0.886"	"0.103"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"400073"	"C12orf76"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"400359"	"C15orf53"	"0.886"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.41"	"1"	"2014"	"2014"	"1"	"13"	"PSYGENET"
"400359"	"C15orf53"	"0.886"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2009"	"2013"	"2"	"0"	"PSYGENET"
"400359"	"C15orf53"	"0.886"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"400500"	"BCAR4"	"0.773"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"400500"	"BCAR4"	"0.773"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2017"	"2"	"0"	"CTD_human"
"400500"	"BCAR4"	"0.773"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2011"	"2"	"0"	"CTD_human"
"400500"	"BCAR4"	"0.773"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2011"	"2"	"0"	"CTD_human"
"400765"	"MIR137HG"	"0.834"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.44"	"0.5"	"2011"	"2018"	"2"	"4"	"PSYGENET"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C0002736"	"Amyotrophic Lateral Sclerosis"	"disease"	"C10;C18"	"Disease or Syndrome"	"0.48"	"0.875"	"2014"	"2018"	"0"	"0"	"ORPHANET"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C0007959"	"Charcot-Marie-Tooth Disease"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C0270960"	"Congenital myopathy (disorder)"	"group"		"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"GENOMICS_ENGLAND"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C3554398"	"SPINAL MUSCULAR ATROPHY, JOKELA TYPE"	"disease"		"Disease or Syndrome"	"0.71"	"1"	"1993"	"2016"	"1"	"1"	"CTD_human;ORPHANET;UNIPROT"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C3888102"	"Frontotemporal Dementia With Motor Neuron Disease"	"disease"	"C10;C18;F03"	"Disease or Syndrome"	"0.33"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C4014648"	"FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2"	"disease"		"Disease or Syndrome"	"0.60"		"2014"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"400916"	"CHCHD10"	"0.642"	"0.345"	"C4015513"	"MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.70"		"1993"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"400931"	"MIRLET7BHG"	"0.886"	"0.069"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"400931"	"MIRLET7BHG"	"0.886"	"0.069"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"400935"	"IL17REL"	"0.886"	"0.172"	"C0009324"	"Ulcerative Colitis"	"disease"	"C06"	"Disease or Syndrome"	"0.41"	"1"	"2010"	"2017"	"1"	"1"	"CTD_human"
"401138"	"AMTN"	"0.886"	"0.138"	"C0002452"	"Amelogenesis Imperfecta"	"disease"	"C07;C16"	"Congenital Abnormality"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"401138"	"AMTN"	"0.886"	"0.138"	"C0399376"	"Amelogenesis Imperfecta, Type III"	"disease"	"C07;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"401138"	"AMTN"	"0.886"	"0.138"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"401145"	"CCSER1"	"0.834"	"0.172"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"401145"	"CCSER1"	"0.834"	"0.172"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"401145"	"CCSER1"	"0.834"	"0.172"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0013146"	"Drug abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0013170"	"Drug habituation"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0013222"	"Drug Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0029231"	"Organic Mental Disorders, Substance-Induced"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0038580"	"Substance Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0038586"	"Substance Use Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0236969"	"Substance-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C0740858"	"Substance abuse problem"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C1510472"	"Drug Dependence"	"phenotype"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401207"	"C5orf63"	"0.857"	"0.069"	"C4316881"	"Prescription Drug Abuse"	"phenotype"	"C25;F03"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"401285"	"TCP10L2"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"GENOMICS_ENGLAND"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0014550"	"Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0338478"	"Idiopathic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0338479"	"Symptomatic Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0393695"	"Early Childhood Epilepsy, Myoclonic"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0393702"	"Myoclonic Astatic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0393703"	"Myoclonic Absence Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0438414"	"Myoclonic Encephalopathy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0751120"	"Benign Infantile Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0751122"	"Infantile Severe Myoclonic Epilepsy"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401474"	"SAMD12"	"0.752"	"0.103"	"C0917800"	"Epilepsy, Myoclonic, Infantile"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"401612"	"SLC25A53"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"402415"	"XKRX"			"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"404281"	"YY2"	"1"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"1"	"UNIPROT"
"404672"	"GTF2H5"	"0.621"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"404672"	"GTF2H5"	"0.621"	"0.69"	"C1955934"	"Trichothiodystrophy Syndromes"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.40"	"0.9736842"	"1992"	"2016"	"0"	"0"	"ORPHANET"
"404672"	"GTF2H5"	"0.621"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"404672"	"GTF2H5"	"0.621"	"0.69"	"C4017171"	"TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE"	"disease"		"Disease or Syndrome"	"0.60"		"2004"	"2004"	"1"	"2"	"CTD_human;UNIPROT"
"405753"	"DUOXA2"	"0.696"	"0.414"	"C0010308"	"Congenital Hypothyroidism"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.39"	"1"	"2008"	"2018"	"5"	"0"	"GENOMICS_ENGLAND"
"405753"	"DUOXA2"	"0.696"	"0.414"	"C0342196"	"Thyroid Dyshormonogenesis 5"	"disease"	"C19"	"Disease or Syndrome"	"0.60"		"2008"	"2015"	"2"	"2"	"CTD_human;UNIPROT"
"405753"	"DUOXA2"	"0.696"	"0.414"	"C0749420"	"Thyroid Agenesis"	"disease"	"C16;C19"	"Congenital Abnormality"	"0.30"		"2008"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"405753"	"DUOXA2"	"0.696"	"0.414"	"C1848805"	"Thyroid Dyshormonogenesis 1"	"disease"	"C05;C16;C19"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406884"	"MIRLET7B"	"0.555"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406885"	"MIRLET7C"	"0.592"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406886"	"MIRLET7D"	"0.663"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406887"	"MIRLET7E"	"0.672"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406887"	"MIRLET7E"	"0.672"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406887"	"MIRLET7E"	"0.672"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406887"	"MIRLET7E"	"0.672"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406890"	"MIRLET7G"	"0.663"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406891"	"MIRLET7I"	"0.63"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406892"	"MIR100"	"0.551"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406893"	"MIR101-1"	"0.799"	"0.103"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406893"	"MIR101-1"	"0.799"	"0.103"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406894"	"MIR101-2"	"0.799"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"406894"	"MIR101-2"	"0.799"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"406894"	"MIR101-2"	"0.799"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406894"	"MIR101-2"	"0.799"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406899"	"MIR106A"	"0.6"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406899"	"MIR106A"	"0.6"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406900"	"MIR106B"	"0.575"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406900"	"MIR106B"	"0.575"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406900"	"MIR106B"	"0.575"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406900"	"MIR106B"	"0.575"	"0.621"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406900"	"MIR106B"	"0.575"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2011"	"2013"	"1"	"0"	"PSYGENET"
"406901"	"MIR107"	"0.586"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406901"	"MIR107"	"0.586"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406902"	"MIR10A"	"0.6"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0017658"	"Glomerulonephritis"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2007"	"2018"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2007"	"2013"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C1704377"	"Bright Disease"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406903"	"MIR10B"	"0.552"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.40"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2017"	"7"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9647059"	"2007"	"2018"	"1"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"406906"	"MIR122"	"0.535"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"7"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.37"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406910"	"MIR125A"	"0.572"	"0.69"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406911"	"MIR125B1"	"0.685"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406912"	"MIR125B2"	"0.685"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2008"	"2018"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2016"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.35"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"0.8888889"	"2008"	"2016"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406913"	"MIR126"	"0.51"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2011"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406914"	"MIR127"	"0.639"	"0.448"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406916"	"MIR128-2"	"0.735"	"0.276"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406919"	"MIR130A"	"0.57"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"0.875"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2007"	"2016"	"1"	"0"	"PSYGENET"
"406920"	"MIR130B"	"0.609"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406920"	"MIR130B"	"0.609"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406921"	"MIR132"	"0.569"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406922"	"MIR133A1"	"0.886"	"0.103"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406922"	"MIR133A1"	"0.886"	"0.103"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406924"	"MIR134"	"0.614"	"0.517"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406927"	"MIR136"	"0.672"	"0.379"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406928"	"MIR137"	"0.561"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"0.6666667"	"2013"	"2015"	"3"	"0"	"PSYGENET"
"406928"	"MIR137"	"0.561"	"0.621"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406928"	"MIR137"	"0.561"	"0.621"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406928"	"MIR137"	"0.561"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9714286"	"2011"	"2018"	"1"	"1"	"CTD_human"
"406928"	"MIR137"	"0.561"	"0.621"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406928"	"MIR137"	"0.561"	"0.621"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406929"	"MIR138-1"	"0.928"	"0.069"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406929"	"MIR138-1"	"0.928"	"0.069"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406929"	"MIR138-1"	"0.928"	"0.069"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406931"	"MIR139"	"0.604"	"0.448"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406931"	"MIR139"	"0.604"	"0.448"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406932"	"MIR140"	"0.627"	"0.483"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406932"	"MIR140"	"0.627"	"0.483"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406933"	"MIR141"	"0.548"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406934"	"MIR142"	"0.557"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2007"	"2012"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0024299"	"Lymphoma"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"1"	"2006"	"2017"	"1"	"0"	"CTD_human"
"406935"	"MIR143"	"0.536"	"0.621"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"406936"	"MIR144"	"0.573"	"0.69"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406936"	"MIR144"	"0.573"	"0.69"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2018"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0011881"	"Diabetic Nephropathy"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0017667"	"Nodular glomerulosclerosis"	"disease"	"C12;C13;C19"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0079731"	"B-Cell Lymphomas"	"group"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406937"	"MIR145"	"0.476"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0001956"	"Alcohol Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0002395"	"Alzheimer's Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.40"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.75"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0011265"	"Presenile dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.36"	"1"	"2013"	"2016"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0276496"	"Familial Alzheimer Disease (FAD)"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0494463"	"Alzheimer Disease, Late Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0546126"	"Acute Confusional Senile Dementia"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.75"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0750900"	"Alzheimer's Disease, Focal Onset"	"disease"	"C10;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C0750901"	"Alzheimer Disease, Early Onset"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406938"	"MIR146A"	"0.452"	"0.759"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.31"	"1"	"2013"	"2017"	"1"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406940"	"MIR148A"	"0.561"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406941"	"MIR149"	"0.604"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406942"	"MIR150"	"0.51"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0003865"	"Arthritis, Adjuvant-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2018"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0971858"	"Arthritis, Collagen-Induced"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C0993582"	"Arthritis, Experimental"	"disease"	"C05"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406943"	"MIR152"	"0.598"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406946"	"MIR154"	"0.681"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"0"	"2014"	"2017"	"2"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"2"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"0.9090909"	"2011"	"2018"	"2"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406947"	"MIR155"	"0.445"	"0.793"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406948"	"MIR15A"	"0.561"	"0.655"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406948"	"MIR15A"	"0.561"	"0.655"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406948"	"MIR15A"	"0.561"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406949"	"MIR15B"	"0.636"	"0.552"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406950"	"MIR16-1"	"0.707"	"0.379"	"C0023487"	"Acute Promyelocytic Leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2012"	"2013"	"1"	"0"	"PSYGENET"
"406952"	"MIR17"	"0.524"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406952"	"MIR17"	"0.524"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406953"	"MIR18A"	"0.586"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406957"	"MIR181C"	"0.645"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406958"	"MIR182"	"0.564"	"0.655"	"C0015408"	"Eye Injuries"	"group"	"C10;C11;C26"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406958"	"MIR182"	"0.564"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406958"	"MIR182"	"0.564"	"0.655"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0015408"	"Eye Injuries"	"group"	"C10;C11;C26"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0085742"	"Injuries, Acute Brain"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0270611"	"Brain Injuries"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0272945"	"Brain Lacerations"	"disease"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C0452047"	"Brain Injuries, Focal"	"group"	"C10;C26"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406959"	"MIR183"	"0.552"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406960"	"MIR184"	"0.614"	"0.517"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406960"	"MIR184"	"0.614"	"0.517"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"406960"	"MIR184"	"0.614"	"0.517"	"C1855670"	"Abnormality of the cornea"	"group"		"Finding"	"0.30"		"2012"	"2016"	"7"	"0"	"GENOMICS_ENGLAND"
"406960"	"MIR184"	"0.614"	"0.517"	"C3280392"	"EDICT syndrome"	"disease"		"Disease or Syndrome"	"0.55"	"1"	"2012"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"406961"	"MIR185"	"0.639"	"0.586"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406961"	"MIR185"	"0.639"	"0.586"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406961"	"MIR185"	"0.639"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"406962"	"MIR186"	"0.648"	"0.414"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406962"	"MIR186"	"0.648"	"0.414"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406964"	"MIR188"	"0.696"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406965"	"MIR190A"	"0.735"	"0.241"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406965"	"MIR190A"	"0.735"	"0.241"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406965"	"MIR190A"	"0.735"	"0.241"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2018"	"2"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406966"	"MIR191"	"0.611"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0027540"	"Necrosis"	"phenotype"	"C23"	"Organ or Tissue Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406967"	"MIR192"	"0.565"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2017"	"4"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406968"	"MIR193A"	"0.594"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406969"	"MIR194-1"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406970"	"MIR194-2"	"1"	"0.069"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406971"	"MIR195"	"0.547"	"0.552"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406974"	"MIR197"	"0.645"	"0.379"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406974"	"MIR197"	"0.645"	"0.379"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406974"	"MIR197"	"0.645"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"0.75"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406974"	"MIR197"	"0.645"	"0.379"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.37"	"0.8571429"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406979"	"MIR19A"	"0.584"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406983"	"MIR200A"	"0.592"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406983"	"MIR200A"	"0.592"	"0.517"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2010"	"2018"	"2"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9166667"	"2010"	"2018"	"2"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"406984"	"MIR200B"	"0.559"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2010"	"2"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9583333"	"2007"	"2018"	"2"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0014170"	"Endometrial Neoplasms"	"group"	"C04;C13"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0476089"	"Endometrial Carcinoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9565217"	"2007"	"2018"	"2"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2010"	"2016"	"2"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406985"	"MIR200C"	"0.536"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406986"	"MIR203A"	"0.524"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406986"	"MIR203A"	"0.524"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9545455"	"2009"	"2018"	"1"	"0"	"CTD_human"
"406986"	"MIR203A"	"0.524"	"0.621"	"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"406986"	"MIR203A"	"0.524"	"0.621"	"C0687132"	"heavy drinking"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"406987"	"MIR204"	"0.57"	"0.621"	"C0009363"	"Congenital ocular coloboma (disorder)"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"406987"	"MIR204"	"0.57"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406987"	"MIR204"	"0.57"	"0.621"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406987"	"MIR204"	"0.57"	"0.621"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406987"	"MIR204"	"0.57"	"0.621"	"C4225233"	"RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT"	"disease"		"Disease or Syndrome"	"0.50"				"0"	"1"	"CTD_human;ORPHANET"
"406988"	"MIR205"	"0.547"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2008"	"2018"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0007137"	"Squamous cell carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.40"	"0.9444444"	"2008"	"2017"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0007138"	"Carcinoma, Transitional Cell"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9285714"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406988"	"MIR205"	"0.547"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"406989"	"MIR206"	"0.557"	"0.621"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.39"	"1"	"2007"	"2015"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"406989"	"MIR206"	"0.557"	"0.621"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.38"	"1"	"2007"	"2014"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C0853193"	"Bipolar I disorder"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"406989"	"MIR206"	"0.557"	"0.621"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"406989"	"MIR206"	"0.557"	"0.621"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406990"	"MIR208A"	"0.713"	"0.31"	"C0876994"	"Cardiotoxicity"	"disease"	"C23;C25;C26"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0018800"	"Cardiomegaly"	"phenotype"	"C14;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0022658"	"Kidney Diseases"	"group"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2014"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C1383860"	"Cardiac Hypertrophy"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406991"	"MIR21"	"0.407"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406992"	"MIR210"	"0.501"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406993"	"MIR211"	"0.624"	"0.414"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406993"	"MIR211"	"0.624"	"0.414"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"406994"	"MIR212"	"0.611"	"0.552"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"406994"	"MIR212"	"0.611"	"0.552"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"2"	"0"	"CTD_human"
"406995"	"MIR181A1"	"0.773"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406995"	"MIR181A1"	"0.773"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406995"	"MIR181A1"	"0.773"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"406996"	"MIR214"	"0.536"	"0.655"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2011"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406997"	"MIR215"	"0.656"	"0.379"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406998"	"MIR216A"	"0.676"	"0.379"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0016059"	"Fibrosis"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C1623038"	"Cirrhosis"	"disease"	"C23"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"406999"	"MIR217"	"0.63"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C0019569"	"Hirschsprung Disease"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C0085758"	"Aganglionosis, Colonic"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C1257840"	"Aganglionosis, Rectosigmoid Colon"	"disease"	"C06;C16"	"Congenital Abnormality"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C3661523"	"Congenital Intestinal Aganglionosis"	"disease"	"C06;C16"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407000"	"MIR218-1"	"0.713"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C0024117"	"Chronic Obstructive Airway Disease"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C0028043"	"Nicotine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C0040332"	"Tobacco Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C0040336"	"Tobacco Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C0376384"	"Nicotine Use Disorder"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407001"	"MIR218-2"	"0.773"	"0.207"	"C1527303"	"Chronic Airflow Obstruction"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407002"	"MIR219A1"	"0.656"	"0.345"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407002"	"MIR219A1"	"0.656"	"0.345"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407003"	"MIR219A2"	"0.857"	"0.207"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"407004"	"MIR22"	"0.554"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C0079773"	"Lymphoma, T-Cell, Cutaneous"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2016"	"1"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C0376407"	"Granulomatous Slack Skin"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407004"	"MIR22"	"0.554"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.34"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407006"	"MIR221"	"0.516"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0040411"	"Tongue Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0153349"	"Malignant neoplasm of tongue"	"disease"	"C04;C07"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.40"	"0.9"	"2010"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C1168401"	"Squamous cell carcinoma of the head and neck"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2008"	"2015"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407007"	"MIR222"	"0.558"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.38"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"407009"	"MIR224"	"0.584"	"0.483"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C0004352"	"Autistic Disorder"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407010"	"MIR23A"	"0.572"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407011"	"MIR23B"	"0.579"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407012"	"MIR24-1"	"0.681"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407013"	"MIR24-2"	"0.799"	"0.207"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"407013"	"MIR24-2"	"0.799"	"0.207"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"407013"	"MIR24-2"	"0.799"	"0.207"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407013"	"MIR24-2"	"0.799"	"0.207"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2012"	"1"	"0"	"CTD_human"
"407014"	"MIR25"	"0.6"	"0.414"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.35"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407017"	"MIR26B"	"0.616"	"0.517"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.34"	"1"	"2012"	"2018"	"1"	"0"	"CTD_human"
"407018"	"MIR27A"	"0.537"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.33"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"407018"	"MIR27A"	"0.537"	"0.655"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407018"	"MIR27A"	"0.537"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407019"	"MIR27B"	"0.59"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2017"	"2"	"0"	"CTD_human"
"407020"	"MIR28"	"0.713"	"0.31"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407020"	"MIR28"	"0.713"	"0.31"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2011"	"2012"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2018"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"407021"	"MIR29A"	"0.523"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"407022"	"MIR296"	"0.667"	"0.379"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407023"	"MIR299"	"0.752"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407023"	"MIR299"	"0.752"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407023"	"MIR299"	"0.752"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407025"	"MIR29B2"	"0.554"	"0.724"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407026"	"MIR29C"	"0.558"	"0.655"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407027"	"MIR301A"	"0.624"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407029"	"MIR30A"	"0.545"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"3"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407030"	"MIR30B"	"0.648"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407031"	"MIR30C1"	"0.636"	"0.621"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.34"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"407032"	"MIR30C2"	"0.621"	"0.621"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407032"	"MIR30C2"	"0.621"	"0.621"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407033"	"MIR30D"	"0.63"	"0.552"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.35"	"1"	"2010"	"2016"	"1"	"0"	"PSYGENET"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"407034"	"MIR30E"	"0.645"	"0.483"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407034"	"MIR30E"	"0.645"	"0.483"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"407035"	"MIR31"	"0.528"	"0.655"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"407035"	"MIR31"	"0.528"	"0.655"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.40"	"0.9333333"	"2009"	"2017"	"1"	"0"	"CTD_human"
"407035"	"MIR31"	"0.528"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407035"	"MIR31"	"0.528"	"0.655"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.37"	"1"	"2010"	"2016"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407037"	"MIR320A"	"0.598"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2011"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.32"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0018799"	"Heart Diseases"	"group"	"C14"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0021368"	"Inflammation"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0028754"	"Obesity"	"disease"	"C18;C23"	"Disease or Syndrome"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0271650"	"Impaired glucose tolerance"	"phenotype"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.35"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407040"	"MIR34A"	"0.47"	"0.759"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2011"	"2014"	"2"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2008"	"2013"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"0.6666667"	"2011"	"2014"	"2"	"0"	"CTD_human"
"407041"	"MIR34B"	"0.558"	"0.69"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407042"	"MIR34C"	"0.602"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407046"	"MIR9-1"	"0.752"	"0.414"	"C0525041"	"Neurobehavioral Manifestations"	"group"	"C10;C23;F01"	"Sign or Symptom"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2015"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407050"	"MIR93"	"0.586"	"0.621"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407053"	"MIR96"	"0.607"	"0.483"	"C0015408"	"Eye Injuries"	"group"	"C10;C11;C26"	"Injury or Poisoning"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407053"	"MIR96"	"0.607"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.35"	"0.8"	"2009"	"2017"	"1"	"0"	"CTD_human"
"407053"	"MIR96"	"0.607"	"0.483"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407053"	"MIR96"	"0.607"	"0.483"	"C1384666"	"hearing impairment"	"phenotype"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"2"	"0"	"CTD_human"
"407053"	"MIR96"	"0.607"	"0.483"	"C3888123"	"DEAFNESS, AUTOSOMAL DOMINANT 50"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"2"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0014859"	"Esophageal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407054"	"MIR98"	"0.656"	"0.379"	"C0546837"	"Malignant neoplasm of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.34"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407055"	"MIR99A"	"0.621"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407056"	"MIR99B"	"0.701"	"0.379"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"407973"	"SCA20"	"1"	"0.069"	"C1837541"	"SPINOCEREBELLAR ATAXIA 20"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0005941"	"Bone Diseases, Developmental"	"group"	"C05"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0010068"	"Coronary heart disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0018273"	"Growth Disorders"	"group"	"C23"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0025958"	"Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0206762"	"Limb Deformities, Congenital"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C0796068"	"Oculodigitoesophagoduodenal syndrome"	"disease"	"C05;C06;C08;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C1956147"	"Microlissencephaly"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C3280489"	"FEINGOLD SYNDROME 2"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2009"	"2016"	"4"	"0"	"GENOMICS_ENGLAND"
"407975"	"MIR17HG"	"0.522"	"0.759"	"C3853041"	"Severe Congenital Microcephaly"	"disease"	"C05;C10;C16"	"Congenital Abnormality; Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0274861"	"Arsenic Poisoning, Inorganic"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0274862"	"Nervous System, Organic Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0311375"	"Arsenic Poisoning"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0751851"	"Arsenic Encephalopathy"	"disease"	"C10;C25"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414062"	"CCL3L3"	"0.785"	"0.207"	"C0751852"	"Arsenic Induced Polyneuropathy"	"disease"	"C10;C25"	"Injury or Poisoning"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"414886"	"SPG27"	"0.857"	"0.207"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"414886"	"SPG27"	"0.857"	"0.207"	"C1836899"	"SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"440138"	"ALG11"	"0.815"	"0.172"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"440138"	"ALG11"	"0.815"	"0.172"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"440138"	"ALG11"	"0.815"	"0.172"	"C3150913"	"CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip"	"disease"		"Congenital Abnormality; Disease or Syndrome"	"0.70"		"2010"	"2012"	"1"	"6"	"CTD_human;ORPHANET;UNIPROT"
"440138"	"ALG11"	"0.815"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2010"	"2013"	"2"	"3"	"CTD_human;GENOMICS_ENGLAND"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0087012"	"Ataxia, Spinocerebellar"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2015"	"2015"	"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752120"	"Spinocerebellar Ataxia Type 1"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752121"	"Spinocerebellar Ataxia Type 2"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752122"	"Spinocerebellar Ataxia Type 4"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752123"	"Spinocerebellar Ataxia Type 5"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752124"	"Spinocerebellar Ataxia Type 6 (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C0752125"	"Spinocerebellar Ataxia Type 7"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440193"	"CCDC88C"	"0.663"	"0.276"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2010"	"2013"	"2"	"0"	"GENOMICS_ENGLAND"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0018500"	"Hair Diseases"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0020542"	"Pulmonary Hypertension"	"phenotype"	"C08"	"Pathologic Function"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0021053"	"Immune System Diseases"	"group"	"C20"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0034091"	"Pulmonary Veno-Occlusive Disease (disorder)"	"disease"	"C08;C14"	"Disease or Syndrome"	"0.64"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0340543"	"Familial primary pulmonary hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0340548"	"Pulmonary capillary hemangiomatosis"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"2014"	"2016"	"0"	"0"	"ORPHANET"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0340848"	"PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE"	"disease"	"C04;C08"	"Disease or Syndrome"	"0.40"		"2014"	"2016"	"2"	"26"	"UNIPROT"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C1701939"	"Familial pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C2973725"	"Pulmonary arterial hypertension"	"disease"		"Disease or Syndrome"	"0.41"	"1"	"2014"	"2018"	"13"	"0"	"GENOMICS_ENGLAND"
"440275"	"EIF2AK4"	"0.696"	"0.414"	"C3203102"	"Idiopathic pulmonary arterial hypertension"	"disease"	"C08"	"Disease or Syndrome"	"0.42"	"1"	"2014"	"2018"	"13"	"0"	"GENOMICS_ENGLAND"
"440387"	"CTRB2"	"1"	"0.034"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.50"		"1991"	"1991"	"0"	"0"	"GENOMICS_ENGLAND"
"440435"	"GPR179"	"0.701"	"0.138"	"C0339535"	"Night blindness, congenital stationary"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.62"	"1"	"2012"	"2017"	"0"	"2"	"CTD_human;ORPHANET"
"440435"	"GPR179"	"0.701"	"0.138"	"C0949804"	"Polyomavirus Infections"	"group"	"C02"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C1848172"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C1850362"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C1864877"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C3281215"	"NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E"	"disease"		"Disease or Syndrome"	"0.60"		"2012"	"2012"	"1"	"12"	"UNIPROT"
"440435"	"GPR179"	"0.701"	"0.138"	"C3495587"	"Night Blindness, Congenital Stationary, Type 1A"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C3501847"	"Night blindness, congenital stationary, type 1"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C3711543"	"X-Linked Csnb"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440435"	"GPR179"	"0.701"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"440435"	"GPR179"	"0.701"	"0.138"	"C4041558"	"Cone-rod synaptic disorder, congenital nonprogressive"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"440822"	"PIWIL3"	"0.886"	"0.069"	"C0028960"	"Oligospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"440823"	"MIAT"	"0.799"	"0.207"	"C0027051"	"Myocardial Infarction"	"disease"	"C14"	"Disease or Syndrome"	"0.42"	"1"	"2007"	"2016"	"1"	"1"	"CTD_human"
"440836"	"ODF3B"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440836"	"ODF3B"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"440854"	"CAPN14"	"0.815"	"0.172"	"C0341106"	"Eosinophilic esophagitis"	"disease"	"C06;C15;C20"	"Disease or Syndrome"	"0.44"	"1"	"2015"	"2018"	"1"	"2"	"CTD_human"
"441151"	"TMEM151B"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441151"	"TMEM151B"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0006118"	"Brain Neoplasms"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0153633"	"Malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0496899"	"Benign neoplasm of brain, unspecified"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0750974"	"Brain Tumor, Primary"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0750977"	"Recurrent Brain Neoplasm"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C0750979"	"Primary malignant neoplasm of brain"	"disease"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441478"	"NRARP"	"0.834"	"0.069"	"C1527390"	"Neoplasms, Intracranial"	"group"	"C04;C10"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"441549"	"CDNF"	"0.928"	"0.103"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.01"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442038"	"SULT1C3"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442184"	"OR2B3"	"1"	"0.034"	"C0162823"	"Dermatitis, Irritant"	"disease"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442721"	"LMOD2"	"0.886"	"0.069"	"C0033975"	"Psychotic Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"442721"	"LMOD2"	"0.886"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"442721"	"LMOD2"	"0.886"	"0.069"	"C0349204"	"Nonorganic psychosis"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2009"	"2009"	"1"	"0"	"PSYGENET"
"442862"	"PRY2"	"0.886"	"0.069"	"C1839071"	"Spermatogenic Failure, Nonobstructive, Y-Linked"	"disease"	"C12;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"442891"	"MIR135B"	"0.609"	"0.483"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442892"	"MIR148B"	"0.672"	"0.379"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442893"	"MIR151A"	"0.701"	"0.276"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442894"	"MIR302B"	"0.72"	"0.241"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442895"	"MIR302C"	"0.762"	"0.172"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442895"	"MIR302C"	"0.762"	"0.172"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442896"	"MIR302D"	"0.799"	"0.207"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442896"	"MIR302D"	"0.799"	"0.207"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442896"	"MIR302D"	"0.799"	"0.207"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442896"	"MIR302D"	"0.799"	"0.207"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442896"	"MIR302D"	"0.799"	"0.207"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442897"	"MIR323A"	"0.762"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442897"	"MIR323A"	"0.762"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442897"	"MIR323A"	"0.762"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442898"	"MIR324"	"0.72"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442899"	"MIR325"	"0.886"	"0.138"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442899"	"MIR325"	"0.886"	"0.138"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442900"	"MIR326"	"0.659"	"0.345"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"442900"	"MIR326"	"0.659"	"0.345"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"442900"	"MIR326"	"0.659"	"0.345"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C0029463"	"Osteosarcoma"	"disease"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"442901"	"MIR328"	"0.63"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442901"	"MIR328"	"0.63"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442902"	"MIR330"	"0.667"	"0.414"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442903"	"MIR331"	"0.727"	"0.241"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442904"	"MIR335"	"0.579"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442905"	"MIR337"	"0.636"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442906"	"MIR338"	"0.611"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442907"	"MIR339"	"0.69"	"0.379"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0020507"	"Hyperplasia"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0025202"	"melanoma"	"disease"	"C04"	"Neoplastic Process"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442908"	"MIR340"	"0.642"	"0.345"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2010"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.32"	"0.5"	"2010"	"2014"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442909"	"MIR342"	"0.636"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442910"	"MIR345"	"0.652"	"0.31"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2017"	"2"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.34"	"1"	"2009"	"2015"	"3"	"0"	"PSYGENET"
"442911"	"MIR346"	"0.713"	"0.414"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"442911"	"MIR346"	"0.713"	"0.414"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442912"	"MIR367"	"0.72"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C0677886"	"Epithelial ovarian cancer"	"disease"	"C04;C13;C19"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442913"	"MIR376C"	"0.69"	"0.276"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442914"	"MIR369"	"0.72"	"0.276"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.33"	"1"	"2009"	"2016"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442915"	"MIR370"	"0.642"	"0.414"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"442920"	"MIR196B"	"0.594"	"0.517"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"449489"	"DFNB47"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"493753"	"COA5"	"0.701"	"0.448"	"C0007194"	"Hypertrophic Cardiomyopathy"	"disease"	"C14"	"Disease or Syndrome"	"0.41"	"1"	"2011"	"2011"	"0"	"0"	"GENOMICS_ENGLAND"
"493753"	"COA5"	"0.701"	"0.448"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.32"	"0.5"	"2005"	"2011"	"0"	"0"	"CTD_human"
"493753"	"COA5"	"0.701"	"0.448"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"493753"	"COA5"	"0.701"	"0.448"	"C1858424"	"Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency"	"disease"	"C05;C10;C14;C16;C18"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"493753"	"COA5"	"0.701"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"493753"	"COA5"	"0.701"	"0.448"	"C4225154"	"CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3"	"disease"		"Disease or Syndrome"	"0.40"		"2011"	"2011"	"1"	"1"	"UNIPROT"
"493818"	"MYMY3"			"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"493856"	"CISD2"	"0.681"	"0.517"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"493856"	"CISD2"	"0.681"	"0.517"	"C0043207"	"Wolfram Syndrome"	"disease"	"C09;C10;C11;C12;C13;C16;C18;C19"	"Disease or Syndrome"	"0.58"	"0.875"	"2001"	"2017"	"6"	"0"	"CLINGEN;ORPHANET"
"493856"	"CISD2"	"0.681"	"0.517"	"C1858028"	"WOLFRAM SYNDROME 2"	"disease"	"C09;C10;C11;C18;C23"	"Disease or Syndrome"	"0.64"	"0.75"	"2000"	"2015"	"1"	"1"	"CTD_human"
"493856"	"CISD2"	"0.681"	"0.517"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"493869"	"GPX8"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494323"	"MIR361"	"0.656"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494324"	"MIR375"	"0.53"	"0.655"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.34"	"0.75"	"2011"	"2017"	"1"	"0"	"CTD_human"
"494324"	"MIR375"	"0.53"	"0.655"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"494324"	"MIR375"	"0.53"	"0.655"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494325"	"MIR376A1"	"0.857"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494325"	"MIR376A1"	"0.857"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494325"	"MIR376A1"	"0.857"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494326"	"MIR377"	"0.672"	"0.31"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"494326"	"MIR377"	"0.672"	"0.31"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494326"	"MIR377"	"0.672"	"0.31"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494326"	"MIR377"	"0.672"	"0.31"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494326"	"MIR377"	"0.672"	"0.31"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494327"	"MIR378A"	"0.602"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494328"	"MIR379"	"0.735"	"0.31"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494328"	"MIR379"	"0.735"	"0.31"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494328"	"MIR379"	"0.735"	"0.31"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494328"	"MIR379"	"0.735"	"0.31"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494328"	"MIR379"	"0.735"	"0.31"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C0035222"	"Respiratory Distress Syndrome, Adult"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494329"	"MIR380"	"0.785"	"0.207"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494330"	"MIR381"	"0.707"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494331"	"MIR382"	"0.663"	"0.414"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"494331"	"MIR382"	"0.663"	"0.414"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494331"	"MIR382"	"0.663"	"0.414"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"494331"	"MIR382"	"0.663"	"0.414"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494331"	"MIR382"	"0.663"	"0.414"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494331"	"MIR382"	"0.663"	"0.414"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494332"	"MIR383"	"0.735"	"0.172"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"494332"	"MIR383"	"0.735"	"0.172"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"494332"	"MIR383"	"0.735"	"0.172"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"494332"	"MIR383"	"0.735"	"0.172"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"494333"	"MIR384"	"0.815"	"0.172"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494333"	"MIR384"	"0.815"	"0.172"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"494333"	"MIR384"	"0.815"	"0.172"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494333"	"MIR384"	"0.815"	"0.172"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"494333"	"MIR384"	"0.815"	"0.172"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C0279626"	"Squamous cell carcinoma of esophagus"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494335"	"MIR423"	"0.642"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"494336"	"MIR424"	"0.6"	"0.552"	"C0001925"	"Albuminuria"	"phenotype"	"C12;C13;C23"	"Finding"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494337"	"MIR425"	"0.676"	"0.276"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C0011052"	"Prelingual Deafness"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C0011053"	"Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C0086395"	"Hearing Loss, Extreme"	"phenotype"	"C09;C10;C23"	"Sign or Symptom"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C0581883"	"Complete Hearing Loss"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C0751068"	"Deafness, Acquired"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C1857744"	"DEAFNESS, AUTOSOMAL RECESSIVE 59"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.80"		"2006"	"2012"	"2"	"4"	"CTD_human;UNIPROT"
"494513"	"PJVK"	"0.762"	"0.172"	"C3665473"	"Bilateral Deafness"	"phenotype"	"C09;C10;C23"	"Finding"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494513"	"PJVK"	"0.762"	"0.172"	"C4082305"	"Deaf Mutism"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"494551"	"WEE2"	"0.928"	"0.069"	"C0278701"	"Gastric Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"494551"	"WEE2"	"0.928"	"0.069"	"C1335167"	"Ovarian Mucinous Adenocarcinoma"	"disease"		"Neoplastic Process"	"0.30"		"2007"	"2007"	"1"	"1"	"UNIPROT"
"541471"	"MIR4435-2HG"	"0.762"	"0.207"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"541471"	"MIR4435-2HG"	"0.762"	"0.207"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"CTD_human"
"552900"	"BOLA2"			"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"553158"	"PRR5-ARHGAP8"	"0.815"	"0.138"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"553158"	"PRR5-ARHGAP8"	"0.815"	"0.138"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"553158"	"PRR5-ARHGAP8"	"0.815"	"0.138"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"553158"	"PRR5-ARHGAP8"	"0.815"	"0.138"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"553158"	"PRR5-ARHGAP8"	"0.815"	"0.138"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2015"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"554210"	"MIR429"	"0.616"	"0.552"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574030"	"MIR362"	"0.69"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574032"	"MIR20B"	"0.727"	"0.379"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574032"	"MIR20B"	"0.727"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"574032"	"MIR20B"	"0.727"	"0.379"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574033"	"MIR18B"	"0.752"	"0.379"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2009"	"2014"	"1"	"0"	"CTD_human"
"574034"	"MIR433"	"0.713"	"0.345"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574034"	"MIR433"	"0.713"	"0.345"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574034"	"MIR433"	"0.713"	"0.345"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574034"	"MIR433"	"0.713"	"0.345"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574034"	"MIR433"	"0.713"	"0.345"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574038"	"MIR431"	"0.834"	"0.069"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574038"	"MIR431"	"0.834"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574038"	"MIR431"	"0.834"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574038"	"MIR431"	"0.834"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574408"	"MIR329-1"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574408"	"MIR329-1"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574408"	"MIR329-1"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574410"	"MIR323B"	"0.815"	"0.172"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574410"	"MIR323B"	"0.815"	"0.172"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574410"	"MIR323B"	"0.815"	"0.172"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574411"	"MIR451A"	"0.577"	"0.69"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574412"	"MIR452"	"0.681"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2016"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574413"	"MIR409"	"0.633"	"0.414"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574433"	"MIR412"	"0.857"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574433"	"MIR412"	"0.857"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574433"	"MIR412"	"0.857"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574434"	"MIR410"	"0.633"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574435"	"MIR376B"	"0.886"	"0.069"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574435"	"MIR376B"	"0.886"	"0.069"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574435"	"MIR376B"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574435"	"MIR376B"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574435"	"MIR376B"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574436"	"MIR485"	"0.681"	"0.483"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574436"	"MIR485"	"0.681"	"0.483"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574436"	"MIR485"	"0.681"	"0.483"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574436"	"MIR485"	"0.681"	"0.483"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574436"	"MIR485"	"0.681"	"0.483"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574441"	"MIR488"	"0.701"	"0.379"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574441"	"MIR488"	"0.701"	"0.379"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574441"	"MIR488"	"0.701"	"0.379"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574442"	"MIR489"	"0.727"	"0.241"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"574442"	"MIR489"	"0.727"	"0.241"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2010"	"2014"	"1"	"0"	"CTD_human"
"574442"	"MIR489"	"0.727"	"0.241"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574442"	"MIR489"	"0.727"	"0.241"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574445"	"MIR511"	"0.735"	"0.414"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574445"	"MIR511"	"0.735"	"0.414"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574445"	"MIR511"	"0.735"	"0.414"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574445"	"MIR511"	"0.735"	"0.414"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574445"	"MIR511"	"0.735"	"0.414"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574447"	"MIR146B"	"0.607"	"0.621"	"C0010054"	"Coronary Arteriosclerosis"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574447"	"MIR146B"	"0.607"	"0.621"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574447"	"MIR146B"	"0.607"	"0.621"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574447"	"MIR146B"	"0.607"	"0.621"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574447"	"MIR146B"	"0.607"	"0.621"	"C1956346"	"Coronary Artery Disease"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574450"	"MIR493"	"0.69"	"0.345"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574450"	"MIR493"	"0.69"	"0.345"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574450"	"MIR493"	"0.69"	"0.345"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574450"	"MIR493"	"0.69"	"0.345"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2015"	"2016"	"1"	"0"	"PSYGENET"
"574451"	"MIR432"	"0.752"	"0.241"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574451"	"MIR432"	"0.752"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2012"	"2014"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574452"	"MIR494"	"0.586"	"0.517"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574453"	"MIR495"	"0.681"	"0.241"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574453"	"MIR495"	"0.681"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574453"	"MIR495"	"0.681"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574453"	"MIR495"	"0.681"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574454"	"MIR496"	"0.834"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574454"	"MIR496"	"0.834"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574454"	"MIR496"	"0.834"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574455"	"MIR193B"	"0.616"	"0.552"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0001430"	"Adenoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0007120"	"Bronchioloalveolar Adenocarcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205646"	"Adenoma, Basal Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205647"	"Follicular adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205648"	"Adenoma, Microcystic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205649"	"Adenoma, Monomorphic"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205650"	"Papillary adenoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0205651"	"Adenoma, Trabecular"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574456"	"MIR497"	"0.58"	"0.586"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574457"	"MIR181D"	"0.707"	"0.31"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574466"	"MIR519C"	"0.928"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"574473"	"MIR520B"	"0.928"	"0.069"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574501"	"MIR499A"	"0.562"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.36"	"1"	"2009"	"2017"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574506"	"MIR503"	"0.624"	"0.483"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574508"	"MIR505"	"0.667"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"574511"	"MIR506"	"0.656"	"0.31"	"C0004509"	"Azoospermia"	"disease"	"C12"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"574511"	"MIR506"	"0.656"	"0.31"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"594857"	"NPS"	"0.652"	"0.655"	"C0003469"	"Anxiety Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.40"	"0.9333333"	"2009"	"2016"	"2"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0011570"	"Mental Depression"	"disease"	"F01"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"594857"	"NPS"	"0.652"	"0.655"	"C0011581"	"Depressive disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"594857"	"NPS"	"0.652"	"0.655"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2014"	"1"	"0"	"PSYGENET"
"594857"	"NPS"	"0.652"	"0.655"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0376280"	"Anxiety States, Neurotic"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0424295"	"Hyperactive behavior"	"phenotype"	"C10;C23"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"3"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C0751217"	"Hyperkinesia, Generalized"	"phenotype"	"C10;C23"	"Sign or Symptom"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"594857"	"NPS"	"0.652"	"0.655"	"C1279420"	"Anxiety neurosis (finding)"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2009"	"2011"	"2"	"0"	"CTD_human"
"606293"	"KLKP1"	"0.834"	"0.103"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"		"2006"	"2008"	"1"	"0"	"CTD_human"
"606293"	"KLKP1"	"0.834"	"0.103"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.33"	"1"	"2006"	"2012"	"1"	"0"	"CTD_human"
"613212"	"CTXN3"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2013"	"2016"	"1"	"0"	"PSYGENET"
"619379"	"SPG29"	"0.928"	"0.069"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2005"	"2005"	"0"	"0"	"GENOMICS_ENGLAND"
"619379"	"SPG29"	"0.928"	"0.069"	"C1857855"	"SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"619465"	"ERVK-8"	"0.681"	"0.621"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"PSYGENET"
"619509"	"WTRS"	"0.886"	"0.172"	"C0796117"	"Pitt-Rogers-Danks Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"619509"	"WTRS"	"0.886"	"0.172"	"C0796202"	"Wittwer syndrome"	"disease"	"C09;C10;C11;C16;C23"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"619509"	"WTRS"	"0.886"	"0.172"	"C1956097"	"Wolf-Hirschhorn Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.31"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619552"	"MIR483"	"0.592"	"0.69"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619553"	"MIR484"	"0.752"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619554"	"MIR486-1"	"0.596"	"0.586"	"C1510586"	"Autism Spectrum Disorders"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"619555"	"MIR487A"	"0.815"	"0.138"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619555"	"MIR487A"	"0.815"	"0.138"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619555"	"MIR487A"	"0.815"	"0.138"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"619556"	"MIR455"	"0.667"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"641339"	"ZNF674"	"0.928"	"0.172"	"C1136249"	"Mental Retardation, X-Linked"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2007"	"2007"	"1"	"0"	"CTD_human"
"641339"	"ZNF674"	"0.928"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.32"	"0.5"	"2007"	"2013"	"3"	"0"	"GENOMICS_ENGLAND"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0019209"	"Hepatomegaly"	"phenotype"	"C06;C23"	"Finding"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"641371"	"ACOT1"	"0.857"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"641372"	"ACOT6"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"643226"	"GRXCR2"	"0.886"	"0.103"	"C1846647"	"DEAFNESS, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C09;C10;C23"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"CLINGEN"
"643226"	"GRXCR2"	"0.886"	"0.103"	"C3892049"	"DEAFNESS, AUTOSOMAL RECESSIVE 101"	"disease"		"Disease or Syndrome"	"0.40"		"2014"	"2014"	"0"	"1"	"CTD_human"
"643418"	"LIPN"	"0.743"	"0.172"	"C0020758"	"Congenital ichthyosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"643418"	"LIPN"	"0.743"	"0.172"	"C0079154"	"Congenital Nonbullous Ichthyosiform Erythroderma"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"643418"	"LIPN"	"0.743"	"0.172"	"C0239849"	"Harlequin Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"643418"	"LIPN"	"0.743"	"0.172"	"C3536797"	"Ichthyosis Congenita II"	"disease"	"C16;C17"	"Congenital Abnormality; Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"643418"	"LIPN"	"0.743"	"0.172"	"C3543867"	"Collodion Fetus"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"643418"	"LIPN"	"0.743"	"0.172"	"C3553029"	"ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"644032"	"PHKG1P2"			"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0007097"	"Carcinoma"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0024667"	"Animal Mammary Neoplasms"	"group"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0024668"	"Mammary Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0205696"	"Anaplastic carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0205697"	"Carcinoma, Spindle-Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0205698"	"Undifferentiated carcinoma"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C0205699"	"Carcinomatosis"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644076"	"GLYCAM1"	"0.886"	"0.069"	"C1257925"	"Mammary Carcinoma, Animal"	"disease"	"C04;C22"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0011269"	"Dementia, Vascular"	"disease"	"C10;C14;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0270786"	"Binswanger Disease"	"disease"	"C10;C14;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0393560"	"Vascular Dementia, Acute Onset"	"disease"	"C10;C14;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0393561"	"Subcortical Vascular Dementia"	"disease"	"C10;C14;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0600359"	"Arteriosclerotic Dementia"	"disease"	"C10;C14;F03"	"Disease or Syndrome"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C1855008"	"Mitochondrial Complex II Deficiency"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.70"		"2010"	"2010"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"644096"	"SDHAF1"	"0.672"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"644165"	"BCRP3"	"0.773"	"0.207"	"C0040053"	"Thrombosis"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"644165"	"BCRP3"	"0.773"	"0.207"	"C0087086"	"Thrombus"	"phenotype"	"C14"	"Pathologic Function"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"644815"	"FAM83G"	"0.928"	"0.069"	"C0022596"	"Palmoplantar Keratosis"	"disease"	"C16;C17"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"644815"	"FAM83G"	"0.928"	"0.069"	"C0432330"	"Erythrokeratoderma"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"645249"	"MNX1-AS1"	"0.815"	"0.172"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"646702"	"HLA-DPA2"	"0.928"	"0.103"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0017605"	"Angle Closure Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.33"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0026010"	"Microphthalmos"	"disease"	"C11;C16"	"Congenital Abnormality"	"0.65"	"1"	"2011"	"2015"	"1"	"0"	"CTD_human;ORPHANET"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0027092"	"Myopia"	"disease"	"C11"	"Disease or Syndrome"	"0.32"	"1"	"2013"	"2015"	"1"	"0"	"CTD_human"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0266524"	"Dysplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0266527"	"Hypoplasia of eye"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"646960"	"PRSS56"	"0.752"	"0.172"	"C0311249"	"Cryptophthalmos"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"646960"	"PRSS56"	"0.752"	"0.172"	"C3150757"	"MICROPHTHALMIA, ISOLATED 6"	"disease"		"Disease or Syndrome"	"0.80"		"2005"	"2013"	"3"	"10"	"CTD_human;UNIPROT"
"646960"	"PRSS56"	"0.752"	"0.172"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"647979"	"NORAD"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"647979"	"NORAD"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"647979"	"NORAD"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"647979"	"NORAD"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"653220"	"XAGE1A"	"0.785"	"0.138"	"C0010606"	"Adenoid Cystic Carcinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0002152"	"Alloxan Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0003873"	"Rheumatoid Arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.34"	"1"	"2004"	"2017"	"2"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0005136"	"Berry Aneurysm"	"phenotype"	"C10;C14"	"Pathologic Function"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0007766"	"Intracranial Aneurysm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0011849"	"Diabetes Mellitus"	"group"	"C18;C19"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2013"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0011853"	"Diabetes Mellitus, Experimental"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0018203"	"Chronic granulomatous disease"	"group"	"C15;C16;C20"	"Disease or Syndrome"	"0.60"	"0.9821429"	"1990"	"2016"	"0"	"0"	"ORPHANET"
"653361"	"NCF1"	"0.546"	"0.759"	"C0020443"	"Hypercholesterolemia"	"disease"	"C18"	"Disease or Syndrome"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0020538"	"Hypertensive disease"	"group"	"C14"	"Disease or Syndrome"	"0.35"	"1"	"2006"	"2014"	"3"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0022661"	"Kidney Failure, Chronic"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0024141"	"Lupus Erythematosus, Systemic"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.32"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0038433"	"Streptozotocin Diabetes"	"disease"	"C18;C19"	"Experimental Model of Disease"	"0.30"		"2004"	"2006"	"2"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0086981"	"Sicca Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0162871"	"Aortic Aneurysm, Abdominal"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0242380"	"Libman-Sacks Disease"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0740385"	"Aneurysm, Middle Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0740386"	"Aneurysm, Anterior Communicating Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0740387"	"Aneurysm, Posterior Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751000"	"Aneurysm, Anterior Cerebral Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751001"	"Aneurysm, Basilar Artery"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751002"	"Aneurysm, Posterior Communicating Artery"	"phenotype"	"C10;C14"	"Anatomical Abnormality"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751003"	"Brain Aneurysm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751004"	"Giant Intracranial Aneurysm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0751005"	"Mycotic Aneurysm, Intracranial"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C0917996"	"Cerebral Aneurysm"	"disease"	"C10;C14"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C1527336"	"Sjogren's Syndrome"	"disease"	"C05;C07;C11;C17;C20"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"653361"	"NCF1"	"0.546"	"0.759"	"C1856251"	"Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I"	"disease"	"C15;C16;C20"	"Disease or Syndrome"	"0.60"		"1991"	"2014"	"2"	"5"	"CTD_human;UNIPROT"
"653509"	"SFTPA1"	"0.596"	"0.483"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"653509"	"SFTPA1"	"0.596"	"0.483"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.54"	"0.5"	"2003"	"2016"	"0"	"0"	"CTD_human;ORPHANET"
"653545"	"DUX4L5"	"0.928"	"0.103"	"C0032460"	"Polycystic Ovary Syndrome"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"653545"	"DUX4L5"	"0.928"	"0.103"	"C1136382"	"Sclerocystic Ovaries"	"disease"	"C04;C13;C19"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2017"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664612"	"MIR539"	"0.72"	"0.172"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664615"	"MIR376A2"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664615"	"MIR376A2"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664615"	"MIR376A2"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.31"	"1"	"2013"	"2014"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664616"	"MIR487B"	"0.743"	"0.207"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"664617"	"MIR542"	"0.707"	"0.276"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"664617"	"MIR542"	"0.707"	"0.276"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"664617"	"MIR542"	"0.707"	"0.276"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"677833"	"SNORA54"	"1"	"0.069"	"C0001973"	"Alcoholic Intoxication, Chronic"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"692088"	"SNORD50B"			"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"692088"	"SNORD50B"			"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"692088"	"SNORD50B"			"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"692088"	"SNORD50B"			"C0596263"	"Carcinogenesis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"692157"	"SNORA16B"	"0.886"	"0.069"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"692157"	"SNORA16B"	"0.886"	"0.069"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"692157"	"SNORA16B"	"0.886"	"0.069"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"692200"	"SNORD103C"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"PSYGENET"
"693120"	"MIR33B"	"0.667"	"0.448"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693120"	"MIR33B"	"0.667"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693121"	"MIR411"	"0.735"	"0.345"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"693121"	"MIR411"	"0.735"	"0.345"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693121"	"MIR411"	"0.735"	"0.345"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693121"	"MIR411"	"0.735"	"0.345"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693121"	"MIR411"	"0.735"	"0.345"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693122"	"MIR421"	"0.696"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693124"	"MIR532"	"0.672"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693128"	"MIR548B"	"1"	"0.034"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693149"	"MIR564"	"0.857"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693159"	"MIR574"	"0.672"	"0.414"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693167"	"MIR582"	"0.743"	"0.276"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693174"	"MIR589"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693177"	"MIR592"	"0.762"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"693180"	"MIR595"	"0.928"	"0.103"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"693183"	"MIR598"	"0.773"	"0.069"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693183"	"MIR598"	"0.773"	"0.069"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693183"	"MIR598"	"0.773"	"0.069"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693183"	"MIR598"	"0.773"	"0.069"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"693183"	"MIR598"	"0.773"	"0.069"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693194"	"MIR609"	"1"	"0.034"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693200"	"MIR615"	"0.773"	"0.31"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693210"	"MIR625"	"0.681"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693212"	"MIR627"	"0.773"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693213"	"MIR628"	"0.815"	"0.276"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693214"	"MIR629"	"0.681"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693223"	"MIR638"	"0.72"	"0.207"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.33"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"693223"	"MIR638"	"0.72"	"0.207"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"693223"	"MIR638"	"0.72"	"0.207"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2009"	"2015"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"693235"	"MIR92B"	"0.707"	"0.345"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"723779"	"MIR651"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724022"	"MIR652"	"0.743"	"0.172"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"724024"	"MIR654"	"0.857"	"0.138"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724024"	"MIR654"	"0.857"	"0.138"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724024"	"MIR654"	"0.857"	"0.138"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724024"	"MIR654"	"0.857"	"0.138"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724024"	"MIR654"	"0.857"	"0.138"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724025"	"MIR655"	"0.752"	"0.241"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724025"	"MIR655"	"0.752"	"0.241"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724025"	"MIR655"	"0.752"	"0.241"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724026"	"MIR656"	"0.834"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724026"	"MIR656"	"0.834"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724026"	"MIR656"	"0.834"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724030"	"MIR660"	"0.735"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"724066"	"ATXN8"	"0.752"	"0.172"	"C0004138"	"Ataxias, Hereditary"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"1999"	"1999"	"1"	"0"	"GENOMICS_ENGLAND"
"724066"	"ATXN8"	"0.752"	"0.172"	"C1837454"	"SPINOCEREBELLAR ATAXIA 8"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.55"	"1"	"2009"	"2013"	"0"	"0"	"CTD_human;ORPHANET"
"724107"	"SPG32"	"0.928"	"0.172"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"724107"	"SPG32"	"0.928"	"0.172"	"C1970009"	"SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE"	"disease"	"C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"724110"	"SPG34"	"0.928"	"0.069"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"724110"	"SPG34"	"0.928"	"0.069"	"C2677897"	"SPASTIC PARAPLEGIA 34, X-LINKED (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"727676"	"SNORD118"	"0.72"	"0.379"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"727676"	"SNORD118"	"0.72"	"0.379"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"727676"	"SNORD118"	"0.72"	"0.379"	"C3281200"	"LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS"	"disease"	"C04;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"6"	"CTD_human"
"727676"	"SNORD118"	"0.72"	"0.379"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"727764"	"MAFIP"	"0.834"	"0.103"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"727857"	"BHLHA9"	"0.713"	"0.138"	"C0152427"	"Polydactyly"	"disease"	"C05;C16"	"Congenital Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"727857"	"BHLHA9"	"0.713"	"0.138"	"C1836206"	"Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.71"	"1"	"1999"	"2015"	"1"	"3"	"CTD_human;ORPHANET;UNIPROT"
"727857"	"BHLHA9"	"0.713"	"0.138"	"C1843758"	"Camptosynpolydactyly, Complex"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.60"		"1999"	"2017"	"1"	"1"	"CTD_human;UNIPROT"
"727857"	"BHLHA9"	"0.713"	"0.138"	"C1861553"	"Split-Hand-Foot Malformation With Long Bone Deficiency 1"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"ORPHANET"
"727857"	"BHLHA9"	"0.713"	"0.138"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"727897"	"MUC5B"	"0.588"	"0.69"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.40"	"1"	"2011"	"2017"	"0"	"0"	"ORPHANET"
"727897"	"MUC5B"	"0.588"	"0.69"	"C0878555"	"Diffuse panbronchiolitis"	"disease"	"C01;C08"	"Disease or Syndrome"	"0.32"	"1"	"2005"	"2010"	"0"	"0"	"ORPHANET"
"727897"	"MUC5B"	"0.588"	"0.69"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.60"	"0.9545455"	"2011"	"2017"	"1"	"0"	"CTD_human;ORPHANET"
"728116"	"ZBTB8B"	"1"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"728118"	"NUTM2A"	"0.886"	"0.103"	"C0206630"	"Endometrial Stromal Sarcoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.36"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"728239"	"MAGED4"	"0.642"	"0.379"	"C0032927"	"Precancerous Conditions"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"728239"	"MAGED4"	"0.642"	"0.379"	"C0282313"	"Condition, Preneoplastic"	"phenotype"	"C04"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C0002514"	"Amino Acid Metabolism, Inborn Errors"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C0750905"	"Amino Acid Metabolism, Inherited Disorders"	"disease"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2005"	"2005"	"1"	"0"	"CTD_human"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C2746066"	"Combined D-2- and L-2-hydroxyglutaric aciduria"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.34"	"1"	"2005"	"2009"	"0"	"0"	"CTD_human"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C3152055"	"D-2-HYDROXYGLUTARIC ACIDURIA 1"	"disease"		"Disease or Syndrome"	"0.63"	"1"	"1993"	"2015"	"3"	"5"	"ORPHANET;UNIPROT"
"728294"	"D2HGDH"	"0.713"	"0.448"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"2005"	"2006"	"2"	"0"	"GENOMICS_ENGLAND"
"728310"	"GOLGA6L7"			"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"728448"	"PPIEL"	"0.928"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2008"	"2008"	"1"	"0"	"PSYGENET"
"728655"	"HULC"	"0.762"	"0.138"	"C0023903"	"Liver neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"728655"	"HULC"	"0.762"	"0.138"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"728655"	"HULC"	"0.762"	"0.138"	"C0345904"	"Malignant neoplasm of liver"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"728724"	"LINC00977"	"1"	"0.034"	"C0023418"	"leukemia"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0020517"	"Hypersensitivity"	"group"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0023895"	"Liver diseases"	"group"	"C06"	"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0032285"	"Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0032300"	"Lobar Pneumonia"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0034069"	"Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.32"	"1"	"2004"	"2016"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0038220"	"Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2014"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0086565"	"Liver Dysfunction"	"phenotype"	"C06"	"Finding"	"0.30"		"2003"	"2003"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0162820"	"Dermatitis, Allergic Contact"	"disease"	"C17;C20"	"Disease or Syndrome"	"0.30"		"2007"	"2007"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0270823"	"Petit mal status"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0311335"	"Grand Mal Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0393734"	"Complex Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0751522"	"Status Epilepticus, Subclinical"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0751523"	"Non-Convulsive Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0751524"	"Simple Partial Status Epilepticus"	"disease"	"C10;C23"	"Disease or Syndrome"	"0.30"		"2009"	"2010"	"2"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C0887898"	"Experimental Lung Inflammation"	"disease"	"C08"	"Experimental Model of Disease"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C1527304"	"Allergic Reaction"	"phenotype"	"C20"	"Pathologic Function"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C3714636"	"Pneumonitis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729230"	"CCR2"	"0.471"	"0.793"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729238"	"SFTPA2"	"0.598"	"0.552"	"C0085786"	"Hamman-Rich syndrome"	"disease"	"C08"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"729238"	"SFTPA2"	"0.598"	"0.552"	"C1800706"	"Idiopathic Pulmonary Fibrosis"	"disease"	"C08"	"Disease or Syndrome"	"0.72"	"1"	"2009"	"2016"	"1"	"2"	"CTD_human;ORPHANET;UNIPROT"
"729262"	"NUTM2B"	"0.928"	"0.103"	"C0206630"	"Endometrial Stromal Sarcoma"	"disease"	"C04;C13"	"Neoplastic Process"	"0.32"	"1"	"2013"	"2015"	"0"	"0"	"ORPHANET"
"729262"	"NUTM2B"	"0.928"	"0.103"	"C0334488"	"Clear cell sarcoma of kidney"	"disease"		"Neoplastic Process"	"0.34"	"1"	"2012"	"2017"	"0"	"0"	"ORPHANET"
"729330"	"OC90"	"1"	"0.034"	"C0042594"	"Vestibular Diseases"	"group"	"C09"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"729582"	"DIRC3"	"0.834"	"0.138"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.40"		"2017"	"2017"	"0"	"1"	"ORPHANET"
"729582"	"DIRC3"	"0.834"	"0.138"	"C1333985"	"Hereditary Clear Cell Renal Cell Carcinoma"	"phenotype"		"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"729920"	"ISPD"	"0.582"	"0.483"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0009451"	"Communicating Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0015393"	"Eye Abnormalities"	"group"	"C11;C16"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0020255"	"Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.60"		"2012"	"2012"	"2"	"0"	"CTD_human;GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0020256"	"Congenital Hydrocephalus"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0026848"	"Myopathy"	"group"	"C05;C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0265221"	"Walker-Warburg congenital muscular dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.54"	"0.75"	"2012"	"2016"	"2"	"0"	"CTD_human;ORPHANET"
"729920"	"ISPD"	"0.582"	"0.483"	"C0266470"	"Cerebellar Hypoplasia"	"disease"	"C10;C16;F03"	"Congenital Abnormality"	"0.40"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0270720"	"Hydrocephalus Ex-Vacuo"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0282577"	"Congenital Disorders of Glycosylation"	"group"	"C16;C18"	"Disease or Syndrome"	"0.30"		"2015"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0410174"	"Fukuyama Type Congenital Muscular Dystrophy"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0457133"	"Muscle eye brain disease"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0477432"	"Post-Traumatic Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0549423"	"Obstructive Hydrocephalus"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.42"	"1"	"2013"	"2015"	"1"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C1531647"	"Cerebral ventriculomegaly"	"phenotype"	"C10"	"Finding"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C1836373"	"MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C2936406"	"alpha-Dystroglycanopathies"	"disease"	"C10;C11;C16"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"2"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C2936718"	"Fetal Cerebral Ventriculomegaly"	"disease"	"C10"	"Congenital Abnormality"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C2936786"	"Aqueductal Stenosis"	"disease"	"C10"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"729920"	"ISPD"	"0.582"	"0.483"	"C3553330"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7"	"disease"		"Disease or Syndrome"	"0.40"		"1990"	"2017"	"5"	"18"	"UNIPROT"
"729920"	"ISPD"	"0.582"	"0.483"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"729920"	"ISPD"	"0.582"	"0.483"	"C4015095"	"MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7"	"disease"		"Disease or Syndrome"	"0.70"		"1990"	"2017"	"3"	"7"	"CTD_human;ORPHANET;UNIPROT"
"768206"	"PRCD"	"0.696"	"0.31"	"C0035334"	"Retinitis Pigmentosa"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.45"	"1"	"1998"	"2014"	"0"	"1"	"ORPHANET"
"768206"	"PRCD"	"0.696"	"0.31"	"C1864621"	"RETINITIS PIGMENTOSA 36"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.60"		"2006"	"2014"	"1"	"3"	"CTD_human;UNIPROT"
"768211"	"RELL1"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"768212"	"MIR758"	"0.857"	"0.138"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"768212"	"MIR758"	"0.857"	"0.138"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768212"	"MIR758"	"0.857"	"0.138"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768212"	"MIR758"	"0.857"	"0.138"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768212"	"MIR758"	"0.857"	"0.138"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768213"	"MIR671"	"0.743"	"0.276"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"768213"	"MIR671"	"0.743"	"0.276"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"768213"	"MIR671"	"0.743"	"0.276"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"768213"	"MIR671"	"0.743"	"0.276"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768218"	"MIR766"	"0.743"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768222"	"MIR770"	"0.834"	"0.103"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768222"	"MIR770"	"0.834"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768222"	"MIR770"	"0.834"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"768222"	"MIR770"	"0.834"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"780851"	"SNORD3A"	"0.886"	"0.069"	"C0022336"	"Creutzfeldt-Jakob disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"780851"	"SNORD3A"	"0.886"	"0.069"	"C0376329"	"New Variant Creutzfeldt-Jakob Disease"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"780851"	"SNORD3A"	"0.886"	"0.069"	"C0751254"	"Creutzfeldt-Jakob Disease, Familial"	"disease"	"C10;F03"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"790955"	"UQCC3"	"0.834"	"0.034"	"C0342778"	"Ubiquinone dehydrogenase deficiency"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"790955"	"UQCC3"	"0.834"	"0.034"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"790955"	"UQCC3"	"0.834"	"0.034"	"C1852372"	"MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)"	"disease"	"C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"790955"	"UQCC3"	"0.834"	"0.034"	"C4015253"	"MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9"	"disease"		"Disease or Syndrome"	"0.40"		"2015"	"2015"	"1"	"1"	"UNIPROT"
"791114"	"PWRN1"	"0.707"	"0.276"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"791114"	"PWRN1"	"0.707"	"0.276"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"791228"	"SPG36"	"0.834"	"0.207"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"791228"	"SPG36"	"0.834"	"0.207"	"C2936879"	"SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100033413"	"SNORD116-1"	"0.707"	"0.276"	"C0032897"	"Prader-Willi Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2002"	"2002"	"0"	"0"	"CTD_human"
"100033413"	"SNORD116-1"	"0.707"	"0.276"	"C0265222"	"Royer Syndrome"	"disease"	"C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0014175"	"Endometriosis"	"disease"	"C13"	"Disease or Syndrome"	"0.45"	"1"	"2010"	"2017"	"1"	"2"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0017612"	"Glaucoma, Open-Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.43"	"1"	"2011"	"2018"	"1"	"6"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0023434"	"Chronic Lymphocytic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0026640"	"Mouth Neoplasms"	"group"	"C04;C07"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0153381"	"Malignant neoplasm of mouth"	"disease"	"C04;C07"	"Neoplastic Process"	"0.40"		"2016"	"2016"	"1"	"1"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0269102"	"Endometrioma"	"disease"	"C13"	"Neoplastic Process"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0271148"	"Secondary Open Angle Glaucoma"	"disease"	"C11"	"Disease or Syndrome"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0333704"	"Chromosome Breaks"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0339573"	"Glaucoma, Primary Open Angle"	"disease"	"C11"	"Disease or Syndrome"	"0.38"	"1"	"2011"	"2016"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C0376628"	"Chromosome Breakage"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100048912"	"CDKN2B-AS1"	"0.55"	"0.586"	"C2931822"	"Nasopharyngeal carcinoma"	"disease"	"C04;C07;C09"	"Neoplastic Process"	"0.31"	"1"	"2017"	"2018"	"1"	"0"	"CTD_human"
"100049159"	"SPG37"	"0.928"	"0.069"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100049159"	"SPG37"	"0.928"	"0.069"	"C2936880"	"SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100049707"	"SPG38"	"0.857"	"0.103"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100049707"	"SPG38"	"0.857"	"0.103"	"C2676732"	"SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT (disorder)"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100124696"	"TEC"	"0.713"	"0.345"	"C0152013"	"Adenocarcinoma of lung (disorder)"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"				"0"	"0"	"UNIPROT"
"100124700"	"HOTAIR"	"0.538"	"0.655"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"0.9090909"	"2014"	"2018"	"1"	"0"	"CTD_human"
"100124700"	"HOTAIR"	"0.538"	"0.655"	"C0027643"	"Neoplasm Recurrence, Local"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100124700"	"HOTAIR"	"0.538"	"0.655"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2017"	"1"	"0"	"CTD_human"
"100124700"	"HOTAIR"	"0.538"	"0.655"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100124700"	"HOTAIR"	"0.538"	"0.655"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.37"	"1"	"2011"	"2018"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126297"	"MIR300"	"0.701"	"0.172"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126309"	"MIR875"	"0.815"	"0.138"	"C0008370"	"Cholestasis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126313"	"MIR744"	"0.72"	"0.379"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2017"	"2"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126314"	"MIR877"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126315"	"MIR665"	"0.834"	"0.138"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126315"	"MIR665"	"0.834"	"0.138"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126315"	"MIR665"	"0.834"	"0.138"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126317"	"MIR374B"	"0.727"	"0.241"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100126318"	"MIR301B"	"0.773"	"0.31"	"C0009171"	"Cocaine Abuse"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126318"	"MIR301B"	"0.773"	"0.31"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100126318"	"MIR301B"	"0.773"	"0.31"	"C0236736"	"Cocaine-Related Disorders"	"group"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126318"	"MIR301B"	"0.773"	"0.31"	"C0600427"	"Cocaine Dependence"	"disease"	"C25;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"CTD_human"
"100126319"	"MIR216B"	"0.707"	"0.31"	"C0030305"	"Pancreatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126327"	"MIR938"	"0.785"	"0.103"	"C0007095"	"Carcinoid Tumor"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"100126327"	"MIR938"	"0.785"	"0.103"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"100126327"	"MIR938"	"0.785"	"0.103"	"C0205695"	"Carcinoid, Goblet Cell"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"100126327"	"MIR938"	"0.785"	"0.103"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"100126327"	"MIR938"	"0.785"	"0.103"	"C0600176"	"Argentaffinoma"	"disease"	"C04"	"Neoplastic Process"	"0.30"		"2014"	"2014"	"1"	"0"	"CTD_human"
"100126328"	"MIR940"	"0.743"	"0.241"	"C0027626"	"Neoplasm Invasiveness"	"phenotype"	"C04;C23"	"Pathologic Function"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126333"	"MIR708"	"0.642"	"0.345"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126333"	"MIR708"	"0.642"	"0.345"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126333"	"MIR708"	"0.642"	"0.345"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126333"	"MIR708"	"0.642"	"0.345"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2018"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0235874"	"Disease Exacerbation"	"phenotype"	"C23"	"Finding"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0524909"	"Hepatitis B, Chronic"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2016"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126334"	"MIR885"	"0.648"	"0.345"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126335"	"MIR543"	"0.735"	"0.207"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126335"	"MIR543"	"0.735"	"0.207"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126335"	"MIR543"	"0.735"	"0.207"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126345"	"MIR889"	"0.834"	"0.103"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126345"	"MIR889"	"0.834"	"0.103"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126345"	"MIR889"	"0.834"	"0.103"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126346"	"MIR190B"	"0.799"	"0.207"	"C0018781"	"Noise-induced hearing loss"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100126346"	"MIR190B"	"0.799"	"0.207"	"C1148522"	"Acoustic Trauma"	"disease"	"C09;C10;C23"	"Injury or Poisoning"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100126348"	"MIR760"	"0.773"	"0.069"	"C0019207"	"Hepatoma, Morris"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126348"	"MIR760"	"0.773"	"0.069"	"C0019208"	"Hepatoma, Novikoff"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126348"	"MIR760"	"0.773"	"0.069"	"C0023904"	"Liver Neoplasms, Experimental"	"group"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126348"	"MIR760"	"0.773"	"0.069"	"C0086404"	"Experimental Hepatoma"	"disease"	"C04;C06"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2011"	"2011"	"1"	"0"	"CTD_human"
"100126351"	"MIR939"	"0.928"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126355"	"MIR365A"	"0.857"	"0.172"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126356"	"MIR365B"	"0.857"	"0.138"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100126572"	"GJE1"	"1"	"0.034"	"C0031117"	"Peripheral Neuropathy"	"group"	"C10"	"Disease or Syndrome"	"0.31"	"1"	"2011"	"2011"	"1"	"0"	"CTD_human"
"100126572"	"GJE1"	"1"	"0.034"	"C0086543"	"Cataract"	"disease"	"C11"	"Acquired Abnormality"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100128252"	"ZNF667-AS1"	"0.928"	"0.069"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100128252"	"ZNF667-AS1"	"0.928"	"0.069"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100128252"	"ZNF667-AS1"	"0.928"	"0.069"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100128252"	"ZNF667-AS1"	"0.928"	"0.069"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100128927"	"ZBTB42"	"1"		"C4015686"	"LETHAL CONGENITAL CONTRACTURE SYNDROME 6"	"disease"		"Disease or Syndrome"	"0.61"	"1"	"2015"	"2015"	"1"	"1"	"CTD_human;UNIPROT"
"100128998"	"C20orf181"	"0.557"	"0.69"	"C0009178"	"Cocaine withdrawal"	"disease"		"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2011"	"2011"	"1"	"0"	"PSYGENET"
"100130890"	"TSTD3"	"1"	"0.034"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100131801"	"PET100"	"0.696"	"0.414"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.42"	"1"	"2014"	"2016"	"0"	"2"	"CTD_human"
"100131801"	"PET100"	"0.696"	"0.414"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100131801"	"PET100"	"0.696"	"0.414"	"C0751651"	"Mitochondrial Diseases"	"group"	"C18"	"Disease or Syndrome"	"0.30"		"2014"	"2014"	"1"	"0"	"GENOMICS_ENGLAND"
"100131801"	"PET100"	"0.696"	"0.414"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"		"1993"	"2016"	"3"	"0"	"GENOMICS_ENGLAND"
"100131814"	"LINC00271"	"0.886"	"0.103"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.33"	"0.6666667"	"2006"	"2010"	"3"	"0"	"PSYGENET"
"100133941"	"CD24"	"0.521"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100133941"	"CD24"	"0.521"	"0.69"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100133941"	"CD24"	"0.521"	"0.69"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.37"	"1"	"2008"	"2017"	"1"	"0"	"CTD_human"
"100134444"	"KCNJ18"	"0.762"	"0.276"	"C0268446"	"Thyrotoxic periodic paralysis"	"disease"		"Disease or Syndrome"	"0.43"	"1"	"1993"	"2017"	"0"	"9"	"ORPHANET"
"100134444"	"KCNJ18"	"0.762"	"0.276"	"C2750473"	"THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2"	"phenotype"		"Finding"	"0.60"		"2010"	"2017"	"3"	"6"	"CTD_human;UNIPROT"
"100137049"	"PLA2G4B"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2006"	"2006"	"1"	"0"	"PSYGENET"
"100144748"	"KLLN"	"0.621"	"0.517"	"C0018553"	"Hamartoma Syndrome, Multiple"	"disease"	"C04;C16"	"Neoplastic Process"	"0.35"	"1"	"2010"	"2016"	"0"	"0"	"ORPHANET"
"100144748"	"KLLN"	"0.621"	"0.517"	"C0346153"	"Breast Cancer, Familial"	"disease"	"C04;C17"	"Neoplastic Process"	"0.30"				"0"	"0"	"ORPHANET"
"100144748"	"KLLN"	"0.621"	"0.517"	"C2676500"	"COWDEN-LIKE SYNDROME (disorder)"	"disease"	"C04;C16;C18"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"0"	"0"	"CTD_human"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C0431350"	"Primary microcephaly"	"disease"		"Congenital Abnormality"	"0.30"		"1993"	"2011"	"2"	"0"	"GENOMICS_ENGLAND"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C0796021"	"Lowry Wood syndrome"	"disease"	"C05;C10;C16;C23;F01;F03"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C1846059"	"Roifman syndrome"	"disease"	"C05;C10;C11;C14;C16;C20"	"Disease or Syndrome"	"0.51"	"1"	"2016"	"2016"	"1"	"7"	"CTD_human;ORPHANET"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C1859452"	"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I"	"disease"	"C05;C10;C13;C16;C19;C23"	"Congenital Abnormality"	"0.37"	"1"	"2011"	"2016"	"1"	"8"	"CTD_human"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.40"				"0"	"0"	"GENOMICS_ENGLAND"
"100151683"	"RNU4ATAC"	"0.577"	"0.655"	"C4319565"	"Microcephalic osteodysplastic primordial dwarfism types I and III"	"disease"		"Congenital Abnormality"	"0.30"				"0"	"0"	"ORPHANET"
"100187828"	"HBD"	"0.762"	"0.207"	"C0010828"	"Cytopenia"	"phenotype"		"Pathologic Function"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100187828"	"HBD"	"0.762"	"0.207"	"C0158995"	"Congenital anemia"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100187828"	"HBD"	"0.762"	"0.207"	"C0271985"	"Delta-Beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100188856"	"DEL22Q11.2"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2012"	"2012"	"1"	"0"	"PSYGENET"
"100216344"	"DYT17"	"1"	"0.034"	"C2676281"	"DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE (disorder)"	"disease"	"C10"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100271837"	"USH1H"	"1"	"0.172"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2009"	"2009"	"0"	"0"	"ORPHANET"
"100272147"	"CMC4"	"0.928"	"0.241"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2014"	"2016"	"2"	"0"	"GENOMICS_ENGLAND"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0003886"	"Arthrogryposis"	"disease"	"C05;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0023452"	"Childhood Acute Lymphoblastic Leukemia"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0023453"	"Leukemia, Lymphocytic, Acute, L2"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0023485"	"Precursor B-Cell Lymphoblastic Leukemia-Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0238288"	"Muscular Dystrophy, Facioscapulohumeral"	"disease"	"C05;C10;C16"	"Disease or Syndrome"	"0.60"	"1"	"2006"	"2018"	"1"	"0"	"CTD_human;ORPHANET"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0686353"	"Muscular Dystrophies, Limb-Girdle"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0699743"	"Congenital muscular dystrophy (disorder)"	"disease"		"Disease or Syndrome"	"0.30"		"2016"	"2017"	"5"	"0"	"GENOMICS_ENGLAND"
"100288687"	"DUX4"	"0.676"	"0.276"	"C0751336"	"Distal Muscular Dystrophies"	"group"	"C05;C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100288687"	"DUX4"	"0.676"	"0.276"	"C1961102"	"Precursor Cell Lymphoblastic Leukemia Lymphoma"	"disease"	"C04;C15;C20"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100288805"	"HYDIN2"			"C0376634"	"Craniofacial Abnormalities"	"group"	"C05;C16"	"Congenital Abnormality"	"0.30"		"2008"	"2008"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302115"	"MIR1468"	"0.799"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302123"	"MIR1275"	"0.773"	"0.31"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100302129"	"MIR1915"	"0.886"	"0.172"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C0007131"	"Non-Small Cell Lung Carcinoma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.32"	"1"	"2012"	"2016"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302142"	"MIR1246"	"0.656"	"0.517"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302145"	"MIR1247"	"0.69"	"0.276"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302149"	"MIR1249"	"0.785"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302150"	"MIR1296"	"0.886"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302174"	"MIR1307"	"0.72"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302197"	"MIR1306"	"0.799"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302201"	"MIR1228"	"0.928"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302218"	"MIR1285-1"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302221"	"MIR1291"	"0.785"	"0.207"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302232"	"MIR1226"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302236"	"MIR1260A"	"0.785"	"0.172"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302240"	"MIR1304"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302246"	"MIR1301"	"0.857"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302250"	"MIR1197"	"0.886"	"0.069"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302250"	"MIR1197"	"0.886"	"0.069"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302250"	"MIR1197"	"0.886"	"0.069"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302258"	"MIR1469"			"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100302259"	"MIR1202"	"0.762"	"0.276"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"100302259"	"MIR1202"	"0.762"	"0.276"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"PSYGENET"
"100302263"	"MIR1908"	"0.815"	"0.172"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302276"	"MIR1290"	"0.672"	"0.448"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302284"	"MIR1303"	"0.773"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100302690"	"DLG2-AS1"	"1"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"100302690"	"DLG2-AS1"	"1"	"0.034"	"C0809983"	"Schizophrenia and related disorders"	"group"		"Disease or Syndrome"	"0.31"	"1"	"2003"	"2003"	"1"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C0041696"	"Unipolar Depression"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C0220702"	"SCHIZOPHRENIA 1 (disorder)"	"disease"		"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2013"	"2013"	"1"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C0525045"	"Mood Disorders"	"group"	"F03"	"Mental or Behavioral Dysfunction"	"0.30"	"1"	"2010"	"2010"	"1"	"0"	"PSYGENET"
"100303453"	"TSNAX-DISC1"	"0.815"	"0.069"	"C1269683"	"Major Depressive Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2010"	"2013"	"2"	"0"	"PSYGENET"
"100303755"	"PET117"	"0.928"	"0.103"	"C0268237"	"Cytochrome-c Oxidase Deficiency"	"disease"	"C16;C18"	"Congenital Abnormality; Disease or Syndrome"	"0.31"	"1"	"2017"	"2017"	"0"	"0"	"ORPHANET"
"100312787"	"VN1R31P"			"C0037274"	"Dermatologic disorders"	"group"	"C17"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C0023890"	"Liver Cirrhosis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C0239946"	"Fibrosis, Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313838"	"MIR764"	"0.785"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313886"	"MIR2116"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100313923"	"MIR449C"	"0.752"	"0.207"	"C0015695"	"Fatty Liver"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100313923"	"MIR449C"	"0.752"	"0.207"	"C2711227"	"Steatohepatitis"	"disease"	"C06"	"Disease or Syndrome"	"0.30"		"2012"	"2012"	"1"	"0"	"CTD_human"
"100359393"	"SCA30"	"0.928"	"0.103"	"C2936793"	"Spinocerebellar ataxia 30"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100359402"	"SPG41"	"0.928"	"0.069"	"C0037773"	"Spastic Paraplegia, Hereditary"	"disease"	"C10;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100359402"	"SPG41"	"0.928"	"0.069"	"C3888208"	"SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100359403"	"PARK16"	"0.928"	"0.069"	"C0030567"	"Parkinson Disease"	"disease"	"C10"	"Disease or Syndrome"	"0.40"	"0.9090909"	"2010"	"2018"	"2"	"0"	"CTD_human"
"100422821"	"MIR1273C"	"0.928"	"0.069"	"C0009402"	"Colorectal Carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100422821"	"MIR1273C"	"0.928"	"0.069"	"C0009404"	"Colorectal Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100422821"	"MIR1273C"	"0.928"	"0.069"	"C0920269"	"Microsatellite Instability"	"phenotype"	"C23"	"Pathologic Function"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100422821"	"MIR1273C"	"0.928"	"0.069"	"C1527249"	"Colorectal Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100422821"	"MIR1273C"	"0.928"	"0.069"	"C1721098"	"Replication Error Phenotype"	"phenotype"	"C23"	"Cell or Molecular Dysfunction"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100422837"	"MIR1193"	"0.815"	"0.172"	"C0027659"	"Neoplasms, Experimental"	"group"	"C04"	"Experimental Model of Disease; Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422837"	"MIR1193"	"0.815"	"0.172"	"C0238463"	"Papillary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422837"	"MIR1193"	"0.815"	"0.172"	"C3501843"	"Non-medullary thyroid carcinoma"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422837"	"MIR1193"	"0.815"	"0.172"	"C3501844"	"Familial Nonmedullary Thyroid Cancer"	"disease"	"C04;C19"	"Neoplastic Process"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422867"	"MIR378C"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422910"	"MIR2861"	"0.834"	"0.138"	"C3150680"	"BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15"	"phenotype"		"Finding"	"0.30"				"0"	"1"	"CTD_human"
"100422981"	"MIR3173"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100422991"	"MIR1260B"	"0.743"	"0.241"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100499467"	"LINC00673"	"0.815"	"0.172"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100499467"	"LINC00673"	"0.815"	"0.172"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C0023891"	"Liver Cirrhosis, Alcoholic"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100500847"	"MIR3615"	"0.799"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0006142"	"Malignant neoplasm of breast"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2004"	"2016"	"2"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0007621"	"Neoplastic Cell Transformation"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0007820"	"Cerebrovascular Disorders"	"group"	"C10;C14"	"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0019156"	"Hepatic Veno-Occlusive Disease"	"disease"	"C06;C14"	"Disease or Syndrome"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0022660"	"Kidney Failure, Acute"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0023520"	"Leukodystrophy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0027651"	"Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0035309"	"Retinal Diseases"	"group"	"C11"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0038002"	"Splenomegaly"	"phenotype"	"C23"	"Finding"	"0.40"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0086692"	"Benign Neoplasm"	"group"	"C04"	"Neoplastic Process"	"0.30"		"2006"	"2006"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0543888"	"Epileptic encephalopathy"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"GENOMICS_ENGLAND"
"100506658"	"OCLN"	"0.57"	"0.69"	"C0678222"	"Breast Carcinoma"	"disease"	"C04;C17"	"Neoplastic Process"	"0.33"	"0.6666667"	"2004"	"2016"	"2"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C1257931"	"Mammary Neoplasms, Human"	"group"	"C04;C17"	"Neoplastic Process"	"0.30"		"2007"	"2013"	"2"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C1458155"	"Mammary Neoplasms"	"group"	"C04;C17"	"Neoplastic Process"	"0.33"	"1"	"2002"	"2013"	"2"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C1565662"	"Acute Kidney Insufficiency"	"disease"	"C12;C13"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C1955869"	"Malformations of Cortical Development"	"group"	"C10;C16"	"Disease or Syndrome"	"0.31"	"1"	"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"100506658"	"OCLN"	"0.57"	"0.69"	"C2609414"	"Acute kidney injury"	"disease"	"C12;C13"	"Injury or Poisoning"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100506658"	"OCLN"	"0.57"	"0.69"	"C2931662"	"Baraitser Brett Piesowicz syndrome"	"disease"	"C05;C10;C16;C18"	"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100506658"	"OCLN"	"0.57"	"0.69"	"C3489725"	"Pseudo-TORCH syndrome"	"disease"	"C10;C16;C20"	"Disease or Syndrome"	"0.73"	"1"	"2010"	"2016"	"1"	"5"	"CTD_human;ORPHANET;UNIPROT"
"100506658"	"OCLN"	"0.57"	"0.69"	"C3714756"	"Intellectual Disability"	"group"	"C10;C23;F01;F03"	"Mental or Behavioral Dysfunction"	"0.30"		"2010"	"2010"	"1"	"0"	"GENOMICS_ENGLAND"
"100506742"	"CASP12"	"0.633"	"0.69"	"C0011854"	"Diabetes Mellitus, Insulin-Dependent"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.51"	"1"	"2005"	"2016"	"1"	"0"	"CTD_human"
"100506742"	"CASP12"	"0.633"	"0.69"	"C0023893"	"Liver Cirrhosis, Experimental"	"disease"	"C06"	"Experimental Model of Disease"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100506742"	"CASP12"	"0.633"	"0.69"	"C0027055"	"Myocardial Reperfusion Injury"	"phenotype"	"C14;C23"	"Pathologic Function"	"0.30"		"2004"	"2004"	"1"	"0"	"CTD_human"
"100506742"	"CASP12"	"0.633"	"0.69"	"C0205734"	"Diabetes, Autoimmune"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100506742"	"CASP12"	"0.633"	"0.69"	"C0342302"	"Brittle diabetes"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100506742"	"CASP12"	"0.633"	"0.69"	"C3837958"	"Diabetes Mellitus, Ketosis-Prone"	"disease"	"C18;C19;C20"	"Disease or Syndrome"	"0.30"		"2013"	"2013"	"1"	"0"	"CTD_human"
"100506965"	"PWAR6"	"1"	"0.069"	"C0345967"	"Malignant mesothelioma"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2015"	"2015"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0007102"	"Malignant tumor of colon"	"disease"	"C04;C06"	"Neoplastic Process"	"0.36"	"1"	"2012"	"2017"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0009375"	"Colonic Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0016978"	"gallbladder neoplasm"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0024121"	"Lung Neoplasms"	"group"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0024623"	"Malignant neoplasm of stomach"	"disease"	"C04;C06"	"Neoplastic Process"	"0.33"	"1"	"2015"	"2017"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0030297"	"Pancreatic Neoplasm"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0038356"	"Stomach Neoplasms"	"group"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0153452"	"Malignant neoplasm of gallbladder"	"disease"	"C04;C06"	"Neoplastic Process"	"0.31"	"1"	"2015"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0242379"	"Malignant neoplasm of lung"	"disease"	"C04;C08"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C0346647"	"Malignant neoplasm of pancreas"	"disease"	"C04;C06;C19"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507056"	"CCAT1"	"0.63"	"0.379"	"C1708349"	"Hereditary Diffuse Gastric Cancer"	"disease"	"C04;C06"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100507436"	"MICA"	"0.499"	"0.759"	"C0010051"	"Coronary Aneurysm"	"disease"	"C14"	"Disease or Syndrome"	"0.30"		"2000"	"2000"	"1"	"0"	"CTD_human"
"100507436"	"MICA"	"0.499"	"0.759"	"C0029172"	"Oral Submucous Fibrosis"	"disease"	"C07"	"Disease or Syndrome"	"0.31"	"1"	"2004"	"2007"	"1"	"0"	"CTD_human"
"100507436"	"MICA"	"0.499"	"0.759"	"C2239176"	"Liver carcinoma"	"disease"	"C04;C06"	"Neoplastic Process"	"0.40"	"1"	"1997"	"2017"	"1"	"1"	"CTD_human"
"100507436"	"MICA"	"0.499"	"0.759"	"C4302111"	"Familial Ménière disease"	"disease"		"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"GENOMICS_ENGLAND"
"100529207"	"RAD51L3-RFFL"	"1"	"0.172"	"C0006826"	"Malignant Neoplasms"	"group"	"C04"	"Neoplastic Process"	"0.30"				"0"	"0"	"CGI"
"100533642"	"FNBP1P1"	"1"	"0.034"	"C0003165"	"Anthracosis"	"disease"	"C08"	"Disease or Syndrome"	"0.30"		"2018"	"2018"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616127"	"MIR4448"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616135"	"MIR4507"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616247"	"MIR151B"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616258"	"MIR4516"	"0.799"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616259"	"MIR378I"	"0.799"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616323"	"MIR4482"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616357"	"MIR3591"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616376"	"MIR4492"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616437"	"MIR1343"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100616452"	"MIR2682"	"0.928"	"0.034"	"C0005586"	"Bipolar Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"0"	"PSYGENET"
"100616452"	"MIR2682"	"0.928"	"0.034"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2015"	"2015"	"1"	"1"	"PSYGENET"
"100616496"	"ERVW-4"	"0.676"	"0.517"	"C0036337"	"Schizoaffective Disorder"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.31"	"1"	"2001"	"2001"	"1"	"0"	"PSYGENET"
"100616496"	"ERVW-4"	"0.676"	"0.517"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.32"	"1"	"2001"	"2006"	"2"	"0"	"PSYGENET"
"100653368"	"SCA32"	"0.834"	"0.138"	"C3151343"	"SPINOCEREBELLAR ATAXIA 32"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"100750225"	"PCAT1"	"0.652"	"0.448"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.30"		"2016"	"2016"	"1"	"0"	"CTD_human"
"100750225"	"PCAT1"	"0.652"	"0.448"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.40"	"1"	"2005"	"2018"	"1"	"0"	"CTD_human"
"100775105"	"ERVK-18"	"0.594"	"0.69"	"C0036341"	"Schizophrenia"	"disease"	"F03"	"Mental or Behavioral Dysfunction"	"0.03"	"1"	"2009"	"2012"	"1"	"0"	"PSYGENET"
"100820829"	"MYZAP"	"0.886"	"0.103"	"C0087031"	"Juvenile-Onset Still Disease"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100820829"	"MYZAP"	"0.886"	"0.103"	"C3495559"	"Juvenile arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100820829"	"MYZAP"	"0.886"	"0.103"	"C3714758"	"Juvenile psoriatic arthritis"	"disease"	"C05;C17;C20"	"Disease or Syndrome"	"0.30"		"2009"	"2009"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847054"	"MIR5588"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100847070"	"MIR5196"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"100885773"	"DYT21"	"0.928"	"0.069"	"C3281236"	"DYSTONIA 21"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"101101692"	"HELLPAR"	"1"	"0.034"	"C0162739"	"HELLP Syndrome"	"disease"	"C13"	"Disease or Syndrome"	"0.31"	"1"	"2016"	"2016"	"0"	"0"	"ORPHANET"
"101180907"	"USH1K"	"1"	"0.172"	"C1568247"	"Usher Syndrome, Type I"	"disease"		"Disease or Syndrome"	"0.31"	"1"	"2013"	"2013"	"0"	"0"	"ORPHANET"
"101669767"	"SCHLAP1"	"0.928"	"0.069"	"C0027627"	"Neoplasm Metastasis"	"phenotype"	"C04;C23"	"Neoplastic Process"	"0.32"	"1"	"2014"	"2015"	"1"	"0"	"CTD_human"
"101669767"	"SCHLAP1"	"0.928"	"0.069"	"C0033578"	"Prostatic Neoplasms"	"group"	"C04;C12"	"Neoplastic Process"	"0.31"	"1"	"2014"	"2014"	"1"	"0"	"CTD_human"
"101669767"	"SCHLAP1"	"0.928"	"0.069"	"C0376358"	"Malignant neoplasm of prostate"	"disease"	"C04;C12"	"Neoplastic Process"	"0.34"	"1"	"2014"	"2018"	"1"	"0"	"CTD_human"
"101926885"	"OCA5"	"1"	"0.138"	"C0078917"	"Albinism, Ocular"	"disease"	"C11;C16;C17;C18"	"Congenital Abnormality"	"0.30"		"2013"	"2017"	"2"	"0"	"GENOMICS_ENGLAND"
"101928376"	"IL12A-AS1"	"0.69"	"0.448"	"C0004943"	"Behcet Syndrome"	"disease"	"C07;C11;C14;C16;C17"	"Disease or Syndrome"	"0.41"	"1"	"2013"	"2016"	"0"	"1"	"ORPHANET"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465489"	"MIR6815"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465513"	"MIR6852"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465530"	"MIR6881"	"1"	"0.069"	"C0019163"	"Hepatitis B"	"disease"	"C02;C06"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465802"	"MIR7704"	"0.799"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465833"	"MIR4433B"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102465858"	"MIR7977"	"0.799"	"0.103"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466247"	"MIR1273H"	"0.815"	"0.069"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466251"	"MIR8061"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C0019193"	"Hepatitis, Toxic"	"disease"	"C06;C25"	"Injury or Poisoning"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C0860207"	"Drug-Induced Liver Disease"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C1262760"	"Hepatitis, Drug-Induced"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C3658290"	"Drug-Induced Acute Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C4277682"	"Chemical and Drug Induced Liver Injury"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466270"	"MIR6741"	"0.799"	"0.138"	"C4279912"	"Chemically-Induced Liver Toxicity"	"disease"	"C06;C25"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"102466739"	"MIR6803"	"1"	"0.069"	"C0011860"	"Diabetes Mellitus, Non-Insulin-Dependent"	"disease"	"C18;C19"	"Disease or Syndrome"	"0.30"		"2017"	"2017"	"1"	"0"	"CTD_human"
"103753527"	"SCA37"	"1"		"C3889636"	"SPINOCEREBELLAR ATAXIA 37"	"disease"		"Disease or Syndrome"	"0.30"				"0"	"0"	"ORPHANET"
"105259599"	"H19-ICR"	"0.672"	"0.483"	"C0004903"	"Beckwith-Wiedemann Syndrome"	"disease"	"C16"	"Disease or Syndrome"	"0.31"	"1"	"2014"	"2014"	"0"	"0"	"CTD_human"
"107305681"	"DHS6S1"	"1"	"0.069"	"C0730294"	"North Carolina macular dystrophy"	"disease"	"C11;C16"	"Disease or Syndrome"	"0.50"				"0"	"0"	"CTD_human;ORPHANET"
"109580095"	"HBB-LCR"	"0.815"	"0.069"	"C0002875"	"Cooley's anemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"109580095"	"HBB-LCR"	"0.815"	"0.069"	"C0005283"	"beta Thalassemia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"109580095"	"HBB-LCR"	"0.815"	"0.069"	"C0019025"	"Hemoglobin F Disease"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"109580095"	"HBB-LCR"	"0.815"	"0.069"	"C0085578"	"Thalassemia Minor"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"
"109580095"	"HBB-LCR"	"0.815"	"0.069"	"C0271979"	"Thalassemia Intermedia"	"disease"	"C15;C16"	"Disease or Syndrome"	"0.30"				"0"	"0"	"CTD_human"